Ginsenoside Rk1
CAS No. 494753-69-4
Ginsenoside Rk1 ( —— )
产品货号. M20267 CAS No. 494753-69-4
人参皂苷 Rk1 是通过高温加工人参植物而产生的成分。 Ginsenoside Rk1 具有抗炎作用,抑制 Jak2/Stat3 信号通路和 NF-κB 的激活。它还具有抗肿瘤作用。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥761 | 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 |
|
| 500MG | 获取报价 | 有现货 |
|
| 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Ginsenoside Rk1
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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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产品简述人参皂苷 Rk1 是通过高温加工人参植物而产生的成分。 Ginsenoside Rk1 具有抗炎作用,抑制 Jak2/Stat3 信号通路和 NF-κB 的激活。它还具有抗肿瘤作用。
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产品描述Ginsenoside Rk1 is a component created by processing the ginseng plant at high temperatures. Ginsenoside Rk1 has an anti-inflammatory effect suppresses the activation of Jak2/Stat3 signaling pathway and NF-κB. It also has an anti-tumor effect.
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体外实验Ginsenoside Rk1 (0-40 μM; 6 hours) inhibits MCP-1 and TNF-α mRNA induced by lipopolysaccharide (LPS), expression of IL-1β is inhibited at 40 μM.Ginsenoside Rk1 (0-40 μM; 24 hours) inhibits phosphorylation of JAK2 and STAT3 (Tyr705 and Ser727) in LPS-induced RAW264.7 cells in a dose-dependent manner.Ginsenoside Rk1 (0-160 μM; 48 hours) results in cell viability significant decrease 75.52 ± 2.51% (40 μM), 52.72 ± 2.54% (80 μM), 17.41 ± 2.94% (120 μM)and 12.63 ± 3.24% (160 μM) compared with control.Ginsenoside Rk1 (0-120 μM; 24 hours) increases G0/G1 phase proportion accompanied with S and G2/M phase proportion decrease in MDA-MB-231 cells.Ginsenoside Rk1 (0-120 μM; 24 hours) promotes the percentage of apoptotic cells in a dose-dependent manner, exhibits to reduction of cell number with nucleus fragmentation, condensation and apoptotic body formation. RT-PCR Cell Line:RAW264.7 cells Concentration:10 μM, 20 μM, 40 μM Incubation Time:6 hours Result: Inhibited JAK2-dependent STAT3 activation in LPS-activated RAW264.7 cells.Western Blot Analysis Cell Line:RAW264.7 cells Concentration:10 μM, 20 μM, 40 μM Incubation Time:6 hours Result:Inhibited JAK2-dependent STAT3 activation in LPS-activated RAW264.7 cells Cell Viability Assay Cell Line:MDA-MB-231 cells Concentration:0 μM, 40 μM, 80 μM, 120 μM Incubation Time:48 hours Result:Inhibited MDA-MB-231 cells proliferation in a dose- and time-dependent manner.Cell Cycle Analysis Cell Line:MDA-MB-231 cells Concentration:0 μM, 40 μM, 80 μM, 120 μM Incubation Time:24 hours Result:Induced G0/G1 phase arrest.Apoptosis Analysis Cell Line:MDA-MB-231 cells Concentration:0 μM, 40 μM, 80 μM, 120 μM Incubation Time:24 hours Result:Induced apoptosis in MDA-MB-231 cells.
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体内实验——
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同义词——
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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——
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适应症——
化学信息
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CAS Number494753-69-4
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分子量767.01
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分子式C42H70O12
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纯度>98% (HPLC)
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溶解度DMSO: 90 mg/mL (117.34 mM)
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SMILES[H][C@@]12[C@H](CC[C@@]1(C)[C@]1(C)CC[C@@]3([H])C(C)(C)[C@H](CC[C@]3(C)[C@@]1([H])C[C@H]2O)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C(=C)CC\C=C(/C)C
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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.Kim JS et al. Induction of apoptosis by ginsenoside Rk1 in SK-MEL-2-human melanoma. Arch Pharm Res. 2012 Mar;35(4):717-22.
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