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BindingDB contains 3.1M data for 1.3M Compounds and 9.6K Targets. Of those, 1.5M data for 698K Compounds and 4.7K Targets were curated by BindingDB curators. BindingDB is a FAIRsharing resource.

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15 articles for thisTarget


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

PMID
Data
Article Title
Organization
First-in-Class Selective Inhibitors of the Lysine Acetyltransferase KAT8.EBI
Sapienza University of Rome
Structure-activity relationship and antitumor activity of 1,4-pyrazine-containing inhibitors of histone acetyltransferases P300/CBP.EBI
Baylor College of Medicine
Histone acetyltransferase inhibitors: An overview in synthesis, structure-activity relationship and molecular mechanism.EBI
Sichuan University
Discovery of Acylsulfonohydrazide-Derived Inhibitors of the Lysine Acetyltransferase, KAT6A, as Potent Senescence-Inducing Anti-Cancer Agents.EBI
Monash University (Parkville Campus)
Discovery of Benzoylsulfonohydrazides as Potent Inhibitors of the Histone Acetyltransferase KAT6A.EBI
Cancer Therapeutics Crc
Discovery, Structure-Activity Relationship, and Biological Activity of Histone-Competitive Inhibitors of Histone Acetyltransferases P300/CBP.EBI
Avera Institute For Human Genetics
Cyclopropyl Fused Thiazin-2-Amine Compounds as Beta-Secretase Inhibitors and Methods of UseBDB
Amgen
Substituted heterocycles as aldehyde dehydrogenase inhibitorsBDB
Kayothera
ERAP INHIBITORSBDB
Universite De Lille
Isoquinolin-3-yl carboxamides and preparation and use thereofBDB
Biosplice Therapeutics
Mu opioid receptor modulatorsBDB
University of California
2,3-dihydrofuro[2,3-b]pyridine compoundsBDB
Eli Lilly
Selective inhibitors of protein arginine methyltransferase 5 (PRMT5)BDB
Prelude Therapeutics
Benzenesulfonamide compounds and their use as therapeutic agentsBDB
Xenon Pharmaceuticals
Methylamine derivatives as lysysl oxidase inhibitors for the treatment of cancerBDB
The Institute of Cancer Research: Royal Cancer Hospital