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Artigo de periodico
Heterobimetallic nickel(II) and palladium(II) complexes derived from S-benzyl-N- (ferrocenyl)methylenedithiocarbazate: Trypanocidal activity and interaction with Trypanosoma cruzi Old Yellow Enzyme (TcOYE) (2019)
Carneiro, Zumira A; Gaspari, Ana P S; Lima, Jackelinne C; Lopes, Carla D; Gaspari, Ana P S; Albuquerque, Sérgio de ; Dinelli, Luis R; Silva, Laudimir Leonardo Walbert Veloso da; Paganelli, Marcella Oliva; Libardi, Silvia Helena; Deflon, Victor Marcelo ; Oliveira, Carolina G; Oliveira, Ronaldo J; Borges, Julio Cesar ; Maia, Pedro I. S
Source: European Journal of Medicinal Chemistry. Unidades: IQSC, FCFRP, FMRP
Assunto: DOENÇA DE CHAGAS
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ABNT
CARNEIRO, Zumira A et al. Heterobimetallic nickel(II) and palladium(II) complexes derived from S-benzyl-N- (ferrocenyl)methylenedithiocarbazate: Trypanocidal activity and interaction with Trypanosoma cruzi Old Yellow Enzyme (TcOYE). European Journal of Medicinal Chemistry, v. 180, p. 213-223, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2019.07.014. Acesso em: 03 nov. 2024.
APA
Carneiro, Z. A., Gaspari, A. P. S., Lima, J. C., Lopes, C. D., Gaspari, A. P. S., Albuquerque, S. de, et al. (2019). Heterobimetallic nickel(II) and palladium(II) complexes derived from S-benzyl-N- (ferrocenyl)methylenedithiocarbazate: Trypanocidal activity and interaction with Trypanosoma cruzi Old Yellow Enzyme (TcOYE). European Journal of Medicinal Chemistry, 180, 213-223. doi:10.1016/j.ejmech.2019.07.014
NLM
Carneiro ZA, Gaspari APS, Lima JC, Lopes CD, Gaspari APS, Albuquerque S de, Dinelli LR, Silva LLWV da, Paganelli MO, Libardi SH, Deflon VM, Oliveira CG, Oliveira RJ, Borges JC, Maia PIS. Heterobimetallic nickel(II) and palladium(II) complexes derived from S-benzyl-N- (ferrocenyl)methylenedithiocarbazate: Trypanocidal activity and interaction with Trypanosoma cruzi Old Yellow Enzyme (TcOYE) [Internet]. European Journal of Medicinal Chemistry. 2019 ; 180 213-223.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.ejmech.2019.07.014
Vancouver
Carneiro ZA, Gaspari APS, Lima JC, Lopes CD, Gaspari APS, Albuquerque S de, Dinelli LR, Silva LLWV da, Paganelli MO, Libardi SH, Deflon VM, Oliveira CG, Oliveira RJ, Borges JC, Maia PIS. Heterobimetallic nickel(II) and palladium(II) complexes derived from S-benzyl-N- (ferrocenyl)methylenedithiocarbazate: Trypanocidal activity and interaction with Trypanosoma cruzi Old Yellow Enzyme (TcOYE) [Internet]. European Journal of Medicinal Chemistry. 2019 ; 180 213-223.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.ejmech.2019.07.014
Artigo de periodico
Natural products as inhibitors of Leishmania major dihydroorotate dehydrogenase (2018)
Chibli, Lucas Apolinário ; Schmidt, Thomas J.; Nonato, Maria Cristina; Calil, Felipe Antunes ; Costa, Fernando Batista da
Source: European Journal of Medicinal Chemistry. Unidade: FCFRP
Subjects: COMPOSITAE, LEISHMANIA, DOENÇAS NEGLIGENCIADAS, SESQUITERPENOS, INIBIDORES DE ENZIMAS, ENZIMAS OXIRREDUTORAS
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CHIBLI, Lucas Apolinário et al. Natural products as inhibitors of Leishmania major dihydroorotate dehydrogenase. European Journal of Medicinal Chemistry, v. 157, p. 852-866, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2018.08.033. Acesso em: 03 nov. 2024.
