<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">PP</journal-id><journal-title-group><journal-title>Pharmacology &amp; Pharmacy</journal-title></journal-title-group><issn pub-type="epub">2157-9423</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/pp.2019.105021</article-id><article-id pub-id-type="publisher-id">PP-92449</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Chemistry&amp;Materials Science</subject><subject> Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Isolated Endophytic Fungi from the Plant &lt;i&gt;Curcuma longa&lt;/i&gt; and Their Potential Bioactivity—A Review
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Kazi</surname><given-names>Jannatul Ferdous</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Farhana</surname><given-names>Afroz</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Md.</surname><given-names>Rakibul Islam</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Md.</surname><given-names>Abdul Mazid</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Md.</surname><given-names>Hossain Sohrab</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff3"><addr-line>Department of Pharmaceutical Chemistry, University of Dhaka, Dhaka, Bangladesh</addr-line></aff><aff id="aff2"><addr-line>Pharmaceutical Sciences Research Division, Bangladesh Council of Scientific and Industrial Research, Dhaka, Bangladesh</addr-line></aff><aff id="aff1"><addr-line>Department of Biochemistry and Molecular Biology, University of Dhaka, Dhaka, Bangladesh</addr-line></aff><pub-date pub-type="epub"><day>14</day><month>05</month><year>2019</year></pub-date><volume>10</volume><issue>05</issue><fpage>244</fpage><lpage>270</lpage><history><date date-type="received"><day>9,</day>	<month>April</month>	<year>2019</year></date><date date-type="rev-recd"><day>14,</day>	<month>May</month>	<year>2019</year>	</date><date date-type="accepted"><day>17,</day>	<month>May</month>	<year>2019</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
   
   Endophytes (both fungi and bacteria) represent a treasure house for bioactive compounds such as anticancer, immunomodulatory, antioxidant, antiparasitic, insecticidal etc. for use in the pharmaceutical and agrochemical industries. Endophytic population is greatly influenced by climatic conditions and location where the host plant grows. Curcuma longa L
   .
    (Turmeric) is a medicinal plant belonging to the Zingiberaceae family 
   that 
   is usually used as spice and preservative. Traditionally it is used to treat various conditions and symptoms such as digestive disorders, arthritis, cardiovascular conditions, cancer, bacterial infections etc. In recent times, there have been different discoveries on endophytic fungi and their biological activity from C. longa. But there is no comprehensive review on endophytic fungi of C. longa. The aim of this review is to analyze the published report based on the endophytic fungi to provide for the first time an updated information about their isolation from different tissues, their biological activities including the phytochemistry of C. longa. This will lead the way to forecast the missing link for future research work. 
  
 
</p></abstract><kwd-group><kwd>&lt;i&gt;Curcuma longa&lt;/i&gt;</kwd><kwd> Endophytes</kwd><kwd> Compounds</kwd><kwd> Bioactivity</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Curcuma longa L. (Turmeric) is a rhizomatous herbaceous perennial plant of the ginger family, Zingiberaceae [<xref ref-type="bibr" rid="scirp.92449-ref1">1</xref>] . It is a naturally grown plant in the Indian subcontinent and Southeast Asia. Turmeric has been used in Asia for thousands of years and is a major part of Ayurveda, Siddha medicine, Unani, and traditional Chinese medicine [<xref ref-type="bibr" rid="scirp.92449-ref2">2</xref>] . A lot of scientific works on pharmacological properties of turmeric have been reported by many scientists and researchers such as anti-inflammatory [<xref ref-type="bibr" rid="scirp.92449-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref4">4</xref>] , antiallergic [<xref ref-type="bibr" rid="scirp.92449-ref5">5</xref>] , antiobesity [<xref ref-type="bibr" rid="scirp.92449-ref6">6</xref>] , lipid-lowering [<xref ref-type="bibr" rid="scirp.92449-ref7">7</xref>] , antiproliferative [<xref ref-type="bibr" rid="scirp.92449-ref8">8</xref>] , anti-microbial [<xref ref-type="bibr" rid="scirp.92449-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref10">10</xref>] , anti-oxidant [<xref ref-type="bibr" rid="scirp.92449-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref12">12</xref>] , anti-diabetic [<xref ref-type="bibr" rid="scirp.92449-ref13">13</xref>] , hypoglycemic [<xref ref-type="bibr" rid="scirp.92449-ref14">14</xref>] , immunomodulating [<xref ref-type="bibr" rid="scirp.92449-ref15">15</xref>] , insecticidal [<xref ref-type="bibr" rid="scirp.92449-ref16">16</xref>] , anti-fungal [<xref ref-type="bibr" rid="scirp.92449-ref17">17</xref>] , neuroprotective [<xref ref-type="bibr" rid="scirp.92449-ref18">18</xref>] , anti-mutagenic [<xref ref-type="bibr" rid="scirp.92449-ref19">19</xref>] , hypolipidemic [<xref ref-type="bibr" rid="scirp.92449-ref20">20</xref>] etc.</p><p>Endophyte, the most important integral part of plant tissues, is a progressively significant area of research in many fields because of their chemical miscellany and their ability to produce many unique secondary metabolites that can be utilized for fuel, medicine, restoration and agriculture. Endophytes are isolated from medicinal plants possess strong fungicidal, bactericidal and cytotoxic metabolites [<xref ref-type="bibr" rid="scirp.92449-ref21">21</xref>] . Previous studies indicate that there have been few investigations done on endophytic microbes of turmeric plant (Curcuma longa). Thus, exploring endophytic microbes from Curcuma longa increases the probability to discover novel compound which is extensive in resistance tissues. There is no review on the endophytic fungi from turmeric plants. Therefore, it is necessary to review the endophytic fungi from Curcuma longa. Hence, this review discusses the current research progresses on endophytic fungi from the turmeric plant, including types of endophytic fungi identified, described bioactive compounds, and biological activities of endophytes to discover the current scope of knowledge of endophytes.</p></sec><sec id="s2"><title>2. Isolated Compounds from Curcuma longa</title><p>A total of 235 compounds with various activities were isolated and identified from the flowers, leaves, roots and rhizomes part of Curcuma longa which is the most phytochemically investigated plant in the world. These compounds are primarily phenolic and terpenoid compounds including diarylheptanoids (including commonly known as curcuminoids), diarylpentanoids, monoterpenes, sesquiterpenes, diterpenes, triterpenes, sterols, fatty acids and also some alkaloidal compounds. A list of isolated compounds from different groups of C. longa is presented in <xref ref-type="table" rid="table1">Table 1</xref>. Curcumin is the key phytochemical compound</p><table-wrap-group id="1"><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Isolated compounds from C. longa</title></caption><table-wrap id="1_1"><table><tbody><thead><tr><th align="center" valign="middle" >Sl.No</th><th align="center" valign="middle" >Compounds</th><th align="center" valign="middle" >Compound type</th><th align="center" valign="middle" >References</th></tr></thead><tr><td align="center" valign="middle" >1</td><td align="center" valign="middle" >curcumin (curcumin I),</td><td