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Recent advances in dopamine D-2 receptor ligands in the treatment of neuropsychiatric disorders

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00179906%3A_____%2F23%3A10452379" target="_blank" >RIV/00179906:_____/23:10452379 - isvavai.cz</a>

  • Alternative codes found

    RIV/00023752:_____/23:43920956 RIV/62690094:18470/23:50019612

  • Result on the web

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=QmLfeXSni1" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=QmLfeXSni1</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/med.21923" target="_blank" >10.1002/med.21923</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Recent advances in dopamine D-2 receptor ligands in the treatment of neuropsychiatric disorders

  • Original language description

    Dopamine is a biologically active amine synthesized in the central and peripheral nervous system. This biogenic monoamine acts by activating five types of dopamine receptors (D(1-5)Rs), which belong to the G protein-coupled receptor family. Antagonists and partial agonists of D(2)Rs are used to treat schizophrenia, Parkinson&apos;s disease, depression, and anxiety. The typical pharmacophore with high D2R affinity comprises four main areas, namely aromatic moiety, cyclic amine, central linker and aromatic/heteroaromatic lipophilic fragment. From the literature reviewed herein, we can conclude that 4-(2,3-dichlorophenyl), 4-(2-methoxyphenyl)-, 4-(benzo[b]thiophen-4-yl)-1-substituted piperazine, and 4-(6-fluorobenzo[d]isoxazol-3-yl)piperidine moieties are critical for high D2R affinity. Four to six atoms chains are optimal for D2R affinity with 4-butoxyl as the most pronounced one. The bicyclic aromatic/heteroaromatic systems are most frequently occurring as lipophilic appendages to retain high D2R affinity. In this review, we provide a thorough overview of the therapeutic potential of D2R modulators in the treatment of the aforementioned disorders. In addition, this review summarizes current knowledge about these diseases, with a focus on the dopaminergic pathway underlying these pathologies. Major attention is paid to the structure, function, and pharmacology of novel D2R ligands, which have been developed in the last decade (2010-2021), and belong to the 1,4-disubstituted aromatic cyclic amine group. Due to the abundance of data, allosteric D2R ligands and D2R modulators from patents are not discussed in this review.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30104 - Pharmacology and pharmacy

Result continuities

  • Project

    <a href="/en/project/GA19-11332S" target="_blank" >GA19-11332S: Specific serotonin-dopamin modulators and their potential in the model of induced psychosis</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2023

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Medicinal Research Reviews

  • ISSN

    0198-6325

  • e-ISSN

    1098-1128

  • Volume of the periodical

    43

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    157

  • Pages from-to

    55-211

  • UT code for WoS article

    000854625800001

  • EID of the result in the Scopus database

    2-s2.0-85138196234