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Brazilian Journal of Pharmaceutical Sciences. . São Paulo: Universidade de São Paulo - USP, Faculdade de Ciências Farmacêuticas - FCF. . Acesso em: 27 jun. 2024. , 2016
APA
Brazilian Journal of Pharmaceutical Sciences. (2016). Brazilian Journal of Pharmaceutical Sciences. São Paulo: Universidade de São Paulo - USP, Faculdade de Ciências Farmacêuticas - FCF.
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Brazilian Journal of Pharmaceutical Sciences. . São Paulo: Universidade de São Paulo - Faculdade de Ciências Farmacêuticas. . Acesso em: 27 jun. 2024. , 2015
APA
Brazilian Journal of Pharmaceutical Sciences. (2015). Brazilian Journal of Pharmaceutical Sciences. São Paulo: Universidade de São Paulo - Faculdade de Ciências Farmacêuticas.
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Brazilian Journal of Pharmaceutical Sciences. . São Paulo: Universidade de São Paulo - Faculdade de Ciências Farmacêuticas. . Acesso em: 27 jun. 2024. , 2014
APA
Brazilian Journal of Pharmaceutical Sciences. (2014). Brazilian Journal of Pharmaceutical Sciences. São Paulo: Universidade de São Paulo - Faculdade de Ciências Farmacêuticas.
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SERAFIM, Ricardo Augusto Massarico et al. Design, synthesis and biological evaluation of hybrid bioisoster derivatives of N-acylhydrazone and furoxan groups with potential and selective anti-Trypanosoma cruzi activity. European Journal of Medicinal Chemistry, v. 82, p. 418-425, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2014.05.077. Acesso em: 27 jun. 2024.
APA
Serafim, R. A. M., Gonçalves, J. E., Souza, F. P. de, Loureiro, A. P. de M., Storpirtis, S., Krogh, R., et al. (2014). Design, synthesis and biological evaluation of hybrid bioisoster derivatives of N-acylhydrazone and furoxan groups with potential and selective anti-Trypanosoma cruzi activity. European Journal of Medicinal Chemistry, 82, 418-425. doi:10.1016/j.ejmech.2014.05.077
NLM
Serafim RAM, Gonçalves JE, Souza FP de, Loureiro AP de M, Storpirtis S, Krogh R, Andricopulo AD, Dias LC, Ferreira EI. Design, synthesis and biological evaluation of hybrid bioisoster derivatives of N-acylhydrazone and furoxan groups with potential and selective anti-Trypanosoma cruzi activity [Internet]. European Journal of Medicinal Chemistry. 2014 ; 82 418-425.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.ejmech.2014.05.077
Vancouver
Serafim RAM, Gonçalves JE, Souza FP de, Loureiro AP de M, Storpirtis S, Krogh R, Andricopulo AD, Dias LC, Ferreira EI. Design, synthesis and biological evaluation of hybrid bioisoster derivatives of N-acylhydrazone and furoxan groups with potential and selective anti-Trypanosoma cruzi activity [Internet]. European Journal of Medicinal Chemistry. 2014 ; 82 418-425.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.ejmech.2014.05.077
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Brazilian Journal of Pharmaceutical Sciences. . São Paulo: Universidade de São Paulo - Faculdade de Ciências Farmacêuticas. . Acesso em: 27 jun. 2024. , 2013
APA
Brazilian Journal of Pharmaceutical Sciences. (2013). Brazilian Journal of Pharmaceutical Sciences. São Paulo: Universidade de São Paulo - Faculdade de Ciências Farmacêuticas.
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Brazilian Journal of Pharmaceutical Sciences. . São Paulo: Universidade de São Paulo - Faculdade de Ciências Farmacêuticas. . Acesso em: 27 jun. 2024. , 2011
APA
Brazilian Journal of Pharmaceutical Sciences. (2011). Brazilian Journal of Pharmaceutical Sciences. São Paulo: Universidade de São Paulo - Faculdade de Ciências Farmacêuticas.
