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Submit ReviewPotent Raf kinase inhibitor (IC50 values are 2.1, 2.5 and 4.2 nM for B-RafV600E, C-Raf and wild-type B-Raf respectively). Also inhibits Abl-1, DDR2, EPHA2 and RET tyrosine kinase activity. Inhibits pERK formation and attenuates tumor growth in melanoma cell xenografts expressing the B-RafV600E mutation in vivo. Orally bioavailable.
分子量 | 611.48 |
公式 | C29H29F3N4O3.2HCl |
储存 | Store at +4°C |
纯度 | ≥98% (HPLC) |
CAS Number | 1237536-18-3 |
PubChem ID | 90488999 |
InChI Key | DNMWHXHMDZCGEX-GHVWMZMZSA-N |
Smiles | O=C(N[C@@H]2CCC(C=CC(OC4=C(CC5)C(NC=C4)=NC5=O)=C3)=C3C2)C1=CC(C(F)(F)F)=CC(C(N)(C)C)=C1.Cl.Cl |
上方提供的技术数据仅供参考。批次相关数据请参见分析证书。
Tocris products are intended for laboratory research use only, unless stated otherwise.
参考文献是支持产品生物活性的出版物。
Gould et al (2011) Design and optimization of potent and orally bioavailable tetrahydronaphthalene Raf inhibitors. J.Med.Chem. 54 1836 PMID: 21341678
Sase et al (2018) Acquired JHDM1D-BRAF fusion confers resistance to FGFR inhibition in FGFR2-amplified gastric cancer. Mol.Cancer Ther. 17 2217 PMID: 30045926
关键词: ML 786 dihydrochloride, ML 786 dihydrochloride supplier, ML786, dihydrochloride, potent, raf, kinase, inhibitors, inhibits, b-raf, c-raf, V600E, mutation, tyrosine, kinases, BGB659, Raf, Kinase, 5036, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 ML 786 dihydrochloride 的部分引用包括:
Sase et al (2018) Acquired JHDM1D-BRAF fusion confers resistance to FGFR inhibition in FGFR2- amplified gastric cancer. Mol.Cancer Ther. PMID: 30045926
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