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http://hub.abes.fr/acs/periodical/jmcmar/1982/volume_25/issue_8/101021jm00350a008/authorship/9
http://hub.abes.fr/acs/periodical/jmcmar/1988/volume_31/issue_1/101021jm00396a014/authorship/8
http://hub.abes.fr/acs/periodical/jmcmar/1995/volume_38/issue_8/101021jm00008a010/authorship/5
http://hub.abes.fr/acs/periodical/jmcmar/1992/volume_35/issue_22/101021jm00100a002/authorship/10
http://hub.abes.fr/acs/periodical/jmcmar/1981/volume_24/issue_8/101021jm00140a002/authorship/5
http://hub.abes.fr/acs/periodical/jmcmar/1984/volume_27/issue_8/101021jm00374a012/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/1987/volume_30/issue_11/101021jm00394a029/authorship/8
http://hub.abes.fr/acs/periodical/jmcmar/1987/volume_30/issue_12/101021jm00395a002/authorship/5
http://hub.abes.fr/acs/periodical/jmcmar/1993/volume_36/issue_21/101021jm00073a021/authorship/4
http://hub.abes.fr/acs/periodical/jmcmar/1979/volume_22/issue_12/101021jm00198a008/authorship/5
http://hub.abes.fr/acs/periodical/jmcmar/1993/volume_36/issue_22/101021jm00074a022/authorship/5
http://hub.abes.fr/acs/periodical/jmcmar/1994/volume_37/issue_17/101021jm00043a013/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/1987/volume_30/issue_4/101021jm00387a004/authorship/6
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http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_26/101021jm010145w/authorship/12
http://hub.abes.fr/acs/periodical/jmcmar/1981/volume_24/issue_4/101021jm00136a012/authorship/9
http://hub.abes.fr/acs/periodical/jmcmar/1989/volume_32/issue_10/101021jm00130a008/authorship/8
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http://hub.abes.fr/acs/periodical/jmcmar/1985/volume_28/issue_8/101021jm00146a012/authorship/8
http://hub.abes.fr/acs/periodical/jmcmar/1981/volume_24/issue_12/101021jm00144a021/authorship/9
http://hub.abes.fr/acs/periodical/jmcmar/1985/volume_28/issue_2/101021jm00380a012/authorship/10
http://hub.abes.fr/acs/periodical/jmcmar/1994/volume_37/issue_20/101021jm00046a010/authorship/8
http://hub.abes.fr/acs/periodical/jmcmar/1995/volume_38/issue_12/101021jm00012a021/authorship/9
http://hub.abes.fr/springer/periodical/702/1994/volume_98/issue_1/B8CBF069E2C75600E053120B220A3371/authorship/6
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http://hub.abes.fr/springer/periodical/702/1991/volume_85/issue_1/B8CBF069DFD25600E053120B220A3371/authorship/3
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http://hub.abes.fr/acs/periodical/jmcmar/1987/volume_30/issue_10/101021jm00393a025/authorship/8
http://hub.abes.fr/acs/periodical/jmcmar/1990/volume_33/issue_3/101021jm00165a020/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/1993/volume_36/issue_15/101021jm00067a002/authorship/9
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3-Phenylpiperidines. Central dopamine-autoreceptor stimulating activity
Pre- and postsynaptic dopaminergic activities of indolizidine and quinolizidine derivatives of 3-(3-hydroxyphenyl)-N-(n-propyl)piperidine (3-PPP). Further developments of a dopamine receptor model
(S)- and (R)-8-(di-n-propylamino)-6,7,8,9-tetrahydro-3H-benz[e]indole-1-carbaldehyde: a new class of orally active 5-HT1A-receptor agonists
Resolved 6,7,8,9-tetrahydro-N,N-dimethyl-3H-benz[e]indol-8-amine: central dopamine and serotonin receptor stimulating properties
Pivaloyl esters of N,N-dialkylated dopamine congeners. Central dopamine-receptor stimulating activity
Substituted 3-phenylpiperidines: new centrally acting dopamine autoreceptor antagonists
Resolved cis- and trans-2-amino-5-methoxy-1-methyltetralins: central dopamine receptor agonists and antagonists
6,7,8,9-Tetrahydro-N,N-di-n-propyl-3H-benzindol-8-amines. Derivatives as Potent and Orally Active Serotonin 5-HT1A Receptor Agonists
substituted (S)-Phenylpiperidines and Rigid Congeners as Preferential Dopamine Autoreceptor Antagonists: Synthesis and Structure-Activity Relationships
(+)-cis-8-Hydroxy-1-methyl-2-(di-n-propylamino)tetralin: a potent and highly stereoselective 5-hydroxytryptamine receptor agonist
