Synthesis And In Vitro Antitumor Activity Of New Nicotinyl-Rhodanine Derivatives
Keywords:
Rhodanine Derivatives, Nicotinaldehydes, Synthesis, Antitumor Activity, Structure-Activity Relations.Abstract
A series of new nicotinyl-rhodanine derivatives were synthesized by condensing various chloronicotinaldehydes with rhodanine and substituted rhodanines. The in vitro antitumor activity for these compounds was screened against MCF-7, A549 and HT29 human cancer cell lines. The results show that compounds 1, 3, 5, 7, 8 and 9 are more potent against MCF-7 cell lines; compounds 9 and 11 are more potent against A549 cell lines; compound 3 is more potent against HT29 cell lines amongst the 14 nicotinyl-rhodanine compounds synthesized. The relationships between structure and antitumor activity were elucidated.
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Published
31.12.2011
How to Cite
BODDU ANANDA RAO, RAVINDRA SINGH RAJPOOT, V. G. M. NAIDU, KOLUPULA SRINIVAS, SISTLA RAMAKRISHNA, & VAIDYA JAYATHIRTHA RAO. (2011). Synthesis And In Vitro Antitumor Activity Of New Nicotinyl-Rhodanine Derivatives. International Journal of Pharma and Bio Sciences, 2(4), 191–202. Retrieved from https://ijpbs.net/index.php/journal/article/view/1012
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