Document Detail


Researches on antibacterial and antifungal agents. I. Analogs of nalidixic acid with a pyrrole moiety.
MedLine Citation:
PMID:  6861999     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The synthesis and antibacterial activities of 4-hydroxyquinoline-3-carboxylic acid and 1,4-dihydro-1-ethyl-4-oxoquinoline-3-carboxylic acid containing a pyrrole or 2,5-dimethylpyrrole group at 6 position are reported. Reaction of 1-(4-aminophenyl)pyrrole or 2,5-dimethyl-1-(4-aminophenyl)-pyrrole with ethoxymethylenemalonate diethyl ester (EMME) afforded the related pyrroleanilinomethylenemalonates, which were subjected to thermal cyclization to give the required quinoline derivatives. These compounds on ethylation furnished at last the quinolonecarboxylic analogs of nalidixic acid.
Authors:
F Corelli; S Massa; G Stefancich; M Artico; S Panico; N Simonetti
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Il Farmaco; edizione scientifica     Volume:  38     ISSN:  0430-0920     ISO Abbreviation:  Farmaco Sci     Publication Date:  1983 Apr 
Date Detail:
Created Date:  1983-08-11     Completed Date:  1983-08-11     Revised Date:  2009-06-05    
Medline Journal Info:
Nlm Unique ID:  0370716     Medline TA:  Farmaco Sci     Country:  ITALY    
Other Details:
Languages:  eng     Pagination:  219-31     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Anti-Bacterial Agents / chemical synthesis*
Antifungal Agents / chemical synthesis*
Bacteria / drug effects
Chemical Phenomena
Chemistry
Nalidixic Acid / analogs & derivatives*,  chemical synthesis,  pharmacology
Chemical
Reg. No./Substance:
0/Anti-Bacterial Agents; 0/Antifungal Agents; 389-08-2/Nalidixic Acid

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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