ID: ALA3752493

Max Phase: Preclinical

Molecular Formula: C22H15N3

Molecular Weight: 321.38

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  N#C/C(=C\c1cccnc1)c1c(-c2ccccc2)[nH]c2ccccc12

Standard InChI:  InChI=1S/C22H15N3/c23-14-18(13-16-7-6-12-24-15-16)21-19-10-4-5-11-20(19)25-22(21)17-8-2-1-3-9-17/h1-13,15,25H/b18-13+

Standard InChI Key:  OSQFEFTUWOOLNC-QGOAFFKASA-N

Associated Targets(Human)

Kinesin-like protein KIF20A 148 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

KB 17409 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: 321.38Molecular Weight (Monoisotopic): 321.1266AlogP: 5.29#Rotatable Bonds: 3
Polar Surface Area: 52.47Molecular Species: NEUTRALHBA: 2HBD: 1
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 13.87CX Basic pKa: 4.76CX LogP: 4.48CX LogD: 4.48
Aromatic Rings: 4Heavy Atoms: 25QED Weighted: 0.52Np Likeness Score: -0.86

References

1. Labrière C, Talapatra SK, Thoret S, Bougeret C, Kozielski F, Guillou C..  (2016)  New MKLP-2 inhibitors in the paprotrain series: Design, synthesis and biological evaluations.,  24  (4): [PMID:26778612] [10.1016/j.bmc.2015.12.042]

Source