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62 articles for thisTarget


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

PMID
Data
Article Title
Organization
Discovery of 2-(((1r,4r)-4-(((4-Chlorophenyl)(phenyl)carbamoyl)oxy)methyl)cyclohexyl)methoxy)acetate (Ralinepag): An Orally Active Prostacyclin Receptor Agonist for the Treatment of Pulmonary Arterial Hypertension.EBI
Arena Pharmaceuticals
Tetrahydroquinoline-based tricyclic amines as potent and selective agonists of the 5-HTEBI
Arena Pharmaceuticals
Discovery of a novel trans-1,4-dioxycyclohexane GPR119 agonist series.EBI
Arena Pharmaceuticals
Discovery of a new series of potent prostacyclin receptor agonists with in vivo activity in rat.EBI
Arena Pharmaceuticals
Design and synthesis of new tricyclic indoles as potent modulators of the S1P1 receptor.EBI
Arena Pharmaceuticals
Discovery and optimization of 5-fluoro-4,6-dialkoxypyrimidine GPR119 agonists.EBI
Arena Pharmaceuticals
(7-Benzyloxy-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-yl)acetic Acids as S1P1 Functional Antagonists.EBI
Arena Pharmaceuticals
Discovery of APD334: Design of a Clinical Stage Functional Antagonist of the Sphingosine-1-phosphate-1 Receptor.EBI
Arena Pharmaceuticals
Discovery of 1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalen-4-carboxamides as potent and selective CB2 receptor agonists.EBI
Arena Pharmaceuticals
Therapeutic utility of cannabinoid receptor type 2 (CB(2)) selective agonists.EBI
Arena Pharmaceuticals
(1aR,5aR)1a,3,5,5a-Tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene-4-carboxylic acid (MK-1903): a potent GPR109a agonist that lowers free fatty acids in humans.EBI
Arena Pharmaceuticals
Fused tricyclic indoles as S1P1 agonists with robust efficacy in animal models of autoimmune disease.EBI
Arena Pharmaceuticals
Nicotinic acid receptor agonists differentially activate downstream effectors.EBI
Arena Pharmaceuticals
A new family of H3 receptor antagonists based on the natural product Conessine.EBI
Arena Pharmaceuticals
Identification of fused bicyclic heterocycles as potent and selective 5-HT(2A) receptor antagonists for the treatment of insomnia.EBI
Arena Pharmaceuticals
Discovery of a second generation agonist of the orphan G-protein coupled receptor GPR119 with an improved profile.EBI
Arena Pharmaceuticals
Identification of biaryl sulfone derivatives as antagonists of the histamine H3 receptor: discovery of (R)-1-(2-(4'-(3-methoxypropylsulfonyl)biphenyl-4-yl)ethyl)-2-methylpyrrolidine (APD916).EBI
Arena Pharmaceuticals
Discovery and characterization of potent and selective 4-oxo-4-(5-(5-phenyl-1,2,4-oxadiazol-3-yl)indolin-1-yl)butanoic acids as S1P¿? agonists.EBI
Arena Pharmaceuticals
Discovery of fused bicyclic agonists of the orphan G-protein coupled receptor GPR119 with in vivo activity in rodent models of glucose control.EBI
Arena Pharmaceuticals
Synthesis and in vivo evaluation of phenethylpiperazine amides: selective 5-hydroxytryptamine(2A) receptor antagonists for the treatment of insomnia.EBI
Arena Pharmaceuticals
Discovery and structure-activity relationship of 3-methoxy-N-(3-(1-methyl-1H-pyrazol-5-yl)-4-(2-morpholinoethoxy)phenyl)benzamide (APD791): a highly selective 5-hydroxytryptamine2A receptor inverse agonist for the treatment of arterial thrombosis.EBI
Arena Pharmaceuticals
Potent tricyclic pyrazole tetrazole agonists of the nicotinic acid receptor (GPR109a).EBI
Arena Pharmaceuticals
Discovery of 1-[3-(4-bromo-2-methyl-2h-pyrazol-3-yl)-4-methoxyphenyl]-3-(2,4-difluorophenyl)urea (nelotanserin) and related 5-hydroxytryptamine2A inverse agonists for the treatment of insomnia.EBI
Arena Pharmaceuticals
Pyrimidine-based antagonists of h-MCH-R1 derived from ATC0175: in vitro profiling and in vivo evaluation.EBI
Arena Pharmaceuticals
Solubilized phenyl-pyrazole ureas as potent, selective 5-HT(2A) inverse-agonists and their application as antiplatelet agents.EBI
Arena Pharmaceuticals
Design and evaluation of novel biphenyl sulfonamide derivatives with potent histamine H(3) receptor inverse agonist activity.EBI
