产品名称 | GW 441756 |
产品货号 | Axon 1251 CAS [504433-23-2] MF C17H13N3OMW 275.30 Purity: 99% Moderately soluble in DMSO Description Potent and orally active TrkA kinase inhibitor (IC50= 2nM) References Certificates Categories Extra info ER Wood et al. Discovery and in vitro evaluation of potent TrkA kinase inhibitors: Oxindole and aza-oxindoles. Bioorg. Med. Chem. Lett. 2004, 14(4), 953-957. J Wang et al. Cellular Assays for High-Throughput Screening for Modulators of Trk Receptor Tyrosine Kinases. Curr. Chem. Genomics, 2008, 1, 27-33. EJ Jung et al. Cytosolic accumulation of γH2AX is associated with tropomyosin-related kinase A-induced cell death in U2OS cells. Exp. Mol. Med. 2008, 40(3), 276–285. Certificate of Analysis Material Safety Data Sheet Cell Signaling & Oncology RTK class VII; EC 2.7.10.1 Trk TrkA inhibitor Chemical name 3-[1-(1-Methyl-1H-indol-3-yl)-meth-(Z)-ylidene]-1,3-dihydro-pyrrolo[3,2-b]pyridin-2-one Parent CAS No. [504433-23-2] Order Size Unit Price Stock 5 mg €75.00 In Stock |
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产品品牌 | axonmedchem |
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GW 441756Axon 1251 CAS [504433-23-2] MF C17H13N3O
Description
Potent and orally active TrkA kinase inhibitor (IC50= 2nM)
TrkA inhibitor
Chemical name3-[1-(1-Methyl-1H-indol-3-yl)-meth-(Z)-ylidene]-1,3-dihydro-pyrrolo[3,2-b]pyridin-2-one Parent CAS No.[504433-23-2] |
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