Synthesis and antiproliferative effect of novel 4-thiazolidinone-, pyridine- and piperazine-based conjugates on human leukemic cells
Data(s) |
2014
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Resumo |
The present work reveals the synthesis and antiproliferative effect of a series of 2, 3 disubstituted 4-thiazolidinone analogues on human leukemic cells. The chemical structures of newly synthesized compounds were confirmed by IR, H-1 NMR, C-13 NMR and mass spectral analysis. Compound methyl 3-methoxy-4-(4-oxo-3-(5-(piperazin-1-yl)pyridin-2-yl)thiazolidin-2-yl)be nzoate (5) displayed potent activity (IC50 9.71, 15.24 and 19.29 mu M) against Nalm6, K562, Jurkat cells. Cell cycle analysis and mitochondrial membrane potential further confirmed that compound 5 is cytotoxic and able to induce cell death. (C) 2014 Elsevier Masson SAS. All rights reserved. |
Formato |
application/pdf |
Identificador |
http://eprints.iisc.ernet.in/49595/1/eur_jou_med_che_81_341_2014.pdf Kumar, Kothanahally Sharath S and Hanumappa, Ananda and Hegde, Mahesh and Narasimhamurthy, Kereyagalahally H and Raghavan, Sathees C and Rangappa, Kanchugarakoppal S (2014) Synthesis and antiproliferative effect of novel 4-thiazolidinone-, pyridine- and piperazine-based conjugates on human leukemic cells. In: EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 81 . pp. 341-349. |
Relação |
http://dx.doi.org/ 10.1016/j.ejmech.2014.05.009 http://eprints.iisc.ernet.in/49595/ |
Palavras-Chave | #Biochemistry |
Tipo |
Journal Article PeerReviewed |