Abstract
In the search for effective, selective, and nontoxic antiviral and antitumor agents, a variety of strategies have been devised to design nucleoside analogues. Here we have described the versatile synthesis of β-L-1,3- thiazolidine nucleoside analogues. These analogues are all derived from the key stereochemically defined intermediate Ntert- butoxy-carbonyl-4-hydroxymethyl-1,3-thiazolidine-2-ol which was accessible in 57% yield starting from L-Cysteine methylester hydrochloride. N-tert-butoxycarbonyl-2-acyloxy-4-trityloxymethyl-1,3-thiazolidine was coupled with the pyrimidine bases in the presence of Lewis acids stannic chloride or trimethyl silyl triflate following Vorbruggen procedure. Proof of the structure and configuration was obtained through 1H NMR, 13C NMR, Mass, elemental analysis and NOE experiments. Docking and antitumor activity of these nucleoside analogues are also reported.
Keywords: β-L-1,3-thiazolidine nucleoside analogues, docking, EAC model, anti-tumor activity
Medicinal Chemistry
Title: Synthesis, Docking and Anti-Tumor Activity of β-L-1,3-Thiazolidine Pyrimidine Nucleoside Analogues
Volume: 3 Issue: 5
Author(s): Shimoga Nagaraj Sriharsha, Karkala Sreedhara Ranganath Pai, Suhas, Sheena Shashikanth, Nagasuma Chandra and Kandigere Ramaiah Prabhu
Affiliation:
Keywords: β-L-1,3-thiazolidine nucleoside analogues, docking, EAC model, anti-tumor activity
Abstract: In the search for effective, selective, and nontoxic antiviral and antitumor agents, a variety of strategies have been devised to design nucleoside analogues. Here we have described the versatile synthesis of β-L-1,3- thiazolidine nucleoside analogues. These analogues are all derived from the key stereochemically defined intermediate Ntert- butoxy-carbonyl-4-hydroxymethyl-1,3-thiazolidine-2-ol which was accessible in 57% yield starting from L-Cysteine methylester hydrochloride. N-tert-butoxycarbonyl-2-acyloxy-4-trityloxymethyl-1,3-thiazolidine was coupled with the pyrimidine bases in the presence of Lewis acids stannic chloride or trimethyl silyl triflate following Vorbruggen procedure. Proof of the structure and configuration was obtained through 1H NMR, 13C NMR, Mass, elemental analysis and NOE experiments. Docking and antitumor activity of these nucleoside analogues are also reported.
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Cite this article as:
Sriharsha Nagaraj Shimoga, Ranganath Pai Sreedhara Karkala, Suhas , Shashikanth Sheena, Chandra Nagasuma and Prabhu Ramaiah Kandigere, Synthesis, Docking and Anti-Tumor Activity of β-L-1,3-Thiazolidine Pyrimidine Nucleoside Analogues, Medicinal Chemistry 2007; 3 (5) . https://dx.doi.org/10.2174/157340607781745500
DOI https://dx.doi.org/10.2174/157340607781745500 |
Print ISSN 1573-4064 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6638 |
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