The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
28319392 |
216 |
Scaffold Repurposing of Nucleosides (Adenosine Receptor Agonists): Enhanced Activity at the Human Dopamine and Norepinephrine Sodium Symporters. |
National Institute of Diabetes and Digestive and Kidney Diseases |
28089699 |
63 |
Investigation of piperazine benzamides as humanß |
Merck |
3560162 |
3 |
Synthesis and antiarrhythmic activity of novel 3-alkyl-1-[omega-[4-[(alkylsulfonyl)amino]phenyl]-omega- hydroxyalkyl]-1H-imidazolium salts and related compounds. |
TBA |
2878080 |
1 |
6,7-Dichloro-1-(3,4,5-trimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline . A structurally novel beta-adrenergic receptor blocking agent. |
TBA |
6124637 |
18 |
Syntheses and adrenergic agonist properties of ring-fluorinated isoproterenols. |
TBA |
11459642 |
39 |
Design and synthesis of novel benzofurans as a new class of antifungal agents targeting fungal N-myristoyltransferase. Part 1. |
Nippon Roche Research Center |
26709102 |
142 |
Discovery of Vibegron: A Potent and Selectiveß3 Adrenergic Receptor Agonist for the Treatment of Overactive Bladder. |
Merck Research Laboratories |
26125514 |
40 |
Discovery of Novel Indazole Derivatives as Highly Potent and Selective Humanß3-Adrenergic Receptor Agonists with the Possibility of Having No Cardiovascular Side Effects. |
Asahi Kasei Pharma |
24835980 |
98 |
Discovery of TD-4306, a long-actingß2-agonist for the treatment of asthma and COPD. |
Theravance |
24813741 |
110 |
Multivalent design of long-actingß(2)-adrenoceptor agonists incorporating biarylamines. |
Theravance |
16640337 |
47 |
Biarylaniline phenethanolamines as potent and selective beta3 adrenergic receptor agonists. |
Glaxosmithkline |
23614528 |
121 |
Synthesis and in vitro and in vivo characterization of highlyß1-selectiveß-adrenoceptor partial agonists. |
University of Nottingham |
21870877 |
119 |
Synthesis and characterization of high-affinity 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene-labeled fluorescent ligands for humanß-adrenoceptors. |
University of Nottingham |
11806709 |
63 |
Synthesis and evaluation of potent and selective beta(3) adrenergic receptor agonists containing acylsulfonamide, sulfonylsulfonamide, and sulfonylurea carboxylic acid isosteres. |
Glaxosmithkline |
12443779 |
44 |
2-(Dimethylaminomethyl)-tetrahydroisoxazolopyridobenzazepine derivatives. Synthesis of a new 5-HT(2C) antagonist with potential anxiolytic properties. |
Janssen-Cilag |
21925889 |
48 |
The discovery of long-acting saligeninß2 adrenergic receptor agonists incorporating a urea group. |
Glaxosmithkline |
21696967 |
51 |
The discovery of long-acting saligeninß2 adrenergic receptor agonists incorporating hydantoin or uracil rings. |
Glaxosmithkline |
20462258 |
50 |
Synthesis and structure-activity relationships of long-acting beta2 adrenergic receptor agonists incorporating metabolic inactivation: an antedrug approach. |
Glaxosmithkline |
19317397 |
62 |
Synthesis and structure-activity relationships of long-acting beta2 adrenergic receptor agonists incorporating arylsulfonamide groups. |
Glaxosmithkline |
15908203 |
23 |
QSAR analysis of thiazole benzenesulfonamide substituted 3-pyridylethanolamines as beta3-adrenergic receptor agonist. |
S.G.S.I.T.S. |
22313227 |
78 |
Radiosynthesis and evaluation of an (18)F-labeled positron emission tomography (PET) radioligand for brain histamine subtype-3 receptors based on a nonimidazole 2-aminoethylbenzofuran chemotype. |
National Institute of Mental Health |
24900353 |
6 |