align="center" valign="middle" >Diarylheptanoid</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref24">24</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref28">28</xref>] - [<xref ref-type="bibr" rid="scirp.92449-ref35">35</xref>]</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >demethoxycurcumin (curcumin II),</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >1-(4-hydroxy-3-methoxyphenyl)-7-(3,4- dihydroxyphenyl)-1,6-heptadiene-3,5-dione,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >1-(4-hydroxyphenyl)-7-(3,4-dihydroxyphenyl)- 1,6-heptadiene-3, 5-dione,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap><table-wrap id="1_2"><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >bisdemethoxycurcumin (curcumin III),</th><th align="center" valign="middle" ></th><th align="center" valign="middle" ></th></tr></thead><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >tetrahydroxycurcumin,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >5-hydroxyl-1-(4-hydroxy-3-methoxyphenyl)-7- (4-hydroxyphenyl)-4,6-heptadiene-3-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >5-hydroxyl-1,7-bis(4-hydroxy-3-methoxyphenyl)- 4,6-heptadiene-3-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >1,7-bis(4-hydroxyphenyl)-1-heptene-3,5-dione,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >5-hydroxyl-7-(4-hydroxy-3-methoxyphenyl)-1- (4-hydroxyphenyl)-4,6-heptadiene-3-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >3-hydroxy-1,7-bis-(4-hydroxyphenyl)-6- heptene-1,5-dione,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >1,5-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)- 7-(4-hydroxyphenyl)-4,6-heptadiene-3-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >1,5-dihydroxy-1-(4-hydroxyphenyl)-7-(4-hydroxy- 3-methoxyphenyl)-4,6-heptadiene-3-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >1,5-dihydroxy-1,7-bis(4-hydroxy-3-methoxyphenyl)-4,6-heptadiene-3-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >1,5-dihydroxy-1,7-bis(4-hydroxyphenyl)- 4,6-heptadiene-3-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >1,5-epoxy-3-carbonyl-1,7-bis(4-hydroxyphenyl)- 4,6-heptadiene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Cyclocurcumin,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >1,7-bis(4-hydroxy-3-methoxyphenyl)-1,4,6- heptatrien-3-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >1,7-bis-(4-hydroxyphenyl)-1,4,6-heptatrien-3-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >1,5-bis(4-hydroxyphenyl)-penta-(1E,4E)- 1,4-dien-3-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >1-(4-hydroxy-3-methoxyphenyl)-5-(4-hydroxyphenyl)-1,4-pentadiene-3-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >1,5-bis(4-hydroxy-3-methoxyphenyl)-penta- (1E,4E)-1,4-dien-3-one</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >2</td><td align="center" valign="middle" >4&quot;-(4&quot;'-hydroxyphenyl)-2&quot;-oxo-3&quot;-butenyl-3- (4'-hydroxyphenyl-3'-methoxy)-propenoate,</td><td align="center" valign="middle" >Phenylpropene</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref28">28</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref35">35</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref36">36</xref>]</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >4&quot;-(4&quot;'-hydroxyphenyl-3-methoxy)-2&quot;-oxo-3&quot;- butenyl-3-(4'-hydroxyphenyl)-propenoate,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >calebin-A,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >(E)-4-(4-hydroxy-3-methoxyphenyl)but-3-en-2-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >(E)-ferulic acid,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >(Z)-ferulic acid</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >3</td><td align="center" valign="middle" >vanillic acid,</td><td align="center" valign="middle" >Phenolic</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref35">35</xref>]</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >vanillin</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >4</td><td align="center" valign="middle" >p-cymene,</td><td align="center" valign="middle" >Monoterpenoid</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref27">27</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>] - [<xref ref-type="bibr" rid="scirp.92449-ref44">44</xref>]</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >m-cymene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >α-terpinene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap><table-wrap id="1_3"><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >γ-terpinene,</th><th align="center" valign="middle" ></th><th align="center" valign="middle" ></th></tr></thead><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >β-phellandrene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >p-mentha-1,4(8)-diene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >terpinen-4-ol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >4-terpinol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Limonene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Terpinolene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Thymol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Phellandrol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Carvacrol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >(E)-carveol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >γ-terpineol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Menthol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >1,3,8-paramenthatriene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >p-methylacetophenone,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Piperitone,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >o-cymene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Carvone,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >p-menth-8-en-2-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >α-thujene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >α-terpineol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >p-cymen-8-ol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >p-meth-8-en-2-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >piperitone epoxide,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Sylvestrene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Menthofuran,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >β, β-dimethylstyrene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Camphor,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Teresantalol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >Benzene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >1-methyl-4-(1-methylpropyl),</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >2-norpinanone,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >borneol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >bornyl acetate,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >(E)-chrysanthenyl acetate,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >(Z)-cinerone,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >(Z)-sabinol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap><table-wrap id="1_4"><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >2-(2,5-dihydroxy-4-methylcyclohex-3-enyl) propanoic acid,</th><th align="center" valign="middle" ></th><th