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Artigo de periodico
Aflavinine alkaloids from Aspergillus sp.: antibacterial activity and inosine 5’-monophosphate dehydrogenase (IMPDH) as a potential target in bacillus subtilis (2025)
Silva-Silva, João Victor ; Feitosa, André O.; Döring, Thiago Henrique ; Watanabe, Luciano Almeida; Siqueira, José Edson de Sousa; Andricopulo, Adriano Defini ; Marinho, Patricia Santana Barbosa ; Marinho, Andrey Moacir do Rosario
Source: Journal of the Brazilian Chemical Society. Unidade: IFSC
Subjects: RESISTÊNCIA MICROBIANA ÀS DROGAS, PLANEJAMENTO DE FÁRMACOS, CRISTALOGRAFIA
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ABNT
SILVA-SILVA, João Victor et al. Aflavinine alkaloids from Aspergillus sp.: antibacterial activity and inosine 5’-monophosphate dehydrogenase (IMPDH) as a potential target in bacillus subtilis. Journal of the Brazilian Chemical Society, v. 36, n. 6, p. e-20250035-1-e-20250035-14, 2025Tradução . . Disponível em: https://doi.org/10.21577/0103-5053.20250035. Acesso em: 30 jul. 2025.
APA
Silva-Silva, J. V., Feitosa, A. O., Döring, T. H., Watanabe, L. A., Siqueira, J. E. de S., Andricopulo, A. D., et al. (2025). Aflavinine alkaloids from Aspergillus sp.: antibacterial activity and inosine 5’-monophosphate dehydrogenase (IMPDH) as a potential target in bacillus subtilis. Journal of the Brazilian Chemical Society, 36( 6), e-20250035-1-e-20250035-14. doi:10.21577/0103-5053.20250035
NLM
Silva-Silva JV, Feitosa AO, Döring TH, Watanabe LA, Siqueira JE de S, Andricopulo AD, Marinho PSB, Marinho AM do R. Aflavinine alkaloids from Aspergillus sp.: antibacterial activity and inosine 5’-monophosphate dehydrogenase (IMPDH) as a potential target in bacillus subtilis [Internet]. Journal of the Brazilian Chemical Society. 2025 ; 36( 6): e-20250035-1-e-20250035-14.[citado 2025 jul. 30 ] Available from: https://doi.org/10.21577/0103-5053.20250035
Vancouver
Silva-Silva JV, Feitosa AO, Döring TH, Watanabe LA, Siqueira JE de S, Andricopulo AD, Marinho PSB, Marinho AM do R. Aflavinine alkaloids from Aspergillus sp.: antibacterial activity and inosine 5’-monophosphate dehydrogenase (IMPDH) as a potential target in bacillus subtilis [Internet]. Journal of the Brazilian Chemical Society. 2025 ; 36( 6): e-20250035-1-e-20250035-14.[citado 2025 jul. 30 ] Available from: https://doi.org/10.21577/0103-5053.20250035
Editor de periodico
Current Topics in Medicinal Chemistry (2025)
Zhou, Jia (Editor); Andricopulo, Adriano Defini (Editor) ; Ferreira, Leonardo Luiz Gomes (Editor) ; Garcia, Célia Regina da Silva (Editor)
Unidades: IFSC, FCF
Assunto: QUÍMICA MÉDICA
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ABNT
Current Topics in Medicinal Chemistry. . Sharjah: Bentham Science. Disponível em: https://repositorio.usp.br/directbitstream/02c01ec1-0d4f-4ecc-8322-929a54f9ca47/3252665.pdf. Acesso em: 30 jul. 2025. , 2025
APA
Current Topics in Medicinal Chemistry. (2025). Current Topics in Medicinal Chemistry. Sharjah: Bentham Science. Recuperado de https://repositorio.usp.br/directbitstream/02c01ec1-0d4f-4ecc-8322-929a54f9ca47/3252665.pdf
NLM
Current Topics in Medicinal Chemistry [Internet]. 2025 ;[citado 2025 jul. 30 ] Available from: https://repositorio.usp.br/directbitstream/02c01ec1-0d4f-4ecc-8322-929a54f9ca47/3252665.pdf
Vancouver
Current Topics in Medicinal Chemistry [Internet]. 2025 ;[citado 2025 jul. 30 ] Available from: https://repositorio.usp.br/directbitstream/02c01ec1-0d4f-4ecc-8322-929a54f9ca47/3252665.pdf
Artigo de periodico
Molecular docking and quantitative structureactivity relationships for a series of Trypanosoma cruzi dihydroorotate dehydrogenase inhibitors (2025)
Jesus, Gabriela Cifelli de; Ribeiro, Tatiana Santana; Andricopulo, Adriano Defini ; Ferreira, Leonardo Luiz Gomes
Source: Brazilian Journal of Pharmaceutical Sciences. Unidade: IFSC
Subjects: TRYPANOSOMA CRUZI, MODELAGEM MOLECULAR, DOENÇA DE CHAGAS, PLANEJAMENTO DE FÁRMACOS, QUÍMICA MÉDICA
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ABNT
JESUS, Gabriela Cifelli de et al. Molecular docking and quantitative structureactivity relationships for a series of Trypanosoma cruzi dihydroorotate dehydrogenase inhibitors. Brazilian Journal of Pharmaceutical Sciences, v. 61, p. e24064-1-e24064-28, 2025Tradução . . Disponível em: https://doi.org/10.1590/s2175-97902025e24064. Acesso em: 30 jul. 2025.
