Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	38256
Common Name:	Retinoyl b-glucuronide
Systematic Name:	(2S,3S,4S,5R,6S)-6-{[(2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)nona-2,4,6,8-tetraenoyl]oxy}-3,4,5-trihydroxyoxane-2-carboxylic acid
RefMet Name:	Retinoyl beta-glucuronide
Synonyms:	[PubChem Synonyms]
Exact Mass:	476.2410 (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:	C26H36O8
InChIKey:	MTGFYEHKPMOVNE-NEFMKCFNSA-N
LIPID MAPS Category:	Prenol Lipids
LIPID MAPS mainclass:	Isoprenoids
LIPID MAPS subclass:	Retinoids
SMILES:	C/C(=CC=CC(=CC(=O)O[C@H]1[C@@H]([C@H]([C@@H]([C@@H](C(=O)O)O1)O)O)O)C)/C=C/C1=C(C)CCCC1(C)C
Studies:	Available studies (via RefMet name)

Select appropriate tab below to view additional details:

All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	5281877
LIPID MAPS ID:	LMPR01090051
CHEBI ID:	28870
HMDB ID:	HMDB0003141
KEGG ID:	C11061
Chemspider ID:	4445170
METLIN ID:	2280
Plant Metabolite Hub(Pmhub):	MS000016373

Calculated physicochemical properties (?):

Heavy Atoms:	34
Rings:	2
Aromatic Rings:	0
Rotatable Bonds:	8
van der Waals Molecular volume:	485.48 Å3 molecule-1
Toplogical Polar Sufrace Area:	135.59 Å2 molecule-1
Hydrogen Bond Donors:	4
Hydrogen Bond Acceptors:	8
logP:	4.39
Molar Refractivity:	129.10
Fraction sp3 Carbons:	0.54
sp3 Carbons:	14

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