<?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">ABC</journal-id><journal-title-group><journal-title>Advances in Biological Chemistry</journal-title></journal-title-group><issn pub-type="epub">2162-2183</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/abc.2022.124009</article-id><article-id pub-id-type="publisher-id">ABC-119514</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></subj-group></article-categories><title-group><article-title>
 
 
  Phytochemical Analysis and Bioactivity Screening of Primary and Secondary Metabolic Products of Medicinal Plants in the Valleys of Medina Region Saudi Arabia
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Safa</surname><given-names>Alsaedi</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>Ghalia</surname><given-names>Aljeddani</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Biology, Collage of Science, University of Jeddah, Jeddah, Saudi Arabia</addr-line></aff><pub-date pub-type="epub"><day>08</day><month>08</month><year>2022</year></pub-date><volume>12</volume><issue>04</issue><fpage>92</fpage><lpage>115</lpage><history><date date-type="received"><day>18,</day>	<month>July</month>	<year>2022</year></date><date date-type="rev-recd"><day>27,</day>	<month>August</month>	<year>2022</year>	</date><date date-type="accepted"><day>30,</day>	<month>August</month>	<year>2022</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>
 
 
  Medicinal plants are highly valued for their active compounds. These
   plants can be used in various fields and preservation of these plants in their environment. The present study aimed to screen medicinal plants used in traditional medicine in Medina valleys for the presence of metabolites, and to answer the following question: is the ethnomedicinal importance of medicinal plants used in Medina valleys conform to their primary and secondary
   meta
  bolite content. Eight plants (Pulicaria incise, Heliotropium arbai
  nense
  , Commicarpus grandiflorus, Rumex vesicarius, Senna alexandrin
  a
  , Rhazya stricta, Withania somnifera 
  and Asphodelus fistulosus) were collected from
   
  the Medina valleys and were biochemically analyzed to determine the different compounds after leaves extraction analyzed statistically to clarify the content of primary compounds. The chemical compounds in the most active fraction were determined using quantitative phytochemical and gas chromatography-mass spectrometry (GC/MS) analytical methods, comparing the mass spectra of the GC/MS identified compounds with those of the Center of Excellence in Environmental Studies (CEES) database library. The result showed 16 aroma compounds representing the GC/MS analysis revealed the presence of various compounds like 4,4-Dimethyl octane, 5H-1-Pyrindine and 1,3-
   
  Cyclopentadiene, 1,2,5,5-tetramethyl- in the ethanolic extract of Pulicaria incisa. The most prevalent plants were Pulicaria incisa, Senna alexandrina and Heliotropium arbainense the study plants have high content of protein. There is a need to focus phytochemical screening on ethnobotanical studies to complete research into traditional medicine which leads to the discovery of new drugs.
 
</p></abstract><kwd-group><kwd>C Phytochemical</kwd><kwd> Medicinal Plants</kwd><kwd> GC-MS Analysis</kwd><kwd> Primary and Secondary Metabolic</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Plants are rich in active compounds or secondary metabolites such as alkaloids, steroids, tannins, glycosides, which are present in their organs such as leaves, flowers, seeds, etc [<xref ref-type="bibr" rid="scirp.119514-ref1">1</xref>]. They are widely distributed in Central Asia and Southern Africa. In Saudi Arabia, they are grown in the Wadi Najran, Taif region, and Al Madinah Al Munawwarah (Abyar Al-Mashy) [<xref ref-type="bibr" rid="scirp.119514-ref2">2</xref>]. The Saudi Arabian flora comprises about 2250 plant species that are distributed throughout the Kingdom [<xref ref-type="bibr" rid="scirp.119514-ref3">3</xref>]. It is well known that Saudi Arabia and the Arabian Peninsula are rich in natural and cultivated plants. The flora of Saudi Arabia contains a total of 2250 plant species belong to 142 families [<xref ref-type="bibr" rid="scirp.119514-ref4">4</xref>].</p><p>Some of these plants were used and still by native people who gain an accumulated experience in the uses of these plants in folk medicine to cure many different diseases. But unfortunately, there is a gap in transferring the indigenous knowledge between old and new generation further to the lack and information scarcity on their uses, further to the difficulties that may be found in identifying the wild medicinal plants as well. However, the gap is still wider between traditional herbal medicine and modern medicine manufacturing. Few studies on medicinal and Ethnomedicinal plants have been done in Saudi Arabia including Al-Baha region among these, studies conducted by Collenette, [<xref ref-type="bibr" rid="scirp.119514-ref5">5</xref>] who described twenty plant species traditionally used as a medicine with their main chemical constituents. Different types of primary and secondary metabolic compounds are used usually divided according to their chemical composition. Active compounds in medicinal plants can be used in medicinal drugs and move society to invest in crop production [<xref ref-type="bibr" rid="scirp.119514-ref6">6</xref>]. And it can be used to treat toxic and bacterial diseases [<xref ref-type="bibr" rid="scirp.119514-ref7">7</xref>]. Medical plants are considered an important economic resource of natural biodiversity [<xref ref-type="bibr" rid="scirp.119514-ref8">8</xref>]. Further, an initial survey on the medicinal plant diversity in the flora of the Kingdom of Saudi Arabia has been made covering seven families [<xref ref-type="bibr" rid="scirp.119514-ref9">9</xref>]. The active compounds can be extracted from medicinal plants this enables and preserving them from human intervention. Medicinal plants have many benefits in health uses and with this study it can prove the validity of their importance. Analysis of some medicinal plants biochemically and find out its medicinal very important to carry out the necessary that help in separating the important primary and secondary metabolic compounds helps in prove their value [<xref ref-type="bibr" rid="scirp.119514-ref10">10</xref>].</p><p>The major goal of this study was to investigate the chemical composition, screen and identify the medicinal plant diversity in Medina valleys to discuss their environmental distribution and work on conservation of these valuable plants to increase their bioavailability. The identified of some the active compounds in the composition of these plants to determine its medicinal and nutritional value. Encouraging the conservation of these important plants and increasing their cultivation in their appropriate environment. Use of these plants in the health and therapeutic field because of their medicinal and nutritional value and can use in the commercial and cosmetic industries due to their useful metabolic compounds.</p></sec><sec id="s2"><title>2. Materials and Methods</title><sec id="s2_1"><title>2.1. Study Area</title><p>Medina region is in the central part of the western sector of the kingdom of Saudi Arabia within the Hijaz Mountain range (<xref ref-type="fig" rid="fig1">Figure 1</xref>), and the southern outskirts</p><p>of Medina are located at the 20 - 24 North latitude and thus it is very close to the northern ends of the tropical zone with thermal surplus and as a result the heat in intense in summer and warm in winter. The annual temperature range is 13.8 degrees, and the average maximum temperature is about 42 degrees [<xref ref-type="bibr" rid="scirp.119514-ref11">11</xref>]. Samples were collected in January 2021 from three valleys (Wadi Al-Baidha, Al-Aqiq, Al-Fora ‘a) in Medina, (<xref ref-type="fig" rid="fig2">Figure 2</xref>).</p></sec><sec id="s2_2"><title>2.2. Maintaining the Integrity of the Specifications</title><p>Samples Collection</p><p>Samples were collected from eight plant species from different location, including 3 valleys from the Medina region during the winter season, and they were placed in plastic bags for preservation. The plant samples were divided into fresh samples that were preserved in ice and samples that were air-dried, milled, and preserved in plastic boxes until carry out the necessary analysis [<xref ref-type="bibr" rid="scirp.119514-ref12">12</xref>].