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Artigo de periodico
Knowing and combating the enemy: a brief review on SARS-CoV-2 and computational approaches applied to the discovery of drug candidates (2021)
Serafim, Mateus Sá Magalhães ; Gertrudes, Jadson Castro ; Costa, Debora M.A.; Oliveira, Patrícia Rufino; Maltarollo, Vinícius Gonçalves ; Honório, Káthia Maria
Fonte: Bioscience Reports. Unidade: EACH
Assuntos: COVID-19, INTELIGÊNCIA ARTIFICIAL, APRENDIZADO COMPUTACIONAL, PLANEJAMENTO DE FÁRMACOS, QUÍMICA MÉDICA
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SERAFIM, Mateus Sá Magalhães et al. Knowing and combating the enemy: a brief review on SARS-CoV-2 and computational approaches applied to the discovery of drug candidates. Bioscience Reports, v. 41, n. 3, p. 01-16, 2021Tradução . . Disponível em: https://doi.org/10.1042/BSR20202616. Acesso em: 01 nov. 2024.
APA
Serafim, M. S. M., Gertrudes, J. C., Costa, D. M. A., Oliveira, P. R., Maltarollo, V. G., & Honório, K. M. (2021). Knowing and combating the enemy: a brief review on SARS-CoV-2 and computational approaches applied to the discovery of drug candidates. Bioscience Reports, 41( 3), 01-16. doi:10.1042/BSR20202616
NLM
Serafim MSM, Gertrudes JC, Costa DMA, Oliveira PR, Maltarollo VG, Honório KM. Knowing and combating the enemy: a brief review on SARS-CoV-2 and computational approaches applied to the discovery of drug candidates [Internet]. Bioscience Reports. 2021 ; 41( 3): 01-16.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1042/BSR20202616
Vancouver
Serafim MSM, Gertrudes JC, Costa DMA, Oliveira PR, Maltarollo VG, Honório KM. Knowing and combating the enemy: a brief review on SARS-CoV-2 and computational approaches applied to the discovery of drug candidates [Internet]. Bioscience Reports. 2021 ; 41( 3): 01-16.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1042/BSR20202616
Artigo de periodico
Inhibition of Mycobacterium tuberculosis tyrosine phosphatase PtpA by synthetic chalcones: kinetics, molecular modeling, toxicity and effect on growth (2010)
Mascarello, Alessandra; Chiaradia, Louise Domeneghini; Vernal, Javier; Villarino, Andrea; Guido, Rafael Victorio Carvalho ; Perizzolo, Paulo; Poirier, Valerie; Wong, Dennis; Martins, Priscila Graziela Alves; Nunes, Ricardo José; Yunes, Rosendo Augusto; Andricopulo, Adriano Defini ; Av-Gay, Yossef; Terenzi, Hernán
Fonte: Bioorganic and Medicinal Chemistry. Unidade: IFSC
Assuntos: PLANEJAMENTO DE FÁRMACOS, MODELAGEM MOLECULAR, INIBIDORES DE ENZIMAS, TUBERCULOSE
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MASCARELLO, Alessandra et al. Inhibition of Mycobacterium tuberculosis tyrosine phosphatase PtpA by synthetic chalcones: kinetics, molecular modeling, toxicity and effect on growth. Bioorganic and Medicinal Chemistry, v. 18, n. 11, p. 3783-3789, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2010.04.051. Acesso em: 01 nov. 2024.
