WARNING: This product is for research use only, not for human or veterinary use.
MedKoo CAT#: 407227
CAS#: 1370001-71-0
Description: BMS-351 is a potent and selective, nonsteroidal CYP17A1 lyase inhibitor with robust selectivity over steroidogenic CYPs 21A2 and 11B1. BMS-351 emerges as an outstanding preclinical candidate to treat CRPC and is likely to minimize the side effects of current therapies due to its exceptional selectivity. BMS-351 is potentially useful for the Treatment of Prostate Cancer.
MedKoo Cat#: 407227
Name: BMS-351
CAS#: 1370001-71-0
Chemical Formula: C15H12F3N3
Exact Mass: 291.0983
Molecular Weight: 291.28
Elemental Analysis: C, 61.85; H, 4.15; F, 19.57; N, 14.43
BMS-351, purity > 98%, is not in stock, may be available through custom synthesis. For cost-effective reason, minimum 1 gram order is requested. The product will be characterized by NMR, HPLC and MS analysis. Purity (HPLC) is usually >98%. CoA, QC data, MSDS will be provided when product is successfully made. The estimated lead time is 2-3 months. Please send email to sales@medkoo.com to inquire quote.
Synonym: BMS-351; BMS 351; BMS351.
IUPAC/Chemical Name: 4-(4-methylpyridin-3-yl)-1-(2,2,2-trifluoroethyl)-1H-benzo[d]imidazole
InChi Key: OFFVLUDFSIUVMI-UHFFFAOYSA-N
InChi Code: InChI=1S/C15H12F3N3/c1-10-5-6-19-7-12(10)11-3-2-4-13-14(11)20-9-21(13)8-15(16,17)18/h2-7,9H,8H2,1H3
SMILES Code: FC(F)(F)CN1C2=CC=CC(C3=C(C)C=CN=C3)=C2N=C1
The following data is based on the product molecular weight 291.28 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 1.15 mL | 5.76 mL | 11.51 mL |
5 mM | 0.23 mL | 1.15 mL | 2.3 mL |
10 mM | 0.12 mL | 0.58 mL | 1.15 mL |
50 mM | 0.02 mL | 0.12 mL | 0.23 mL |
Audris Huang, Lata Jayaraman, Aberra Fura, Gregory D. Vite, George L. Trainor, Marco M. Gottardis, Thomas E. Spires, Vanessa M. Spires, Cheryl A. Rizzo, Mary T. Obermeier, Paul A. Elzinga, Gordon Todderud, Yi Fan, John A. Newitt, Sophie M. Beyer, Yongxin Zhu, Bethanne M. Warrack, Angela K. Goodenough, Andrew J. Tebben, Arthur M. Doweyko, David L. Gold, and Aaron Balog. Discovery of the Selective CYP17A1 Lyase Inhibitor BMS-351 for the Treatment of Prostate Cancer. ACS Med. Chem. Lett. Articles ASAP (As Soon As Publishable); Publication Date (Web): December 2, 2015 (Letter); DOI: 10.1021/acsmedchemlett.5b00310