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Registro Completo |
Biblioteca(s): |
Embrapa Meio Ambiente. |
Data corrente: |
23/04/2013 |
Data da última atualização: |
23/04/2013 |
Tipo da produção científica: |
Resumo em Anais de Congresso |
Autoria: |
QUEIROZ, S. C. do N. de; CANTRELL, C. L.; DUKE, S. O.; MORAES, R. M.; CERDEIRA, A. L.; NANDULA, V. |
Afiliação: |
SONIA CLAUDIA DO N DE QUEIROZ, CNPMA; C. L. CANTRELL, USDA-ARS; S. O. DUKE, USDA-ARS; R. M. MORAES, University of Mississippi-USA; ANTONIO LUIZ CERDEIRA, CNPMA; V. NANDULA, USDA-ARS. |
Título: |
Bioassay-directed isolation and identification of phytotoxic terpenoids from horseweed (Conyza Canadensis). |
Ano de publicação: |
2012 |
Fonte/Imprenta: |
Thieme eJournals - Abstract. |
Idioma: |
Inglês |
Conteúdo: |
Horseweed [Conyza canadensis (L.) Cronquist, syn. Erigeron canadensis L.], Asteraceae, is a common weed with known allelopathic effects but few studies on the isolation and identification of the phytotoxic compounds have been reported [1]. C. canadensis infests orchards, vineyards, field crops such as corn, soybean and cotton, particularly in herbicide-resistant crops where conservation tillage or no-till systems are used. The objective of this study was to identify the phytotoxic compounds present by systematically performing bioassay-directed isolation and subsequent identification of the bioactive constituents according to Dayan et al. [2]. No significant phytotoxic activity against Lactuca sativa or Agrostis stolonifera was detected in methanol, or water extracts when tested at 1.0mg·mL-1; however, the dichloromethane extract was active. Further fractionation using liquid-liquid partitioning with hexane, chloroform, ethyl acetate and water was performed with the DCM extract. The most active extract (chloroform) was subjected to preparative HPLC and the fractions were tested again. The active compounds were isolated and identified by GC-MS and 1H- and 13C-NMR. The isolated compounds (Figure 1) were identified as (2Z,8Z)-matricaria acid methyl ester, (4Z,8Z)-matricarialactone and (4Z)-lachnophyllumlactone. Compound 3 shows similar activity as |
Palavras-Chave: |
Horseweed; Phytotoxic terpenoids. |
Thesaurus Nal: |
Conyza canadensis. |
Categoria do assunto: |
W Química e Física |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/81863/1/RA-QueirozSCN-PlantaMedica-....pdf
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Marc: |
LEADER 01992nam a2200205 a 4500 001 1956433 005 2013-04-23 008 2012 bl uuuu u00u1 u #d 100 1 $aQUEIROZ, S. C. do N. de 245 $aBioassay-directed isolation and identification of phytotoxic terpenoids from horseweed (Conyza Canadensis).$h[electronic resource] 260 $aThieme eJournals - Abstract.$c2012 520 $aHorseweed [Conyza canadensis (L.) Cronquist, syn. Erigeron canadensis L.], Asteraceae, is a common weed with known allelopathic effects but few studies on the isolation and identification of the phytotoxic compounds have been reported [1]. C. canadensis infests orchards, vineyards, field crops such as corn, soybean and cotton, particularly in herbicide-resistant crops where conservation tillage or no-till systems are used. The objective of this study was to identify the phytotoxic compounds present by systematically performing bioassay-directed isolation and subsequent identification of the bioactive constituents according to Dayan et al. [2]. No significant phytotoxic activity against Lactuca sativa or Agrostis stolonifera was detected in methanol, or water extracts when tested at 1.0mg·mL-1; however, the dichloromethane extract was active. Further fractionation using liquid-liquid partitioning with hexane, chloroform, ethyl acetate and water was performed with the DCM extract. The most active extract (chloroform) was subjected to preparative HPLC and the fractions were tested again. The active compounds were isolated and identified by GC-MS and 1H- and 13C-NMR. The isolated compounds (Figure 1) were identified as (2Z,8Z)-matricaria acid methyl ester, (4Z,8Z)-matricarialactone and (4Z)-lachnophyllumlactone. Compound 3 shows similar activity as 650 $aConyza canadensis 653 $aHorseweed 653 $aPhytotoxic terpenoids 700 1 $aCANTRELL, C. L. 700 1 $aDUKE, S. O. 700 1 $aMORAES, R. M. 700 1 $aCERDEIRA, A. L. 700 1 $aNANDULA, V.
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Embrapa Meio Ambiente (CNPMA) |
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Registros recuperados : 35 | |
9. | | CERDEIRA, A. L.; DUKE, S. O. Transgenic herbicide-resistant crops. In: CONGRESSO BRASILEIRO DE BIOSSEGURANÇA, 5.; SIMPÓSIO LATINO-AMERICANO DE PRODUTOS TRANSGÊNICOS, 5., 2007, Ouro Preto. Anais dos eventos. Rio de Janeiro: Associação Nacional de Biossegurança, 2007. p.39-40.Tipo: Artigo em Anais de Congresso / Nota Técnica |
Biblioteca(s): Embrapa Meio Ambiente. |
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14. | | CERDEIRA, A. L.; CANTRELL, C. L.; BYRD, J. D.; DUKE, S. O. Phytotoxic Activity of Imperata cylindrica (L.) P. Beauv. Extracts. Planta Medica, v. 77, n. 6, 2011. 10th Annual Oxford International Conference on the Science of Botanicals ICBS, 11-14 April, 2011, University of Mississippi, USA. Poster 39.Tipo: Resumo em Anais de Congresso |
Biblioteca(s): Embrapa Meio Ambiente. |
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15. | | CERDEIRA, A. L.; GAZZIERO, D. L. P.; DUKE, S. O.; MATALLO, M. B.; SPADOTTO, C. A. Review of potential environmental impacts of transgenic glyphosate-resistant soybean in Brazil. Journal of Environmental Science and Health. Part B. Pesticides, Food Contaminants and Agricultural Wastes, New Yrok, v. 42, n. 5, p. 539-549, 2007.Tipo: Artigo em Periódico Indexado | Circulação/Nível: Internacional - A |
Biblioteca(s): Embrapa Meio Ambiente; Embrapa Soja. |
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20. | | CERDEIRA, A. L.; CANTRELL, C. L.; DAYAN, F. E.; BYRD, J. D.; DUKE, S. O. Tabanone, a new phytotoxic constituent of cogongrass (Imperata cylindrica). Weed Science, Champaign, v. 60, n. 2, p. 212-218, 2012.Tipo: Artigo em Periódico Indexado | Circulação/Nível: A - 2 |
Biblioteca(s): Embrapa Meio Ambiente. |
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Registros recuperados : 35 | |
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Nenhum registro encontrado para a expressão de busca informada. |
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