Structure Database (LMSD)

O HO OH OH N H H H O OH H H H H
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


Main

Classification

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
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

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Created at
-
Updated at
24th Apr 2024