align="center" valign="middle" ></th></tr></thead><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >camphene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >3-carene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >2-carene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >ascaridole,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >α-pinene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >β-pinene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >cineole,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >cis-ocimene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >citronellal,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >geranial,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >neral,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >myrcene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >R-citronellene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >citronellylpentanoate,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >nerol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >geraniol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >iso-artemisia ketone,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >trans-ocimene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >linalool,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >neryl acetate,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >geranic acid,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >geranyl acetate,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >3-bornanone,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >4,8-dimethyl-3,7-nonadien-2-ol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >3,4,5,6-tetramethyl-2,5-octadiene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >3,7-dimethyl-6-nonenal,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >2,6-dimethyl-2,6-octadiene-1,8-diol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >4,5-dimethyl-2,6-octadiene</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >5</td><td align="center" valign="middle" >ar-turmerone,</td><td align="center" valign="middle" >Bisabolane</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref25">25</xref>]</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >α-turmerone,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref26">26</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref35">35</xref>] - [<xref ref-type="bibr" rid="scirp.92449-ref52">52</xref>]</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >β-turmerone,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >2-methyl-6-(4-hydroxyphenyl)-2-hepten-4-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >2-methyl-6-(4-hydroxy-3-methylphenyl)-2- hepten-4-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >2-methoxy-5-hydroxybisabola-3,10-diene-9-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap><table-wrap id="1_5"><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >2-methyl-6-(4-formylphenyl)-2-hepten-4-one,</th><th align="center" valign="middle" ></th><th align="center" valign="middle" ></th></tr></thead><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >5-hydroxyl-ar-turmerone,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >4-methylene-5-hydroxybisabola-2,10-diene-9-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >ar-curcumene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >ar-turmerol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >bisabola-3,10-diene-2-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >bisabolone,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >4, 5-dihydroxybisabola-2,10-diene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >4-hydroxybisabola-2,10-diene-9-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >4-methoxy-5-hydroxy-bisabola-2,10-diene-9-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >bisacurone,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >bisacurone A,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >bisacurone B,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >bisacurone C,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >bisabolone-9-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >bisacumol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >turmeronol A,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >turmeronol B,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >α-oxobisabolene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >α-zingiberene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >xanthorrhizol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >zingerone,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >dehydrozingerone,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >(Z)-α-atlantone,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >(E)-α-atlantone,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >β-bisabolene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >(6S,7R)-bisabolene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >γ-bisabolene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >γ-curcumene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >β-curcumene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >α-curcumene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >β-sesquiphellandrene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >(Z)-γ-atlantone,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >(E)-γ-atlantone,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >(6S)-2-methyl-6-[(1R,5S)-(4-methene-5- hydroxyl-2-cyclohexen)-2-hepten-4-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >curcuphenol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >curlone,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap><table-wrap id="1_6"><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >curculonone C,</th><th align="center" valign="middle" ></th><th align="center" valign="middle" ></th></tr></thead><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >curculonone D,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >curculonone B,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >curculonone A, 2, 5-dihydroxybisabola-3, 10-diene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >(6R)-[(1R)-1,5-dimethylhex-4-enyl]-3- methylcyclohex-2-en-1-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >β-atlantone,2,8-epoxy-5-hydroxybisabola- 3,10-diene-9-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >α-bisabolol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >dihydro-ar-turmerone,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >dehydrocurcumene</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >6</td><td align="center" valign="middle" >(4S,5S)-germacrone-4,5-epoxide,</td><td align="center" valign="middle" >Germacrane</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref39">39</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref40">40</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref49">49</xref>]</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >dehydrocurdione,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >germacrene D,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >germacrone,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >germacrone-13-al,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >β-germacene</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >7</td><td align="center" valign="middle" >1,10-dehydro-10-deoxy-9-oxozedoarondiol,</td><td align="center" valign="middle" >Guaiane</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref35">35</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref49">49</xref>]</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >curcumenol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >epiprocurcumenol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >isoprocurcumenol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >zedoaronediol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >procurcumadiol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >procurcumenol</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >8</td><td align="center" valign="middle" >naphthalene,1,2,3,4,4a,5,6,8a-octahydro-4a,8- dimethyl-2-(1-methylethylidene),</td><td