Biological evaluation of isothiazoloquinolones containing aromatic heterocycles at the 7-position: In vitro activity of a series of potent antibacterial agents that are effective against methicillin-resistant Staphylococcus aureus.
Bioorg Med Chem Lett
; 16(5): 1277-81, 2006 Mar 01.
Article
in En
| MEDLINE
| ID: mdl-16337789
We synthesized a diverse series of 9H-isothiazolo[5,4-b]quinoline-3,4-diones containing heteroaromatic groups at the 7-position via palladium-catalyzed cross-coupling. Many of these compounds demonstrated potent antistaphylococcal activity (MICs 2 microg/mL) against a multi-drug-resistant strain (ATCC 700699) and low cytotoxic activity (CC(50)>100 microM) against the human cell line Hep2 (laryngeal carcinoma).
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Staphylococcus aureus
/
Sulfhydryl Compounds
/
Azo Compounds
/
Methicillin Resistance
/
Quinolones
/
Anti-Bacterial Agents
Limits:
Humans
Language:
En
Journal:
Bioorg Med Chem Lett
Journal subject:
BIOQUIMICA
/
QUIMICA
Year:
2006
Document type:
Article
Affiliation country:
United States
Country of publication:
United kingdom