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] |
---|
Links: |
---|
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 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM233858415 | ||
003 | DE-627 | ||
005 | 20231224100014.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231224s2014 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.4155/fmc.13.158 |2 doi | |
028 | 5 | 2 | |a pubmed24n0779.xml |
035 | |a (DE-627)NLM233858415 | ||
035 | |a (NLM)24358948 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Zajdel, Pawel |e verfasserin |4 aut | |
245 | 1 | 0 | |a Quinoline- and isoquinoline-sulfonamide analogs of aripiprazole |b novel antipsychotic agents? |
264 | 1 | |c 2014 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 06.08.2014 | ||
500 | |a Date Revised 19.11.2015 | ||
500 | |a published: Print | ||
500 | |a Citation Status MEDLINE | ||
520 | |a 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 | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Review | |
650 | 7 | |a Antipsychotic Agents |2 NLM | |
650 | 7 | |a Isoquinolines |2 NLM | |
650 | 7 | |a Piperazines |2 NLM | |
650 | 7 | |a Quinolines |2 NLM | |
650 | 7 | |a Quinolones |2 NLM | |
650 | 7 | |a Receptors, Dopamine |2 NLM | |
650 | 7 | |a Receptors, Serotonin |2 NLM | |
650 | 7 | |a Sulfonamides |2 NLM | |
650 | 7 | |a Aripiprazole |2 NLM | |
650 | 7 | |a 82VFR53I78 |2 NLM | |
650 | 7 | |a quinoline |2 NLM | |
650 | 7 | |a E66400VT9R |2 NLM | |
650 | 7 | |a isoquinoline |2 NLM | |
650 | 7 | |a JGX76Y85M6 |2 NLM | |
700 | 1 | |a Partyka, Anna |e verfasserin |4 aut | |
700 | 1 | |a Marciniec, Krzysztof |e verfasserin |4 aut | |
700 | 1 | |a Bojarski, Andrzej J |e verfasserin |4 aut | |
700 | 1 | |a Pawlowski, Maciej |e verfasserin |4 aut | |
700 | 1 | |a Wesolowska, Anna |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Future medicinal chemistry |d 2009 |g 6(2014), 1 vom: 08. Jan., Seite 57-75 |w (DE-627)NLM194822109 |x 1756-8927 |7 nnns |
773 | 1 | 8 | |g volume:6 |g year:2014 |g number:1 |g day:08 |g month:01 |g pages:57-75 |
856 | 4 | 0 | |u http://dx.doi.org/10.4155/fmc.13.158 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 6 |j 2014 |e 1 |b 08 |c 01 |h 57-75 |