APA
Jesus, G. C. de, Ribeiro, T. S., Andricopulo, A. D., & Ferreira, L. L. G. (2025). Molecular docking and quantitative structureactivity relationships for a series of Trypanosoma cruzi dihydroorotate dehydrogenase inhibitors. Brazilian Journal of Pharmaceutical Sciences, 61, e24064-1-e24064-28. doi:10.1590/s2175-97902025e24064
NLM
Jesus GC de, Ribeiro TS, Andricopulo AD, Ferreira LLG. Molecular docking and quantitative structureactivity relationships for a series of Trypanosoma cruzi dihydroorotate dehydrogenase inhibitors [Internet]. Brazilian Journal of Pharmaceutical Sciences. 2025 ; 61 e24064-1-e24064-28.[citado 2025 jul. 30 ] Available from: https://doi.org/10.1590/s2175-97902025e24064
Vancouver
Jesus GC de, Ribeiro TS, Andricopulo AD, Ferreira LLG. Molecular docking and quantitative structureactivity relationships for a series of Trypanosoma cruzi dihydroorotate dehydrogenase inhibitors [Internet]. Brazilian Journal of Pharmaceutical Sciences. 2025 ; 61 e24064-1-e24064-28.[citado 2025 jul. 30 ] Available from: https://doi.org/10.1590/s2175-97902025e24064
Trabalho de evento-resumo
Pyrrole derivatives as new compounds for breast and prostate cancer (2025)
Kawatoko, Tayla Hiroki; Costa, Analu Rocha ; Silva-Silva, João Victor ; Santos, Hugo; Lima, Sâmia Rocha; Coelho, Fernando; Ferreira, Leonardo Luiz Gomes ; Andricopulo, Adriano Defini
Source: Anais. Conference titles: Reunião Anual da Sociedade Brasileira de Química - RASBQ. Unidade: IFSC
Subjects: NEOPLASIAS, PLANEJAMENTO DE FÁRMACOS, CRISTALOGRAFIA
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ABNT
KAWATOKO, Tayla Hiroki et al. Pyrrole derivatives as new compounds for breast and prostate cancer. 2025, Anais.. São Paulo: Sociedade Brasileira de Química - SBQ, 2025. Disponível em: https://repositorio.usp.br/directbitstream/63f8d9e6-6bba-48a0-8ab8-6cc0b3473bda/3259928.pdf. Acesso em: 30 jul. 2025.
APA
Kawatoko, T. H., Costa, A. R., Silva-Silva, J. V., Santos, H., Lima, S. R., Coelho, F., et al. (2025). Pyrrole derivatives as new compounds for breast and prostate cancer. In Anais. São Paulo: Sociedade Brasileira de Química - SBQ. Recuperado de https://repositorio.usp.br/directbitstream/63f8d9e6-6bba-48a0-8ab8-6cc0b3473bda/3259928.pdf
NLM
Kawatoko TH, Costa AR, Silva-Silva JV, Santos H, Lima SR, Coelho F, Ferreira LLG, Andricopulo AD. Pyrrole derivatives as new compounds for breast and prostate cancer [Internet]. Anais. 2025 ;[citado 2025 jul. 30 ] Available from: https://repositorio.usp.br/directbitstream/63f8d9e6-6bba-48a0-8ab8-6cc0b3473bda/3259928.pdf
Vancouver
Kawatoko TH, Costa AR, Silva-Silva JV, Santos H, Lima SR, Coelho F, Ferreira LLG, Andricopulo AD. Pyrrole derivatives as new compounds for breast and prostate cancer [Internet]. Anais. 2025 ;[citado 2025 jul. 30 ] Available from: https://repositorio.usp.br/directbitstream/63f8d9e6-6bba-48a0-8ab8-6cc0b3473bda/3259928.pdf
Artigo de periodico
Non-mutagenic Ru(II)-phosphine-based complexes induce mitochondria-mediated apoptosis in breast cancer cells: from 2D to 3D investigations (2025)
Mello, Marcos Vinícius Palmeira de ; Teixeira, Tamara; Costa, Analu Rocha ; Machado, Aline Maria; Grandis, Rone A. De; Oliveira, Letícia Pires de ; Moraes, Carlos A. F.; de Araujo Neto, João Honorato ; Deflon, Victor Marcelo ; Andricopulo, Adriano Defini ; Ellena, Javier ; Selistre-de-Araujo, Heloisa Sobreiro ; Rocha, Fillipe Vieira ; Batista, Alzir Azevedo
Source: Inorganic Chemistry Frontiers. Unidades: IQSC, IFSC
Subjects: RUTÊNIO, NEOPLASIAS
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ABNT
MELLO, Marcos Vinícius Palmeira de et al. Non-mutagenic Ru(II)-phosphine-based complexes induce mitochondria-mediated apoptosis in breast cancer cells: from 2D to 3D investigations. Inorganic Chemistry Frontiers, 2025Tradução . . Disponível em: https://doi.org/10.1039/d5qi00546a. Acesso em: 30 jul. 2025.