Combination of a Beta adrenoceptor modulator and a norepinephrine-serotonin uptake inhibitor for the treatment of obesity. |
TBA |
21207959 |
69 |
Syntheses of 2-amino and 2-halothiazole derivatives as high-affinity metabotropic glutamate receptor subtype 5 ligands and potential radioligands for in vivo imaging. |
National Institute of Mental Health |
20181479 |
177 |
Heterocyclic acetamide and benzamide derivatives as potent and selective beta3-adrenergic receptor agonists with improved rodent pharmacokinetic profiles. |
Merck Research Laboratories |
19963380 |
38 |
Synthetic studies and pharmacological evaluations on the MDMA ('Ecstasy') antagonist nantenine. |
Hunter College and The Graduate Center of The City University of New York |
19608416 |
29 |
Discovery of highly potent and selective biphenylacylsulfonamide-based beta3-adrenergic receptor agonists and molecular modeling based on the solved X-ray structure of the beta2-adrenergic receptor: part 6. |
Astellas Pharma |
19581100 |
162 |
Discovery of novel thiourea derivatives as potent and selective beta3-adrenergic receptor agonists. |
Astellas Pharma |
19232786 |
72 |
Discovery of novel acetanilide derivatives as potent and selective beta3-adrenergic receptor agonists. |
Astellas Pharma |
18651730 |
123 |
Discovery of a novel series of benzoic acid derivatives as potent and selective human beta3 adrenergic receptor agonists with good oral bioavailability. 3. Phenylethanolaminotetraline (PEAT) skeleton containing biphenyl or biphenyl ether moiety. |
Astellas Pharma |
18083578 |
16 |
Stereospecific synthesis and bio-activity of novel beta(3)-adrenoceptor agonists and inverse agonists. |
Universit£ |
18307290 |
97 |
Discovery of a novel series of biphenyl benzoic acid derivatives as potent and selective human beta3-adrenergic receptor agonists with good oral bioavailability. Part I. |
Astellas Pharma |
15603933 |
28 |
Discovery of a novel, potent and selective human beta3-adrenergic receptor agonist. |
Fujisawa Pharmaceutical |
15482914 |
25 |
Azaadamantane benzamide 5-HT4 agonists: gastrointestinal prokinetic SC-54750. |
Pfizer |
12502364 |
17 |
Relationship between stereochemistry and the beta3-adrenoceptor agonistic activity of 4'-hydroxynorephedrine derivative as an agent for treatment of frequent urination and urinary incontinence. |
Kissei Pharmaceutical |
11311069 |
64 |
(4-Piperidin-1-yl)phenyl amides: potent and selective human beta(3) agonists. |
Wyeth-Ayerst Research |
1976812 |
62 |
Synthesis of novel (aryloxy)propanolamines and related compounds possessing both class II and class III antiarrhythmic activity. |
Berlex Laboratories |
15149682 |
25 |
Potent and selective, sulfamide-based human beta 3-adrenergic receptor agonists. |
Pfizer |
11714605 |
39 |
Beta 3 agonists. Part 1: evolution from inception to BMS-194449. |
Bristol-Myers Squibb Pharmaceutical Research Institute |
| 13 |
A simplified template approach towards the synthesis of a potent beta-3 adrenoceptor agonist at the human receptor |
TBA |
21615150 |
14 |
Progress in structure based drug design for G protein-coupled receptors. |
Heptares Therapeutics |
21353541 |
25 |
Design of a novel pyrrolidine scaffold utilized in the discovery of potent and selective humanß3 adrenergic receptor agonists. |
Merck Research Laboratories |
20833036 |
221 |
Thienopyrimidines asß3-adrenoceptor agonists: hit-to-lead optimization. |
4Sc |
20813948 |
63 |
Spiroindolones, a potent compound class for the treatment of malaria. |
Swiss Tropical and Public Health Institute |
20434333 |
111 |