APA
Chibli, L. A., Schmidt, T. J., Nonato, M. C., Calil, F. A., & Costa, F. B. da. (2018). Natural products as inhibitors of Leishmania major dihydroorotate dehydrogenase. European Journal of Medicinal Chemistry, 157, 852-866. doi:10.1016/j.ejmech.2018.08.033
NLM
Chibli LA, Schmidt TJ, Nonato MC, Calil FA, Costa FB da. Natural products as inhibitors of Leishmania major dihydroorotate dehydrogenase [Internet]. European Journal of Medicinal Chemistry. 2018 ; 157 852-866.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.ejmech.2018.08.033
Vancouver
Chibli LA, Schmidt TJ, Nonato MC, Calil FA, Costa FB da. Natural products as inhibitors of Leishmania major dihydroorotate dehydrogenase [Internet]. European Journal of Medicinal Chemistry. 2018 ; 157 852-866.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.ejmech.2018.08.033
Artigo de periodico
Chameleon-like behavior of indolylpiperidines in complex with cholinesterases targets: potent butyrylcholinesterase inhibitors (2018)
Chierrito, Talita Perez Cantuaria; Pedersoli-Mantoani, Susimaire; Roca, Carlos; Sebastian-Pérez, Victor; Martínez-Gonzalez, Loreto; Pérez, Daniel I.; Perez, Concepción; Canales, Angeles; Cañada, F. Javier; Campillo, Nuria E.; Carvalho, Ivone; Martinez, Ana
Source: European Journal of Medicinal Chemistry. Unidade: FCFRP
Subjects: DOENÇA DE ALZHEIMER, FARMACOTÉCNICA
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ABNT
CHIERRITO, Talita Perez Cantuaria et al. Chameleon-like behavior of indolylpiperidines in complex with cholinesterases targets: potent butyrylcholinesterase inhibitors. European Journal of Medicinal Chemistry, v. 145, p. 431-444, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2018.01.007. Acesso em: 03 nov. 2024.
APA
Chierrito, T. P. C., Pedersoli-Mantoani, S., Roca, C., Sebastian-Pérez, V., Martínez-Gonzalez, L., Pérez, D. I., et al. (2018). Chameleon-like behavior of indolylpiperidines in complex with cholinesterases targets: potent butyrylcholinesterase inhibitors. European Journal of Medicinal Chemistry, 145, 431-444. doi:10.1016/j.ejmech.2018.01.007
NLM
Chierrito TPC, Pedersoli-Mantoani S, Roca C, Sebastian-Pérez V, Martínez-Gonzalez L, Pérez DI, Perez C, Canales A, Cañada FJ, Campillo NE, Carvalho I, Martinez A. Chameleon-like behavior of indolylpiperidines in complex with cholinesterases targets: potent butyrylcholinesterase inhibitors [Internet]. European Journal of Medicinal Chemistry. 2018 ; 145 431-444.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.ejmech.2018.01.007
Vancouver
Chierrito TPC, Pedersoli-Mantoani S, Roca C, Sebastian-Pérez V, Martínez-Gonzalez L, Pérez DI, Perez C, Canales A, Cañada FJ, Campillo NE, Carvalho I, Martinez A. Chameleon-like behavior of indolylpiperidines in complex with cholinesterases targets: potent butyrylcholinesterase inhibitors [Internet]. European Journal of Medicinal Chemistry. 2018 ; 145 431-444.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.ejmech.2018.01.007
Artigo de periodico
Evaluation of 7-arylaminopyrazolo[1,5- a ]pyrimidines as anti- Plasmodium falciparum , antimalarial, and Pf- dihydroorotate dehydrogenase inhibitors (2017)
Azeredo, Luís Felipe S. P.; Coutinho, Julia P.; Jabor, Valquíria Aparecida Polisel; Feliciano, Patricia R.; Nonato, Maria Cristina; Kaiser, Carlos R.; Menezes, Carla Maria S.; Hammes, Amanda S. O.; Caffarena, Ernesto Raul; Hoelz, Lucas V. B.; Souza, Nicolli B. de; Pereira, Glaécia A. N.; Cerávolo, Isabela P.; Krettli, Antoniana U.; Boechat, Nubia
Source: European Journal of Medicinal Chemistry. Unidade: FCFRP
Subjects: ANTIMALÁRICOS, INIBIDORES DE ENZIMAS
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ABNT
AZEREDO, Luís Felipe S. P. et al. Evaluation of 7-arylaminopyrazolo[1,5- a ]pyrimidines as anti- Plasmodium falciparum , antimalarial, and Pf- dihydroorotate dehydrogenase inhibitors. European Journal of Medicinal Chemistry, v. 126, p. 72-83, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2016.09.073. Acesso em: 03 nov. 2024.