APA
Mello, M. V. P. de, Teixeira, T., Costa, A. R., Machado, A. M., Grandis, R. A. D., Oliveira, L. P. de, et al. (2025). Non-mutagenic Ru(II)-phosphine-based complexes induce mitochondria-mediated apoptosis in breast cancer cells: from 2D to 3D investigations. Inorganic Chemistry Frontiers. doi:10.1039/d5qi00546a
NLM
Mello MVP de, Teixeira T, Costa AR, Machado AM, Grandis RAD, Oliveira LP de, Moraes CAF, de Araujo Neto JH, Deflon VM, Andricopulo AD, Ellena J, Selistre-de-Araujo HS, Rocha FV, Batista AA. Non-mutagenic Ru(II)-phosphine-based complexes induce mitochondria-mediated apoptosis in breast cancer cells: from 2D to 3D investigations [Internet]. Inorganic Chemistry Frontiers. 2025 ;[citado 2025 jul. 30 ] Available from: https://doi.org/10.1039/d5qi00546a
Vancouver
Mello MVP de, Teixeira T, Costa AR, Machado AM, Grandis RAD, Oliveira LP de, Moraes CAF, de Araujo Neto JH, Deflon VM, Andricopulo AD, Ellena J, Selistre-de-Araujo HS, Rocha FV, Batista AA. Non-mutagenic Ru(II)-phosphine-based complexes induce mitochondria-mediated apoptosis in breast cancer cells: from 2D to 3D investigations [Internet]. Inorganic Chemistry Frontiers. 2025 ;[citado 2025 jul. 30 ] Available from: https://doi.org/10.1039/d5qi00546a
Artigo de periodico
Design, synthesis, and in vitro evaluation of 4-(arylchalcogenyl)methyl)-1H-1,2,3-triazol-1-yl-menadione: exploring their potential against tuberculosis (2025)
Santos, Nathália L. B.; Gomes, Luana Silva ; Ribeiro, Ruan C. B.; Carvalho, Alcione Silva de; Lourenço, Maria Cristina da Silva; Marins, Laís Machado; Valle, Sandy Polycarpo; Döring, Thiago Henrique ; Andricopulo, Adriano Defini ; Oliveira, Aldo Sena de ; Ferreira, Vitor Francisco ; Silva, Fernando de Carvalho da ; Forezi, Luana da Silva Magalhães ; Nascimento, Vanessa
Source: Pharmaceuticals. Unidade: IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, TUBERCULOSE, RESISTÊNCIA MICROBIANA ÀS DROGAS
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ABNT
SANTOS, Nathália L. B. et al. Design, synthesis, and in vitro evaluation of 4-(arylchalcogenyl)methyl)-1H-1,2,3-triazol-1-yl-menadione: exploring their potential against tuberculosis. Pharmaceuticals, v. 18, n. 6, p. 797-1-797-21 + supplementary materials, 2025Tradução . . Disponível em: https://doi.org/10.3390/ph18060797. Acesso em: 30 jul. 2025.
APA
Santos, N. L. B., Gomes, L. S., Ribeiro, R. C. B., Carvalho, A. S. de, Lourenço, M. C. da S., Marins, L. M., et al. (2025). Design, synthesis, and in vitro evaluation of 4-(arylchalcogenyl)methyl)-1H-1,2,3-triazol-1-yl-menadione: exploring their potential against tuberculosis. Pharmaceuticals, 18( 6), 797-1-797-21 + supplementary materials. doi:10.3390/ph18060797
NLM
Santos NLB, Gomes LS, Ribeiro RCB, Carvalho AS de, Lourenço MC da S, Marins LM, Valle SP, Döring TH, Andricopulo AD, Oliveira AS de, Ferreira VF, Silva F de C da, Forezi L da SM, Nascimento V. Design, synthesis, and in vitro evaluation of 4-(arylchalcogenyl)methyl)-1H-1,2,3-triazol-1-yl-menadione: exploring their potential against tuberculosis [Internet]. Pharmaceuticals. 2025 ; 18( 6): 797-1-797-21 + supplementary materials.[citado 2025 jul. 30 ] Available from: https://doi.org/10.3390/ph18060797
Vancouver
Santos NLB, Gomes LS, Ribeiro RCB, Carvalho AS de, Lourenço MC da S, Marins LM, Valle SP, Döring TH, Andricopulo AD, Oliveira AS de, Ferreira VF, Silva F de C da, Forezi L da SM, Nascimento V. Design, synthesis, and in vitro evaluation of 4-(arylchalcogenyl)methyl)-1H-1,2,3-triazol-1-yl-menadione: exploring their potential against tuberculosis [Internet]. Pharmaceuticals. 2025 ; 18( 6): 797-1-797-21 + supplementary materials.[citado 2025 jul. 30 ] Available from: https://doi.org/10.3390/ph18060797
Artigo de periodico
Phenotypic screening of H1-antihistamines identifies promethazine and rupatadine as active compounds against Toxocara canis infective larvae (2025)
Silva, Tais C.; Silva, Julia Godoy; Amaro, Monique C.; Silva-Silva, João Victor ; Döring, Thiago Henrique ; Ferreira, Leonardo Luiz Gomes ; Andricopulo, Adriano Defini ; Moraes, Josué de
Source: Pharmaceuticals. Unidade: IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, TOXOCARA CANIS, RESISTÊNCIA MICROBIANA ÀS DROGAS
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ABNT
SILVA, Tais C. et al. Phenotypic screening of H1-antihistamines identifies promethazine and rupatadine as active compounds against Toxocara canis infective larvae. Pharmaceuticals, v. 18, n. 7, p. 997-1-997-14 + supplementary materials, 2025Tradução . . Disponível em: https://doi.org/10.3390/ph18070997. Acesso em: 30 jul. 2025.
