| Literature DB >> 3005577 |
M Ogata, H Matsumoto, S Shimizu, S Kida, T Wada, M Shiro, K Sato.
Abstract
To find antiviral agents, various sulfonamidobenzophenone oximes (II) were synthesized from the appropriate m-sulfonamidobenzophenones by hydroxylamine reaction. The reaction products were generally obtained as syn/anti mixtures which were separable by fractional crystallization. The anti isomer had more potent antipoliovirus activity than the syn isomer. Various sulfonamidobenzamides (III) which were structurally related to II were synthesized by the reactions of amino-substituted benzamides with sulfuryl chloride or amines with (aminosulfonyl)benzoyl chloride. Antiviral activity was examined by the plaque-inhibition test. Compounds 5, 36, and 69 exhibited strong antipicornavirus activity. The structure-activity relationships are discussed.Entities:
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Year: 1986 PMID: 3005577 DOI: 10.1021/jm00153a018
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446