4,6,7-TRIMETHYL-2H-CHROMEN-2-ONE

ID: ALA2259698

Max Phase: Preclinical

Molecular Formula: C12H12O2

Molecular Weight: 188.23

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1cc2oc(=O)cc(C)c2cc1C

Standard InChI:  InChI=1S/C12H12O2/c1-7-4-10-9(3)6-12(13)14-11(10)5-8(7)2/h4-6H,1-3H3

Standard InChI Key:  RYGXMOYSSBNDQZ-UHFFFAOYSA-N

Associated Targets(non-human)

Setaria cervi 263 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Gamma-glutamyltranspeptidase 21 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Glutathione synthetase 20 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Glutamate--cysteine ligase 130 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 188.23Molecular Weight (Monoisotopic): 188.0837AlogP: 2.72#Rotatable Bonds: 0
Polar Surface Area: 30.21Molecular Species: NEUTRALHBA: 2HBD: 0
#RO5 Violations: 0HBA (Lipinski): 2HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 3.11CX LogD: 3.11
Aromatic Rings: 2Heavy Atoms: 14QED Weighted: 0.59Np Likeness Score: -0.08

References

1. Gupta S, Arora K, Tiwari V, Katiyar D, Tripathi R, Srivastava AK, Walter RD.  (2004)  INHIBITORS OF FILARIAL GAMMA-GLUTAMYL CYCLE ENZYMES AS POSSIBLE MACROFILARICIDAL AGENTS,  13  (8): [10.1007/s00044-004-0112-9]

Source