APA
Silva, T. C., Silva, J. G., Amaro, M. C., Silva-Silva, J. V., Döring, T. H., Ferreira, L. L. G., et al. (2025). Phenotypic screening of H1-antihistamines identifies promethazine and rupatadine as active compounds against Toxocara canis infective larvae. Pharmaceuticals, 18( 7), 997-1-997-14 + supplementary materials. doi:10.3390/ph18070997
NLM
Silva TC, Silva JG, Amaro MC, Silva-Silva JV, Döring TH, Ferreira LLG, Andricopulo AD, Moraes J de. Phenotypic screening of H1-antihistamines identifies promethazine and rupatadine as active compounds against Toxocara canis infective larvae [Internet]. Pharmaceuticals. 2025 ; 18( 7): 997-1-997-14 + supplementary materials.[citado 2025 jul. 30 ] Available from: https://doi.org/10.3390/ph18070997
Vancouver
Silva TC, Silva JG, Amaro MC, Silva-Silva JV, Döring TH, Ferreira LLG, Andricopulo AD, Moraes J de. Phenotypic screening of H1-antihistamines identifies promethazine and rupatadine as active compounds against Toxocara canis infective larvae [Internet]. Pharmaceuticals. 2025 ; 18( 7): 997-1-997-14 + supplementary materials.[citado 2025 jul. 30 ] Available from: https://doi.org/10.3390/ph18070997
Trabalho de evento-resumo
Leishmanicidal benzodiazepines as DHFR-TS inhibitors: in vitro and in silico analysis (2025)
Silva-Silva, João Victor ; Queiroz, Karla Valéria Maia de; Costa, Analu Rocha ; Nascimento, Vinicius Rodrigues do ; Graebin, Cedric S.; Ferreira, Leonardo Luiz Gomes ; Andricopulo, Adriano Defini
Source: Anais. Conference titles: Reunião Anual da Sociedade Brasileira de Química - RASBQ. Unidade: IFSC
Subjects: DOENÇAS NEGLIGENCIADAS, ANTIPARASITÁRIOS, PLANEJAMENTO DE FÁRMACOS
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ABNT
SILVA-SILVA, João Victor et al. Leishmanicidal benzodiazepines as DHFR-TS inhibitors: in vitro and in silico analysis. 2025, Anais.. São Paulo: Sociedade Brasileira de Química - SBQ, 2025. Disponível em: https://repositorio.usp.br/directbitstream/cdbc83db-50bf-4ab7-927c-54b32822fafe/3259748.pdf. Acesso em: 30 jul. 2025.
APA
Silva-Silva, J. V., Queiroz, K. V. M. de, Costa, A. R., Nascimento, V. R. do, Graebin, C. S., Ferreira, L. L. G., & Andricopulo, A. D. (2025). Leishmanicidal benzodiazepines as DHFR-TS inhibitors: in vitro and in silico analysis. In Anais. São Paulo: Sociedade Brasileira de Química - SBQ. Recuperado de https://repositorio.usp.br/directbitstream/cdbc83db-50bf-4ab7-927c-54b32822fafe/3259748.pdf
NLM
Silva-Silva JV, Queiroz KVM de, Costa AR, Nascimento VR do, Graebin CS, Ferreira LLG, Andricopulo AD. Leishmanicidal benzodiazepines as DHFR-TS inhibitors: in vitro and in silico analysis [Internet]. Anais. 2025 ;[citado 2025 jul. 30 ] Available from: https://repositorio.usp.br/directbitstream/cdbc83db-50bf-4ab7-927c-54b32822fafe/3259748.pdf
Vancouver
Silva-Silva JV, Queiroz KVM de, Costa AR, Nascimento VR do, Graebin CS, Ferreira LLG, Andricopulo AD. Leishmanicidal benzodiazepines as DHFR-TS inhibitors: in vitro and in silico analysis [Internet]. Anais. 2025 ;[citado 2025 jul. 30 ] Available from: https://repositorio.usp.br/directbitstream/cdbc83db-50bf-4ab7-927c-54b32822fafe/3259748.pdf
Trabalho de evento-resumo
Design, synthesis and in vitro evaluation of a series of arylmorpholine derivative compounds against chagas disease (2025)
Farago, Danilo Nascimento; Resende, Daniela de Melo ; Chelucci, Rafael Consolin ; Andricopulo, Adriano Defini ; Ferreira, Leonardo Luiz Gomes ; Murta, Silvane Maria Fonseca ; Rezende Junior, Celso de Oliveira
Source: Anais. Conference titles: Reunião Anual da Sociedade Brasileira de Química - RASBQ. Unidade: IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, DOENÇA DE CHAGAS
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ABNT
FARAGO, Danilo Nascimento et al. Design, synthesis and in vitro evaluation of a series of arylmorpholine derivative compounds against chagas disease. 2025, Anais.. São Paulo: Sociedade Brasileira de Química - SBQ, 2025. Disponível em: https://repositorio.usp.br/directbitstream/488b6113-cf75-4d55-a443-c3d253019b10/3259726.pdf. Acesso em: 30 jul. 2025.
