首页 > 产品目录 > 对照品 > 中药对照品 > 人参系列 > 人参皂苷CK/20(S)-人参皂苷CK/人参皂苷C-K/人参皂苷K/20(S)-人参皂苷C-K/(2S,3R,4S,5S,6R)-2-(((S)-2-((3S,5R,8R,9R,10R,12R,13R,14R,17S)-3,12-二羟基-4,4,8,10,14-五甲基十六氢-1H-环戊二稀并[a]菲-17-基)-6-甲基庚-5-烯-2-基)氧基)-6-(羟甲基)四氢-2H-吡喃-3,4,5-三醇

人参皂苷CK/20(S)-人参皂苷CK/人参皂苷C-K/人参皂苷K/20(S)-人参皂苷C-K/(2S,3R,4S,5S,6R)-2-(((S)-2-((3S,5R,8R,9R,10R,12R,13R,14R,17S)-3,12-二羟基-4,4,8,10,14-五甲基十六氢-1H-环戊二稀并[a]菲-17-基)-6-甲基庚-5-烯-2-基)氧基)-6-(羟甲基)四氢-2H-吡喃-3,4,5-三醇

Compound CK

产品编号:WKQ-0000459 CAS No.:39262-14-1 纯度:HPLC≥98% 分子式:C36H62O8

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基本信息
英文名称 Compound CK
中文名称人参皂苷CK/20(S)-人参皂苷CK/人参皂苷C-K/人参皂苷K/20(S)-人参皂苷C-K/(2S,3R,4S,5S,6R)-2-(((S)-2-((3S,5R,8R,9R,10R,12R,13R,14R,17S)-3,12-二羟基-4,4,8,10,14-五甲基十六氢-1H-环戊二稀并[a]菲-17-基)-6-甲基庚-5-烯-2-基)氧基)-6-(羟甲基)四氢-2H-吡喃-3,4,5-三醇
CAS号39262-14-1
分子式C36H62O8
分子量622.87
外观 白色粉末
熔点181-183 °C
沸点723.1±60.0 °C | Condition: Press: 760 Torr
酸度系数pKa12.94±0.70 | Condition: Most Acidic Temp: 25 °C
产品详情

WKQ-0000459

中文名称:人参皂苷CK

中文别名:20(S)-人参皂苷CK;人参皂苷C-K;人参皂苷K;20(S)-人参皂苷C-K;(2S,3R,4S,5S,6R)-2-(((S)-2-((3S,5R,8R,9R,10R,12R,13R,14R,17S)-3,12-二羟基-4,4,8,10,14-五甲基十六氢-1H-环戊二稀并[a]菲-17-基)-6-甲基庚-5-烯-2-基)氧基)-6-(羟甲基)四氢-2H-吡喃-3,4,5-三醇

英文名称:Compound CK

英文别名:(3β,12β)-3,12-Dihydroxydammar-24-en-20-yl β-D-glucopyranoside;20(S)-Protopanaxadiol 20-O-D-glucopyranoside;20(S)-Protopanaxadiol 20-O-β-D-glucopyranoside;20-O-β-D-Glucopyranosyl-20(S)-protopanaxadiol;20-O-β-Glucopyranosyl-20(S)-protopanaxadiol;20S-Protopanaxadiol 20-O-β-D-glucopyranoside;3-O-Deglucosylginsenoside F2;Compound k;Ginsenoside C-K;Ginsenoside IH901;Ginsenoside K;Ginsenoside M1;Ginsenoside compound K;Ginsenoside metabolite M1;IH 901;LCHK 168;NT3 VAN SC6;Protopanaxadiol 20-O-glucoside;

分子式:C36H62O8

分子量:622.87

CAS号:39262-14-1

纯度:HPLC≥98%

熔点:181-183 °C

沸点:723.1±60.0 °C | Condition: Press: 760 Torr

密度:1.19±0.1 g/cm3 | Condition: Temp: 20 °C Press: 760 Torr

酸系度数:12.94±0.70 | Condition: Most Acidic Temp: 25 °C

储存条件:-20℃,干燥、避光、密封

规格:5mg10mg20mg50mg100mg500mg1g2g等应客户需求包装

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相关文献
Ginsenoside compound K exerts antitumour effects in renal cell carcinoma via regulation of ROS and lncRNA THOR
来源:SCI:ONCOLOGY REPORTS 作者:Shuqiu Chen 备注:影响因子:3.906
引用描述

All cells were cultured in RPMI-1640 medium (Gibco; Thermo Fisher Scientific, Inc.) with 10% heat-inactivated foetal bovine serum (FBS; HyClone; Cytiva), 100 U/ml penicillin and 100 µg/ml streptomycin (Sigma-Aldrich; Merck KGaA) at 37°C in a humidified 5% CO2 atmosphere. CK was purchased from Sichuan WeiKeqi Biological Technology Co., Ltd. Pan-caspase inhibitor z-VAD was obtained from Sigma-Aldrich (Merck KGaA) and was used at a concentration of 10 µM at 37°C.