</p></sec><sec id="s2_3"><title>2.3. Plant Material</title><p>Eight plants (Pulicariaincise, Heliotropiumarbainense, Commicarpusgrandiflorus, Rumexvesicarius, Sennaalexandrina, Rhazyastricta, Withaniasomnifera and Asphodelusfistulosus) as show in <xref ref-type="fig" rid="fig3">Figure 3</xref> were identified according to Saudi Arabia flora and authenticated by the method of Chaudhary plant Protection. Plants were collected, dried and deposited at the herbarium of Jeddah university [<xref ref-type="bibr" rid="scirp.119514-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.119514-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.119514-ref15">15</xref>].</p></sec><sec id="s2_4"><title>2.4. Aqueous Extracts of Plant for Primary Metabolic Analysis</title><p>A sample of the fresh plant was taken from each plant species 1:20 and then ground into a porcelain mortar using distilled water; the volume was completed in a standard flask, and the extract was kept at very low temperature until perform the necessary analysis The extracts were filtered through a filter paper several times and kept at 4˚C in the dark until use [<xref ref-type="bibr" rid="scirp.119514-ref16">16</xref>].</p></sec><sec id="s2_5"><title>2.5. Ethanolic Extraction for Secondary Metabolic Analysis</title><p>Dried plant at flask with about 1:15 of ethanol 75% after the first filtration, the Ethanolic extract was kept in the refrigerator. Repeat the same steps 2 day. Then samples were heating the extract using water bath under condenser. The extracts were filtered through a filter paper several times after 24 hours and kept at 4˚C in the dark until use [<xref ref-type="bibr" rid="scirp.119514-ref17">17</xref>].</p></sec><sec id="s2_6"><title>2.6. Tests of Primary Compounds</title><sec id="s2_6_1"><title>2.6.1. Protein</title><p>0.2 ml of fresh plant extract was added to 5 ml Coomassie brilliant blue using an electric stirrer and measured in a spectrophotometer (NOVA SPCC II SECTROPHOTOMETER) [<xref ref-type="bibr" rid="scirp.119514-ref18">18</xref>].</p></sec><sec id="s2_6_2"><title>2.6.2. Proline</title><p>0.5 ml of plant extract with 2.5 ml of sulfosalicylic acid with 2 ml ninhydrin with 2 ml of glacial acetic acid, the closed with a pulp and placed in water bath for 1 hour [<xref ref-type="bibr" rid="scirp.119514-ref19">19</xref>].</p></sec><sec id="s2_6_3"><title>2.6.3. Amino Acids</title><p>Take 2 ml of plant extract with 1 ml of ninhydrin 1% with 2.4 ml of glycerin with 0.4 ml of buffer [<xref ref-type="bibr" rid="scirp.119514-ref20">20</xref>].</p></sec><sec id="s2_6_4"><title>2.6.4. Carbohydrates</title><p>0.4 ml of plant extract mixed with 3.6 ml of carbohydrate reagent and immediately put in a boiling water bath covered with pulp for 30 seconds [<xref ref-type="bibr" rid="scirp.119514-ref21">21</xref>].</p></sec></sec><sec id="s2_7"><title>2.7. Tests of Secondary Compounds</title><sec id="s2_7_1"><title>2.7.1. Phytosterols</title><p>Drops of each of the plant extract in a test tube was added drops of concentrated H<sub>2</sub>SO<sub>4</sub> Reddish brown color in chloroform layer indicates the presence of phytosterols [<xref ref-type="bibr" rid="scirp.119514-ref22">22</xref>].</p></sec><sec id="s2_7_2"><title>2.7.2. Triterpenoids</title><p>Plant extracts were treated with few drops of acetic anhydride, boil and cool. Red color indicated the presence of triterpenoids [<xref ref-type="bibr" rid="scirp.119514-ref23">23</xref>].</p></sec><sec id="s2_7_3"><title>2.7.3. Saponins</title><p>Small amount of the plant extract with little quantity of water and shaken vigorously. Appearance of foam persisting for 10 min indicated presence of saponins [<xref ref-type="bibr" rid="scirp.119514-ref24">24</xref>].</p></sec><sec id="s2_7_4"><title>2.7.4. Alkaloids</title><p>Little of plant extract were dissolved in few drops of conc. HCL and adding few drops of Mayer’s reagent. Appearance of white precipitate indicated presence of alkaloids [<xref ref-type="bibr" rid="scirp.119514-ref25">25</xref>].</p></sec><sec id="s2_7_5"><title>2.7.5. Flavonoids</title><p>Extract mix with few drops of ferric chloride. Appearance of blackish red color indicated presence of flavonoids [<xref ref-type="bibr" rid="scirp.119514-ref26">26</xref>].</p></sec><sec id="s2_7_6"><title>2.7.6. Coumarins</title><p>Small amount of the plant extracts with little drops of NaOH 10% and chloroform. Appearance of yellow color indicated presence of coumarin [<xref ref-type="bibr" rid="scirp.119514-ref27">27</xref>].</p></sec><sec id="s2_7_7"><title>2.7.7. Tannins</title><p>Few drops of ferric chloride were added to plant extract. Appear of black precipitate gives positive result [<xref ref-type="bibr" rid="scirp.119514-ref28">28</xref>].</p></sec><sec id="s2_7_8"><title>2.7.8. Gas Chromatography-Mass Spectrometry (GC/MS) Analysis</title><p>Plant extracts were selected for gas chromatography-mass spectroscopy (GC-MS) analysis in order to identify the active compound present. Analysis was conducted using the database of Center of Excellence in Environmental Studies (CEES), with the spectrum of the unknown components being compared with the spectrum of known components stored in the (CEES) library. Before identifying the compounds in the extracts 0.1 ml of each plant extract was mixed with 1ml of ethanol (HPLC grade) (WINLAB, UK) and filtered using a 0.22 μ Millipore filter (Millex-HV) to obtain a crystal-clear solution. The identification of the compounds was done by injecting 1&#188; l of crystal-clear sample into an RTx -5 columns (the initial temperature of the column oven was 250&#176;C. A HP 5 ms, 30 m capillary column was used (30 m &#215; 0.25 mm i.d. &#215; 0.25 m, 5% phenylmethylsiloxane, RTx -5MS)) with (30 &#215; 0.32 nm) of GC-MS model (Perkin Elmer, Clarus 500, USA) and helium (3 ml/min) was used as a carrier gas. The following temperature gradient program was used (75˚C for 2 min followed by an increase from 75˚C to 175˚C at a rate of 50˚C per min and finally 7 min at 175˚C). The fractions were compared with those in the mass spectrum library of the corresponding organic compounds. The chemical components of the plant extracts were analyzed in the central laboratory of (CEES) [<xref ref-type="bibr" rid="scirp.119514-ref29">29</xref>].</p></sec></sec></sec><sec id="s3"><title>3. Result</title><p>The result in <xref ref-type="table" rid="table1">Table 1</xref> shows the different types of plants with their families that were counted in the three valleys (Wadi Al-Baidha, Al-Aqiq, Al-Fora ‘a) of Medina region from which the study plants were collected (P. incise, H. arbainense, C. grandiflorus, R. vesicarius, S. alexandrina, R. stricta, W. somnifera and A. fistulosus). Showed prevalent plants were (S. alexandrina, P. incise, H. arbainense).</p><p>A sample. The results of phytochemical screening of aqueous and ethanol plant extract showed the existence of Protein, Proline, Amino acids and carbohydrates (<xref ref-type="table" rid="table2">Table 2</xref>) for Primary Compounds and Phytosterols, Triterpenoids, saponins, alkaloids, flavonoids, coumarins and tannins (<xref ref-type="table" rid="table3">Table 3</xref>) for secondary compounds.</p><p><xref ref-type="table" rid="table2">Table 2</xref> shows the statistical results of the primary metabolic compounds in the form of the mean and standard deviation. There is a high protein content in</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Inventory of some medicinal plants in valleys of medina region (Wadi 1-Al-Baidha, 2-Al-Aqiq, 3-Al-Fora ‘a) presence (+) and absence (−) of plant study</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Plant species</th><th align="center" valign="middle"  rowspan="2"  >Families</th><th align="center" valign="middle"  rowspan="2"  >Life form</th><th align="center" valign="middle"  rowspan="2"  >Life growth</th><th align="center" valign="middle"  colspan="3"  >Sites</th></tr></thead><tr><td align="center" valign="middle" >1</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >3</td></tr><tr><td align="center" valign="middle" >Asphodelus fistulosus</td><td align="center" valign="middle" >Asphodelaceae</td><td align="center" valign="middle" >Herb</td><td align="center" valign="middle" >Annual</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >Commicarpus grandiflorus</td><td align="center" valign="middle" >Nyctaginaceae</td><td align="center" valign="middle" >Herb</td><td align="center" valign="middle" >Perrenial</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td></tr><tr><td align="center" valign="middle" >Heliotropium arbainense</td><td align="center" valign="middle" >Boraginaceae</td><td align="center" valign="middle" >Herb</td><td align="center" valign="middle" >Perrenial</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td></tr><tr><td align="center" valign="middle" >Pulicaria incisa</td><td align="center" valign="middle" >Asteraceae</td><td align="center" valign="middle" >Herb</td><td align="center" valign="middle" >Annual</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td></tr><tr><td align="center" valign="middle" >Rhazya