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| Product | Description | |
|---|---|---|
| Enzastaurin | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| Enzastaurin | Enzastaurin. Group: Biochemicals. Alternative Names: 3-(1-Methyl-1H-indol-3-yl)-4-[1-[1-(2-pyridinylmethyl)-4-piperidinyl]-1H-indol-3-yl]-1H-pyrrole-2,5-dione. Grades: Highly Purified. CAS No. 170364-57-5. Pack Sizes: 25mg, 50mg, 100mg, 250mg, 500mg. Molecular Formula: C32H29N5O2. US Biological Life Sciences. |  Worldwide |
| Enzastaurin | Enzastaurin is a protein kinase C beta inhibitor with 6- to 20-fold selectivity against PKCα, PKCγ and PKC&epsilon. Binding to the ATP-binding site, enzastaurin selectively inhibits protein kinase C beta, an enzyme involved in the induction of vascular endothelial growth factor (VEGF)-stimulated neo-angiogenesis. This agent may decrease tumor blood supply and so tumor burden. Synonyms: 3-(1-Methyl-1H-indol-3-yl)-4-(1-(1-(pyridin-2-ylmethyl)piperidin-4-yl)-1H-indol-3-yl)-1H-pyrrole-2,5-dione; LY-317615. CAS No. 170364-57-5. Molecular formula: C32H29N5O2. Mole weight: 515.617. |  |
| Enzastaurin | Enzastaurin (LY317615) is a potent and selective PKCβ inhibitor with an IC 50 of 6 nM, showing 6- to 20-fold selectivity over PKCα, PKCγ and PKCε [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LY317615. CAS No. 170364-57-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-10342. |  |
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