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Artigo de periodico
Antileishmanial activity evaluation of a natural amide and its synthetic analogs against Leishmania (V.) braziliensis: an integrated approach in vitro and in silico (2021)
Silva, Minelly A. da ; Fokoue, Harold H; Fialho, Saara N; Santos, Ana Paula de A. dos; Rossi, Norton R. D. L. P; Gouveia, Aurileya de J; Ferreira, Amália S; Passarini, Guilherme M; Garay, Ana F. G; Alfonso, Jorge J; Soares, Andreimar M ; Zanchi, Fernando Berton ; Kato, Massuo Jorge ; Teles, Carolina B. G ; Kuehn, Christian C
Fonte: Parasitology Research. Unidade: IQ
Assuntos: LEISHMANIA BRASILIENSIS, AMIDAS, ANTIPROTOZOÁRIOS
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ABNT
SILVA, Minelly A. da et al. Antileishmanial activity evaluation of a natural amide and its synthetic analogs against Leishmania (V.) braziliensis: an integrated approach in vitro and in silico. Parasitology Research, v. 120, p. 2199–2218, 2021Tradução . . Disponível em: https://doi.org/10.1007/s00436-021-07169-w. Acesso em: 16 nov. 2024.
APA
Silva, M. A. da, Fokoue, H. H., Fialho, S. N., Santos, A. P. de A. dos, Rossi, N. R. D. L. P., Gouveia, A. de J., et al. (2021). Antileishmanial activity evaluation of a natural amide and its synthetic analogs against Leishmania (V.) braziliensis: an integrated approach in vitro and in silico. Parasitology Research, 120, 2199–2218. doi:10.1007/s00436-021-07169-w
NLM
Silva MA da, Fokoue HH, Fialho SN, Santos AP de A dos, Rossi NRDLP, Gouveia A de J, Ferreira AS, Passarini GM, Garay AFG, Alfonso JJ, Soares AM, Zanchi FB, Kato MJ, Teles CBG, Kuehn CC. Antileishmanial activity evaluation of a natural amide and its synthetic analogs against Leishmania (V.) braziliensis: an integrated approach in vitro and in silico [Internet]. Parasitology Research. 2021 ; 120 2199–2218.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1007/s00436-021-07169-w
Vancouver
Silva MA da, Fokoue HH, Fialho SN, Santos AP de A dos, Rossi NRDLP, Gouveia A de J, Ferreira AS, Passarini GM, Garay AFG, Alfonso JJ, Soares AM, Zanchi FB, Kato MJ, Teles CBG, Kuehn CC. Antileishmanial activity evaluation of a natural amide and its synthetic analogs against Leishmania (V.) braziliensis: an integrated approach in vitro and in silico [Internet]. Parasitology Research. 2021 ; 120 2199–2218.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1007/s00436-021-07169-w
Artigo de periodico
Effect of isoxazole derivatives of tetrahydrofuran neolignans on intracellular amastigotes of Leishmania (Leishmania) amazonensis: a structure-activity relationship comparative study with triazole-neolignan-based compounds (2019)
Neves, Amarith R. das; Trefzger, Ozildéia S; Barbosa, Natália V; Honorato, Antonio M; Carvalho, Diego B; Moslaves, Iluska S; Kadri, Monica C. T; Yoshida, Nidia Cristiane; Kato, Massuo Jorge ; Arruda, Carla C. P; Baroni, Adriano César de Moraes
Fonte: Chemical Biology & Drug Design. Unidade: IQ
Assuntos: LEISHMANIA, ANTIPROTOZOÁRIOS
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ABNT
NEVES, Amarith R. das et al. Effect of isoxazole derivatives of tetrahydrofuran neolignans on intracellular amastigotes of Leishmania (Leishmania) amazonensis: a structure-activity relationship comparative study with triazole-neolignan-based compounds. Chemical Biology & Drug Design, v. 94, n. 6, p. 2004-2012, 2019Tradução . . Disponível em: https://doi.org/10.1111/cbdd.13609. Acesso em: 16 nov. 2024.
