ID: ALA4168349

Max Phase: Preclinical

Molecular Formula: C24H27NO5

Molecular Weight: 409.48

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1cc(/C=C2\CN(C)C/C(=C\c3cc(OC)cc(OC)c3)C2=O)cc(OC)c1

Standard InChI:  InChI=1S/C24H27NO5/c1-25-14-18(6-16-8-20(27-2)12-21(9-16)28-3)24(26)19(15-25)7-17-10-22(29-4)13-23(11-17)30-5/h6-13H,14-15H2,1-5H3/b18-6+,19-7+

Standard InChI Key:  UINOSMFXESPUJK-JRGWAENISA-N

Associated Targets(non-human)

Luciferin 4-monooxygenase 66902 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: 409.48Molecular Weight (Monoisotopic): 409.1889AlogP: 3.70#Rotatable Bonds: 6
Polar Surface Area: 57.23Molecular Species: NEUTRALHBA: 6HBD: 0
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 4.97CX LogP: 3.65CX LogD: 3.65
Aromatic Rings: 2Heavy Atoms: 30QED Weighted: 0.68Np Likeness Score: -0.16

References

1. Deck LM, Hunsaker LA, Vander Jagt TA, Whalen LJ, Royer RE, Vander Jagt DL..  (2018)  Activation of anti-oxidant Nrf2 signaling by enone analogues of curcumin.,  143  [PMID:29223100] [10.1016/j.ejmech.2017.11.048]

Source