Metabolomics Structure Database

 
MW REGNO: 37540
Common Name:dUDP
Systematic Name:[({[(2R,3S,5R)-5-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)-3-hydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy]phosphonic acid
RefMet Name:dUDP
Synonyms: [PubChem Synonyms]
Exact Mass:
388.0073 (neutral)    Calculate m/z:
Formula:C9H14N2O11P2
InChIKey:QHWZTVCCBMIIKE-SHYZEUOFSA-N
ClassyFire superclass:Nucleosides, nucleotides, and analogues [C0000289]
ClassyFire class:Pyrimidine nucleotides [C0001509]
ClassyFire subclass:Pyrimidine deoxyribonucleotides [C0002148]
ClassyFire direct parent:Pyrimidine 2'-deoxyribonucleoside diphosphates [C0002156]
Massbank MS spectra:View MS spectra
SMILES:c1cn([C@H]2C[C@@H]([C@@H](COP(=O)(O)OP(=O)(O)O)O2)O)c(=O)[nH]c1=O
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:145729
CHEBI ID:28850
HMDB ID:HMDB0001000
KEGG ID:C01346
Chemspider ID:128553
METLIN ID:5931
MetaCyc ID:DUDP
Plant Metabolite Hub(Pmhub):MS000015937

Calculated physicochemical properties (?):

Heavy Atoms: 24  
Rings: 2  
Aromatic Rings: 1  
Rotatable Bonds: 6  
van der Waals Molecular volume: 279.07 Å3 molecule-1  
Toplogical Polar Sufrace Area: 199.68 Å2 molecule-1  
Hydrogen Bond Donors: 5  
Hydrogen Bond Acceptors: 12  
logP: 1.42  
Molar Refractivity: 76.01  
Fraction sp3 Carbons: 0.56  
sp3 Carbons: 5  

Human Pathway links:

HMDB and KEGG pathways containing this metabolite

REACTOME 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

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