APA
Neves, A. R. das, Trefzger, O. S., Barbosa, N. V., Honorato, A. M., Carvalho, D. B., Moslaves, I. S., et al. (2019). Effect of isoxazole derivatives of tetrahydrofuran neolignans on intracellular amastigotes of Leishmania (Leishmania) amazonensis: a structure-activity relationship comparative study with triazole-neolignan-based compounds. Chemical Biology & Drug Design, 94( 6), 2004-2012. doi:10.1111/cbdd.13609
NLM
Neves AR das, Trefzger OS, Barbosa NV, Honorato AM, Carvalho DB, Moslaves IS, Kadri MCT, Yoshida NC, Kato MJ, Arruda CCP, Baroni AC de M. Effect of isoxazole derivatives of tetrahydrofuran neolignans on intracellular amastigotes of Leishmania (Leishmania) amazonensis: a structure-activity relationship comparative study with triazole-neolignan-based compounds [Internet]. Chemical Biology & Drug Design. 2019 ; 94( 6): 2004-2012.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/cbdd.13609
Vancouver
Neves AR das, Trefzger OS, Barbosa NV, Honorato AM, Carvalho DB, Moslaves IS, Kadri MCT, Yoshida NC, Kato MJ, Arruda CCP, Baroni AC de M. Effect of isoxazole derivatives of tetrahydrofuran neolignans on intracellular amastigotes of Leishmania (Leishmania) amazonensis: a structure-activity relationship comparative study with triazole-neolignan-based compounds [Internet]. Chemical Biology & Drug Design. 2019 ; 94( 6): 2004-2012.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/cbdd.13609
Artigo de periodico
Design, synthesis and antitrypanosomatid activities of 3,5-diaryl-isoxazole analogues based on neolignans veraguensin, grandisin and machilin G (2019)
Trefzger, Ozildeia S; Neves, Amarith R. das; Barbosa, Natalia V; Carvalho, Diego B; Pereira, Indiara C; Perdomo, Renata T; Matos, Maria F. C; Yoshida, Nidia C; Kato, Massuo Jorge ; Albuquerque, Sérgio de; Arruda, Carla C. P; Baroni, Adriano C. M
Fonte: Chemical Biology and Drug Design. Unidades: IQ, FCFRP
Assuntos: FITOQUÍMICA, ANTIPROTOZOÁRIOS
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ABNT
TREFZGER, Ozildeia S et al. Design, synthesis and antitrypanosomatid activities of 3,5-diaryl-isoxazole analogues based on neolignans veraguensin, grandisin and machilin G. Chemical Biology and Drug Design, v. 93, n. 3, p. 313-324, 2019Tradução . . Disponível em: https://doi.org/10.1111/cbdd.13417. Acesso em: 16 nov. 2024.
APA
Trefzger, O. S., Neves, A. R. das, Barbosa, N. V., Carvalho, D. B., Pereira, I. C., Perdomo, R. T., et al. (2019). Design, synthesis and antitrypanosomatid activities of 3,5-diaryl-isoxazole analogues based on neolignans veraguensin, grandisin and machilin G. Chemical Biology and Drug Design, 93( 3), 313-324. doi:10.1111/cbdd.13417
NLM
Trefzger OS, Neves AR das, Barbosa NV, Carvalho DB, Pereira IC, Perdomo RT, Matos MFC, Yoshida NC, Kato MJ, Albuquerque S de, Arruda CCP, Baroni ACM. Design, synthesis and antitrypanosomatid activities of 3,5-diaryl-isoxazole analogues based on neolignans veraguensin, grandisin and machilin G [Internet]. Chemical Biology and Drug Design. 2019 ; 93( 3): 313-324.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/cbdd.13417
Vancouver
Trefzger OS, Neves AR das, Barbosa NV, Carvalho DB, Pereira IC, Perdomo RT, Matos MFC, Yoshida NC, Kato MJ, Albuquerque S de, Arruda CCP, Baroni ACM. Design, synthesis and antitrypanosomatid activities of 3,5-diaryl-isoxazole analogues based on neolignans veraguensin, grandisin and machilin G [Internet]. Chemical Biology and Drug Design. 2019 ; 93( 3): 313-324.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/cbdd.13417
Artigo de periodico
Bioactivity-guided isolation of laevicarpin, an antitrypanosomal and anticryptococcal lactam from Piper laevicarpu (Piperaceae) (2016)
Maciel, Dayany da Silva Alves; Freitas, Viviane P; Conserva, Geanne A. Alves; Alexandre, Tatiana R; Purisco, Sonia U; Tempone, André Gustavo; Melhem, Márcia Souza C; Kato, Massuo Jorge ; Guimarães, Elsie Franklin; Lago, João Henrique Ghilardi
Fonte: Fitoterapia. Unidade: IQ
Assuntos: TRYPANOSOMA CRUZI, CRYPTOCOCCUS, ANTIPROTOZOÁRIOS, FITOTERAPIA
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ABNT
MACIEL, Dayany da Silva Alves et al. Bioactivity-guided isolation of laevicarpin, an antitrypanosomal and anticryptococcal lactam from Piper laevicarpu (Piperaceae). Fitoterapia, v. 111, p. 24-28, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.fitote.2016.04.005. Acesso em: 16 nov. 2024.