Arena Pharmaceuticals
5-N,N-Disubstituted 5-aminopyrazole-3-carboxylic acids are highly potent agonists of GPR109b.EBI
Arena Pharmaceuticals
Nicotinic acid receptor agonists.EBI
Arena Pharmaceuticals
Discovery of the first potent and orally efficacious agonist of the orphan G-protein coupled receptor 119.EBI
Arena Pharmaceuticals
3-(1H-tetrazol-5-yl)-1,4,5,6-tetrahydro-cyclopentapyrazole (MK-0354): a partial agonist of the nicotinic acid receptor, G-protein coupled receptor 109a, with antilipolytic but no vasodilatory activity in mice.EBI
Arena Pharmaceuticals
Novel H3 receptor antagonists with improved pharmacokinetic profiles.EBI
Arena Pharmaceuticals
3-Nitro-4-amino benzoic acids and 6-amino nicotinic acids are highly selective agonists of GPR109b.EBI
Arena Pharmaceuticals
Fluorinated pyrazole acids are agonists of the high affinity niacin receptor GPR109a.EBI
Arena Pharmaceuticals
Agonist lead identification for the high affinity niacin receptor GPR109a.EBI
Arena Pharmaceuticals
Analogues of acifran: agonists of the high and low affinity niacin receptors, GPR109a and GPR109b.EBI
Arena Pharmaceuticals
Discovery and SAR of new benzazepines as potent and selective 5-HT(2C) receptor agonists for the treatment of obesity.EBI
Arena Pharmaceuticals
Novel (R)-6,6a,7,8,9,10-hexahydro-5H-pyrazino[1,2-a][1,n]naphthyridines as potent and selective agonists of the 5-HTEBI
Arena Pharmaceuticals
Discovery of a lead series of potent benzodiazepine 5-HTEBI
Arena Pharmaceuticals
Discovery and structure-activity relationship of (1R)-8-chloro-2,3,4,5-tetrahydro-1-methyl-1H-3-benzazepine (Lorcaserin), a selective serotonin 5-HT2C receptor agonist for the treatment of obesity.EBI
Arena Pharmaceuticals
Discovery of APD371: Identification of a Highly Potent and Selective CBEBI
Arena Pharmaceuticals
CYCLOPROPANECARBOXAMIDE-CONTAINING COMPOUNDS AND APPLICATION THEREOFBDB
Cgenetech (Suzhou, China)
1,7-naphthyridine derivative and preparation method and use thereforBDB
Cspc Zhongqi Pharmaceutical Technology (Shijiazhuang)
HDAC inhibitor compounds and methods of treatmentBDB
University of Florida Research Foundation
Sulfinylpyridines and their use in the treatment of cancerBDB
Oblique Therapeutics
Methods of use for trisubstituted benzotriazole derivatives as dihydroorotate oxygenase inhibitorsBDB
Aurigene Discovery Technologies
Compounds that participate in cooperative binding and uses thereofBDB
Revolution Medicines
Compounds and uses thereofBDB
Yumanity Therapeutics
Thiophene, manufacturing method thereof, and pharmaceutical application of sameBDB
Cstone Pharmaceutical (Suzhou)
TYK2 inhibitors and uses thereofBDB
Nimbus Lakshmi
Method of treatment using substituted pyrazolo[1,5-A] pyrimidine compoundsBDB
Array Biopharma
ASK1 isoindolin-1-one inhibitors and methods of use thereofBDB
Hepatikos Therapeutics
Sulfonyl piperidine derivatives and their use for treating prokineticin mediated diseasesBDB
Takeda Pharmaceutical
Susceptibility of cord blood antioxidant enzymes glutathione reductase, glutathione peroxidase and glutathione S-transferase to different antibiotics: in vitro approach.BDB
Ondokuz Mayis University
Identification and structure-activity relationship of purine derivatives as novel MTH1 inhibitors.BDB
Riken Center For Life Science Technologies
Synthesis of 4-thiazolidinone analogs as potent in vitro anti-urease agents.BDB
Hazara University
2,5-methano- and 2,5-ethano-tetrahydrobenzazepine derivatives and use thereof to block reuptake of norepinephrine, dopamine, and serotoninBDB
Albany Molecular Research
Substituted quinolines and their use as medicamentsBDB
Boehringer Ingelheim International
Compounds and their use as BACE inhibitorsBDB
Astrazeneca
Anti-infective agents against intracellular pathogensBDB
The Ohio State University Research Foundation
Heterologous expression of human {alpha}6{beta}4{beta}3{alpha}5 nicotinic acetylcholine receptors: binding properties consistent with their natural expression require quaternary subunit assembly including the {alpha}5 subunit.BDB
Targacept