Metabolomics Structure Database

 
MW REGNO: 42796
Common Name:Gemcitabine
Systematic Name:4-amino-1-[(2R,4R,5R)-3,3-difluoro-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2-dihydropyrimidin-2-one
RefMet Name:Gemcitabine
Synonyms: [PubChem Synonyms]
Exact Mass:
263.0718 (neutral)    Calculate m/z:
Formula:C9H11F2N3O4
InChIKey:SDUQYLNIPVEERB-QPPQHZFASA-N
ClassyFire superclass:Nucleosides, nucleotides, and analogues
ClassyFire class:Pyrimidine nucleosides
ClassyFire subclass:Pyrimidine 2'-deoxyribonucleosides
ClassyFire direct parent:Pyrimidine 2'-deoxyribonucleosides
Massbank MS spectra:View MS spectra
SMILES:c1cn([C@H]2C([C@@H]([C@@H](CO)O2)O)(F)F)c(=O)nc1N
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:60750
CHEBI ID:175901
HMDB ID:HMDB0014584
KEGG ID:C07650
Chemspider ID:54753
EPA CompTox DB:DTXCID70197239
Plant Metabolite Hub(Pmhub):MS000002031

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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