Chemical Structure : R1530
CAS No.: 882531-87-5
Catalog No.: PC-28544Not For Human Use, Lab Use Only.
R1530 (R-1530) is a highly potent, orally active mitosis/angiogenesis inhibitor, inhibits angiogenesis-related receptor tyrosine kinases (KDR, FGFR) with IC50 of 10 nM and 28 nM, also inhibits PLK4 with IC50 of 7.06 nM.
| Packing | Price | Stock | Quantity |
|---|---|---|---|
| 5 mg | $88 | In stock | |
| 10 mg | $128 | In stock | |
| 25 mg | $198 | In stock | |
| 50 mg | Get quote | ||
| 100 mg | Get quote |
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R1530 (R-1530) is a highly potent, orally active mitosis/angiogenesis inhibitor, inhibits angiogenesis-related receptor tyrosine kinases (KDR, FGFR) with IC50 of 10 nM and 28 nM, also inhibits PLK4 with IC50 of 7.06 nM.
R1530 shows much weaker activities against CDK2 and CDK4.
R1530 inhibits the kinase activities of vascular endothelial growth factor receptor 2 (VGFr2), FGFR1, and PDGFR-β.
R1530 exhibits potent in vitro antiproliferative activity in various human tumor tissues including breast, colon, lung, prostate, melanoma, and oral epidermoid (IC50= 0.2-3.4 μM).
R1530 (25 or 50 mg/kg) produced significant tumor growth inhibition in MDA-MB-435 human tumor xenograft model.
| M.Wt | 356.79 | |
| Formula | C18H14ClFN4O | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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| Chemical Name/SMILES |
5-(2-Chlorophenyl)-7-fluoro-8-methoxy-3-methyl-1,2-dihydrobenzo[e]pyrazolo[4,3-b][1,4]diazepine |
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1. Liu JJ, et al. ACS Med Chem Lett. 2013 Jan 15;4(2):259-63.
2. Kolinsky K, et al. Cancer Chemother Pharmacol. 2011 Dec;68(6):1585-94.
3. Tovar C, et al. Cell Cycle. 2010 Aug 15;9(16):3364-75.

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