stricta</td><td align="center" valign="middle" >Apocynaceae</td><td align="center" valign="middle" >Shrub</td><td align="center" valign="middle" >Perrenial</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >Rumex vesicarius</td><td align="center" valign="middle" >Polygonaceae</td><td align="center" valign="middle" >Herb</td><td align="center" valign="middle" >Annual</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >Senna alexandrina</td><td align="center" valign="middle" >Leguminosae</td><td align="center" valign="middle" >Shrub</td><td align="center" valign="middle" >Perrenial</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td></tr><tr><td align="center" valign="middle" >Withania somnifera</td><td align="center" valign="middle" >Solanaceae</td><td align="center" valign="middle" >Shrub</td><td align="center" valign="middle" >Perrenial</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td></tr></tbody></table></table-wrap><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> The averages and standard deviations of the primary compounds in the study plants (mg/g f.wt.) n = 3</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Plant species</th><th align="center" valign="middle"  colspan="2"  >Protein</th><th align="center" valign="middle"  colspan="2"  >Proline</th><th align="center" valign="middle"  colspan="2"  >Amino acids</th><th align="center" valign="middle"  colspan="2"  >Carbohydrates</th></tr></thead><tr><td align="center" valign="middle" >Pulicaria incisa</td><td align="center" valign="middle"  colspan="2"  >3.23<sup>d</sup> &#177; 0.02 (0.01)</td><td align="center" valign="middle"  colspan="2"  >0.03<sup>g</sup> &#177; 0.0 (0.0)</td><td align="center" valign="middle"  colspan="2"  >0.01<sup>e</sup> &#177; 0.0 (0.0)</td><td align="center" valign="middle"  colspan="2"  >0.04<sup>e</sup> &#177; 0.01 (0.003)</td></tr><tr><td align="center" valign="middle" >Heliotropium arbainense</td><td align="center" valign="middle"  colspan="2"  >3.62<sup>a</sup> &#177; 0.02 (0.01)</td><td align="center" valign="middle"  colspan="2"  >0.12<sup>d</sup> &#177; 0.0 (0.0)</td><td align="center" valign="middle"  colspan="2"  >0.03<sup>e</sup> &#177; 0.0 (0.0)</td><td align="center" valign="middle"  colspan="2"  >0.10<sup>c</sup> &#177; 0.0 (0.0)</td></tr><tr><td align="center" valign="middle" >Commicarpus grandiflorus</td><td align="center" valign="middle"  colspan="2"  >3.54<sup>b</sup> &#177; 0.02 (0.01)</td><td align="center" valign="middle"  colspan="2"  >0.12<sup>d</sup> &#177; 0.0 (0.0)</td><td align="center" valign="middle"  colspan="2"  >0.03<sup>e</sup> &#177; 0.0 (0.0)</td><td align="center" valign="middle"  colspan="2"  >0.07<sup>d</sup> &#177; 0.01 (0.003)</td></tr><tr><td align="center" valign="middle" >Rumex vesicarius</td><td align="center" valign="middle"  colspan="2"  >3.03<sup>e</sup> &#177; 0.01 (0.01)</td><td align="center" valign="middle"  colspan="2"  >0.36<sup>a</sup> &#177; 0.01 (0.0)</td><td align="center" valign="middle"  colspan="2"  >3.15<sup>b</sup> &#177; 0.28 (0.16)</td><td align="center" valign="middle"  colspan="2"  >0.03<sup>f</sup> &#177; 0.01 (0.003)</td></tr><tr><td align="center" valign="middle" >Senna alexandrina</td><td align="center" valign="middle"  colspan="2"  >2.86<sup>f</sup> &#177; 0.02 (0.01)</td><td align="center" valign="middle"  colspan="2"  >0.11<sup>e</sup> &#177; 0.0 (0.0)</td><td align="center" valign="middle"  colspan="2"  >7.69<sup>a</sup> &#177; 0.28 (0.16)</td><td align="center" valign="middle"  colspan="2"  >0.19<sup>b</sup> &#177; 0.01 (0.003)</td></tr><tr><td align="center" valign="middle" >Rhazya stricta</td><td align="center" valign="middle"  colspan="2"  >3.06<sup>e</sup> &#177; 0.02 (0.01)</td><td align="center" valign="middle"  colspan="2"  >0.13<sup>c</sup> &#177; 0.0 (0.0)</td><td align="center" valign="middle"  colspan="2"  >2.17<sup>c</sup> &#177; 0.08 (0.04)</td><td align="center" valign="middle"  colspan="2"  >0.03<sup>ef</sup> &#177; 0.0 (0.0)</td></tr><tr><td align="center" valign="middle" >Withania somnifera</td><td align="center" valign="middle"  colspan="2"  >3.07<sup>e</sup> &#177; 0.03 (0.02)</td><td align="center" valign="middle"  colspan="2"  >0.21<sup>b</sup> &#177; 0.01 (0.0)</td><td align="center" valign="middle"  colspan="2"  >2.0<sup>c</sup> &#177; 0.14 (0.08)</td><td align="center" valign="middle"  colspan="2"  >0.04<sup>ef</sup> &#177; 0.0 (0.0)</td></tr><tr><td align="center" valign="middle" >Asphodelus fistulosus</td><td align="center" valign="middle"  colspan="2"  >3.34<sup>c</sup> &#177; 0.01 (0.0)</td><td align="center" valign="middle"  colspan="2"  >0.04<sup>f</sup> &#177; 0.0 (0.0)</td><td align="center" valign="middle"  colspan="2"  >1.42<sup>d</sup> &#177; 0.28 (0.16)</td><td align="center" valign="middle"  colspan="2"  >0.64<sup>a</sup> &#177; 0.01 (0.01)</td></tr><tr><td align="center" valign="middle" >F (p)</td><td align="center" valign="middle" >628.698*</td><td align="center" valign="middle" >(&lt;0.001*)</td><td align="center" valign="middle" >3920.0*</td><td align="center" valign="middle" >(&lt;0.001*)</td><td align="center" valign="middle" >614.698*</td><td align="center" valign="middle" >(&lt;0.001*)</td><td align="center" valign="middle" >4444.33*</td><td align="center" valign="middle" >(&lt;0.001*)</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> List of presence (+) and presence in high concentration (++) and absence (−) of secondary compounds in plant study</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Plant species</th><th align="center" valign="middle" >Phytosterols</th><th align="center" valign="middle" >Triterpenoids</th><th align="center" valign="middle" >Saponins</th><th align="center" valign="middle" >Alkaloids</th><th align="center" valign="middle" >Flavonoids</th><th align="center" valign="middle" >Coumarins</th><th align="center" valign="middle" >Tannins</th></tr></thead><tr><td align="center" valign="middle" >Pulicaria incisa</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td></tr><tr><td align="center" valign="middle" >Heliotropium arbainense</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td></tr><tr><td align="center" valign="middle" >Commicarpus grandiflorus</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td></tr><tr><td align="center" valign="middle" >Rumex vesicarius</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >++</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td></tr><tr><td align="center" valign="middle" >Senna alexandrina</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td></tr><tr><td align="center" valign="middle" >Rhazya stricta</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td></tr><tr><td align="center" valign="middle" >Withania somnifera</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td></tr><tr><td align="center" valign="middle" >Asphodelus fistulosus</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td></tr></tbody></table></table-wrap><p>the study samples. The changes in the soluble protein content of the different plant species shows in <xref ref-type="table" rid="table2">Table 2</xref>, and they retained the largest amount of it significantly and the highest of protein is the plant H. arbainense, and the lowest plant is S. alexandrina.</p><p>The saponins sowed little content for R. stricta, R. vesicarius and A. fistulosus but, moderate level was showed for P. incise, H. arbainense, C. grandiflorus and S. alexandrina. Also R. vesicarius extract showed a high content of flavonoids, but P. incisa, S. alexandrina and A. fistulosus have the moderate content and the little amount was observed in R. stricta, C. grandiflorus and H. arbainense. All plant extract has moderate content of alkaloids, Triterpenoids, coumarins and tannins respectively.