SCH772984

    98%

SCH772984

源叶(MedMol)
S81143
942183-80-4
C33H33N9O2
587.67
3-Pyrrolidinecarboxamide, 1-[2-oxo-2-[4-[4-(2-pyrimidinyl)phenyl]-1-piperazinyl]ethyl]-N-(3-phenyl-1H-indazol-5-yl)-, (3R)-
品牌 货号 产品规格 价格(RMB) 库存(上海) 北京 武汉 南京 购买数量
源叶(MedMol) S81143-2mg 98% ¥408.00元 预计交期:2-3天 - - -
源叶(MedMol) S81143-5mg 98% ¥598.40元 1 - - -
源叶(MedMol) S81143-10mg 98% ¥1020.00元 7 - - -
源叶(MedMol) S81143-25mg 98% ¥2040.00元 6 - - -
源叶(MedMol) S81143-50mg 98% ¥3400.00元 预计交期:2-3天 - - -
源叶(MedMol) S81143-100mg 98% ¥5440.00元 预计交期:2-3天 - - -
源叶(MedMol) S81143-200mg 98% ¥7800.00元 预计交期:2-3天 - - -
产品介绍 参考文献(1篇) 质检证书(COA) 摩尔浓度计算器 相关产品

产品介绍

SCH772984 is a highly selective and ATP-competitive ERK inhibitor, with IC50s of 4 and 1 nM for ERK1 and ERK2, respectively. SCH772984 has antitumor activity in MAPK inhibitor-naïve and MAPK inhibitor-resistant cells containing BRAF or RAS mutations

产品描述:

SCH772984 is a highly selective and ATP-competitive ERK inhibitor, with IC50s of 4 and 1 nM for ERK1 and ERK2, respectively. SCH772984 has antitumor activity in MAPK inhibitor-naïve and MAPK inhibitor-resistant cells containing BRAF or RAS mutations

靶点: ERK2:1 nM (IC50);ERK1:4 nM (IC50);ERK; MEK
体内研究: SCH772984 (12.5-50 mg/kg; i.p.; twice daily for 14 days) leads to 98% tumor regression. Dose-dependent antitumor activity is also observed in the KRAS-mutant pancreatic MiaPaCa model, with 36% regression at 50 mg/kg twice daily. Importantly, tumor regression is accompanied by robust inhibition of ERK phosphorylation in tumor tissue. SCH772984 is well tolerated on this schedule as measured by morbidity, lethality, or body weight loss。
参考文献: 1. Morris EJ, et al. Discovery of a novel ERK inhibitor with activity in models of acquired resistance to BRAF and MEK inhibitors. Cancer Discov. 2013 Jul;3(7):742-50.
溶解性: DMSO  :  48  mg/mL  (81.68  mM;  Need  ultrasonic)
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 1.702 ml 8.508 ml 17.016 ml
5 mM 0.34 ml 1.702 ml 3.403 ml
10 mM 0.17 ml 0.851 ml 1.702 ml
50 mM 0.034 ml 0.17 ml 0.34 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

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