U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C26H43NO4
Molecular Weight 433.6239
Optical Activity UNSPECIFIED
Defined Stereocenters 9 / 9
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GLYCOLITHOCHOLIC ACID

SMILES

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

InChI

InChIKey=XBSQTYHEGZTYJE-OETIFKLTSA-N
InChI=1S/C26H43NO4/c1-16(4-9-23(29)27-15-24(30)31)20-7-8-21-19-6-5-17-14-18(28)10-12-25(17,2)22(19)11-13-26(20,21)3/h16-22,28H,4-15H2,1-3H3,(H,27,29)(H,30,31)/t16-,17-,18-,19+,20-,21+,22+,25+,26-/m1/s1

HIDE SMILES / InChI

Molecular Formula C26H43NO4
Molecular Weight 433.6239
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 9 / 9
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 19:41:44 GMT 2023
Edited
by admin
on Fri Dec 15 19:41:44 GMT 2023
Record UNII
Q53GV75CJG
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GLYCOLITHOCHOLIC ACID
Common Name English
3.ALPHA.-HYDROXY-5.BETA.-CHOLANIC ACID GLYCINE ESTER
Systematic Name English
3.ALPHA.-HYDROXY-N-(CARBOXYMETHYL)-5.BETA.-CHOLAN-24-AMIDE
Systematic Name English
5.BETA.-CHOLAN-24-AMIDE, N-(CARBOXYMETHYL)-3.ALPHA.-HYDROXY-
Systematic Name English
LITHOCHOLIC ACID GLYCINE CONJUGATE
Systematic Name English
N-((3.ALPHA.,5.BETA.)-3-HYDROXY-24-OXOCHOLAN-24-YL)GLYCINE
Systematic Name English
LITHOCHOLYLGLYCINE
Systematic Name English
3.ALPHA.-HYDROXY-5.BETA.-CHOLANOYLGLYCINE
Systematic Name English
GLYCINE, N-((3.ALPHA.,5.BETA.)-3-HYDROXY-24-OXOCHOLAN-24-YL)-
Systematic Name English
N-(3.ALPHA.-HYDROXY-5.BETA.-CHOLANOYL)GLYCINE
Systematic Name English
GLYCINE, N-(3.ALPHA.-HYDROXY-5.BETA.-CHOLAN-24-OYL)-
Systematic Name English
Code System Code Type Description
CAS
474-74-8
Created by admin on Fri Dec 15 19:41:44 GMT 2023 , Edited by admin on Fri Dec 15 19:41:44 GMT 2023
PRIMARY
EPA CompTox
DTXSID00963828
Created by admin on Fri Dec 15 19:41:44 GMT 2023 , Edited by admin on Fri Dec 15 19:41:44 GMT 2023
PRIMARY
PUBCHEM
115245
Created by admin on Fri Dec 15 19:41:44 GMT 2023 , Edited by admin on Fri Dec 15 19:41:44 GMT 2023
PRIMARY
CHEBI
37998
Created by admin on Fri Dec 15 19:41:44 GMT 2023 , Edited by admin on Fri Dec 15 19:41:44 GMT 2023
PRIMARY
FDA UNII
Q53GV75CJG
Created by admin on Fri Dec 15 19:41:44 GMT 2023 , Edited by admin on Fri Dec 15 19:41:44 GMT 2023
PRIMARY