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Chemical Structure : Motesanib diphosphate
CAS No.: 857876-30-3
Catalog No.: PC-42472Not For Human Use, Lab Use Only.
A potent, orally bioavailable, multikinase inhibitor inhibitor of VEGFR1/2/3, PDGFR and c-Kit with IC50 of 2-6 nM, 84 nM and 8 nM, respectively.
| Packing | Price | Stock | Quantity |
|---|---|---|---|
| 50 mg | $128 | In stock | |
| 100 mg | $224 | In stock |
Bulk size, bulk discount!
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A potent, orally bioavailable, multikinase inhibitor inhibitor of VEGFR1/2/3, PDGFR and c-Kit with IC50 of 2-6 nM, 84 nM and 8 nM, respectively; also displays activity against Ret (IC50=59 nM), no activities against EGFR, Src, and p38; inhibits human endothelial cell proliferation induced by VEGF, but not by bFGF in vitro; potently inhibits VEGF-induced angiogenesis in the rat models.
Lung Cancer
Phase 3 Discontinued
| M.Wt | 569.4413 | |
| Formula | C22H29N5O9P2 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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| Chemical Name/SMILES |
3-Pyridinecarboxamide, N-(2,3-dihydro-3,3-dimethyl-1H-indol-6-yl)-2-[(4-pyridinylmethyl)amino]-, phosphate (1:2) |
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1. Polverino A, et al. Cancer Res. 2006 Sep 1;66(17):8715-21.
2. Sherman SI, et al. N Engl J Med. 2008 Jul 3;359(1):31-42.
3. Coxon A, et al. lin Cancer Res. 2009 Jan 1;15(1):110-8.
4. Caenepeel S, et al. J Exp Clin Cancer Res. 2010 Jul 15;29:96.
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