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Registros recuperados : 11 | |
2. | | CHAVES, F. C. M.; CAMARGO, J. V. S.; PINTO, A. C. DA S.; NOGUEIRA, K. L.; POHLIT, A. M. Produção de biomassa, teor e rendimento de extrato de Piper peltata em função de arranjos espaciais. In: INTERNATIONAL SYMPOSIUM ON MEDICINAL AND NUTRACEUTICAL PLANTS, 3.; CONFERENCE OF NATIONAL INSTITUTE OF SCIENCE & TECHNOLOGY FOR TROPICAL FRUITS, 3., 2012, Aracaju. [Abstracts...]. Aracaju: ISHS; UFS; SBCTA, 2012. 1 CD-ROM. Biblioteca(s): Embrapa Amazônia Ocidental. |
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3. | | PINTO, A. C. da S.; LUCENA, J. F. de; NOGUEIRA, K. L.; POHLIT, A. M.; CHAVES, F. C. M. Preparação de derivados semi-sintéticos de catecol e 4-nerolidilcatecol e atividade citotóxica em Artemia franciscana. In: REUNIÃO ANUAL DA SOCIEDADE BRASILEIRA DE QUÍMICA, 30., 2007, Águas de Lindóia, SP. Resumos... Águas de Lindóia: Sociedade Brasileira de Química, 2007. Biblioteca(s): Embrapa Amazônia Ocidental. |
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6. | | PINTO, A. C. S.; NOGUEIRA, K. L.; CHAVES, F. C. M.; SILVA, L. V. S. da; TADEI, W. P.; POHLIT, A. M. Adulticidal activity of dillapiol and semi-synthetic derivatives of dillapiol against adults of Aedes aegypti (L.) (Culicidae). Journal of Mosquito Research, v. 2, n. 1, p. 1-7, jun. 2012. Biblioteca(s): Embrapa Amazônia Ocidental. |
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8. | | LIMA, E. S.; PINTO, A. C. S.; NOGUEIRA, K. L.; SILVA, L. F. R. e; ALMEIDA, P. D. O. de; VASCONCELLOS, M. C. de; CHAVES, F. C. M.; TADEI, W. P.; POHLIT, A. M. Stability and Antioxidant Activity of Semi-synthetic Derivatives of 4-Nerolidylcatechol. Molecules, v. 18, n. 1, p. 178-189, jan. 2013. Biblioteca(s): Embrapa Amazônia Ocidental. |
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9. | | POHLIT, A. M.; PINTO, A. C. da S.; CAVALCANTI, B. C.; PESSOA, C. do O.; SILVA, E. C. C. e; CHAVES, F. C. M.; NOGUEIRA, K. L.; LOTUFO, L.; SILVA, L. F. R. e; MELO, M. R. S.; VIEIRA, P. P. R.; MAUSE, R.; AMORIM, R. C. da N.; TADEI, W. P.; ANDRADE-NETO, V. de. Biopharmaceuticals synthesis. In: CARIOCA, J. O. B. (Ed.). Brazilian network on green chemistry - awareness, responsability and action. Benfica: UFC, 2008. p. 347-372. Biblioteca(s): Embrapa Amazônia Ocidental. |
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10. | | SILVA, L. F. R. e; NOGUEIRA, K. L.; PINTO, A. C. da S.; KATZIN, A. M.; SUSSMANN, R. A. C.; MUNIZ, M. P.; ANDRADE NETO, V. F. de; CHAVES, F. C. M.; COUTINHO, J. P.; LIMA, E. S.; KRETTLI, A. U.; TADEI, W. P.; POHLIT, A. M. In vivo antimalarial activity and mechanisms of action of 4-Nerolidylcatechol derivatives. Antimicrobial Agents and Chemotherapy, v. 59, n. 6, p. 3271-80, Jun. 2015. Biblioteca(s): Embrapa Amazônia Ocidental. |
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11. | | ANDRADE-NETO, V. F. de; POHLIT, A. M.; PINTO, A. C. S.; SILVA, E. C. C.; NOGUEIRA, K. L.; MELO, M. R. S.; HENRIQUE, M. C.; AMORIM, R. C. N.; SILVA, L. F. R.; COSTA, M. R. F.; NUNOMURA, R. C. S.; NUNOMURA, S. M.; ALECRIM, W. D.; ALECRIM, M. das G. C.; CHAVES, F. C. M.; VIEIRA, P. P. R. In vitro inhibition of Plasmodium falciparum by substances isolated from Amazonian antimalarial plants. Memórias do Instituto Oswaldo Cruz, Rio de Janeiro, v. 102, n. 3, p. 359-365, jun. 2007. Biblioteca(s): Embrapa Amazônia Ocidental. |
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Registros recuperados : 11 | |
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Registro Completo