</p><p>The proposed chemical structures of these compounds are indicated in Figures 4-11. The names of the probable bio molecules present with their RT, Retention Time, Values, and peak areas are indicated in <xref ref-type="table" rid="table4">Table 4</xref>. GC-MS analysis the results of GC-MS analysis of ethanol extracts of P. incisa are given in <xref ref-type="table" rid="table4">Table 4</xref> and <xref ref-type="fig" rid="fig4">Figure 4</xref>, the GC-MS analysis of P. incisa, the compounds found were -</p><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> GC/MS analysis of plant study Ethanolic extracts</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Compounds</th><th align="center" valign="middle" >RT (min)</th><th align="center" valign="middle" >Area (mAU*s)</th><th align="center" valign="middle" >Height</th></tr></thead><tr><td align="center" valign="middle"  colspan="4"  >Pulicaria incisa</td></tr><tr><td align="center" valign="middle" >2-Propanone, 1,1-dimethoxy-</td><td align="center" valign="middle" >3.342</td><td align="center" valign="middle" >357,977</td><td align="center" valign="middle" >133,535</td></tr><tr><td align="center" valign="middle" >1,2,4-Benzenetricarboxylic acid, 1,2-dimethyl ester</td><td align="center" valign="middle" >3.483</td><td align="center" valign="middle" >51,547</td><td align="center" valign="middle" >9336</td></tr><tr><td align="center" valign="middle" >3-Hexanol, 2-methyl-</td><td align="center" valign="middle" >4.315</td><td align="center" valign="middle" >30,558</td><td align="center" valign="middle" >13,107</td></tr><tr><td align="center" valign="middle" >2-Propenoic acid, butyl ester</td><td align="center" valign="middle" >5.147</td><td align="center" valign="middle" >144,967</td><td align="center" valign="middle" >39,482</td></tr><tr><td align="center" valign="middle" >2-Butenoic acid, 2-methyl-, (Z)-</td><td align="center" valign="middle" >5.263</td><td align="center" valign="middle" >228,272</td><td align="center" valign="middle" >49,700</td></tr><tr><td align="center" valign="middle" >5H-1-Pyrindine</td><td align="center" valign="middle" >11.525</td><td align="center" valign="middle" >3,032,157</td><td align="center" valign="middle" >440,220</td></tr><tr><td align="center" valign="middle" >Acrylic acid, (5-cyclopropylidenepentyl) ester</td><td align="center" valign="middle" >12.575</td><td align="center" valign="middle" >47,653</td><td align="center" valign="middle" >10,055</td></tr><tr><td align="center" valign="middle" >1,3-Cyclopentadiene, 1,2,5,5-tetramethyl-</td><td align="center" valign="middle" >13.461</td><td align="center" valign="middle" >914,482</td><td align="center" valign="middle" >273,337</td></tr><tr><td align="center" valign="middle" >1,3-Cyclopentadiene, 1,2,5,5-tetramethyl-</td><td align="center" valign="middle" >13.544</td><td align="center" valign="middle" >2,706,387</td><td align="center" valign="middle" >773,527</td></tr><tr><td align="center" valign="middle" >2-Hydroxy-2,6-dimethyl-hept-6-en-3-one</td><td align="center" valign="middle" >16.641</td><td align="center" valign="middle" >59,827</td><td align="center" valign="middle" >15,683</td></tr><tr><td align="center" valign="middle" >Heptane, 4,4-dimethyl-</td><td align="center" valign="middle" >3.144</td><td align="center" valign="middle" >1,462,217</td><td align="center" valign="middle" >976,610</td></tr><tr><td align="center" valign="middle" >Ethylbenzene</td><td align="center" valign="middle" >4.439</td><td align="center" valign="middle" >18,637</td><td align="center" valign="middle" >8779</td></tr><tr><td align="center" valign="middle" >Ethanone, 1-cyclobutyl-</td><td align="center" valign="middle" >4.733</td><td align="center" valign="middle" >17,488</td><td align="center" valign="middle" >2260</td></tr><tr><td align="center" valign="middle" >4,4-Dimethyl octane</td><td align="center" valign="middle" >5.197</td><td align="center" valign="middle" >6,939,195</td><td align="center" valign="middle" >3,301,821</td></tr><tr><td align="center" valign="middle" >Pentane, 2,2-dimethyl-</td><td align="center" valign="middle" >12.641</td><td align="center" valign="middle" >32,434</td><td align="center" valign="middle" >11,081</td></tr><tr><td align="center" valign="middle" >Heptane, 4,4-dimethyl-</td><td align="center" valign="middle" >3.144</td><td align="center" valign="middle" >1,462,217</td><td align="center" valign="middle" >976,610</td></tr><tr><td align="center" valign="middle"  colspan="4"  >Heliotropium arbainense</td></tr><tr><td align="center" valign="middle" >Butanoic acid, anhydride</td><td align="center" valign="middle" >3.131</td><td align="center" valign="middle" >9464</td><td align="center" valign="middle" >5471</td></tr><tr><td align="center" valign="middle" >2-Propanone, 1,1-dimethoxy-</td><td align="center" valign="middle" >3.326</td><td align="center" valign="middle" >125,502</td><td align="center" valign="middle" >52,314</td></tr><tr><td align="center" valign="middle" >Acetic acid, butyl ester</td><td align="center" valign="middle" >3.45</td><td align="center" valign="middle" >57,268</td><td align="center" valign="middle" >15,950</td></tr><tr><td align="center" valign="middle" >2-Propenoic acid, butyl ester</td><td align="center" valign="middle" >5.155</td><td align="center" valign="middle" >212,791</td><td align="center" valign="middle" >55,756</td></tr><tr><td align="center" valign="middle" >1,3-Cyclopentadiene, 1,2,5,5-tetramethyl-</td><td align="center" valign="middle" >13.529</td><td align="center" valign="middle" >2,570,446</td><td align="center" valign="middle" >717,552</td></tr><tr><td align="center" valign="middle" >1,3-Dioxolane-2-methanol</td><td align="center" valign="middle" >15.289</td><td align="center" valign="middle" >37,964</td><td align="center" valign="middle" >10,627</td></tr><tr><td align="center" valign="middle" >Bicyclo[2.2.1]heptane, 2-(2-propenyl)-</td><td align="center" valign="middle" >16.076</td><td align="center" valign="middle" >44,160</td><td align="center" valign="middle" >10,578</td></tr><tr><td align="center" valign="middle" >1-Undecene, 9-methyl-</td><td align="center" valign="middle" >16.44</td><td align="center" valign="middle" >54,827</td><td align="center" valign="middle" >17,210</td></tr><tr><td align="center" valign="middle" >Isophthalaldehyde</td><td align="center" valign="middle" >17.191</td><td align="center" valign="middle" >15,120</td><td align="center" valign="middle" >5174</td></tr><tr><td align="center" valign="middle" >4,6-Heptadienoic acid, 3,3,6-trimethyl-, ethyl ester</td><td align="center" valign="middle" >17.892</td><td align="center" valign="middle" >359,433</td><td align="center" valign="middle" >62,759</td></tr><tr><td align="center" valign="middle" >Heptane, 4,4-dimethyl-</td><td align="center" valign="middle" >3.148</td><td align="center" valign="middle" >1,517,641</td><td align="center" valign="middle" >1,024,671</td></tr><tr><td align="center" valign="middle" >Ethylbenzene</td><td align="center" valign="middle" >4.443</td><td align="center" valign="middle" >11,865</td><td align="center" valign="middle" >7807</td></tr><tr><td align="center" valign="middle" >Undecane</td><td align="center" valign="middle" >5.2</td><td align="center" valign="middle" >7,194,793</td><td align="center" valign="middle" >3,497,076</td></tr><tr><td align="center" valign="middle" >3-Hexanone, 2,5-dimethyl-</td><td align="center" valign="middle" >12.643</td><td align="center" valign="middle" >21,693</td><td align="center" valign="middle" >8316</td></tr><tr><td align="center" valign="middle" >Phenol, 3-(1,1-dimethylethyl)-4-methoxy-</td><td align="center" valign="middle" >16.465</td><td align="center" valign="middle" >2,787,397</td><td align="center" valign="middle" >193,202</td></tr><tr><td align="center" valign="middle"  colspan="4"  >Commicarpus grandiflorus</td></tr><tr><td align="center" valign="middle" >2-Propanone, 1,1-dimethoxy-</td><td align="center" valign="middle" >3.136</td><td align="center" valign="middle" >102,048</td><td align="center" valign="middle" >37,944</td></tr><tr><td align="center" valign="middle" >2-Propenoic acid, butyl ester</td><td align="center" valign="middle" >5.035</td><td align="center" valign="middle" >33,535</td><td align="center" valign="middle" >12,867</td></tr><tr><td align="center" valign="middle" >2-Butenoic acid, 2-methyl-, (Z)-</td><td align="center" valign="middle" >5.178</td><td align="center" valign="middle" >323,558</td><td align="center" valign="middle" >57,313</td></tr><tr><td align="center" valign="middle" >2,4-Dihydroxy-2,5-dimethyl-3(2H)-furan-3-one</td><td align="center" valign="middle" >7.547</td><td align="center" valign="middle" >29,364</td><td align="center" valign="middle" >8863</td></tr><tr><td align="center" valign="middle" >5H-1-Pyrindine</td><td align="center" valign="middle" >11.508</td><td align="center" valign="middle" >2,996,333</td><td align="center" valign="middle" >446,081</td></tr><tr><td align="center" valign="middle" >1,3-Cyclopentadiene, 1,2,5,5-tetramethyl-</td><td align="center" valign="middle" >13.534</td><td align="center" valign="middle" >61,177</td><td align="center" valign="middle" >21,525</td></tr><tr><td align="center" valign="middle" >4H-Pyran-4-one, 2,3-dihydro-3,5-dihydroxy-6-methyl-</td><td align="center" valign="middle" >14.305</td><td align="center" valign="middle" >256,448</td><td align="center" valign="middle" >42,365</td></tr><tr><td align="center" valign="middle" >(S)-(+)-1-(2-Pyrrolidinylmethyl)-pyrrolidine</td><td align="center" valign="middle" >16.45</td><td align="center" valign="middle" >61,558</td><td align="center" valign="middle" >9967</td></tr><tr><td align="center" valign="middle" >1-Butanol, 3-methyl-, acetate</td><td align="center" valign="middle" >16.837</td><td align="center" valign="middle" >323,177</td><td