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| Product | Description | |
|---|---|---|
| L-779450 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| L-779450 | L-779450 is a potent, selective and ATP-competitive Raf kinase inhibitor (IC50 = 10 nM). L-779450 suppresses DNA synthesis and induces apoptosis in cells that proliferate in response to Raf-1 and A-Raf but not B-Raf. Synonyms: L-779450; L779450; L 779450; L-779,450; L 779,450; L779,450. Grades: >98%. CAS No. 303727-31-3. Molecular formula: C20H14ClN3O. Mole weight: 347.8. |  |
| L-779450 | Raf kinase inhibitor, a potential treatment for neurotraumatic diseases. Its effects also suppress DNA synthesis and induce apoptosis in targeted cells, presenting new applications in treating certain types of cancers. Group: Biochemicals. Alternative Names: 2-Chloro-5-[2-phenyl-5-(4-pyridinyl)-1H-imidazol-4-yl]phenol; 4-(4-Chloro-3-hydroxyphenyl)-2-phenyl-5-(4-pyridyl)-1H-imidazole. Grades: Highly Purified. CAS No. 303727-31-3. Pack Sizes: 10mg. US Biological Life Sciences. |  Worldwide |
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