Biblioteca(s): |
Embrapa Amazônia Ocidental. |
Data corrente: |
04/04/2013 |
Data da última atualização: |
29/01/2018 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Circulação/Nível: |
A - 1 |
Autoria: |
LIMA, E. S.; PINTO, A. C. S.; NOGUEIRA, K. L.; SILVA, L. F. R. e; ALMEIDA, P. D. O. de; VASCONCELLOS, M. C. de; CHAVES, F. C. M.; TADEI, W. P.; POHLIT, A. M. |
Afiliação: |
Emerson Silva Lima, UFAM; Ana Cristina Silva Pinto, INPA; Karla Lagos Nogueira, INPA; Luiz Francisco Rocha e Silva, INPA; Patricia Danielle Oliveira de Almeida, UFAM; Marne Carvalho de Vasconcellos, UFAM; FRANCISCO CELIO MAIA CHAVES, CPAA; Wanderli Pedro Tadei, INPA; Adrian Martin Pohlit, INPA. |
Título: |
Stability and Antioxidant Activity of Semi-synthetic Derivatives of 4-Nerolidylcatechol. |
Ano de publicação: |
2013 |
Fonte/Imprenta: |
Molecules, v. 18, n. 1, p. 178-189, jan. 2013. |
ISSN: |
1420-3049 |
DOI: |
10.3390/molecules18010178 |
Idioma: |
Inglês |
Conteúdo: |
4-nerolidylcatechol (4-NC) is an unstable natural product that exhibits important antioxidant, anti-inflammatory and other properties. It is readily obtainable on a multi-gram scale through straightforward solvent extraction of the roots of cultivated Piper peltatum or P. umbellatum, followed by column chromatography on the resulting extract. Semi-synthetic derivatives of 4-NC with one or two substituent groups (methyl, acetyl, benzyl, benzoyl) on the O atoms have been introduced that have increased stability compared to 4-NC and significant in vitro inhibitory activity against the human malaria parasite Plasmodium falciparum. Antioxidant and anti-inflammatory properties may be important for the antiplasmodial mode of action of 4-NC derivatives. Thus, we decided to investigate the antioxidant properties, cytotoxicity and stability of 4-NC derivatives as a means to explore the potential utility of these compounds. 4-NC showed high antioxidant activity in the DPPH and ABTS assays and in 3T3-L1 cells (mouse embryonic fibroblast), however 4-NC was more cytotoxic (IC50 = 31.4 µM) and more unstable than its derivatives and lost more than 80% of its antioxidant activity upon storage in solution at −20 °C for 30 days. DMSO solutions of mono-O-substituted derivatives of 4-NC exhibited antioxidant activity and radical scavenging activity in the DPPH and ABTS assays that was comparable to that of BHA and BHT. In the cell-based antioxidant model, most DMSO solutions of derivatives of 4-NC were less active on day 1 than 4-NC, quercetin and BHA and more active antioxidants than BHT. After storage for 30 days at −20 °C, DMSO solutions of most of the derivatives of 4-NC were more stable and exhibited more antioxidant activity than 4-NC, quercetin and BHA and exhibited comparable antioxidant activity to BHT. These findings point to the potential of derivatives of 4-NC as antioxidant compounds. Menos4-nerolidylcatechol (4-NC) is an unstable natural product that exhibits important antioxidant, anti-inflammatory and other properties. It is readily obtainable on a multi-gram scale through straightforward solvent extraction of the roots of cultivated Piper peltatum or P. umbellatum, followed by column chromatography on the resulting extract. Semi-synthetic derivatives of 4-NC with one or two substituent groups (methyl, acetyl, benzyl, benzoyl) on the O atoms have been introduced that have increased stability compared to 4-NC and significant in vitro inhibitory activity against the human malaria parasite Plasmodium falciparum. Antioxidant and anti-inflammatory properties may be important for the antiplasmodial mode of action of 4-NC derivatives. Thus, we decided to investigate the antioxidant properties, cytotoxicity and stability of 4-NC derivatives as a means to explore the potential utility of these compounds. 