Solamargine
CAS No. 20311-51-7
Solamargine ( Solamargin | δ-Solanigrine )
产品货号. M17419 CAS No. 20311-51-7
Solamargine 是从中药 Solanum nigrum L. (SNL) 中提取的主要甾体生物碱苷;已被证明可以抑制多种癌细胞的生长并诱导其凋亡。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥889 | 有现货 |
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| 10MG | ¥1416 | 有现货 |
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| 25MG | ¥2753 | 有现货 |
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| 50MG | ¥4064 | 有现货 |
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| 100MG | ¥5607 | 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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| 1 mL x 10 mM in DMSO | ¥1349 | 有现货 |
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生物学信息
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产品名称Solamargine
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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Solamargine 是从中药 Solanum nigrum L. (SNL) 中提取的主要甾体生物碱苷;已被证明可以抑制多种癌细胞的生长并诱导其凋亡。
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产品描述Solamargine is a major steroidal alkaloid glycoside extracted from a traditional Chinese medicine herb, Solanum nigrum L. (SNL); has been shown to inhibit growth and induce apoptosis of various cancer cells.
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体外实验Solamargine (15 μg/ml; 72 hours) predominantly stimulates the cells of the G2/M phase to apoptosis.Solamargine (72 hours) dramatically inhibits the proliferation of SMMC-7721 and HepG2 cells in a dose- and time-dependent manner. The IC50s are 9.21 and 19.88 μg/ml, respectively. Cell Viability Assay Cell Line:SMMC-7721cells Concentration:15 μg/ml.Incubation Time:72 hours Result:Displayed a significant increase of sub-G1.
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体内实验Solamargine (10 mg/kg; intragastric administration; once daily for 8 days) exhibits an antitumor effect and promotes the apoptosis of GC in vivo. Animal Model:Female specific pathogen-free BALB/c nude mice weighing 18-20 g (6-8-weeks-old) Dosage:10 mg/kg Administration:Intragastric administration; once daily for 8 days Result:Tumor growth was significantly inhibited .
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同义词Solamargin | δ-Solanigrine
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通路Angiogenesis
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靶点PKC
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受体p38 MAPK| STAT3
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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 Number20311-51-7
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分子量868.07
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分子式C45H73NO15
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纯度>98% (HPLC)
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溶解度DMSO : ≥ 8.8 mg/mL; 10.14 mM
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SMILES[C@H]1([C@H]([C@@H]([C@H]([C@@H](O1)O[C@@H]1CC2=CC[C@H]3[C@@H]4C[C@@H]5O[C@]6([C@H]([C@@H]5[C@]4(CC[C@@H]3[C@]2(CC1)C)C)C)NC[C@@H](CC6)C)O[C@H]1[C@@H]([C@@H]([C@H]([C@@H](O1)C)O)O)O)O)O[C@H]1[C@@H]([C@@H]([C@H]([C@@H](O1)C)O)O)O)CO
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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
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Protein kinase inhib...
Protein kinase inhibitor H-7 dihydrochloride 是一种有效的 PKC 蛋白激酶 C 抑制剂。在 100 μM 时,Protein kinase inhibitor H-7 dihydrochloride 完全抑制 TPA (皮肤肿瘤启动子,12-O-tetradecanoylphorbol-13-acetate) 和磷脂酶 C 诱导的 ODC (鸟氨酸脱羧酶)。
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Delcasertib
Delcasertib 是一种有效的选择性 δ-蛋白激酶 C (δPKC) 抑制剂。
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PKC β pseudosubstrat...
Selective cell-permeable peptide inhibitor of protein kinase C (IC50 ~ 0.5 μM). Consists of amino acids 19 - 31 of PKC pseudosubstrate domain linked by a disulphide bridge to a cell permeabilisation Antennapedia domain vector peptide. The Antennapedia peptide is actively taken up by intact cells, at 4 or 37°C, ensuring rapid and effective uptake of the inhibitor peptide. Once inside the cell, the disulphide bonds are subjected to reduction in the cytoplasm leading to release of the inhibitor peptide.
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