ID: ALA5275648

Max Phase: Preclinical

Molecular Formula: C19H24FN7O

Molecular Weight: 385.45

Associated Items:

Representations

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

Standard InChI:  InChI=1S/C19H24FN7O/c1-18(2,3)10-23-17(28)19(4,5)26-14-9-24-27-16(25-14)13-8-22-15-12(13)6-11(20)7-21-15/h6-9H,10H2,1-5H3,(H,21,22)(H,23,28)(H,25,26,27)

Standard InChI Key:  YYQPWCZIULWLQY-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: 385.45Molecular Weight (Monoisotopic): 385.2026AlogP: 2.91#Rotatable Bonds: 5
Polar Surface Area: 108.48Molecular Species: NEUTRALHBA: 6HBD: 3
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.19CX Basic pKa: 4.02CX LogP: 2.25CX LogD: 2.25
Aromatic Rings: 3Heavy Atoms: 28QED Weighted: 0.62Np Likeness Score: -1.36

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