4-NC showed high antioxidant activity in the DPPH and ABTS assays and in 3T3-L1 cells (mouse embryonic fibroblast), however 4-NC was more cytotoxic (IC50 = 31.4 µM) and more unstable than its derivatives and lost more than 80% of its antioxidant activity upon storage in solution at −20 °C for 30 days. DMSO solutions of mono-O-substituted derivatives of 4-NC exhibited antioxidant activity and radical scavenging activity in the DPPH and ABTS assays that was comparable to that of BHA and BHT. In the cell-based antioxidant model, most DMSO solutions of derivatives... Mostrar Tudo |
Palavras-Chave: |
Antioxidantes; Piper peltatum. |
Categoria do assunto: |
-- |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/80487/1/molecules-18-00178-v2.pdf
|
Marc: |
LEADER 02680naa a2200265 a 4500 001 1954997 005 2018-01-29 008 2013 bl uuuu u00u1 u #d 022 $a1420-3049 024 7 $a10.3390/molecules18010178$2DOI 100 1 $aLIMA, E. S. 245 $aStability and Antioxidant Activity of Semi-synthetic Derivatives of 4-Nerolidylcatechol. 260 $c2013 520 $a4-nerolidylcatechol (4-NC) is an unstable natural product that exhibits important antioxidant, anti-inflammatory and other properties. It is readily obtainable on a multi-gram scale through straightforward solvent extraction of the roots of cultivated Piper peltatum or P. umbellatum, followed by column chromatography on the resulting extract. Semi-synthetic derivatives of 4-NC with one or two substituent groups (methyl, acetyl, benzyl, benzoyl) on the O atoms have been introduced that have increased stability compared to 4-NC and significant in vitro inhibitory activity against the human malaria parasite Plasmodium falciparum. Antioxidant and anti-inflammatory properties may be important for the antiplasmodial mode of action of 4-NC derivatives. Thus, we decided to investigate the antioxidant properties, cytotoxicity and stability of 4-NC derivatives as a means to explore the potential utility of these compounds. 4-NC showed high antioxidant activity in the DPPH and ABTS assays and in 3T3-L1 cells (mouse embryonic fibroblast), however 4-NC was more cytotoxic (IC50 = 31.4 µM) and more unstable than its derivatives and lost more than 80% of its antioxidant activity upon storage in solution at −20 °C for 30 days. DMSO solutions of mono-O-substituted derivatives of 4-NC exhibited antioxidant activity and radical scavenging activity in the DPPH and ABTS assays that was comparable to that of BHA and BHT. In the cell-based antioxidant model, most DMSO solutions of derivatives of 4-NC were less active on day 1 than 4-NC, quercetin and BHA and more active antioxidants than BHT. After storage for 30 days at −20 °C, DMSO solutions of most of the derivatives of 4-NC were more stable and exhibited more antioxidant activity than 4-NC, quercetin and BHA and exhibited comparable antioxidant activity to BHT. These findings point to the potential of derivatives of 4-NC as antioxidant compounds. 653 $aAntioxidantes 653 $aPiper peltatum 700 1 $aPINTO, A. C. S. 700 1 $aNOGUEIRA, K. L. 700 1 $aSILVA, L. F. R. e 700 1 $aALMEIDA, P. D. O. de 700 1 $aVASCONCELLOS, M. C. de 700 1 $aCHAVES, F. C. M. 700 1 $aTADEI, W. P. 700 1 $aPOHLIT, A. M. 773 $tMolecules$gv. 18, n. 1, p. 178-189, jan. 2013.
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