Literature DB >> 11200287

Synthesis and structure activity relationships of 5-substituted-4'-thio-beta-D-arabinofuranosylcytosines.

K N Tiwari1, A T Shortnacy-Fowler, L Cappellacci, W R Waud, W B Parker, J A Montgomery, J A Secrist.   

Abstract

Four 5-substituted (chloro, fluoro, bromo, methyl) 1-(4-thio-beta-D-arabinofuranosyl)cytosines and their alpha anomers were synthesized by a facile route in high yields. All of these nucleosides were evaluated for cytotoxicity against a panel of human tumor cell lines in vitro. Only 5-fluoro-1-(4-thio-beta-D-arabinofuranosyl)cytosine was found to be highly cytotoxic in all the cell lines and was further evaluated in vivo.

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Year:  2000        PMID: 11200287     DOI: 10.1080/15257770008045474

Source DB:  PubMed          Journal:  Nucleosides Nucleotides Nucleic Acids        ISSN: 1525-7770            Impact factor:   1.381


  2 in total

1.  Inhibition of herpesvirus replication by 5-substituted 4'-thiopyrimidine nucleosides.

Authors:  Mark N Prichard; Debra C Quenelle; Caroll B Hartline; Emma A Harden; Geraldine Jefferson; Samuel L Frederick; Shannon L Daily; Richard J Whitley; Kamal N Tiwari; Joseph A Maddry; John A Secrist; Earl R Kern
Journal:  Antimicrob Agents Chemother       Date:  2009-09-21       Impact factor: 5.191

2.  Activities of certain 5-substituted 4'-thiopyrimidine nucleosides against orthopoxvirus infections.

Authors:  Earl R Kern; Mark N Prichard; Debra C Quenelle; Kathy A Keith; Kamal N Tiwari; Joseph A Maddry; John A Secrist
Journal:  Antimicrob Agents Chemother       Date:  2008-11-24       Impact factor: 5.191

  2 in total

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