ML 786 dihydrochloride

Discontinued Product

5036 has been discontinued.

View all Raf Kinases products.
说明: Potent Raf kinase inhibitor; orally bioavailable
别名: BGB659
化学名: 3-(1-Amino-1-methylethyl)-N-[(2R)-1,2,3,4-tetrahydro-7-oxo-1,8-naphthryridin-4-yl)oxy]-2-naphthalenyl]-5-benzamide dihydrochloride
纯度: ≥98% (HPLC)
说明书
引用文献 (1)
评论

生物活性 for ML 786 dihydrochloride

Potent 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.

技术数据 for ML 786 dihydrochloride

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.

产品说明书 for ML 786 dihydrochloride

参考文献 for ML 786 dihydrochloride

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

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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

1 篇 ML 786 dihydrochloride 的引用文献

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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