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

Details

Stereochemistry ABSOLUTE
Molecular Formula C26H43NO5
Molecular Weight 449.6233
Optical Activity UNSPECIFIED
Defined Stereocenters 10 / 10
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of URSODEOXYCHOLYLGLYCINE

SMILES

[H][C@@]1(CC[C@@]2([H])[C@]3([H])[C@@H](O)C[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=GHCZAUBVMUEKKP-XROMFQGDSA-N
InChI=1S/C26H43NO5/c1-15(4-7-22(30)27-14-23(31)32)18-5-6-19-24-20(9-11-26(18,19)3)25(2)10-8-17(28)12-16(25)13-21(24)29/h15-21,24,28-29H,4-14H2,1-3H3,(H,27,30)(H,31,32)/t15-,16+,17-,18-,19+,20+,21+,24+,25+,26-/m1/s1

HIDE SMILES / InChI

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
PubMed

PubMed

TitleDatePubMed
Positions of conjugation of bile acids with glucose and N-acetylglucosamine in vitro.
1994 Sep
Expression and transport properties of the human ileal and renal sodium-dependent bile acid transporter.
1998 Jan
Whole-cell response characteristics of ciliated and microvillous olfactory receptor neurons to amino acids, pheromone candidates and urine in rainbow trout.
2001 Nov
Patents
Name Type Language
URSODEOXYCHOLYLGLYCINE
Common Name English
3.ALPHA.,7.BETA.-DIHYDROXY-5.BETA.-CHOLANOYLGLYCINE
Systematic Name English
N-((3.ALPHA.,5.BETA.,7.BETA.)-3,7-DIHYDROXY-24-OXOCHOLAN-24-YL)GLYCINE
Systematic Name English
GLYCOURSODEOXYCHOLIC ACID
Common Name English
N-(3.ALPHA.,7.BETA.-DIHYDROXY-5.BETA.-CHOLAN-24-OYL)GLYCINE
Systematic Name English
GLYCINE, N-((3.ALPHA.,5.BETA.,7.BETA.)-3,7-DIHYDROXY-24-OXOCHOLAN-24-YL)-
Systematic Name English
GLYCYLURSODEOXYCHOLIC ACID
Common Name English
URSODEOXYCHOLYLGLYCINE, (+)-
Common Name English
Code System Code Type Description
CHEBI
89929
Created by admin on Sat Dec 16 09:30:00 GMT 2023 , Edited by admin on Sat Dec 16 09:30:00 GMT 2023
PRIMARY
PUBCHEM
12310288
Created by admin on Sat Dec 16 09:30:00 GMT 2023 , Edited by admin on Sat Dec 16 09:30:00 GMT 2023
PRIMARY
FDA UNII
PF1G5J2X2A
Created by admin on Sat Dec 16 09:30:00 GMT 2023 , Edited by admin on Sat Dec 16 09:30:00 GMT 2023
PRIMARY
EPA CompTox
DTXSID20862344
Created by admin on Sat Dec 16 09:30:00 GMT 2023 , Edited by admin on Sat Dec 16 09:30:00 GMT 2023
PRIMARY
CAS
64480-66-6
Created by admin on Sat Dec 16 09:30:00 GMT 2023 , Edited by admin on Sat Dec 16 09:30:00 GMT 2023
PRIMARY