APA
Maciel, D. da S. A., Freitas, V. P., Conserva, G. A. A., Alexandre, T. R., Purisco, S. U., Tempone, A. G., et al. (2016). Bioactivity-guided isolation of laevicarpin, an antitrypanosomal and anticryptococcal lactam from Piper laevicarpu (Piperaceae). Fitoterapia, 111, 24-28. doi:10.1016/j.fitote.2016.04.005
NLM
Maciel D da SA, Freitas VP, Conserva GAA, Alexandre TR, Purisco SU, Tempone AG, Melhem MSC, Kato MJ, Guimarães EF, Lago JHG. Bioactivity-guided isolation of laevicarpin, an antitrypanosomal and anticryptococcal lactam from Piper laevicarpu (Piperaceae) [Internet]. Fitoterapia. 2016 ; 111 24-28.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.fitote.2016.04.005
Vancouver
Maciel D da SA, Freitas VP, Conserva GAA, Alexandre TR, Purisco SU, Tempone AG, Melhem MSC, Kato MJ, Guimarães EF, Lago JHG. Bioactivity-guided isolation of laevicarpin, an antitrypanosomal and anticryptococcal lactam from Piper laevicarpu (Piperaceae) [Internet]. Fitoterapia. 2016 ; 111 24-28.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.fitote.2016.04.005
Artigo de periodico
Trypanocidal activity of Piper arboreum and Piper tuberculatum (Piperaceae) (2009)
Regasini, Luis Octávio; Silva, Fernando Cotinguiba da; Passerini, Gabriela Duó; Bolzani, Vanderlan da Silva; Cicarelli, Regina Maria Barretto; Kato, Massuo Jorge ; Furlan, Maysa
Fonte: Revista Brasileira de Farmacognosia. Unidade: IQ
Assuntos: ANTIPROTOZOÁRIOS, TRIPANOSSOMICIDAS, TRYPANOSOMA CRUZI
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ABNT
REGASINI, Luis Octávio et al. Trypanocidal activity of Piper arboreum and Piper tuberculatum (Piperaceae). Revista Brasileira de Farmacognosia, v. 19, n. 1B, p. 199-203, 2009Tradução . . Disponível em: https://doi.org/10.1590/s0102-695x2009000200003. Acesso em: 16 nov. 2024.
APA
Regasini, L. O., Silva, F. C. da, Passerini, G. D., Bolzani, V. da S., Cicarelli, R. M. B., Kato, M. J., & Furlan, M. (2009). Trypanocidal activity of Piper arboreum and Piper tuberculatum (Piperaceae). Revista Brasileira de Farmacognosia, 19( 1B), 199-203. doi:10.1590/s0102-695x2009000200003
NLM
Regasini LO, Silva FC da, Passerini GD, Bolzani V da S, Cicarelli RMB, Kato MJ, Furlan M. Trypanocidal activity of Piper arboreum and Piper tuberculatum (Piperaceae) [Internet]. Revista Brasileira de Farmacognosia. 2009 ; 19( 1B): 199-203.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1590/s0102-695x2009000200003
Vancouver
Regasini LO, Silva FC da, Passerini GD, Bolzani V da S, Cicarelli RMB, Kato MJ, Furlan M. Trypanocidal activity of Piper arboreum and Piper tuberculatum (Piperaceae) [Internet]. Revista Brasileira de Farmacognosia. 2009 ; 19( 1B): 199-203.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1590/s0102-695x2009000200003
Artigo de periodico
Piperamides and their derivatives as potential anti-trypanosomal agents (2009)
Cotinguiba, Fernando; Regasini, Luis Octávio; Bolzani, Vanderlan da Silva; Debonsi, Hosana Maria; Passerini, Gabriela Duó; Cicarelli, Regina Maria Barretto; Kato, Massuo Jorge ; Furlan, Maysa
Fonte: Medicinal Chemistry Research. Unidades: FCFRP, IQ
Assuntos: TRYPANOSOMA CRUZI, DOENÇA DE CHAGAS, ANTIPROTOZOÁRIOS
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ABNT
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.
APA
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

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