C3-Methylated 5-hydroxy-2-(dipropylamino)tetralins: conformational and steric parameters of importance for central dopamine receptor activation
Synthesis and Evaluation of Pharmacological and Pharmacokinetic Properties of Monopropyl Analogs of 5-, 7-, and 8-[[(Trifluoromethyl)sulfonyl]oxy]-2-aminotetralins: Central Dopamine and Serotonin Receptor Activity
8-Hydroxy-2-(alkylamino)tetralins and related compounds as central 5-hydroxytryptamine receptor agonists
Dopamine receptors, controlling dopamine levels in rat adrenal glands — comparison with central dopaminergic autoreceptors
Dopamine D3 Receptor Antagonists. 1. Synthesis and Structure−ActivityRelationships of 5,6-Dimethoxy-N-alkyl- and N-Alkylaryl-Substituted2-Aminoindans
I. c. v. dopamine fails to alter adrenomedullary function in rats
Differential effects of dopamine D2 and D3 receptor antagonists in regard to dopamine release, in vivo receptor displacement and behaviour
Evidence for an increased catecholamine synthesis in rat adrenal glands following stimulation of peripheral dopamine receptors
The dopamine D3-receptor: A postsynaptic receptor inhibitory on rat locomotor activity
Effects of the partial dopamine receptor agonists SDZ 208-911, SDZ 208-912 and terguride on central monoamine receptors
Monophenolic octahydrobenzo[f]quinolines: central dopamine- and serotonin-receptor stimulating activity
6-Hydroxy-3-propyl-2,3,4,5-tetrahydro-1H-3-benzazepine and analogs: new centrally acting 5-HT1a receptor agonists
C1- and C3-methyl-substituted derivatives of 7-hydroxy-2-(di-n-propylamino)tetralin: activities at central dopamine receptors
8-Hydroxy-2-(dipropylamino)tetralin, a new centrally acting 5-hydroxytryptamine receptor agonist
Resolved monophenolic 2-aminotetralins and 1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolines: structural and stereochemical considerations for centrally acting pre- and postsynaptic dopamine-receptor agonists
N-Substituted 1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolines and 3-phenylpiperidines: effects on central dopamine and .sigma. receptors
N,N-Dialkylated monophenolic trans-2-phenylcyclopropylamines: novel central 5-hydroxytryptamine-receptor agonists
C1-Methylated 5-hydroxy-2-(dipropylamino)tetralins: central dopamine-receptor stimulating activity
Novel dopamine receptor agonists and antagonists with preferential action on autoreceptors
Structure-Activity Relationships in the 8-Amino-6,7,8,9-tetrahydro-3H-benz[e]indole Ring System. Part 1: Effects of Substituents in the Aromatic System on Serotonin and Dopamine Receptor Subtypes
N-Alkylated 2-aminotetralins: central dopamine-receptor stimulating activity
Monophenolic 2-(dipropylamino)indans and related compounds: central dopamine-receptor stimulating activity
Synthesis and biological activity of cis-(3aR)-(-)-2,3,3a,4,5,9b-hexahydro-3-propyl-1H-benz[e]indole-9-carboxamide: A potent and selective 5-HT1A receptor agonist with good oral availability
Synergistic interactions between the NMDA antagonist dizocilpine and the preferential dopamine autoreceptor antagonists (+)-AJ 76 and (+)-UH 232 with regard to locomotor stimulation in monoamine-depleted mice
On the roles of dopamine D-1 vs. D-2 receptors for the hyperactivity response elicited by MK-801
Synergistic interactions between muscarinic antagonists, adrenergic agonists and NMDA antagonists with respect to locomotor stimulatory effects in monoamine-depleted mice
Locomotor inhibition by the D3 ligand R-(+)-7-OH-DPAT is independent of changes in dopamine release
Differential locomotor interactions between dopamine D1/D2 receptor agonists and the NMDA antagonist dizocilpine in monoamine-depleted mice
Effects of MPP+ on catecholamine levels in adrenal glands and heart of rats
Orally active central dopamine and serotonin receptor ligands: 5-, 6-, 7-, and 8-[[(trifluoromethyl)sulfonyl]oxy]-2-(di-n-propylamino)tetralins and the formation of active metabolites in vivo
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