Metabolomics Structure Database

 
MW REGNO: 37187
Common Name:Xanthosine 5-triphosphate
Systematic Name:({[({[(2R,3S,4R,5R)-5-(2,6-dihydroxy-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)phosphonic acid
RefMet Name:Xanthosine 5-triphosphate
Synonyms: [PubChem Synonyms]
Exact Mass:
523.9747 (neutral)    Calculate m/z:
Formula:C10H15N4O15P3
InChIKey:CAEFEWVYEZABLA-UUOKFMHZSA-N
ClassyFire superclass:Nucleosides, nucleotides, and analogues [C0000289]
ClassyFire class:Purine nucleotides [C0001506]
ClassyFire subclass:Purine ribonucleotides [C0001544]
ClassyFire direct parent:Purine ribonucleoside triphosphates [C0001619]
SMILES:C([C@@H]1[C@H]([C@H]([C@H](n2cnc3c2[nH]c(=O)[nH]c3=O)O1)O)O)OP(=O)(O)OP(=O)(O)OP(=O)(O)O
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:439296
CHEBI ID:10049
HMDB ID:HMDB0000293
KEGG ID:C00700
Chemspider ID:388429
Plant Metabolite Hub(Pmhub):MS000016945

Calculated physicochemical properties (?):

Heavy Atoms: 32  
Rings: 3  
Aromatic Rings: 2  
Rotatable Bonds: 8  
van der Waals Molecular volume: 347.46 Å3 molecule-1  
Toplogical Polar Sufrace Area: 295.12 Å2 molecule-1  
Hydrogen Bond Donors: 8  
Hydrogen Bond Acceptors: 17  
logP: 0.69  
Molar Refractivity: 98.27  
Fraction sp3 Carbons: 0.50  
sp3 Carbons: 5  

Human Pathway links:

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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