SB-590885

本公司产品仅用于科研实验，不得用于人体或动物的临床与诊断

一种有效的选择性 B-Raf 抑制剂，Kd 为 0.3 nM。

A potent and selective B-Raf inhibitor with Kd of 0.3 nM; >1000 fold selectivity over p38a, GSK3b and Lck.

SB-590885 displays significant selectivity for B-Raf over c-Raf with Ki?of 0.16 nM over 1.72 nM. SB-590885 is a more potent inhibitor than the previously described Raf/VEGFR kinase inhibitor BAY 439006 (Ki=38 nM for mutant B-Raf, 6 nM for c-Raf). SB-590885 displays potent selectivity over 46 other kinases. Unlike the multi-kinase inhibitor BAY43-9006, SB-590885 stabilizes the oncogenic B-Raf kinase domain in an active configuration. In Colo205, HT29, A375P, SKMEL28, and MALME-3M cells expressing oncogenic B-RafV600E, SB-590885 treatment potently inhibits ERK phosphorylation with EC50 of 28 nM, 58 nM, 290 nM, 58 nM, and 190 nM, respectively, and consistently, inhibits the proliferation with EC50 of 0.1 μM, 0.87 μM, 0.37 μM, 0.12 μM, and 0.15 μM, respectively. SB-590885 decreases anchorage-independent growth of melanoma cell lines in a BRAF mutant-selective manner.?SB-590885 displays high affinity for B-Raf with Kd of 0.3 nM.?Most of the melanoma cell lines that harbor the BRAF V600E mutation and lack CDK4 mutations (451Lu, WM35, and WM983) are highly sensitive to SB-590885 with IC50 of <1 μM. Increased levels of cyclin D1 resulting from genomic amplification mediate SB-590885 resistance in B-Raf V600E-mutated melanomas.

Administration of SB-590885 potently decreases tumorigenesis in murine xenografts established from mutant B-Raf-expressing A375P melanoma cells, and modestly inhibits tumor growth.

SB590885 | SB 590885

MAPK/ERK Signaling

Raf

B-Raf

Cancer

——

405554-55-4

453.5356

C27H27N5O2

>98% (HPLC)

10 mM in DMSO

CN(C)CCOC1=CC=C(C=C1)C2=N/C(=C/3\C=CC4=C(CCC4=C3)N=O)/C(=C5C=CNC=C5)N2

1H-Inden-1-one, 5-[2-[4-[2-(dimethylamino)ethoxy]phenyl]-5-(4-pyridinyl)-1H-imidazol-4-yl]-2,3-dihydro-, oxime

(-20℃)

With Ice Pack

≥ 2 years