APA
Mascarello, A., Chiaradia, L. D., Vernal, J., Villarino, A., Guido, R. V. C., Perizzolo, P., et al. (2010). Inhibition of Mycobacterium tuberculosis tyrosine phosphatase PtpA by synthetic chalcones: kinetics, molecular modeling, toxicity and effect on growth. Bioorganic and Medicinal Chemistry, 18( 11), 3783-3789. doi:10.1016/j.bmc.2010.04.051
NLM
Mascarello A, Chiaradia LD, Vernal J, Villarino A, Guido RVC, Perizzolo P, Poirier V, Wong D, Martins PGA, Nunes RJ, Yunes RA, Andricopulo AD, Av-Gay Y, Terenzi H. Inhibition of Mycobacterium tuberculosis tyrosine phosphatase PtpA by synthetic chalcones: kinetics, molecular modeling, toxicity and effect on growth [Internet]. Bioorganic and Medicinal Chemistry. 2010 ; 18( 11): 3783-3789.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.bmc.2010.04.051
Vancouver
Mascarello A, Chiaradia LD, Vernal J, Villarino A, Guido RVC, Perizzolo P, Poirier V, Wong D, Martins PGA, Nunes RJ, Yunes RA, Andricopulo AD, Av-Gay Y, Terenzi H. Inhibition of Mycobacterium tuberculosis tyrosine phosphatase PtpA by synthetic chalcones: kinetics, molecular modeling, toxicity and effect on growth [Internet]. Bioorganic and Medicinal Chemistry. 2010 ; 18( 11): 3783-3789.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.bmc.2010.04.051
Artigo de periodico
Structural basis for selective inhibition of purine nucleoside phosphorylase from Schistosoma mansoni: kinetic and structural studies (2010)
Castilho, Marcelo S.; Postigo, Matheus P.; Pereira, Humberto d'Muniz; Oliva, Glaucius ; Andricopulo, Adriano Defini
Fonte: Bioorganic and Medicinal Chemistry. Unidade: IFSC
Assuntos: PLANEJAMENTO DE FÁRMACOS, QUÍMICA MÉDICA, INIBIDORES DE ENZIMAS, SCHISTOSOMA MANSONI
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CASTILHO, Marcelo S. et al. Structural basis for selective inhibition of purine nucleoside phosphorylase from Schistosoma mansoni: kinetic and structural studies. Bioorganic and Medicinal Chemistry, v. 18, n. 4, p. 1421-1427, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2010.01.022. Acesso em: 01 nov. 2024.
APA
Castilho, M. S., Postigo, M. P., Pereira, H. d'M., Oliva, G., & Andricopulo, A. D. (2010). Structural basis for selective inhibition of purine nucleoside phosphorylase from Schistosoma mansoni: kinetic and structural studies. Bioorganic and Medicinal Chemistry, 18( 4), 1421-1427. doi:10.1016/j.bmc.2010.01.022
NLM
Castilho MS, Postigo MP, Pereira H d'M, Oliva G, Andricopulo AD. Structural basis for selective inhibition of purine nucleoside phosphorylase from Schistosoma mansoni: kinetic and structural studies [Internet]. Bioorganic and Medicinal Chemistry. 2010 ; 18( 4): 1421-1427.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.bmc.2010.01.022
Vancouver
Castilho MS, Postigo MP, Pereira H d'M, Oliva G, Andricopulo AD. Structural basis for selective inhibition of purine nucleoside phosphorylase from Schistosoma mansoni: kinetic and structural studies [Internet]. Bioorganic and Medicinal Chemistry. 2010 ; 18( 4): 1421-1427.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.bmc.2010.01.022
Artigo de periodico
Fragment-based QSAR strategies in drug design (2010)
Salum, Livia B.; Andricopulo, Adriano Defini
Fonte: Expert Opinion on Drug Discovery. Unidade: IFSC
Assuntos: QUÍMICA MÉDICA, RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA, PLANEJAMENTO DE FÁRMACOS
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SALUM, Livia B. e ANDRICOPULO, Adriano Defini. Fragment-based QSAR strategies in drug design. Expert Opinion on Drug Discovery, v. 5, n. 5, p. 405-412, 2010Tradução . . Disponível em: https://doi.org/10.1517/17460441003782277. Acesso em: 01 nov. 2024.
APA
Salum, L. B., & Andricopulo, A. D. (2010). Fragment-based QSAR strategies in drug design. Expert Opinion on Drug Discovery, 5( 5), 405-412. doi:10.1517/17460441003782277
NLM
Salum LB, Andricopulo AD. Fragment-based QSAR strategies in drug design [Internet]. Expert Opinion on Drug Discovery. 2010 ; 5( 5): 405-412.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1517/17460441003782277
Vancouver
Salum LB, Andricopulo AD. Fragment-based QSAR strategies in drug design [Internet]. Expert Opinion on Drug Discovery. 2010 ; 5( 5): 405-412.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1517/17460441003782277
Trabalho de evento-resumo
Study of the solid-state properties of two non-bioequivalent forms of 5e-phenylethenylbenzofuroxan (2010)
Gonzalez, Mercedes; Cerecetto, Hugo; Honorato, Sara B.; Ellena, Javier ; Ayala, Alejandro P.
