ID: ALA5282427

Max Phase: Preclinical

Molecular Formula: C20H26N8O2

Molecular Weight: 410.48

Associated Items:

Representations

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

Standard InChI:  InChI=1S/C20H26N8O2/c1-19(2,3)10-24-18(30)20(4,5)27-14-9-25-28-17(26-14)13-8-23-16-12(13)6-11(7-22-16)15(21)29/h6-9H,10H2,1-5H3,(H2,21,29)(H,22,23)(H,24,30)(H,26,27,28)

Standard InChI Key:  JJNUPUXMDNEBER-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: 410.48Molecular Weight (Monoisotopic): 410.2179AlogP: 1.87#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: 4.02CX LogP: 0.88CX LogD: 0.88
Aromatic Rings: 3Heavy Atoms: 30QED Weighted: 0.48Np Likeness Score: -1.24

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