Metabolomics Structure Database

 
MW REGNO: 38470
Common Name:Adenylylselenate
Systematic Name:[({[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy]selenonic acid
RefMet Name:Adenylylselenate
Synonyms: [PubChem Synonyms]
Exact Mass:
474.9644 (neutral)    Calculate m/z:
Formula:C10H14N5O10PSe
InChIKey:XCADVMZZFPIERR-KQYNXXCUSA-N
ClassyFire superclass:Nucleosides, nucleotides, and analogues [C0000289]
ClassyFire class:Purine nucleotides [C0001506]
ClassyFire subclass:Purine ribonucleotides [C0001544]
ClassyFire direct parent:Purine ribonucleoside monophosphates [C0001617]
SMILES:Nc1ncnc2c1ncn2[C@@H]1O[C@H](COP(=O)(O)O[Se](=O)(=O)O)[C@@H](O)[C@H]1O
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:440758
CHEBI ID:2485
HMDB ID:HMDB0004112
KEGG ID:C05686
Chemspider ID:389628
Plant Metabolite Hub(Pmhub):MS000018827

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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