Fonte: Abstracts. Nome do evento: Reunión Anual de la Asociación Argentina de Cristalografia - AACr. Unidade: IFSC
Assuntos: DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI, PLANEJAMENTO DE FÁRMACOS, DIFRAÇÃO POR RAIOS X
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GONZALEZ, Mercedes et al. Study of the solid-state properties of two non-bioequivalent forms of 5e-phenylethenylbenzofuroxan. 2010, Anais.. Chester: International Union of Crystallography - IUCr, 2010. . Acesso em: 01 nov. 2024.
APA
Gonzalez, M., Cerecetto, H., Honorato, S. B., Ellena, J., & Ayala, A. P. (2010). Study of the solid-state properties of two non-bioequivalent forms of 5e-phenylethenylbenzofuroxan. In Abstracts. Chester: International Union of Crystallography - IUCr.
NLM
Gonzalez M, Cerecetto H, Honorato SB, Ellena J, Ayala AP. Study of the solid-state properties of two non-bioequivalent forms of 5e-phenylethenylbenzofuroxan. Abstracts. 2010 ;[citado 2024 nov. 01 ]
Vancouver
Gonzalez M, Cerecetto H, Honorato SB, Ellena J, Ayala AP. Study of the solid-state properties of two non-bioequivalent forms of 5e-phenylethenylbenzofuroxan. Abstracts. 2010 ;[citado 2024 nov. 01 ]
Artigo de periodico
Effectiveness of commercial inhibitors against subtype F HIV-1 protease (2009)
Krauchenco, Sandra; Martins, Nádia H.; Sanches, Mario; Polikarpov, Igor
Fonte: Journal of Enzyme Inhibition and Medicinal Chemistry. Unidade: IFSC
Assuntos: INIBIDORES DE ENZIMAS, HIV, PLANEJAMENTO DE FÁRMACOS, SÍNDROME DE IMUNODEFICIÊNCIA ADQUIRIDA, POLIMORFISMO
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ABNT
KRAUCHENCO, Sandra et al. Effectiveness of commercial inhibitors against subtype F HIV-1 protease. Journal of Enzyme Inhibition and Medicinal Chemistry, v. 24, n. 3, p. 638-645, 2009Tradução . . Disponível em: https://doi.org/10.1080/14756360802321740. Acesso em: 01 nov. 2024.
APA
Krauchenco, S., Martins, N. H., Sanches, M., & Polikarpov, I. (2009). Effectiveness of commercial inhibitors against subtype F HIV-1 protease. Journal of Enzyme Inhibition and Medicinal Chemistry, 24( 3), 638-645. doi:10.1080/14756360802321740
NLM
Krauchenco S, Martins NH, Sanches M, Polikarpov I. Effectiveness of commercial inhibitors against subtype F HIV-1 protease [Internet]. Journal of Enzyme Inhibition and Medicinal Chemistry. 2009 ; 24( 3): 638-645.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1080/14756360802321740
Vancouver
Krauchenco S, Martins NH, Sanches M, Polikarpov I. Effectiveness of commercial inhibitors against subtype F HIV-1 protease [Internet]. Journal of Enzyme Inhibition and Medicinal Chemistry. 2009 ; 24( 3): 638-645.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1080/14756360802321740
Artigo de periodico
Inhibition of Trypanosoma brucei glucose-6-phosphate dehydrogenase by human steroids and their effects on the viability of cultured parasites (2009)
Cordeiro, Artur T.; Thiemann, Otávio Henrique ; Michels, Paul A. M.
Fonte: Bioorganic and Medicinal Chemistry. Unidade: IFSC
Assuntos: TRYPANOSOMA, ESTEROIDES (HUMANO), INIBIDORES DE ENZIMAS, MOLÉCULA (ESTRUTURA), PLANEJAMENTO DE FÁRMACOS
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CORDEIRO, Artur T. e THIEMANN, Otávio Henrique e MICHELS, Paul A. M. Inhibition of Trypanosoma brucei glucose-6-phosphate dehydrogenase by human steroids and their effects on the viability of cultured parasites. Bioorganic and Medicinal Chemistry, v. 17, n. 6, p. 2483-2489, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2009.01.068. Acesso em: 01 nov. 2024.
