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Ginsenoside CK

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    Ginsenoside CK
  • Ginsenoside CK
Cat No: 29926
Biochemicals - Kinase Inhibitors
Cayman

Ginsenoside CK is a metabolite of the saponin ginsenoside Rb1 (Item No. 15319) that has diverse biological activities.{52367,52368,52369,52370} Ginsenoside CK is formed from ginsenoside Rb1 via intestinal bacterial exo-β-D-glucosidase.{52367} It reduc...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • (3?,12?)-3,12-dihydroxydammar-24-en-20-yl, ?-D-glucopyranoside
Correlated keywords:
  • 79104-63-5 852637-00-4 IH-901 mmp2 MMP9 MHCC97H Rb-1
Product Overview:
Ginsenoside CK is a metabolite of the saponin ginsenoside Rb1 (Item No. 15319) that has diverse biological activities.{52367,52368,52369,52370} Ginsenoside CK is formed from ginsenoside Rb1 via intestinal bacterial exo-β-D-glucosidase.{52367} It reduces protein levels of matrix metalloproteinase-2 (MMP-2) and pro-MMP-9 in, and inhibits growth, adhesion, and invasion of, MHCC97-H human hepatocellular carcinoma cells (HCCs) when used at concentrations of 50 and 75 µM.{52368} It inhibits metastasis in an MHCC97-H mouse xenograft model but does not reduce tumor growth. Ginsenoside CK reduces the percentage of memory B cells in the spleen, the number of swollen joints, and lymph node hyperplasia in an adjuvant-induced model of rheumatoid arthritis.{52369} It increases the activity of pSer9-glycogen synthase kinase and insulin degrading enzyme (IDE) and reduces the accumulation of amyloid-β (1-42) (Aβ42; Item No. 20574) in the rat hippocampal CA1 and CA3 regions in a model of vascular dementia induced by chronic cerebral hypofusion.{52370} It also increases the percentage of time spent in the target quadrant of the Morris water maze when administered at doses of 100 and 200 mg/kg in the same model.
Size 5 mg
Shipping dry ice
CAS Number 39262-14-1
Molecular Formula C36H62O8
SMILES O[C@H]1[C@@]2([H])[C@](CC[C@]2([H])[C@@](CC/C=C(C)/C)(C)O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)(C)[C@]4(C)CC[C@]5([H])[C@@](CC[C@H](O)C5(C)C)(C)[C@@]4([H])C1
Molecular Weight 622,9
Formulation A crystalline solid
Purity ≥95%
Custom Code 2938.90
UNSPSC code 12352100

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Cayman Chemical's mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.

Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

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ISO/IEC 17025:2005
ISO Guide 34:2009

Cayman is a leader in the field of emerging drugs of abuse, providing high-purity Schedule I-V Controlled Substances to federally-licensed laboratories and qualified academic research institutions for forensic analyses. We are certified by ACLASS Accreditation Services with dual accreditation to ISO/IEC 17025:2005 and ISO Guide 34:2009.

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