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Details

Stereochemistry ABSOLUTE
Molecular Formula C24H38O3
Molecular Weight 374.5567
Optical Activity UNSPECIFIED
Defined Stereocenters 8 / 8
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DEHYDROLITHOCHOLIC ACID

SMILES

[H][C@@]1(CC[C@@]2([H])[C@]3([H])CC[C@]4([H])CC(=O)CC[C@]4(C)[C@@]3([H])CC[C@]12C)[C@H](C)CCC(O)=O

InChI

InChIKey=KIQFUORWRVZTHT-OPTMKGCMSA-N
InChI=1S/C24H38O3/c1-15(4-9-22(26)27)19-7-8-20-18-6-5-16-14-17(25)10-12-23(16,2)21(18)11-13-24(19,20)3/h15-16,18-21H,4-14H2,1-3H3,(H,26,27)/t15-,16-,18+,19-,20+,21+,23+,24-/m1/s1

HIDE SMILES / InChI

Molecular Formula C24H38O3
Molecular Weight 374.5567
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 8 / 8
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
St. John's wort induces hepatic drug metabolism through activation of the pregnane X receptor.
2000 Jun 20
The nuclear receptor PXR is a lithocholic acid sensor that protects against liver toxicity.
2001 Mar 13
Vitamin D receptor as an intestinal bile acid sensor.
2002 May 17
Specificity of human alcohol dehydrogenase 1C*2 (gamma2gamma2) for steroids and simulation of the uncompetitive inhibition of ethanol metabolism.
2003 Feb 1
Novel pathways of bile acid metabolism involving CYP3A4.
2005 Feb 21
Evolution of the pregnane x receptor: adaptation to cross-species differences in biliary bile salts.
2005 Jul
Evolutionary selection across the nuclear hormone receptor superfamily with a focus on the NR1I subfamily (vitamin D, pregnane X, and constitutive androstane receptors).
2005 Sep 30
In silico prediction of pregnane X receptor activators by machine learning approaches.
2007 Jan
Rapid and drastic induction of CYP3A4 mRNA expression via vitamin D receptor in human intestinal LS180 cells.
2007 Oct
Characterization of an oligomeric carbonyl reductase of dog liver: its identity with peroxisomal tetrameric carbonyl reductase.
2007 Sep
Biotransformation of lithocholic acid by rat hepatic microsomes: metabolite analysis by liquid chromatography/mass spectrometry.
2008 Feb
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 18:30:32 GMT 2023
Edited
by admin
on Fri Dec 15 18:30:32 GMT 2023
Record UNII
96JBM35FXF
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DEHYDROLITHOCHOLIC ACID
Common Name English
3-OXOLITHOCHOLIC ACID
Common Name English
CHOLAN-24-OIC ACID, 3-OXO-, (5.BETA.)-
Common Name English
3-KETOLITHOCHOLIC ACID
Common Name English
3-KETO-5.BETA.-CHOLAN-24-OIC ACID
Systematic Name English
5.BETA.-CHOLANIC ACID-3-ONE
Common Name English
5.BETA.-CHOLANIC ACID, 3-OXO-
Common Name English
3-OXO-5.BETA.-CHOLAN-24-OIC ACID
Systematic Name English
5.BETA.-CHOLAN-24-OIC ACID, 3-OXO-
Common Name English
3-KETO-5.BETA.-CHOLANIC ACID
Systematic Name English
3-OXOCHOLANIC ACID
Systematic Name English
Code System Code Type Description
PUBCHEM
5283906
Created by admin on Fri Dec 15 18:30:32 GMT 2023 , Edited by admin on Fri Dec 15 18:30:32 GMT 2023
PRIMARY
CHEBI
17639
Created by admin on Fri Dec 15 18:30:32 GMT 2023 , Edited by admin on Fri Dec 15 18:30:32 GMT 2023
PRIMARY
FDA UNII
96JBM35FXF
Created by admin on Fri Dec 15 18:30:32 GMT 2023 , Edited by admin on Fri Dec 15 18:30:32 GMT 2023
PRIMARY
CAS
1553-56-6
Created by admin on Fri Dec 15 18:30:32 GMT 2023 , Edited by admin on Fri Dec 15 18:30:32 GMT 2023
PRIMARY
EPA CompTox
DTXSID60935182
Created by admin on Fri Dec 15 18:30:32 GMT 2023 , Edited by admin on Fri Dec 15 18:30:32 GMT 2023
PRIMARY
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