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Glycolithocholic acid

Cat. No. M11304
Glycolithocholic acid  Structure
Size Price Availability Quantity
5mg USD 120  USD120 In stock
10mg USD 200  USD200 In stock
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Quality Control & Documentation
Biological Activity

Glycolithocholic acid, an endogenous metabolite, is a glycine conjugated secondary bile acid. Glycolithocholic acid can be used to study ulcerative colitis (UC), non-alcoholic steatohepatitis (NASH0) and primary sclerosing cholangitis (PSC).

Chemical Information
Molecular Weight 433.63
Formula C26H43NO4
CAS Number 474-74-8
Solubility (25°C) DMSO 45 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Alessandro Mantovani, et al. Metabolites. Plasma Bile Acid Profile in Patients with and without Type 2 Diabetes

[2] Sumit Bansal, et al. J Pharmacol Exp Ther. Inhibition of Human Sulfotransferase 2A1-Catalyzed Sulfonation of Lithocholic Acid, Glycolithocholic Acid, and Taurolithocholic Acid by Selective Estrogen Receptor Modulators and Various Analogs and Metabolites

[3] F Kuipers, et al. Clin Sci (Lond). Cholestasis induced by sulphated glycolithocholic acid in the rat: protection by endogenous bile acids

[4] F Kuipers, et al. Biochim Biophys Acta. Biliary lipid secretion in the rat. The uncoupling of biliary cholesterol and phospholipid secretion from bile acid secretion by sulfated glycolithocholic acid

[5] K Y Tserng, et al. J Lipid Res. Synthesis of sulfate esters of lithocholic acid, glycolithocholic acid, and taurolithocholic acid with sulfur trioxide-triethylamine

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