Filtros : "Indexado no Science Citation Index" "Kato, Massuo Jorge" Removidos: "Indexado no Commonwealth Agricultural Bureau (CAB) Abstracts" "Phytochemical Analysis" Limpar

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  • Source: Planta Medica. Unidade: IQ

    Subjects: TRYPANOSOMA CRUZI, PRODUTOS NATURAIS

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      MOTA, Jonas da Silva et al. In vitro trypanocidal activity of phenolic derivatives from Peperomia obtusifolia. Planta Medica, v. 75, n. 6, p. 620-623, 2009Tradução . . Disponível em: http://www.thieme-connect.de/ejournals/pdf/plantamedica/doi/10.1055/s-0029-1185364.pdf. Acesso em: 16 nov. 2024.
    • APA

      Mota, J. da S., Leite, A. C., Batista Junior, J. M., López, S. N., Ambrósio, D. L., Passerini, G. D., et al. (2009). In vitro trypanocidal activity of phenolic derivatives from Peperomia obtusifolia. Planta Medica, 75( 6), 620-623. Recuperado de http://www.thieme-connect.de/ejournals/pdf/plantamedica/doi/10.1055/s-0029-1185364.pdf
    • NLM

      Mota J da S, Leite AC, Batista Junior JM, López SN, Ambrósio DL, Passerini GD, Kato MJ, Bolzani V da S, Cicarelli RMB, Furlan M. In vitro trypanocidal activity of phenolic derivatives from Peperomia obtusifolia [Internet]. Planta Medica. 2009 ; 75( 6): 620-623.[citado 2024 nov. 16 ] Available from: http://www.thieme-connect.de/ejournals/pdf/plantamedica/doi/10.1055/s-0029-1185364.pdf
    • Vancouver

      Mota J da S, Leite AC, Batista Junior JM, López SN, Ambrósio DL, Passerini GD, Kato MJ, Bolzani V da S, Cicarelli RMB, Furlan M. In vitro trypanocidal activity of phenolic derivatives from Peperomia obtusifolia [Internet]. Planta Medica. 2009 ; 75( 6): 620-623.[citado 2024 nov. 16 ] Available from: http://www.thieme-connect.de/ejournals/pdf/plantamedica/doi/10.1055/s-0029-1185364.pdf
  • Source: Chirality. Unidade: IQ

    Assunto: PRODUTOS NATURAIS (BIOSSÍNTESE)

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      BATISTA JR., João Marcos et al. Resolution and absolute configuration assignment of a natural racemic chromane from Peperomia obtusifolia (Piperaceae). Chirality, v. 21, n. 9, p. 799-801, 2009Tradução . . Disponível em: https://doi.org/10.1002/chir.20676. Acesso em: 16 nov. 2024.
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      Batista Jr., J. M., López, S. N., Mota, J. da S., Vanzolini, K. L., Cass, Q. B., Rinaldo, D., et al. (2009). Resolution and absolute configuration assignment of a natural racemic chromane from Peperomia obtusifolia (Piperaceae). Chirality, 21( 9), 799-801. doi:10.1002/chir.20676
    • NLM

      Batista Jr. JM, López SN, Mota J da S, Vanzolini KL, Cass QB, Rinaldo D, Vilegas W, Bolzani V da S, Kato MJ, Furlan M. Resolution and absolute configuration assignment of a natural racemic chromane from Peperomia obtusifolia (Piperaceae) [Internet]. Chirality. 2009 ; 21( 9): 799-801.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/chir.20676
    • Vancouver

      Batista Jr. JM, López SN, Mota J da S, Vanzolini KL, Cass QB, Rinaldo D, Vilegas W, Bolzani V da S, Kato MJ, Furlan M. Resolution and absolute configuration assignment of a natural racemic chromane from Peperomia obtusifolia (Piperaceae) [Internet]. Chirality. 2009 ; 21( 9): 799-801.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/chir.20676
  • Source: Journal of the Brazilian Chemical Society. Unidade: IQ

