Synthesis of progesterone heterocyclic derivatives of potential antimicrobial activity

17Citations
Citations of this article
23Readers
Mendeley users who have this article in their library.

Abstract

The aim of this work was to synthesize steroidal heterocycles and to elucidate the potential role of these compounds as antimicrobial agents. The synthesis of steroidal heterocycles containing the pyrazole, isoxazole, thiazole, pyrane, pyridine, pyridazine, or benzopyrane ring attached to the pregnene nucleus is reported. Progesterone (1) reacts with dimethyl formamide dimethyl acetal to form enamine 2. Heterocyclization of 2 with hydrazines, hydroxylamine, glycine, ethyl acetoacetate or cyanomethylene afforded novel steroidal heterocyclic derivatives. The in vitro antimicrobial evaluation showed that all synthesized compounds show activity against the used strains of Gram positive bacteria and fungi.

Cite

CITATION STYLE

APA

Mohareb, R. M., & Hana, H. Y. (2008). Synthesis of progesterone heterocyclic derivatives of potential antimicrobial activity. Acta Pharmaceutica, 58(1), 29–42. https://doi.org/10.2478/v10007-007-0043-3

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