| Company Name: |
TargetMol |
| Tel: |
400-821-0310 15002144251 |
| Email: |
xuexiang.shao@tsbiochem.com |
|
| | CytochroMe P450 14a-deMethylase inhibitor 1h Basic information |
| | CytochroMe P450 14a-deMethylase inhibitor 1h Chemical Properties |
| Melting point | 67.3-68.8 °C | | Boiling point | 590.771±60.00 °C(Press: 760.00 Torr)(predicted) | | density | 1.379±0.14 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted) | | pka | 11.925±0.29(predicted) |
| | CytochroMe P450 14a-deMethylase inhibitor 1h Usage And Synthesis |
| Uses | CYP51-IN-2 (compound 1h), a Fluconazole (HY-B0101) analog, is a potent antifungal agent. CYP51-IN-2 shows MIC80s of 15.6 and 62.5 ng/mL for Microsporum gypseum and Candida albicans, respectively[1]. | | References | [1] Chai X, et, al. Design, synthesis, and biological evaluation of novel triazole derivatives as inhibitors of cytochrome P450 14alpha-demethylase. Eur J Med Chem. 2009 May;44(5):1913-20. DOI:10.1016/j.ejmech.2008.11.007 |
| | CytochroMe P450 14a-deMethylase inhibitor 1h Preparation Products And Raw materials |
|