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| Product | Description | |
|---|---|---|
| Telatinib | Telatinib (Bay 57-9352) is an orally active, small molecule inhibitor of VEGFR2 , VEGFR3 , PDGFα , and c-Kit with IC 50 s of 6, 4, 15 and 1 nM, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Bay 57-9352. CAS No. 332012-40-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10527. |  |
| Telatinib | Telatinib is a potent inhibitor of VEGFR2/3, c-Kit and PDGFRα with IC50 of 6 nM/4 nM, 1 nM and 15 nM, respectively. Synonyms: BAY 57-9352; BAY579352; BAY-57-9352. Grades: >98%. CAS No. 332012-40-5. Molecular formula: C20H16ClN5O3. Mole weight: 409.83. |  |
| Telatinib mesylate | Telatinib mesylate (Bay 57-9352 mesylate) is a potent and orally active VEGFR2 , VEGFR3 , PDGFα , and c-Kit inhibitor with IC 50 s of 6 nM, 4 nM, 15 nM and 1 nM, respectively [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Bay 57-9352 mesylate. CAS No. 332013-26-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10527C. | |
| 17-AAG (17-allylamino-17-demethoxygeldanamycin, Telatinib, Tanespimycin, NSC-330507, CNF-101, KOS-953, GLD-36, CP 127374) | Semi-synthetic derivative of geldanamycin, demonstrating greater stability and lower in vivo toxicity than its parent compound. 17-AAG binds specifically to heat shock protein Hsp90 in a manner similar to geldanamycin, but the binding is weaker. Group: Biochemicals. Grades: Highly Purified. CAS No. 75747-14-7. Pack Sizes: 250mg. US Biological Life Sciences. |  Worldwide |
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