ID: ALA473115

Max Phase: Preclinical

Molecular Formula: C21H18N6O

Molecular Weight: 370.42

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1ccc(NC(=O)c2ccncc2)cc1Nc1nc(-c2cccnc2)c[nH]1

Standard InChI:  InChI=1S/C21H18N6O/c1-14-4-5-17(25-20(28)15-6-9-22-10-7-15)11-18(14)26-21-24-13-19(27-21)16-3-2-8-23-12-16/h2-13H,1H3,(H,25,28)(H2,24,26,27)

Standard InChI Key:  FYOSYDULSRCSNA-UHFFFAOYSA-N

Associated Targets(Human)

Tyrosine-protein kinase receptor FLT3 13481 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Platelet-derived growth factor receptor 285 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: 370.42Molecular Weight (Monoisotopic): 370.1542AlogP: 4.17#Rotatable Bonds: 5
Polar Surface Area: 95.59Molecular Species: NEUTRALHBA: 5HBD: 3
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.14CX Basic pKa: 7.53CX LogP: 3.18CX LogD: 2.83
Aromatic Rings: 4Heavy Atoms: 28QED Weighted: 0.49Np Likeness Score: -1.67

References

1. Mahboobi S, Sellmer A, Eswayah A, Elz S, Uecker A, Böhmer FD..  (2008)  Inhibition of PDGFR tyrosine kinase activity by a series of novel N-(3-(4-(pyridin-3-yl)-1H-imidazol-2-ylamino)phenyl)amides: a SAR study on the bioisosterism of pyrimidine and imidazole.,  43  (7): [PMID:17983688] [10.1016/j.ejmech.2007.09.021]

Source