Structure Database (LMSD)
Common Name
Glycocholic Acid
Systematic Name
N-(3α,7α,12α-trihydroxy-5β-cholan-24-oyl)-glycine
Synonyms
- Cholylglycine
- GCA
LM ID
LMST05030001
Formula
Exact Mass
Calculate m/z
465.309039
Sum Composition
Status
Active
3D model of Glycocholic Acid
Please note: Where there are chiral atoms but the stereochemistry is undefined, the 3D model takes an arbitrary conformation
Main
Classification
Category
Main Class
Sub Class
String Representations
InChiKey (Click to copy)
RFDAIACWWDREDC-FRVQLJSFSA-N
InChi (Click to copy)
InChI=1S/C26H43NO6/c1-14(4-7-22(31)27-13-23(32)33)17-5-6-18-24-19(12-21(30)26(17,18)3)25(2)9-8-16(28)10-15(25)11-20(24)29/h14-21,24,28-30H,4-13H2,1-3H3,(H,27,31)(H,32,33)/t14-,15+,16-,17-,18+,19+,20-,21+,24+,25+,26-/m1/s1
SMILES (Click to copy)
[C@]12([C@H](O)C[C@]3([H])C[C@H](O)CC[C@]3(C)[C@@]1([H])C[C@H](O)[C@]1(C)[C@@]([H])([C@@](C)([H])CCC(NCC(O)=O)=O)CC[C@@]21[H])[H]
References
Taxonomy Information
Curated from
NCBI taxonomy class
Reference
Homo sapiens
(#9606)
Mammalia
(#40674)
The capacity of human liver homogenates to synthesize taurocholic and glycocholic acid in vitro.,
Scand J Clin Lab Invest, 1966
Scand J Clin Lab Invest, 1966
Pubmed ID:
5959320
Other Databases
Wikipedia
KEGG ID
HMDB ID
CHEBI ID
PubChem CID
SwissLipids ID
Cayman ID
PDB ID
GuidePharm ID
Calculated Physicochemical Properties
Heavy Atoms
33
Rings
4
Aromatic Rings
0
Rotatable Bonds
6
Van der Waals Molecular Volume
467.38
Topological Polar Surface Area
127.09
Hydrogen Bond Donors
5
Hydrogen Bond Acceptors
7
logP
3.71
Molar Refractivity
125.07
Admin
Created at
-
Updated at
24th Apr 2024