ethyl 3-(4-chlorophenyl)-2-[(4-chlorophenyl)methyl]-4-hydroxy-5-oxo-2,5-dihydrofuran-2-carboxylate

ID: ALA5285400

Chembl Id: CHEMBL5285400

Max Phase: Preclinical

Molecular Formula: C20H16Cl2O5

Molecular Weight: 407.25

Associated Items:

Names and Identifiers

Canonical SMILES:  CCOC(=O)C1(Cc2ccc(Cl)cc2)OC(=O)C(O)=C1c1ccc(Cl)cc1

Standard InChI:  InChI=1S/C20H16Cl2O5/c1-2-26-19(25)20(11-12-3-7-14(21)8-4-12)16(17(23)18(24)27-20)13-5-9-15(22)10-6-13/h3-10,23H,2,11H2,1H3

Standard InChI Key:  UGAZATBCWQPKGM-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA5285400

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Associated Targets(Human)

SNCA Tchem Alpha-synuclein (10960 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: 407.25Molecular Weight (Monoisotopic): 406.0375AlogP: 4.36#Rotatable Bonds: 5
Polar Surface Area: 72.83Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: 8.28CX Basic pKa: CX LogP: 5.02CX LogD: 4.97
Aromatic Rings: 2Heavy Atoms: 27QED Weighted: 0.75Np Likeness Score: 0.69

References

1. Prebble DW, Holland DC, Hayton JB, Ferretti F, Jennings LK, Everson J, Xu M, Kiefel MJ, Mellick GD, Carroll AR..  (2023)  α-Synuclein Aggregation Inhibitory Procerolides and Diphenylalkanes from the Ascidian Polycarpa procera.,  86  (3): [PMID:36787528] [10.1021/acs.jnatprod.2c01140]

Source