APA
Farago, D. N., Resende, D. de M., Chelucci, R. C., Andricopulo, A. D., Ferreira, L. L. G., Murta, S. M. F., & Rezende Junior, C. de O. (2025). Design, synthesis and in vitro evaluation of a series of arylmorpholine derivative compounds against chagas disease. In Anais. São Paulo: Sociedade Brasileira de Química - SBQ. Recuperado de https://repositorio.usp.br/directbitstream/488b6113-cf75-4d55-a443-c3d253019b10/3259726.pdf
NLM
Farago DN, Resende D de M, Chelucci RC, Andricopulo AD, Ferreira LLG, Murta SMF, Rezende Junior C de O. Design, synthesis and in vitro evaluation of a series of arylmorpholine derivative compounds against chagas disease [Internet]. Anais. 2025 ;[citado 2025 jul. 30 ] Available from: https://repositorio.usp.br/directbitstream/488b6113-cf75-4d55-a443-c3d253019b10/3259726.pdf
Vancouver
Farago DN, Resende D de M, Chelucci RC, Andricopulo AD, Ferreira LLG, Murta SMF, Rezende Junior C de O. Design, synthesis and in vitro evaluation of a series of arylmorpholine derivative compounds against chagas disease [Internet]. Anais. 2025 ;[citado 2025 jul. 30 ] Available from: https://repositorio.usp.br/directbitstream/488b6113-cf75-4d55-a443-c3d253019b10/3259726.pdf
Artigo de periodico
Discovery and early optimization of 1H-indole-2-carboxamides with anti-trypanosoma cruzi activity (2025)
Oliveira, Ramon Guerra de ; Duarte, Simone Michelan ; Krogh, Renata ; Ferreira, Leonardo Luiz Gomes ; Chelucci, Rafael Consolin ; Feltrin, Clarissa ; Silva, Adriana Corrêa da ; Santos, Benedito Matheus dos ; Broering, Milena Fronza ; Moraes, Carolina Borsoi ; Andricopulo, Adriano Defini
Source: Journal of Medicinal Chemistry. Unidades: IFSC, FCF, ICB
Subjects: DOENÇA DE CHAGAS, QUÍMICA MÉDICA, PLANEJAMENTO DE FÁRMACOS, ANTIPARASITÁRIOS, TRYPANOSOMA CRUZI
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ABNT
OLIVEIRA, Ramon Guerra de et al. Discovery and early optimization of 1H-indole-2-carboxamides with anti-trypanosoma cruzi activity. Journal of Medicinal Chemistry, v. 68, n. 7, p. 7313-7340 + supporting information, 2025Tradução . . Disponível em: https://doi.org/10.1021/acs.jmedchem.4c02942. Acesso em: 30 jul. 2025.
APA
Oliveira, R. G. de, Duarte, S. M., Krogh, R., Ferreira, L. L. G., Chelucci, R. C., Feltrin, C., et al. (2025). Discovery and early optimization of 1H-indole-2-carboxamides with anti-trypanosoma cruzi activity. Journal of Medicinal Chemistry, 68( 7), 7313-7340 + supporting information. doi:10.1021/acs.jmedchem.4c02942
NLM
Oliveira RG de, Duarte SM, Krogh R, Ferreira LLG, Chelucci RC, Feltrin C, Silva AC da, Santos BM dos, Broering MF, Moraes CB, Andricopulo AD. Discovery and early optimization of 1H-indole-2-carboxamides with anti-trypanosoma cruzi activity [Internet]. Journal of Medicinal Chemistry. 2025 ; 68( 7): 7313-7340 + supporting information.[citado 2025 jul. 30 ] Available from: https://doi.org/10.1021/acs.jmedchem.4c02942
Vancouver
Oliveira RG de, Duarte SM, Krogh R, Ferreira LLG, Chelucci RC, Feltrin C, Silva AC da, Santos BM dos, Broering MF, Moraes CB, Andricopulo AD. Discovery and early optimization of 1H-indole-2-carboxamides with anti-trypanosoma cruzi activity [Internet]. Journal of Medicinal Chemistry. 2025 ; 68( 7): 7313-7340 + supporting information.[citado 2025 jul. 30 ] Available from: https://doi.org/10.1021/acs.jmedchem.4c02942
Trabalho de evento-resumo
Hit-to-Lead optimization of pyridylpiperazine derivatives: promising antimalarial candidates with notable ADME profiles and metabolic stability (2025)
Oliveira, Douglas Davison da Silva ; Krüger, Arne ; Chelucci, Rafael Consolin ; Ferreira, Leonardo Luiz Gomes ; Andricopulo, Adriano Defini ; Wunderlich, Gerhard ; Silva, Neide Maria da; Rezende Junior, Celso de Oliveira
Source: Anais. Conference titles: Reunião Anual da Sociedade Brasileira de Química - RASBQ. Unidades: IFSC, ICB
Subjects: MALÁRIA, PLASMODIUM FALCIPARUM, PLANEJAMENTO DE FÁRMACOS
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ABNT
OLIVEIRA, Douglas Davison da Silva et al. Hit-to-Lead optimization of pyridylpiperazine derivatives: promising antimalarial candidates with notable ADME profiles and metabolic stability. 2025, Anais.. São Paulo: Sociedade Brasileira de Química - SBQ, 2025. Disponível em: https://repositorio.usp.br/directbitstream/f179559b-b0ab-49da-8d2d-69b170cab755/3259728.pdf. Acesso em: 30 jul. 2025.
