Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	50056
Common Name:	Succinyl-CoA
Systematic Name:	3'-phosphoadenosine 5'-{3-[(3R)-4-{[3-({2-[(3-carboxypropanoyl)sulfanyl]ethyl}amino)-3-oxopropyl]amino}-3-hydroxy-2,2-dimethyl-4-oxobutyl] dihydrogen diphosphate}
RefMet Name:	Succinyl-CoA
Synonyms:	Coenzyme A, S-(hydrogen butanedioate); S-(3-Carboxy-propionyl)-coenzym-A; S-(3-carboxy-propionyl)-CoA; S-(3-carboxypropionyl)-coenzyme-A; S-(Hydrogen succinyl)coenzyme A; S-(hydrogen succinyl)-CoA; Succinyl-coenzyme A; succinyl-CoA [PubChem Synonyms]
Exact Mass:	867.1313 (neutral)    Calculate m/z: (Choose adduct) [M+H]+ [M+H-H2O]+ [M.]+ [M+2H]2+ [M+3H]3+ [M+4H]4+ [M+K]+ [M+2K]2+ [M-H+2K]+ [M+Na]+ [M+2Na]2+ [M-H+2Na]+ [M+Li]+ [M+2Li]2+ [M+NH4]+ [M-H]- [M-2H]2- [M-3H]3- [M-4H]4- [M+Cl]- [M+OAc]- [M+HCOO]- M(neutral)
Formula:	C25H40N7O19P3S
InChIKey:	VNOYUJKHFWYWIR-ITIYDSSPSA-N
LIPID MAPS Category:	Fatty Acyls [FA]
LIPID MAPS mainclass:	Fatty esters [FA07]
LIPID MAPS subclass:	Fatty acyl CoAs [FA0705]
MoNA MS spectra:	View MS spectra
SMILES:	CC(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)[C@H](C(=O)NCCC(=O)NCCSC(=O)CCC(=O)O)O
Studies:	Available studies (via RefMet name)

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All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	92133
LIPID MAPS ID:	LMFA07050370
CHEBI ID:	15380
HMDB ID:	HMDB0001022
KEGG ID:	C00091
MetaCyc ID:	SUC-COA
Plant Metabolite Hub(Pmhub):	MS000016795

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