26 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Novel C-aryl glucoside SGLT2 inhibitors as potential antidiabetic agents: 1,3,4-Thiadiazolylmethylphenyl glucoside congeners.

Green Cross
Novel thiophenyl C-aryl glucoside SGLT2 inhibitors as potential antidiabetic agents.

Green Cross
Design and synthesis of novel arylpiperazine derivatives containing the imidazole core targeting 5-HT(2A) receptor and 5-HT transporter.

Green Cross
Novel macrocyclic C-aryl glucoside SGLT2 inhibitors as potential antidiabetic agents.

Green Cross
Glucosides with cyclic diarylpolynoid as novel C-aryl glucoside SGLT2 inhibitors.

Green Cross
Exploration of SAR regarding glucose moiety in novel C-aryl glucoside inhibitors of SGLT2.

Green Cross
Pyrimidinylmethylphenyl glucoside as novel C-aryl glucoside SGLT2 inhibitors.

Green Cross
Arylpiperazine-containing pyrimidine 4-carboxamide derivatives targeting serotonin 5-HT(2A), 5-HT(2C), and the serotonin transporter as a potential antidepressant.

Green Cross
Discovery of 2-(4-((1H-1,2,4-triazol-1-yl)methyl)-5-(4-bromophenyl)-1-(2-chlorophenyl)-1H-pyrazol-3-yl)-5-tert-butyl-1,3,4-thiadiazole (GCC2680) as a potent, selective and orally efficacious cannabinoid-1 receptor antagonist.

Green Cross
Synthesis of pyridazine and thiazole analogs as SGLT2 inhibitors.

Green Cross
Further optimization of novel pyrrole 3-carboxamides for targeting serotonin 5-HT(2A), 5-HT(2C), and the serotonin transporter as a potential antidepressant.

Green Cross
Novel C-aryl glucoside SGLT2 inhibitors as potential antidiabetic agents: Pyridazinylmethylphenyl glucoside congeners.

Green Cross
Arylpiperazine-containing pyrrole 3-carboxamide derivatives targeting serotonin 5-HT(2A), 5-HT(2C), and the serotonin transporter as a potential antidepressant.

Green Cross
Synthesis and structure-activity relationship of 1,2,4-triazole-containing diarylpyrazolyl carboxamide as CB1 cannabinoid receptor-ligand.

Green Cross
Pentacycle derivatives as cannabinoid CB1 receptor ligands.

Green Cross
Substituted pyrimidines as cannabinoid CB1 receptor ligands.

Green Cross
Synthesis and structure-activity relationship of novel diarylpyrazole imide analogues as CB1 cannabinoid receptor ligands.

Green Cross
Oxadiazole-diarylpyrazole 4-carboxamides as cannabinoid CB1 receptor ligands.

Green Cross
Diarylimidazolyl oxadiazole and thiadiazole derivatives as cannabinoid CB1 receptor antagonists.

Green Cross
Biarylpyrazolyl oxadiazole as potent, selective, orally bioavailable cannabinoid-1 receptor antagonists for the treatment of obesity.

Green Cross
Substituted 3-arylsulfonyl-pyrazolo[1,5-A]pyrimidines, serotonin 5-HT6 receptor antagonists and methods for the production and use thereof

TBA
Inactivation of a novel neuropeptide Y/peptide YY receptor gene in primate species.

Yamanouchi Pharmaceutical
Heme oxygenase inhibition by 2-oxy-substituted 1-azolyl-4-phenylbutanes: effect of variation of the azole moiety. X-ray crystal structure of human heme oxygenase-1 in complex with 4-phenyl-1-(1H-1,2,4-triazol-1-yl)-2-butanone.

Queen'S University
A new potent and selective non-peptide gastrin antagonist and brain cholecystokinin receptor (CCK-B) ligand: L-365,260.

Merck Sharp & Dohme Research Laboratories
Affinity reagents that target a specific inactive form of protein kinases.

University of Washington