APA
Oliveira, D. D. da S., Krüger, A., Chelucci, R. C., Ferreira, L. L. G., Andricopulo, A. D., Wunderlich, G., et al. (2025). Hit-to-Lead optimization of pyridylpiperazine derivatives: promising antimalarial candidates with notable ADME profiles and metabolic stability. In Anais. São Paulo: Sociedade Brasileira de Química - SBQ. Recuperado de https://repositorio.usp.br/directbitstream/f179559b-b0ab-49da-8d2d-69b170cab755/3259728.pdf
NLM
Oliveira DD da S, Krüger A, Chelucci RC, Ferreira LLG, Andricopulo AD, Wunderlich G, Silva NM da, Rezende Junior C de O. Hit-to-Lead optimization of pyridylpiperazine derivatives: promising antimalarial candidates with notable ADME profiles and metabolic stability [Internet]. Anais. 2025 ;[citado 2025 jul. 30 ] Available from: https://repositorio.usp.br/directbitstream/f179559b-b0ab-49da-8d2d-69b170cab755/3259728.pdf
Vancouver
Oliveira DD da S, Krüger A, Chelucci RC, Ferreira LLG, Andricopulo AD, Wunderlich G, Silva NM da, Rezende Junior C de O. Hit-to-Lead optimization of pyridylpiperazine derivatives: promising antimalarial candidates with notable ADME profiles and metabolic stability [Internet]. Anais. 2025 ;[citado 2025 jul. 30 ] Available from: https://repositorio.usp.br/directbitstream/f179559b-b0ab-49da-8d2d-69b170cab755/3259728.pdf
Trabalho de evento-resumo
Identification of a novel antileishmanial compound through combined in vitro and in silico approaches (2025)
Afonso, Maynara; Costa, Analu Rocha ; Silva-Silva, João Victor ; Duarte, Simone Michelan ; Chelucci, Rafael Consolin ; Döring, Thiago Henrique ; Ferreira, Leonardo Luiz Gomes ; Andricopulo, Adriano Defini
Source: Anais. Conference titles: Reunião Anual da Sociedade Brasileira de Química - RASBQ. Unidade: IFSC
Subjects: DOENÇAS NEGLIGENCIADAS, ANTIPARASITÁRIOS, PLANEJAMENTO DE FÁRMACOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
AFONSO, Maynara et al. Identification of a novel antileishmanial compound through combined in vitro and in silico approaches. 2025, Anais.. São Paulo: Sociedade Brasileira de Química - SBQ, 2025. Disponível em: https://repositorio.usp.br/directbitstream/3d9b2aa3-ff6f-424c-b97d-4b1f3267ebe8/3259733.pdf. Acesso em: 30 jul. 2025.
APA
Afonso, M., Costa, A. R., Silva-Silva, J. V., Duarte, S. M., Chelucci, R. C., Döring, T. H., et al. (2025). Identification of a novel antileishmanial compound through combined in vitro and in silico approaches. In Anais. São Paulo: Sociedade Brasileira de Química - SBQ. Recuperado de https://repositorio.usp.br/directbitstream/3d9b2aa3-ff6f-424c-b97d-4b1f3267ebe8/3259733.pdf
NLM
Afonso M, Costa AR, Silva-Silva JV, Duarte SM, Chelucci RC, Döring TH, Ferreira LLG, Andricopulo AD. Identification of a novel antileishmanial compound through combined in vitro and in silico approaches [Internet]. Anais. 2025 ;[citado 2025 jul. 30 ] Available from: https://repositorio.usp.br/directbitstream/3d9b2aa3-ff6f-424c-b97d-4b1f3267ebe8/3259733.pdf
Vancouver
Afonso M, Costa AR, Silva-Silva JV, Duarte SM, Chelucci RC, Döring TH, Ferreira LLG, Andricopulo AD. Identification of a novel antileishmanial compound through combined in vitro and in silico approaches [Internet]. Anais. 2025 ;[citado 2025 jul. 30 ] Available from: https://repositorio.usp.br/directbitstream/3d9b2aa3-ff6f-424c-b97d-4b1f3267ebe8/3259733.pdf
Artigo de periodico
In vitro and in vivo evaluation of the antischistosomal activity of polygodial and 9-deoxymuzigadial isolated from drimys brasiliensis branches (2025)
Umehara, Eric; Cajas, Rayssa Araújo; Conceição, Gabriel B.; Antar, Guilherme Medeiros ; Andricopulo, Adriano Defini ; Moraes, Josué de ; Lago, João Henrique Ghilardi
Source: Molecules. Unidade: IFSC
Subjects: SCHISTOSOMA MANSONI, FÁRMACOS, PLANEJAMENTO DE FÁRMACOS
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ABNT
UMEHARA, Eric et al. In vitro and in vivo evaluation of the antischistosomal activity of polygodial and 9-deoxymuzigadial isolated from drimys brasiliensis branches. Molecules, v. 30, n. Ja 2025, p. 267-1-267-11 + supplementary materials, 2025Tradução . . Disponível em: https://doi.org/10.3390/molecules30020267. Acesso em: 30 jul. 2025.
APA
Umehara, E., Cajas, R. A., Conceição, G. B., Antar, G. M., Andricopulo, A. D., Moraes, J. de, & Lago, J. H. G. (2025). In vitro and in vivo evaluation of the antischistosomal activity of polygodial and 9-deoxymuzigadial isolated from drimys brasiliensis branches. Molecules, 30( Ja 2025), 267-1-267-11 + supplementary materials. doi:10.3390/molecules30020267
NLM
Umehara E, Cajas RA, Conceição GB, Antar GM, Andricopulo AD, Moraes J de, Lago JHG. In vitro and in vivo evaluation of the antischistosomal activity of polygodial and 9-deoxymuzigadial isolated from drimys brasiliensis branches [Internet]. Molecules. 2025 ; 30( Ja 2025): 267-1-267-11 + supplementary materials.[citado 2025 jul. 30 ] Available from: https://doi.org/10.3390/molecules30020267
Vancouver
Umehara E, Cajas RA, Conceição GB, Antar GM, Andricopulo AD, Moraes J de, Lago JHG. In vitro and in vivo evaluation of the antischistosomal activity of polygodial and 9-deoxymuzigadial isolated from drimys brasiliensis branches [Internet]. Molecules. 2025 ; 30( Ja 2025): 267-1-267-11 + supplementary materials.[citado 2025 jul. 30 ] Available from: https://doi.org/10.3390/molecules30020267
Artigo de periodico
Discovery of arylpiperazines with broad-spectrum antimicrobial activity and favorable pharmacokinetic profiles (2025)
Oliveira, Douglas Davison da Silva ; Silva, Nagela Bernadelli Sousa; Lapierre, Thibault Joseph William Jacques Dit ; Souza, Sara Lemes de; Brito, Nícolas Peterson Ferreira ; Martinho, Ana Clara Cassiano ; Dias, Renieidy Flávia Clemente; Farago, Danilo Nascimento; Duarte, Simone Michelan ; Chelucci, Rafael Consolin; Cruz, Mariza Gabriela Faleiro de Moura Lodi; Resende, Daniela de Melo ; Andricopulo, Adriano Defini ; Murta, Silvane Maria Fonseca ; Ferreira, Leonardo Luiz Gomes ; Martins, Carlos Henrique Gomes ; Rezende Junior, Celso de Oliveira
Source: Chemistry and Biodiversity. Unidade: IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, RESISTÊNCIA MICROBIANA ÀS DROGAS, CITOTOXINAS
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ABNT
OLIVEIRA, Douglas Davison da Silva et al. Discovery of arylpiperazines with broad-spectrum antimicrobial activity and favorable pharmacokinetic profiles. Chemistry and Biodiversity, v. 22, n. 2, p. e202402100-1-e202402100-14, 2025Tradução . . Disponível em: https://doi.org/10.1002/cbdv.202402100. Acesso em: 30 jul. 2025.
