Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	71323
Common Name:	Militarinone B
Systematic Name:	(3E)-5-[hydroxy-(4-hydroxyphenyl)methyl]-3-[(2E,4E,6E,8R,10R)-1-hydroxy-6,8,10-trimethyl-dodeca-2,4,6-trienylidene]pyrrolidine-2,4-dione
RefMet Name:	Militarinone B
Synonyms:	CHEBI:70184; AC1NQZHZ; CHEMBL478579; C12334 [PubChem Synonyms]
Exact Mass:	439.2359 (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:	C26H33NO5
InChIKey:	NKHVQSJVSMTQID-YNUTZCEOSA-N
ClassyFire superclass:	Lipids and lipid-like molecules [C0000012]
NP-MRD NMR spectra:	View NMR spectra
SMILES:	CC[C@@H](C)C[C@@H](C)/C=C(C)/C=C/C=C/C(=C /C(=O)C(C(c2ccc(cc2)O)O)NC1=O)/O
Studies:	Available studies (via RefMet name)

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All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	54691340
KEGG ID:	C12334
Natural Products Atlas ID:	NP017821
NP-MRD ID(NMR):	NP0004553
Plant Metabolite Hub(Pmhub):	MS000023014

Calculated physicochemical properties (?):

Heavy Atoms:	32
Rings:	2
Aromatic Rings:	1
Rotatable Bonds:	9
van der Waals Molecular volume:	453.93 Å3 molecule-1
Toplogical Polar Sufrace Area:	106.86 Å2 molecule-1
Hydrogen Bond Donors:	4
Hydrogen Bond Acceptors:	5
logP:	4.72
Molar Refractivity:	125.44
Fraction sp3 Carbons:	0.38
sp3 Carbons:	10

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