1
|
SL651498: an anxioselective compound with functional selectivity for alpha2- and alpha3-containing gamma-aminobutyric acid(A) (GABA(A)) receptors.
|
J Pharmacol Exp Ther
|
2001
|
0.97
|
2
|
Structural elements of the gamma-aminobutyric acid type A receptor conferring subtype selectivity for benzodiazepine site ligands.
|
J Biol Chem
|
1999
|
0.83
|
3
|
Molecular structure and stereoelectronic properties of sarmazenil--a weak inverse agonist at the omega modulatory sites (benzodiazepine receptors): comparison with bretazenil and flumazenil.
|
Bioorg Med Chem
|
1998
|
0.78
|
4
|
SL 84.0418: a novel, potent and selective alpha-2 adrenoceptor antagonist: in vitro pharmacological profile.
|
J Pharmacol Exp Ther
|
1992
|
0.76
|
5
|
Synthesis and benzodiazepine receptor (omega receptor) affinities of 3-substituted derivatives of pyrrolo[2,3-c]pyridine-5-carboxylate, a novel class of omega1 selective ligands.
|
Bioorg Med Chem
|
1999
|
0.75
|
6
|
Enantioselective desymmetrization of meso bicyclic hydrazines: a novel approach to the asymmetric synthesis of polysubstituted amino cyclopentanic cores.
|
J Org Chem
|
2002
|
0.75
|