ID: ALA4105595

Max Phase: Preclinical

Molecular Formula: C31H34FN7O4

Molecular Weight: 587.66

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cn1nc(-c2cccc(-n3ncc4cc(C(C)(C)C)cc(F)c4c3=O)c2CO)cc(Nc2cnn(CC(C)(C)O)c2)c1=O

Standard InChI:  InChI=1S/C31H34FN7O4/c1-30(2,3)19-10-18-13-34-39(29(42)27(18)23(32)11-19)26-9-7-8-21(22(26)16-40)24-12-25(28(41)37(6)36-24)35-20-14-33-38(15-20)17-31(4,5)43/h7-15,35,40,43H,16-17H2,1-6H3

Standard InChI Key:  GQDXSWUIDLYPBF-UHFFFAOYSA-N

Associated Targets(Human)

Liver 3974 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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: 587.66Molecular Weight (Monoisotopic): 587.2656AlogP: 3.79#Rotatable Bonds: 7
Polar Surface Area: 140.09Molecular Species: NEUTRALHBA: 11HBD: 3
#RO5 Violations: 2HBA (Lipinski): 11HBD (Lipinski): 3#RO5 Violations (Lipinski): 2
CX Acidic pKa: 11.29CX Basic pKa: 1.45CX LogP: 3.02CX LogD: 3.02
Aromatic Rings: 5Heavy Atoms: 43QED Weighted: 0.26Np Likeness Score: -1.05

References

1. Lou Y, Lopez F, Jiang Y, Han X, Brotherton C, Billedeau R, Gabriel S, Gleason S, Goldstein DM, Hilgenkamp R, Kocer B, Orzechowski L, Tan J, Wovkulich P, Wen B, Fry D, Di Lello P, Chen L, Zhang FJ, Fretland J, Nangia A, Yang T, Owens TD..  (2017)  Mitigation of reactive metabolite formation for a series of 3-amino-2-pyridone inhibitors of Bruton's tyrosine kinase (BTK).,  27  (3): [PMID:28025004] [10.1016/j.bmcl.2016.11.092]

Source