align="center" valign="middle" >Selinane</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref41">41</xref>]</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >α-selinene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >juniper camphor,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >corymbolone</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >9</td><td align="center" valign="middle" >α-santalol,</td><td align="center" valign="middle" >Santalane</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >α-santalene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >β-santalene</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >10</td><td align="center" valign="middle" >(E)-caryophyllene,</td><td align="center" valign="middle" >Caryophyllane</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref43">43</xref>]</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >caryophyllene oxide</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >11</td><td align="center" valign="middle" >β-elemene,</td><td align="center" valign="middle" >Elemane</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref41">41</xref>]</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >γ-elemene</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >12</td><td align="center" valign="middle" >acoradiene</td><td align="center" valign="middle" >Acorane</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" >13</td><td align="center" valign="middle" >aristolene</td><td align="center" valign="middle" >Aristolene</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" >14</td><td align="center" valign="middle" >(Z)-α-bergamotene</td><td align="center" valign="middle" >Bergamotane</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref43">43</xref>]</td></tr></tbody></table></table-wrap><table-wrap id="1_7"><table><tbody><thead><tr><th align="center" valign="middle" >15</th><th align="center" valign="middle" >curcumenone</th><th align="center" valign="middle" >Carabrane</th><th align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref49">49</xref>]</th></tr></thead><tr><td align="center" valign="middle" >16</td><td align="center" valign="middle" >di-epi-cedrene</td><td align="center" valign="middle" >Cedrane</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" >17</td><td align="center" valign="middle" >himachalene</td><td align="center" valign="middle" >Himachalene</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" >18</td><td align="center" valign="middle" >(E)-sesquisabinene hydrate</td><td align="center" valign="middle" >Sesquisabinane</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref43">43</xref>]</td></tr><tr><td align="center" valign="middle" >19</td><td align="center" valign="middle" >bicyclo [7.2.0] undecane,10,10-dimethyl-2,6-bis(methylene),</td><td align="center" valign="middle" >Sesquiterpene</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref35">35</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref37">37</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref39">39</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref40">40</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref41">41</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref43">43</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref51">51</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref53">53</xref>]</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >10,10-dimethyl-2,6-bis(methylene),</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >γ-gurjunen epoxide,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >1-epi-cubenol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >cubebene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >7-epi-sesquithujene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >caryophyllene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >6α-hydroxycurcumanolide A,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >curcumanolide A,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >curcumanolide B,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >curcumin L,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >α-humulene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >12-oxabicyclo [9.1.0]dodeca-3,7-diene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >1,5,5,8-tetramethyl,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >adoxal,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >2,6,10-dodecatrien-1-ol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >3,7,11-trimethyl,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >(E,E)-α-farnesene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >5,9-undecadien-2-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >6,10-dimethyl-, (Z),</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >hxadecane-1,2-diol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >nerolidal,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >(Z)-β-farnesene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >nerolidyl propionate</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >20</td><td align="center" valign="middle" >Phytol,</td><td align="center" valign="middle" >Diterpenoid</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref41">41</xref>]</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >(E,E,E)-3,7,11,15-tetramethylhexadeca- 1,3,6,10,14-pentaene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >2,6,11,15-tetramethyl-hexadeca-2,6,8,10,14-pentaene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >1,6,10,14-hexadecatetraen-3-ol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >3,7,11,15-tetramethyl-,(E,E)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >21</td><td align="center" valign="middle" >hopenone I,</td><td align="center" valign="middle" >Triterpenoid</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref54">54</xref>]</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >hop-17(21)-en-3β-ol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >hop-17(21)-en-3β-yl acetate</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap><table-wrap id="1_8"><table><tbody><thead><tr><th align="center" valign="middle" >22</th><th align="center" valign="middle" >β-sitosterol,</th><th align="center" valign="middle" >Steroid</th><th align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref35">35</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</th></tr></thead><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >stigmasterol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >gitoxigenin,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >20-oxopregn-16-en-12-yl acetate</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >23</td><td align="center" valign="middle" >linoleic acid,</td><td align="center" valign="middle" >Fatty acid</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref41">41</xref>]</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >8,11-Octadecadienoic acid,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >methyl ester,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >palmitic acid (n-hexadecanoic acid),</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >oleic acid,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >stearic acid</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >24</td><td align="center" valign="middle" >curcuma-J,</td><td align="center" valign="middle" >Miscellaneous</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref50">50</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref55">55</xref>]</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >2-(2'-methyl-1'-propenyl)-4,6- dimethyl-7-hydroxyquinoline,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >2,3,5-trimethylfuran,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >(1,2,3-trimethyl-cyclopent-2-enyl)-methanol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >dicumyl