A vHTS approach for the identification of beta-adrenoceptor ligands. |
4Sc |
19767208 |
33 |
Discovery and optimization of novel 4-[(aminocarbonyl)amino]-N-[4-(2-aminoethyl)phenyl]benzenesulfonamide ghrelin receptor antagonists. |
Merck Research Laboratories |
19646882 |
72 |
Novel delta opioid receptor agonists exhibit differential stimulation of signaling pathways. |
University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School and The Informatics Institute of Umdnj |
| 21 |
Serotonin 5-HT4 agonist activity of a series of meso-azanoradamantane benzamides |
TBA |
| 38 |
Carboxyl-promoted enhancement of selectivity for the β3 adrenergic receptor. Negative charge of the sulfonic acid BMS-187413 introduces-β3 binding selectivity |
TBA |
| 32 |
The synthesis and biological activity of some known and putative metabolites of the atypical antipsychotic agent olanzapine (LY170053) |
TBA |
| 26 |
BMS-187257, a potent, selective, and novel heterocyclic β3 adrenergic receptor agonist |
TBA |
| 37 |
The discovery of CP-96,021 and CP-96,486, balanced, combined, potent and orally active leukotriene D4 (LTD4)/platelet activating factor (PAF) receptor antagonists. |
TBA |
19492813 |
56 |
Antagonists of the calcium receptor I. Amino alcohol-based parathyroid hormone secretagogues. |
Glaxosmithkline |
19366244 |
138 |
Discovery of highly potent and selective biphenylacylsulfonamide-based beta3-adrenergic receptor agonists and evaluation of physical properties as potential overactive bladder therapies: part 5. |
Astellas Pharma |
19362005 |
74 |
Synthesis and evaluation of novel phenoxypropanolamine derivatives containing acetanilides as potent and selective beta3-adrenergic receptor agonists. |
Astellas Pharma |
19329329 |
183 |
Synthesis and in vitro affinities of various MDL 100907 derivatives as potential 18F-radioligands for 5-HT2A receptor imaging with PET. |
Institute of Nuclear Chemistry Johannes Gutenberg-University Mainz |
19081260 |
10 |
Substituted 1,2,3,4-tetrahydroquinolin-6-yloxypropanes as beta3-adrenergic receptor agonists: design, synthesis, biological evaluation and pharmacophore modeling. |
Central Drug Research Institute |
18752946 |
47 |
Discovery of novel series of benzoic acid derivatives containing biphenyl ether moiety as potent and selective human beta(3)-adrenergic receptor agonists: Part IV. |
Astellas Pharma |
18701276 |
97 |
Highly functionalized 7-azaindoles as selective PPAR gamma modulators. |
Merck Research Laboratories |
18553954 |
126 |
Discovery of a novel series of biphenyl benzoic acid derivatives as highly potent and selective human beta3 adrenergic receptor agonists with good oral bioavailability. Part II. |
Astellas Pharma |
17911024 |
37 |
Potent oxindole based human beta3 adrenergic receptor agonists. |
Eli Lilly |
17632003 |
55 |
Discovery of potent and orally bioavailable heterocycle-based beta3-adrenergic receptor agonists, potential therapeutics for the treatment of obesity. |
Pfizer |
17533126 |
78 |
Arylpropanolamines: selective beta3 agonists arising from strategies to mitigate phase I metabolic transformations. |
Bristol-Myers Squibb Pharmaceutical Research Institute |
17303428 |
22 |
Novel chiral isoxazole derivatives: synthesis and pharmacological characterization at human beta-adrenergic receptor subtypes. |
Università |
16931005 |
21 |
Potent benzimidazolone based human beta(3)-adrenergic receptor agonists. |
Eli Lilly |
16722631 |
87 |
An integrated in silico 3D model-driven discovery of a novel, potent, and selective amidosulfonamide 5-HT1A agonist (PRX-00023) for the treatment of anxiety and depression. |
