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1,4-Benzothiazine and 1,4-benzoxazine imidazole derivatives with antifungal activity: a docking study.

作者信息

Macchiarulo Antonio, Costantino Gabriele, Fringuelli Daniele, Vecchiarelli Anna, Schiaffella Fausto, Fringuelli Renata

机构信息

Department of Drug Chemistry and Technology, Via del Liceo 1, University of Perugia, Perugia, Italy.

出版信息

Bioorg Med Chem. 2002 Nov;10(11):3415-23. doi: 10.1016/s0968-0896(02)00263-8.

Abstract

We have recently described the synthesis and antifungal activity of a series of 1,4-benzothiazine and 1,4-benzoxazine imidazole derivatives that mainly showed in vivo activity against a murine experimental model of candidiasis but that very often lacked in vitro activity. Here, we report a docking study of a representative set of our molecules in a 3D model of CYP51 of Candida albicans (CA-CYP51). The model was constructed on the basis of the sequence homology relationship with the recently reported crystal structure of the CYP51 of Mycobacterium tuberculosis (MT- CYP51).

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