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Glycolithocholic acid

Catalog No.
C8620
An endogenous metabolite and belongs to the category of glycine-binding secondary bile acids
Grouped product items
SizePriceStock Qty
1mg
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In stock
5mg
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In stock
10mg
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In stock
For scientific research use only and should not be used for diagnostic or medical purposes.

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Background

Glycolithocholic acid (Lithocholylglycine) is an endogenous metabolite and belongs to the category of glycine-binding secondary bile acids. It is formed by the metabolism of primary bile acids into choline by intestinal microorganisms, which then combines with glycine. Studies have shown that this compound is abnormally expressed in diseases such as ulcerative colitis (UC), non-alcoholic steatohepatitis (NASH), and primary sclerosing cholangitis (PSC), and can serve as a potential diagnostic marker - the disorder of intestinal flora in UC patients may lead to metabolic imbalance, and liver damage in NASH is accompanied by changes in its concentration The level of PSC patients will also fluctuate abnormally in the state of cholestasis. As a secondary bile acid, it has both liposoluble and polar characteristics and plays a role in the metabolic regulation of the gut-liver axis. Abnormal concentration of it may reflect the disorder of host-microbe interaction and the pathological process of liver, gallbladder and intestinal diseases.

Chemical Properties

Physical AppearanceA solid
StorageStore at -20°C for 3 years.
M.Wt433.62
Cas No.474-74-8
FormulaC26H43NO4
SynonymsLithocholylglycine
Solubility≥52 mg/mL in DMSO; ≥50.6 mg/mL in EtOH; insoluble in H2O
Chemical Name((R)-4-((3R,5R,8R,9S,10S,13R,14S,17R)-3-hydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoyl)glycine
SDFDownload SDF
Canonical SMILESO=C(NCC(O)=O)CC[C@@H](C)[C@H]1CC[C@@]2([H])[C@]3([H])CC[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])CC[C@@]21C
Shipping ConditionSmall Molecules with Blue Ice, Modified Nucleotides with Dry Ice.
General tips We do not recommend long-term storage for the solution, please use it up soon.

Quality Control

Chemical structure

Glycolithocholic acid