Mefentrifluconazole is a novel azole derivative and used as an agrochemical broad-spectrum antifungal agent. 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 µM)[1].
Molecular Weight:
397.78
Purity:
99.61
CAS Number:
[1417782-03-6]
Formula:
C18H15ClF3N3O2
Target:
Cytochrome P450,Fungal
Application Notes:
MCE Product type: Reference compound
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