Predix Pharmaceuticals |
16392798 |
46 |
Synthesis and in vivo validation of [O-methyl-11C]2-{4-[4-(7-methoxynaphthalen-1-yl)piperazin- 1-yl]butyl}-4-methyl-2H-[1,2,4]triazine-3,5-dione: a novel 5-HT1A receptor agonist positron emission tomography ligand. |
Columbia University College of Physicians and Surgeons |
15686912 |
35 |
Tryptamine-based human beta3-adrenergic receptor agonists. Part 3: improved oral bioavailability via modification of the sulfonamide moiety. |
Dainippon Pharmaceutical |
15546708 |
35 |
Tryptamine-based human beta3-adrenergic receptor agonists. Part 2: SAR of the methylene derivatives. |
Dainippon Pharmaceutical |
15546707 |
60 |
Tryptamine-based human beta3-adrenergic receptor agonists. Part 1: SAR studies of the 7-position of the indole ring. |
Dainippon Pharmaceutical |
15177466 |
74 |
BMS-201620: a selective beta 3 agonist. |
Bristol-Myers Squibb Pharmaceutical Research Institute |
15149647 |
10 |
Bridgehead-methyl analog of SC-53116 as a 5-HT4 agonist. |
Pfizer |
12852947 |
36 |
Development of 3D-QSAR models in cyclic ureidobenzenesulfonamides: human beta3-adrenergic receptor agonist. |
Central Drug Research Institute |
12798332 |
35 |
Cyclic amine sulfonamides as linkers in the design and synthesis of novel human beta(3) adrenergic receptor agonists. |
Wyeth Research |
12657269 |
52 |
Novel and potent human and rat beta3-adrenergic receptor agonists containing substituted 3-indolylalkylamines. |
Dainippon Pharmaceutical |
12270184 |
34 |
Novel substituted 4-aminomethylpiperidines as potent and selective human beta3-agonists. Part 2: arylethanolaminomethylpiperidines. |
Wyeth Research |
12270183 |
45 |
Novel substituted 4-aminomethylpiperidines as potent and selective human beta3-agonists. Part 1: aryloxypropanolaminomethylpiperidines. |
Wyeth Research |
11720857 |
37 |
4-Aminopiperidine ureas as potent selective agonists of the human beta(3)-adrenergic receptor. |
Wyeth-Ayerst Research |
11714606 |
31 |
BMS-196085: a potent and selective full agonist of the human beta(3) adrenergic receptor. |
Bristol-Myers Squibb Pharmaceutical Research Institute |
11327605 |
27 |
New oxadiazolidinedione derivatives as potent and selective human beta3 agonists. |
Wyeth-Ayerst Research |
11277513 |
25 |
2,4-Thiazolidinediones as potent and selective human beta3 agonists. |
Wyeth-Ayerst Research |
11212115 |
72 |
Human beta3 adrenergic receptor agonists containing cyanoguanidine and nitroethylenediamine moieties. |
Merck Research Laboratories |
11055339 |
59 |
Tetrahydroisoquinoline derivatives containing a benzenesulfonamide moiety as potent, selective human beta3 adrenergic receptor agonists. |
Merck Research Laboratories |
11052788 |
33 |
Discovery of a potent, orally bioavailable beta(3) adrenergic receptor agonist, (R)-N-[4-[2-[[2-hydroxy-2-(3-pyridinyl)ethyl]amino]ethyl]phenyl]-4-[4 -[4-(trifluoromethyl)phenyl]thiazol-2-yl]benzenesulfonamide. |
Merck Research Laboratories |
10999482 |
52 |
Human beta3-adrenergic receptor agonists containing 1,2,3-triazole-substituted benzenesulfonamides. |
Merck Research Laboratories |
10987429 |
69 |
Potent, selective 3-pyridylethanolamine beta3 adrenergic receptor agonists possessing a thiazole benzenesulfonamide pharmacophore. |
Merck Research Laboratories |
10915043 |
69 |
Substituted oxazole benzenesulfonamides as potent human beta3 adrenergic receptor agonists. |
Merck Research Laboratories |
10888325 |
90 |
Synthesis and SAR of benzyl and phenoxymethylene oxadiazole benzenesulfonamides as selective beta3 adrenergic receptor agonist antiobesity agents. |
