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1.
J Med Chem ; 22(9): 1055-9, 1979 Sep.
Article in English | MEDLINE | ID: mdl-114657

ABSTRACT

Alcohol, ketone, aldehyde, and oxime analogues of ambruticin (1) were prepared. The analogues were tested against Histoplasma capsulatum, Microsporum fulvum, Candida albicans, and Streptococcus pyogenes. Structure-activity relationships are described. Increasing the bulk of substituent at C1 and C5 reduces antifungal activity.


Subject(s)
Antifungal Agents/chemical synthesis , Alcohols/chemical synthesis , Alcohols/pharmacology , Aldehydes/chemical synthesis , Aldehydes/pharmacology , Bacteria/drug effects , Fungi/drug effects , Ketones/chemical synthesis , Ketones/pharmacology , Myxococcales , Oximes/chemical synthesis , Oximes/pharmacology , Pyrans/chemical synthesis , Structure-Activity Relationship
2.
J Med Chem ; 22(9): 1144-7, 1979 Sep.
Article in English | MEDLINE | ID: mdl-114661

ABSTRACT

A series of ester and amide analogues of ambruticin (1) was prepared. The analogues were tested against Histoplasma capsulatum, Microsporum fulvum, Candida albicans and Streptococcus pyogenes. Structure-activity relationships are described.


Subject(s)
Amides/chemical synthesis , Antifungal Agents/chemical synthesis , Antifungal Agents/pharmacology , Bacteria/drug effects , Esters/chemical synthesis , Fungi/drug effects , Myxococcales , Pyrans/chemical synthesis , Pyrans/pharmacology , Structure-Activity Relationship
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