| 常用名 | N-[3-[[2,3-二氢-2-氧代-3-(1H-吡咯-2-基亚甲基)-1H-吲哚-6-基]氨基]-4-甲基苯基]-N'-[2-氟-5-(三氟甲基)苯基]-脲 | CAS号 | 1033769-28-6 |
|---|---|---|---|
| 价格 | ¥需询单/1kg ¥需询单/1g ¥需询单/1mg | 纯度 | 98.0% |
| 备货期 | 需询单 | 库存 | 询单 |
| 产品详情(用途,包装等)
用途: GNF-5837 is a potent pan-Trk inhibitor which display antiproliferative effects in cellular Ba/F3 assays (IC50 values are 7, 9 and 11 nM for cells containing the fusion proteins Tel-TrkC, Tel-TrkB and Tel-TrkA, respectively).IC50 Value: 7/9/11 nM (Tel-TrkC/Tel-TrkB/Tel-TrkA) [1]Target: pan-TrkGNF-5837 is an orally bioavailable oxindole compound that and acts as a potent, reversible and type II DFG-out inhibitor of pan-Trk activity (IC50 = 8 and 12 nM for TrkA and TrkB). Shown to target Trk (tropomyosin receptor kinase) ATP binding cleft and an immediately adjacent hydrophobic pocket. Preferentially arrests the proliferation of Ba/F3 cells fused with Tel-TrkA, Tel-TrkB and Tel-TrkC (IC50 = 11, 9 and 7 nM, respectively) and in Ba/F3 and RIE cells expressing both TrkA and NGF (IC50 = 42 and 17 nM, respectively) over Mo7e-c-Kit and Rat-A10-PDGFR (IC50 = 1 and 0.5 μM) and Ba/F3-Tel-KDR and wt-Ba/F3 cells (IC50 = 3.0 and 5.6 μM). GNF-5837 displays ~100-fold greater selectivity among a panel of 59 closely related kinases and in 33 cellular kinase assays. GNF-5837 weakly antagonize relevant cytochrome P450 isozymes and hERG channel, and exhibit adequate microsomal stability, pharmacokinetic profile and efficacy in mice and rats. GNF-5837 suppresses tumor growth in a mouse RIE-TrkAmNGF xenograft model (50 mg/kg, p.o.) [1]. 物理化学性质: CAS号:1033769-28-6 常用中文名:N-[3-[[2,3-二氢-2-氧代-3-(1H-吡咯-2-基亚甲基)-1H-吲哚-6-基]氨基]-4-甲基苯基]-N'-[2-氟-5-(三氟甲基)苯基]-脲 常用英文名:GNF-5837 分子式:C28H21F4N5O2 分子量:535.492 密度:1.5±0.1 g/cm3 沸点:616.0±55.0 °C at 760 mmHg 熔点:N/A 闪点:326.4±31.5 °C 储存条件:2-8°C |