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LA-SCALEA, Mauro Aquiles et al. Electrochemical reduction using glassy carbon electrode in aqueous medium of a potential anti-Chagas drug: NFOH. Journal of the Electrochemical Society, v. 156, n. 7, p. F93-F97, 2009Tradução . . Disponível em: http://scitation.aip.org/getpdf/servlet/GetPDFServlet?filetype=pdf&id=JESOAN000156000007000F93000001&idtype=cvips&prog=normal. Acesso em: 27 jun. 2024.
APA
La-Scalea, M. A., Trossini, G. H. G., Menezes, C. M. de S., Chung, M. C., & Ferreira, E. I. (2009). Electrochemical reduction using glassy carbon electrode in aqueous medium of a potential anti-Chagas drug: NFOH. Journal of the Electrochemical Society, 156( 7), F93-F97. Recuperado de http://scitation.aip.org/getpdf/servlet/GetPDFServlet?filetype=pdf&id=JESOAN000156000007000F93000001&idtype=cvips&prog=normal
NLM
La-Scalea MA, Trossini GHG, Menezes CM de S, Chung MC, Ferreira EI. Electrochemical reduction using glassy carbon electrode in aqueous medium of a potential anti-Chagas drug: NFOH [Internet]. Journal of the Electrochemical Society. 2009 ; 156( 7): F93-F97.[citado 2024 jun. 27 ] Available from: http://scitation.aip.org/getpdf/servlet/GetPDFServlet?filetype=pdf&id=JESOAN000156000007000F93000001&idtype=cvips&prog=normal
Vancouver
La-Scalea MA, Trossini GHG, Menezes CM de S, Chung MC, Ferreira EI. Electrochemical reduction using glassy carbon electrode in aqueous medium of a potential anti-Chagas drug: NFOH [Internet]. Journal of the Electrochemical Society. 2009 ; 156( 7): F93-F97.[citado 2024 jun. 27 ] Available from: http://scitation.aip.org/getpdf/servlet/GetPDFServlet?filetype=pdf&id=JESOAN000156000007000F93000001&idtype=cvips&prog=normal
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TROSSINI, Gustavo Henrique Goulart et al. Quantitative structure-activity relationships for a series of inhibitors of cruzain from Trypanosoma cruzi: molecular modeling, CoMFA and CoMSIA studies. Journal of Molecular Graphics and Modelling, v. 28, n. 1, p. 3-11, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.jmgm.2009.03.001. Acesso em: 27 jun. 2024.
APA
Trossini, G. H. G., Guido, R. V. C., Oliva, G., Ferreira, E. I., & Andricopulo, A. D. (2009). Quantitative structure-activity relationships for a series of inhibitors of cruzain from Trypanosoma cruzi: molecular modeling, CoMFA and CoMSIA studies. Journal of Molecular Graphics and Modelling, 28( 1), 3-11. doi:10.1016/j.jmgm.2009.03.001
NLM
Trossini GHG, Guido RVC, Oliva G, Ferreira EI, Andricopulo AD. Quantitative structure-activity relationships for a series of inhibitors of cruzain from Trypanosoma cruzi: molecular modeling, CoMFA and CoMSIA studies [Internet]. Journal of Molecular Graphics and Modelling. 2009 ; 28( 1): 3-11.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.jmgm.2009.03.001
Vancouver
Trossini GHG, Guido RVC, Oliva G, Ferreira EI, Andricopulo AD. Quantitative structure-activity relationships for a series of inhibitors of cruzain from Trypanosoma cruzi: molecular modeling, CoMFA and CoMSIA studies [Internet]. Journal of Molecular Graphics and Modelling. 2009 ; 28( 1): 3-11.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.jmgm.2009.03.001
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SILVA, Márcia da et al. Topliss method in the optimization of salicylic acid derivatives as potential antimycobacterial agents. Chemical Biology & Drug Design, v. 71, n. 2, p. 167-172, 2008Tradução . . Acesso em: 27 jun. 2024.
APA
Silva, M. da, Menezes, C. M. de S., Ferreira, E. I., Leite, C. Q. F., Sato, D. N., Correia, C. C., et al. (2008). Topliss method in the optimization of salicylic acid derivatives as potential antimycobacterial agents. Chemical Biology & Drug Design, 71( 2), 167-172.
