ANIMAL CELL;
ARTICLE;
BINDING AFFINITY;
CONTROLLED STUDY;
DRUG PROTEIN BINDING;
DRUG STRUCTURE;
DRUG SYNTHESIS;
HUMAN;
HUMAN CELL;
LIGAND BINDING;
NONHUMAN;
Dopamine/ Serotonin receptor ligands. Part VIII: The dopamine receptor antagonist le
Decker, M.; Schleifer, K. J.; Nieger, M.; Lehmann, J. Dopamine/ Serotonin receptor ligands. Part VIII: the dopamine receptor antagonist LE. Eur. J. Med. Chem. 2004, 39, 481-489.
7-Methyl-6,7,8,9,14,15-hexahydro-5H-benz[d]indolo[2,3-g]azecine: A new heterocyclic system and a new lead compound for dopamine receptor antagonists
Witt, T.; Hock, F. J.; Lehmann, J. 7-Methyl-6,7,8,9,14,15-hexahydro-5H- benz[d]indolo[2,3-g]azecine: a new heterocyclic system and a new lead compound for dopamine receptor antagonists. J. Med. Chem. 2000, 43, 2079-2081.
TransHexahydroindolo[4,3-ab]phenanthridines ("benzergolines"), the first structural class of potent and selective dopamine D1 receptor agonists lacking a catechol group
Seiler, M. P.; Hagenbach, A.; Wuthrich, H. J.; Markstein, R. transHexahydroindolo[4,3-ab]phenanthridines ("benzergolines"), the first structural class of potent and selective dopamine D1 receptor agonists lacking a catechol group. J. Med. Chem. 1991, 34, 303-307.
5 receptor agonist high affinity and constitutive activity profile conferred by carboxyl-terminal tail sequence
5 receptor agonist high affinity and constitutive activity profile conferred by carboxyl-terminal tail sequence. J. Biol. Chem. 2000, 275, 23446-23455.
Antiparkinsonian activity of CY 208-243, a partial D-1 dopamine receptor agonist, in MPTP-treated marmosets and patients with Parkinson's disease
Temlett, J. A.; Quinn, N. P.; Jenner, P. G.; Marsden, C. D.; Pourcher, E.; Bonnet, A. M.; Agid, Y.; Markstein, R.; Lataste, X. Antiparkinsonian activity of CY 208-243, a partial D-1 dopamine receptor agonist, in MPTP-treated marmosets and patients with Parkinson's disease. Mov. Disord. 1989, 4, 261-265.
Dopamine/ serotonin receptor ligands. 12(1): SAR studies on hexahydrodibenz[d,g]azecines lead to 4-chloro-7-methyl-5,6,7,8,9,14- hexahydrodibenz[d,g]azecin-3-ol, the first picomolar D5-selective dopamine-receptor antagonist
Mohr, P.; Decker, M.; Enzensperger, C.; Lehmann, J. Dopamine/ serotonin receptor ligands. 12(1): SAR studies on hexahydrodibenz[d,g]azecines lead to 4-chloro-7-methyl-5,6,7,8,9,14-hexahydrodibenz[d,g]azecin-3-ol, the first picomolar D5-selective dopamine-receptor antagonist. J. Med. Chem. 2006, 49, 2110-2116.
A chemogenomic analysis of the transmembrane binding cavity of human G-protein-coupled receptors
Surgand, J. S.; Rodrigo, J.; Kellenberger, E.; Rognan, D. A chemogenomic analysis of the transmembrane binding cavity of human G-protein-coupled receptors. Proteins 2006, 62, 509-538.
3,4-Bridgedindoles: Part 2. Synthesis of 6-keto-1,5-dihydro-4, 5diazepino[6,5,4-cd]indoles and 3,4-disubstituted indoles as 5-HT antagonists
Ananthanarayanan, C. V.; Rastogi, S. N.; Patnaik, G. K.; Anand, N. 3,4-Bridgedindoles: Part 2. Synthesis of 6-keto-1,5-dihydro-4,5diazepino[6,5,4- cd]indoles and 3,4-disubstituted indoles as 5-HT antagonists. Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 1977, 15,710-714.
Highly efficient catalysts for epoxidation mediated by iminium salts
Page, P. C. B.; Buckley, B. R.; Appleby, L. F.; Alsters, P. A. Highly efficient catalysts for epoxidation mediated by iminium salts. Synthesis 2005, 3405-3411.
Synthetic indole compounds. V. Syntheses of indoles with (2-aminoethyl)-, (2-aminopropyl)-, or alkanolamine side chains on the six-membered ring
Troxler, F.; Harnisch, A.; Bormann, G.; Seemann, F.; Szabo, L. Synthetic indole compounds. V. Syntheses of indoles with (2-aminoethyl)-, (2-aminopropyl)-, or alkanolamine side chains on the six-membered ring. Helv. Chim. Acta 1968, 51,1616-1628.