Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	68752
Common Name:	Dimethylenetriurea
Systematic Name:	1,3-bis(ureidomethyl)urea
RefMet Name:	Dimethylenetriurea
Synonyms:	AC1L9ADA; C06385; CTK0E7734; 1,3-bis[(carbamoylamino)methyl]urea; 2,4,6,8-Tetraazanonanediamide, 5-oxo- [PubChem Synonyms]
Exact Mass:	204.0971 (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:	C5H12N6O3
InChIKey:	OKNSZPQWMKXIEO-UHFFFAOYSA-N
ClassyFire superclass:	Organic acids and derivatives [C0000264]
ClassyFire class:	Carboxylic acids and derivatives [C0000265]
ClassyFire subclass:	Amino acids, peptides, and analogues [C0000013]
ClassyFire direct parent:	Oligourea amides [C0001952]
SMILES:	C(NC(=O)N)NC(=O)NCNC(=O)N
Studies:	Available studies (via RefMet name)

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All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	441000
CHEBI ID:	4621
KEGG ID:	C06385
EPA CompTox DB:	DTXCID20282649
Plant Metabolite Hub(Pmhub):	MS000019117

Calculated physicochemical properties (?):

Heavy Atoms:	14
Rings:	0
Aromatic Rings:	0
Rotatable Bonds:	8
van der Waals Molecular volume:	179.51 Å3 molecule-1
Toplogical Polar Sufrace Area:	151.37 Å2 molecule-1
Hydrogen Bond Donors:	6
Hydrogen Bond Acceptors:	3
logP:	-2.46
Molar Refractivity:	46.84
Fraction sp3 Carbons:	0.40
sp3 Carbons:	2

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