NLM
Silva M da, Menezes CM de S, Ferreira EI, Leite CQF, Sato DN, Correia CC, Pimenta CP, Botelho KCA. Topliss method in the optimization of salicylic acid derivatives as potential antimycobacterial agents. Chemical Biology & Drug Design. 2008 ;71( 2): 167-172.[citado 2024 jun. 27 ]
Vancouver
Silva M da, Menezes CM de S, Ferreira EI, Leite CQF, Sato DN, Correia CC, Pimenta CP, Botelho KCA. Topliss method in the optimization of salicylic acid derivatives as potential antimycobacterial agents. Chemical Biology & Drug Design. 2008 ;71( 2): 167-172.[citado 2024 jun. 27 ]
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RANDO, Daniela Gonçales et al. Antileishmanial activity screening of 5-nitro-2-heterocyclic benzylidene hydrazides. Bioorganic and Medicinal Chemistry, v. 16, n. 14, p. 6724-6731, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2008.05.076. Acesso em: 27 jun. 2024.
APA
Rando, D. G., Avery, M. A., Tekwani, B. L., Khan, S. I., & Ferreira, E. I. (2008). Antileishmanial activity screening of 5-nitro-2-heterocyclic benzylidene hydrazides. Bioorganic and Medicinal Chemistry, 16( 14), 6724-6731. doi:10.1016/j.bmc.2008.05.076
NLM
Rando DG, Avery MA, Tekwani BL, Khan SI, Ferreira EI. Antileishmanial activity screening of 5-nitro-2-heterocyclic benzylidene hydrazides [Internet]. Bioorganic and Medicinal Chemistry. 2008 ; 16( 14): 6724-6731.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.bmc.2008.05.076
Vancouver
Rando DG, Avery MA, Tekwani BL, Khan SI, Ferreira EI. Antileishmanial activity screening of 5-nitro-2-heterocyclic benzylidene hydrazides [Internet]. Bioorganic and Medicinal Chemistry. 2008 ; 16( 14): 6724-6731.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.bmc.2008.05.076
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ANDRADE, Carolina Horta et al. Tree-dimensional quantitative structure-activity relationships for a large series of potent antitubercular agents. Letters in Drug Design and Discovery, v. 5, n. 6, p. 377-387, 2008Tradução . . Disponível em: https://doi.org/10.2174/157018008785777289. Acesso em: 27 jun. 2024.
APA
Andrade, C. H., Salum, L. de B., Pasqualoto, K. F. M., Ferreira, E. I., & Andricopulo, A. D. (2008). Tree-dimensional quantitative structure-activity relationships for a large series of potent antitubercular agents. Letters in Drug Design and Discovery, 5( 6), 377-387. doi:10.2174/157018008785777289
NLM
Andrade CH, Salum L de B, Pasqualoto KFM, Ferreira EI, Andricopulo AD. Tree-dimensional quantitative structure-activity relationships for a large series of potent antitubercular agents [Internet]. Letters in Drug Design and Discovery. 2008 ; 5( 6): 377-387.[citado 2024 jun. 27 ] Available from: https://doi.org/10.2174/157018008785777289
Vancouver
Andrade CH, Salum L de B, Pasqualoto KFM, Ferreira EI, Andricopulo AD. Tree-dimensional quantitative structure-activity relationships for a large series of potent antitubercular agents [Internet]. Letters in Drug Design and Discovery. 2008 ; 5( 6): 377-387.[citado 2024 jun. 27 ] Available from: https://doi.org/10.2174/157018008785777289
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BRAGA, Mara Elga Medeiros et al. Supercritical solvent impregnation of ophthalmic drugs on chitosan derivatives. Journal of Supercritical Fluids, v. 44, n. 2, p. 245-257, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.supflu.2007.10.002. Acesso em: 27 jun. 2024.
