Quinoline- and isoquinoline-sulfonamide analogs of aripiprazole : novel antipsychotic agents?

The introduction of typical antipsychotics over six decades ago signaled an important milestone in psychiatry. However, second-generation antipsychotics ameliorated the positive symptoms of schizophrenia but displayed limited effectiveness for the negative and cognitive symptoms. In addition, while the newer antipsychotics produced fewer motor side effects, the atypical antipsychotics still induced weight gain and endocrinopathies. In recent years, a third generation of antipsychotics was identified. Aripiprazole was the first approved drug acting as a D2 partial agonist/functionally selective ligand. This review presents the state of the development of novel antipsychotic dopaminergic and non-dopaminergic agents, supported by an overview of the compounds evaluated under advanced preclinical and clinical development (e.g., cariprazine and brexpiprazole). In line with the recent trends in the development of modern atypical antipsychotics, we present our strategic development of long-chain arylpiperazine-derived quinoline- and isoquinoline-sulfonamide displaying a multireceptor binding profile and partial D2 receptor agonism.

Medienart:

E-Artikel

Erscheinungsjahr:

2014

Erschienen:

2014

Enthalten in:

Zur Gesamtaufnahme - volume:6

Enthalten in:

Future medicinal chemistry - 6(2014), 1 vom: 08. Jan., Seite 57-75

Sprache:

Englisch

Beteiligte Personen:

Zajdel, Pawel [VerfasserIn]
Partyka, Anna [VerfasserIn]
Marciniec, Krzysztof [VerfasserIn]
Bojarski, Andrzej J [VerfasserIn]
Pawlowski, Maciej [VerfasserIn]
Wesolowska, Anna [VerfasserIn]

Links:

Volltext

Themen:

82VFR53I78
Antipsychotic Agents
Aripiprazole
E66400VT9R
Isoquinoline
Isoquinolines
JGX76Y85M6
Journal Article
Piperazines
Quinoline
Quinolines
Quinolones
Receptors, Dopamine
Receptors, Serotonin
Review
Sulfonamides

Anmerkungen:

Date Completed 06.08.2014

Date Revised 19.11.2015

published: Print

Citation Status MEDLINE

doi:

10.4155/fmc.13.158

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM233858415