ID: ALA3393157

Max Phase: Preclinical

Molecular Formula: C14H15BrN2O3

Molecular Weight: 339.19

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCCNC(=O)/C(C#N)=C/c1cc(Br)c(O)c(OC)c1

Standard InChI:  InChI=1S/C14H15BrN2O3/c1-3-4-17-14(19)10(8-16)5-9-6-11(15)13(18)12(7-9)20-2/h5-7,18H,3-4H2,1-2H3,(H,17,19)/b10-5+

Standard InChI Key:  VWQNCAFFUAYTFX-BJMVGYQFSA-N

Associated Targets(Human)

Protein-tyrosine phosphatase 4A3 173 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Protein tyrosine phosphatase type IVA 2 36 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Protein tyrosine phosphatase type IVA 1 47 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: 339.19Molecular Weight (Monoisotopic): 338.0266AlogP: 2.60#Rotatable Bonds: 5
Polar Surface Area: 82.35Molecular Species: NEUTRALHBA: 4HBD: 2
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.59CX Basic pKa: CX LogP: 2.55CX LogD: 2.34
Aromatic Rings: 1Heavy Atoms: 20QED Weighted: 0.64Np Likeness Score: -0.59

References

1. Hoeger B, Diether M, Ballester PJ, Köhn M..  (2014)  Biochemical evaluation of virtual screening methods reveals a cell-active inhibitor of the cancer-promoting phosphatases of regenerating liver.,  88  [PMID:25159123] [10.1016/j.ejmech.2014.08.060]

Source