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TAS-115 mesylate (TAS-115 methanesulfonate) (Synonyms: TAS-115 mesylate)

カタログ番号GC33273

パムフェチニブ (TAS-115) メシル酸塩は、強力な VEGFR および肝細胞増殖因子受容体 (c-Met/HGFR) を標的とするキナーゼ阻害剤であり、rVEGFR2 および rMET の IC50 はそれぞれ 30 および 32 nM です。

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TAS-115 mesylate (TAS-115 methanesulfonate) 化学構造

Cas No.: 1688673-09-7

サイズ 価格 在庫数 個数
10mM (in 1mL DMSO)
$243.00
在庫あり
5mg
$180.00
在庫あり
10mg
$315.00
在庫あり
25mg
$608.00
在庫あり
50mg
$810.00
在庫あり
100mg
$1,350.00
在庫あり

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Sample solution is provided at 25 µL, 10mM.

Description Protocol Chemical Properties Product Documents Related Products

TAS-115 mesylate is a potent vascular endothelial growth factor (VEGFR) and hepatocyte growth factor receptor (c-Met/HGFR)-targeted kinase inhibitor, with IC50s of 30 and 32 nM for rVEGFR2 and rMET, respectively.

TAS-115 powerfully suppresses the VEGF-dependent proliferation of HUVECs (IC50=0.019 μM) as a VEGFR-targeted inhibitor and powerfully suppresses the proliferation of MET-amplified cancer cells (GI50=0.032-0.362 μM) as a MET-targeted inhibitor. TAS-115 has much less toxicity in various normal cell lines when compared with other VEGFR-targeted kinase inhibitors[1]. Crizotinib and TAS-115 inhibit Met phosphorylation and reverse erlotinib resistance and VEGF production triggered by HGF in PC-9 and HCC827 cells[2].

TAS-115 completely suppresses the progression of MET-inactivated tumor by blocking angiogenesis without toxicity when given every day for 6 weeks, even at a serum-saturating dose of TAS-115. TAS-115 induces marked tumor shrinkage and prolonges survival in MET-amplified human cancer-bearing mice[1].

[1]. Fujita H, et al. The novel VEGF receptor/MET-targeted kinase inhibitor TAS-115 has marked in vivo antitumor properties and a favorable tolerability profile. Mol Cancer Ther. 2013 Dec;12(12):2685-96. [2]. Nakade J, et al. Triple inhibition of EGFR, Met, and VEGF suppresses regrowth of HGF-triggered, erlotinib-resistant lung cancer harboring an EGFR mutation. J Thorac Oncol. 2014 Jun;9(6):775-83.

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Average Rating: 5 ★★★★★ (Based on Reviews and 18 reference(s) in Google Scholar.)

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