Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	67702
Common Name:	Vitamin E Nicotinate
Systematic Name:	[(2R)-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]chroman-6-yl] pyridine-3-carboxylate
RefMet Name:	Vitamin E Nicotinate
Synonyms:	Renascin; tocopherol nicotinate; TOCOPHERYL NICOTINATE; DL-alpha tocopheryl nicotinate; D-alpha tocopheryl nicotinate [PubChem Synonyms]
Exact Mass:	535.4025 (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:	C35H53NO3
InChIKey:	MSCCTZZBYHQMQJ-AZAGJHQNSA-N
LIPID MAPS Category:	Prenol Lipids
LIPID MAPS mainclass:	Quinones and hydroquinones
LIPID MAPS subclass:	Vitamin E
SMILES:	CC(C)CCC[C@@H](C)CCC[C@@H](C)CCC[C@]1(C)CCc2c(O1)c(C)c(C)c(OC(=O)c1c[n]ccc1)c2C
Studies:	Available studies (via RefMet name)

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All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	27990
CHEBI ID:	32239
HMDB ID:	HMDB0259853
KEGG ID:	C12981
Plant Metabolite Hub(Pmhub):	MS000023192

Calculated physicochemical properties (?):

Heavy Atoms:	39
Rings:	3
Aromatic Rings:	2
Rotatable Bonds:	15
van der Waals Molecular volume:	574.07 Å3 molecule-1
Toplogical Polar Sufrace Area:	50.49 Å2 molecule-1
Hydrogen Bond Donors:	0
Hydrogen Bond Acceptors:	4
logP:	10.04
Molar Refractivity:	162.43
Fraction sp3 Carbons:	0.66
sp3 Carbons:	23

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