    Subjects: BIOTRANSFORMAÇÃO, PRODUTOS NATURAIS

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      RAMOS, Clécio Sousa e KATO, Massuo Jorge. Hydrolysis of methyl benzoate from Piper arboreum by Naupactus bipes Beetle. Journal of the Brazilian Chemical Society, v. 20, n. 3, p. 560-563, 2009Tradução . . Disponível em: https://doi.org/10.1590/s0103-50532009000300022. Acesso em: 16 nov. 2024.
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      Ramos, C. S., & Kato, M. J. (2009). Hydrolysis of methyl benzoate from Piper arboreum by Naupactus bipes Beetle. Journal of the Brazilian Chemical Society, 20( 3), 560-563. doi:10.1590/s0103-50532009000300022
    • NLM

      Ramos CS, Kato MJ. Hydrolysis of methyl benzoate from Piper arboreum by Naupactus bipes Beetle [Internet]. Journal of the Brazilian Chemical Society. 2009 ; 20( 3): 560-563.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1590/s0103-50532009000300022
    • Vancouver

      Ramos CS, Kato MJ. Hydrolysis of methyl benzoate from Piper arboreum by Naupactus bipes Beetle [Internet]. Journal of the Brazilian Chemical Society. 2009 ; 20( 3): 560-563.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1590/s0103-50532009000300022
  • Source: Journal of Inclusion Phenomena and Macrocyclic Chemistry. Unidade: IQ

    Subjects: ANTIOXIDANTES, METABÓLITOS SECUNDÁRIOS

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      SOARES, Lílian Amélia et al. Host-guest system of 4-nerolidylcatechol in 2-hydroxypropyl 'beta'-cyclodextrin: preparation, characterization and molecular modeling. Journal of Inclusion Phenomena and Macrocyclic Chemistry, v. 64, n. 1-2, p. 23-35, 2009Tradução . . Disponível em: http://www.springerlink.com.w10077.dotlib.com.br/content/ku4h8574977u25g1/fulltext.pdf. Acesso em: 16 nov. 2024.
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      Soares, L. A., Leal, A. F. V. B., Fraceto, L. F., Maia, E. R., Resck, I. S., Kato, M. J., et al. (2009). Host-guest system of 4-nerolidylcatechol in 2-hydroxypropyl 'beta'-cyclodextrin: preparation, characterization and molecular modeling. Journal of Inclusion Phenomena and Macrocyclic Chemistry, 64( 1-2), 23-35. Recuperado de http://www.springerlink.com.w10077.dotlib.com.br/content/ku4h8574977u25g1/fulltext.pdf
    • NLM

      Soares LA, Leal AFVB, Fraceto LF, Maia ER, Resck IS, Kato MJ, Gil E de S, Sousa AR de, Cunha LC da, Rezende KR. Host-guest system of 4-nerolidylcatechol in 2-hydroxypropyl 'beta'-cyclodextrin: preparation, characterization and molecular modeling [Internet]. Journal of Inclusion Phenomena and Macrocyclic Chemistry. 2009 ; 64( 1-2): 23-35.[citado 2024 nov. 16 ] Available from: http://www.springerlink.com.w10077.dotlib.com.br/content/ku4h8574977u25g1/fulltext.pdf
    • Vancouver

      Soares LA, Leal AFVB, Fraceto LF, Maia ER, Resck IS, Kato MJ, Gil E de S, Sousa AR de, Cunha LC da, Rezende KR. Host-guest system of 4-nerolidylcatechol in 2-hydroxypropyl 'beta'-cyclodextrin: preparation, characterization and molecular modeling [Internet]. Journal of Inclusion Phenomena and Macrocyclic Chemistry. 2009 ; 64( 1-2): 23-35.[citado 2024 nov. 16 ] Available from: http://www.springerlink.com.w10077.dotlib.com.br/content/ku4h8574977u25g1/fulltext.pdf
  • Source: Medicinal Chemistry Research. Unidades: FCFRP, IQ

