ID: ALA4102309

Max Phase: Preclinical

Molecular Formula: C23H18Cl2N4O

Molecular Weight: 437.33

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Nc1cccc(C(c2cccnc2)C(O)c2cccnc2-c2cc(Cl)cc(Cl)c2)n1

Standard InChI:  InChI=1S/C23H18Cl2N4O/c24-16-10-15(11-17(25)12-16)22-18(5-3-9-28-22)23(30)21(14-4-2-8-27-13-14)19-6-1-7-20(26)29-19/h1-13,21,23,30H,(H2,26,29)

Standard InChI Key:  IHBTZOMDMPJGFK-UHFFFAOYSA-N

Associated Targets(Human)

Voltage-gated potassium channel subunit Kv1.5 1353 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

HERG 29587 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: 437.33Molecular Weight (Monoisotopic): 436.0858AlogP: 5.29#Rotatable Bonds: 5
Polar Surface Area: 84.92Molecular Species: NEUTRALHBA: 5HBD: 2
#RO5 Violations: 1HBA (Lipinski): 5HBD (Lipinski): 3#RO5 Violations (Lipinski): 1
CX Acidic pKa: 13.79CX Basic pKa: 6.07CX LogP: 4.34CX LogD: 4.32
Aromatic Rings: 4Heavy Atoms: 30QED Weighted: 0.44Np Likeness Score: -0.59

References

1. Wolkenberg SE, Nolt MB, Bilodeau MT, Trotter BW, Manley PJ, Kett NR, Nanda KK, Wu Z, Cato MJ, Kane SA, Kiss L, Spencer RH, Wang J, Lynch JJ, Regan CP, Stump GL, Li B, White R, Yeh S, Dinsmore CJ, Lindsley CW, Hartman GD..  (2017)  Discovery of MK-1832, a Kv1.5 inhibitor with improved selectivity and pharmacokinetics.,  27  (4): [PMID:28131713] [10.1016/j.bmcl.2016.12.054]

Source