Description
B-Raf IN 1 inhibits both B-Raf and c-Raf, likely displaying anticancer activity.
| Product Unit Size | Cost | Quantity | Stock |
|---|
B-Raf IN 1 inhibits both B-Raf and c-Raf, likely displaying anticancer activity.
| Cas No. | 950736-05-7 |
|---|---|
| Purity | ≥98% |
| Formula | C29H24F3N5O |
| Formula Wt. | 515.54 |
| IUPAC Name | N-[3-(3-{4-[(Dimethylamino)methyl]phenyl}pyrazolo[1,5-a]pyrimidin-7-yl)phenyl]-3-(trifluoromethyl)benzamide |
| Solubility | DMSO: ≥ 53 mg/mL |
| Store Temp | -20°C |
|---|---|
| Ship Temp | Ambient |
| MSDS | |
|---|---|
| Info Sheet | |
| Brochures |
Berger DM, Torres N, Dutia M, et al. Non-hinge-binding pyrazolo[1,5-a]pyrimidines as potent B-Raf kinase inhibitors. Bioorg Med Chem Lett. 2009 Dec 1;19(23):6519-23. PMID: 19864136.
Isoquinoline alkaloid found in a variety of pla...
β-lactamase inhibitor.
Trichothecene mycotoxin produced by Fusarium, a...
Epoxomicin analog; proteasome inhibitor.
Triterpene sapogenin found in species of Panax;...
BH3 mimetic; Bcl-2 and Bcl-xl inhibitor.
Histamine H2 inverse agonist.
β1/2-adrenergic antagonist.
Fermentation impurity
Fluoroquinolone; topoisomerase IV and bacterial...
FAK inhibitor.
HDAC6 inhibitor.
Nucleoside (deoxyuridine) analog; DNA chain ter...
Mixture of glycopeptide bleomycin sulfate salts...
STING inhibitor
Endogenous peptide, involved in stress signalin...
Synthesis impurity
Optically active isomer of ibuprofen, NSAID; CO...
Type A trichothecene mycotoxin produced by Fusa...
Synthetic progestogen; PR agonist.