    Subjects: TRYPANOSOMA CRUZI, DOENÇA DE CHAGAS, ANTIPROTOZOÁRIOS

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      COTINGUIBA, Fernando et al. Piperamides and their derivatives as potential anti-trypanosomal agents. Medicinal Chemistry Research, n. ja 2009, 2009Tradução . . Disponível em: https://doi.org/10.1007/s00044-008-9161-9. Acesso em: 16 nov. 2024.
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      Cotinguiba, F., Regasini, L. O., Bolzani, V. da S., Debonsi, H. M., Passerini, G. D., Cicarelli, R. M. B., et al. (2009). Piperamides and their derivatives as potential anti-trypanosomal agents. Medicinal Chemistry Research, ( ja 2009). doi:10.1007/s00044-008-9161-9
    • NLM

      Cotinguiba F, Regasini LO, Bolzani V da S, Debonsi HM, Passerini GD, Cicarelli RMB, Kato MJ, Furlan M. Piperamides and their derivatives as potential anti-trypanosomal agents [Internet]. Medicinal Chemistry Research. 2009 ;( ja 2009):[citado 2024 nov. 16 ] Available from: https://doi.org/10.1007/s00044-008-9161-9
    • Vancouver

      Cotinguiba F, Regasini LO, Bolzani V da S, Debonsi HM, Passerini GD, Cicarelli RMB, Kato MJ, Furlan M. Piperamides and their derivatives as potential anti-trypanosomal agents [Internet]. Medicinal Chemistry Research. 2009 ;( ja 2009):[citado 2024 nov. 16 ] Available from: https://doi.org/10.1007/s00044-008-9161-9
  • Source: Biological & Pharmaceutical Bulletin. Unidade: IQ

    Subjects: TRYPANOSOMA CRUZI, DOENÇA DE CHAGAS, PRODUTOS NATURAIS

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      BATISTA JUNIOR, João Marcos et al. Natural chromenes and chromene derivatives as potential anti-trypanosomal agents. Biological & Pharmaceutical Bulletin, v. 31, n. 3, p. 538-540, 2008Tradução . . Acesso em: 16 nov. 2024.
    • APA

      Batista Junior, J. M., Lopes, A. A., Ambrósio, D. L., Regasini, L. O., Kato, M. J., Bolzani, V. da S., et al. (2008). Natural chromenes and chromene derivatives as potential anti-trypanosomal agents. Biological & Pharmaceutical Bulletin, 31( 3), 538-540.
    • NLM

      Batista Junior JM, Lopes AA, Ambrósio DL, Regasini LO, Kato MJ, Bolzani V da S, Cicarelli RMB, Furlan M. Natural chromenes and chromene derivatives as potential anti-trypanosomal agents. Biological & Pharmaceutical Bulletin. 2008 ;31( 3): 538-540.[citado 2024 nov. 16 ]
    • Vancouver

      Batista Junior JM, Lopes AA, Ambrósio DL, Regasini LO, Kato MJ, Bolzani V da S, Cicarelli RMB, Furlan M. Natural chromenes and chromene derivatives as potential anti-trypanosomal agents. Biological & Pharmaceutical Bulletin. 2008 ;31( 3): 538-540.[citado 2024 nov. 16 ]
  • Source: Pure and Applied Chemistry. Unidade: IQ

    Subjects: METABÓLITOS SECUNDÁRIOS, AMIDO, LIGNINA, MIMETISMO

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      KATO, Massuo Jorge e FURLAN, Maysa. Chemistry and evolution of the Piperaceae. Pure and Applied Chemistry, v. 79, n. 4, p. 529-538, 2007Tradução . . Disponível em: https://doi.org/10.1351/pac200779040529. Acesso em: 16 nov. 2024.
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      Kato, M. J., & Furlan, M. (2007). Chemistry and evolution of the Piperaceae. Pure and Applied Chemistry, 79( 4), 529-538. doi:10.1351/pac200779040529
    • NLM

      Kato MJ, Furlan M. Chemistry and evolution of the Piperaceae [Internet]. Pure and Applied Chemistry. 2007 ; 79( 4): 529-538.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1351/pac200779040529
    • Vancouver

      Kato MJ, Furlan M. Chemistry and evolution of the Piperaceae [Internet]. Pure and Applied Chemistry. 2007 ; 79( 4): 529-538.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1351/pac200779040529
  • Source: Journal of the Brazilian Chemical Society. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, PRODUTOS NATURAIS

