3-butyl-6-((2'-hydroxybenzyl)oxy)isobenzofuran-1(3H)-one

ID: ALA5193286

Chembl Id: CHEMBL5193286

PubChem CID: 168284627

Max Phase: Preclinical

Molecular Formula: C19H20O4

Molecular Weight: 312.37

Associated Items:

Names and Identifiers

Canonical SMILES:  CCCCC1OC(=O)c2cc(OCc3ccccc3O)ccc21

Standard InChI:  InChI=1S/C19H20O4/c1-2-3-8-18-15-10-9-14(11-16(15)19(21)23-18)22-12-13-6-4-5-7-17(13)20/h4-7,9-11,18,20H,2-3,8,12H2,1H3

Standard InChI Key:  ZQDCTTYBLWOZJJ-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA5193286

    ---

Associated Targets(Human)

MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAOB Tclin Monoamine oxidase B (8835 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

ache Acetylcholinesterase (12221 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bche Butyrylcholinesterase (745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 312.37Molecular Weight (Monoisotopic): 312.1362AlogP: 4.37#Rotatable Bonds: 6
Polar Surface Area: 55.76Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: 9.11CX Basic pKa: CX LogP: 4.62CX LogD: 4.61
Aromatic Rings: 2Heavy Atoms: 23QED Weighted: 0.80Np Likeness Score: 0.73

References

1. Liu Z, Shi Y, Zhang X, Yu G, Li J, Cong S, Deng Y..  (2022)  Discovery of novel 3-butyl-6-benzyloxyphthalide Mannich base derivatives as multifunctional agents against Alzheimer's disease.,  58  [PMID:35183029] [10.1016/j.bmc.2022.116660]

Source