TCS JNK 6o

    98%

TCS JNK 6o

源叶(MedMol)
S89992
894804-07-0
C₁₈H₂₀N₄O₄
356.38
;TCS JNK 6o;JNK Inhibitor VIII
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) S89992-1mg 98% ¥150.00元 9 - - -
源叶(MedMol) S89992-5mg 98% ¥250.00元 8 - - -
源叶(MedMol) S89992-25mg 98% ¥530.00元 6 - - -
源叶(MedMol) S89992-100mg 98% ¥1640.00元 1 - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品

产品介绍

JNK Inhibitor VIII (TCS JNK 6o) 是一种 c-Jun N-terminal kinases 的抑制剂,对JNK-1和JNK-2的IC50值分别为45 nM和160 nM。JNK Inhibitor VIII (TCS JNK 6o) 可抑制JNK-1、JNK-2和JNK-3,对应的Ki值分别为2 nM、4 nM和52 nM
产品描述: JNK Inhibitor VIII (TCS JNK 6o) 是一种 c-Jun N-terminal kinases 的抑制剂,对JNK-1和JNK-2的IC50值分别为45 nM和160 nM。JNK Inhibitor VIII (TCS JNK 6o) 可抑制JNK-1、JNK-2和JNK-3,对应的Ki值分别为2 nM、4 nM和52 nM
靶点: JNK1(Cell-free assay):2 nM(Ki); JNK2(Cell-free assay):4 nM(Ki); JNK1(Cell-free assay):45 nM; JNK3(Cell-free assay):52 nM(Ki); JNK2(Cell-free assay):160 nM;JNK
体内研究: Pharmacokinetic profiles are determined for JNK Inhibitor VIII (TCS-JNK-6o) in Sprague-Dawley rats. JNK Inhibitor VIII (TCS-JNK-6o) showes a short half-life of roughly 1 h, with rapid clearance and barely measurable bioavailability. Microsomal incubation studies revealed that oxidative metabolism is very rapid with this compound
细胞实验: Cell lines: hepG2 cells Concentrations: Serial concentrations Incubation Time: 1 h Method: HepG2 human hepatoma cells (ATCC) are cultured in low glucose MEM supplemented with 1×NEAA, 1×sodium pyruvate, and 10% FBS. For P-c-Jun assays, cells are plated at 5×104 cells/well in 500 μL of complete media on 24-well collagen-coated plates and incubated overnight. Serial compound dilutions are made in DMSO at 100×, and then 5 μL is added directly to the media on the cells to provide the final inhibitor concentrations. After 1 h, cells are stimulated with vehicle control or TNFR for 30 min and harvested in 70μL of lysis buffer (TBS (54 mM Tris-HCl, pH 7.6, 150 mM NaCl), 1% TritonX-100,0.5% Nonidet P-40, 0.25% sodium deoxycholate, 1 mM EDTA, 1 mM EGTA, 0.5 mM sodium fluoride, 1 mM pervanadate, 1 μM microcystin, 1 mM AEBSF, 1 tablet of complete EDTA Free-Mini inhibitor cocktail) and frozen at -80 °C prior to use in the P-c-Jun assay.
动物实验: Animal Models: Sprague-Dawley rat Dosages: 5 mg/kg Administration: IV, Oral gavage
参考文献: 1. Bruce G Szczepankiewicz, et al. J Med Chem. 2006 Jun 15;49(12):3563-80.
溶解性: Soluble  in  DMSO
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.806 ml 14.03 ml 28.06 ml
5 mM 0.561 ml 2.806 ml 5.612 ml
10 mM 0.281 ml 1.403 ml 2.806 ml
50 mM 0.056 ml 0.281 ml 0.561 ml
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参考文献

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