18 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
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TYK2 inhibitors and uses thereof

Nimbus Lakshmi
H3 antagonists containing phenoxypiperidine core structure

Richter Gedeon
Dual inhibitor compounds for use in the treatment of neurodegenerative disorders and alzheimer''s disease

Fondazione Istituto Itaiano Di Tecnologia
8-(piperazin-1-yl)-1,2,3,4-tetrahydro-isoquinoline derivatives

Idorsia Pharmaceuticals
Heterocyclic inhibitors of PTPN11

The University of Texas System
Selective targeting of lysosomal cysteine proteases with radiolabeled electrophilic substrate analogs.

University of California San Francisco
Antibiotic sensitization using biphenyl tetrazoles as potent inhibitors of Bacteroides fragilis metallo-beta-lactamase.

Merck Research Laboratories
Splicing factor SF3b as a target of the antitumor natural product pladienolide.

Eisai
Rigid duplex alpha-cyclodextrin reversibly connected with disulfide bonds. Synthesis and inclusion complexes.

Institute of Organic Chemistry and Biochemistry As Cr
Thermodynamics of molecular recognition by cyclodextrins. 1. Calorimetric titration of inclusion complexation of naphthalenesulfonates with .alpha.-, .beta.-, and .gamma.-cyclodextrins: enthalpy-entropy compensation

Himeji Institute of Technology
Chiral Recognition Thermodynamics of β-Cyclodextrin: The Thermodynamic Origin of Enantioselectivity and the Enthalpy-Entropy Compensation Effect

Japan Science and Technology Agency
Aroylguanidine-based factor Xa inhibitors: the discovery of BMS-344577.

Bristol-Myers Squibb
Discovery of begacestat, a Notch-1-sparing gamma-secretase inhibitor for the treatment of Alzheimer's disease.

Wyeth Research
Structural analysis of ARC-type inhibitor (ARC-1034) binding to protein kinase A catalytic subunit and rational design of bisubstrate analogue inhibitors of basophilic protein kinases.

University of Tartu
Discovery of novel spirocyclopropyl hydroxamate and carboxylate compounds as TACE inhibitors.

Schering-Plough Research Institute
Synthesis and biological evaluation of 4-amino derivatives of benzimidazoquinoxaline, benzimidazoquinoline, and benzopyrazoloquinazoline as potent IKK inhibitors.

Bristol-Myers Squibb