Metabolomics Structure Database

 
MW REGNO: 51820
Common Name:trans-hex-2-enoyl-CoA
Systematic Name:3'-phosphoadenosine 5'-{3-[(3R)-4-({3-[(2-{[(2E)-hex-2-enoyl]sulfanyl}ethyl)amino]-3-oxopropyl}amino)-3-hydroxy-2,2-dimethyl-4-oxobutyl] dihydrogen diphosphate}
RefMet Name:2E-Hexenoyl-CoA
Synonyms:(2E)-hexenoyl-coenzyme A; 2E-hexenoyl-CoA; 2E-hexenoyl-coenzyme A; trans-2,3-dehydrohexanoyl-CoA; trans-2,3-dehydrohexanoyl-coenzyme A; trans-2-hexenoyl-coenzyme A; trans-hex-2-enoyl-coenzyme A [PubChem Synonyms]
Exact Mass:
863.1727 (neutral)    Calculate m/z:
Formula:C27H44N7O17P3S
InChIKey:OINXHIBNZUUIMR-IXUYQXAASA-N
LIPID MAPS Category:Fatty Acyls [FA]
LIPID MAPS mainclass:Fatty esters [FA07]
LIPID MAPS subclass:Fatty acyl CoAs [FA0705]
SMILES:CCC/C=C/C(=O)SCCNC(=O)CCNC(=O)[C@@H](C(C)(C)COP(=O)(O)OP(=O)(O)OC[C@@H]1[C@H]([C@H]([C@H](n2cnc3c(N)ncnc23)O1)O)OP(=O)(O)O)O
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:11966204
LIPID MAPS ID:LMFA07050393
CHEBI ID:28706
HMDB ID:HMDB0003944
KEGG ID:C05271
MetaCyc ID:CPD0-2121
Plant Metabolite Hub(Pmhub):MS000018635

Calculated physicochemical properties (?):

Heavy Atoms: 55  
Rings: 3  
Aromatic Rings: 2  
Rotatable Bonds: 23  
van der Waals Molecular volume: 700.09 Å3 molecule-1  
Toplogical Polar Sufrace Area: 365.70 Å2 molecule-1  
Hydrogen Bond Donors: 9  
Hydrogen Bond Acceptors: 21  
logP: 3.27  
Molar Refractivity: 195.09  
Fraction sp3 Carbons: 0.63  
sp3 Carbons: 17  

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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