Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	70312
Common Name:	Laserpitin
Systematic Name:	[(3R,3aS,4S,6R,8S,8aS)-3,6-dihydroxy-3-isopropyl-6,8a-dimethyl-8-[(Z)-2-methylbut-2-enoyl]oxy-7-oxo-1,2,3a,4,5,8-hexahydroazulen-4-yl] (Z)-2-methylbut-2-enoate
RefMet Name:	Laserpitin
Synonyms:	AC1NQYKY; SureCN5334359; MEGxp0_001744; ACon1_000435 [PubChem Synonyms]
Exact Mass:	450.2618 (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:	C25H38O7
InChIKey:	LYTPVRMVQVQYGM-NVWKHIKUSA-N
LIPID MAPS Category:	Prenol Lipids
LIPID MAPS mainclass:	Isoprenoids
LIPID MAPS subclass:	C15 isoprenoids
SMILES:	C/C=C(/C)C(=O)O[C@H]1C[C@](C)(C(=O)[C@H]([C@@]2(C)CC[C@@](C(C)C)([C@H]12)O)OC(=O)/C(=CC)/C)O
Studies:	Available studies (via RefMet name)

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All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	5281524
CHEBI ID:	6381
KEGG ID:	C09697
Plant Metabolite Hub(Pmhub):	MS000020947

Calculated physicochemical properties (?):

Heavy Atoms:	32
Rings:	2
Aromatic Rings:	0
Rotatable Bonds:	7
van der Waals Molecular volume:	464.67 Å3 molecule-1
Toplogical Polar Sufrace Area:	110.13 Å2 molecule-1
Hydrogen Bond Donors:	2
Hydrogen Bond Acceptors:	7
logP:	4.42
Molar Refractivity:	121.54
Fraction sp3 Carbons:	0.72
sp3 Carbons:	18

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