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My Cart> Small Molecule Compounds > Inhibitors & Antagonists & Agonists > Immunology & Inflammation > Ginsenoside CKCAS：39262-14-1
Molecular Formula：C36H62O8
Molecular Weight：622.87
Storage：Powder:2-8℃，2 years;Insolvent(Mother Liquid):-20℃，6 months;-80℃，1 year
Purity：HPLC≥98%
Appearance：White to off-white Solid
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| CAS | 39262-14-1 |
| Name | Ginsenoside CK |
| Molecular Formula | C36H62O8 |
| Molecular Weight | 622.87 |
| Solubility | Soluble in DMSO ≥10mg/mL |
| Purity | HPLC≥98% |
| Appearance | White to off-white Solid |
| Storage | Powder:2-8℃，2 years;Insolvent(Mother Liquid):-20℃，6 months;-80℃，1 year |
| MDL | MFCD07772261 |
| SMILES | C[C@@]([C@@]12C)(CC[C@@]3([H])C4(C)C)[C@@](C[C@@H](O)[C@]1([H])[C@]([C@@](CC/C=C(C)/C)(C)O[C@@H]([C@@H]([C@@H](O)[C@@H]5O)O)O[C@@H]5CO)([H])CC2)([H])[C@]3(CC[C@@H]4O)C |
| InChIKey | FVIZARNDLVOMSU-IRFFNABBSA-N |
| InChI | 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-/m0/s1 |
| PubChem CID | 9852086 |
| Target Point | COX;iNOS |
| Passage | Immunology & Inflammation |
| Background | It exerts anti-inflammatory effects by inhibiting inducible nitric oxide synthase (iNOS) and COX-2. |
| Biological Activity | Ginsenoside C-K 是一种 Ginsenoside Rb1 的细菌代谢物。Ginsenoside C-K 通过抑制诱生型一氧化氮合酶 (iNOS) 和 COX-2 来发挥抗炎作用。在人肝微粒体中，Ginsenoside C-K 抑制 CYP2C9 和 CYP2A6 活性，IC50 分别为 32.0±3.6 μM和 63.6±4.2 μM。[1-4] |
| Data Literature Source | [1]. Kim JH，et al. Role of ginsenosides，the main active components of Panax ginseng，in inflammatory responsesand diseases. J Ginseng Res. 2017 Oct;41(4):435-443. [2]. Zhang J，et al. Ginsenosides Regulate PXR/NF-κB Signaling and Attenuate Dextran Sulfate Sodium-Induced Colitis. Drug Metab Dispos. 2015 Aug;43(8):1181-9. [3]. Liu KK，et al. Ginsenoside compound K suppresses the abnormal activation of T lymphocytes in mice with collagen-induced arthritis. Acta Pharmacol Sin. 2014 May;35(5):599-612. [4]. Liu Y，et al. Ginsenoside metabolites，rather than naturally occurring ginsenosides，lead to inhibition of human cytochrome P450 enzymes. Toxicol Sci. 2006 Jun;91(2):356-64 |
| Unit | Bottle |
| Specification | 5mg 10mM*1mL in DMSO 10mg |
Remark：These protocols are for reference only. Solarbio does not independently validate these methods.
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