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      LEITE, Ana C. et al. Biosynthetic origin of the isoprene units in chromenes of Piper aduncum (piperaceae). Journal of the Brazilian Chemical Society, v. 18, n. 8, p. 1500-1503, 2007Tradução . . Disponível em: https://doi.org/10.1590/s0103-50532007000800008. Acesso em: 16 nov. 2024.
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      Leite, A. C., Lopes, A. A., Kato, M. J., Bolzani, V. da S., & Furlan, M. (2007). Biosynthetic origin of the isoprene units in chromenes of Piper aduncum (piperaceae). Journal of the Brazilian Chemical Society, 18( 8), 1500-1503. doi:10.1590/s0103-50532007000800008
    • NLM

      Leite AC, Lopes AA, Kato MJ, Bolzani V da S, Furlan M. Biosynthetic origin of the isoprene units in chromenes of Piper aduncum (piperaceae) [Internet]. Journal of the Brazilian Chemical Society. 2007 ; 18( 8): 1500-1503.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1590/s0103-50532007000800008
    • Vancouver

      Leite AC, Lopes AA, Kato MJ, Bolzani V da S, Furlan M. Biosynthetic origin of the isoprene units in chromenes of Piper aduncum (piperaceae) [Internet]. Journal of the Brazilian Chemical Society. 2007 ; 18( 8): 1500-1503.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1590/s0103-50532007000800008
  • Source: Pest Management Science. Unidades: FCFRP, IQ

    Subjects: INSETICIDAS (ATIVIDADE), AMIDO, PESTICIDAS, PRODUTOS NATURAIS

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      NAVICKIENE, Hosana Maria Debonsi et al. Toxicity of extracts and isobutyl amides from Piper tuberculatum: potent compounds with potential for the control of the velvetbean caterpillar, Anticarsia gemmatalis. Pest Management Science, v. 63, n. 4, p. 399-403, 2007Tradução . . Disponível em: https://doi.org/10.1002/ps.1340. Acesso em: 16 nov. 2024.
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      Navickiene, H. M. D., Miranda, J. E., De Bortoli, S. A., Kato, M. J., Bolzani, V. da S., & Furlan, M. (2007). Toxicity of extracts and isobutyl amides from Piper tuberculatum: potent compounds with potential for the control of the velvetbean caterpillar, Anticarsia gemmatalis. Pest Management Science, 63( 4), 399-403. doi:10.1002/ps.1340
    • NLM

      Navickiene HMD, Miranda JE, De Bortoli SA, Kato MJ, Bolzani V da S, Furlan M. Toxicity of extracts and isobutyl amides from Piper tuberculatum: potent compounds with potential for the control of the velvetbean caterpillar, Anticarsia gemmatalis [Internet]. Pest Management Science. 2007 ; 63( 4): 399-403.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/ps.1340
    • Vancouver

      Navickiene HMD, Miranda JE, De Bortoli SA, Kato MJ, Bolzani V da S, Furlan M. Toxicity of extracts and isobutyl amides from Piper tuberculatum: potent compounds with potential for the control of the velvetbean caterpillar, Anticarsia gemmatalis [Internet]. Pest Management Science. 2007 ; 63( 4): 399-403.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/ps.1340
  • Source: Journal of Natural Products. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, PRODUTOS NATURAIS

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      MARQUES, Joaquim Vogt et al. Antifungal Amides from Piper scutifolium and Piper hoffmanseggianum. Journal of Natural Products, v. 70, n. 12, p. 2036-2039, 2007Tradução . . Disponível em: https://doi.org/10.1021/np070347g. Acesso em: 16 nov. 2024.
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      Marques, J. V., Kitamura, R. O. S., Lago, J. H. G., Young, M. C. M., Guimarães, E. F., & Kato, M. J. (2007). Antifungal Amides from Piper scutifolium and Piper hoffmanseggianum. Journal of Natural Products, 70( 12), 2036-2039. doi:10.1021/np070347g
    • NLM

      Marques JV, Kitamura ROS, Lago JHG, Young MCM, Guimarães EF, Kato MJ. Antifungal Amides from Piper scutifolium and Piper hoffmanseggianum [Internet]. Journal of Natural Products. 2007 ; 70( 12): 2036-2039.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1021/np070347g
    • Vancouver

