3-(2-bromo-4,5-dimethoxyphenyl)-1-(4-bromophenyl)prop-2-en-1-one oxime

ID: ALA5279164

Chembl Id: CHEMBL5279164

Max Phase: Preclinical

Molecular Formula: C17H15Br2NO3

Molecular Weight: 441.12

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1cc(Br)c(/C=C/C(=N/O)c2ccc(Br)cc2)cc1OC

Standard InChI:  InChI=1S/C17H15Br2NO3/c1-22-16-9-12(14(19)10-17(16)23-2)5-8-15(20-21)11-3-6-13(18)7-4-11/h3-10,21H,1-2H3/b8-5+,20-15-

Standard InChI Key:  SUKZUBWYMMGLIB-ZEUYVESBSA-N

Alternative Forms

  1. Parent:

    ALA5279164

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Associated Targets(non-human)

LLC-PK1 (2135 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: 441.12Molecular Weight (Monoisotopic): 438.9419AlogP: 5.12#Rotatable Bonds: 5
Polar Surface Area: 51.05Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 6.72CX Basic pKa: 1.79CX LogP: 5.12CX LogD: 4.37
Aromatic Rings: 2Heavy Atoms: 23QED Weighted: 0.40Np Likeness Score: -0.32

References

1. Lee D, Hyuk Lee S, Lee H, Choi YK, Sung Kang K, Wook Lee J..  (2023)  Elucidation of protective effects of oxime derivatives against cisplatin-induced cytotoxicity in LLC-PK1 kidney cells.,  80  [PMID:36574854] [10.1016/j.bmcl.2022.129114]

Source