3-((4-boraneylphenyl)thio)-3-(4-chlorophenyl)-1-(4-hydroxy-3-methylphenyl)propan-1-one

ID: ALA5286851

Chembl Id: CHEMBL5286851

Max Phase: Preclinical

Molecular Formula: C22H20BClO2S

Molecular Weight: 394.73

Associated Items:

Names and Identifiers

Canonical SMILES:  Bc1ccc(SC(CC(=O)c2ccc(O)c(C)c2)c2ccc(Cl)cc2)cc1

Standard InChI:  InChI=1S/C22H20BClO2S/c1-14-12-16(4-11-20(14)25)21(26)13-22(15-2-7-18(24)8-3-15)27-19-9-5-17(23)6-10-19/h2-12,22,25H,13,23H2,1H3

Standard InChI Key:  MDXNDHXZQVENPU-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA5286851

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Associated Targets(non-human)

Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bacillus anthracis (2936 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Enterococcus faecalis (29875 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: 394.73Molecular Weight (Monoisotopic): 394.0966AlogP: #Rotatable Bonds:
Polar Surface Area: Molecular Species: HBA: HBD:
#RO5 Violations: HBA (Lipinski): HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: CX LogD:
Aromatic Rings: Heavy Atoms: QED Weighted: Np Likeness Score:

References

1. Dan W, Dai J..  (2020)  Recent developments of chalcones as potential antibacterial agents in medicinal chemistry.,  187  [PMID:31877539] [10.1016/j.ejmech.2019.111980]

Source