Metabolomics Structure Database

 
MW REGNO: 69502
Common Name:Evoxanthidine
Systematic Name:11-methoxy-5H-[1,3]dioxolo[4,5-b]acridin-10-one
RefMet Name:Evoxanthidine
Synonyms:AC1L9DLT; C10668; CTK8J9393; 11-methoxy-5H-[1,3]dioxolo[4,5-b]acridin-10-one; 1,3-Dioxolo[4,5-b]acridin-10(5H)-one, 11-methoxy- [PubChem Synonyms]
Exact Mass:
269.0688 (neutral)    Calculate m/z:
Formula:C15H11NO4
InChIKey:HHCAZEOWGVDROC-UHFFFAOYSA-N
ClassyFire superclass:Organoheterocyclic compounds
ClassyFire class:Quinolines and derivatives
ClassyFire subclass:Benzoquinolines
ClassyFire direct parent:Acridones
SMILES:COc1c2c(cc3c1OCO3)[nH]c1ccccc1c2=O
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:442899
CHEBI ID:4951
KEGG ID:C10668
EPA CompTox DB:DTXCID20283090
Plant Metabolite Hub(Pmhub):MS000021822

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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