Development in research of CYP51 as the target of triazoles / 药学实践杂志
Journal of Pharmaceutical Practice
; (6): 106-109, 2016.
Article
Dans Zh
| WPRIM
| ID: wpr-790569
Responsable en Bibliothèque :
WPRO
ABSTRACT
Triazoles are the most widely used antifungal drugs in clinic with broad spectrum and high efficacy,which targets sterol 14α-demethylase (CYP51),an enzyme expressed by the gene EGR11,which is a key enzyme in the fungi ergos-terol biosynthesis.On the one hand,the CYP51 belongs to a transmembrane protein.It is difficult to get the exact functional structure conformation which becomes a big challenge for the development of new drugs.On the other hand,it becomes con-sensus that EGR11 exon mutation cause CYP51 structural change is one of the major reasons for antifungal drugs resistance. Therefore,study of the structural changes toward the antifungal drug resistance is quite important.The review authors have summarized the research progress on CYP51 over the recent years.
Texte intégral:
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Indice:
WPRIM
langue:
Zh
Texte intégral:
Journal of Pharmaceutical Practice
Année:
2016
Type:
Article