Metabolomics Structure Database

 
MW REGNO: 37094
Common Name:Guanosine
Systematic Name:2-amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-6,9-dihydro-1H-purin-6-one
RefMet Name:Guanosine
Synonyms: [PubChem Synonyms]
Exact Mass:
283.0917 (neutral)    Calculate m/z:
Formula:C10H13N5O5
InChIKey:NYHBQMYGNKIUIF-UUOKFMHZSA-N
ClassyFire superclass:Nucleosides, nucleotides, and analogues [C0000289]
ClassyFire class:Purine nucleosides [C0000479]
ClassyFire subclass:Purine nucleosides [C0000479]
ClassyFire direct parent:Aromatic heteropolycyclic compounds
Massbank MS spectra:View MS spectra
NP-MRD NMR spectra:View NMR spectra
SMILES:C([C@@H]1[C@H]([C@H]([C@H](n2cnc3c2nc(N)[nH]c3=O)O1)O)O)O
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:135398635
CHEBI ID:16750
HMDB ID:HMDB0000133
KEGG ID:C00387
Chemspider ID:6544
METLIN ID:87
BMRB ID:bmse001018
MetaCyc ID:GUANOSINE
NP-MRD ID(NMR):NP0001335
EPA CompTox DB:DTXCID90223741
Plant Metabolite Hub(Pmhub):MS000000863

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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