化合物BMS794833 T2419
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Product IntroductionBioactivity英文名: BMS-794833描述: BMS794833 是一种 VEGFR2 和 Met 的抑制剂，它们的 IC50值分别为 15 和 1.7 nM。细胞实验: GTL-16 c
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Product Introduction
Bioactivity
英文名: BMS-794833
描述: BMS794833 是一种 VEGFR2 和 Met 的抑制剂，它们的 IC50值分别为 15 和 1.7 nM。
细胞实验: GTL-16 cells are seeded into 96 well plates and incubated for 24 hours. BMS798433 is dissolved in DMSO at 10 mM and diluted with culture medium before use. Then BMS798433 is added to the cells for 72 hours. After that, MTS assay is used to measure the IC50.(Only for Reference)
激酶实验: Met kinase assay: BMS798433 is dissolved in DMSO and diluted by water before use. The reaction solution contains baculovirus expressed GST-Met kinase, 20 mM Tris-HCl (pH 7.4), 1 mM MnCl2, 1 mM DTT, 0.1 mg BSA, 0.1 mg polyGlu4/tyr, 1 μM ATP and 0.2μCi γ–ATP. Reactions are incubated at 30 °C for 1 hour and stopped by 8% TCA. TCA precipitates are collected onto GF/C plates using a universal harvester and the filters are quantitated using liquid scintillation counter.
体外活性: BMS798433在25 mg/kg的剂量下对U87胶质母细胞瘤模型也显示完全抑制肿瘤生长作用.在GTL-16人胃肿瘤异种移植模型中,BMS798433处理14天,在至少一个肿瘤倍增时间内显示大于50％的TGI,期间没有观察到明显的毒性.
体内活性: BMS794833抑制Met受体激活的胃癌细胞系GTL-16,IC50 为39 nM。
存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: H2O : < 1 mg/mL (insoluble or slightly soluble)
DMSO : 87 mg/mL (185.6 mM)
Ethanol : < 1 mg/mL (insoluble or slightly soluble)
关键字: VEGFR | BMS794833 | Inhibitor | c-Met/HGFR | inhibit | Vascular endothelial growth factor receptor | BMS 794833 | BMS-794833
相关产品: VEGFR-2-IN-35 | Ningetinib | Dovitinib lactate hydrate | Dovitinib | Cabozantinib | NVP-ACC789 | URMC-099 | TIE-2/VEGFR-2 kinase-IN-5 | SKLB 610 | Sprengerinin C
相关库: Anti-Prostate Cancer Compound Library | ReFRAME Related Library | Angiogenesis related Compound Library | Membrane Protein-targeted Compound Library | Bioactive Compounds Library Max | Kinase Inhibitor Library | Inhibitor Library | Anti-Colorectal Cancer Compound Library | Tyrosine Kinase Inhibitor Library | Anti-Cancer Active Compound Library
Bioactivity
英文名: BMS-794833
描述: BMS794833 是一种 VEGFR2 和 Met 的抑制剂，它们的 IC50值分别为 15 和 1.7 nM。
细胞实验: GTL-16 cells are seeded into 96 well plates and incubated for 24 hours. BMS798433 is dissolved in DMSO at 10 mM and diluted with culture medium before use. Then BMS798433 is added to the cells for 72 hours. After that, MTS assay is used to measure the IC50.(Only for Reference)
激酶实验: Met kinase assay: BMS798433 is dissolved in DMSO and diluted by water before use. The reaction solution contains baculovirus expressed GST-Met kinase, 20 mM Tris-HCl (pH 7.4), 1 mM MnCl2, 1 mM DTT, 0.1 mg BSA, 0.1 mg polyGlu4/tyr, 1 μM ATP and 0.2μCi γ–ATP. Reactions are incubated at 30 °C for 1 hour and stopped by 8% TCA. TCA precipitates are collected onto GF/C plates using a universal harvester and the filters are quantitated using liquid scintillation counter.
体外活性: BMS798433在25 mg/kg的剂量下对U87胶质母细胞瘤模型也显示完全抑制肿瘤生长作用.在GTL-16人胃肿瘤异种移植模型中,BMS798433处理14天,在至少一个肿瘤倍增时间内显示大于50％的TGI,期间没有观察到明显的毒性.
体内活性: BMS794833抑制Met受体激活的胃癌细胞系GTL-16,IC50 为39 nM。
存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: H2O : < 1 mg/mL (insoluble or slightly soluble)
DMSO : 87 mg/mL (185.6 mM)
Ethanol : < 1 mg/mL (insoluble or slightly soluble)
关键字: VEGFR | BMS794833 | Inhibitor | c-Met/HGFR | inhibit | Vascular endothelial growth factor receptor | BMS 794833 | BMS-794833
相关产品: VEGFR-2-IN-35 | Ningetinib | Dovitinib lactate hydrate | Dovitinib | Cabozantinib | NVP-ACC789 | URMC-099 | TIE-2/VEGFR-2 kinase-IN-5 | SKLB 610 | Sprengerinin C
相关库: Anti-Prostate Cancer Compound Library | ReFRAME Related Library | Angiogenesis related Compound Library | Membrane Protein-targeted Compound Library | Bioactive Compounds Library Max | Kinase Inhibitor Library | Inhibitor Library | Anti-Colorectal Cancer Compound Library | Tyrosine Kinase Inhibitor Library | Anti-Cancer Active Compound Library
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