APA
Azeredo, L. F. S. P., Coutinho, J. P., Jabor, V. A. P., Feliciano, P. R., Nonato, M. C., Kaiser, C. R., et al. (2017). Evaluation of 7-arylaminopyrazolo[1,5- a ]pyrimidines as anti- Plasmodium falciparum , antimalarial, and Pf- dihydroorotate dehydrogenase inhibitors. European Journal of Medicinal Chemistry, 126, 72-83. doi:10.1016/j.ejmech.2016.09.073
NLM
Azeredo LFSP, Coutinho JP, Jabor VAP, Feliciano PR, Nonato MC, Kaiser CR, Menezes CMS, Hammes ASO, Caffarena ER, Hoelz LVB, Souza NB de, Pereira GAN, Cerávolo IP, Krettli AU, Boechat N. Evaluation of 7-arylaminopyrazolo[1,5- a ]pyrimidines as anti- Plasmodium falciparum , antimalarial, and Pf- dihydroorotate dehydrogenase inhibitors [Internet]. European Journal of Medicinal Chemistry. 2017 ; 126 72-83.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.ejmech.2016.09.073
Vancouver
Azeredo LFSP, Coutinho JP, Jabor VAP, Feliciano PR, Nonato MC, Kaiser CR, Menezes CMS, Hammes ASO, Caffarena ER, Hoelz LVB, Souza NB de, Pereira GAN, Cerávolo IP, Krettli AU, Boechat N. Evaluation of 7-arylaminopyrazolo[1,5- a ]pyrimidines as anti- Plasmodium falciparum , antimalarial, and Pf- dihydroorotate dehydrogenase inhibitors [Internet]. European Journal of Medicinal Chemistry. 2017 ; 126 72-83.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.ejmech.2016.09.073
Artigo de periodico
From dual binding site acetylcholinesterase inhibitors to allosteric modulators: a new avenue for disease-modifying drugs in Alzheimer's disease (2017)
Chierrito, Talita P. C.; Mantoani, Susimaire Pedersoli; Roca, Carlos; Requena, Carlos; Perez, Victor Sebastian; Castillo, Willian O.; Moreira, Natalia C. S.; Pérez, Concepción; Sakamoto-Hojo, Elza Tiemi; Takahashi, Catarina Satie; Barbero, Jesús Jiménez; Cañada, F. Javier; Campillo, Nuria E.; Martinez, Ana; Carvalho, Ivone
Source: European Journal of Medicinal Chemistry. Unidades: FFCLRP, FCFRP
Subjects: DOENÇA DE ALZHEIMER, INIBIDORES DE ENZIMAS, PROLIFERAÇÃO CELULAR
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ABNT
CHIERRITO, Talita P. C. et al. From dual binding site acetylcholinesterase inhibitors to allosteric modulators: a new avenue for disease-modifying drugs in Alzheimer's disease. European Journal of Medicinal Chemistry, v. 139, p. 773-791, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2017.08.051. Acesso em: 03 nov. 2024.