APA
Cordeiro, A. T., Thiemann, O. H., & Michels, P. A. M. (2009). Inhibition of Trypanosoma brucei glucose-6-phosphate dehydrogenase by human steroids and their effects on the viability of cultured parasites. Bioorganic and Medicinal Chemistry, 17( 6), 2483-2489. doi:10.1016/j.bmc.2009.01.068
NLM
Cordeiro AT, Thiemann OH, Michels PAM. Inhibition of Trypanosoma brucei glucose-6-phosphate dehydrogenase by human steroids and their effects on the viability of cultured parasites [Internet]. Bioorganic and Medicinal Chemistry. 2009 ; 17( 6): 2483-2489.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.bmc.2009.01.068
Vancouver
Cordeiro AT, Thiemann OH, Michels PAM. Inhibition of Trypanosoma brucei glucose-6-phosphate dehydrogenase by human steroids and their effects on the viability of cultured parasites [Internet]. Bioorganic and Medicinal Chemistry. 2009 ; 17( 6): 2483-2489.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.bmc.2009.01.068
Artigo de periodico
Vanadium complexes with thiosemicarbazones: synthesis, characterization, crystal structures and anti-Mycobacterium tuberculosis activity (2009)
Maia, Pedro I. S.; Pavan, Fernando R.; Leite, Clarice Q. F.; Lemos, Sebastião S.; Sousa, Gerimário F.; Batista, Alzir A.; Nascimento, Otaciro Rangel ; Ellena, Javier ; Castellano, Eduardo Ernesto ; Niquet, Elke; Deflon, Victor Marcelo
Fonte: Polyhedron. Unidades: IFSC, IQSC
Assuntos: PLANEJAMENTO DE FÁRMACOS, FARMACODINÂMICA, CRISTALOGRAFIA (ESTRUTURA), TUBERCULOSE, DIFRAÇÃO POR RAIOS X, MICOBACTERIOSE (ATIVIDADE;TESTES)
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MAIA, Pedro I. S. et al. Vanadium complexes with thiosemicarbazones: synthesis, characterization, crystal structures and anti-Mycobacterium tuberculosis activity. Polyhedron, v. 28, n. 2, p. 398-406, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.poly.2008.11.017. Acesso em: 01 nov. 2024.
APA
Maia, P. I. S., Pavan, F. R., Leite, C. Q. F., Lemos, S. S., Sousa, G. F., Batista, A. A., et al. (2009). Vanadium complexes with thiosemicarbazones: synthesis, characterization, crystal structures and anti-Mycobacterium tuberculosis activity. Polyhedron, 28( 2), 398-406. doi:10.1016/j.poly.2008.11.017
NLM
Maia PIS, Pavan FR, Leite CQF, Lemos SS, Sousa GF, Batista AA, Nascimento OR, Ellena J, Castellano EE, Niquet E, Deflon VM. Vanadium complexes with thiosemicarbazones: synthesis, characterization, crystal structures and anti-Mycobacterium tuberculosis activity [Internet]. Polyhedron. 2009 ; 28( 2): 398-406.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.poly.2008.11.017
Vancouver
Maia PIS, Pavan FR, Leite CQF, Lemos SS, Sousa GF, Batista AA, Nascimento OR, Ellena J, Castellano EE, Niquet E, Deflon VM. Vanadium complexes with thiosemicarbazones: synthesis, characterization, crystal structures and anti-Mycobacterium tuberculosis activity [Internet]. Polyhedron. 2009 ; 28( 2): 398-406.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.poly.2008.11.017
Artigo de periodico
Novel 6-methanesulfonamide-3,4-methylenedioxyphenyl-N-acylhydrazones: orally effective anti-inflammatory drug candidates (2009)
Tributino, Jorge L. M.; Duarte, Carolina D.; Corrêa, Rodrigo S.; Doriguetto, Antonio C.; Ellena, Javier ; Romeiro, Nelilma C.; Castro, Newton G.; Miranda, Ana Luisa P.; Barreiro, Eliezer J.; Fraga, Carlos A. M.
Fonte: Bioorganic and Medicinal Chemistry. Unidade: IFSC
Assuntos: ANTI-INFLAMATÓRIOS (ESTUDO), QUÍMICA MÉDICA, MOLÉCULA (ESTRUTURA), PLANEJAMENTO DE FÁRMACOS, FARMACODINÂMICA
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TRIBUTINO, Jorge L. M. et al. Novel 6-methanesulfonamide-3,4-methylenedioxyphenyl-N-acylhydrazones: orally effective anti-inflammatory drug candidates. Bioorganic and Medicinal Chemistry, v. 17, n. 3, p. 1125-1131, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2008.12.045. Acesso em: 01 nov. 2024.