APA
Braga, M. E. M., Pato, M. T. V., Silva, H. S. R. C., Ferreira, E. I., Gil, M. H., Duarte, C. M. M., & Sousa, H. C. de. (2008). Supercritical solvent impregnation of ophthalmic drugs on chitosan derivatives. Journal of Supercritical Fluids, 44( 2), 245-257. doi:10.1016/j.supflu.2007.10.002
NLM
Braga MEM, Pato MTV, Silva HSRC, Ferreira EI, Gil MH, Duarte CMM, Sousa HC de. Supercritical solvent impregnation of ophthalmic drugs on chitosan derivatives [Internet]. Journal of Supercritical Fluids. 2008 ;44( 2): 245-257.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.supflu.2007.10.002
Vancouver
Braga MEM, Pato MTV, Silva HSRC, Ferreira EI, Gil MH, Duarte CMM, Sousa HC de. Supercritical solvent impregnation of ophthalmic drugs on chitosan derivatives [Internet]. Journal of Supercritical Fluids. 2008 ;44( 2): 245-257.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.supflu.2007.10.002
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ANDRADE, Carolina H. et al. Fragment-based and classical quantitative structure-activity relationships for a series of hydrazides as antituberculosis agents. Molecular Diversity, v. 12, n. 1, p. 47-59, 2008Tradução . . Disponível em: https://doi.org/10.1007/s11030-008-9074-z. Acesso em: 27 jun. 2024.
APA
Andrade, C. H., Salum, L. B., Castilho, M. S., Pasqualoto, K. F. M., Ferreira, E. I., & Andricopulo, A. D. (2008). Fragment-based and classical quantitative structure-activity relationships for a series of hydrazides as antituberculosis agents. Molecular Diversity, 12( 1), 47-59. doi:10.1007/s11030-008-9074-z
NLM
Andrade CH, Salum LB, Castilho MS, Pasqualoto KFM, Ferreira EI, Andricopulo AD. Fragment-based and classical quantitative structure-activity relationships for a series of hydrazides as antituberculosis agents [Internet]. Molecular Diversity. 2008 ; 12( 1): 47-59.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1007/s11030-008-9074-z
Vancouver
Andrade CH, Salum LB, Castilho MS, Pasqualoto KFM, Ferreira EI, Andricopulo AD. Fragment-based and classical quantitative structure-activity relationships for a series of hydrazides as antituberculosis agents [Internet]. Molecular Diversity. 2008 ; 12( 1): 47-59.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1007/s11030-008-9074-z
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GUIDO, Rafael V. C. et al. Structure-activity relationships for a class of selective inhibitors of the major cysteine protease from Trypanosoma cruzi. Journal of Enzyme Inhibition and Medicinal Chemistry, v. 23, n. 6, p. 964-973, 2008Tradução . . Disponível em: https://doi.org/10.1080/14756360701810322. Acesso em: 27 jun. 2024.
APA
Guido, R. V. C., Trossini, G. H. G., Castilho, M. S., Oliva, G., Ferreira, E. I., & Andricopulo, A. D. (2008). Structure-activity relationships for a class of selective inhibitors of the major cysteine protease from Trypanosoma cruzi. Journal of Enzyme Inhibition and Medicinal Chemistry, 23( 6), 964-973. doi:10.1080/14756360701810322
NLM
Guido RVC, Trossini GHG, Castilho MS, Oliva G, Ferreira EI, Andricopulo AD. Structure-activity relationships for a class of selective inhibitors of the major cysteine protease from Trypanosoma cruzi [Internet]. Journal of Enzyme Inhibition and Medicinal Chemistry. 2008 ; 23( 6): 964-973.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1080/14756360701810322
Vancouver
Guido RVC, Trossini GHG, Castilho MS, Oliva G, Ferreira EI, Andricopulo AD. Structure-activity relationships for a class of selective inhibitors of the major cysteine protease from Trypanosoma cruzi [Internet]. Journal of Enzyme Inhibition and Medicinal Chemistry. 2008 ; 23( 6): 964-973.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1080/14756360701810322
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BARBOSA, Carolina Fregonesi et al. Rapid test for the evaluation of the activity of the prodrug hydroxymethylnitrofurazone in the processing of Trypanosoma cruzi messenger RNAs. Brazilian Journal of Medical and Biological Research, v. 40, n. 1, p. 33-39, 2007Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2007000100005. Acesso em: 27 jun. 2024.