Merck Research Laboratories |
10888324 |
48 |
Discovery of an orally bioavailable alkyl oxadiazole beta3 adrenergic receptor agonist. |
Merck Research Laboratories |
32342685 |
325 |
Discovery, Optimization, and Characterization of ML417: A Novel and Highly Selective D |
National Institute of Neurological Disorders and Stroke |
10406657 |
91 |
Potent, elective human beta3 adrenergic receptor agonists containing a substituted indoline-5-sulfonamide pharmacophore. |
Merck Research Laboratories |
10340609 |
15 |
L-770,644: a potent and selective human beta3 adrenergic receptor agonist with improved oral bioavailability. |
Merck Research Laboratories |
10201842 |
69 |
Human beta3 adrenergic receptor agonists containing imidazolidinone and imidazolone benzenesulfonamides. |
Merck Research Laboratories |
10201841 |
47 |
Human beta3 adrenergic receptor agonists containing cyclic ureidobenzenesulfonamides. |
Merck Research Laboratories |
9925722 |
18 |
Pharmacological treatment of obesity: therapeutic strategies. |
The R. W. Johnson Pharmaceutical Research Institute |
9873681 |
65 |
3-Pyridylethanolamines: potent and selective human beta 3 adrenergic receptor agonists. |
Merck Research Laboratories |
30605331 |
236 |
Design and in Vivo Characterization of A |
Medical College of Wisconsin |
9873496 |
80 |
3-Pyridyloxypropanolamine agonists of the beta 3 adrenergic receptor with improved pharmacokinetic properties. |
Merck Research Laboratories |
9871717 |
72 |
Discovery of L-755,507: a subnanomolar human beta 3 adrenergic receptor agonist. |
Merck Research Laboratories |
9871716 |
94 |
Potent, selective benzenesulfonamide agonists of the human beta 3 adrenergic receptor. |
Merck Research Laboratories |
31620230 |
283 |
3-Amino-chromanes and Tetrahydroquinolines as Selective 5-HT |
University of Minnesota Twin Cities |
26590100 |
42 |
Discovery of benzamides as potent human ?3 adrenergic receptor agonists. |
Merck And |
21170122 |
84 |
Comparative 3D QSAR study on ?(1)-, ?(2)-, and ?(3)-adrenoceptor agonists. |
National Institute of Pharmaceutical Education and Research |
21075638 |
105 |
Synthesis and pharmacological properties of novel hydrophilic 5-HT4 receptor antagonists. |
Drug Discovery Laboratory |
17560786 |
48 |
Synthesis and evaluation of potent and selective beta3 adrenergic receptor agonists containing heterobiaryl carboxylic acids. |
Glaxosmithkline |
10377236 |
15 |
2-Amino-4-benzyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridines: novel selective beta3-adrenoceptor agonists. |
University of Tennessee |
29751236 |
46 |
Synthesis and biological evaluation of ? |
Shenyang Pharmaceutical University |
30389290 |
146 |
Analogs of penfluridol as chemotherapeutic agents with reduced central nervous system activity. |
Texas Tech University Health Sciences Center |
29574204 |
54 |
Design and synthesis of aryloxypropanolamine as ? |
East China Normal University |
29767967 |
74 |
Structure-Guided Modification of Heterocyclic Antagonists of the P2Y |
National Institute of Diabetes and Digestive and Kidney Diseases |
28355078 |
34 |
Discovery of Novel Indazole Derivatives as Orally Available? |
Asahi Kasei Pharma |
27128689 |
28 |
Deazaflavin Inhibitors of Tyrosyl-DNA Phosphodiesterase 2 (TDP2) Specific for the Human Enzyme and Active against Cellular TDP2. |
National Institutes of Health |
2172674 |
5 |
Amplification of the rat M2 muscarinic receptor gene by the polymerase chain reaction: functional expression of the M2 muscarinic receptor. |
University of Arizona |