APA
Tributino, J. L. M., Duarte, C. D., Corrêa, R. S., Doriguetto, A. C., Ellena, J., Romeiro, N. C., et al. (2009). Novel 6-methanesulfonamide-3,4-methylenedioxyphenyl-N-acylhydrazones: orally effective anti-inflammatory drug candidates. Bioorganic and Medicinal Chemistry, 17( 3), 1125-1131. doi:10.1016/j.bmc.2008.12.045
NLM
Tributino JLM, Duarte CD, Corrêa RS, Doriguetto AC, Ellena J, Romeiro NC, Castro NG, Miranda ALP, Barreiro EJ, Fraga CAM. Novel 6-methanesulfonamide-3,4-methylenedioxyphenyl-N-acylhydrazones: orally effective anti-inflammatory drug candidates [Internet]. Bioorganic and Medicinal Chemistry. 2009 ; 17( 3): 1125-1131.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.bmc.2008.12.045
Vancouver
Tributino JLM, Duarte CD, Corrêa RS, Doriguetto AC, Ellena J, Romeiro NC, Castro NG, Miranda ALP, Barreiro EJ, Fraga CAM. Novel 6-methanesulfonamide-3,4-methylenedioxyphenyl-N-acylhydrazones: orally effective anti-inflammatory drug candidates [Internet]. Bioorganic and Medicinal Chemistry. 2009 ; 17( 3): 1125-1131.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.bmc.2008.12.045
Artigo de periodico
The genome of the blood fluke Schistosoma mansoni (2009)
Berriman, Matthew; Hass, Brian, J.; LoVerde, Philip T.; Wilson, R. Alan; Dillon, Gary P.; Cerqueira, Gustavo C.; Mashiyama, Susan T.; Al-Lazikani, Bissan; Andradre, Luiza F.; Ashton, Peter D.; Aslett, Martin A.; Bartholomeu, Daniella C.; Blandin, Gaelle; Caffrey, Conor R.; Coghlan, Avril; Coulson, Richard; Day, Tim A.; Delcher, Art; De Marco, Ricardo; Djikeng, Appolinaire; Eyre, Tina; Gamble, John A.; Ghedin, Elodie; Gu, Young; Fowler, Christiane Hertz; Hirai, Hirohisha; Hirai, Yuriko; Houston, Robin; Ivens, Alasdair; Johnston, David A.; Lacerda, Daniela; Macedo, Camila D.; McVeigh, Paul; Ning, Zemin; Oliveira, Guilherme; Overington, John P.; Parkhill, Julian; Pertea, Mihaela; Pierce, Raymond J.; Protasio, Anna V.; Quail, Michael A.; Rajandream, Marie-Adèle; Rogers, Jane; Sajid, Mohammed; Salzberg, Steven L.; Stanke, Mario; Tivey, Adrian R.; White, Owen; Williams, David L.; Wortman, Jennifer; Wu, Wenjie; Zamanian, Mostafa; Zerlotini, Adhemar; Liggett, Claire M. Fraser; Barrell, Barclay G.; El-Sayed, Najib M.
Fonte: Nature. Unidade: IFSC
Assuntos: SCHISTOSOMA MANSONI, SEQUENCIAMENTO GENÉTICO, PLANEJAMENTO DE FÁRMACOS, ESQUISTOSSOMOSE (TRATAMENTO)
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ABNT
BERRIMAN, Matthew et al. The genome of the blood fluke Schistosoma mansoni. Nature, v. 460, n. 7253, p. 352-358 : + supplementary materials, 2009Tradução . . Disponível em: https://doi.org/10.1038/nature08160. Acesso em: 01 nov. 2024.
