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Key Documents

SMB00348

Sigma-Aldrich

人参皂苷化合物 K

≥96% (HPLC)

同義詞:

(3B,12B)-3,12-二羟基达马-24-烯-20-基 β-D-吡喃葡萄糖苷, 20 (S)-人参皂苷 Ck, 人参皂苷 K, 原人参二醇 20-O-葡萄糖苷

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About This Item

經驗公式(希爾表示法):
C36H62O8
CAS號碼:
分子量::
622.87
分類程式碼代碼:
12352205
PubChem物質ID:
NACRES:
NA.25

化驗

≥96% (HPLC)

形狀

powder

應用

metabolomics
vitamins, nutraceuticals, and natural products

SMILES 字串

CC(C)=CCC[C@](C1C2[C@H](O)CC3[C@@]([C@]2(C)CC1)(C)CCC4C(C)(C)[C@@H](O)CC[C@@]43C)(C)O[C@@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@H]5O

InChI

1S/C36H62O8/c1-20(2)10-9-14-36(8,44-31-30(42)29(41)28(40)23(19-37)43-31)21-11-16-35(7)27(21)22(38)18-25-33(5)15-13-26(39)32(3,4)24(33)12-17-34(25,35)6/h10,21-31,37-42H,9,11-19H2,1-8H3/t21?,22-,23-,24?,25?,26+,27?,28-,29+,30-,31+,33+,34-,35-,36+/m1/s1

InChI 密鑰

FVIZARNDLVOMSU-KJULZEBLSA-N

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一般說明

人参皂苷化合物K是在人参根中发现的一种四环达玛烷型三萜皂苷。它是人参的主要成分,人参传统上用于增加对压力和衰老的抵抗力。

應用


  • Combination of Electrochemistry and Mass Spectrometry to Study Nitric Oxide Metabolism and Its Modulation by Compound K in Breast Cancer Cells.: This research explores the interaction of Ginsenoside Compound K with nitric oxide metabolism in breast cancer cells, employing a combination of electrochemical techniques and mass spectrometry to elucidate the metabolic pathways and potential therapeutic effects of Compound K (Zhao et al., 2022).

  • Metabolic analysis of Panax notoginseng saponins with gut microbiota-mediated biotransformation by HPLC-DAD-Q-TOF-MS/MS.: This article investigates the gut microbiota-mediated biotransformation of Panax notoginseng saponins, including Compound K, detailing the complex interactions and metabolic profiles in a biological system, which could inform their therapeutic use and bioavailability (Chen et al., 2018).

生化/生理作用

人参皂苷化合物K具有很多药理性质,包括抗糖尿病、抗炎、肝脏保护、抗过敏和抗癌作用。它在大鼠中也具有神经保护性质,可以从突触丧失和记忆损害中恢复。人参皂苷化合物K可以抑制人脐静脉内皮细胞(HUVEC)中多种基因表达,从而抑制内皮细胞的迁移和血管生成。

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Oral

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

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Catherine Hu et al.
European journal of pharmacology, 815, 501-511 (2017-10-17)
Conflicting data exist on the effect of ginsenosides on transactivation of human glucocorticoid receptor α (herein referred to as glucocorticoid receptor), and relatively little is known regarding the effect of these chemicals on transrepression of this receptor. We investigated the

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