Mechanisms of action of atypical antipsychotic drugs: implications for novel therapeutic strategies for schizophrenia

AY Deutch, B Moghaddam, RB Innis, JH Krystal… - Schizophrenia …, 1991 - Elsevier
The mechanisms which contribute to the actions of atypical antipsychotic drugs, such as
clozapine and the putative atypical agents remoxipride and raclopride, are reviewed …

Metabotropic glutamate receptors for new treatments in schizophrenia

EJ Herman, M Bubser, PJ Conn, CK Jones - Novel Antischizophrenia …, 2012 - Springer
Metabotropic glutamate receptors (mGluRs) represent exciting targets for the development
of novel therapeutic agents for schizophrenia. Recent studies indicate that selective …

Dopamine autoreceptor agonists as potential antipsychotics. 3. 6-Propyl-4, 5, 5a, 6, 7, 8-hexahydrothiazolo [4, 5-f] quinolin-2-amine

BW Caprathe, JC Jaen, LD Wise… - Journal of medicinal …, 1991 - ACS Publications
A series of rigid tricyclic analogues of the dopamine (DA) agonist PD 118440 [4-(l, 2, 5, 6-
tetrahydro-l-propyl-3-pyridinyl)-2-thiazolamine] was synthesized and evaluated for …

Dopamine autoreceptor agonists as potential antipsychotics. 2.(Aminoalkoxy)-4H-1-benzopyran-4-ones

JC Jaen, LD Wise, TG Heffner… - Journal of medicinal …, 1991 - ACS Publications
The synthesis and pharmacological properties of a novel type of [(arylpiperazinyl) alkoxy]-
4H-l-benzopyran-4-ones with dopaminergic activity are described. The nature of the …

Aryl 1-But-3-ynyl-4-phenyl-1, 2, 3, 6-tetrahydropyridines as Potential Antipsychotic Agents: Synthesis and Structure− Activity Relationships

SA Glase, HC Akunne, TG Heffner… - Journal of medicinal …, 1996 - ACS Publications
A novel series of aryl 1-but-3-ynyl-4-phenyl-1, 2, 3, 6-tetrahydropyridines with dopaminergic
activity is described. The structure− activity relationships of this series were studied by …

Structure‐activity and conformational studies of a series of modified C‐terminal hexapeptide neurotensin analogues

DL HEYL, NM SEFLER, JX HE… - … journal of peptide …, 1994 - Wiley Online Library
Neurotensin (NT), is a linear tetradecapeptide (pGlu1‐Leu2‐Tyr3‐Glu4‐Asn5‐Lys6‐Pro7‐
Arg8‐Arg9‐Pro10‐Tyr11‐Ile12‐Leu13) that has been found in the central nervous system …

The discovery and structure-activity relationships of 1, 2, 3, 6-tetrahydro-4-phenyl-1-[(arylcyclohexenyl) alkyl] pyridines. Dopamine autoreceptor agonists and potential …

JL Wright, BW Caprathe, DM Downing… - Journal of medicinal …, 1994 - ACS Publications
A novel dopamine (DA) autoreceptoragonist, l, 2, 3, 6-tetrahydro-4-phenyl-l-[(3-phenyl-3-
cyclohexen-l-yl) methyl] pyridine (14), was identified. The structure-activity relationships …

Differential effects of the nonpeptide neurotensin antagonist, SR 48692, on the pharmacological effects of neurotensin agonists

TA Pugsley, HC Akunne, SZ Whetzel, S Demattos… - Peptides, 1995 - Elsevier
In in vitro studies, SR 48692, a nonpeptide neurotensin receptor antagonist, inhibited the
binding of [3H] or [125I] neurotensin to membrane preparations from 10-day-old mouse …

Synthesis of the enantiomers of reduced haloperidol

JC Jaen, BW Caprathe, S Priebe, LD Wise - Pharmaceutical research, 1991 - Springer
Reduced haloperidol (RHAL) is the best known metabolite of haloperidol (HAL), having
been identified in humans, rats, and guinea pigs. Since RHAL contains an asymmetric …

Lack of involvement of haloperidol-sensitive sigma binding sites in modulation of dopamine neuronal activity and induction of dystonias by antipsychotic drugs

LT Meltzer, CL Christoffersen, KA Serpa, TA Pugsley… - …, 1992 - Elsevier
The present studies evaluated previous suggestions that haloperidol-sensitive sigma
binding sites are involved in the modulation of dopamine (DA) neuronal activity and in the …