Synthesis, antioxidant, and cytotoxic activities of n-azole substituted thiomorpholine Derivatives

12Citations
Citations of this article
12Readers
Mendeley users who have this article in their library.
Get full text

Abstract

A new class of N-azole substituted thiomorpholine derivatives were prepared and their antioxidant and cytotoxic activities were studied. The methyl substituted oxazolyl thiomorpholine dioxide 9b exhibited radical scavenging activity greater than the standard ascorbic acid. On the other hand, the thiazolyl thiomorpholine 10c having a chloro substituent on the aromatic ring was identified as a remarkable lead molecule for cytotoxic activity against A549 and HeLa cells, with IC50 values of 10.1 and 30.0 μM, respectively. A new series of N-azole substituted thiomorpholine derivatives were prepared to study their antioxidant and cytotoxic activities. The methyl substituted oxazolyl thiomorpholine dioxide 9b exhibited excellent radical scavenging activity greater than ascorbic acid. The thiazolyl thiomorpholine 10c showed noticeable cytotoxic activity against A549 and HeLa cells. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Cite

CITATION STYLE

APA

Reddy, P. R., Reddy, G. M., Padmaja, A., Padmavathi, V., Kondaiah, P., & Krishna, N. S. (2014). Synthesis, antioxidant, and cytotoxic activities of n-azole substituted thiomorpholine Derivatives. Archiv Der Pharmazie, 347(3), 221–228. https://doi.org/10.1002/ardp.201300299

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free