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Results: 1-10 |
Results: 10
THE CHEMICAL-STRUCTURE OF U99194A
Authors: HAADSMASVENSSON SR SMITH MW SVENSSON K WATERS N CARLSSON A
Citation: Sr. Haadsmasvensson et al., THE CHEMICAL-STRUCTURE OF U99194A, Journal of neural transmission, 99(1-3), 1995, pp. 1-1
C-9 AND N-SUBSTITUTED ANALOGS OF -HEXAHYDRO-3-PROPYL-1H-BENZ[E]INDOLE-9-CARBOXAMIDE - 5-HT1A RECEPTOR AGONISTS WITH VARIOUS DEGREES OF METABOLIC STABILITY
Authors: HAADSMASVENSSON SR SVENSSON K DUNCAN N SMITH MW LIN CH
Citation: Sr. Haadsmasvensson et al., C-9 AND N-SUBSTITUTED ANALOGS OF -HEXAHYDRO-3-PROPYL-1H-BENZ[E]INDOLE-9-CARBOXAMIDE - 5-HT1A RECEPTOR AGONISTS WITH VARIOUS DEGREES OF METABOLIC STABILITY, Journal of medicinal chemistry, 38(4), 1995, pp. 725-734
STRUCTURE-ACTIVITY-RELATIONSHIPS IN THE 8-AMINO-6,7,8,9-TETRAHYDRO-3H-BENZ[E]INDOLE RING-SYSTEM .2. EFFECT OF 8-AMINO NITROGEN SUBSTITUTIONON SEROTONIN RECEPTOR-BINDING AND PHARMACOLOGY
Authors: ENNIS MD STJERNLOF P HOFFMAN RL GHAZAL NB SMITH MW SVENSSON K WIKSTROM H HAADSMASVENSSON SR LIN CH
Citation: Md. Ennis et al., STRUCTURE-ACTIVITY-RELATIONSHIPS IN THE 8-AMINO-6,7,8,9-TETRAHYDRO-3H-BENZ[E]INDOLE RING-SYSTEM .2. EFFECT OF 8-AMINO NITROGEN SUBSTITUTIONON SEROTONIN RECEPTOR-BINDING AND PHARMACOLOGY, Journal of medicinal chemistry, 38(12), 1995, pp. 2217-2230
SYNTHESIS AND BIOLOGICAL-ACTIVITY OF C-5 MODIFIED DERIVATIVES OF (-AJ76 AND (+)-UH232 - INCREASED DOPAMINE D3 RECEPTOR PREFERENCE AND IMPROVED PHARMACOKINETIC PROPERTIES())
Authors: HAADSMASVENSSON SR SMITH MW LIN CH DUNCAN JN
Citation: Sr. Haadsmasvensson et al., SYNTHESIS AND BIOLOGICAL-ACTIVITY OF C-5 MODIFIED DERIVATIVES OF (-AJ76 AND (+)-UH232 - INCREASED DOPAMINE D3 RECEPTOR PREFERENCE AND IMPROVED PHARMACOKINETIC PROPERTIES()), Bioorganic & medicinal chemistry letters, 4(5), 1994, pp. 689-694
SYNTHESIS OF (R) AND TETRAHYDRO-N,N-(DIPROPYL)-3H-BENZ[E]INDOL-8-AMINES - POTENT AND ORALLY-ACTIVE 5-HT1A RECEPTOR AGONISTS
Authors: LIN CH ENNIS MD HOFFMAN RL PHILLIPS G HAADSMASVENSSON SR GHAZAL NB CHIDESTER CG
Citation: Ch. Lin et al., SYNTHESIS OF (R) AND TETRAHYDRO-N,N-(DIPROPYL)-3H-BENZ[E]INDOL-8-AMINES - POTENT AND ORALLY-ACTIVE 5-HT1A RECEPTOR AGONISTS, Journal of heterocyclic chemistry, 31(1), 1994, pp. 129-139
THE DOPAMINE D3-RECEPTOR - A POSTSYNAPTIC RECEPTOR INHIBITORY ON RAT LOCOMOTOR-ACTIVITY