Antidepressant-like effects of ginsenosides: A comparison of ginsenoside Rb3 and its four deglycosylated derivatives, Rg3, Rh2, compound K, and 20(S)-protopanaxadiol in mice models of despair
来源:SCI:PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR 作者:Hualin Zhang 备注:影响因子:2.781
引用描述

The ginsenoside Rb3 (Rb3) was isolated from SCLPN, and its structure was characterized by spectroscopic analysis with both ESI-MS and 13C NMR. 20(S)-Ginsenoside Rg3 (Rg3, Lot No.: 14,197–60-5-15-1), 20(S)-ginsenoside Rh2 (Rh2, Lot No.: 78214-33-2-14-6), compound K (C-K, Lot No.: 39262-14-1-14-9) and 20(S)-protopanaxadiol (PPD, Lot No.: 30636-90-9-14-2) were supplied by Sichuan Weikeqi Biological Technology Co. Ltd. (Chengdu, China). These compounds are white powders with a purity of 98%, which was verified by high

Effects of compound K, a metabolite of ginsenosides, on memory and cognitive dysfunction in db/db mice involve the inhibition of ER stress and the NLRP3 inflammasome pathway
来源:SCI:Food & Function 作者:Chu-Wen Li 备注:影响因子:4.171
引用描述

Ginsenoside compound K (CK, purity: UV ≥ 98%) was obtained from Weikeqi

Biological Technology (Sichuan, China), while sodium carboxymethylcellulose (CMCNa), glucose and insulin solutions were acquired from Sigma-Aldrich (MO, USA)


Effects of ginsenoside compound K combined with cisplatin on the proliferation, apoptosis and epithelial mesenchymal transition in MCF-7 cells of human breast cancer
来源:SCI:PHARMACEUTICAL BIOLOGY 作者:Keqiang Zhang 备注:影响因子:1.241
引用描述

CK (purity > 98%) was provided by Weikeqi Biological Technology Co. (Shichuan, China). DDP was purchased from Haosen Pharmaceutical Co., Ltd. (Jiangsu, China).

Structure–inhibition relationship of ginsenosides towards UDP-glucuronosyltransferases (UGTs)
来源:SCI:TOXICOLOGY AND APPLIED PHARMACOLOGY 作者:Zhong-Ze Fang 备注:影响因子:3.975
引用描述

Recombinant human UGT isoforms (UGT1A1, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10, UGT2B7, UGT2B15) expressed in baculovirus-infected insect cells were obtained from BD Gentest Corp. (Woburn, MA, USA). Ginsenosides Rb1, Rb2, Rc, Rd, Rg3, Rh2, C-K, ppd, ppt, Re, Rg1, Rh1, F1, and F2 were purchased from Sichuan Weikeqi Biotechnology Company (Chengdu, Sichuan, China). The purity of these compounds was above 95%. All other reagents were of HPLC grade or of the highest grade commercially available.

Effect of steam-processing of the Panax ginseng root on its inducible activity on granulocyte-colony stimulating factor secretion in intestinal epithelial cells in vitro
来源:SCI:JOURNAL OF ETHNOPHARMACOLOGY 作者:Kewen Ding 备注:影响因子:4.36
引用描述

Isomaltose was purchased from Tokyo Chemical Industry (Tokyo, Japan). Protopanaxatriol and protopanaxadiol were obtained from ChromaDex (Irvine, CA). Compound K, ginsenosides Rh1, Rd, F1, F2, Rg3, and Rh2 were obtained from Sichuan Weikeqi Biological Technology (Chengdu, Sichuam, China). Lectin from Phytolacca americana (pokeweed mitogen, PWM), dextran standards certified according to Deutsches Institut für Normung (molecular weight; 668 kDa), Dulbecco’s modified Eagle’s medium

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