ID: ALA3753280

Max Phase: Preclinical

Molecular Formula: C19H15N3O

Molecular Weight: 301.35

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccc2[nH]cc(/C(C#N)=C/C=C/c3cccnc3)c2c1

Standard InChI:  InChI=1S/C19H15N3O/c1-23-16-7-8-19-17(10-16)18(13-22-19)15(11-20)6-2-4-14-5-3-9-21-12-14/h2-10,12-13,22H,1H3/b4-2+,15-6+

Standard InChI Key:  SYXIRBKBFLVFJC-XEXQVEHGSA-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: 301.35Molecular Weight (Monoisotopic): 301.1215AlogP: 4.19#Rotatable Bonds: 4
Polar Surface Area: 61.70Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 4.88CX LogP: 3.28CX LogD: 3.28
Aromatic Rings: 3Heavy Atoms: 23QED Weighted: 0.58Np Likeness Score: -0.66

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