Page last updated: 2024-08-17

quinoxalines and exenatide

quinoxalines has been researched along with exenatide in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's3 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Flatt, PR; Green, BD; Irwin, N; Patterson, S1
Cheong, YH; Kaang, BK; Kim, MK; Son, MH1
Guan, S; Li, X; Liu, Y; Ma, X; Meng, J; Qu, D; Wang, L; Wang, N; Wang, X; Zhang, H; Zhou, S; Zhou, Y1

Other Studies

3 other study(ies) available for quinoxalines and exenatide

ArticleYear
Insulin-releasing and metabolic effects of small molecule GLP-1 receptor agonist 6,7-dichloro-2-methylsulfonyl-3-N-tert-butylaminoquinoxaline.
    European journal of pharmacology, 2010, Feb-25, Volume: 628, Issue:1-3

    Topics: Animals; Biomimetic Materials; Blood Glucose; Cell Line; Exenatide; Glucagon-Like Peptide 1; Glucagon-Like Peptide-1 Receptor; Hypoglycemic Agents; Insulin; Insulin Secretion; Liraglutide; Mice; Molecular Weight; Peptides; Quinoxalines; Receptors, Glucagon; Sulfones; Venoms

2010
Two small molecule agonists of glucagon-like peptide-1 receptor modulate the receptor activation response differently.
    Biochemical and biophysical research communications, 2012, Jan-06, Volume: 417, Issue:1

    Topics: Animals; Calcium; CHO Cells; Cricetinae; Exenatide; Glucagon-Like Peptide 1; Glucagon-Like Peptide-1 Receptor; Humans; Hypoglycemic Agents; Peptides; Pyrimidines; Quinoxalines; Receptors, Glucagon; Sulfones; Venoms

2012
An Orally Active Allosteric GLP-1 Receptor Agonist Is Neuroprotective in Cellular and Rodent Models of Stroke.
    PloS one, 2016, Volume: 11, Issue:2

    Topics: Administration, Oral; Allosteric Regulation; Animals; Apoptosis; Blood Glucose; Brain; Cell Survival; Cells, Cultured; Drug Evaluation, Preclinical; Exenatide; Glucagon-Like Peptide-1 Receptor; Infarction, Middle Cerebral Artery; Inhibitory Concentration 50; Insulin; Male; Mice, Inbred C57BL; Neurons; Neuroprotective Agents; Peptides; Primary Cell Culture; Quinoxalines; Reperfusion Injury; Sulfones; Venoms

2016