ID: ALA4069088

Max Phase: Preclinical

Molecular Formula: C13H10ClN3

Molecular Weight: 243.70

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Nc1cc(-c2c[nH]c3cc(Cl)ccc23)ccn1

Standard InChI:  InChI=1S/C13H10ClN3/c14-9-1-2-10-11(7-17-12(10)6-9)8-3-4-16-13(15)5-8/h1-7,17H,(H2,15,16)

Standard InChI Key:  IYRXLUOYVGHRDZ-UHFFFAOYSA-N

Associated Targets(Human)

Nuclear factor of activated T-cells cytoplasmic 1 86 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Dual-specificity tyrosine-phosphorylation regulated kinase 1A 6484 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Glycogen synthase kinase-3 beta 11785 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: 243.70Molecular Weight (Monoisotopic): 243.0563AlogP: 3.47#Rotatable Bonds: 1
Polar Surface Area: 54.70Molecular Species: NEUTRALHBA: 2HBD: 2
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 6.42CX LogP: 2.87CX LogD: 2.83
Aromatic Rings: 3Heavy Atoms: 17QED Weighted: 0.69Np Likeness Score: 0.02

References

1. Shaw SJ, Goff DA, Lin N, Singh R, Li W, McLaughlin J, Baltgalvis KA, Payan DG, Kinsella TM..  (2017)  Developing DYRK inhibitors derived from the meridianins as a means of increasing levels of NFAT in the nucleus.,  27  (11): [PMID:28408219] [10.1016/j.bmcl.2017.03.037]

Source