ID: ALA5180154

Max Phase: Preclinical

Molecular Formula: C20H14Br2N2

Molecular Weight: 442.15

Associated Items:

Representations

Canonical SMILES:  Brc1ccc(C2=NC(c3ccc(Br)cc3)Nc3ccccc32)cc1

Standard InChI:  InChI=1S/C20H14Br2N2/c21-15-9-5-13(6-10-15)19-17-3-1-2-4-18(17)23-20(24-19)14-7-11-16(22)12-8-14/h1-12,20,23H

Standard InChI Key:  GTMROVIXUHQFDL-UHFFFAOYSA-N

Associated Targets(non-human)

Quinolone resistance protein norA 2171 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Staphylococcus aureus 210822 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

Properties

Molecular Weight: 442.15Molecular Weight (Monoisotopic): 439.9524AlogP: 6.17#Rotatable Bonds: 2
Polar Surface Area: 24.39Molecular Species: NEUTRALHBA: 2HBD: 1
#RO5 Violations: 1HBA (Lipinski): 2HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 3.38CX LogP: 6.56CX LogD: 6.56
Aromatic Rings: 3Heavy Atoms: 24QED Weighted: 0.50Np Likeness Score: -0.30

References

1. Deka B, Suri M, Sarma S, Devi MV, Bora A, Sen T, Dihingia A, Pahari P, Singh AK..  (2022)  Potentiating the intracellular killing of Staphylococcus aureus by dihydroquinazoline analogues as NorA efflux pump inhibitor.,  54  [PMID:34953341] [10.1016/j.bmc.2021.116580]

Source