      Marques JV, Kitamura ROS, Lago JHG, Young MCM, Guimarães EF, Kato MJ. Antifungal Amides from Piper scutifolium and Piper hoffmanseggianum [Internet]. Journal of Natural Products. 2007 ; 70( 12): 2036-2039.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1021/np070347g
  • Source: Journal of the Brazilian Chemical Society. Unidade: IQ

    Subjects: ÓLEOS ESSENCIAIS, SESQUITERPENOS

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      LAGO, João Henrique Ghilardi et al. 3-Ishwarone and 3-Ishwarol, rare sesquiterpenes in essential oil from leaves of Peperomia oreophila Hensch. Journal of the Brazilian Chemical Society, v. 18, n. 3, p. 638-642, 2007Tradução . . Disponível em: https://doi.org/10.1590/s0103-50532007000300022. Acesso em: 16 nov. 2024.
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      Lago, J. H. G., Oliveira, A. de, Guimarães, E. F., & Kato, M. J. (2007). 3-Ishwarone and 3-Ishwarol, rare sesquiterpenes in essential oil from leaves of Peperomia oreophila Hensch. Journal of the Brazilian Chemical Society, 18( 3), 638-642. doi:10.1590/s0103-50532007000300022
    • NLM

      Lago JHG, Oliveira A de, Guimarães EF, Kato MJ. 3-Ishwarone and 3-Ishwarol, rare sesquiterpenes in essential oil from leaves of Peperomia oreophila Hensch [Internet]. Journal of the Brazilian Chemical Society. 2007 ; 18( 3): 638-642.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1590/s0103-50532007000300022
    • Vancouver

      Lago JHG, Oliveira A de, Guimarães EF, Kato MJ. 3-Ishwarone and 3-Ishwarol, rare sesquiterpenes in essential oil from leaves of Peperomia oreophila Hensch [Internet]. Journal of the Brazilian Chemical Society. 2007 ; 18( 3): 638-642.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1590/s0103-50532007000300022
  • Source: Natural Product Research. Unidade: IQ

    Subjects: PRODUTOS NATURAIS, PLANTAS MEDICINAIS

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      LAGO, João Henrique Ghilardi e KATO, Massuo Jorge. 3'alpha',4'alpha'-Epoxy-2-piperidone, a new minor derivative from leaves of Piper crassinervium Kunth (Piperaceae). Natural Product Research, v. 21, n. 10, p. 910-914, 2007Tradução . . Acesso em: 16 nov. 2024.
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      Lago, J. H. G., & Kato, M. J. (2007). 3'alpha',4'alpha'-Epoxy-2-piperidone, a new minor derivative from leaves of Piper crassinervium Kunth (Piperaceae). Natural Product Research, 21( 10), 910-914.
    • NLM

      Lago JHG, Kato MJ. 3'alpha',4'alpha'-Epoxy-2-piperidone, a new minor derivative from leaves of Piper crassinervium Kunth (Piperaceae). Natural Product Research. 2007 ;21( 10): 910-914.[citado 2024 nov. 16 ]
    • Vancouver

      Lago JHG, Kato MJ. 3'alpha',4'alpha'-Epoxy-2-piperidone, a new minor derivative from leaves of Piper crassinervium Kunth (Piperaceae). Natural Product Research. 2007 ;21( 10): 910-914.[citado 2024 nov. 16 ]
  • Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC

    Subjects: ANTIFÚNGICOS (ATIVIDADE), CANDIDA, PRODUTOS NATURAIS

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      REIGADA, Juliana Beltrame et al. Chemical constituents from Piper marginatum Jacq. (Piperaceae) - antifungal activities and kinetic resolution of (RS)-marginatumol by Candida antarctica lipase (Novozym 435). Tetrahedron - Asymmetry, v. 18, n. 9, p. 1054-1058, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2007.05.006. Acesso em: 16 nov. 2024.
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      Reigada, J. B., Tcacenco, C. M., Andrade, L. H., Kato, M. J., Porto, A. L. M., & Lago, J. H. G. (2007). Chemical constituents from Piper marginatum Jacq. (Piperaceae) - antifungal activities and kinetic resolution of (RS)-marginatumol by Candida antarctica lipase (Novozym 435). Tetrahedron - Asymmetry, 18( 9), 1054-1058. doi:10.1016/j.tetasy.2007.05.006
    • NLM