align="center" valign="middle" >32,881</td></tr><tr><td align="center" valign="middle" >12-Hydroxy-3-keto-bisnor-4-cholenic acid</td><td align="center" valign="middle" >17.889</td><td align="center" valign="middle" >361,988</td><td align="center" valign="middle" >59,190</td></tr><tr><td align="center" valign="middle" >Heptane, 4,4-dimethyl-</td><td align="center" valign="middle" >3.153</td><td align="center" valign="middle" >1,603,394</td><td align="center" valign="middle" >1,044,918</td></tr><tr><td align="center" valign="middle" >Benzene, 1,3-dimethyl-</td><td align="center" valign="middle" >4.445</td><td align="center" valign="middle" >50,368</td><td align="center" valign="middle" >25,880</td></tr><tr><td align="center" valign="middle" >4,4-Dimethyl octane</td><td align="center" valign="middle" >5.202</td><td align="center" valign="middle" >7,576,894</td><td align="center" valign="middle" >3,621,189</td></tr><tr><td align="center" valign="middle" >8-Hydroxy-2,2,8-trimethyldeca-5,9-dien-3-one</td><td align="center" valign="middle" >12.63</td><td align="center" valign="middle" >64,037</td><td align="center" valign="middle" >22,688</td></tr><tr><td align="center" valign="middle" >1,3-Cyclopentadiene, 5,5-dimethyl-2-ethyl-</td><td align="center" valign="middle" >13.533</td><td align="center" valign="middle" >2,937,389</td><td align="center" valign="middle" >917,337</td></tr><tr><td align="center" valign="middle"  colspan="4"  >Rumex vesicarius</td></tr><tr><td align="center" valign="middle" >2-Propanone, 1,1-dimethoxy-</td><td align="center" valign="middle" >3.159</td><td align="center" valign="middle" >120,361</td><td align="center" valign="middle" >59,949</td></tr><tr><td align="center" valign="middle" >2-Propenoic acid, butyl ester</td><td align="center" valign="middle" >5.049</td><td align="center" valign="middle" >45,284</td><td align="center" valign="middle" >18,451</td></tr><tr><td align="center" valign="middle" >2,4-Dihydroxy-2,5-dimethyl-3(2H)-furan-3-one</td><td align="center" valign="middle" >7.563</td><td align="center" valign="middle" >43,099</td><td align="center" valign="middle" >12,345</td></tr><tr><td align="center" valign="middle" >5H-1-Pyrindine</td><td align="center" valign="middle" >11.5</td><td align="center" valign="middle" >393,080</td><td align="center" valign="middle" >105,109</td></tr><tr><td align="center" valign="middle" >4H-Pyran-4-one, 2,3-dihydro-3,5-dihydroxy-6-methyl-</td><td align="center" valign="middle" >14.313</td><td align="center" valign="middle" >372,536</td><td align="center" valign="middle" >62,756</td></tr><tr><td align="center" valign="middle" >1-Heptanol, 3-methyl-</td><td align="center" valign="middle" >16.45</td><td align="center" valign="middle" >83,592</td><td align="center" valign="middle" >10,852</td></tr><tr><td align="center" valign="middle" >Octane, 1-ethoxy-</td><td align="center" valign="middle" >16.6</td><td align="center" valign="middle" >221,363</td><td align="center" valign="middle" >15,146</td></tr><tr><td align="center" valign="middle" >1-Butanol, 3-methyl-, acetate</td><td align="center" valign="middle" >16.992</td><td align="center" valign="middle" >617,214</td><td align="center" valign="middle" >38,696</td></tr><tr><td align="center" valign="middle" >9-Octadecenoic acid, (2-phenyl-1,3-dioxolan-4-yl)methyl ester, trans-</td><td align="center" valign="middle" >17.198</td><td align="center" valign="middle" >462,205</td><td align="center" valign="middle" >44,485</td></tr><tr><td align="center" valign="middle" >Sulfurous acid, hexyl 2-propyl ester</td><td align="center" valign="middle" >17.475</td><td align="center" valign="middle" >51,454</td><td align="center" valign="middle" >6142</td></tr><tr><td align="center" valign="middle" >Heptane, 4,4-dimethyl-</td><td align="center" valign="middle" >3.159</td><td align="center" valign="middle" >1,645,515</td><td align="center" valign="middle" >1,120,801</td></tr><tr><td align="center" valign="middle" >Undecane</td><td align="center" valign="middle" >5.206</td><td align="center" valign="middle" >7,634,942</td><td align="center" valign="middle" >3,654,061</td></tr><tr><td align="center" valign="middle" >Butane, 2,2-dimethyl-</td><td align="center" valign="middle" >12.64</td><td align="center" valign="middle" >36,668</td><td align="center" valign="middle" >11,532</td></tr><tr><td align="center" valign="middle" >n-Tridecan-1-ol</td><td align="center" valign="middle" >16.537</td><td align="center" valign="middle" >814,164</td><td align="center" valign="middle" >42,294</td></tr><tr><td align="center" valign="middle" >5,8-Decadien-2-one, 5,9-dimethyl-, (E)-</td><td align="center" valign="middle" >17.895</td><td align="center" valign="middle" >387,599</td><td align="center" valign="middle" >71,229</td></tr><tr><td align="center" valign="middle"  colspan="4"  >Senna alexandrina</td></tr><tr><td align="center" valign="middle" >Furan, 2-butyltetrahydro-</td><td align="center" valign="middle" >3.153</td><td align="center" valign="middle" >11,528</td><td align="center" valign="middle" >8192</td></tr><tr><td align="center" valign="middle" >2-Propanone, 1,1-dimethoxy-</td><td align="center" valign="middle" >3.349</td><td align="center" valign="middle" >203,673</td><td align="center" valign="middle" >78,579</td></tr><tr><td align="center" valign="middle" >Acetic acid, butyl ester</td><td align="center" valign="middle" >3.467</td><td align="center" valign="middle" >39,942</td><td align="center" valign="middle" >9713</td></tr><tr><td align="center" valign="middle" >2-Propenoic acid, butyl ester</td><td align="center" valign="middle" >5.145</td><td align="center" valign="middle" >182,112</td><td align="center" valign="middle" >49,726</td></tr><tr><td align="center" valign="middle" >2,4-Dihydroxy-2,5-dimethyl-3(2H)-furan-3-one</td><td align="center" valign="middle" >7.606</td><td align="center" valign="middle" >25,143</td><td align="center" valign="middle" >9151</td></tr><tr><td align="center" valign="middle" >Propanoic acid</td><td align="center" valign="middle" >8.055</td><td align="center" valign="middle" >38,578</td><td align="center" valign="middle" >15,228</td></tr><tr><td align="center" valign="middle" >1-Pentene, 4,4-dimethyl-</td><td align="center" valign="middle" >9.604</td><td align="center" valign="middle" >62,706</td><td align="center" valign="middle" >9678</td></tr><tr><td align="center" valign="middle" >Benzeneacetaldehyde</td><td align="center" valign="middle" >9.98</td><td align="center" valign="middle" >49,835</td><td align="center" valign="middle" >15,902</td></tr><tr><td align="center" valign="middle" >4H-Pyran-4-one, 2,3-dihydro-3,5-dihydroxy-6-methyl-</td><td align="center" valign="middle" >14.347</td><td align="center" valign="middle" >96,211</td><td align="center" valign="middle" >17,843</td></tr><tr><td align="center" valign="middle" >Octane, 2-chloro-</td><td align="center" valign="middle" >16.454</td><td align="center" valign="middle" >87,489</td><td align="center" valign="middle" >18,523</td></tr><tr><td align="center" valign="middle" >2-Hexanone</td><td align="center" valign="middle" >3.043</td><td align="center" valign="middle" >50,170</td><td align="center" valign="middle" >17,244</td></tr><tr><td align="center" valign="middle" >Heptane, 4,4-dimethyl-</td><td align="center" valign="middle" >3.197</td><td align="center" valign="middle" >2,060,280</td><td align="center" valign="middle" >1,357,310</td></tr><tr><td align="center" valign="middle" >Benzene, 1,3-dimethyl-</td><td align="center" valign="middle" >4.477</td><td align="center" valign="middle" >23,469</td><td align="center" valign="middle" >12,631</td></tr><tr><td align="center" valign="middle" >4,4-Dimethyl octane</td><td align="center" valign="middle" >5.229</td><td align="center" valign="middle" >9,288,316</td><td align="center" valign="middle" >4,340,129</td></tr><tr><td align="center" valign="middle" >Butane, 2,2-dimethyl-</td><td align="center" valign="middle" >12.645</td><td align="center" valign="middle" >40,835</td><td align="center" valign="middle" >14,779</td></tr><tr><td align="center" valign="middle"  colspan="4"  >Rhazya stricta</td></tr><tr><td align="center" valign="middle" >2-Propanone, 1,1-dimethoxy-</td><td align="center" valign="middle" >3.133</td><td align="center" valign="middle" >25,949</td><td align="center" valign="middle" >13,582</td></tr><tr><td align="center" valign="middle" >2-Propanone, 1,1-dimethoxy-</td><td align="center" valign="middle" >3.171</td><td align="center" valign="middle" >37,558</td><td align="center" valign="middle" >21,506</td></tr><tr><td align="center" valign="middle" >Acetic acid, butyl ester</td><td align="center" valign="middle" >3.311</td><td align="center" valign="middle" >28,369</td><td align="center" valign="middle" >9479</td></tr><tr><td