peroxide,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >1-(3-cyclopentylpropyl)-2,4-dimethy-benzene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >1,4-dimethyl-2-(2-methylpropyl)-benzene,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >2,2'-oxybis [octahydro-7,8,8-trimethyl- 4,7-methanobenzofuran,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >cyclohexylformate,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >methyleugenol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >3,3,5-trimethyl-cyclohexanol acetate,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >2,4-dimethyl-8-oxabicyclo [3.2.1]oct-6-en-3-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >2,6-dimethyl-6-(4-methyl-3-pentenyl)-2- cyclohexene-1-carboxaldehyde,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >bicyclo [3.3.1]nonan-9-one,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >2,4-dimethyl-3-nitro-(exo),</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >2,2,4-trimethyl-3-(3,8,12,16-tetramethyl-heptadeca- 3,7,11,15-tetraenyl)-cyclohexanol,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >pyrazolo [1,5-a]pyridine,</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >3,3a,4,7-tetrahydro-3,3-dimethyl-, (3aS)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap></table-wrap-group><p>responsible for many of turmeric’s eccentric properties and bright yellow colouring. Curcumin has been shown to reveal antioxidant, anti-inflammatory, antiviral, antibacterial, antifungal, and anticancer activities and thus, has a potential against various malignant diseases, diabetes, allergies, arthritis, Alzheimer’s disease, and other chronic illnesses [<xref ref-type="bibr" rid="scirp.92449-ref22">22</xref>] . Ar-turmerone and curlone have antimutagenic activity [<xref ref-type="bibr" rid="scirp.92449-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref23">23</xref>] whereas sodium curcuminate has anti-inflammatory activity [<xref ref-type="bibr" rid="scirp.92449-ref2">2</xref>] . The structures of some bioactive compounds from C. longa are given in <xref ref-type="table" rid="table2">Table 2</xref>.</p><table-wrap-group id="2"><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Structures of some bioactive compounds from C. longa</title></caption><table-wrap id="2_1"><table><tbody><thead><tr><th align="center" valign="middle" >Compound type</th><th align="center" valign="middle" >References</th></tr></thead><tr><td align="center" valign="middle" >Diarylheptanoid</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.92449-ref28">28</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref29">29</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x2.png" xlink:type="simple"/></inline-formula> curcumin Ι</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x3.png" xlink:type="simple"/></inline-formula> curcumin ΙΙ</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref28">28</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref29">29</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x4.png" xlink:type="simple"/></inline-formula> curcumin ΙΙΙ</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref28">28</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x5.png" xlink:type="simple"/></inline-formula> tetrahydroxycurcumin</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref28">28</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x6.png" xlink:type="simple"/></inline-formula> 1,7-bis(4-hydroxyphenyl)-1-heptene-3,5-dione</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref31">31</xref>]</td></tr><tr><td align="center" valign="middle" >Phenylpropene</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.92449-ref36">36</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x7.png" xlink:type="simple"/></inline-formula> 4&quot;-(4&quot;'-hydroxyphenyl)-2&quot;-oxo-3&quot;-butenyl-3- (4'-hydroxyphenyl-3'-methoxy)-propenoate</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x8.png" xlink:type="simple"/></inline-formula> 4&quot;-(4&quot;'-hydroxyphenyl-3-methoxy)-2&quot;-oxo-3&quot;- butenyl-3-(4'-hydroxyphenyl)-propenoate</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref36">36</xref>]</td></tr></tbody></table></table-wrap><table-wrap id="2_2"><table><tbody><thead><tr><th align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x9.png" xlink:type="simple"/></inline-formula> calebin-A</th><th align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref28">28</xref>]</th></tr></thead><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x10.png" xlink:type="simple"/></inline-formula> (E)-4-(4-hydroxy-3-methoxyphenyl)but-3-en-2-one</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref35">35</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x11.png" xlink:type="simple"/></inline-formula> (E)-ferulic acid</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref35">35</xref>]</td></tr><tr><td align="center" valign="middle" >Phenolic</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.92449-ref35">35</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x12.png" xlink:type="simple"/></inline-formula> vanillic acid</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x13.png" xlink:type="simple"/></inline-formula> vanillin</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref35">35</xref>]</td></tr><tr><td align="center" valign="middle" >Monoterpenoid</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.92449-ref40">40</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x14.png" xlink:type="simple"/></inline-formula> thymol</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x15.png" xlink:type="simple"/></inline-formula> menthol</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr></tbody></table></table-wrap><table-wrap id="2_3"><table><tbody><thead><tr><th align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x16.png" xlink:type="simple"/></inline-formula> piperitone</th><th align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</th></tr></thead><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x17.png" xlink:type="simple"/></inline-formula> geraniol</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x18.png" xlink:type="simple"/></inline-formula> geranic acid</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" >Bisabolane</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.92449-ref25">25</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref47">47</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x19.png" xlink:type="simple"/></inline-formula> ar-turmerone</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x20.png" xlink:type="simple"/></inline-formula> zingerone</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref34">34</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x21.png" xlink:type="simple"/></inline-formula> curlone</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref35">35</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x22.png" xlink:type="simple"/></inline-formula> 2,5-dihydroxybisabola-3,10-diene</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref34">34</xref>]</td></tr></tbody></table></table-wrap><table-wrap id="2_4"><table><tbody><thead><tr><th align="center" valign="middle" >Germacrane</th><th