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Schisandrin C
CAS No. 61301-33-5
Schisandrin C ( Schizandrin C | Schizandrin-C )
产品货号. M18896 CAS No. 61301-33-5
Schisandrin C 是一种从五味子 (Schizandra chinensis Baill) 中分离出来的植物化学木脂素;显示出对人类白血病 U937 细胞的抗癌作用。
纯度: >98% (HPLC)
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规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥441 | 有现货 |
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10MG | ¥1332 | 有现货 |
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100MG | 获取报价 | 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Schisandrin C
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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Schisandrin C 是一种从五味子 (Schizandra chinensis Baill) 中分离出来的植物化学木脂素;显示出对人类白血病 U937 细胞的抗癌作用。
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产品描述Schizandrin C is a compound that exerts anti-neuroinflammatory effects by upregulating phase II detoxifying/antioxidant enzymes in microglia.(In Vitro):Schisandrin C (25-100 μM; 48 hours) down-regulates expression levels of Bcl-2, Bcl-xL and a concomitant degradation of poly(ADP-ribose) polymerase (PARP). It also activates caspase-3 and -9 in U937 cells.Schisandrin C (25-100 μM; 48 hours) induces apoptosis in a dose-dependent manner. And the fragmentation of genomic DNA is also increased in U937 cells.Schisandrin C (25-100 μM; 72 hours) induces G1 arrest, it down-regulates cyclin D1, cyclin E, cyclin-dependent kinase (Cdk) 4 and E2Fs expression, and also exhibits inhibition of pRB, and up-regulation of the Cdk inhibitor p21(WAF1/CIP1).(In Vivo):Schisandrin C (lateral ventricle injection (i.c.v.); 15-150 μg/kg; 5 days) reduces Aβ1-42-induced memory deficits in the Y-maze test. Neurons in the hippocampus of SCH-C (15 μg/kg)-treated group returned to normal level, and and SCH-C group (150 μg/kg) has slight neuroprotective effects Aβ1-42-induced group. SCH-C (15 μg/kg) recoveres the activities of SOD and GSHPx and the ratios of GSH, decreases the levels of ChEtotal in the brain of the Aβ1–42-induced amnesic mice simultaneously.
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体外实验Schisandrin C (25-100 μM; 48 hours) down-regulates expression levels of Bcl-2, Bcl-xL and a concomitant degradation of poly(ADP-ribose) polymerase (PARP). It also activates caspase-3 and -9 in U937 cells.Schisandrin C (25-100 μM; 48 hours) induces apoptosis in a dose-dependent manner. And the fragmentation of genomic DNA is also increased in U937 cells.Schisandrin C (25-100 μM; 72 hours) induces G1 arrest, it down-regulates cyclin D1, cyclin E, cyclin-dependent kinase (Cdk) 4 and E2Fs expression, and also exhibitsinhibition of pRB, and up-regulation of the Cdk inhibitor p21(WAF1/CIP1). Western Blot Analysis Cell Line:U937 cells Concentration:25 μM,50 μM,100 μM Incubation Time:48 hours Result:Decreased the expression of apoptosis related proteins.Apoptosis Analysis Cell Line:U937 cells Concentration:25 μM,50 μM,100 μM Incubation Time:48 hours Result:Induced cell apoptosis. Cell Cycle Analysis Cell Line:U937 cells Concentration:25 μM,50 μM,100 μM Incubation Time:48 hoursResult:Induced growth inhibition and G1 arrest of U937 cells.
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体内实验Schisandrin C (lateral ventricle injection (i.c.v.); 15-150 μg/kg; 5 days) reducesAβ1-42-induced memory deficits in the Y-maze test. Neurons in the hippocampus of SCH-C (15 μg/kg)-treated group returned to normal level, and and SCH-C group (150 μg/kg) has slight neuroprotective effects Aβ1-42-induced group. SCH-C (15 μg/kg) recoveres the activities of SOD and GSHPx and the ratios of GSH, decreases the levels of ChEtotal in the brain of the Aβ1–42-induced amnesic mice simultaneously. Animal Model:Aβ1-42-induced Alzheimer’s disease mice Dosage:15-150 μg/kg Administration:Lateral ventricle injection (i.c.v.); 15-150 μg/kg; 5 days Result:Exhibited potent neuroprotective effects linking to anti-ChEtotal activities and anti-oxidative mechanisms in Aβ1-42-induced amnestic mice.
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同义词Schizandrin C | Schizandrin-C
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通路Others
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靶点Other Targets
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受体Others
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研究领域Cancer
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适应症——
化学信息
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CAS Number61301-33-5
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分子量384.42
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分子式C22H24O6
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 8.33 mg/mL (21.67 mM)
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SMILESC[C@H]1Cc4cc5OCOc5c(OC)c4c2c(OC)c3OCOc3cc2C[C@H]1C
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化学全称A name could not be generated for this structure.
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.E Q, Tang M, et al.Cell Biol Int. 2015 Dec;39(12):1418-24.
产品手册
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