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.
Synthetic quinone CoQ analog, promotes mitochon...
Endogenous cardiomodulatory peptide; NPR-A agon...
Endogenous peptide neurotransmitter, involved i...
Antacid; pepsin inhibitor. Assay (Polysaccharid...
Recombinant HCV antigen fragment.
Chaetocin is naturally produced by Chaetomium s...
Endogenous peptide, involved in stress signalin...
Stem cell neurogenesis inducer.
Flavonol found in fruits and vegetables; COMT i...
Cysteine derivative found in Allium; NMDA NR2A/...
Endogenous pyrimidine base required for product...
Isoflavone daidzein derivative found in Puerari...
Mycotoxin produced by species of Fusarium; pote...
Dibenzofuran produced by lichens.
Wnt/beta-catenin/CBP inhibitor
NSAID; COX-1/2 inhibitor.
Pt-based DNA cross-linker.
Resveratrol prodrug; potential SIRT1 activator....
Antioxidant; Nrf2 activator.
Synthetic peptice; μOR agonist.