Contact us: +91 9550333722 040 - 40102781
Structured search
India
Choose your country
Different countries will display different contents
Try our best to find the right business for you.
My chemicalbook

Welcome back!

HomeProduct name listGlycocholic acid

Glycocholic acid

Synonym(s):3α,7α,12α-Trihydroxy-5β-cholan-24-oic acid N-(carboxymethyl)amide;Cholylglycine;N-(3α,7α,12α-Trihydroxy-24-oxocholan-24-yl)-glycine

  • CAS NO.:475-31-0
  • Empirical Formula: C26H43NO6
  • Molecular Weight: 465.63
  • MDL number: MFCD00065902
  • EINECS: 207-494-9
  • SAFETY DATA SHEET (SDS)
  • Update Date: 2024-11-26 17:46:08
Glycocholic acid Structural

What is Glycocholic acid?

Description

Glycocholic acid is a glycine-conjugated form of the primary bile acid cholic acid and has roles in the emulsification of fats. It reduces expression of the gene encoding the farnesoid X receptor (FXR) and increases expression of the genes encoding the bile acid receptors TGR5 and S1PR2 in SNU-245 cells when used at a concentration of 1.6 μmol/ml. Glycocholic acid (250 μM) increases the intracellular accumulation and cytotoxicity of epirubicin in Caco-2 cells, as well as decreases expression of the genes encoding multidrug resistance protein 1 (MDR1), MDR-associated protein 1 (MRP1), and MRP2 when used alone or in combination with epirubicin. It increases absorption of epirubicin into everted sacs of rat ileum and jejunum when used at a concentration of 250 μM. The bile acid composition ratio of glycocholic acid is elevated in bile of patients with cholangiocarcinoma compared with patients with pancreatic cancer or benign biliary diseases. Serum levels of glycocholic acid are elevated in patients with hepatocellular carcinoma compared with healthy individuals.

Description

N-Cholylglycine. Bile salt, conjugate of cholate and glycine, usually as the sodium salt. It acts as a detergent to solubilize fats for absorption and is itself absorbed. It is used as a cholagogue and choleretic.

Chemical properties

Off-White Solid

The Uses of Glycocholic acid

Labelled Glycocholic Acid. The product of conjugation of cholic acid with glycine; chief ingredient of the bile of herbivorous animals. In the weakly alkaline bile fluid glycocholic acid exists as the sodium salt.

What are the applications of Application

Glycocholic acid is a conjugate of cholic acid and glycine

Definition

ChEBI: A bile acid glycine conjugate having cholic acid as the bile acid component.

Purification Methods

Glycocholic acid crystallises from hot water as the sesquihydrate. Dry it at 110o in vacuo. An analytical sample is prepared by suspending the acid (4g) in H2O (400mL) at ~20o, heating to boiling with slow stirring, filtering hot and allowing to cool to ~20o. The acid is filtered off, washed with H2O, dried in air, recrystallised from 5% aqueous EtOH, washed well and dried over P2O5 in a moderate vacuum to constant weight. Recrystallisation from EtOH/EtOAc, and drying, gave the anhydrous acid. [Cortese & Bauman J Am Chem Soc 57 1393 1935, Bergstrom & Norman Acta Chem Scand 7 1126 1953, Beilstein 10 IV 2077.]

Properties of Glycocholic acid

Melting point: 128°C
Boiling point: 568.76°C (rough estimate)
Density  1.1336 (rough estimate)
refractive index  1.6000 (estimate)
storage temp.  Refrigerator
solubility  methanol: 0.1 g/mL, clear, colorless
form  Solid
pka 4.4(at 25℃)
color  White to Off-White
Water Solubility  329.9mg/L(20 ºC)
Merck  13,4507
Stability: Hygroscopic
CAS DataBase Reference 475-31-0(CAS DataBase Reference)
NIST Chemistry Reference Glycocholic acid(475-31-0)

Safety information for Glycocholic acid

Signal word Warning
Pictogram(s)
ghs
Exclamation Mark
Irritant
GHS07
Precautionary Statement Codes P280:Wear protective gloves/protective clothing/eye protection/face protection.

Computed Descriptors for Glycocholic acid

InChIKey RFDAIACWWDREDC-NSPZZGDONA-N

Related products of tetrahydrofuran

You may like

Statement: All products displayed on this website are only used for non medical purposes such as industrial applications or scientific research, and cannot be used for clinical diagnosis or treatment of humans or animals. They are not medicinal or edible.