ID: ALA3393158

Max Phase: Preclinical

Molecular Formula: C16H18BrNO5

Molecular Weight: 384.23

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCOc1c(Br)cc(/C=C(\C#N)C(=O)OCCOC)cc1OC

Standard InChI:  InChI=1S/C16H18BrNO5/c1-4-22-15-13(17)8-11(9-14(15)21-3)7-12(10-18)16(19)23-6-5-20-2/h7-9H,4-6H2,1-3H3/b12-7+

Standard InChI Key:  IILCKUYLITZKAQ-KPKJPENVSA-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: 384.23Molecular Weight (Monoisotopic): 383.0368AlogP: 2.95#Rotatable Bonds: 8
Polar Surface Area: 77.78Molecular Species: NEUTRALHBA: 6HBD: 0
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 3.09CX LogD: 3.09
Aromatic Rings: 1Heavy Atoms: 23QED Weighted: 0.30Np Likeness Score: -0.76

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