Síntese quimioenzimática do levetiracetam e análogos
| Ano de defesa: | 2015 |
|---|---|
| Autor(a) principal: | |
| Orientador(a): | |
| Banca de defesa: | |
| Tipo de documento: | Dissertação |
| Tipo de acesso: | Acesso aberto |
| Idioma: | por |
| Instituição de defesa: |
Universidade Estadual Paulista (Unesp)
|
| Programa de Pós-Graduação: |
Não Informado pela instituição
|
| Departamento: |
Não Informado pela instituição
|
| País: |
Não Informado pela instituição
|
| Palavras-chave em Português: | |
| Link de acesso: | http://hdl.handle.net/11449/124450 |
Resumo: | Biocatalysts (enzymes and/or microorganisms) are widely used in the synthesis of bioactive molecules, in particular pharmaceuticals, to generate or resolve chiral centers. Levetiracetam, commercially known as Keppra®, is a chiral compound with anticonvulsant properties whose pharmacological activity is related to the (S)-enantiomer. The increase in option for the use of levetiracetam over the others anticonvulsant drugs is closely associated with low incidence of side effects caused by this. Several chemosynthetic routes for its production are reported in the literature. Most of them involve numerous synthetic steps, high energy consumption, use of metal catalysts and low overall yields. On the other hand, this project aims to develop a chemoenzymatic route, with fewer steps, milder conditions and environmentally friendly reaction for the synthesis of levetiracetam and analogues (aliphatic series). The respective aromatic series was also synthesized, since it is chiral building blocks for the synthesis of compounds with known antimalarial activity. The first step was the synthesis of racemic cyanohydrin followed by substitution of the hydroxyl group by nitrogen heterocycles. Collections of nitrile hydratase enzymes type (EC 4.2.1.84) were used to catalyze the conversion of N-heterocycles α-substituted nitriles in the respective chiral amides. The enzymes were used both in isolated form (obtained commercially) as in whole cells bacteria and yeast Collection of Microorganisms of Biocatalysis Laboratory of IQ-UNESP Araraquara. The enzymatic reactions were performed in buffered aqueous medium and ionic liquid : buffer (10, 20, 40 and 80%) binary systems in order to evaluate the influence of the solvent on the enantioselectivity and yield of these reactions. The ionic liquids synthesized and used in this work were 1-butyl-3-methylimidazolium tetrafluoroborate, 1-butyl-3-methylimidazolium... |
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Síntese quimioenzimática do levetiracetam e análogosBiocatáliseSintese assimetricaMetaloenzimasEnantiomerosLíquidos iônicosAsymmetric synthesisBiocatalysts (enzymes and/or microorganisms) are widely used in the synthesis of bioactive molecules, in particular pharmaceuticals, to generate or resolve chiral centers. Levetiracetam, commercially known as Keppra®, is a chiral compound with anticonvulsant properties whose pharmacological activity is related to the (S)-enantiomer. The increase in option for the use of levetiracetam over the others anticonvulsant drugs is closely associated with low incidence of side effects caused by this. Several chemosynthetic routes for its production are reported in the literature. Most of them involve numerous synthetic steps, high energy consumption, use of metal catalysts and low overall yields. On the other hand, this project aims to develop a chemoenzymatic route, with fewer steps, milder conditions and environmentally friendly reaction for the synthesis of levetiracetam and analogues (aliphatic series). The respective aromatic series was also synthesized, since it is chiral building blocks for the synthesis of compounds with known antimalarial activity. The first step was the synthesis of racemic cyanohydrin followed by substitution of the hydroxyl group by nitrogen heterocycles. Collections of nitrile hydratase enzymes type (EC 4.2.1.84) were used to catalyze the conversion of N-heterocycles α-substituted nitriles in the respective chiral amides. The enzymes were used both in isolated form (obtained commercially) as in whole cells bacteria and yeast Collection of Microorganisms of Biocatalysis Laboratory of IQ-UNESP Araraquara. The enzymatic