Fluconazole analogues containing 2H-1,4-benzothiazin-3(4H)-one or 2H-1,4-benzoxazin-3(4H)-one moieties, a novel class of anti-Candida agents

As a part of our program to develop new antifungal agents, a series of fluconazole analogues was designed and synthesized wherein one of the triazole moieties in fluconazole was replaced with 2H-1,4-benzothiazin-3(4H)-one or 2H-1,4-benzoxazin-3(4H)-one moiety. The new chemical entities thus synthesi...

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Veröffentlicht in:Bioorganic & medicinal chemistry letters 2010-01, Vol.20 (2), p.722-725
Hauptverfasser: BORATE, Hanumant B, MAUJAN, Suleman R, KUNTE, Sunita S, SAWARGAVE, Sangmeshwer P, CHANDAVARKAR, Mohan A, VAIUDE, Sharangi R, JOSHI, Vinay A, WAKHARKAR, Radhika D, IYER, Ramki, KELKAR, Ramesh G, CHAVAN, Subhash P
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Sprache:eng
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Zusammenfassung:As a part of our program to develop new antifungal agents, a series of fluconazole analogues was designed and synthesized wherein one of the triazole moieties in fluconazole was replaced with 2H-1,4-benzothiazin-3(4H)-one or 2H-1,4-benzoxazin-3(4H)-one moiety. The new chemical entities thus synthesized were screened against various fungi and it was observed that the compounds 4a and 4i are potent inhibitors of Candida strains. The structure-activity relationship for these compounds is discussed.
ISSN:0960-894X
1464-3405
DOI:10.1016/j.bmcl.2009.11.071