APA
Barbosa, C. F., Okuda, E. S., Chung, M. C., Ferreira, E. I., & Cicarelli, R. M. B. (2007). Rapid test for the evaluation of the activity of the prodrug hydroxymethylnitrofurazone in the processing of Trypanosoma cruzi messenger RNAs. Brazilian Journal of Medical and Biological Research, 40( 1), 33-39. doi:10.1590/s0100-879x2007000100005
NLM
Barbosa CF, Okuda ES, Chung MC, Ferreira EI, Cicarelli RMB. Rapid test for the evaluation of the activity of the prodrug hydroxymethylnitrofurazone in the processing of Trypanosoma cruzi messenger RNAs [Internet]. Brazilian Journal of Medical and Biological Research. 2007 ; 40( 1): 33-39.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1590/s0100-879x2007000100005
Vancouver
Barbosa CF, Okuda ES, Chung MC, Ferreira EI, Cicarelli RMB. Rapid test for the evaluation of the activity of the prodrug hydroxymethylnitrofurazone in the processing of Trypanosoma cruzi messenger RNAs [Internet]. Brazilian Journal of Medical and Biological Research. 2007 ; 40( 1): 33-39.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1590/s0100-879x2007000100005
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SCOTTI, Luciana et al. Quantitative elucidation of the structure-bitterness relationship of cynaropicrin and grosheimin derivatives. Food Chemistry, v. 105, n. 1, p. 77-83, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.foodchem.2007.03.038. Acesso em: 27 jun. 2024.
APA
Scotti, L., Scotti, M. T., Ishiki, H. M., Ferreira, M. J. P., Emerenciano, V. de P., Menezes, C. M. de S., & Ferreira, E. I. (2007). Quantitative elucidation of the structure-bitterness relationship of cynaropicrin and grosheimin derivatives. Food Chemistry, 105( 1), 77-83. doi:10.1016/j.foodchem.2007.03.038
NLM
Scotti L, Scotti MT, Ishiki HM, Ferreira MJP, Emerenciano V de P, Menezes CM de S, Ferreira EI. Quantitative elucidation of the structure-bitterness relationship of cynaropicrin and grosheimin derivatives [Internet]. Food Chemistry. 2007 ; 105( 1): 77-83.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.foodchem.2007.03.038
Vancouver
Scotti L, Scotti MT, Ishiki HM, Ferreira MJP, Emerenciano V de P, Menezes CM de S, Ferreira EI. Quantitative elucidation of the structure-bitterness relationship of cynaropicrin and grosheimin derivatives [Internet]. Food Chemistry. 2007 ; 105( 1): 77-83.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.foodchem.2007.03.038
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SILVA, Márcia da et al. Preparation of polymeric Micelles for use as carries of tuberculostatic drugs. Tropical Journal of Pharmaceutical Research, v. 6, n. 4, p. 815-824, 2007Tradução . . Disponível em: http://www.tjpr.org/vol6_no4/644Marcia.pdf. Acesso em: 27 jun. 2024.
APA
Silva, M. da, Ferreira, E. I., Leite, C. Q. F., & Sato, D. N. (2007). Preparation of polymeric Micelles for use as carries of tuberculostatic drugs. Tropical Journal of Pharmaceutical Research, 6( 4), 815-824. Recuperado de http://www.tjpr.org/vol6_no4/644Marcia.pdf
NLM
Silva M da, Ferreira EI, Leite CQF, Sato DN. Preparation of polymeric Micelles for use as carries of tuberculostatic drugs [Internet]. Tropical Journal of Pharmaceutical Research. 2007 ; 6( 4): 815-824.[citado 2024 jun. 27 ] Available from: http://www.tjpr.org/vol6_no4/644Marcia.pdf
Vancouver
Silva M da, Ferreira EI, Leite CQF, Sato DN. Preparation of polymeric Micelles for use as carries of tuberculostatic drugs [Internet]. Tropical Journal of Pharmaceutical Research. 2007 ; 6( 4): 815-824.[citado 2024 jun. 27 ] Available from: http://www.tjpr.org/vol6_no4/644Marcia.pdf
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RANDO, D. G. et al. A duplicated nitrotienyl derivative with antimycobacterial activity synthesis, x-ray crystallography, biological and mutagenic activity tests. European Journal of Medicinal Chemistry, v. 41, n. 10, p. 1196-1200, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2006.04.009. Acesso em: 27 jun. 2024.
