Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/5060
Title: Antimycobacterial compounds. Optimization of the BM212 structure, the lead compound for a new pyrrole derivative class
Authors: Biava, M
Porretta, Gc
Poce, G
Deidda, D
Pompei, R
Tafi, Andrea 
Manetti, Fabrizio 
Keywords: Antimycobacterial activity; Pharmacophore model; Pyrrole derivatives; , Thiomorpholinomethyl substituent
Issue Date: 2005
Project: None 
Journal: BIOORGANIC & MEDICINAL CHEMISTRY
Abstract: 
Our work on antitubercular agents led to the identification of BM 212 as a lead compound among a series of pyrrole derivatives with good in vitro activity against mycobacteria and candidae. Further studies led us to synthesize additional pyrroles bearing the thiomorpholinomethyl moiety and different aryl substituents at N1 and C5. Some of them revealed very active, prompting us to design the new pyrrole derivatives 5-20 in the hope of increasing the activity and better understanding the influence of ortho halogens on the antimycobacterial activity. Microbiological data showed interesting in vitro activity toward Mycobacterium tuberculosis and atypical mycobacteria.
Description: 
36856
URI: http://hdl.handle.net/20.500.12779/5060
ISSN: 0968-0896
DOI: 10.1016/j.bmc.2004.11.018
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