align="center" valign="middle" >2-Propenoic acid, butyl ester</td><td align="center" valign="middle" >5.057</td><td align="center" valign="middle" >51,816</td><td align="center" valign="middle" >19,997</td></tr><tr><td align="center" valign="middle" >2,4-Dihydroxy-2,5-dimethyl-3(2H)-furan-3-one</td><td align="center" valign="middle" >7.564</td><td align="center" valign="middle" >62,619</td><td align="center" valign="middle" >15,279</td></tr><tr><td align="center" valign="middle" >Acetic acid, pentyl ester</td><td align="center" valign="middle" >12.475</td><td align="center" valign="middle" >99,794</td><td align="center" valign="middle" >8983</td></tr><tr><td align="center" valign="middle" >Diazene, bis(1,1-dimethylethyl)-</td><td align="center" valign="middle" >12.55</td><td align="center" valign="middle" >38,618</td><td align="center" valign="middle" >6718</td></tr><tr><td align="center" valign="middle" >4H-Pyran-4-one, 2,3-dihydro-3,5-dihydroxy-6-methyl-</td><td align="center" valign="middle" >14.315</td><td align="center" valign="middle" >326,506</td><td align="center" valign="middle" >59,466</td></tr><tr><td align="center" valign="middle" >Urazole</td><td align="center" valign="middle" >14.517</td><td align="center" valign="middle" >19,727</td><td align="center" valign="middle" >4249</td></tr><tr><td align="center" valign="middle" >Diisopropyl(methoxy)silane</td><td align="center" valign="middle" >15.054</td><td align="center" valign="middle" >44,535</td><td align="center" valign="middle" >12,398</td></tr><tr><td align="center" valign="middle" >Heptane, 4,4-dimethyl-</td><td align="center" valign="middle" >3.218</td><td align="center" valign="middle" >2,326,418</td><td align="center" valign="middle" >1,594,435</td></tr><tr><td align="center" valign="middle" >Ethylbenzene</td><td align="center" valign="middle" >4.317</td><td align="center" valign="middle" >4953</td><td align="center" valign="middle" >7110</td></tr><tr><td align="center" valign="middle" >Benzene, 1,3-dimethyl-</td><td align="center" valign="middle" >4.492</td><td align="center" valign="middle" >25,204</td><td align="center" valign="middle" >13,065</td></tr><tr><td align="center" valign="middle" >Undecane</td><td align="center" valign="middle" >5.242</td><td align="center" valign="middle" >10,019,914</td><td align="center" valign="middle" >4,839,199</td></tr><tr><td align="center" valign="middle" >Pentane, 2,2-dimethyl-</td><td align="center" valign="middle" >12.644</td><td align="center" valign="middle" >44,962</td><td align="center" valign="middle" >15,107</td></tr><tr><td align="center" valign="middle"  colspan="4"  >Withania somnifera</td></tr><tr><td align="center" valign="middle" >2-Propanone, 1,1-dimethoxy-</td><td align="center" valign="middle" >3.298</td><td align="center" valign="middle" >166,182</td><td align="center" valign="middle" >69,608</td></tr><tr><td align="center" valign="middle" >Acetic acid, butyl ester</td><td align="center" valign="middle" >3.411</td><td align="center" valign="middle" >28,083</td><td align="center" valign="middle" >10,727</td></tr><tr><td align="center" valign="middle" >2-Propenoic acid, butyl ester</td><td align="center" valign="middle" >5.117</td><td align="center" valign="middle" >165,834</td><td align="center" valign="middle" >55,952</td></tr><tr><td align="center" valign="middle" >Pyridine, 3-ethyl-</td><td align="center" valign="middle" >6.883</td><td align="center" valign="middle" >34,106</td><td align="center" valign="middle" >9710</td></tr><tr><td align="center" valign="middle" >2,4-Dihydroxy-2,5-dimethyl-3(2H)-furan-3-one</td><td align="center" valign="middle" >7.595</td><td align="center" valign="middle" >27,639</td><td align="center" valign="middle" >9230</td></tr><tr><td align="center" valign="middle" >Propanoic acid</td><td align="center" valign="middle" >8.048</td><td align="center" valign="middle" >30,208</td><td align="center" valign="middle" >11,163</td></tr><tr><td align="center" valign="middle" >Formic acid, 2-propylpentyl ester</td><td align="center" valign="middle" >9.576</td><td align="center" valign="middle" >57,843</td><td align="center" valign="middle" >12,413</td></tr><tr><td align="center" valign="middle" >4H-Pyran-4-one, 2,3-dihydro-3,5-dihydroxy-6-methyl-</td><td align="center" valign="middle" >14.332</td><td align="center" valign="middle" >154,754</td><td align="center" valign="middle" >30,031</td></tr><tr><td align="center" valign="middle" >Acetate, 2-hydroxy-2-(3-chloro-4,5-dihydro-5-isoxazolyl)-, ethyl ester</td><td align="center" valign="middle" >15.072</td><td align="center" valign="middle" >39,594</td><td align="center" valign="middle" >12,349</td></tr><tr><td align="center" valign="middle" >1-Heptanol, 3-methyl-</td><td align="center" valign="middle" >16.458</td><td align="center" valign="middle" >37,852</td><td align="center" valign="middle" >13,249</td></tr><tr><td align="center" valign="middle" >Heptane, 4,4-dimethyl-</td><td align="center" valign="middle" >3.159</td><td align="center" valign="middle" >1,616,307</td><td align="center" valign="middle" >1,104,565</td></tr><tr><td align="center" valign="middle" >p-Xylene</td><td align="center" valign="middle" >4.45</td><td align="center" valign="middle" >22,523</td><td align="center" valign="middle" >11,159</td></tr><tr><td align="center" valign="middle" >Undecane</td><td align="center" valign="middle" >5.205</td><td align="center" valign="middle" >7,482,419</td><td align="center" valign="middle" >3,490,731</td></tr><tr><td align="center" valign="middle" >Pentane, 2,2-dimethyl-</td><td align="center" valign="middle" >12.637</td><td align="center" valign="middle" >39,647</td><td align="center" valign="middle" >11,939</td></tr><tr><td align="center" valign="middle" >Phenol, 5-methyl-2-(1-methylethyl)-, acetate</td><td align="center" valign="middle" >16.478</td><td align="center" valign="middle" >176,498</td><td align="center" valign="middle" >11,942</td></tr><tr><td align="center" valign="middle"  colspan="4"  >Asphodelus fistulosus</td></tr><tr><td align="center" valign="middle" >2-Propanone, 1,1-dimethoxy-</td><td align="center" valign="middle" >3.346</td><td align="center" valign="middle" >294,890</td><td align="center" valign="middle" >93,973</td></tr><tr><td align="center" valign="middle" >3-Furanmethanol</td><td align="center" valign="middle" >4.529</td><td align="center" valign="middle" >133,436</td><td align="center" valign="middle" >26,256</td></tr><tr><td align="center" valign="middle" >2-Propenoic acid, butyl ester</td><td align="center" valign="middle" >5.134</td><td align="center" valign="middle" >202,046</td><td align="center" valign="middle" >54,975</td></tr><tr><td align="center" valign="middle" >2,4-Dihydroxy-2,5-dimethyl-3(2H)-furan-3-one</td><td align="center" valign="middle" >7.59</td><td align="center" valign="middle" >60,182</td><td align="center" valign="middle" >15,462</td></tr><tr><td align="center" valign="middle" >Formic acid, 2-propylpentyl ester</td><td align="center" valign="middle" >9.565</td><td align="center" valign="middle" >100,012</td><td align="center" valign="middle" >17,130</td></tr><tr><td align="center" valign="middle" >4H-Pyran-4-one, 2,3-dihydro-3,5-dihydroxy-6-methyl-</td><td align="center" valign="middle" >14.347</td><td align="center" valign="middle" >299,297</td><td align="center" valign="middle" >40,393</td></tr><tr><td align="center" valign="middle" >Phosphonofluoridic acid, methyl-, 3,3-dimethylbutyl ester</td><td align="center" valign="middle" >14.562</td><td align="center" valign="middle" >147,540</td><td align="center" valign="middle" >24,060</td></tr><tr><td align="center" valign="middle" >dl-Erythro-O-methylthreonine</td><td align="center" valign="middle" >15.892</td><td align="center" valign="middle" >105,398</td><td align="center" valign="middle" >12,480</td></tr><tr><td align="center" valign="middle" >1H,5H,7H,11H-Dipyrazolo[1,2-a:1',2'-d][1,2,4,5] tetrazine, tetrahydro-</td><td align="center" valign="middle" >16.11</td><td align="center" valign="middle" >78,817</td><td align="center" valign="middle" >9909</td></tr><tr><td align="center" valign="middle" >1-Heptanol, 3-methyl-</td><td align="center" valign="middle" >16.454</td><td align="center" valign="middle" >68,031</td><td align="center" valign="middle" >16,568</td></tr><tr><td align="center" valign="middle" >Heptane, 4,4-dimethyl-</td><td align="center" valign="middle" >3.19</td><td align="center" valign="middle" >1,949,351</td><td align="center" valign="middle" >1,309,283</td></tr><tr><td align="center" valign="middle" >p-Xylene</td><td align="center" valign="middle" >4.47</td><td align="center" valign="middle" >25,669</td><td align="center" valign="middle" >11,960</td></tr><tr><td align="center" valign="middle" >Undecane</td><td align="center" valign="middle" >5.223</td><td align="center" valign="middle" >8,546,527</td><td align="center" valign="middle" >4,089,618</td></tr><tr><td align="center" valign="middle" >Pentane, 2,2-dimethyl-</td><td align="center" valign="middle" >12.641</td><td align="center" valign="middle" >44,432</td><td align="center" valign="middle" >13,159</td></tr><tr><td align="center" valign="middle" >(SS)- or (RR)-2,3-hexanediol</td><td align="center" valign="middle" >15.29</td><td align="center" valign="middle" >13,811</td><td align="center" valign="middle" >5761</td></tr></tbody></table></table-wrap><p>Propanone, 1,1-dimethoxy-, 1,2,4-Benzenetricarboxylic acid, 1,2-dimethyl ester,3-Hexanol, 2-methyl-, 2-Propenoic acid, butyl ester, 2-Butenoic acid, 2-methyl-, (Z)-, 5H-1-Pyrindine, Acrylic acid, (5-cyclopropylidenepentyl) ester, 1,3-Cyclopentadiene, 1,2,5,5-tetramethyl-, 1,3-Cyclopentadiene, 1,2,5,5-tetramethyl-, 2-Hydroxy-2,6-dimethyl-hept-6-en-3-one, Heptane, 4,4-dimethyl-, Ethylbenzene, Ethanone, 1-cyclobutyl-, 4,4-Dimethyl octane, Pentane, 2,2-dimethyl- and Heptane, 4,4-dimethyl.