APA
Chierrito, T. P. C., Mantoani, S. P., Roca, C., Requena, C., Perez, V. S., Castillo, W. O., et al. (2017). From dual binding site acetylcholinesterase inhibitors to allosteric modulators: a new avenue for disease-modifying drugs in Alzheimer's disease. European Journal of Medicinal Chemistry, 139, 773-791. doi:10.1016/j.ejmech.2017.08.051
NLM
Chierrito TPC, Mantoani SP, Roca C, Requena C, Perez VS, Castillo WO, Moreira NCS, Pérez C, Sakamoto-Hojo ET, Takahashi CS, Barbero JJ, Cañada FJ, Campillo NE, Martinez A, Carvalho I. From dual binding site acetylcholinesterase inhibitors to allosteric modulators: a new avenue for disease-modifying drugs in Alzheimer's disease [Internet]. European Journal of Medicinal Chemistry. 2017 ; 139 773-791.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.ejmech.2017.08.051
Vancouver
Chierrito TPC, Mantoani SP, Roca C, Requena C, Perez VS, Castillo WO, Moreira NCS, Pérez C, Sakamoto-Hojo ET, Takahashi CS, Barbero JJ, Cañada FJ, Campillo NE, Martinez A, Carvalho I. From dual binding site acetylcholinesterase inhibitors to allosteric modulators: a new avenue for disease-modifying drugs in Alzheimer's disease [Internet]. European Journal of Medicinal Chemistry. 2017 ; 139 773-791.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.ejmech.2017.08.051
Artigo de periodico
Synthesis and 2D-QSAR studies of neolignan-based diaryl-tetrahydrofuran and -furan analogues with remarkable activity against Trypanosoma cruzi and assessment of the trypanothione reductase activity (2017)
Hartmann, Ana Paula; Carvalho, Marcelo Rodrigues de; Bernardes, Lilian Sibelle Campos; Moraes, Milena Hoehr de; Melo, Eduardo Borges de; Lopes, Carla Duque; Steindel, Mario; Silva, João Santana da; Carvalho, Ivone
Source: European Journal of Medicinal Chemistry. Unidades: FCFRP, FMRP
Subjects: DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI, INIBIDORES DE ENZIMAS
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ABNT
HARTMANN, Ana Paula et al. Synthesis and 2D-QSAR studies of neolignan-based diaryl-tetrahydrofuran and -furan analogues with remarkable activity against Trypanosoma cruzi and assessment of the trypanothione reductase activity. European Journal of Medicinal Chemistry, v. 140, p. 187-199, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2017.08.064. Acesso em: 03 nov. 2024.
APA
Hartmann, A. P., Carvalho, M. R. de, Bernardes, L. S. C., Moraes, M. H. de, Melo, E. B. de, Lopes, C. D., et al. (2017). Synthesis and 2D-QSAR studies of neolignan-based diaryl-tetrahydrofuran and -furan analogues with remarkable activity against Trypanosoma cruzi and assessment of the trypanothione reductase activity. European Journal of Medicinal Chemistry, 140, 187-199. doi:10.1016/j.ejmech.2017.08.064
NLM
Hartmann AP, Carvalho MR de, Bernardes LSC, Moraes MH de, Melo EB de, Lopes CD, Steindel M, Silva JS da, Carvalho I. Synthesis and 2D-QSAR studies of neolignan-based diaryl-tetrahydrofuran and -furan analogues with remarkable activity against Trypanosoma cruzi and assessment of the trypanothione reductase activity [Internet]. European Journal of Medicinal Chemistry. 2017 ; 140 187-199.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.ejmech.2017.08.064
Vancouver
Hartmann AP, Carvalho MR de, Bernardes LSC, Moraes MH de, Melo EB de, Lopes CD, Steindel M, Silva JS da, Carvalho I. Synthesis and 2D-QSAR studies of neolignan-based diaryl-tetrahydrofuran and -furan analogues with remarkable activity against Trypanosoma cruzi and assessment of the trypanothione reductase activity [Internet]. European Journal of Medicinal Chemistry. 2017 ; 140 187-199.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.ejmech.2017.08.064
Artigo de periodico
Use of self-organizing maps and molecular descriptors to predict the cytotoxic activity of sesquiterpene lactones (2008)
Fernandes, Mariane Ballerini; Scotti, Marcus Tullius; Ferreira, Marcelo J. P ; Emerenciano, Vicente de Paulo
Source: European Journal of Medicinal Chemistry. Unidade: IQ
Subjects: SESQUITERPENOS, REDES NEURAIS
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ABNT
FERNANDES, Mariane Ballerini et al. Use of self-organizing maps and molecular descriptors to predict the cytotoxic activity of sesquiterpene lactones. European Journal of Medicinal Chemistry, v. 43, n. 10, p. 2197-2205, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2008.01.003. Acesso em: 03 nov. 2024.
