3,5-bis(3-bromo-4-hydroxybenzylidene)-1-methylpiperidin-4-one

ID: ALA259459

Chembl Id: CHEMBL259459

PubChem CID: 24827450

Max Phase: Preclinical

Molecular Formula: C20H17Br2NO3

Molecular Weight: 479.17

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CN1C/C(=C\c2ccc(O)c(Br)c2)C(=O)/C(=C/c2ccc(O)c(Br)c2)C1

Standard InChI:  InChI=1S/C20H17Br2NO3/c1-23-10-14(6-12-2-4-18(24)16(21)8-12)20(26)15(11-23)7-13-3-5-19(25)17(22)9-13/h2-9,24-25H,10-11H2,1H3/b14-6+,15-7+

Standard InChI Key:  ZRUNGEBRUZSURT-MKFXEVHTSA-N

Associated Targets(Human)

U-937 (7138 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

rmtA RmtA (95 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

Calculated Properties

Molecular Weight: 479.17Molecular Weight (Monoisotopic): 476.9575AlogP: 4.60#Rotatable Bonds: 2
Polar Surface Area: 60.77Molecular Species: NEUTRALHBA: 4HBD: 2
#RO5 Violations: HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski):
CX Acidic pKa: 7.34CX Basic pKa: 5.08CX LogP: 5.21CX LogD: 4.81
Aromatic Rings: 2Heavy Atoms: 26QED Weighted: 0.62Np Likeness Score: 0.01

References

1. Mai A, Cheng D, Bedford MT, Valente S, Nebbioso A, Perrone A, Brosch G, Sbardella G, De Bellis F, Miceli M, Altucci L..  (2008)  epigenetic multiple ligands: mixed histone/protein methyltransferase, acetyltransferase, and class III deacetylase (sirtuin) inhibitors.,  51  (7): [PMID:18348515] [10.1021/jm701595q]

Source