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KP-103, a novel topical antifungal triazole: structure-activity relationships of azolylamine derivatives.

Ogura H, Kobayashi H, Nagai K, Nishida T, Naito T, Tatsumi Y, Yokoo M, Arika T; Interscience Conference on Antimicrobial Agents and Chemotherapy.

Abstr Intersci Conf Antimicrob Agents Chemother Intersci Conf Antimicrob Agents Chemother. 1996 Sep 15-18; 113 (abstract no. F78).

Kaken Pharmaceutical Company, LTD., Kyoto, Japan.

In a search for an antifungal agent, we have prepared a variety of new azolylamine derivatives with general formula (I) and measured in vitro activity. MIC values (micrograms/ml) were shown below. (Table: see text) We found that the cyclic amine having methylene group at the 3 position is necessary for a broad antifungal spectrum and a potent activity. KP-103 which has a (2R,3R)-absolute configuration and a 4-methylenepiperidine moiety, showed the most potent activity and significantly lower MIC values than clotrimazole (CTZ). (Table: see text).

Publication Types:
  • Meeting Abstracts
Keywords:
  • Antifungal Agents
  • Clotrimazole
  • In Vitro
  • KP 103
  • Miconazole
  • Microbial Sensitivity Tests
  • Structure-Activity Relationship
  • Triazoles
Other ID:
  • 98927675
UI: 102234849

From Meeting Abstracts




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