CytochroMe P450 14a-deMethylase inhibitor 1h

CytochroMe P450 14a-deMethylase inhibitor 1h Suppliers list
Company Name: Shanghai civi chemical technology co.,Ltd  
Tel: 86-21-34053660
Email: sale@labgogo.com
Company Name: TargetMol  
Tel: 400-821-0310 15002144251
Email: xuexiang.shao@tsbiochem.com
CytochroMe P450 14a-deMethylase inhibitor 1h Basic information
Product Name:CytochroMe P450 14a-deMethylase inhibitor 1h
Synonyms:CytochroMe P450 14a-deMethylase inhibitor 1h;1H-1,2,4-Triazole-1-ethanol, α-[[[(2-bromophenyl)methyl]-2-propen-1-ylamino]methyl]-α-(2,4-difluorophenyl)-;CYP51-IN-8
CAS:1155361-06-0
MF:C21H21BrF2N4O
MW:463.32
EINECS:
Product Categories:
Mol File:1155361-06-0.mol
CytochroMe P450 14a-deMethylase inhibitor 1h Structure
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)
pka11.925±0.29(predicted)
Safety Information
MSDS Information
CytochroMe P450 14a-deMethylase inhibitor 1h Usage And Synthesis
UsesCYP51-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
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