Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	28987
Common Name:	Antheraxanthin
Systematic Name:	(1R,3S,6S)-6-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-3-ol
RefMet Name:	Antheraxanthin
Synonyms:	[PubChem Synonyms]
Exact Mass:	584.4229 (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:	C40H56O3
InChIKey:	OFNSUWBAQRCHAV-OYQUVCAXSA-N
LIPID MAPS Category:	Prenol Lipids [PR]
LIPID MAPS mainclass:	Isoprenoids [PR01]
LIPID MAPS subclass:	C40 isoprenoids (tetraterpenes) [PR0107]
Massbank MS spectra:	View MS spectra
SMILES:	C/C(=CC=CC=C(/C)C=CC=C(/C)C=C[C@]12C(C)(C)C[C@@H](C[C@@]1(C)O2)O)/C=C/C=C(C)/C=C/C1=C(C)C[C@H](CC1(C)C)O
Studies:	Available studies (via RefMet name)

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All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	5281223
LIPID MAPS ID:	LMPR01070262
CHEBI ID:	27867
KEGG ID:	C08579
Plant Metabolite Hub(Pmhub):	MS000010867
PhytoHub ID:	PHUB000343

Calculated physicochemical properties (?):

Heavy Atoms:	43
Rings:	3
Aromatic Rings:	0
Rotatable Bonds:	10
van der Waals Molecular volume:	663.45 Å3 molecule-1
Toplogical Polar Sufrace Area:	52.99 Å2 molecule-1
Hydrogen Bond Donors:	2
Hydrogen Bond Acceptors:	3
logP:	10.90
Molar Refractivity:	185.74
Fraction sp3 Carbons:	0.50
sp3 Carbons:	20

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