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BindingDB contains 3.2M data for 1.4M Compounds and 11.5K Targets. Of those, 1.6M data for 765K Compounds and 4.8K Targets were curated by BindingDB curators. BindingDB is a FAIRsharing resource.

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49 articles for thisTarget


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

PMID
Cmpds
Data
Article Title
Organization
33
3-oxadiazolyl substituted pyrazolo[1,5,a]pyrimidines for ROS1, NTRK, and ALK mediated diseasesBDB
Tyk Medicines
104
NEUROPEPTIDE Y1 RECEPTOR (NPY1R) TARGETED THERAPEUTICS AND USES THEREOFBDB
Radionetics Oncology
6
Pyrimidine Heterocyclic Compound, Preparation Method Thereof and use Thereof in MedicineBDB
Insilico Medicine IP
493
Pyrazolopyridinone CompoundsBDB
Beigene
108
NITROGEN-CONTAINING POLYCYCLIC FUSED RING COMPOUND, PHARMACEUTICAL COMPOSITION THEREOF, PREPARATION METHOD THEREFOR, AND USE THEREOFBDB
Applied Pharmaceutical Science
172
AMINOHETEROARYL KINASE INHIBITORSBDB
Anrui Biomedical Technology (Guangzhou) Co.
12
N-CYANOPYRROLIDINES WITH ACTIVITY AS USP30 INHIBITORSBDB
Mission Therapeutics
93
SARS-CoV-2 inhibitors for treating coronavirus infectionsBDB
Insilico Medicine IP
159
Pyridone amides as modulators of sodium channelsBDB
Vertex Pharmaceuticals
46
Sting modulator compounds, and methods of making and usingBDB
Takeda Pharmaceutical
140
Compounds for inhibiting TNIK and medical uses thereofBDB
Korea Research Institute of Chemical Technology
80
CIS-morpholinone and other compounds as MDM2 inhibitors for the treatment of cancerBDB
Amgen
26
Combination therapy for treatment of hematological diseasesBDB
Incyte
708
Substituted carboxamides as inhibitors of WDR5 protein-protein bindingBDB
Propellon Therapeutics
23
Compositions and methods for treating KIT- and PDGFRA-mediated diseasesBDB
Blueprint Medicines
25
Iso-citrate dehydrogenase (IDH) inhibitorBDB
Shanghai Meton Pharmaceutical
196
Indole derivatives and their use in neurodegenerative diseasesBDB
Merck Patent
51
Pharmacokinetically improved compoundsBDB
Surface Logix
51
Heterocyclic sulfonamide derivative and medicine containing sameBDB
Ea Pharma
1143
TYK2 inhibitors and uses thereofBDB
Nimbus Lakshimi
302
Isoquinolin-3-YL carboxamides and preparation and use thereofBDB
Samumed
191
SGC stimulatorsBDB
Ironwood Pharmaceuticals
52
Bicyclic aromatic carboxamide compounds useful as Pim kinase inhibitorsBDB
Incyte
1
Polymorphs of N-[(R)-1-[(S)-1-(4-aminomethyl-benzylcarbamoyl)-2-phenyl-ethylcarbamoyl]-2-(4-ethoxy-phenyl)-ethyl]-benzamide hydrochlorideBDB
Kalvista Pharmaceuticals
11
Carbonic anhydrase inhibitors: in vitro inhibition of a isoforms (hCA I, hCA II, bCA III, hCA IV) by flavonoids.BDB
Ondokuz Mayis University
64
Tricyclic compounds as modulators of TNF-alpha synthesis and as PDE4 inhibitorsBDB
Vtv Therapeutics
19
Glucagon receptor antagonist compounds, compositions containing such compounds and methods of useBDB
Merck Sharp & Dohme
13
Monocyclic heteroaryl cycloalkyldiamine derivativesBDB
Novartis
137
Selective NR2B antagonistsBDB
Bristol Myers Squibb
50
Quinoline derivatives as PDE10A enzyme inhibitorsBDB
H. Lundbeck
20
Discovery of isoalloxazine derivatives as a new class of potential anti-Alzheimer agents and their synthesis.BDB
The M. S. University of Baroda
115
Bicyclic compound or salt thereofBDB
Taiho Pharmaceutical
111
Aminopyrazole derivativeBDB
Chugai Seiyaku Kabushiki Kaisha
36
Substituted spiro[cycloalkyl-1,3′-indo]-2′(1′H)-one derivatives and their use as P38 mitogen-activated kinase inhibitorsBDB
Almirall
26
1,4-oxazepines as BACE1 and/or BACE2 inhibitorsBDB
Hoffmann-La Roche
11
 
Identification of a Novel Series of Potent TrkA Receptor Tyrosine Kinase InhibitorsBDB
Methylgene
21
Monoamine oxidase inhibition by C4-substituted phthalonitriles.BDB
North-West University
8
Pharmacological characterization of a novel nonpeptide antagonist radioligand, (+/-)-N-[2-methyl-4-methoxyphenyl]-1-(1-(methoxymethyl) propyl)-6-methyl-1H-1,2,3-triazolo[4,5-c]pyridin-4-amine ([3H]SN003) for corticotropin-releasing factor1 receptors.BDB
Bristol Myers Squibb
15
Identification of a novel hypothalamic neuropeptide Y receptor associated with feeding behavior.BDB
Bayer
24
Characterization of 5-hydroxytryptamine1B receptors in rat spinal cord via [125I]iodocyanopindolol binding and inhibition of [3H]-5-hydroxytryptamine release.BDB
University of Texas
20
CYCLIN-DEPENDENT KINASE INHIBITORSBDB
Novartis
30
A novel class of carbonic anhydrase inhibitors: glycoconjugate benzene sulfonamides prepared by "click-tailing".BDB
Griffith University
12
Synthesis and pharmacological evaluation of huprine-tacrine heterodimers: subnanomolar dual binding site acetylcholinesterase inhibitors.BDB
Universitat De Barcelona
25
Dual-site binding of bivalent 4-aminopyridine- and 4-aminoquinoline-based AChE inhibitors: contribution of the hydrophobic alkylene tether to monomer and dimer affinities.BDB
Hong Kong University of Science and Technology
3
Acetylcholinesterase complexed with bivalent ligands related to huperzine a: experimental evidence for species-dependent protein-ligand complementarity.BDB
Weizmann Institute of Science