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Agric Biol Chem ; 55(10): 2615-21, 1991 Oct.
Article in English | MEDLINE | ID: mdl-1368759

ABSTRACT

Starting from milbemycin D (1), milbemycin A4 (2) and milbemycin A3 (3), a series of 5-keto-5-oxime derivatives were synthesized by selective oximation at the alpha,beta-conjugated carbonyl function of the 5-ketomilbemycins (4-6). The activities of the synthesized compounds were studied in dogs naturally infested with microfilariae of Dirofilaria immitis. The 5-keto-5-oximes of milbemycin D (7), A4 (8) and A3 (9) had quite high efficacy to control the microfilariae and more potency than their parents, while the 5-O-acyl oximes (11-15) also exhibited high activity.


Subject(s)
Anti-Bacterial Agents/chemical synthesis , Dirofilaria immitis/drug effects , Dirofilariasis/drug therapy , Oximes/chemical synthesis , Animals , Anti-Bacterial Agents/pharmacology , Dogs , Macrolides , Microfilariae/drug effects , Oximes/pharmacology , Structure-Activity Relationship
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