      Reigada JB, Tcacenco CM, Andrade LH, Kato MJ, Porto ALM, Lago JHG. Chemical constituents from Piper marginatum Jacq. (Piperaceae) - antifungal activities and kinetic resolution of (RS)-marginatumol by Candida antarctica lipase (Novozym 435) [Internet]. Tetrahedron - Asymmetry. 2007 ; 18( 9): 1054-1058.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.tetasy.2007.05.006
    • Vancouver

      Reigada JB, Tcacenco CM, Andrade LH, Kato MJ, Porto ALM, Lago JHG. Chemical constituents from Piper marginatum Jacq. (Piperaceae) - antifungal activities and kinetic resolution of (RS)-marginatumol by Candida antarctica lipase (Novozym 435) [Internet]. Tetrahedron - Asymmetry. 2007 ; 18( 9): 1054-1058.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.tetasy.2007.05.006
  • Source: Parasitology Research. Unidades: IQ, FM

    Subjects: JACARANDÁ, PRODUTOS NATURAIS, ANTIPROTOZOÁRIOS (ATIVIDADE)

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      PASSERO, Luiz Felipe Domingues et al. Anti-leishmania activity of semi-purified fraction of Jacaranda puberula leaves. Parasitology Research, v. 101, n. 3, p. 677-680, 2007Tradução . . Disponível em: https://doi.org/10.1007/s00436-007-0530-y. Acesso em: 16 nov. 2024.
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      Passero, L. F. D., Castro, A. A. de, Tomokane, T. Y., Kato, M. J., Paulinetti, T. F., Corbett, C. E. P., & Laurenti, M. D. (2007). Anti-leishmania activity of semi-purified fraction of Jacaranda puberula leaves. Parasitology Research, 101( 3), 677-680. doi:10.1007/s00436-007-0530-y
    • NLM

      Passero LFD, Castro AA de, Tomokane TY, Kato MJ, Paulinetti TF, Corbett CEP, Laurenti MD. Anti-leishmania activity of semi-purified fraction of Jacaranda puberula leaves [Internet]. Parasitology Research. 2007 ;101( 3): 677-680.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1007/s00436-007-0530-y
    • Vancouver

      Passero LFD, Castro AA de, Tomokane TY, Kato MJ, Paulinetti TF, Corbett CEP, Laurenti MD. Anti-leishmania activity of semi-purified fraction of Jacaranda puberula leaves [Internet]. Parasitology Research. 2007 ;101( 3): 677-680.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1007/s00436-007-0530-y
  • Source: Tetrahedron. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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      NIHEI, Ken-ichi et al. An efficient and versatile synthesis of all structural types of acylpolyamine spider toxins. Tetrahedron, v. 62, n. 35, p. 8335-8350, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2006.06.051. Acesso em: 16 nov. 2024.
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      Nihei, K. -ichi, Kato, M. J., Yamane, T., & Konno, K. (2006). An efficient and versatile synthesis of all structural types of acylpolyamine spider toxins. Tetrahedron, 62( 35), 8335-8350. doi:10.1016/j.tet.2006.06.051
    • NLM

      Nihei K-ichi, Kato MJ, Yamane T, Konno K. An efficient and versatile synthesis of all structural types of acylpolyamine spider toxins [Internet]. Tetrahedron. 2006 ; 62( 35): 8335-8350.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.tet.2006.06.051
    • Vancouver

      Nihei K-ichi, Kato MJ, Yamane T, Konno K. An efficient and versatile synthesis of all structural types of acylpolyamine spider toxins [Internet]. Tetrahedron. 2006 ; 62( 35): 8335-8350.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.tet.2006.06.051
  • Source: Journal of the Brazilian Chemical Society. Unidades: IQ, IFSC

