20 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
Organization
Disulfiram derivatives as ALDH1A1 and MAGL inhibitors

Batterjee Medical College
Substituted 3-azabicyclo[3.1.0]hexanes as ketohexokinase inhibitors

Pfizer
Pyridylamino substituted heterotricyclic compounds, and preparation method and pharmaceutical use thereof

TBA
Pyrazolo[1,5-a]pyrazin-4-yl derivatives

Pfizer
Piperidine derivatives as inhibitors of ubiquitin specific protease 7

Almac Discovery
Heterocyclylamines as PI3K inhibitors

Incyte
Heteroaromatic compounds as BTK inhibitors

Boehringer Ingelheim International
Isoxazole derivatives as FXR agonists and methods of use therof

Enanta Pharmaceuticals
Heterocyclic compounds as PI3K-γ inhibitors

Incyte
Binding of rasagiline-related inhibitors to human monoamine oxidases: a kinetic and crystallographic analysis.

University of Pavia
Inhibitors of protein kinase C. 2. Substituted bisindolylmaleimides with improved potency and selectivity.

Roche Products
Ring Size effect in the PKC inhibitory activities of perhydroazepine analogs of balanol.

Sphinx Laboratories
An ethylenamine inhibitor binds tightly to both wild type and mutant HIV-1 proteases. Structure and energy study.

Academy of Sciences of The Czech Republic
In vitro anti-human immunodeficiency virus (HIV) activities of transition state mimetic HIV protease inhibitors containing allophenylnorstatine.

National Cancer Institute-Bethesda
Use of medium-sized cycloalkyl rings to enhance secondary binding: discovery of a new class of human immunodeficiency virus (HIV) protease inhibitors.

Upjohn
Structure-based design of sulfonamide-substituted non-peptidic HIV protease inhibitors.

Upjohn
L-735,524: an orally bioavailable human immunodeficiency virus type 1 protease inhibitor.

Merck Research Laboratories
L-687,908, a potent hydroxyethylene-containing HIV protease inhibitor.

Merck Research Laboratories
Structure-activity relationship of small-sized HIV protease inhibitors containing allophenylnorstatine.

Japan Energy
Understanding binding affinity: a combined isothermal titration calorimetry/molecular dynamics study of the binding of a series of hydrophobically modified benzamidinium chloride inhibitors to trypsin.

University of Groningen