align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.92449-ref49">49</xref>]</th></tr></thead><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x23.png" xlink:type="simple"/></inline-formula> (4S,5S)-germacrone-4,5-epoxide</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x24.png" xlink:type="simple"/></inline-formula> dehydrocurdione</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref49">49</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x25.png" xlink:type="simple"/></inline-formula> germacrene D</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref39">39</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x26.png" xlink:type="simple"/></inline-formula> germacrone</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref49">49</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x27.png" xlink:type="simple"/></inline-formula> germacrone-13-al</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref49">49</xref>]</td></tr><tr><td align="center" valign="middle" >Guaiane</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.92449-ref49">49</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x28.png" xlink:type="simple"/></inline-formula> epiprocurcumenol</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x29.png" xlink:type="simple"/></inline-formula> isoprocurcumenol</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref49">49</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x30.png" xlink:type="simple"/></inline-formula> zedoaronediol</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref49">49</xref>]</td></tr></tbody></table></table-wrap><table-wrap id="2_5"><table><tbody><thead><tr><th align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x31.png" xlink:type="simple"/></inline-formula> procurcumadiol</th><th align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref49">49</xref>]</th></tr></thead><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x32.png" xlink:type="simple"/></inline-formula> procurcumenol</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref49">49</xref>]</td></tr><tr><td align="center" valign="middle" >Selinane</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x33.png" xlink:type="simple"/></inline-formula> naphthalene,1,2,3,4,4a,5,6,8a-octahydro-4a,8- dimethyl-2-(1-methylethylidene)</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x34.png" xlink:type="simple"/></inline-formula> α-selinene</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x35.png" xlink:type="simple"/></inline-formula> juniper camphor</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x36.png" xlink:type="simple"/></inline-formula> corymbolone</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" >Santalane</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x37.png" xlink:type="simple"/></inline-formula> α-santalol</td></tr></tbody></table></table-wrap><table-wrap id="2_6"><table><tbody><thead><tr><th align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x38.png" xlink:type="simple"/></inline-formula> α-santalene</th><th align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</th></tr></thead><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x39.png" xlink:type="simple"/></inline-formula> β-santalene</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" >Caryophyllane</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.92449-ref43">43</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x40.png" xlink:type="simple"/></inline-formula> (E)-caryophyllene</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x41.png" xlink:type="simple"/></inline-formula> caryophyllene oxide</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" >Elemane</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.92449-ref41">41</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x42.png" xlink:type="simple"/></inline-formula> β-elemene</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x43.png" xlink:type="simple"/></inline-formula> γ-elemene</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" >Acorane</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x44.png" xlink:type="simple"/></inline-formula> acoradiene</td></tr></tbody></table></table-wrap><table-wrap id="2_7"><table><tbody><thead><tr><th align="center" valign="middle" >Aristolene</th><th align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</th></tr></thead><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x45.png" xlink:type="simple"/></inline-formula> aristolene</td></tr><tr><td align="center" valign="middle" >Bergamotane</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.92449-ref43">43</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x46.png" xlink:type="simple"/></inline-formula> (Z)-α-bergamotene</td></tr><tr><td align="center" valign="middle" >Carabrane</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.92449-ref49">49</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x47.png" xlink:type="simple"/></inline-formula> curcumenone</td></tr><tr><td align="center" valign="middle" >Cedrane</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x48.png" xlink:type="simple"/></inline-formula> di-epi-cedrene</td></tr><tr><td align="center" valign="middle" >Himachalene</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x49.png" xlink:type="simple"/></inline-formula> himachalene</td></tr><tr><td align="center" valign="middle" >Sesquisabinane</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.92449-ref43">43</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x50.png" xlink:type="simple"/></inline-formula> (E)-sesquisabinene hydrate</td></tr><tr><td align="center" valign="middle" >Sesquiterpene</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.92449-ref43">43</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x51.png" xlink:type="simple"/></inline-formula> 7-epi-sesquithujene</td></tr></tbody></table></table-wrap><table-wrap id="2_8"><table><tbody><thead><tr><th align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x52.png" xlink:type="simple"/></inline-formula> caryophyllene</th><th align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref39">39</xref>]</th></tr></thead><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x53.png" xlink:type="simple"/></inline-formula> adoxal</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x54.png" xlink:type="simple"/></inline-formula> nerolidal</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref37">37</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x55.png" xlink:type="simple"/></inline-formula> nerolidyl propionate</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" >Diterpenoid</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.92449-ref41">41</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x56.png" xlink:type="simple"/></inline-formula> phytol</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x57.png" xlink:type="simple"/></inline-formula> (E,E,E)-3,7,11,15-tetramethylhexadeca-1,3,6,10,14-pentaene</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x58.png" xlink:type="simple"/></inline-formula> 2,6,11,15-tetramethyl-hexadeca-2,6,8,10,14-pentaene</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x59.png" xlink:type="simple"/></inline-formula> 1,6,10,14-hexadecatetraen-3-ol,3,7,11,15-tetramethyl-,(E,E)-</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" >Triterpenoid</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.92449-ref54">54</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x60.png" xlink:type="simple"/></inline-formula> hopenone I</td></tr></tbody></table></table-wrap><table-wrap id="2_9"><table><tbody><thead><tr><th align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x61.png" xlink:type="simple"/></inline-formula> hop-17(21)-en-3β-ol</th><th align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref54">54</xref>]</th></tr></thead><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x62.png" xlink:type="simple"/></inline-formula> hop-17(21)-en-3β-yl