ID: ALA3751920

Max Phase: Preclinical

Molecular Formula: C19H15N3O2

Molecular Weight: 317.35

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccc2c(c1)c(/C(C#N)=C/c1cccnc1)cn2C(C)=O

Standard InChI:  InChI=1S/C19H15N3O2/c1-13(23)22-12-18(17-9-16(24-2)5-6-19(17)22)15(10-20)8-14-4-3-7-21-11-14/h3-9,11-12H,1-2H3/b15-8+

Standard InChI Key:  CDFDOYUTJLRZOX-OVCLIPMQSA-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: 317.35Molecular Weight (Monoisotopic): 317.1164AlogP: 3.77#Rotatable Bonds: 3
Polar Surface Area: 67.91Molecular Species: NEUTRALHBA: 5HBD: 0
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 4.76CX LogP: 2.07CX LogD: 2.07
Aromatic Rings: 3Heavy Atoms: 24QED Weighted: 0.69Np Likeness Score: -1.18

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