ID: ALA5291189

Max Phase: Preclinical

Molecular Formula: C19H24N8O2

Molecular Weight: 396.46

Associated Items:

Representations

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

Standard InChI:  InChI=1S/C19H24N8O2/c1-10(18(29)23-9-19(2,3)4)25-14-8-24-27-17(26-14)13-7-22-16-12(13)5-11(6-21-16)15(20)28/h5-8,10H,9H2,1-4H3,(H2,20,28)(H,21,22)(H,23,29)(H,25,26,27)

Standard InChI Key:  FQZKDZIINPUTOS-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: 396.46Molecular Weight (Monoisotopic): 396.2022AlogP: 1.48#Rotatable Bonds: 6
Polar Surface Area: 151.57Molecular Species: NEUTRALHBA: 7HBD: 4
#RO5 Violations: 0HBA (Lipinski): 10HBD (Lipinski): 5#RO5 Violations (Lipinski): 0
CX Acidic pKa: 11.60CX Basic pKa: 4.05CX LogP: 0.61CX LogD: 0.61
Aromatic Rings: 3Heavy Atoms: 29QED Weighted: 0.49Np Likeness Score: -1.39

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