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CAS号 | 1029872-54-5 | 货号 | BCP43160 |
关联产品 | 918504-65-1(维罗非尼) | ||
中文名 | 维罗非尼 | ||
英文名 | Vemurafenib | ||
中文别名 | |||
英文别名 | PLX4032;PLX-4032;PLX 4032; | ||
SMILES | CCCS(=O)(=O)NC1=C(C(=C(C=C1)F)C(=O)C2=CNC3=C2C=C(C=N3)C4=CC=C(C=C4)Cl)F | ||
化学名称 | |||
分子式 | C23H18ClF2N3O3S | 分子量 | 489.92 |
纯度 | 98% | 配送 | 惯例下常温包邮 |
产品描述 | Vemurafenib is an orally bioavailable, ATP-competitive, small-molecule inhibitor of BRAF(V600E) kinase with potential antineoplastic activity. Vemurafenib selectively binds to the ATP-binding site of BRAF(V600E) kinase and inhibits its activity, which may result in an inhibition of an over-activated MAPK signaling pathway downstream in BRAF(V600E) kinase-expressing tumor cells and a reduction in tumor cell proliferation. Approximately 90% of BRAF gene mutations involve a valine-to-glutamic acid mutation at residue 600 (V600E); the oncogene protein product, BRAF(V600E) kinase, exhibits a markedly elevated activity that over-activates the MAPK signaling pathway. The BRAF(V600E) gene mutation has been found to occur in approximately 60% of melanomas, and in about 8% of all solid tumors, including melanoma, colorectal, thyroid and other cancers. |
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