Why do aromatic interactions matter of compound: 86404-63-9

There is still a lot of research devoted to this compound(SMILES:FC1=CC=C(C(CN2N=CN=C2)=O)C(F)=C1)SDS of cas: 86404-63-9, and with the development of science, more effects of this compound(86404-63-9) can be discovered.

SDS of cas: 86404-63-9. The reaction of aromatic heterocyclic molecules with protons is called protonation. Aromatic heterocycles are more basic than benzene due to the participation of heteroatoms. Compound: 1-(2,4-Difluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanone, is researched, Molecular C10H7F2N3O, CAS is 86404-63-9, about Improved model of lanosterol 14α-demethylase by ligand-supported homology modeling: validation by virtual screening and azole optimization. Author is Sheng, Chunquan; Wang, Wenya; Che, Xiaoying; Dong, Guoqiang; Wang, Shengzheng; Ji, Haitao; Miao, Zhenyuan; Yao, Jianzhong; Zhang, Wannian.

Lanosterol 14α-demethylase (CYP51) is an important target for antifungal drugs. An improved three-dimensional model of CYP51 from Candida albicans (CACYP51) was constructed by ligand-supported homol. modeling and mol. dynamics simulations. The accuracy of the constructed model was evaluated by its performance in a small-scale virtual screen. The results show that known CYP51 inhibitors were efficiently discriminated by the model, and it performed better than our previous CACYP51 model. The active site of CACYP51 was characterized by multiple copy simultaneous search (MCSS) calculations On the basis of the MCSS results, a series of novel azoles were designed and synthesized, and they showed good in vitro antifungal activity with a broad spectrum. The MIC80 value of four of these compounds against C. albicans is 0.001 μg mL-1, indicating that they are promising leads for the discovery of novel antifungal agents.

There is still a lot of research devoted to this compound(SMILES:FC1=CC=C(C(CN2N=CN=C2)=O)C(F)=C1)SDS of cas: 86404-63-9, and with the development of science, more effects of this compound(86404-63-9) can be discovered.

Reference:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics