ID: ALA3393152

Max Phase: Preclinical

Molecular Formula: C11H8BrNO3

Molecular Weight: 282.09

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COC(=O)/C(C#N)=C/c1ccc(O)c(Br)c1

Standard InChI:  InChI=1S/C11H8BrNO3/c1-16-11(15)8(6-13)4-7-2-3-10(14)9(12)5-7/h2-5,14H,1H3/b8-4+

Standard InChI Key:  VUQRSPUHSQPQJB-XBXARRHUSA-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: 282.09Molecular Weight (Monoisotopic): 280.9688AlogP: 2.23#Rotatable Bonds: 2
Polar Surface Area: 70.32Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.03CX Basic pKa: CX LogP: 2.79CX LogD: 2.27
Aromatic Rings: 1Heavy Atoms: 16QED Weighted: 0.51Np Likeness Score: -0.12

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