Synthesis, Characterization and Anti-HIV Evaluation of Some Novel 2-(substitutedphenyl)-5-methyl-3-(pyridin-4-yl)-1,3-thiazolidin-4-ones

A series of novel 2-(substituted phenyl)-5-methyl-3-(pyridin-4-yl)-1,3-thiazolidin-4-ones (4a-g) were synthesized, structurally confirmed by elemental analysis, IR, 1H NMR and MS spectral analysis, further evaluated for their anti-HIV activity and cytotoxicity in MT-4 cells infected with wild-type HIV-1 strain IIIB and HIV-2 strain ROD in comparison with nevirapine (NVP), azidothymidine (AZT), dideoxycytidine (DDC) and dideoxyinosine (DDI), which were used as reference drugs. The experimental results indicated that none of the synthesized compounds inhibited the replication of HIV-1 (IIIB) and HIV-2 (ROD) in MT-4 cell cultures at subtoxic concentration.

Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2024-12-11
DOI
https://doi.org/10.5281/zenodo.14382287
Primary Topic
Synthesis and biological activity
Type
article
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article

Synthesis, Characterization and Anti-HIV Evaluation of Some Novel 2-(substitutedphenyl)-5-methyl-3-(pyridin-4-yl)-1,3-thiazolidin-4-ones

Zenodo (CERN European Organization for Nuclear Research)
Synthesis and biological activity
article

Synthesis, Characterization and Anti-HIV Evaluation of Some Novel 2-(substitutedphenyl)-5-methyl-3-(pyridin-4-yl)-1,3-thiazolidin-4-ones

article en

Abstract

A series of novel 2-(substituted phenyl)-5-methyl-3-(pyridin-4-yl)-1,3-thiazolidin-4-ones (4a-g) were synthesized, structurally confirmed by elemental analysis, IR, 1H NMR and MS spectral analysis, further evaluated for their anti-HIV activity and cytotoxicity in MT-4 cells infected with wild-type HIV-1 strain IIIB and HIV-2 strain ROD in comparison with nevirapine (NVP), azidothymidine (AZT), dideoxycytidine (DDC) and dideoxyinosine (DDI), which were used as reference drugs. The experimental results indicated that none of the synthesized compounds inhibited the replication of HIV-1 (IIIB) and HIV-2 (ROD) in MT-4 cell cultures at subtoxic concentration.

Zenodo (CERN European Organization for Nuclear Research)
Good health and well-being
Openalex Percentile: Top 59%
Synthesis and biological activity
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