ID: ALA3752183

Max Phase: Preclinical

Molecular Formula: C18H15N3O

Molecular Weight: 289.34

Molecule Type: Small molecule

Associated Items:

Representations

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

Standard InChI:  InChI=1S/C18H15N3O/c1-12-18(14(10-19)8-13-4-3-7-20-11-13)16-9-15(22-2)5-6-17(16)21-12/h3-9,11,21H,1-2H3/b14-8+

Standard InChI Key:  PZCYBMUUVCANMJ-RIYZIHGNSA-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: 289.34Molecular Weight (Monoisotopic): 289.1215AlogP: 3.94#Rotatable Bonds: 3
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: 4.76CX LogP: 2.95CX LogD: 2.95
Aromatic Rings: 3Heavy Atoms: 22QED Weighted: 0.74Np Likeness Score: -1.23

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