ID: ALA2047846

Max Phase: Preclinical

Molecular Formula: C12H9ClFN3O

Molecular Weight: 265.68

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1ccc(C(=O)Nc2cnc(Cl)nc2)cc1F

Standard InChI:  InChI=1S/C12H9ClFN3O/c1-7-2-3-8(4-10(7)14)11(18)17-9-5-15-12(13)16-6-9/h2-6H,1H3,(H,17,18)

Standard InChI Key:  QDPHEMQSIMZQRG-UHFFFAOYSA-N

Associated Targets(Human)

Voltage-gated potassium channel, KQT; KCNQ2(Kv7.2)/KCNQ3(Kv7.3) 372 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Voltage-gated potassium channel, IKs; KCNQ1(Kv7.1)/KCNE1(MinK) 185 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Voltage-gated potassium channel KCNQ3/KCNQ5 37 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: 265.68Molecular Weight (Monoisotopic): 265.0418AlogP: 2.83#Rotatable Bonds: 2
Polar Surface Area: 54.88Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 2.71CX LogD: 2.71
Aromatic Rings: 2Heavy Atoms: 18QED Weighted: 0.85Np Likeness Score: -2.22

References

1. Amato G, Roeloffs R, Rigdon GC, Antonio B, Mersch T, McNaughton-Smith G, Wickenden AD, Fritch P, Suto MJ..  (2011)  N-Pyridyl and Pyrimidine Benzamides as KCNQ2/Q3 Potassium Channel Openers for the Treatment of Epilepsy.,  (6): [PMID:24900334] [10.1021/ml200053x]

Source