ID: ALA5276235

Max Phase: Preclinical

Molecular Formula: C20H24N8O

Molecular Weight: 392.47

Associated Items:

Representations

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

Standard InChI:  InChI=1S/C20H24N8O/c1-19(2,3)11-24-18(29)20(4,5)27-15-10-25-28-17(26-15)14-9-23-16-13(14)6-12(7-21)8-22-16/h6,8-10H,11H2,1-5H3,(H,22,23)(H,24,29)(H,26,27,28)

Standard InChI Key:  GJPPGMWXEGSNII-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: 392.47Molecular Weight (Monoisotopic): 392.2073AlogP: 2.64#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: 11.79CX Basic pKa: 4.02CX LogP: 1.96CX LogD: 1.96
Aromatic Rings: 3Heavy Atoms: 29QED Weighted: 0.61Np Likeness Score: -1.40

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