The following articles (labelled with PubMed ID or TBD) are for your review
||Synthesis and in silico studies of novel sulfonamides having oxadiazole ring: As ß-glucuronidase inhibitors.
||Universiti Teknologi MARA (UiTM)
||Agonist-induced up-regulation of alpha4beta2 nicotinic acetylcholine receptors in M10 cells: pharmacological and spatial definition.
||University of Bath
||Mediation by 5-hydroxytryptamine2B receptors of endothelium-dependent relaxation in rat jugular vein.
||SmithKline Beecham Pharmaceuticals
||Molecular pharmacology of somatostatin receptors.
||Sandoz Pharma Ltd.
||Structural requirements for the occupancy of rat brain PACAP receptors and adenylate cyclase activation.
||Université Libre de Bruxelles
||PET examination of [11C]NNC 687 and [11C]NNC 756 as new radioligands for the D1-dopamine receptor.
||Design, synthesis, and X-ray crystal structures of 2,4-diaminofuro[2,3-d]pyrimidines as multireceptor tyrosine kinase and dihydrofolate reductase inhibitors.
||Think twice: understanding the high potency of bis(phenyl)methane inhibitors of thrombin.
||Crystal structure of human carboxylesterase 1 complexed with the Alzheimer's drug tacrine: from binding promiscuity to selective inhibition.
||University of North Carolina at Chapel Hill
||Identification of 4-aminopyrazolylpyrimidines as potent inhibitors of Trk kinases.
||Discovery of pyrrolopyridine-pyridone based inhibitors of Met kinase: synthesis, X-ray crystallographic analysis, and biological activities.
||Bristol-Myers Squibb Company
||Development of potent, orally active 1-substituted-3,4-dihydro-2-quinolone glycogen phosphorylase inhibitors.
||A series of potent and selective, triazolylphenyl-based histone deacetylases inhibitors with activity against pancreatic cancer cells and Plasmodium falciparum.
||University of Illinois at Chicago
||Dual aromatase-steroid sulfatase inhibitors.
||University of Bath
||2-Pyridinone derivatives: a new class of nonnucleoside, HIV-1-specific reverse transcriptase inhibitors.
||Merck Sharp and Dohme Research Laboratories
||Human Plasma Lecithin-Cholesterol Acyltransferase