Author/Authors :
Tatar, Esra Marmara University - Faculty of Pharmacy - Department of Pharmaceutical Chemistry, Turkey , Küçükgüzel, İlkay Marmara University - Faculty of Pharmacy - Department of Pharmaceutical Chemistry, Turkey , Clercq, Erik De Katholieke Universiteit - Rega Institute for Medical Research, Belgium , Krishnan, Ramalingam University of Medicine and Dentistry of New Jersey - Medical School - Department of Biochemistry and Molecular Biology, USA , Kaushik-Basu, Neerja University of Medicine and Dentistry of New Jersey - Medical School - Department of Biochemistry and Molecular Biology, USA
Title Of Article :
Synthesis, characterization and antiviral evaluation of 1,3-Thiazolidine-4-one derivatives bearing L-Valine side chain
شماره ركورد :
18741
Abstract :
1,3-Thiazolidine-4-ones have been known to possess anti-HIV and anti-HCV activity as they are, respectively, HIV-1 non-nucleoside reverse transcriptase inhibitors and HCV NS5B RNA-dependent RNA-polymerase inhibitors. Some novel 1-[2-(benzoylamino)- 3-methylbutyryl]-4-alkyl/arylalkylthiosemicarbazides, 2-[2-(benzoylamino)-3-methylbutyrylhydrazono]- 3-alkyl-/arylalkyl- 5-non substituted/methyl-1,3-thiazolidinones, were synthesized and evaluated for their antiviral activity. Antiviral activity of the synthesized compounds were screened against various types of viruses (Feline Corona Virus (FIPV), Feline Herpes Virus, HSV-1(KOS), HSV-1(TK-KOS ACVr), HSV-2(G), Vaccinia virus, Vesicular stomatitis virus, Varicella- ZosterVirus TK+VZV, Varicella-ZosterVirus TK-VZV, Cytomegalovirus, Respiratory syncytial virus, Coxsackie B4 virus, Parainfluenza-3 virus, Reovirus-1, Sindbis virus and Punta Toro virus) in CRFK, HEL, HeLa and Vero cell cultures. Anti-HIV and cytotoxicity data were also obtained with the compounds using the strains HIV-1 (IIIB) and HIV-2 (ROD) in an MT-4/MTT based assay. None of the tested compounds showed antiviral activity at subtoxic concentrations. For all the synthesized compounds anti-HCV NS5B RdRp activity was not observed at the concentration of 100 μM which was the highest concentration tested.
From Page :
181
NaturalLanguageKeyword :
4 , Thiazolidinones , L , valine , anti , HIV activity , anti , HCV activity
JournalTitle :
Journal of Research in Pharmacy
To Page :
193
Link To Document :
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