</p><p>The GC-MS analysis of H. arbainense, was shown in <xref ref-type="table" rid="table4">Table 4</xref> and <xref ref-type="fig" rid="fig5">Figure 5</xref> the compounds found were Butanoic acid, anhydride, 2-Propanone, 1,1-dimethoxy-Acetic acid, butyl ester, 2-Propenoic acid, butyl ester, 1,3-Cyclopentadiene, 1,2,5,5-tetramethyl, 1,3-Dioxolane-2-methanol, Bicyclo [2.2.1]heptane, 2-(2-propenyl), 1-Undecene, 9-methyl, Isophthalaldehyde, 4,6-Heptadienoic acid, 3,3,6-trimethyl-, ethyl ester Heptane, 4,4-dimethyl, Ethylbenzene, Undecane, 3-Hexanone, 2,5-dimethyl and Phenol, 3-(1,1-dimethylethyl)-4-methoxy.</p><p>Fifteen compounds (2-Propanone, 1,1-dimethoxy-, 2-Propenoic acid, butyl ester, 2-Butenoic acid, 2-methyl-, (Z)-, 2,4-Dihydroxy-2,5-dimethyl-3(2H)-furan-3-one, 5H-1-Pyrindine, 1,3-Cyclopentadiene, 1,2,5,5-tetramethyl, 4H-Pyran-4-one, 2,3-dihydro-3,5-dihydroxy-6-methyl, (S)-(+)-1-(2-Pyrrolidinylmethyl)-pyrrolidine, 1-Butanol, 3-methyl-, acetate, 12-Hydroxy-3-keto-bisnor-4-cholenic acid, Heptane, 4,4-dimethyl, Benzene, 1,3-dimethyl, 4,4-Dimethyl octane, 8-Hydroxy-2,2,8-trimethyldeca-5,9-dien-3-one, 1,3-Cyclopentadiene, 5,5-dimethyl-2-ethyl-) ware appear from C. grandiflorus extract, the data reported in <xref ref-type="table" rid="table4">Table 4</xref> and <xref ref-type="fig" rid="fig6">Figure 6</xref>.</p><p>Results revealed in <xref ref-type="table" rid="table4">Table 4</xref> and <xref ref-type="fig" rid="fig7">Figure 7</xref> the identification of 15 compounds (2-Propanone, 1,1-dimethoxy-, 2-Propenoic acid, butyl ester, 2,4-Dihydroxy-2,5-dimethyl-3(2H)-furan-3-one, 5H-1-Pyrindine, 4H-Pyran-4-one, 2,3-dihydro-3,5-dihydroxy-6-methyl-, 1-Heptanol, 3-methyl-, Octane, 1-ethoxy-, 1-Bu-tanol, 3-methyl-, acetate, 9-Octadecenoic acid, (2-phenyl-1,3-dioxolan-4-yl) methyl ester, trans-, Sulfurous acid, hexyl 2-propyl ester, Heptane, 4,4-dimethyl, Undecane, Butane, 2,2-dimethyl-, n-Tridecan-1-ol, 5,8-Decadien-2-one and 5,9-dimethyl-) in R. vesicarius extract. Previous phytochemical investigation revealed the presence of anthraquinones, flavonoids and minerals.</p><p>The GC/MS data and spectrum of the chemical constituents in ethanol extract of S. alexandrina are shown in <xref ref-type="table" rid="table4">Table 4</xref> and <xref ref-type="fig" rid="fig8">Figure 8</xref> The chromatogram showed that ethanol leaf fraction contained 15 compounds and they are Furan, 2-butyltetrahydro-, 2-Propanone, 1,1-dimethoxy, Acetic acid, butyl ester, 2-Propenoic acid, butyl ester 2,4-Dihydroxy-2,5-dimethyl-3(2H)-furan-3-one, Propanoic acid, 1-Pentene, 4,4-dimethyl, Benzeneacetaldehyde 4H-Pyran-4-one, 2,3-dihydro-3,5-dihydroxy-6-methyl, Octane, 2-chloro, 2-Hexanone, Heptane, 4,4-dimethyl, Butane, Benzene, 1,3-dimethyl, 4,4-Dimethyl octane, 2,2-dimethyl.</p><p>We detected 15 peaks associated with segregated constituents by GC−MS in the R. stricta extract. Composites are listed in <xref ref-type="table" rid="table4">Table 4</xref> and <xref ref-type="fig" rid="fig9">Figure 9</xref>. 2-Propanone, 1,1-dimethoxy, 2-Propanone, 1,1-dimethoxy, Acetic acid, butyl ester, 2-Propenoic acid, butyl ester, 2,4-Dihydroxy-2,5-dimethyl-3(2H)-furan-3-one, Acetic acid, pentyl ester, Diazene, bis(1,1-dimethylethyl), 4H-Pyran-4-one, 2,3-dihydro-3,5-dihydroxy-6-methyl, Urazole, Diisopropyl (methoxy)silane, Heptane, 4,4-dimethyl, Ethylbenzene, Benzene, 1,3-dimethyl, Undecane and Pentane, 2,2-dimethyl, were the major components present in the extract.</p><p>The GC/MS data and spectrum of the chemical constituents in ethanol extract of W. somnifera are shown in <xref ref-type="table" rid="table4">Table 4</xref> and <xref ref-type="fig" rid="fig1">Figure 1</xref>0 respectively.</p></sec><sec id="s4"><title>4. Discussion</title><p>Widely distributed in Central Asia and Southern Africa. In Saudi Arabia, they are grown in the Wadi Najran, Taif region, and Al Madinah Al Munawwarah (Abyar Al-Mashy) [<xref ref-type="bibr" rid="scirp.119514-ref13">13</xref>]. Teucrium polium L. occurs throughout the Mediterranean and Irano-Turanian regions [<xref ref-type="bibr" rid="scirp.119514-ref14">14</xref>]. In Saudi Arabia, it is widely distributed in Aljuf, Hail, and Al Madinah Al Munawwarah (Gabal Al-aquiq) [<xref ref-type="bibr" rid="scirp.119514-ref14">14</xref>]. Many of these Species that are distributed throughout the Kingdom have been used by the local communities for the treatment of a large number of ailments [<xref ref-type="bibr" rid="scirp.119514-ref15">15</xref>]. This result sagest the report of Migahid (16). Primary metabolic compounds are important compounds in the processes of transporting and storing energy, regulating growth and respiration, and they are the primary compounds to produce secondary metabolic compounds [<xref ref-type="bibr" rid="scirp.119514-ref30">30</xref>].</p><p>The protein parts are used as therapeutic agents in combination with other chemicals, which makes them have a high medicinal value [<xref ref-type="bibr" rid="scirp.119514-ref30">30</xref>]. In <xref ref-type="table" rid="table2">Table 2</xref> it shows the changes in the soluble proline content of different plant species, the largest amount of which was retained significantly, and the highest plant was R. vesicarius it is very clear, and the lowest plant are P. incisa and A. fistulosus. Low levels of proline ensure that girls are in a favorable environment that is not subject to stress [<xref ref-type="bibr" rid="scirp.119514-ref31">31</xref>].</p><p>On the other hand, the result in <xref ref-type="table" rid="table2">Table 2</xref> shows the decrease in the amino acid content in P. incise, H. arbainense and C. grandiflorus, and then the observed increase in the plant sample R. vesicarius and S. alexandrina then the average decrease in the rest of the samples. Amino acids are the main component of protein, contribute to cellular digestion and osmotic pressure, and are an essential component in the synthesis of the alkaloid secondary metabolite, which gives it medicinal value in therapeutic uses [<xref ref-type="bibr" rid="scirp.119514-ref32">32</xref>]. Also, the result shows the decrease in carbohydrate content in the plant samples and the observed increase in the plant sample A. fistulosus then S. alexandrina. The carbohydrate content in the plant affects the plant’s immunity, and it has sugar molecules that can be extracted and used to increase the plant’s immunity and protect it from diseases [<xref ref-type="bibr" rid="scirp.119514-ref33">33</xref>].</p><p>The result in <xref ref-type="table" rid="table3">Table 3</xref> showed secondary compounds in the ethanol plant extract, the result clears that, phytosterol compound appeared in all plant extract, which this compound has types as sitosterol and stigmasterol usually abundant in many plant foods such as fruits and vegetables and has a common role in reducing harmful cholesterol (LDL) [<xref ref-type="bibr" rid="scirp.119514-ref34">34</xref>]. Thus, protects against many heart and cancer diseases [<xref ref-type="bibr" rid="scirp.119514-ref35">35</xref>]. All plant samples have triterpenoids compound. This compound has played several roles in immunity against bacteria and allergies, the most important of which is regulating and controlling the proliferation of cancer cells [<xref ref-type="bibr" rid="scirp.119514-ref36">36</xref>]. The results are agreement with Pathak who suggested that quantitative phytochemical study indicated an appreciable number of polyphenols, flavonoids, flavonols, proanthocyanidins, tannins, saponins and alkaloids. The presence of these phytochemicals has been reported to exert profound stabilizing effect on lysosomal membrane while tannins and saponins bind cations, thereby stabilizing erythrocyte membranes and other biological macromolecules [<xref ref-type="bibr" rid="scirp.119514-ref37">37</xref>].