ID: ALA187150

Max Phase: Preclinical

Molecular Formula: C17H14O3

Molecular Weight: 266.30

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C1/C(=C/c2ccc(O)cc2)CCc2cc(O)ccc21

Standard InChI:  InChI=1S/C17H14O3/c18-14-5-1-11(2-6-14)9-13-4-3-12-10-15(19)7-8-16(12)17(13)20/h1-2,5-10,18-19H,3-4H2/b13-9+

Standard InChI Key:  KORCTUWODUQVTH-UKTHLTGXSA-N

Associated Targets(Human)

Cytochrome P450 26A1 308 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Cytochrome P450 24A1 20 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Liver microsomes 8692 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

RAW264.7 28094 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: 266.30Molecular Weight (Monoisotopic): 266.0943AlogP: 3.31#Rotatable Bonds: 1
Polar Surface Area: 57.53Molecular Species: NEUTRALHBA: 3HBD: 2
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.91CX Basic pKa: CX LogP: 3.73CX LogD: 3.61
Aromatic Rings: 2Heavy Atoms: 20QED Weighted: 0.78Np Likeness Score: 0.39

References

1. Yee SW, Simons C..  (2004)  Synthesis and CYP24 inhibitory activity of 2-substituted-3,4-dihydro-2H-naphthalen-1-one (tetralone) derivatives.,  14  (22): [PMID:15482941] [10.1016/j.bmcl.2004.08.040]
2. Yee SW, Jarno L, Gomaa MS, Elford C, Ooi LL, Coogan MP, McClelland R, Nicholson RI, Evans BA, Brancale A, Simons C..  (2005)  Novel tetralone-derived retinoic acid metabolism blocking agents: synthesis and in vitro evaluation with liver microsomal and MCF-7 CYP26A1 cell assays.,  48  (23): [PMID:16279770] [10.1021/jm0501681]
3. Kunwar S, Min Lee S, Man Kadayat T, Shrestha A, Park PH, Lee ES..  (2022)  Potent inhibitory activity of hydroxylated 2-benzylidene-3,4-dihydronaphthalen-1(2H)-ones on LPS-stimulated reactive oxygen species production in RAW 264.7 macrophages.,  73  [PMID:35932905] [10.1016/j.bmcl.2022.128921]

Source