Structural analogues of ZAPA as GABA~A agonists

Autor: Allan, R. D., Dickenson, H. W., Johnston, G. A. R., Kazlauskas, R., Mewett, K. N.

Publikováno v: Neurochemistry International; 1997, Vol. 30 Issue: 6 p583-591, 9p

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ChemInform Abstract: A New Synthesis, Resolution and in vitro Activities of (R)- and (S)-β-Phenyl-GABA.

Autor: ALLAN, R. D., BATES, M. C., DREW, C. A., DUKE, R. K., HAMBLEY, T. W., JOHNSTON, G. A. R., MEWETT, K. N., SPENCE, I.

Publikováno v: ChemInform; Jul1990, Vol. 21 Issue 31, pno-no, 1p

(+)- and (-)-cis-2-aminomethylcyclopropanecarboxylic acids show opposite pharmacology at recombinant rho(1) and rho(2) GABA(C) receptors.

Autor: Duke RK; Adrien Albert Laboratory of Medicinal Chemistry, Department of Pharmacology, University of Sydney, New South Wales, Australia. rujeek@pharmacol.usyd.edu.au, Chebib M, Balcar VJ, Allan RD, Mewett KN, Johnston GA

Publikováno v: Journal of neurochemistry [J Neurochem] 2000 Dec; Vol. 75 (6), pp. 2602-10.

R-(-)-beta-phenyl-GABA is a full agonist at GABAB receptors in brain slices but a partial agonist in the ileum.

Autor: Ong J; Department of Anaesthesia and Intensive Care, University of Adelaide, South Australia., Kerr DI, Doolette DJ, Duke RK, Mewett KN, Allen RD, Johnston GA

Publikováno v: European journal of pharmacology [Eur J Pharmacol] 1993 Mar 16; Vol. 233 (1), pp. 169-72.