27 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Exploring the Existing Drug Space for Novel pTyr Mimetic and SHP2 Inhibitors.

Indiana University School of Medicine
Identification of new inhibitors for low molecular weight protein tyrosine phosphatase isoform B.

Saint John'S University
Calix[4]arene methylenebisphosphonic acids as inhibitors of protein tyrosine phosphatase 1B.

National Academy of Sciences of Ukraine
A potent and selective small-molecule inhibitor for the lymphoid-specific tyrosine phosphatase (LYP), a target associated with autoimmune diseases.

Indiana University School of Medicine
Arylstibonic acids are potent and isoform-selective inhibitors of Cdc25a and Cdc25b phosphatases.

Imperial College
Identification and characterization of novel inhibitors of mPTPB, an essential virulent phosphatase from Mycobacterium tuberculosis.

Indiana University School of Medicine
Identification of novel inhibitors for a low molecular weight protein tyrosine phosphatase via virtual screening.

Purdue University
5-Arylidene-2,4-thiazolidinediones as inhibitors of protein tyrosine phosphatases.

University of Messina
Structure of protein tyrosine phosphatase 1B in complex with inhibitors bearing two phosphotyrosine mimetics.

University of Waterloo
Fragment-based discovery of selective inhibitors of the Mycobacterium tuberculosis protein tyrosine phosphatase PtpA.

University of California
Recent advances in the discovery of competitive protein tyrosine phosphatase 1B inhibitors for the treatment of diabetes, obesity, and cancer.

Incyte
Inhibition of Yersinia protein tyrosine phosphatase by phosphonate derivatives of calixarenes.

National Academy of Sciences of Ukraine
Knowledge-based characterization of similarity relationships in the human protein-tyrosine phosphatase family for rational inhibitor design.

University of Miami
Recent developments in fragment-based drug discovery.

Astex Therapeutics
Structure-Based Design of Active-Site-Directed, Highly Potent, Selective, and Orally Bioavailable Low-Molecular-Weight Protein Tyrosine Phosphatase Inhibitors.

Eli Lilly
Design and synthesis of potent, non-peptidic inhibitors of HPTPbeta.

Procter & Gamble Pharmaceuticals
Inhibition of Low Molecular Weight Protein Tyrosine Phosphatase by an Induced-Fit Mechanism.

Purdue University
Highly Potent and Selective

Purdue University
PTP1B inhibition and antihyperglycemic activity in the ob/ob mouse model of novel 11-arylbenzo[b]naphtho[2,3-d]furans and 11-arylbenzo[b]naphtho[2,3-d]thiophenes.

Wyeth-Ayerst Research
Study of triaryl-based sulfamic acid derivatives as HPTPβ inhibitors.

National Engineering Research Center For The Emergency Strategic Drug
CXCR4-TARGETED DIAGNOSTIC AND THERAPEUTIC AGENTS WITH REDUCED SPECIES SELECTIVITY

Technische University Munchen
SALT CONTAINING PIPERAZINE POLYCYCLIC DERIVATIVE, CRYSTAL FORM THEREOF, PREPARATION METHOD THEREFOR, AND USE THEREOF

Shanghai Hansoh Biomedical
ALK2 inhibitors and methods for inhibiting BMP signaling

The Brigham and Women'S Hospital
Pyrazolopyridine compounds and uses thereof

Incyte
Nurr1:RXR activating compounds for simultaneous treatment of symptoms and pathology of Parkinson's disease

TBA
Specific inhibitors and active site probes for legumain

The Leland Stanford Junior University