ID: ALA2023327

Max Phase: Preclinical

Molecular Formula: C20H20ClFN4O3

Molecular Weight: 382.40

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cl.O=[N+]([O-])c1cc(CN2CCN(c3ccc(F)cc3)CC2)c(O)c2ncccc12

Standard InChI:  InChI=1S/C20H19FN4O3.ClH/c21-15-3-5-16(6-4-15)24-10-8-23(9-11-24)13-14-12-18(25(27)28)17-2-1-7-22-19(17)20(14)26;/h1-7,12,26H,8-11,13H2;1H

Standard InChI Key:  WIKFITPFWNTEAR-UHFFFAOYSA-N

Associated Targets(non-human)

Tyrosine-protein phosphatase yopH 57 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

Properties

Molecular Weight: 382.40Molecular Weight (Monoisotopic): 382.1441AlogP: 3.31#Rotatable Bonds: 4
Polar Surface Area: 82.74Molecular Species: ACIDHBA: 6HBD: 1
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 5.77CX Basic pKa: 8.01CX LogP: 2.36CX LogD: 2.33
Aromatic Rings: 3Heavy Atoms: 28QED Weighted: 0.55Np Likeness Score: -1.61

References

1. Enquist PA, Gylfe A, Hägglund U, Lindström P, Norberg-Scherman H, Sundin C, Elofsson M..  (2012)  Derivatives of 8-hydroxyquinoline--antibacterial agents that target intra- and extracellular Gram-negative pathogens.,  22  (10): [PMID:22525317] [10.1016/j.bmcl.2012.03.096]

Source