(+/-)-(6-Hydroxy-1,2,3,4-tetrahydronaphthalen-2-yl)(2-hydroxy-4-methoxyphenyl)methanone

ID: ALA4470333

Chembl Id: CHEMBL4470333

PubChem CID: 155534322

Max Phase: Preclinical

Molecular Formula: C18H18O4

Molecular Weight: 298.34

Molecule Type: Unknown

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1ccc(C(=O)C2CCc3cc(O)ccc3C2)c(O)c1

Standard InChI:  InChI=1S/C18H18O4/c1-22-15-6-7-16(17(20)10-15)18(21)13-3-2-12-9-14(19)5-4-11(12)8-13/h4-7,9-10,13,19-20H,2-3,8H2,1H3

Standard InChI Key:  BGMJTNBUDVDZRO-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA4470333

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Associated Targets(Human)

NOTCH1 Tchem Neurogenic locus notch homolog protein 1 (161 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KOPTK1 (43 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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

Calculated Properties

Molecular Weight: 298.34Molecular Weight (Monoisotopic): 298.1205AlogP: 3.09#Rotatable Bonds: 3
Polar Surface Area: 66.76Molecular Species: NEUTRALHBA: 4HBD: 2
#RO5 Violations: HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski):
CX Acidic pKa: 8.88CX Basic pKa: CX LogP: 4.29CX LogD: 4.27
Aromatic Rings: 2Heavy Atoms: 22QED Weighted: 0.85Np Likeness Score: 0.45

References

1. Quaglio D, Zhdanovskaya N, Tobajas G, Cuartas V, Balducci S, Christodoulou MS, Fabrizi G, Gargantilla M, Priego EM, Carmona Pestaña Á, Passarella D, Screpanti I, Botta B, Palermo R, Mori M, Ghirga F, Pérez-Pérez MJ..  (2019)  Chalcones and Chalcone-mimetic Derivatives as Notch Inhibitors in a Model of T-cell Acute Lymphoblastic Leukemia.,  10  (4): [PMID:30996810] [10.1021/acsmedchemlett.8b00608]

Source