The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
28103022 |
36 |
Discovery of a Novel Series of Orally Bioavailable and CNS Penetrant Glucagon-like Peptide-1 Receptor (GLP-1R) Noncompetitive Antagonists Based on a 1,3-Disubstituted-7-aryl-5,5-bis(trifluoromethyl)-5,8-dihydropyrimido[4,5-d]pyrimidine-2,4(1H,3H)-dione Core. |
Vanderbilt University |
27161876 |
41 |
Design, synthesis, structure-activity relationships, and docking studies of pyrazole-containing derivatives as a novel series of potent glucagon receptor antagonists. |
Shanghai Institute Of Materia Medica |
26303893 |
93 |
A novel series of indazole-/indole-based glucagon receptor antagonists. |
Merck Research Laboratories |
26271588 |
19 |
Recent progress in the development of small-molecule glucagon receptor antagonists. |
Pfizer |
25127101 |
26 |
Discovery of furan-2-carbohydrazides as orally active glucagon receptor antagonists. |
Dainippon Sumitomo Pharma |
24881566 |
140 |
Identification of diarylsulfonamides as agonists of the free fatty acid receptor 4 (FFA4/GPR120). |
Glaxosmithkline |
24527772 |
262 |
The discovery of N-((2H-tetrazol-5-yl)methyl)-4-((R)-1-((5r,8R)-8-(tert-butyl)-3-(3,5-dichlorophenyl)-2-oxo-1,4-diazaspiro[4.5]dec-3-en-1-yl)-4,4-dimethylpentyl)benzamide (SCH 900822): a potent and selective glucagon receptor antagonist. |
Merck Research Laboratories |
23562063 |
32 |
The design and synthesis of a potent glucagon receptor antagonist with favorable physicochemical and pharmacokinetic properties as a candidate for the treatment of type 2 diabetes mellitus. |
Pfizer |
22650618 |
4 |
Rediocide A, an Insecticide, induces G-protein-coupled receptor desensitization via activation of conventional protein kinase C. |
Chinese Academy Of Sciences |
22708876 |
106 |
Discovery of a novel glucagon receptor antagonist N-[(4-{(1S)-1-[3-(3, 5-dichlorophenyl)-5-(6-methoxynaphthalen-2-yl)-1H-pyrazol-1-yl]ethyl}phenyl)carbonyl]-ß-alanine (MK-0893) for the treatment of type II diabetes. |
Merck Research Laboratories |
19597507 |
62 |
A new glucagon and GLP-1 co-agonist eliminates obesity in rodents. |
Indiana University |
19702274 |
31 |
Eleven amino acid glucagon-like peptide-1 receptor agonists with antidiabetic activity. |
Bristol-Myers Squibb |
22119466 |
38 |
A novel series of glucagon receptor antagonists with reduced molecular weight and lipophilicity. |
Pfizer |
22030028 |
55 |
Discovery of N-aryl-2-acylindole human glucagon receptor antagonists. |
Merck Research Laboratories |
22001094 |
78 |
Discovery of cyclic guanidines as potent, orally active, human glucagon receptor antagonists. |
Merck Research Laboratories |
21147532 |
82 |
Discovery of novel, potent, selective, and orally active human glucagon receptor antagonists containing a pyrazole core. |
Merck Research Laboratories |
20813948 |
63 |
Spiroindolones, a potent compound class for the treatment of malaria. |
Swiss Tropical And Public Health Institute |
18707090 |
68 |
Novel glucagon receptor antagonists with improved selectivity over the glucose-dependent insulinotropic polypeptide receptor. |
Novo Nordisk |
18539028 |
81 |
Discovery of potent, orally active benzimidazole glucagon receptor antagonists. |
Merck Research Laboratories |
15387654 |
3 |
BI-32169, a bicyclic 19-peptide with strong glucagon receptor antagonist activity from Streptomyces sp. |
Boehringer Ingelheim Pharma Gmbh And |
17201415 |
47 |
New beta-alanine derivatives are orally available glucagon receptor antagonists. |
Novo Nordisk |
17126016 |
69 |
Design and synthesis of conformationally constrained tri-substituted ureas as potent antagonists of the human glucagon receptor. |
Merck Research Laboratories |
16500101 |
3 |
Novel substituted naphthalen-1-yl-methanone derivatives as anti-hyperglycemic agents. |
Central Drug Research Institute |
16250656 |
4 |
Fast small molecule similarity searching with multiple alignment profiles of molecules represented in one-dimension. |
Pharmacopeia |
16102966 |
55 |
Discovery of novel, potent, and orally active spiro-urea human glucagon receptor antagonists. |
Merck Research Laboratories |
15713396 |
22 |
Discovery and investigation of a novel class of thiophene-derived antagonists of the human glucagon receptor. |
Merck Research Laboratories |
15080976 |
43 |
Biaryl amide glucagon receptor antagonists. |
Abbott Laboratories |
12477359 |
78 |
Optimization of alkylidene hydrazide based human glucagon receptor antagonists. Discovery of the highly potent and orally available 3-cyano-4-hydroxybenzoic acid [1-(2,3,5,6-tetramethylbenzyl)-1H-indol-4-ylmethylene]hydrazide. |
Novo Nordisk |
12419375 |
21 |
Integration of optimized substituent patterns to produce highly potent 4-aryl-pyridine glucagon receptor antagonists. |
Bayer Research Center |
11965376 |
19 |
Optimization of the 4-aryl group of 4-aryl-pyridine glucagon antagonists: development of an efficient, alternative synthesis. |
Bayer Research Center |
11844695 |
35 |
Human glucagon receptor antagonists based on alkylidene hydrazides. |
Pfizer |
11814820 |
28 |
Discovery of 5-hydroxyalkyl-4-phenylpyridines as a new class of glucagon receptor antagonists. |
Bayer Research Center |
11549467 |
85 |
Substituted imidazoles as glucagon receptor antagonists. |
Merck Research Laboratories |
11543683 |
42 |
Identification of alkylidene hydrazides as glucagon receptor antagonists. |
Pfizer |
10201821 |
166 |
Potent, orally absorbed glucagon receptor antagonists. |
Merck Research Laboratories |
9857085 |
33 |
Discovery and structure-activity relationship of the first non-peptide competitive human glucagon receptor antagonists. |
Novo Nordisk |
28376304 |
26 |
Origins of PDZ Binding Specificity. A Computational and Experimental Study Using NHERF1 and the Parathyroid Hormone Receptor. |
The University Of Queensland |
21108268 |
67 |
Biological evaluation and structural determinants of p38α mitogen-activated-protein kinase and c-Jun-N-terminal kinase 3 inhibition by flavonoids. |
Eberhard Karls University Of Tuebingen |