Authors: WATERS N SVENSSON K HAADSMASVENSSON SR SMITH MW CARLSSON A
Citation: N. Waters et al., THE DOPAMINE D3-RECEPTOR - A POSTSYNAPTIC RECEPTOR INHIBITORY ON RAT LOCOMOTOR-ACTIVITY, Journal of neural transmission, 94(1), 1993, pp. 11-19
CENTRALLY ACTING SEROTONERGIC AND DOPAMINERGIC AGENTS .1. SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF 2,3,3A,4,5,9B-HEXAHYDRO-1H-BENZ[E]INDOLE DERIVATIVES
Authors: LIN CH HAADSMASVENSSON SR LAHTI RA MCCALL RB PIERCEY MF SCHREUR PJKD VONVOIGTLANDER PF SMITH MW CHIDESTER CG
Citation: Ch. Lin et al., CENTRALLY ACTING SEROTONERGIC AND DOPAMINERGIC AGENTS .1. SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF 2,3,3A,4,5,9B-HEXAHYDRO-1H-BENZ[E]INDOLE DERIVATIVES, Journal of medicinal chemistry, 36(8), 1993, pp. 1053-1068
CENTRALLY ACTING SEROTONERGIC AND DOPAMINERGIC AGENTS .2. SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF 2,3,3A,4,9,9A-HEXAHYDRO-1H-BENZ[F]INDOLE DERIVATIVES
Authors: LIN CH HAADSMASVENSSON SR PHILLIPS G LAHTI RA MCCALL RB PIERCEY MF SCHREUR PJKD VONVOIGTLANDER PF SMITH MW CHIDESTER CG
Citation: Ch. Lin et al., CENTRALLY ACTING SEROTONERGIC AND DOPAMINERGIC AGENTS .2. SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF 2,3,3A,4,9,9A-HEXAHYDRO-1H-BENZ[F]INDOLE DERIVATIVES, Journal of medicinal chemistry, 36(8), 1993, pp. 1069-1083
SYNTHESIS AND BIOLOGICAL-ACTIVITY OF -HEXAHYDRO-3-PROPYL-1H-BENZ[E]INDOLE-9-CARBOXAMIDE - A POTENT AND SELECTIVE 5-HT(1A) RECEPTOR AGONIST WITH GOOD ORAL AVAILABILITY
Authors: LIN CH HAADSMASVENSSON SR PHILLIPS G MCCALL RB PIERCEY MF SMITH MW SVENSSON K CARLSSON A CHIDESTER CG VONVOIGTLANDER PF
Citation: Ch. Lin et al., SYNTHESIS AND BIOLOGICAL-ACTIVITY OF -HEXAHYDRO-3-PROPYL-1H-BENZ[E]INDOLE-9-CARBOXAMIDE - A POTENT AND SELECTIVE 5-HT(1A) RECEPTOR AGONIST WITH GOOD ORAL AVAILABILITY, Journal of medicinal chemistry, 36(15), 1993, pp. 2208-2218
COMPARISON OF 5-HT(1A) AND DOPAMINE-D(2) PHARMACOPHORES - X-RAY STRUCTURES AND AFFINITIES OF CONFORMATIONALLY CONSTRAINED LIGANDS
Authors: CHIDESTER CG LIN CH LAHTI RA HAADSMASVENSSON SR SMITH MW
Citation: Cg. Chidester et al., COMPARISON OF 5-HT(1A) AND DOPAMINE-D(2) PHARMACOPHORES - X-RAY STRUCTURES AND AFFINITIES OF CONFORMATIONALLY CONSTRAINED LIGANDS, Journal of medicinal chemistry, 36(10), 1993, pp. 1301-1315
Risultati: 1-10 |