APA
Oliveira, D. D. da S., Silva, N. B. S., Lapierre, T. J. W. J. D., Souza, S. L. de, Brito, N. P. F., Martinho, A. C. C., et al. (2025). Discovery of arylpiperazines with broad-spectrum antimicrobial activity and favorable pharmacokinetic profiles. Chemistry and Biodiversity, 22( 2), e202402100-1-e202402100-14. doi:10.1002/cbdv.202402100
NLM
Oliveira DD da S, Silva NBS, Lapierre TJWJD, Souza SL de, Brito NPF, Martinho ACC, Dias RFC, Farago DN, Duarte SM, Chelucci RC, Cruz MGF de ML, Resende D de M, Andricopulo AD, Murta SMF, Ferreira LLG, Martins CHG, Rezende Junior C de O. Discovery of arylpiperazines with broad-spectrum antimicrobial activity and favorable pharmacokinetic profiles [Internet]. Chemistry and Biodiversity. 2025 ; 22( 2): e202402100-1-e202402100-14.[citado 2025 jul. 30 ] Available from: https://doi.org/10.1002/cbdv.202402100
Vancouver
Oliveira DD da S, Silva NBS, Lapierre TJWJD, Souza SL de, Brito NPF, Martinho ACC, Dias RFC, Farago DN, Duarte SM, Chelucci RC, Cruz MGF de ML, Resende D de M, Andricopulo AD, Murta SMF, Ferreira LLG, Martins CHG, Rezende Junior C de O. Discovery of arylpiperazines with broad-spectrum antimicrobial activity and favorable pharmacokinetic profiles [Internet]. Chemistry and Biodiversity. 2025 ; 22( 2): e202402100-1-e202402100-14.[citado 2025 jul. 30 ] Available from: https://doi.org/10.1002/cbdv.202402100
Artigo de periodico
Synthesis and in vitro leishmanicidal activity of novel n-arylspermidine derivatives (2025)
Mollo, María Cruz ; Cambiaso, Mariana L.; Ferreira, Leonardo Luiz Gomes ; Kilimciler, Natalia Beatriz; Bisceglia, Juan A.; Andricopulo, Adriano Defini ; Orelli, Liliana R.
Source: Bioorganic Chemistry. Unidade: IFSC
Subjects: LEISHMANIA INFANTUM, DOENÇAS NEGLIGENCIADAS, CRISTALOGRAFIA
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ABNT
MOLLO, María Cruz et al. Synthesis and in vitro leishmanicidal activity of novel n-arylspermidine derivatives. Bioorganic Chemistry, v. 154, n. Ja 2025, p. 108083-1-108083-8 + supplementary data, 2025Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2024.108083. Acesso em: 30 jul. 2025.
APA
Mollo, M. C., Cambiaso, M. L., Ferreira, L. L. G., Kilimciler, N. B., Bisceglia, J. A., Andricopulo, A. D., & Orelli, L. R. (2025). Synthesis and in vitro leishmanicidal activity of novel n-arylspermidine derivatives. Bioorganic Chemistry, 154( Ja 2025), 108083-1-108083-8 + supplementary data. doi:10.1016/j.bioorg.2024.108083
NLM
Mollo MC, Cambiaso ML, Ferreira LLG, Kilimciler NB, Bisceglia JA, Andricopulo AD, Orelli LR. Synthesis and in vitro leishmanicidal activity of novel n-arylspermidine derivatives [Internet]. Bioorganic Chemistry. 2025 ; 154( Ja 2025): 108083-1-108083-8 + supplementary data.[citado 2025 jul. 30 ] Available from: https://doi.org/10.1016/j.bioorg.2024.108083
Vancouver
Mollo MC, Cambiaso ML, Ferreira LLG, Kilimciler NB, Bisceglia JA, Andricopulo AD, Orelli LR. Synthesis and in vitro leishmanicidal activity of novel n-arylspermidine derivatives [Internet]. Bioorganic Chemistry. 2025 ; 154( Ja 2025): 108083-1-108083-8 + supplementary data.[citado 2025 jul. 30 ] Available from: https://doi.org/10.1016/j.bioorg.2024.108083
Trabalho de evento-resumo
The effect of Ru(II)-phosphine complexes on triple-negative breast cancer cells (2025)
Costa, Analu Rocha ; Oliveira, Letícia Pires de ; Demidoff, Felipe Cerqueira ; Daher Netto, Chaquip ; Andricopulo, Adriano Defini ; Batista, Alzir Azevedo
Source: Anais. Conference titles: Reunião Anual da Sociedade Brasileira de Química - RASBQ. Unidade: IFSC
Subjects: RUTÊNIO, NEOPLASIAS MAMÁRIAS, ANTINEOPLÁSICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COSTA, Analu Rocha et al. The effect of Ru(II)-phosphine complexes on triple-negative breast cancer cells. 2025, Anais.. São Paulo: Sociedade Brasileira de Química - SBQ, 2025. Disponível em: https://repositorio.usp.br/directbitstream/c8c103f0-66ef-42a9-a5e2-02b9ba0569ac/3259719.pdf. Acesso em: 30 jul. 2025.