reactions were performed in buffered aqueous medium and ionic liquid : buffer (10, 20, 40 and 80%) binary systems in order to evaluate the influence of the solvent on the enantioselectivity and yield of these reactions. The ionic liquids synthesized and used in this work were 1-butyl-3-methylimidazolium tetrafluoroborate, 1-butyl-3-methylimidazolium...Os biocatalisadores (enzimas e/ou micro-organismos) são amplamente utilizados na síntese de moléculas bioativas, em especial os fármacos, para gerar ou resolver centros quirais. O levetiracetam, comercialmente conhecido como Keppra®, é um composto quiral com propriedades anticonvulsivantes cuja atividade farmacológica está relacionada ao enantiômero (S). O aumento da opção pelo uso do levetiracetam em detrimento a outros fármacos anticonvulsivantes está intimamente associado à baixa ocorrência de efeitos colaterais provocados por este. Diversas rotas quimiossintéticas para sua produção são relatadas na literatura. A maioria delas envolve um elevado número de etapas, alto consumo energético, uso de catalisadores metálicos e baixos rendimentos globais. Em contrapartida, este projeto teve por objetivo empregar uma rota quimioenzimática, com menor número de etapas, condições mais brandas e ambientalmente amigáveis de reação para a síntese do levetiracetam e análogos (série alifática). A respectiva série aromática também foi sintetizada, uma vez que trata-se de blocos construtores quirais para a síntese de compostos com reconhecida atividade anti-malária. A primeira etapa consistiu na síntese das cianidrinas racêmicas seguida da substiuição da hidroxila destas por heterociclos nitrogenados. Uma coleção de enzimas do tipo nitrila hidratases (E.C. 4.2.1.84) foi empregada para catalisar a conversão das nitrilas α-substituidas por N-heterociclos nas respectivas amidas quirais. As enzimas foram utilizadas tanto na forma isolada (obtidas comercialmente) quanto em células íntegras de bactérias e leveduras da Coleção de Micro-organismos do Laboratório de Biocatálise do IQ-UNESP Araraquara. As reações enzimáticas foram conduzidas em meio aquoso tamponado e em sistemas binários líquido iônico : solução tampão (10, 20, 40 e 80%) a fim de avaliar a influência do...Universidade Estadual Paulista (Unesp)Milagre, Cintia Duarte de Freitas [UNESP]Universidade Estadual Paulista (Unesp)Amaral, Bruno Sérgio do [UNESP]2015-07-13T12:10:18Z2015-07-13T12:10:18Z2015-02-23info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesis212 f. : il. -application/pdfAMARAL, Bruno Sérgio do. Síntese quimioenzimática do levetiracetam e análogos. 2015. 212 f. Dissertação (mestrado) - Universidade Estadual Paulista, Instituto de Química, 2015.http://hdl.handle.net/11449/124450000825064000825064.pdf33004030072P833004030072P814257489168493760000-0001-5627-8616Alephreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPporinfo:eu-repo/semantics/openAccess2025-05-28T11:23:55Zoai:repositorio.unesp.br:11449/124450Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-05-28T11:23:55Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
| dc.title.none.fl_str_mv |
Síntese quimioenzimática do levetiracetam e análogos |
| title |
Síntese quimioenzimática do levetiracetam e análogos |
| spellingShingle |
Síntese quimioenzimática do levetiracetam e análogos Amaral, Bruno Sérgio do [UNESP] Biocatálise Sintese assimetrica Metaloenzimas Enantiomeros Líquidos iônicos Asymmetric synthesis |
| title_short |
Síntese quimioenzimática do levetiracetam e análogos |
| title_full |
Síntese quimioenzimática do levetiracetam e análogos |
| title_fullStr |
Síntese quimioenzimática do levetiracetam e análogos |
| title_full_unstemmed |
Síntese quimioenzimática do levetiracetam e análogos |
| title_sort |
Síntese quimioenzimática do levetiracetam e análogos |
| author |
Amaral, Bruno Sérgio do [UNESP] |
| author_facet |
Amaral, Bruno Sérgio do [UNESP] |
| author_role |
author |
| dc.contributor.none.fl_str_mv |
Milagre, Cintia Duarte de Freitas [UNESP] Universidade Estadual Paulista (Unesp) |
| dc.contributor.author.fl_str_mv |
Amaral, Bruno Sérgio do [UNESP] |
| dc.subject.por.fl_str_mv |
Biocatálise Sintese assimetrica Metaloenzimas Enantiomeros Líquidos iônicos Asymmetric synthesis |
| topic |
