
M50054
CAS No. 54135-60-3
M50054 ( Apoptosis Inhibitor )
产品货号. M27486 CAS No. 54135-60-3
细胞凋亡抑制剂是一种与 caspase-3 抑制相关的程序性细胞死亡的新型抑制剂。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥446 | 有现货 |
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10MG | ¥640 | 有现货 |
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25MG | ¥1312 | 有现货 |
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50MG | ¥1968 | 有现货 |
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100MG | ¥2900 | 有现货 |
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200MG | 获取报价 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称M50054
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述细胞凋亡抑制剂是一种与 caspase-3 抑制相关的程序性细胞死亡的新型抑制剂。
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产品描述Apoptosis Inhibitor was a novel inhibitor of programmed cell death associate with caspase-3 inhibition.(In Vitro):Apoptosis Inhibitor was identified as a novel inhibitor of apoptosis (programmed cell death) using an in vitro cell death assay system induced in human Fas-expressing WC8 cells by soluble human Fas ligand.
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体外实验M50054 inhibits the caspase-3 activation by Etoposide in a dose-dependent manner. The IC50 value of M50054 against Etoposide-induced caspase-3 activation of U937 cells is 79 μg/mL. However, M50054 does not directly inhibit the enzymatic activity of caspase-3 at all concentrations up to 1000 μg/mL.M50054 (1-300 μg/mL) inhibits soluble human Fas ligand-induced cell death of human Fas-expressing WC8 cells in a dose-dependent manner, and the IC50 of 67 μg/mL.M50054 (30-300 μg/mL) inhibits the death of U937 cells induced by etoposide (10 μg/mL) in a dose-dependent manner, and the IC50 value of M50054 against Etoposide-induced cell death of U937 cells is 130 μg/mL. The IC50 value of M50054 against etoposide-induced DNA fragmentation of U937 cells was 54 μg/mL. Cell Proliferation Assay Cell Line:Human Fas-expressing WC8 cells Concentration:1, 3, 10, 30, 100, 300 μg/mL Incubation Time:Pre-incubated for 30 min Result:Inhibited soluble human Fas ligand-induced cell death of human Fas-expressing WC8 cells in a dose-dependent manner, and the IC50 of 67 μg/mL.
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体内实验M50054 (10-300 mg/kg; oral administration 30 min before anti-Fas antibody injection) inhibits the elevation of alanine aminotransferase and aspartate aminotransferase in a dose-dependent manner.M50054 (topical treatment; given daily beginning on day 5 after birth and ending on day 14) significantly improves alopecia (hair loss) symptoms. Animal Model:Female BALB/c miceDosage:10, 30, 100 or 300 mg/kg Administration:Orally administered in a volume of 10 mL/kg Result:Inhibited the elevation of alanine aminotransferase and aspartate aminotransferase in a dose-dependent manner. Significantly improved these parameters at doses of 100 mg/kg and 300 mg/kg.Animal Model:Five-day-old SD rats Dosage:Administration:Topically applied to the head and back of 5-day-old rats once daily for 10 days Result:Alopecia scores significantly decreased throughout the entire observation period compared with the control group.
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同义词Apoptosis Inhibitor
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通路Apoptosis
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靶点Caspase
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受体CYP1A2|CYP2B6
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研究领域——
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适应症——
化学信息
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CAS Number54135-60-3
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分子量236.26
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分子式C13H16O4
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纯度>98% (HPLC)
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溶解度——
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SMILESO=C(CCC1)C(CC(C(CCC2)=O)C2=O)C1=O
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.L E Korhonen, et al. New potent and selective cytochrome P450 2B6 (CYP2B6) inhibitors based on three-dimensional quantitative structure-activity relationship (3D-QSAR) analysis. Br J Pharmacol. 2007 Apr;150(7):932-42.
产品手册




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