Metabolomics Structure Database

 
MW REGNO: 36826
Common Name:3alpha,7alpha-dihydroxy-5beta-cholestan-26-al
Systematic Name:3alpha,7alpha-dihydroxy-5beta-cholestan-26-al
RefMet Name:3alpha,7alpha-Dihydroxy-5beta-cholestan-26-al
Synonyms:3alpha,7alpha-Dihydroxy-5beta-cholestan-26-al; 3alpha,7alpha-dihydroxy-5beta-cholestan-26-al [PubChem Synonyms]
Exact Mass:
418.3447 (neutral)    Calculate m/z:
Formula:C27H46O3
InChIKey:YWGOKHMOJTZGBN-UGMUFZQESA-N
LIPID MAPS Category:Sterol Lipids [ST]
LIPID MAPS mainclass:Bile acids and derivatives [ST04]
LIPID MAPS subclass:C27 bile acids, alcohols, and derivatives [ST0403]
SMILES:CC(CCC[C@@H](C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@H](C[C@H]1C[C@H]3O)O)C=O
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:5460041
LIPID MAPS ID:LMST04030162
CHEBI ID:27428
HMDB ID:HMDB0006894
KEGG ID:C05445
MetaCyc ID:CPD-10587
Plant Metabolite Hub(Pmhub):MS000018713

Calculated physicochemical properties (?):

Heavy Atoms: 30  
Rings: 4  
Aromatic Rings: 0  
Rotatable Bonds: 6  
van der Waals Molecular volume: 449.95 Å3 molecule-1  
Toplogical Polar Sufrace Area: 57.53 Å2 molecule-1  
Hydrogen Bond Donors: 2  
Hydrogen Bond Acceptors: 3  
logP: 6.19  
Molar Refractivity: 121.88  
Fraction sp3 Carbons: 0.96  
sp3 Carbons: 26  

Human Pathway links:

REACTOME pathways containing this metabolite

References

LIPID MAPS classification: "Update of the LIPID MAPS comprehensive classification system for lipids", Fahy E, Subramaniam S, Murphy RC, Nishijima M, Raetz CR, Shimizu T, Spener F, van Meer G, Wakelam MJ, and Dennis EA, J. Lipid Res. (2009) 50: S9-S14. DOI: 10.1194/jlr.R800095-JLR200
ClassyFire classification: "ClassyFire: automated chemical classification with a comprehensive, computable taxonomy", Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS, J. Cheminformatics (2016) 8:61. DOI: 10.1186/s13321-016-0174-y

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