Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	56188
Common Name:	Dinotefuran
Systematic Name:	1-methyl-2-nitro-3-(tetrahydrofuran-3-ylmethyl)guanidine
RefMet Name:	Dinotefuran
Synonyms:	1-methyl-2-nitro-3-(tetrahydro-3-furylmethyl)guanidine; Dinotefuran [PubChem Synonyms]
Exact Mass:	202.1066 (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:	C7H14N4O3
InChIKey:	YKBZOVFACRVRJN-UHFFFAOYSA-N
ClassyFire superclass:	Organic nitrogen compounds [C0004707]
ClassyFire class:	Organonitrogen compounds [C0000278]
ClassyFire subclass:	Guanidines [C0000375]
ClassyFire direct parent:	Nitroguanidines [C0004667]
Massbank MS spectra:	View MS spectra
SMILES:	CN/C(=N/[N+](=O)[O-])/NCC1CCOC1
Studies:	Available studies (via RefMet name)

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All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	135779803
CHEBI ID:	39183
HMDB ID:	HMDB0244741
KEGG ID:	C18509
EPA CompTox DB:	DTXCID5014549
Plant Metabolite Hub(Pmhub):	MS000002582

Calculated physicochemical properties (?):

Heavy Atoms:	14
Rings:	1
Aromatic Rings:	0
Rotatable Bonds:	5
van der Waals Molecular volume:	182.39 Å3 molecule-1
Toplogical Polar Sufrace Area:	90.86 Å2 molecule-1
Hydrogen Bond Donors:	2
Hydrogen Bond Acceptors:	5
logP:	0.23
Molar Refractivity:	51.89
Fraction sp3 Carbons:	0.86
sp3 Carbons:	6

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