Rogaratinib是一种有效且有选择性的成纤维细胞生长因子受体(FGFR)抑制剂。
CAS：1443530-05-9
分子式：C23H26N6O3S
分子量：466.56
纯度：98%
存储：Store at -20°C

Background:

Rogaratinib is a potent and selective fibroblast growth factor receptor (FGFR) inhibitor.

Of the 24 cell lines, 2 FGFR1-amplified lung cancer (LC) cell lines, H1581 and DMS114, show extreme sensitivity to Rogaratinib (BAY1163877) (GI50 values ranging from 36 to 244 nM). Treatment with Rogaratinib results in a significant decrease in colonies formed by H1581P cells, but not by H1581AR and BR cells. Ectopic expression of Met significantly induces resistance to Rogaratinib in MTT assays. Met overexpression induces activation of downstream extracellular signal-regulated kinase 1/2 (ERK1/2) and AKT, which cannot be abrogated by Rogaratinib treatment[1].

[1]. Kim SM, et al. Activation of the Met kinase confers acquired drug resistance in FGFR-targeted lung cancer therapy. Oncogenesis. 2016 Jul 18;5(7):e241.