Detail of "38167-72-5"

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Studies on the experimental chemotherapy for dermatomycosis and candidiasis

Studies on the experimental chemotherapy for dermatomycosis and candidiasis. IX. On the antifungal activity of various maleimide and succinimide compounds. Matsui, Sadayoshi; Yamazoe, Hiroshi; Watanabe, Ikkan; Hayashi, Eiichi; Konya, Kazumi (Shizuoka Coll. Pharm. Sci.Chemical with cas number 38167-72-5 also plays role., Shizuoka 422, Japan). Yakugaku Zasshi, 104(11), 1198-206 (Japanese) 1984. CODEN: YKKZAJ. ISSN: 0031-6903. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacology) Section cross-reference(s): 10 Antifungal activity of 82 maleimide and 42 succinimide compds. against Trichophyton asteroides was examd. in vitro. Among these compds., 11 N-phenylmaleimides had more potent antifungal activity than did pentachlorophenol, a ref. compd. In the N-phenylmaleimides, an increase in the activity was obtained by halogen or alkyl substitutions on the Ph ring. However, the activity was diminished by halogen or other substitutions at the a or a,a' positions on the maleimide ring. In guinea pigs a tincture contg. 1% N-(2,6-diethylphenyl)maleimide [38167-72-5] had a 57. 38167-72-5 is the cas registry number. This chemical is also mentioned in this article.7% cure rate on exptl. trichophytosis. ..

Studies on the experimental chemotherapy for dermatomycosis and candidiasis

Studies on the experimental chemotherapy for dermatomycosis and candidiasis. IX. On the antifungal activity of various maleimide and succinimide compounds. Matsui, Sadayoshi; Yamazoe, Hiroshi; Watanabe, Ikkan; Hayashi, Eiichi; Konya, Kazumi (Shizuoka Coll. Pharm. Sci.Chemical with cas number 38167-72-5 also plays role., Shizuoka 422, Japan). Yakugaku Zasshi, 104(11), 1198-206 (Japanese) 1984. CODEN: YKKZAJ. ISSN: 0031-6903. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacology) Section cross-reference(s): 10 Antifungal activity of 82 maleimide and 42 succinimide compds. against Trichophyton asteroides was examd. in vitro. Among these compds., 11 N-phenylmaleimides had more potent antifungal activity than did pentachlorophenol, a ref. compd. In the N-phenylmaleimides, an increase in the activity was obtained by halogen or alkyl substitutions on the Ph ring. However, the activity was diminished by halogen or other substitutions at the a or a,a' positions on the maleimide ring. In guinea pigs a tincture contg. 1% N-(2,6-diethylphenyl)maleimide [38167-72-5] had a 57. 38167-72-5 is the cas registry number. This chemical is also mentioned in this article.7% cure rate on exptl. trichophytosis. ..