APA
Rando, D. G., Doriguetto, A. C., Silva, C. H. T. de P. da, Ellena, J., Sato, D. N., Leite, C. Q. F., et al. (2006). A duplicated nitrotienyl derivative with antimycobacterial activity synthesis, x-ray crystallography, biological and mutagenic activity tests. European Journal of Medicinal Chemistry, 41( 10), 1196-1200. doi:10.1016/j.ejmech.2006.04.009
NLM
Rando DG, Doriguetto AC, Silva CHT de P da, Ellena J, Sato DN, Leite CQF, Varanda EA, Ferreira EI. A duplicated nitrotienyl derivative with antimycobacterial activity synthesis, x-ray crystallography, biological and mutagenic activity tests [Internet]. European Journal of Medicinal Chemistry. 2006 ; 41( 10): 1196-1200.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.ejmech.2006.04.009
Vancouver
Rando DG, Doriguetto AC, Silva CHT de P da, Ellena J, Sato DN, Leite CQF, Varanda EA, Ferreira EI. A duplicated nitrotienyl derivative with antimycobacterial activity synthesis, x-ray crystallography, biological and mutagenic activity tests [Internet]. European Journal of Medicinal Chemistry. 2006 ; 41( 10): 1196-1200.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.ejmech.2006.04.009
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ABNT
LA-SCALEA, Mauro Aquiles et al. Molecular modeling of the voltammetric oxidation at a glassy carbon electrode of the antimalarial drug primaquine and its prodrugs succinylprimaquine and maleylprimaquine. Electrochimica Acta, v. 51, n. 24, p. 5103-5111, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.electacta.2006.03.085. Acesso em: 27 jun. 2024.
APA
La-Scalea, M. A., Menezes, C. M. de S., Matsutani, G. C., Polli, M. C., Serrano, S. H. P., & Ferreira, E. I. (2006). Molecular modeling of the voltammetric oxidation at a glassy carbon electrode of the antimalarial drug primaquine and its prodrugs succinylprimaquine and maleylprimaquine. Electrochimica Acta, 51( 24), 5103-5111. doi:10.1016/j.electacta.2006.03.085
NLM
La-Scalea MA, Menezes CM de S, Matsutani GC, Polli MC, Serrano SHP, Ferreira EI. Molecular modeling of the voltammetric oxidation at a glassy carbon electrode of the antimalarial drug primaquine and its prodrugs succinylprimaquine and maleylprimaquine [Internet]. Electrochimica Acta. 2006 ; 51( 24): 5103-5111.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.electacta.2006.03.085
Vancouver
La-Scalea MA, Menezes CM de S, Matsutani GC, Polli MC, Serrano SHP, Ferreira EI. Molecular modeling of the voltammetric oxidation at a glassy carbon electrode of the antimalarial drug primaquine and its prodrugs succinylprimaquine and maleylprimaquine [Internet]. Electrochimica Acta. 2006 ; 51( 24): 5103-5111.[citado 2024 jun. 27 ] Available from: https://doi.org/10.1016/j.electacta.2006.03.085
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ABNT
SILVA, Marcia et al. Potential tuberculostatic agent: Micelle-forming pyrazinamide prodrug. Archiv der Pharmazie, v. 339, n. 6, p. 283-290, 2006Tradução . . Acesso em: 27 jun. 2024.
APA
Silva, M., Ricelli, N. L., El Seoud, O. A., Valentim, C. S., Ferreira, A. G., Sato, D. N., et al. (2006). Potential tuberculostatic agent: Micelle-forming pyrazinamide prodrug. Archiv der Pharmazie, 339( 6), 283-290.
NLM
Silva M, Ricelli NL, El Seoud OA, Valentim CS, Ferreira AG, Sato DN, Leite CQF, Ferreira EI. Potential tuberculostatic agent: Micelle-forming pyrazinamide prodrug. Archiv der Pharmazie. 2006 ; 339( 6): 283-290.[citado 2024 jun. 27 ]
Vancouver
Silva M, Ricelli NL, El Seoud OA, Valentim CS, Ferreira AG, Sato DN, Leite CQF, Ferreira EI. Potential tuberculostatic agent: Micelle-forming pyrazinamide prodrug. Archiv der Pharmazie. 2006 ; 339( 6): 283-290.[citado 2024 jun. 27 ]