Summary

IMPPAT Phytochemical identifier: IMPHY014095

Phytochemical name: 1-Hydroxy-10-methylacridone

Synonymous chemical names:
1-hydroxy-10-methyl-acridin-9-(10h)-one, 1-hydroxy-10-methylacridin-9(10h)-one, 1-hydroxy-n-methylacridone

External chemical identifiers:
CID:5376484, ChEMBL:CHEMBL1288799, ZINC:ZINC000006523722, SureChEMBL:SCHEMBL9352178, MolPort-002-872-482

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Chemical structure information

SMILES:
Cn1c2ccccc2c(=O)c2c1cccc2O

InChI:
InChI=1S/C14H11NO2/c1-15-10-6-3-2-5-9(10)14(17)13-11(15)7-4-8-12(13)16/h2-8,16H,1H3

InChIKey:
NHYDBJFGZCQFEO-UHFFFAOYSA-N

DeepSMILES:
Cncccccc6c=O)cc%10cccc6O

Functional groups:
c=O, cO, cn(c)C

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Molecular scaffolds

Scaffold Graph/Node/Bond level:
O=c1c2ccccc2[nH]c2ccccc12

Scaffold Graph/Node level:
OC1C2CCCCC2NC2CCCCC21

Scaffold Graph level:
CC1C2CCCCC2CC2CCCCC21

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Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass: Organoheterocyclic compounds

ClassyFire Class: Quinolines and derivatives

ClassyFire Subclass: Benzoquinolines

NP Classifier Biosynthetic pathway: Alkaloids

NP Classifier Superclass: Anthranilic acid alkaloids

NP Classifier Class: Acridone alkaloids

NP-Likeness score: 0.55

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Chemical structure download