    Subjects: MOLÉCULA, BANCO DE DADOS, PLANTAS MEDICINAIS, MEDICINA POPULAR, DIFRAÇÃO POR RAIOS X, ANTIASMÁTICOS

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      SOARES, Marisi Gomes et al. 2-Hydroxy-4,6-dimethoxyacetophenone from leaves of perperomia glabella. Journal of the Brazilian Chemical Society, v. No/Dec. 2006, n. 7, p. 1205-1210, 2006Tradução . . Disponível em: https://doi.org/10.1590/s0103-50532006000700002. Acesso em: 16 nov. 2024.
    • APA

      Soares, M. G., Felippe, A. P. V., Guimarães, E. F., Kato, M. J., Ellena, J., & Doriguetto, A. C. (2006). 2-Hydroxy-4,6-dimethoxyacetophenone from leaves of perperomia glabella. Journal of the Brazilian Chemical Society, No/Dec. 2006( 7), 1205-1210. doi:10.1590/s0103-50532006000700002
    • NLM

      Soares MG, Felippe APV, Guimarães EF, Kato MJ, Ellena J, Doriguetto AC. 2-Hydroxy-4,6-dimethoxyacetophenone from leaves of perperomia glabella [Internet]. Journal of the Brazilian Chemical Society. 2006 ; No/Dec. 2006( 7): 1205-1210.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1590/s0103-50532006000700002
    • Vancouver

      Soares MG, Felippe APV, Guimarães EF, Kato MJ, Ellena J, Doriguetto AC. 2-Hydroxy-4,6-dimethoxyacetophenone from leaves of perperomia glabella [Internet]. Journal of the Brazilian Chemical Society. 2006 ; No/Dec. 2006( 7): 1205-1210.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1590/s0103-50532006000700002
  • Source: Bioorganic and Medicinal Chemistry. Unidades: IQ, FCFRP

    Subjects: ANTIPARASITÁRIOS, PRODUTOS NATURAIS, TRYPANOSOMA CRUZI

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      BERNARDES, Lilian Sibelle Campos et al. Synthesis and trypanocidal activity of 1,4-bis(3,4,5-trimethoxy-phenyl)-1,4-butanediol and 1,4-bis-(3,4-dimethoxyphenyl)-1,4-butanediol. Bioorganic and Medicinal Chemistry, v. 14, p. 7075-7082, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2006.07.006. Acesso em: 16 nov. 2024.
    • APA

      Bernardes, L. S. C., Kato, M. J., Albuquerque, S. de, & Carvalho, I. (2006). Synthesis and trypanocidal activity of 1,4-bis(3,4,5-trimethoxy-phenyl)-1,4-butanediol and 1,4-bis-(3,4-dimethoxyphenyl)-1,4-butanediol. Bioorganic and Medicinal Chemistry, 14, 7075-7082. doi:10.1016/j.bmc.2006.07.006
    • NLM

      Bernardes LSC, Kato MJ, Albuquerque S de, Carvalho I. Synthesis and trypanocidal activity of 1,4-bis(3,4,5-trimethoxy-phenyl)-1,4-butanediol and 1,4-bis-(3,4-dimethoxyphenyl)-1,4-butanediol [Internet]. Bioorganic and Medicinal Chemistry. 2006 ; 14 7075-7082.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.bmc.2006.07.006
    • Vancouver

      Bernardes LSC, Kato MJ, Albuquerque S de, Carvalho I. Synthesis and trypanocidal activity of 1,4-bis(3,4,5-trimethoxy-phenyl)-1,4-butanediol and 1,4-bis-(3,4-dimethoxyphenyl)-1,4-butanediol [Internet]. Bioorganic and Medicinal Chemistry. 2006 ; 14 7075-7082.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.bmc.2006.07.006
  • Source: Journal of the Brazilian Chemical Society. Unidade: IQ

    Subjects: SESQUITERPENOS, PRODUTOS NATURAIS

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      BERGAMO, Debora Cristina Baldoqui et al. Biosynthetic origins of the isoprene units of 4-nerolidylcatechol in Potomorphe umbellata. Journal of the Brazilian Chemical Society, v. 16, n. 6B, p. 1406-1409, 2005Tradução . . Disponível em: https://doi.org/10.1590/s0103-50532005000800018. Acesso em: 16 nov. 2024.
    • APA

