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 diseases

Tyk Medicines
104
NEUROPEPTIDE Y1 RECEPTOR (NPY1R) TARGETED THERAPEUTICS AND USES THEREOF

Radionetics Oncology
6
Pyrimidine Heterocyclic Compound, Preparation Method Thereof and use Thereof in Medicine

Insilico Medicine IP
493
Pyrazolopyridinone Compounds

Beigene
108
NITROGEN-CONTAINING POLYCYCLIC FUSED RING COMPOUND, PHARMACEUTICAL COMPOSITION THEREOF, PREPARATION METHOD THEREFOR, AND USE THEREOF

Applied Pharmaceutical Science
172
AMINOHETEROARYL KINASE INHIBITORS

Anrui Biomedical Technology (Guangzhou) Co.
12
N-CYANOPYRROLIDINES WITH ACTIVITY AS USP30 INHIBITORS

Mission Therapeutics
93
SARS-CoV-2 inhibitors for treating coronavirus infections

Insilico Medicine IP
159
Pyridone amides as modulators of sodium channels

Vertex Pharmaceuticals
46
Sting modulator compounds, and methods of making and using

Takeda Pharmaceutical
140
Compounds for inhibiting TNIK and medical uses thereof

Korea Research Institute of Chemical Technology
80
CIS-morpholinone and other compounds as MDM2 inhibitors for the treatment of cancer

Amgen
26
Combination therapy for treatment of hematological diseases

Incyte
708
Substituted carboxamides as inhibitors of WDR5 protein-protein binding

Propellon Therapeutics
23
Compositions and methods for treating KIT- and PDGFRA-mediated diseases

Blueprint Medicines
25
Iso-citrate dehydrogenase (IDH) inhibitor

Shanghai Meton Pharmaceutical
196
Indole derivatives and their use in neurodegenerative diseases

Merck Patent
51
Pharmacokinetically improved compounds

Surface Logix
51
Heterocyclic sulfonamide derivative and medicine containing same

Ea Pharma
1143
TYK2 inhibitors and uses thereof

Nimbus Lakshimi
302
Isoquinolin-3-YL carboxamides and preparation and use thereof

Samumed
191
SGC stimulators

Ironwood Pharmaceuticals
52
Bicyclic aromatic carboxamide compounds useful as Pim kinase inhibitors

Incyte
1
Polymorphs of N-[(R)-1-[(S)-1-(4-aminomethyl-benzylcarbamoyl)-2-phenyl-ethylcarbamoyl]-2-(4-ethoxy-phenyl)-ethyl]-benzamide hydrochloride

Kalvista Pharmaceuticals
11
Carbonic anhydrase inhibitors: in vitro inhibition of a isoforms (hCA I, hCA II, bCA III, hCA IV) by flavonoids.

Ondokuz Mayis University
64
Tricyclic compounds as modulators of TNF-alpha synthesis and as PDE4 inhibitors

Vtv Therapeutics
19
Glucagon receptor antagonist compounds, compositions containing such compounds and methods of use

Merck Sharp & Dohme
13
Monocyclic heteroaryl cycloalkyldiamine derivatives

Novartis
137
Selective NR2B antagonists

Bristol Myers Squibb
50
Quinoline derivatives as PDE10A enzyme inhibitors

H. Lundbeck
20
Discovery of isoalloxazine derivatives as a new class of potential anti-Alzheimer agents and their synthesis.

The M. S. University of Baroda
115
Bicyclic compound or salt thereof

Taiho Pharmaceutical
111
Aminopyrazole derivative

Chugai Seiyaku Kabushiki Kaisha
36
Substituted spiro[cycloalkyl-1,3′-indo]-2′(1′H)-one derivatives and their use as P38 mitogen-activated kinase inhibitors

Almirall
26
1,4-oxazepines as BACE1 and/or BACE2 inhibitors

Hoffmann-La Roche
11
Identification of a Novel Series of Potent TrkA Receptor Tyrosine Kinase Inhibitors

Methylgene
21
Monoamine oxidase inhibition by C4-substituted phthalonitriles.

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.

Bristol Myers Squibb
15
Identification of a novel hypothalamic neuropeptide Y receptor associated with feeding behavior.

Bayer
24
Characterization of 5-hydroxytryptamine1B receptors in rat spinal cord via [125I]iodocyanopindolol binding and inhibition of [3H]-5-hydroxytryptamine release.

University of Texas
20
CYCLIN-DEPENDENT KINASE INHIBITORS

Novartis
30
A novel class of carbonic anhydrase inhibitors: glycoconjugate benzene sulfonamides prepared by "click-tailing".

Griffith University
12
Synthesis and pharmacological evaluation of huprine-tacrine heterodimers: subnanomolar dual binding site acetylcholinesterase inhibitors.

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.

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.

Weizmann Institute of Science