Antinociceptive Profile of 2,3,6-Trisubstituted Piperidine Alkaloids : 3-O-Acetyl-spectaline and Semi-synthetic Derivatives of (-)-Spectaline
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概要
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In early studies, we have reported the antinociceptive profile of (-)-spectaline, a piperidine alkaloid from Cassia spectabilis. The present study describes the synthesis, the antinociceptive and anti-inflammatory activities of a series of 2,3,6-trialkyl-piperidine alkaloids: the natural (-)-3-O-acetyl-spectaline (LASSBio-755) and ten semi-synthetic spectaline derivatives. Structure-activity relationship (SARs) studies were performed. The structures of all synthesized derivatives were confirmed by means of nuclear magnetic resonance. Compounds were evaluated for their analgesic (acetic acid-induced mouse abdominal constrictions, hot-plate test, formalin-induced pain test) and some of them for the anti-inflammatory activities (carrageenan-induced rat paw edema test). The pharmacological results showed that several of the new compounds given orally at a dose of 100μmol/kg significantly inhibited the acetic acid-induced abdominal constrictions, but they were less active than (-)-spectaline. LASSBio-755 and LASSBio-776 were the most actives with 37% and 31.7% of inhibition. In the formalin-induced pain only LASSBio-776 was able to inhibit by 34.4% the paw licking response of the inflammatory phase, (-)-spectaline and LASSBio-755 did show any activity. In the carrageenan-induced rat paw edema, only (-)-spectaline exhibited an anti-inflammatory profile, showing an ED_<50> value of 56.6μmol/kg. Our results suggest different mechanisms of action for the analgesic activity observed for LASSBio-776 (3-O-Boc-spectaline), LASSBio-755 (3-O-acetyl-spectaline) and (-)-spectaline (LASSBio-754). The antinociceptive profile of some of the semi-synthetic spectaline derivatives extends our research concerning the chemical and pharmacological optimization of isolated natural products in the search of new drug candidates from brazilian biodiversity.
- 公益社団法人日本薬学会の論文
- 2008-04-01
著者
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Bolzani Vanderlan
ブラジル
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VIEGAS Jr.
Laboratorio de Fitoquimica e Quimica Medicinal, Departamento de Ciencias Exatas, Universidade Federa
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ALEXANDRE-MOREIRA Magna
Laboratorio de Farmacologia e Imunidade, Departamento de Fisiologia, Centro de Ciencias Biologicas,
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FRAGA Carlos
Laboratorio de Avaliacao e Sintese de Substancias Bioativas, Departamento de Farmacos, Faculdade de
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BARREIRO Eliezer
Laboratorio de Avaliacao e Sintese de Substancias Bioativas, Departamento de Farmacos, Faculdade de
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BOLZANI Vanderlan
Nucleo de Bioensaios, Biossintese e Ecofisiologia de Produtos Naturals, Institute de Quimica, Univer
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MIRANDA Ana
Laboratorio de Avaliacao e Sintese de Substancias Bioativas, Departamento de Farmacos, Faculdade de
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Viegas Jr.
Laboratorio De Fitoquimica E Quimica Medicinal Departamento De Ciencias Exatas Universidade Federal
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Miranda Ana
Laboratorio De Avaliacao E Sintese De Substancias Bioativas Departamento De Farmacos Faculdade De Fa
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Miranda Ana
Laboratorio De Avaliacao E Sintese De Substancias Bioativas (lassbio) Faculdade De Farmacia Universi
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Fraga Carlos
Laboratorio De Avaliacao E Sintese De Substancias Bioativas Departamento De Farmacos Faculdade De Fa
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Fraga Carlos
Laboratorio De Avaliacao E Sintese De Substancias Bioativas (lassbio) Faculdade De Farmacia Universi
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Barreiro Eliezer
Laboratorio De Avaliacao E Sintese De Substancias Bioativas Departamento De Farmacos Faculdade De Fa
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Barreiro Eliezer
Laboratorio De Avaliacao E Sintese De Substancias Bioativas (lassbio) Faculdade De Farmacia Universi
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Alexandre-moreira Magna
Laboratorio De Farmacologia E Imunidade Departamento De Fisiologia Centro De Ciencias Biologicas Uni
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Bolzani Vanderlan
Nucleo De Bioensaios Biossintese E Ecofisiologia De Produtos Naturals Institute De Quimica Universidade Estadual Paulista
関連論文
- Antinociceptive Profile of 2,3,6-Trisubstituted Piperidine Alkaloids : 3-O-Acetyl-spectaline and Semi-synthetic Derivatives of (-)-Spectaline
- Design and Synthesis of a New 4-Oxa-8ω-11-deoxy-5,6-dihydroprostacyclin Analogue