</p><p>Alkaloids are known anti-inflammatory effects. Flavonoid and phenolic compounds are potent antioxidants which prevent oxidative cell damage and possess anti-inflammatory, anti-allergic and anti-thrombotic [<xref ref-type="bibr" rid="scirp.119514-ref38">38</xref>]. Proanthocyanidins are a type of bioflavonoid that has been shown to have very potent antioxidant activity [<xref ref-type="bibr" rid="scirp.119514-ref39">39</xref>]. Previous studies had also shown that plant extracts possessing anti-inflammatory properties may contain phytochemicals with antioxidant activity against deleterious chain reactions triggered by reactive oxygen species associated with inflammations [<xref ref-type="bibr" rid="scirp.119514-ref40">40</xref>].</p><p>Some plant samples haves saponins compound this benefit in role of lowering cholesterol and regulating glucose in the blood, which makes it anti-diabetic [<xref ref-type="bibr" rid="scirp.119514-ref41">41</xref>]. Plants differed in flavonoid content and were only in plant R. vesicarius, P. incisa and S. alexandrina. It protects against cell damage, cancer, and liver diseases, and helps in the dilation of blood vessel [<xref ref-type="bibr" rid="scirp.119514-ref42">42</xref>]. And has antioxidant activity [<xref ref-type="bibr" rid="scirp.119514-ref43">43</xref>]. The coumarin compound appeared in all the samples it’s benefit as an anti-inflammatory and usually found in the peels of fruits; it gives role in protecting and preservation them from rotting [<xref ref-type="bibr" rid="scirp.119514-ref44">44</xref>]. Also gives the samples a distinctive aromatic smell upon concentration varies, and this effective compound is useful in the perfume industry [<xref ref-type="bibr" rid="scirp.119514-ref1">1</xref>]. The tannin compound has many uses in dyes and leather tanning [<xref ref-type="bibr" rid="scirp.119514-ref45">45</xref>], health benefits as antioxidant, anti-allergic, anti-helminthic and usually us as astringent [<xref ref-type="bibr" rid="scirp.119514-ref46">46</xref>]. There are a number of reports on the phytochemical constituents of Pulicariaincisa. The presences of Sixty-six compounds representing 89.4% of total oil were identified. The main components were α-Ocimene (15.17%), τ-Cadinol (6.79%), α-Cadinol (4.51%), Alloaromadendrene (4.45%) δ-Cadinene, (+) - (4.13% [<xref ref-type="bibr" rid="scirp.119514-ref29">29</xref>]. Some more reports indicate the presence of compounds such as dl-limonene, bcaryophyllene, 5, 30-dihydroxy-3, 7, 40, 50-tetramethoxy flavone, myricetin-7,30,40-trimethyl ether, and a di-C-glycosyl flavone, vicenin 3 [<xref ref-type="bibr" rid="scirp.119514-ref29">29</xref>]. For example, the study of Muhammad [<xref ref-type="bibr" rid="scirp.119514-ref46">46</xref>] a large number of extracts and bioactive constituents of different species of genus Heliotropium revealed significant biological activities such as antimicrobial, antitumor, antiviral, antiinflammatory, wound healing, cytotoxicity and phytotoxicity [<xref ref-type="bibr" rid="scirp.119514-ref47">47</xref>].</p><p>This is in accordance with the previous findings with respect sample, where had major quantitative changes in C. digitatum after processing; a special combinations of volatile compounds which gives the aroma of the processed C. digitatum have also other benefits as functional food ingredients; some of them with additional activity as natural food additives, analgesic or antioxidant which participate in the reasonably high antioxidant capacity of C. digitatum that were previously determined [<xref ref-type="bibr" rid="scirp.119514-ref48">48</xref>]. However, the hepatic protective activity of R. vesicarius extract was not previously studied [<xref ref-type="bibr" rid="scirp.119514-ref49">49</xref>]. Chemical composition: Senna contains anthraquinonoid compounds flavonoid, saccharide, naphthalene derivatives, phytosterols, essential oils, waxes, tannins, mineral salts, resins, and mucilage [<xref ref-type="bibr" rid="scirp.119514-ref50">50</xref>]. These values are considered high when compared to other plants, corresponding to a previous work [<xref ref-type="bibr" rid="scirp.119514-ref51">51</xref>]. Iqbal et al. have reported that the antioxidant capability of the methanolic extracts of R. stricta leaves was significantly elevated when compared to the α-tocopherol or the synthetic antioxidant BHA [<xref ref-type="bibr" rid="scirp.119514-ref51">51</xref>]. Another study conducted in Saudi Arabia has demonstrated the high TPC of R. stricta extract [<xref ref-type="bibr" rid="scirp.119514-ref52">52</xref>].</p><p>The chromatogram showed that ethanol leaf fraction contained 15 compounds and they are 2-Propanone, 1,1-dimethoxy-, Acetic acid, butyl ester, 2-Propenoic acid, butyl ester, Pyridine, 3-ethyl-2,4-Dihydroxy-2,5-dimethyl-3(2H)-furan-3-one Propanoic acid, Formic acid, 2-propylpentyl ester, 4H-Pyran-4-one, 2,3-dihydr-3,5-dihydroxy-6-methyl-Acetate, 2-hydroxy-2-(3-chloro-4,5-dihydro-5-isoxazolyl)-, ethyl ester, 1-Heptanol, 3-methyl-, Heptane, 4,4-dimethyl-p-Xylene, Undecane, Pentane, 2,2-dimethyl-Phenol and 5-methyl-2-(1-methylethyl)-, acetate. The chemistry of Withania species has been extensively studied and several groups of chemical constituents such as steroidal lactones, alkaloids, flavonoids, and tannins have been extracted and identified [<xref ref-type="bibr" rid="scirp.119514-ref53">53</xref>]. A qualitative analysis of constituents present in ethanol extract was performed by GC/MS. As shown in <xref ref-type="table" rid="table4">Table 4</xref> and <xref ref-type="fig" rid="fig1">Figure 1</xref>1, the full scan revealed the presence of several phenolic compounds, based on the over15 major peaks detected. 2-Propanone, 1,1-dimethoxy-, 3-Furanmethanol, 2-Propenoic acid, butyl ester, 2,4-Dihydroxy-2,5-dimethyl-3(2H)-furan-3-one, Formic acid, 2-propylpentyl ester, 4H-Pyran-4-one, 2,3-dihydro-3,5-dihydroxy-6-methyl-Phosphonofluoridic acid, methyl-, 3,3-dimethylbutyl ester, dl-Erythro-O-methyl threonine, 1H,5H,7H,11H-Dipyrazolo [1,2-a:1',2'-d][1, 2,4,5]tetrazine, tetrahydro, 1-Heptanol, 3-methyl, Heptane, 4,4-dimethyl, p-Xylene Undecane, Pentane, 2,2-dimethyl- and (SS)- or (RR)-2,3-hexanediol. In fact, different results obtained from lyophilized samples of A. tenuifolius harvested from septentrional Algerian Sahara [<xref ref-type="bibr" rid="scirp.119514-ref54">54</xref>].</p></sec><sec id="s5"><title>5. Conclusion and Recommendation</title><p>Medicinal plants are of great medicinal and nutritional importance, as they highly contain content of proteins and secondary compounds of phytosterols, triterpenoids, tannins, etc. That extracted from leaves, enabling them to be used in several cosmetic, medicinal, and commercial fields. Alkaloid compound, which makes them anti-diseases and the most prominent role of them is to be a rich source for the manufacture of pharmaceutical drugs and vitamins. Phytochemical screening is an important step in the detection of the bioactive components existing in medicinal plants that are used in traditional medicine. There is a need to focus phytochemical screening on ethnobotanical studies to complete research into traditional medicine which leads to the discovery of new drugs. The flora of Kingdom of Saudi Arabia contains many medicinal plants, some of them were studied in research to discover their importance, and the field is still open for many studies to identify the important components in these plants and how to use them in industry to produce medical and cosmetic materials that benefit humanity.</p></sec><sec id="s6"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s7"><title>Cite this paper</title><p>Alsaedi, S. and Aljeddani, G. (2022) Phytochemical Analysis and Bioactivity Screening of Primary and Secondary Metabolic Products of Medicinal Plants in the Valleys of Medina Region Saudi Arabia. Advances in Biological Chemistry, 12, 92-115. https://doi.org/10.4236/abc.2022.124009</p></sec></body><back><ref-list><title>References</title><ref id="scirp.119514-ref1"><label>1</label><mixed-citation publication-type="book" xlink:type="simple">Hussein, R.A. and El-Anssary, A.A. (2019) Plants Secondary Metabolites: The Key Drivers of the Pharmacological Actions of Medicinal Plants. In: Builders, P.F., Ed., Herbal Medicine, IntechOpen, London, 11-30. https://doi.org/10.5772/intechopen.76139</mixed-citation></ref><ref id="scirp.119514-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Vieira, A.A. (2010) Comparison of Traditional Anti-Inflammation and Anti-Infection Medicinal Plants with Current Evidence from Biomedical Research: Results from a Regional Study. 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