Metabolomics Structure Database

 
MW REGNO: 68534
Common Name:2-AminoAMP
Systematic Name:[(2R,3S,4R,5R)-4-amino-5-(6-aminopurin-9-yl)-3-hydroxy-tetrahydrofuran-2-yl]methyl dihydrogen phosphate
RefMet Name:2-Amino-AMP
Synonyms:C01655; AC1L97JZ; CTK1J0497; 5'-Adenylic acid, 2'-amino-2'-deoxy- [PubChem Synonyms]
Exact Mass:
346.0791 (neutral)    Calculate m/z:
Formula:C10H15N6O6P
InChIKey:WCNLOVDQFDDWLB-QYYRPYCUSA-N
ClassyFire superclass:Nucleosides, nucleotides, and analogues
ClassyFire class:Purine nucleotides
ClassyFire subclass:Purine deoxyribonucleotides
ClassyFire direct parent:Purine 2'-deoxyribonucleoside monophosphates
SMILES:C([C@@H]1[C@H]([C@H]([C@H](n2cnc3c(N)ncnc23)O1)N)O)OP(=O)(O)O
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:439541
CHEBI ID:1012
KEGG ID:C01655
EPA CompTox DB:DTXCID20964034
Plant Metabolite Hub(Pmhub):MS000017304

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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