Taurocholic acid
Names | |
---|---|
IUPAC name
2-{[(3α,5β,7α,12α)-3,7,12-trihydroxy-24-oxocholan-24-yl]amino}ethanesulfonic acid | |
Identifiers | |
81-24-3 | |
3D model (Jmol) | Interactive image |
ChEBI | CHEBI:28865 |
ChEMBL | ChEMBL224867 |
ChemSpider | 6423 |
ECHA InfoCard | 100.001.216 |
4547 | |
PubChem | 6675 |
| |
| |
Properties | |
C26H45NO7S | |
Molar mass | 515.7058 g/mol |
Melting point | 125.0 °C (257.0 °F; 398.1 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references | |
Taurocholic acid, known also as cholaic acid, cholyltaurine, or acidum cholatauricum, is a deliquescent yellowish crystalline bile acid involved in the emulsification of fats. It occurs as a sodium salt in the bile of mammals. It is a conjugate of cholic acid with taurine. In medical use, it is administered as a cholagogue and choleretic.
Hydrolysis of taurocholic acid yields taurine.
For commercial use, taurocholic acid is manufactured from cattle bile, a byproduct of the meat-processing industry.[1]
This acid is also one of the many molecules in the body that has cholesterol as its precursor.
Toxicity
The median lethal dose of taurocholic acid in newborn rats is 380 mg/kg.
See also
References
- ↑ Taurocholic acid, sodium salt at GlycoFineChem.com
This article is issued from Wikipedia - version of the 8/8/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.