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Highly lipophilic benzoxazoles with potential antibacterial activity
J. Vinšová, V. Horák, V. Buchta, J. Kaustová
Jazyk angličtina Země Švýcarsko
Grantová podpora
1A8238
MZ0
CEP - Centrální evidence projektů
NLK
Directory of Open Access Journals
od 1997
Free Medical Journals
od 1997
PubMed Central
od 2001
Europe PubMed Central
od 2001
ProQuest Central
od 1997-01-01
Open Access Digital Library
od 1997-01-01
Health & Medicine (ProQuest)
od 1997-01-01
PubMed
18007347
DOI
10.3390/10070783
Knihovny.cz E-zdroje
- MeSH
- antibakteriální látky farmakologie MeSH
- antifungální látky farmakologie MeSH
- antituberkulotika farmakologie MeSH
- benzoxazoly farmakologie chemie MeSH
- financování organizované MeSH
- isomerie MeSH
- isoniazid farmakologie MeSH
- molekulární konformace MeSH
- molekulární modely MeSH
- Mycobacterium tuberculosis účinky léků MeSH
- rozpustnost MeSH
- vztahy mezi strukturou a aktivitou MeSH
A series of lipophilic 2-substituted 5,7-di-tert-butylbenzoxazoles was prepared in average yields by the reaction of 3,5-di-tert-butyl-1,2-benzoquinone with amino acids and dipeptides bearing N-terminal glycine. Dipeptides having other N-terminal amino acids undergo oxidative deamination. 5,7-Di-tert-butylbenzoxazoles have shown activity against Mycobacterium tuberculosis and some nontuberculous strains where isoniazid has been inactive. Antifungal activity was mediocre.
Citace poskytuje Crossref.org
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- $a A series of lipophilic 2-substituted 5,7-di-tert-butylbenzoxazoles was prepared in average yields by the reaction of 3,5-di-tert-butyl-1,2-benzoquinone with amino acids and dipeptides bearing N-terminal glycine. Dipeptides having other N-terminal amino acids undergo oxidative deamination. 5,7-Di-tert-butylbenzoxazoles have shown activity against Mycobacterium tuberculosis and some nontuberculous strains where isoniazid has been inactive. Antifungal activity was mediocre.
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