Taurocholic acid
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Taurocholic acid | |
---|---|
IUPAC name | 2-{[(3alpha,5beta, 7alpha,12alpha) -3,7,12-trihydroxy- 24-oxocholan-24-yl] amino} ethanesulfonic acid |
Identifiers | |
CAS number | [81-24-3] |
SMILES | C[C@@]34[C@] (CC[C@@H]4[C@@H] (CCC(NCCS(O) (=O)=O)=O)C) ([H])[C@]2([H]) [C@H](O)C[C@]1 ([H])C[C@H](O)CC [C@@](C)1[C@] ([H])2C[C@@H]3O |
Properties | |
Molecular formula | C26H45NO7S |
Molar mass | 515.7058 g/mol |
Density | x.xxx g/cm3 |
Melting point |
125.0 °C |
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and 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, a nonessential amino acid.
For commercial use, taurocholic acid is manufactured from cattle bile, a byproduct of the meat-processing industry.
[edit] See also
[edit] References
The references in this article would be clearer with a different or consistent style of citation, footnoting, or external linking. |
- Formula, model
- PubChem. Retrieved on February 5, 2006.
- http://www.chemexper.com/. Retrieved on February 5, 2006.