The first public molecular recognition database, BindingDB supports research, education and practice in drug discovery, pharmacology and related fields.

BindingDB contains 2.9M data for 1.2M Compounds and 9.3K Targets. Of those, 1,352K data for 627K Compounds and 4.5K Targets were curated by BindingDB curators. BindingDB is a FAIRsharing resource.

If BindingDB was of value to your research, please take a moment to donate to this nonprofit project. Your donation will let us provide you with more data and improved service.

Advanced Search

24 articles for thisTarget


The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Data
Article Title
Organization
Development of new Malt1 inhibitors and probes.EBI
Leiden University
MALT1 Inhibitors May Potentially Treat Lymphomas and Autoimmune Disorders.EBI
Therachem Research Medilab (India)
Identification of฿-Lapachone Analogs as Novel MALT1 Inhibitors To Treat an Aggressive Subtype of Diffuse Large B-Cell Lymphoma.EBI
Institute of Basic Science (Ibs)
Discovery and optimization of cyclohexane-1,4-diamines as allosteric MALT1 inhibitors.EBI
Astrazeneca
Identification of Novel Fused Heteroaromatics-Based MALT1 Inhibitors by High-Throughput Screening to Treat B Cell Lymphoma.EBI
Chinese Academy of Sciences
Structure-activity relationship studies of 3-substituted pyrazoles as novel allosteric inhibitors of MALT1 protease.EBI
Toray Industries
Optimization of the EBI
Novartis Pharma
Discovery of Potent, Highly Selective, and EBI
Novartis Institutes For Biomedical Research
Quinoline and thiazolopyridine allosteric inhibitors of MALT1.EBI
Harvard Medical School
Secondary Metabolites from the Fungus Dictyosporium sp. and Their MALT1 Inhibitory Activities.EBI
National Cancer Institute
Discovery and optimization of a series of small-molecule allosteric inhibitors of MALT1 protease.EBI
Janssen Research & Development
Use of Non-Natural Amino Acids for the Design and Synthesis of a Selective, Cell-Permeable MALT1 Activity-Based Probe.EBI
Ku Leuven
Peptide-based covalent inhibitors of MALT1 paracaspase.EBI
Harvard Medical School
N-aryl-piperidine-4-carboxamides as a novel class of potent inhibitors of MALT1 proteolytic activity.EBI
Novartis Institutes For Biomedical Research