Bioactivity:

Mefentrifluconazole is a potent, selective and orally active fungal CYP51 (Kd= 0.5 nM) inhibitor, but shows less inhibitory activity on human aromatase (IC50=0.92 _M).�Mefentrifluconazole is a novel azole derivative and used as an agrochemical broad-spect

CAS nr:

1417782-03-6

Purity:

98%

Molecular Weight:

397,78

SMILES:

OC(C)(C1=CC=C(OC2=CC=C(Cl)C=C2)C=C1C(F)(F)F)CN3N=CN=C3

Formula:

C18H15ClF3N3O2

Pathway:

Microbiology/Virology,Metabolism

Target:

Antifungal,P450