acetate</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref54">54</xref>]</td></tr><tr><td align="center" valign="middle" >Steroid</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.92449-ref35">35</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x63.png" xlink:type="simple"/></inline-formula> β-sitosterol</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x64.png" xlink:type="simple"/></inline-formula> stigmasterol</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref35">35</xref>]</td></tr><tr><td align="center" valign="middle" >Fatty acid</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.92449-ref41">41</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x65.png" xlink:type="simple"/></inline-formula> linoleic acid</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x66.png" xlink:type="simple"/></inline-formula> palmitic acid (n-hexadecanoic acid)</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref41">41</xref>]</td></tr></tbody></table></table-wrap><table-wrap id="2_10"><table><tbody><thead><tr><th align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x67.png" xlink:type="simple"/></inline-formula> oleic acid</th><th align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref41">41</xref>]</th></tr></thead><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x68.png" xlink:type="simple"/></inline-formula> stearic acid</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref41">41</xref>]</td></tr><tr><td align="center" valign="middle" >Miscellaneous</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.92449-ref55">55</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x69.png" xlink:type="simple"/></inline-formula> curcuma-J</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x70.png" xlink:type="simple"/></inline-formula> 2-(2'-methyl-1'-propenyl)-4,6-dimethyl-7-hydroxyquinoline</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref34">34</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x71.png" xlink:type="simple"/></inline-formula> 2,3,5-trimethylfuran</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x72.png" xlink:type="simple"/></inline-formula> methyleugenol</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" ><inline-formula><inline-graphic xlink:href="/html.scirp.org/file/3-2501014x73.png" xlink:type="simple"/></inline-formula> 3,3,5-trimethyl-cyclohexanol acetate</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref38">38</xref>]</td></tr></tbody></table></table-wrap></table-wrap-group></sec><sec id="s3"><title>3. Isolated Endophytic Fungi from Curcuma longa</title><p>Endophytic fungi Fusarium nivale, Fusarium solani, Doratomyces stemonitis, Penicillium, Diaphorte sp. were isolated from Curcuma longa [<xref ref-type="bibr" rid="scirp.92449-ref56">56</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref57">57</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref58">58</xref>] . Various studies have been identified the prospective of endophytic fungi from this plant as antioxidant, antidiabetic, anti-microbial and antitumor [<xref ref-type="bibr" rid="scirp.92449-ref62">62</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref63">63</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref64">64</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref65">65</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref66">66</xref>] . Therefore, in this section, endophytic fungi from different parts of C. longa is reviewed and presented in <xref ref-type="table" rid="table3">Table 3</xref>.</p><sec id="s3_1"><title>3.1. Endophytic Fungi of Rhizome</title><p>From the rhizome of C. longa several endophytic fungi have been isolated [<xref ref-type="bibr" rid="scirp.92449-ref62">62</xref>] . Exactly 207 endophytic fungi were found to be isolated in one of the study that belongs to the seven genera namely, Acremonium, Aspergillus, Exophiala, Fusarium, Penicillium, Phoma, and Stachybotrys. Among the species F. solani, F. delphinoides, F. verticillioides and A. versicolor, A. venenatus bearing the genus of Fusarium sp. and Aspergillus sp. were recovered from rhizomes of C. longa. The rest of the genera were isolated as single species. From them, Exophiala lecanii the fungal endophyte was isolated for the first time from the rhizome of C. longa [<xref ref-type="bibr" rid="scirp.92449-ref59">59</xref>] . Another investigation reported 31 endophytic fungi from the rhizome of C. longa [<xref ref-type="bibr" rid="scirp.92449-ref60">60</xref>] . In most studies of endophytic fungi, the sterile mycelia fungi are reported as mycelia-sterile. Unlike those one mycelia-sterile was identified as Phaeosphaeria ammophilae from rhizome by Eris et al., [<xref ref-type="bibr" rid="scirp.92449-ref61">61</xref>] . One of the genus Eurotium sp. was also noted from the healthy rhizomes of C. longa [<xref ref-type="bibr" rid="scirp.92449-ref63">63</xref>] .</p></sec><sec id="s3_2"><title>3.2. Endophytic Fungi of Leaf</title><p>A total of 6 endophytic fungi have been isolated from leaves of C. longa through a study [<xref ref-type="bibr" rid="scirp.92449-ref64">64</xref>] . Another study carried by Eris et al., have isolated one fungus Daldinia eschscholzii from leaf of C. longa [<xref ref-type="bibr" rid="scirp.92449-ref61">61</xref>] .</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Endophytic fungi from different parts of turmeric plant</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Genus</th><th align="center" valign="middle" >Identified by</th><th align="center" valign="middle" >Plant tissue</th><th align="center" valign="middle" >References</th></tr></thead><tr><td align="center" valign="middle" >Acremonium sp.</td><td align="center" valign="middle" >ITS-5.8s r-DNA analysis</td><td align="center" valign="middle" >Rh</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref59">59</xref>]</td></tr><tr><td align="center" valign="middle" >Aspergillus versicolor and Aspergillus venenatus</td><td align="center" valign="middle" >ITS-5.8s r-DNA analysis</td><td align="center" valign="middle" >Rh</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref59">59</xref>]</td></tr><tr><td align="center" valign="middle" >Exophiala lecanii</td><td align="center" valign="middle" >ITS-5.8s r-DNA analysis</td><td align="center" valign="middle" >Rh</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref59">59</xref>]</td></tr><tr><td align="center" valign="middle" >Fusarium Solani, Fusarium proliferatum, Fusarium oxysporum</td><td align="center" valign="middle" >ITS-5.8s r-DNA analysis</td><td align="center" valign="middle" >Rh, S, Fl, In</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref59">59</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref60">60</xref>] [<xref ref-type="bibr" rid="scirp.92449-ref61">61</xref>]</td></tr><tr><td align="center" valign="middle" >Trichoderma harzianum, Trichoderma atroviride, Trichoderma asperellum</td><td align="center" valign="middle" >ITS-5.8s r-DNA analysis</td><td align="center" valign="middle" >Rh</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref60">60</xref>]</td></tr><tr><td align="center" valign="middle" >Penicillium citrinum</td><td align="center" valign="middle" >ITS-5.8s r-DNA analysis</td><td align="center" valign="middle" >Rh</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref59">59</xref>]</td></tr><tr><td align="center" valign="middle" >Phoma herbarum</td><td align="center" valign="middle" >ITS-5.8s r-DNA analysis</td><td align="center" valign="middle" >Rh</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref59">59</xref>]</td></tr><tr><td align="center" valign="middle" >Stachybotrys sp.</td><td align="center" valign="middle" >ITS-5.8s r-DNA analysis</td><td align="center" valign="middle" >Rh</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref59">59</xref>]</td></tr><tr><td align="center" valign="middle" >Pestalopsis microspora</td><td align="center" valign="middle" >ITS-5.8s r-DNA analysis</td><td align="center" valign="middle" >Rh</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref60">60</xref>]</td></tr><tr><td align="center" valign="middle" >Phaeosphaeria ammophilae</td><td align="center" valign="middle" >ITS-5.8s r-DNA analysis</td><td align="center" valign="middle" >Rh</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref61">61</xref>]</td></tr><tr><td align="center" valign="middle" >Daldinia eschscholzii</td><td align="center" valign="middle" >ITS-5.8s r-DNA analysis</td><td align="center" valign="middle" >L</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref61">61</xref>]</td></tr><tr><td align="center" valign="middle" >Arthrobotrys foliicola</td><td align="center" valign="middle" >ITS-5.8s r-DNA analysis</td><td align="center" valign="middle" >R</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref61">61</xref>]</td></tr><tr><td align="center" valign="middle" >Drechslera kusanoi</td><td align="center" valign="middle" >ITS-5.8s r-DNA analysis</td><td align="center" valign="middle" >In</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.92449-ref61">61</xref>]</td></tr></tbody></table></table-wrap><p>Rh = Rhizome, S = Stem, Fl = Flower, In = Inflorescence, L = Leaf, R = Root.</p></sec><sec id="s3_3"><title>3.3. Endophytic Fungi of Stem</title><p>Several endophytic fungi from fresh stem of C. longa have been isolated [<xref ref-type="bibr" rid="scirp.92449-ref62">62</xref>] . The endophytic fungus Fusarium proliferatum was isolated from stems of healthy C. longa collected in Indonesia [<xref ref-type="bibr" rid="scirp.92449-ref61">61</xref>] .</p></sec><sec id="s3_4"><title>3.4. Endophytic Fungi of Root</title><p>The endophytic fungus Arthrobotrys foliicola was isolated from the roots of C. longa [<xref ref-type="bibr" rid="scirp.92449-ref61">61</xref>] . Some endophytic fungi have also been isolated from roots of C. longa [<xref ref-type="bibr" rid="scirp.92449-ref62">62</xref>] .</p></sec><sec id="s3_5"><title>3.5. Endophytic Fungi of other Parts</title><p>Some endophytic fungi from tubers and young tubers of C. longa have been isolated [<xref ref-type="bibr" rid="scirp.92449-ref62">62</xref>] . Eris et al., have isolated Fusarium verticillioides and Phanerochaete chrysosporium from the flowers of C. longa of which the later fungus is reported as mycelia-sterile. The group also isolated Cochliobolus kusanoi and Fusarium proliferatum from the inflorescence part of the plant. Cochliobolus kusanoi is the teleomorph stage of Drechslera kusanoi [<xref ref-type="bibr" rid="scirp.92449-ref61">61</xref>] .</p></sec></sec><sec id="s4"><title>4. Reported Bioactivity on Endophytic Fungi Isolated from Turmeric Plant</title><sec id="s4_1"><title>4.1. Antioxidant Activity</title><p>44 endophytic fungi from several parts of turmeric plant were investigated by a research group Bustanussalam et al., for their antioxidant bioactive compounds. They observed both filtrate and biomass ethylacetate extracts of endophytic fungi have antioxidant activity. On the basis of DPPH free radical scavenging method filtrate extracts gave higher antioxidant activity than biomass extracts. Due to presence of fatty acids, biomass extracts are less active as antioxidant. Filtrate extracts contain many secondary metabolites that may act as protection for the endophytic fungi of host plant [<xref ref-type="bibr" rid="scirp.92449-ref62">62</xref>] .</p></sec><sec id="s4_2"><title>4.2. Anticancer Activity</title><p>A study carried out by Ratih et al., have shown inhibitory activity of 4 isolates of endophytic fungi towards human breast cancer MCF-7 cell line [<xref ref-type="bibr" rid="scirp.92449-ref65">65</xref>] . Endophytic fungus Eurotium sp. was isolated from rhizomes of C. longa by Ruby and Raghunath and it is utilized for the production of anticancer enzyme asparaginase for the first time [<xref ref-type="bibr" rid="scirp.92449-ref63">63</xref>] . The enzyme is considered to participate in major role in the asparaginase metabolism of the cells. It’s a likely therapeutic agent for acute lymphocytic leukemia, acute lymphoblastic leukemia and chronic myelogenous leukemia also reported to be an effective antilymphoma agent in humans.</p></sec><sec id="s4_3"><title>4.3. Antifungal Activity</title><p>Suruchi et al., have separated endophytic fungi from C. longa for antifungal activity. The group reported the active constituent Gentisyl alcohol which is an anti-phytopathogenic molecule from fungal isolate P. herbarum. The purified compound showed antagonistic activity against C. gloeosporioides causing leaf spot of turmeric and could, therefore, be explored as a biocontrol agent for the host-specific phytopathogen [<xref ref-type="bibr" rid="scirp.92449-ref59">59</xref>] . Similarly, Vinayarani and Prakash have isolated T. harzianum from the rhizome of turmeric and they concluded that this can be exploited as a potential biocontrol agent for suppressing rhizome rot and leaf blight diseases in turmeric [<xref ref-type="bibr" rid="scirp.92449-ref60">60</xref>] .</p><disp-formula id="scirp.92449-formula4"><graphic  xlink:href="//html.scirp.org/file/3-2501014x74.png"  xlink:type="simple"/></disp-formula></sec><sec id="s4_4"><title>4.4. Antibacterial Activity</title><p>Endophytic fungi could be a promising source for antibacterial bioactive agents. A study carried out by Sharmila et al., found that the endophytic fungus Chaetomium sp. isolated from C. longa exhibited protruding antibacterial activity against three different human pathogenic bacteria such as Proteus sp., Pseudomonas sp. and Staphylococcus aureus [<xref ref-type="bibr" rid="scirp.92449-ref66">66</xref>] .</p></sec></sec><sec id="s5"><title>5. Conclusion</title><p>Till today, the chemical composition of C. longa has thoroughly been investigated and a number of different active substances have been identified, which exhibit a wide range of medicinal value. But, very few structures of bioactive compounds are characterized and identified from endophytic fungi of C. longa. Most of the investigations are restricted to the level of fungal identification and bioactivity assay. But, endophytic fungi, producer of a wide array of secondary bioactive metabolites with their peculiar potential compounds, namely, antioxidant, antibacterial, antifungal, anticancer, etc., are the ideal targets for further drug discovery. These leads may play a major role in the recovery of infectious, inflammatory and also certain kinds of cancer diseases. So, extensive research is necessary in the area of endophytic fungi isolation and characterization of the compounds from C. longa.</p></sec><sec id="s6"><title>Cite this paper</title><p>Ferdous, K.J., Afroz, F., Islam, M.R., Mazid, M.A. and Sohrab, M.H. (2019) Isolated Endophytic Fungi from the Plant Curcuma longa and Their Potential Bioactivity—A Review. Pharmacology &amp; Pharmacy, 10, 244-270. https://doi.org/10.4236/pp.2019.105021</p></sec></body><back><ref-list><title>References</title><ref id="scirp.92449-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Priyadarsini, K.I. (2014) The Chemistry of Curcumin: From Extraction to Therapeutic Agent. Molecules, 19, 20091-20112. https://doi.org/10.3390/molecules191220091</mixed-citation></ref><ref id="scirp.92449-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Chattopadhyay, I., Kaushik, B., Uday, B. and Ranajit, K.B. 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