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Journal of Medicinal Chemistry|November 1, 1979
Substituted 3-amino-1,1-diaryl-2-propanols as potential antidepressant agentsJ A Clark, M S Clark, D V Gardner, et al.Journal of Medicinal Chemistry|December 1, 1978
4-(6-Methoxy-2-naphthyl)butan-2-one and related analogues, a novel structural class of antiinflammatory compoundsA C Goudie, L M Gaster, A W Lake, et al.Bioorganic & Medicinal Chemistry|February 1, 1996
Azabicyclic indole esters as potent 5-HT4 receptor antagonistsP A Wyman, L M Gaster, F D King, et al.Naunyn-Schmiedeberg'S Archives of Pharmacology|August 29, 2000
The effect of SB-236057-A, a selective 5-HT1B receptor inverse agonist, on in vivo extracellular 5-HT levels in the freely-moving guinea-pigC Roberts, P Hatcher, J J Hagan, et al.Diabetologia|August 23, 2008
Transcriptional profiling of myotubes from patients with type 2 diabetes: no evidence for a primary defect in oxidative phosphorylation genesC M Frederiksen, K Højlund, L Hansen, et al.Molecular Pharmacology|June 18, 2002
SB-431542 is a potent and specific inhibitor of transforming growth factor-beta superfamily type I activin receptor-like kinase (ALK) receptors ALK4, ALK5, and ALK7Gareth J Inman, Francisco J Nicolás, James F Callahan, et al.Journal of Medicinal Chemistry|December 10, 1993
Synthesis of novel modified dipeptide inhibitors of human collagenase: beta-mercapto carboxylic acid derivativesB Beszant, J Bird, L M Gaster, et al.European Journal of Pharmacology|August 12, 1999
SB-236057, a selective 5-HT1B receptor inverse agonist, blocks the 5-HT human terminal autoreceptorD N Middlemiss, M Göthert, E Schlicker, et al.British Journal of Pharmacology|October 17, 1998
SB-224289--a novel selective (human) 5-HT1B receptor antagonist with negative intrinsic activityJ V Selkirk, C Scott, M Ho, et al.Diabetologia|February 19, 2010
Glucosamine-induced endoplasmic reticulum stress affects GLUT4 expression via activating transcription factor 6 in rat and human skeletal muscle cellsG A Raciti, C Iadicicco, L Ulianich, et al.Pageof 4