ALLOSTERISM;
ANIMAL CELL;
ARTICLE;
CONTROLLED STUDY;
DRUG BINDING SITE;
DRUG EFFICACY;
DRUG IDENTIFICATION;
DRUG MECHANISM;
DRUG POTENCY;
DRUG RESEARCH;
DRUG STRUCTURE;
DRUG SYNTHESIS;
FEMALE;
IC 50;
IN VITRO STUDY;
MOLECULAR MODEL;
NONHUMAN;
OOCYTE;
PRIORITY JOURNAL;
PROTEIN EXPRESSION;
QUANTITATIVE STRUCTURE ACTIVITY RELATION;
VOLTAGE CLAMP;
XENOPUS LAEVIS;
A receptor isoforms by a diazepam analogue provides evidence for a novel benzodiazepine binding site that prevents modulation by these drugs
A receptor isoforms by a diazepam analogue provides evidence for a novel benzodiazepine binding site that prevents modulation by these drugs. J Neurochem 106: 2353-2363.
In vivo determination of efficacy of pyrazoloquinolinones at the benzodiazepine receptor
Brown C, Martin I, Jones B, Oakley N, (1984). In vivo determination of efficacy of pyrazoloquinolinones at the benzodiazepine receptor. Eur J Pharmacol 103: 139-143.
Stoichiometry of a ligand-gated ion channel determined by fluorescence energy transfer
Farrar SJ, Whiting PJ, Bonnert TP, McKernan RM, (1999). Stoichiometry of a ligand-gated ion channel determined by fluorescence energy transfer. J Biol Chem 274: 10100-10104.
Structure-activity relationship studies at the benzodiazepine receptor (BZR): A comparison of the substituent effects of pyrazoloquinolinone analogs
Fryer R, Zhang P, Rios R, Gu ZQ, Basile AS, Skolnick P, (1993). Structure-activity relationship studies at the benzodiazepine receptor (BZR): a comparison of the substituent effects of pyrazoloquinolinone analogs. J Med Chem 36: 1669-1673.
A/BzR subtypes: Binding affinities of symmetrically substituted pyrazolo[4,3-c]quinolin-3-ones at recombinant alpha x beta 3 gamma 2 subtypes and quantitative structure-activity relationship studies via a comparative molecular field analysis
A/BzR subtypes: binding affinities of symmetrically substituted pyrazolo[4,3-c]quinolin-3-ones at recombinant alpha x beta 3 gamma 2 subtypes and quantitative structure-activity relationship studies via a comparative molecular field analysis. Drug Des Discov 16: 77-91.
Heterocyclen durch Anellierung an 4-Pyridinole, II Thieno[3,2-c]pyridin- 3-ole
Hoerlein G, Boerries S, Studeneer A, Salbeck G, (1979). Heterocyclen durch Anellierung an 4-Pyridinole, II Thieno[3,2-c]pyridin-3-ole. Liebigs Anna Chem 3: 387-391.
35S]TBPS binding to the chloride channel. Noncompetitive inhibition of classical benzodiazepines and competitive inhibition of the partial agonist, CGS 9895, by CGS 8216
35S]TBPS binding to the chloride channel. Noncompetitive inhibition of classical benzodiazepines and competitive inhibition of the partial agonist, CGS 9895, by CGS 8216. Neuropharmacology 26 (7A): 775-778.
Williams M, Bennett DA, Loo PS, Braunwalder AF, Amrick CL, Wilson DE, et al. (1989). CGS 20625, a novel pyrazolopyridine anxiolytic. J Pharmacol Exp Ther 248: 89-96.