Metabolomics Structure Database

 
MW REGNO: 68628
Common Name:Inosine tetraphosphate
Systematic Name:[[(2R,3S,4R,5R)-3,4-dihydroxy-5-(6-oxo-3H-purin-9-yl)tetrahydrofuran-2-yl]methoxy-hydroxy-phosphoryl] [hydroxy(phosphonooxy)phosphoryl] hydrogen phosphate
Synonyms:Inosine 5'-tetraphosphate; C03614; AC1L98LM; CTK2F4319 [PubChem Synonyms]
Exact Mass:
587.9461 (neutral)    Calculate m/z:
Formula:C10H16N4O17P4
InChIKey:CNCKBPIZHHRXIO-KQYNXXCUSA-N
ClassyFire superclass:Nucleosides, nucleotides, and analogues
ClassyFire class:Purine nucleotides
ClassyFire subclass:Purine ribonucleotides
ClassyFire direct parent:Purine ribonucleoside polyphosphates
SMILES:C([C@@H]1[C@H]([C@H]([C@H](n2cnc3c2[nH]cnc3=O)O1)O)O)OP(=O)(O)OP(=O)(O)OP(=O)(O)OP(=O)(O)O
Studies:Available studies(via PubChem CID)

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External database links:

PubChem CID:135398694
KEGG ID:C03614
EPA CompTox DB:DTXCID40964051
Plant Metabolite Hub(Pmhub):MS000018005

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
NPClassifier classification: "NPClassifier: A Deep Neural Network-Based Structural Classification Tool for Natural Products", Kim HW, Wang M, Leber CA, Nothias LF, Reher R, Kang KB, van der Hooft JJJ, Dorrestein PC, Gerwick WH and Cottrell GW. J Nat Prod. 2021 Nov 26;84(11):2795-2807.DOI: 10.1021/acs.jnatprod.1c00399.

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