Chemical Structure : Motesanib
CAS No.: 453562-69-1
货号: PC-42471Not For Human Use, Lab Use Only.
Motesanib (AMG706) is 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.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
10 mg | ¥580 | In stock | |
25 mg | ¥880 | In stock | |
50 mg | ¥1280 | In stock | |
100 mg | ¥1980 | In stock | |
250 mg | Get quote |
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Motesanib (AMG706) is 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.
Motesanib (AMG706) also displays activity against Ret (IC50=59 nM), no activities against EGFR, Src, and p38.
Motesanib (AMG706) inhibits human endothelial cell proliferation induced by VEGF, but not by bFGF in vitro.
Motesanib (AMG706) potently inhibits VEGF-induced angiogenesis in the rat models.
分子量 | 373.4509 | |
分子式 | C22H23N5O | |
外观性状 | Solid | |
储存条件 |
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Solubility |
DMSO: ≥ 30 mg/mL |
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Chemical Name/SMILES |
3-Pyridinecarboxamide, N-(2,3-dihydro-3,3-dimethyl-1H-indol-6-yl)-2-[(4-pyridinylmethyl)amino]- |
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. Clin 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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