ID: ALA3885381

Max Phase: Preclinical

Molecular Formula: C22H23F3N4O2

Molecular Weight: 432.45

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C1C(=O)N(CCN2CCN(NCc3ccccc3C(F)(F)F)CC2)c2ccccc21

Standard InChI:  InChI=1S/C22H23F3N4O2/c23-22(24,25)18-7-3-1-5-16(18)15-26-28-12-9-27(10-13-28)11-14-29-19-8-4-2-6-17(19)20(30)21(29)31/h1-8,26H,9-15H2

Standard InChI Key:  QKGCUHXFPFLLGT-UHFFFAOYSA-N

Associated Targets(non-human)

DNA gyrase subunit A/DNA gyrase subunit B 505 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

DNA gyrase subunit B 445 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mus musculus 284745 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: 432.45Molecular Weight (Monoisotopic): 432.1773AlogP: 2.56#Rotatable Bonds: 6
Polar Surface Area: 55.89Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 5.48CX LogP: 2.45CX LogD: 2.44
Aromatic Rings: 2Heavy Atoms: 31QED Weighted: 0.71Np Likeness Score: -1.20

References

1. Chaudhari K, Surana S, Jain P, Patel HM..  (2016)  Mycobacterium Tuberculosis (MTB) GyrB inhibitors: An attractive approach for developing novel drugs against TB.,  124  [PMID:27569197] [10.1016/j.ejmech.2016.08.034]

Source