Metabolomics Structure Database

 
MW REGNO: 43203
Common Name:Zalcitabine
Systematic Name:4-amino-1-[(2R,5S)-5-(hydroxymethyl)oxolan-2-yl]-1,2-dihydropyrimidin-2-one
RefMet Name:Zalcitabine
Synonyms: [PubChem Synonyms]
Exact Mass:
211.0957 (neutral)    Calculate m/z:
Formula:C9H13N3O3
InChIKey:WREGKURFCTUGRC-POYBYMJQSA-N
ClassyFire superclass:Nucleosides, nucleotides, and analogues
ClassyFire class:Pyrimidine nucleosides
ClassyFire subclass:Pyrimidine 2',3'-dideoxyribonucleosides
ClassyFire direct parent:Pyrimidine 2',3'-dideoxyribonucleosides
Massbank MS spectra:View MS spectra
NP-MRD NMR spectra:View NMR spectra
SMILES:C1C[C@H](n2ccc(N)nc2=O)O[C@@H]1CO
Studies:Available studies (via RefMet name)

Select appropriate tab below to view additional details:

External database links:

PubChem CID:24066
CHEBI ID:10101
HMDB ID:HMDB0015078
KEGG ID:C07207
Chemspider ID:22498
BMRB ID:bmse000712
NP-MRD ID(NMR):NP0002865
EPA CompTox DB:DTXCID20209351
Plant Metabolite Hub(Pmhub):MS000001442

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.

  logo