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S88447

GSK2982772

源叶(MedMol) 98%
  • 英文名:
  • (S)-5-Benzyl-N-(5-methyl-4-oxo-2,3,4,5-tetrahydrobenzo[b]-[1,4]oxazepin-3-yl)-4H-1,2,4-triazole-3-carboxamide
  • 别名:
  • GSK2982772; GSK-2982772; GSK 2982772.
  • CAS号:
  • 1622848-92-3
  • 分子式:
  • C20H19N5O3
  • 分子量:
  • 377.39656
  • 核磁/质谱:
品牌货号产品规格价格(RMB) 库存(上海) 北京 武汉 南京 数量计量单位 加入购物车...
源叶(MedMol) S88447-5mg 98% ¥800.00元 5 - - - EA 加入购物车
源叶(MedMol) S88447-10mg 98% ¥1280.00元 5 - - - EA 加入购物车
源叶(MedMol) S88447-25mg 98% ¥2400.00元 6 - - - EA 加入购物车
源叶(MedMol) S88447-100mg 98% ¥9120.00元 预计交期:2-3天 - - - EA 加入购物车
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参考文献

质检证书(COA)

摩尔浓度计算器

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  • 产品描述: GSK2982772 is a potent, orally active and ATP competitive RIP1 kinase inhibitor with IC50 values of 16 nM and 20 nM for human and monkey RIP1, respectively
  • 靶点: IC50: 16 nM (human RIP1 FP) IC50: 20 nM (monkey RIP1 FP) IC50: 2 μM (rat RIP1 FP) IC50: 2.5 μM (mouse RIP1 FP);RIPkinase
  • 体外研究:
    GSK2982772 shows more than 1,000-fold selectivity for ERK5 over a panel of over 339 kinases at 10 μM. In stimulated cellular systems,GSK2982772 is also able to reduce spontaneous production of cytokines (IL-1β and IL-6) in a concentration-dependent fashion from ulcerative colitis explant tissue in overnight incubations. GSK2982772 produces a weak concentration dependent inhibition of hERG in human embryonic kidney (HEK-293) cells, with an estimated IC50 of 195 μM, and also shows a weak activation of the human Pregnane X receptor (hPXR) with an EC50 of 13 μM.
  • 体内研究:
    GSK2982772 is dosed orally 15 min prior to TNF and shows 68, 80, and 87% protection from temperature loss over 6 h, at doses of 3, 10, and 50 mg/kg, respectively. In the corresponding TNF/zVAD model, GSK2982772 shows 13, 63, and 93% protection from temperature loss over 3 h. GSK2982772 displays a good free fraction in blood in rats (4.2%), dogs (11%), cynomolgus monkeys (11%), and humans (7.4%). The inhibitor has a good pharmacokinetic profile across both rats and monkeys. GSK2982772 distributes into a range of tissues including the colon, liver, kidney, and heart at concentrations comparable to those of blood. However, GSK2982772 has low brain penetration in rat (4%) despite possessing good cell permeability (21×10-6 cm/s).
  • 参考文献:
    1. Harris PA, et al. Discovery of a First-in-Class Receptor Interacting Protein 1 (RIP1) Kinase Specific Clinical Candidate (GSK2982772) for the Treatment of Inflammatory Diseases. J Med Chem. 2017 Feb 23;60(4):1247-1261.
  • 溶解性: Soluble  in  DMSO
  • 保存条件: -20℃
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 2.65 ml 13.249 ml 26.497 ml
    5 mM 0.53 ml 2.65 ml 5.299 ml
    10 mM 0.265 ml 1.325 ml 2.65 ml
    50 mM 0.053 ml 0.265 ml 0.53 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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