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| Product | Description | |
|---|---|---|
| ZM 336372 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| ZM 336372 | Cell-permeable. A potent, selective and ATP-competitive inhibitor of c-Raf in vitro (IC50 = 70nM for inhibition of human c-Raf). Displays 10-fold selectivity over B-Raf. Also inhibits SAPK2/p38 (IC50= 2uM). Group: Biochemicals. Alternative Names: 3- (Dimethylamino) -N- [3- [ (4-hydroxybenzoyl) -amino] -4-methylphenyl] benzamide. Grades: Highly Purified. CAS No. 208260-29-1. Pack Sizes: 1mg. US Biological Life Sciences. |  Worldwide |
| ZM 336372 | ZM 336372 is a potent inhibitor of the protein kinase c-Raf. The IC 50 value is 0.07 μM in the standard assay, which contains 0.1 mM ATP. Uses: Scientific research. Group: Signaling pathways. CAS No. 208260-29-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-13343. |  |
| ZM 336372 - CAS 208260-29-1 | A potent, cell-permeable, reversible, ATP-competitive and specific inhibitor of the protein kinase c-Raf (IC?? = 70 nM). Group: Fluorescence/luminescence spectroscopy. | |
| ZM336372 | ZM336372 is a Raf-1 activating agent, has been shown to cause growth inhibition and suppression of hormone secretion in a neuroendocrine cell line. ZM336372 causes growth inhibition, suppression of hormone secretion, and up-regulation of cell cycle inhibitors in a human hepatocellular carcinoma cell line, similar to that previously seen in NETs. Synonyms: ZM-336372; ZM 336372. Grades: 0.98. CAS No. 208260-29-1. Molecular formula: C23H23N3O3. Mole weight: 389.45. |  |
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