ID: ALA5278860

Max Phase: Preclinical

Molecular Formula: C19H22N8O

Molecular Weight: 378.44

Associated Items:

Representations

Canonical SMILES:  CC(Nc1cnnc(-c2c[nH]c3ncc(C#N)cc23)n1)C(=O)NCC(C)(C)C

Standard InChI:  InChI=1S/C19H22N8O/c1-11(18(28)23-10-19(2,3)4)25-15-9-24-27-17(26-15)14-8-22-16-13(14)5-12(6-20)7-21-16/h5,7-9,11H,10H2,1-4H3,(H,21,22)(H,23,28)(H,25,26,27)

Standard InChI Key:  RVWMDKQIEVFKCP-UHFFFAOYSA-N

Associated Targets(Human)

Tyrosine-protein kinase JAK2 12915 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Tyrosine-protein kinase JAK3 8349 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 378.44Molecular Weight (Monoisotopic): 378.1917AlogP: 2.25#Rotatable Bonds: 5
Polar Surface Area: 132.27Molecular Species: NEUTRALHBA: 7HBD: 3
#RO5 Violations: 0HBA (Lipinski): 9HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 11.80CX Basic pKa: 4.04CX LogP: 1.69CX LogD: 1.69
Aromatic Rings: 3Heavy Atoms: 28QED Weighted: 0.62Np Likeness Score: -1.55

References

1. Cascioferro S, Parrino B, Spanò V, Carbone A, Montalbano A, Barraja P, Diana P, Cirrincione G..  (2017)  An overview on the recent developments of 1,2,4-triazine derivatives as anticancer compounds.,  142  [PMID:28851503] [10.1016/j.ejmech.2017.08.009]

Source