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Bertaccini, E.J. (2010) The Molecular Mechanisms of Anesthetic Action: Updates and Cutting Edge Developments from the Field of Molecular Modeling. Pharmaceuticals, 3, 2178-2196.
https://doi.org/10.3390/ph3072178

has been cited by the following article:

• TITLE: Molecular Similarity within Carcinogen and Guanine Cyclic Nucleotide Structures

  AUTHORS: Wynford Robert Williams

  KEYWORDS: Anesthetics, Cancer, Carcinogens, Guanosine Cyclic Monophosphate, Molecular Similarity

  JOURNAL NAME: Journal of Biosciences and Medicines, Vol.10 No.5, May 25, 2022

  ABSTRACT: Tumor promoters, apoptosis and autophagy modulators, chemotherapy drugs, and endogenous steroids demonstrate molecular similarity relative to cyclic nucleotide structure. This study explores relative molecular similarity within established human carcinogen structures using computational chemistry software. Molecular structures of conventional carcinogenic drugs and industrial agents demonstrate molecular similarity with a focus on the guanine base and nucleotide cyclized ring. Structures of volatile and gaseous anesthetic carcinogens do not conform to conventional 3-point pharmacophore-based fits characteristic of receptor-binding drugs. The results of this study provide some insight into how carcinogen structures may interact with endogenous compounds to disrupt cyclic nucleotide-driven homeostatic mechanisms.