      Bergamo, D. C. B., Kato, M. J., Bolzani, V. da S., & Furlan, M. (2005). Biosynthetic origins of the isoprene units of 4-nerolidylcatechol in Potomorphe umbellata. Journal of the Brazilian Chemical Society, 16( 6B), 1406-1409. doi:10.1590/s0103-50532005000800018
    • NLM

      Bergamo DCB, Kato MJ, Bolzani V da S, Furlan M. Biosynthetic origins of the isoprene units of 4-nerolidylcatechol in Potomorphe umbellata [Internet]. Journal of the Brazilian Chemical Society. 2005 ; 16( 6B): 1406-1409.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1590/s0103-50532005000800018
    • Vancouver

      Bergamo DCB, Kato MJ, Bolzani V da S, Furlan M. Biosynthetic origins of the isoprene units of 4-nerolidylcatechol in Potomorphe umbellata [Internet]. Journal of the Brazilian Chemical Society. 2005 ; 16( 6B): 1406-1409.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1590/s0103-50532005000800018
  • Source: Journal of the Brazilian Chemical Society. Unidade: IQ

    Subjects: METABÓLITOS SECUNDÁRIOS, PRODUTOS NATURAIS

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      DANELUTTE, Ana Paula et al. Divergence of secondary metabolism in cell suspension cultures and differentiated plants of Piper cernuum and P.crassinervium. Journal of the Brazilian Chemical Society, v. 16, n. 6B, p. 1425-1430, 2005Tradução . . Disponível em: https://doi.org/10.1590/s0103-50532005000800022. Acesso em: 16 nov. 2024.
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      Danelutte, A. P., Costantin, M. B., Delgado, G. E., Braz-Filho, R., & Kato, M. J. (2005). Divergence of secondary metabolism in cell suspension cultures and differentiated plants of Piper cernuum and P.crassinervium. Journal of the Brazilian Chemical Society, 16( 6B), 1425-1430. doi:10.1590/s0103-50532005000800022
    • NLM

      Danelutte AP, Costantin MB, Delgado GE, Braz-Filho R, Kato MJ. Divergence of secondary metabolism in cell suspension cultures and differentiated plants of Piper cernuum and P.crassinervium [Internet]. Journal of the Brazilian Chemical Society. 2005 ; 16( 6B): 1425-1430.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1590/s0103-50532005000800022
    • Vancouver

      Danelutte AP, Costantin MB, Delgado GE, Braz-Filho R, Kato MJ. Divergence of secondary metabolism in cell suspension cultures and differentiated plants of Piper cernuum and P.crassinervium [Internet]. Journal of the Brazilian Chemical Society. 2005 ; 16( 6B): 1425-1430.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1590/s0103-50532005000800022
  • Source: Natural Product Research. Unidades: FCF, IQ

    Subjects: PLANTAS MEDICINAIS, ANTIOXIDANTES (ATIVIDADE), LIGNINA

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      REZENDE, Kênnia Rocha et al. Antioxidant activity of aryltetralone lignans and derivatives from Virola sebifera (Aubl.). Natural Product Research, v. 19, n. 7, p. 661-666, 2005Tradução . . Disponível em: https://doi.org/10.1080/14786410412331302118. Acesso em: 16 nov. 2024.
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      Rezende, K. R., Davino, S. C., Barros, S. B. de M., & Kato, M. J. (2005). Antioxidant activity of aryltetralone lignans and derivatives from Virola sebifera (Aubl.). Natural Product Research, 19( 7), 661-666. doi:10.1080/14786410412331302118
    • NLM

      Rezende KR, Davino SC, Barros SB de M, Kato MJ. Antioxidant activity of aryltetralone lignans and derivatives from Virola sebifera (Aubl.) [Internet]. Natural Product Research. 2005 ; 19( 7): 661-666.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1080/14786410412331302118
    • Vancouver

      Rezende KR, Davino SC, Barros SB de M, Kato MJ. Antioxidant activity of aryltetralone lignans and derivatives from Virola sebifera (Aubl.) [Internet]. Natural Product Research. 2005 ; 19( 7): 661-666.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1080/14786410412331302118

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