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Design, synthesis, molecular docking and anti-hepatocellular carcinoma evaluation of novel acyclic pyridine thioglycosides
Journal article   Peer reviewed

Design, synthesis, molecular docking and anti-hepatocellular carcinoma evaluation of novel acyclic pyridine thioglycosides

Galal H. Elgemeie, Nahed M. Fathy, Ayman B. Farag and Sheikha A. Alkhursani
Nucleosides, nucleotides & nucleic acids, Vol.37(3), pp.186-198
04/03/2018
PMID: 29608403

Abstract

Acyclic pyridine thioglycosides anti-tumor activity cytotoxic activity docking studies thioglycosides thymidylate synthase dihydrofolate reductase (TS-DHFR)
A novel series of acyclic pyridine thioglycosides has been synthesized. Evaluation of the anti proliferative activity of these compounds against HEPG-2 cell lines (liver carcinoma cell lines) shows that most of the compounds have high anti-tumor activities especially 6b, 6c, 7b and 7c. Furthermore, in the modeling study, these compounds showed that they have high binding affinity with thymidylate synthase dihydrofolate reductase (TS-DHFR).

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