APA
Berriman, M., Hass, B., LoVerde, P. T., Wilson, R. A., Dillon, G. P., Cerqueira, G. C., et al. (2009). The genome of the blood fluke Schistosoma mansoni. Nature, 460( 7253), 352-358 : + supplementary materials. doi:10.1038/nature08160
NLM
Berriman M, Hass B, LoVerde PT, Wilson RA, Dillon GP, Cerqueira GC, Mashiyama ST, Al-Lazikani B, Andradre LF, Ashton PD, Aslett MA, Bartholomeu DC, Blandin G, Caffrey CR, Coghlan A, Coulson R, Day TA, Delcher A, De Marco R, Djikeng A, Eyre T, Gamble JA, Ghedin E, Gu Y, Fowler CH, Hirai H, Hirai Y, Houston R, Ivens A, Johnston DA, Lacerda D, Macedo CD, McVeigh P, Ning Z, Oliveira G, Overington JP, Parkhill J, Pertea M, Pierce RJ, Protasio AV, Quail MA, Rajandream M-A, Rogers J, Sajid M, Salzberg SL, Stanke M, Tivey AR, White O, Williams DL, Wortman J, Wu W, Zamanian M, Zerlotini A, Liggett CMF, Barrell BG, El-Sayed NM. The genome of the blood fluke Schistosoma mansoni [Internet]. Nature. 2009 ; 460( 7253): 352-358 : + supplementary materials.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1038/nature08160
Vancouver
Berriman M, Hass B, LoVerde PT, Wilson RA, Dillon GP, Cerqueira GC, Mashiyama ST, Al-Lazikani B, Andradre LF, Ashton PD, Aslett MA, Bartholomeu DC, Blandin G, Caffrey CR, Coghlan A, Coulson R, Day TA, Delcher A, De Marco R, Djikeng A, Eyre T, Gamble JA, Ghedin E, Gu Y, Fowler CH, Hirai H, Hirai Y, Houston R, Ivens A, Johnston DA, Lacerda D, Macedo CD, McVeigh P, Ning Z, Oliveira G, Overington JP, Parkhill J, Pertea M, Pierce RJ, Protasio AV, Quail MA, Rajandream M-A, Rogers J, Sajid M, Salzberg SL, Stanke M, Tivey AR, White O, Williams DL, Wortman J, Wu W, Zamanian M, Zerlotini A, Liggett CMF, Barrell BG, El-Sayed NM. The genome of the blood fluke Schistosoma mansoni [Internet]. Nature. 2009 ; 460( 7253): 352-358 : + supplementary materials.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1038/nature08160
Artigo de periodico
Structure-activity relationships for a class of selective inhibitors of the major cysteine protease from Trypanosoma cruzi (2008)
Guido, Rafael Victorio Carvalho ; Trossini, Gustavo Henrique Goulart ; Castilho, Marcelo S.; Oliva, Glaucius ; Ferreira, Elizabeth Igne ; Andricopulo, Adriano Defini
Fonte: Journal of Enzyme Inhibition and Medicinal Chemistry. Unidades: IFSC, FCF
Assuntos: INIBIDORES DE ENZIMAS, DOENÇA DE CHAGAS, PLANEJAMENTO DE FÁRMACOS, QUIMIOTERAPIA, RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA, TRYPANOSOMA CRUZI
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ABNT
GUIDO, Rafael Victorio Carvalho 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: 01 nov. 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 nov. 01 ] 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 nov. 01 ] Available from: https://doi.org/10.1080/14756360701810322
Artigo de periodico
Hologram QSAR model for the prediction of human oral bioavailability (2007)
Moda, Tiago L.; Montanari, Carlos Alberto ; Andricopulo, Adriano Defini
Fonte: Bioorganic and Medicinal Chemistry. Unidades: IQSC, IFSC
Assuntos: RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA, FARMACOCINÉTICA, FÁRMACOS (DESENVOLVIMENTO), HOLOGRAMAS, PLANEJAMENTO DE FÁRMACOS
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ABNT
MODA, Tiago L. e MONTANARI, Carlos Alberto e ANDRICOPULO, Adriano Defini. Hologram QSAR model for the prediction of human oral bioavailability. Bioorganic and Medicinal Chemistry, v. 15, n. 24, p. 7738-7745, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2007.08.060. Acesso em: 01 nov. 2024.