Biocatálise Sintese assimetrica Metaloenzimas Enantiomeros Líquidos iônicos Asymmetric synthesis |
| description |
Biocatalysts (enzymes and/or microorganisms) are widely used in the synthesis of bioactive molecules, in particular pharmaceuticals, to generate or resolve chiral centers. Levetiracetam, commercially known as Keppra®, is a chiral compound with anticonvulsant properties whose pharmacological activity is related to the (S)-enantiomer. The increase in option for the use of levetiracetam over the others anticonvulsant drugs is closely associated with low incidence of side effects caused by this. Several chemosynthetic routes for its production are reported in the literature. Most of them involve numerous synthetic steps, high energy consumption, use of metal catalysts and low overall yields. On the other hand, this project aims to develop a chemoenzymatic route, with fewer steps, milder conditions and environmentally friendly reaction for the synthesis of levetiracetam and analogues (aliphatic series). The respective aromatic series was also synthesized, since it is chiral building blocks for the synthesis of compounds with known antimalarial activity. The first step was the synthesis of racemic cyanohydrin followed by substitution of the hydroxyl group by nitrogen heterocycles. Collections of nitrile hydratase enzymes type (EC 4.2.1.84) were used to catalyze the conversion of N-heterocycles α-substituted nitriles in the respective chiral amides. The enzymes were used both in isolated form (obtained commercially) as in whole cells bacteria and yeast Collection of Microorganisms of Biocatalysis Laboratory of IQ-UNESP Araraquara. The enzymatic reactions were performed in buffered aqueous medium and ionic liquid : buffer (10, 20, 40 and 80%) binary systems in order to evaluate the influence of the solvent on the enantioselectivity and yield of these reactions. The ionic liquids synthesized and used in this work were 1-butyl-3-methylimidazolium tetrafluoroborate, 1-butyl-3-methylimidazolium... |
| publishDate |
2015 |
| dc.date.none.fl_str_mv |
2015-07-13T12:10:18Z 2015-07-13T12:10:18Z 2015-02-23 |
| dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
| dc.type.driver.fl_str_mv |
info:eu-repo/semantics/masterThesis |
| format |
masterThesis |
| status_str |
publishedVersion |
| dc.identifier.uri.fl_str_mv |
AMARAL, Bruno Sérgio do. Síntese quimioenzimática do levetiracetam e análogos. 2015. 212 f. Dissertação (mestrado) - Universidade Estadual Paulista, Instituto de Química, 2015. http://hdl.handle.net/11449/124450 000825064 000825064.pdf 33004030072P8 33004030072P8 1425748916849376 0000-0001-5627-8616 |
| identifier_str_mv |
AMARAL, Bruno Sérgio do. Síntese quimioenzimática do levetiracetam e análogos. 2015. 212 f. Dissertação (mestrado) - Universidade Estadual Paulista, Instituto de Química, 2015. 000825064 000825064.pdf 33004030072P8 1425748916849376 0000-0001-5627-8616 |
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http://hdl.handle.net/11449/124450 |
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por |
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por |
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info:eu-repo/semantics/openAccess |
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openAccess |
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212 f. : il. - application/pdf |
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Universidade Estadual Paulista (Unesp) |
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Universidade Estadual Paulista (Unesp) |
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Aleph reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
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Universidade Estadual Paulista (UNESP) |
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UNESP |
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UNESP |
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Repositório Institucional da UNESP |
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Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
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repositoriounesp@unesp.br |
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1854954619339276288 |