том 20 издание 4 страницы 1545-1556

Quinoline- and isoquinoline-sulfonamide derivatives of LCAP as potent CNS multi-receptor—5-HT1A/5-HT2A/5-HT7 and D2/D3/D4—agents: The synthesis and pharmacological evaluation

Тип публикацииJournal Article
Дата публикации2012-02-01
scimago Q2
wos Q1
БС1
SJR0.608
CiteScore6.7
Impact factor3
ISSN09680896, 14643391
Organic Chemistry
Drug Discovery
Biochemistry
Molecular Biology
Pharmaceutical Science
Clinical Biochemistry
Molecular Medicine
Краткое описание
Two series of arylpiperazinyl-alkyl quinoline-, isoquinoline-, naphthalene-sulfonamides with flexible (13-26) and semi-rigid (33-36) alkylene spacer were synthesized and evaluated for 5-HT(1A), 5-HT(2A), 5-HT(6), 5-HT(7) and selected compounds for D(2), D(3), D(4) receptors. The compounds with a mixed 5-HT and D receptors profile 16 (N-{4-[4-(3-chlorophenyl)-piperazin-1-yl]-butyl}-3-quinolinesulfonamide) and 36 (4-(4-{2-[4-(4-chloro-phenyl)-piperazin-1-yl]-ethyl}-piperidine-1-sulfonyl)-isoquinoline), displaying antagonistic activity at 5-HT(7), 5-HT(2A), D(2) postsynaptic sites, produced antidepressant-like effects in the forced swim test in mice and showed significant anxiolytic activity in the plus-maze test in rats. The lead compound 36, a multi-receptor 5-HT(2A)/5-HT(7)/D(2)/D(3)/D(4) agent, also displayed significant antipsychotic properties in the MK-801-induced hyperlocomotor activity in mice.
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ГОСТ |
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Zajdel P. et al. Quinoline- and isoquinoline-sulfonamide derivatives of LCAP as potent CNS multi-receptor—5-HT1A/5-HT2A/5-HT7 and D2/D3/D4—agents: The synthesis and pharmacological evaluation // Bioorganic and Medicinal Chemistry. 2012. Vol. 20. No. 4. pp. 1545-1556.
ГОСТ со всеми авторами (до 50) Скопировать
Zajdel P., Marciniec K., Maślankiewicz [] A., Satała G., Duszyńska B., Bojarski A. J., Partyka A., Jastrzębska-Więsek M., Wróbel D., Wesołowska A., Pawłowski M. Quinoline- and isoquinoline-sulfonamide derivatives of LCAP as potent CNS multi-receptor—5-HT1A/5-HT2A/5-HT7 and D2/D3/D4—agents: The synthesis and pharmacological evaluation // Bioorganic and Medicinal Chemistry. 2012. Vol. 20. No. 4. pp. 1545-1556.
RIS |
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TY - JOUR
DO - 10.1016/j.bmc.2011.12.039
UR - https://doi.org/10.1016/j.bmc.2011.12.039
TI - Quinoline- and isoquinoline-sulfonamide derivatives of LCAP as potent CNS multi-receptor—5-HT1A/5-HT2A/5-HT7 and D2/D3/D4—agents: The synthesis and pharmacological evaluation
T2 - Bioorganic and Medicinal Chemistry
AU - Zajdel, P.
AU - Marciniec, Krzysztof
AU - Maślankiewicz [], Andrzej
AU - Satała, Grzegorz
AU - Duszyńska, Beata
AU - Bojarski, Andrzej J
AU - Partyka, Anna
AU - Jastrzębska-Więsek, Magdalena
AU - Wróbel, Dagmara
AU - Wesołowska, Anna
AU - Pawłowski, M.
PY - 2012
DA - 2012/02/01
PB - Elsevier
SP - 1545-1556
IS - 4
VL - 20
PMID - 22277589
SN - 0968-0896
SN - 1464-3391
ER -
BibTex |
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@article{2012_Zajdel,
author = {P. Zajdel and Krzysztof Marciniec and Andrzej Maślankiewicz [] and Grzegorz Satała and Beata Duszyńska and Andrzej J Bojarski and Anna Partyka and Magdalena Jastrzębska-Więsek and Dagmara Wróbel and Anna Wesołowska and M. Pawłowski},
title = {Quinoline- and isoquinoline-sulfonamide derivatives of LCAP as potent CNS multi-receptor—5-HT1A/5-HT2A/5-HT7 and D2/D3/D4—agents: The synthesis and pharmacological evaluation},
journal = {Bioorganic and Medicinal Chemistry},
year = {2012},
volume = {20},
publisher = {Elsevier},
month = {feb},
url = {https://doi.org/10.1016/j.bmc.2011.12.039},
number = {4},
pages = {1545--1556},
doi = {10.1016/j.bmc.2011.12.039}
}
MLA
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Zajdel, P., et al. “Quinoline- and isoquinoline-sulfonamide derivatives of LCAP as potent CNS multi-receptor—5-HT1A/5-HT2A/5-HT7 and D2/D3/D4—agents: The synthesis and pharmacological evaluation.” Bioorganic and Medicinal Chemistry, vol. 20, no. 4, Feb. 2012, pp. 1545-1556. https://doi.org/10.1016/j.bmc.2011.12.039.