APA
Moda, T. L., Montanari, C. A., & Andricopulo, A. D. (2007). Hologram QSAR model for the prediction of human oral bioavailability. Bioorganic and Medicinal Chemistry, 15( 24), 7738-7745. doi:10.1016/j.bmc.2007.08.060
NLM
Moda TL, Montanari CA, Andricopulo AD. Hologram QSAR model for the prediction of human oral bioavailability [Internet]. Bioorganic and Medicinal Chemistry. 2007 ; 15( 24): 7738-7745.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.bmc.2007.08.060
Vancouver
Moda TL, Montanari CA, Andricopulo AD. Hologram QSAR model for the prediction of human oral bioavailability [Internet]. Bioorganic and Medicinal Chemistry. 2007 ; 15( 24): 7738-7745.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.bmc.2007.08.060
Artigo de periodico
Quantitative structure-activity relationships for a series of selective estrogen receptor-beta modulators (2007)
Salum, L.; Polikarpov, Igor ; Andricopulo, Adriano Defini
Fonte: Sar and Qsar in Envitonmental Research. Unidade: IFSC
Assuntos: RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA, ESTRÓGENOS (ESTRUTURA), RECEPTORES HORMONAIS, PLANEJAMENTO DE FÁRMACOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SALUM, L. e POLIKARPOV, Igor e ANDRICOPULO, Adriano Defini. Quantitative structure-activity relationships for a series of selective estrogen receptor-beta modulators. Sar and Qsar in Envitonmental Research, v. 18, n. 7/8 p. 711-727, 2007Tradução . . Disponível em: https://doi.org/10.1080/10629360701698811. Acesso em: 01 nov. 2024.
APA
Salum, L., Polikarpov, I., & Andricopulo, A. D. (2007). Quantitative structure-activity relationships for a series of selective estrogen receptor-beta modulators. Sar and Qsar in Envitonmental Research, 18( 7/8 p. 711-727). doi:10.1080/10629360701698811
NLM
Salum L, Polikarpov I, Andricopulo AD. Quantitative structure-activity relationships for a series of selective estrogen receptor-beta modulators [Internet]. Sar and Qsar in Envitonmental Research. 2007 ; 18( 7/8 p. 711-727):[citado 2024 nov. 01 ] Available from: https://doi.org/10.1080/10629360701698811
Vancouver
Salum L, Polikarpov I, Andricopulo AD. Quantitative structure-activity relationships for a series of selective estrogen receptor-beta modulators [Internet]. Sar and Qsar in Envitonmental Research. 2007 ; 18( 7/8 p. 711-727):[citado 2024 nov. 01 ] Available from: https://doi.org/10.1080/10629360701698811
Artigo de periodico
New acetylenic furan derivates: synthesis and anti-inflammatory activity (2001)
Zeni, Gilson; Lüdtke, Diogo S.; Nogueira, Cristina W.; Panatieri, Rodrigo B.; Braga, Antônio L.; Silveira, Claudio C.; Stefani, Hélio Alexandre ; Rocha, João B. T.
Fonte: Tetrahedron Letters. Unidade: FCF
Assuntos: ANTI-INFLAMATÓRIOS (SÍNTESE), MEDICAMENTO (ANÁLISE;AVALIAÇÃO), PLANEJAMENTO DE FÁRMACOS, COMPOSTOS HETEROCÍCLICOS (SÍNTESE QUÍMICA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZENI, Gilson et al. New acetylenic furan derivates: synthesis and anti-inflammatory activity. Tetrahedron Letters, v. 42, n. 51, p. 8927-8930, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0040-4039(01)01984-0. Acesso em: 01 nov. 2024.
APA
Zeni, G., Lüdtke, D. S., Nogueira, C. W., Panatieri, R. B., Braga, A. L., Silveira, C. C., et al. (2001). New acetylenic furan derivates: synthesis and anti-inflammatory activity. Tetrahedron Letters, 42( 51), 8927-8930. doi:10.1016/s0040-4039(01)01984-0
NLM
Zeni G, Lüdtke DS, Nogueira CW, Panatieri RB, Braga AL, Silveira CC, Stefani HA, Rocha JBT. New acetylenic furan derivates: synthesis and anti-inflammatory activity [Internet]. Tetrahedron Letters. 2001 ; 42( 51): 8927-8930.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/s0040-4039(01)01984-0
Vancouver
Zeni G, Lüdtke DS, Nogueira CW, Panatieri RB, Braga AL, Silveira CC, Stefani HA, Rocha JBT. New acetylenic furan derivates: synthesis and anti-inflammatory activity [Internet]. Tetrahedron Letters. 2001 ; 42( 51): 8927-8930.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/s0040-4039(01)01984-0

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