Metabolomics Structure Database

 
MW REGNO: 50152
Common Name:Stearoyl-CoA
Systematic Name:3'-phosphoadenosine 5'-(3-{(3R)-3-hydroxy-2,2-dimethyl-4-[(3-{[2-(octadecanoylsulfanyl)ethyl]amino}-3-oxopropyl)amino]-4-oxobutyl} dihydrogen diphosphate)
RefMet Name:Stearoyl-CoA
Synonyms:C18:0-CoA; C18:0-coenzyme A; S-stearoyl-CoA; S-stearoylcoenzyme A; octadecanoyl-CoA; octadecanoyl-coenzyme A; stearoyl-coenzyme A [PubChem Synonyms]
Exact Mass:
1033.3762 (neutral)    Calculate m/z:
Formula:C39H70N7O17P3S
InChIKey:SIARJEKBADXQJG-LFZQUHGESA-N
LIPID MAPS Category:Fatty Acyls [FA]
LIPID MAPS mainclass:Fatty esters [FA07]
LIPID MAPS subclass:Fatty acyl CoAs [FA0705]
SMILES:CCCCCCCCCCCCCCCCCC(=O)SCCNC(=O)CCNC(=O)[C@@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@@H]1O[C@@H]([C@@H](O)[C@H]1OP(O)(O)=O)[n]1c[n]c2c(N)[n]c[n]c12
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:94140
LIPID MAPS ID:LMFA07050369
CHEBI ID:15541
HMDB ID:HMDB0001114
KEGG ID:C00412
MetaCyc ID:STEAROYL-COA
Plant Metabolite Hub(Pmhub):MS000016864

Calculated physicochemical properties (?):

Heavy Atoms: 67  
Rings: 3  
Aromatic Rings: 2  
Rotatable Bonds: 36  
van der Waals Molecular volume: 910.33 Å3 molecule-1  
Toplogical Polar Sufrace Area: 365.70 Å2 molecule-1  
Hydrogen Bond Donors: 9  
Hydrogen Bond Acceptors: 21  
logP: 8.18  
Molar Refractivity: 250.59  
Fraction sp3 Carbons: 0.79  
sp3 Carbons: 31  

Human Pathway links:

HMDB and KEGG 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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