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Trudell, M.L., Lifer, S.L., Tan, Y.C., Martin, M.J., Deng, L., Skolnick, P. and Cook, J.M. (1990) Synthesis of substituted 7,12-dihydropyrido[3,2-b:5,4-b’]diindoles: Rigid planar benzodiazepine receptor ligands with inverse agonist/antagonist properties. Journal of Medicinal Chemistry, 33, 2412-2420. doi:10.1021/jm00171a015

has been cited by the following article:

• TITLE: 3-Arylisothiazoloquinols As Potent Ligands for the Benzodiazepine Site of GABAA Receptors

  AUTHORS: Jakob Nilsson, Elsebet Østergaard Nielsen, Tommy Liljefors, Mogens Nielsen, Olov Sterner

  KEYWORDS: Isothiazolo[5, 4-b]quinolin-4(9H)-ones; Isoxazolo[5, 4-b]quinolin-4(9H)-ones; Benzodiazepine binding site; GABAA Receptors; GABAA Receptor Subtypes; Pharmacophore Model

  JOURNAL NAME: Journal of Biomedical Science and Engineering, Vol.5 No.1, January 12, 2012

  ABSTRACT: 3-Arylisothiazolo[5,4-b]quinolin-4(9H)-ones and 3-arylisoxazolo[5,4-b]quinolin-4(9H)-ones were synthesized and assayed for affinity for the benzodiazepine binding site of the GABAA receptors. While the 3-arylisothiazoloquinolin-4-ones were found to be potent ligands, with affinities (expressed as the affinity Ki value) down to 1 nM, the 3-arylisoxazoloquinolin-4-ones are less potent. This is suggested to depend on sterical repulsive interaction of the 3-arylisoxazoloquinolin-4-ones with the receptor essential volume of the binding site, and a higher electron density at the nitrogen in the azole ring (N-2) as well as the carbonyl oxygen in the isothiazoloquinolin-4-ones enabling them to interact stronger with hydrogen bond donor sites at the binding site.