Macchiarulo Antonio, Costantino Gabriele, Fringuelli Daniele, Vecchiarelli Anna, Schiaffella Fausto, Fringuelli Renata
Department of Drug Chemistry and Technology, Via del Liceo 1, University of Perugia, Perugia, Italy.
Bioorg Med Chem. 2002 Nov;10(11):3415-23. doi: 10.1016/s0968-0896(02)00263-8.
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).