ID: ALA2431703

Max Phase: Preclinical

Molecular Formula: C16H17F2O4P

Molecular Weight: 342.28

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)c1ccc(O)c(-c2cccc(C(F)(F)P(=O)(O)O)c2)c1

Standard InChI:  InChI=1S/C16H17F2O4P/c1-10(2)11-6-7-15(19)14(9-11)12-4-3-5-13(8-12)16(17,18)23(20,21)22/h3-10,19H,1-2H3,(H2,20,21,22)

Standard InChI Key:  GXLZUGCQUQEUCW-UHFFFAOYSA-N

Associated Targets(Human)

Tyrosine-protein phosphatase non-receptor type 5 536 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: 342.28Molecular Weight (Monoisotopic): 342.0833AlogP: 4.41#Rotatable Bonds: 4
Polar Surface Area: 77.76Molecular Species: ACIDHBA: 2HBD: 3
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 0.49CX Basic pKa: CX LogP: 3.91CX LogD: 1.15
Aromatic Rings: 2Heavy Atoms: 23QED Weighted: 0.72Np Likeness Score: -0.06

References

1. Baguley TD, Xu HC, Chatterjee M, Nairn AC, Lombroso PJ, Ellman JA..  (2013)  Substrate-based fragment identification for the development of selective, nonpeptidic inhibitors of striatal-enriched protein tyrosine phosphatase.,  56  (19): [PMID:24083656] [10.1021/jm401037h]

Source