APA
Fernandes, M. B., Scotti, M. T., Ferreira, M. J. P., & Emerenciano, V. de P. (2008). Use of self-organizing maps and molecular descriptors to predict the cytotoxic activity of sesquiterpene lactones. European Journal of Medicinal Chemistry, 43( 10), 2197-2205. doi:10.1016/j.ejmech.2008.01.003
NLM
Fernandes MB, Scotti MT, Ferreira MJP, Emerenciano V de P. Use of self-organizing maps and molecular descriptors to predict the cytotoxic activity of sesquiterpene lactones [Internet]. European Journal of Medicinal Chemistry. 2008 ; 43( 10): 2197-2205.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.ejmech.2008.01.003
Vancouver
Fernandes MB, Scotti MT, Ferreira MJP, Emerenciano V de P. Use of self-organizing maps and molecular descriptors to predict the cytotoxic activity of sesquiterpene lactones [Internet]. European Journal of Medicinal Chemistry. 2008 ; 43( 10): 2197-2205.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.ejmech.2008.01.003
Artigo de periodico
Dihydropyrimidin-(2H)-ones obtained by ultrasound irradiation: a new class of potential antioxidant agents (2006)
Stefani, Hélio Alexandre ; Oliveira, Carlindo Baeta de; Almeida, Roberta Bernardo de; Pereira, Claudio Martim Pereira de; Braga, Rodolpho de Campos; Cella, Rodrigo; Borges, Vanessa Corralo; Savegnago, Lucielli; Nogueira, Cristina Wayne
Source: European Journal of Medicinal Chemistry. Unidade: FCF
Subjects: QUÍMICA FARMACÊUTICA, FARMACOLOGIA, ANTIOXIDANTES (ATIVIDADE), ULTRASSONOGRAFIA
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ABNT
STEFANI, Hélio Alexandre et al. Dihydropyrimidin-(2H)-ones obtained by ultrasound irradiation: a new class of potential antioxidant agents. European Journal of Medicinal Chemistry, v. 41, n. 4, p. 513-518, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2006.01.007. Acesso em: 03 nov. 2024.
APA
Stefani, H. A., Oliveira, C. B. de, Almeida, R. B. de, Pereira, C. M. P. de, Braga, R. de C., Cella, R., et al. (2006). Dihydropyrimidin-(2H)-ones obtained by ultrasound irradiation: a new class of potential antioxidant agents. European Journal of Medicinal Chemistry, 41( 4), 513-518. doi:10.1016/j.ejmech.2006.01.007
NLM
Stefani HA, Oliveira CB de, Almeida RB de, Pereira CMP de, Braga R de C, Cella R, Borges VC, Savegnago L, Nogueira CW. Dihydropyrimidin-(2H)-ones obtained by ultrasound irradiation: a new class of potential antioxidant agents [Internet]. European Journal of Medicinal Chemistry. 2006 ; 41( 4): 513-518.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.ejmech.2006.01.007
Vancouver
Stefani HA, Oliveira CB de, Almeida RB de, Pereira CMP de, Braga R de C, Cella R, Borges VC, Savegnago L, Nogueira CW. Dihydropyrimidin-(2H)-ones obtained by ultrasound irradiation: a new class of potential antioxidant agents [Internet]. European Journal of Medicinal Chemistry. 2006 ; 41( 4): 513-518.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.ejmech.2006.01.007

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