Metabolomics Structure Database

 
MW REGNO: 42620
Common Name:Moxifloxacin
Systematic Name:7-[(4aS,7aS)-octahydro-1H-pyrrolo[3,4-b]pyridin-6-yl]-1-cyclopropyl-6-fluoro-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid
RefMet Name:Moxifloxacin
Synonyms: [PubChem Synonyms]
Exact Mass:
401.1751 (neutral)    Calculate m/z:
Formula:C21H24FN3O4
InChIKey:FABPRXSRWADJSP-MEDUHNTESA-N
ClassyFire superclass:Organoheterocyclic compounds
ClassyFire class:Quinolines and derivatives
ClassyFire subclass:Quinoline carboxylic acids
ClassyFire direct parent:Quinoline carboxylic acids
SMILES:COc1c2c(cc(c1N1C[C@@H]3CCCN[C@@H]3C1)F)c(=O)c(cn2C1CC1)C(=O)O
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:152946
CHEBI ID:63611
HMDB ID:HMDB0014363
KEGG ID:C07663
Chemspider ID:134802
EPA CompTox DB:DTXCID70197113
Plant Metabolite Hub(Pmhub):MS000003489

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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