APA
Costa, A. R., Oliveira, L. P. de, Demidoff, F. C., Daher Netto, C., Andricopulo, A. D., & Batista, A. A. (2025). The effect of Ru(II)-phosphine complexes on triple-negative breast cancer cells. In Anais. São Paulo: Sociedade Brasileira de Química - SBQ. Recuperado de https://repositorio.usp.br/directbitstream/c8c103f0-66ef-42a9-a5e2-02b9ba0569ac/3259719.pdf
NLM
Costa AR, Oliveira LP de, Demidoff FC, Daher Netto C, Andricopulo AD, Batista AA. The effect of Ru(II)-phosphine complexes on triple-negative breast cancer cells [Internet]. Anais. 2025 ;[citado 2025 jul. 30 ] Available from: https://repositorio.usp.br/directbitstream/c8c103f0-66ef-42a9-a5e2-02b9ba0569ac/3259719.pdf
Vancouver
Costa AR, Oliveira LP de, Demidoff FC, Daher Netto C, Andricopulo AD, Batista AA. The effect of Ru(II)-phosphine complexes on triple-negative breast cancer cells [Internet]. Anais. 2025 ;[citado 2025 jul. 30 ] Available from: https://repositorio.usp.br/directbitstream/c8c103f0-66ef-42a9-a5e2-02b9ba0569ac/3259719.pdf
Artigo de periodico
Structure-activity relationships of novel N-imidazoylpiperazines with potent anti-trypanosoma cruzi activity (2024)
Chávez, Rocio Marisol Espinoza ; Rezende Junior, Celso de Oliveira ; Souza, Mariana Laureano de ; Pauli, Ivani; Valli, Marilia ; Ferreira, Leonardo Luiz Gomes ; Chelucci, Rafael Consolin; Duarte, Simone Michelan ; Krogh, Renata; Silva, Fernando Bezerra Romualdo da; Cruz, Fábio Cardoso; Oliveira, Aldo Sena de ; Andricopulo, Adriano Defini ; Dias, Luiz Carlos
Source: Future Medicinal Chemistry. Unidade: IFSC
Subjects: FÁRMACOS, PLANEJAMENTO DE FÁRMACOS, DOENÇAS PARASITÁRIAS, DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CHÁVEZ, Rocio Marisol Espinoza et al. Structure-activity relationships of novel N-imidazoylpiperazines with potent anti-trypanosoma cruzi activity. Future Medicinal Chemistry, v. 16, n. Ja 2024, p. 253-269, 2024Tradução . . Disponível em: https://doi.org/10.4155/fmc-2023-0185. Acesso em: 30 jul. 2025.
APA
Chávez, R. M. E., Rezende Junior, C. de O., Souza, M. L. de, Pauli, I., Valli, M., Ferreira, L. L. G., et al. (2024). Structure-activity relationships of novel N-imidazoylpiperazines with potent anti-trypanosoma cruzi activity. Future Medicinal Chemistry, 16( Ja 2024), 253-269. doi:10.4155/fmc-2023-0185
NLM
Chávez RME, Rezende Junior C de O, Souza ML de, Pauli I, Valli M, Ferreira LLG, Chelucci RC, Duarte SM, Krogh R, Silva FBR da, Cruz FC, Oliveira AS de, Andricopulo AD, Dias LC. Structure-activity relationships of novel N-imidazoylpiperazines with potent anti-trypanosoma cruzi activity [Internet]. Future Medicinal Chemistry. 2024 ; 16( Ja 2024): 253-269.[citado 2025 jul. 30 ] Available from: https://doi.org/10.4155/fmc-2023-0185
Vancouver
Chávez RME, Rezende Junior C de O, Souza ML de, Pauli I, Valli M, Ferreira LLG, Chelucci RC, Duarte SM, Krogh R, Silva FBR da, Cruz FC, Oliveira AS de, Andricopulo AD, Dias LC. Structure-activity relationships of novel N-imidazoylpiperazines with potent anti-trypanosoma cruzi activity [Internet]. Future Medicinal Chemistry. 2024 ; 16( Ja 2024): 253-269.[citado 2025 jul. 30 ] Available from: https://doi.org/10.4155/fmc-2023-0185
Artigo de periodico
Synthesis and anti-trypanosoma cruzi activity of 3-cyanopyridine derivatives (2024)
Slafer, Brian Wayne ; Dessoy, Marco Aurélio ; Oliveira, Ramon Guerra de ; Mollo, María Cruz ; Lee, Eun ; Matheeussen, An ; Maes, Louis ; Caljon, Guy ; Ferreira, Leonardo Luiz Gomes ; Krogh, Renata ; Andricopulo, Adriano Defini ; Cruz, Luiza dos Reis ; Mowbray, Charles E. ; Kratz, Jadel M. ; Dias, Luiz Carlos
Source: ACS Omega. Unidade: IFSC
Subjects: TRYPANOSOMA CRUZI, COMPOSTOS AROMÁTICOS, CRISTALOGRAFIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SLAFER, Brian Wayne et al. Synthesis and anti-trypanosoma cruzi activity of 3-cyanopyridine derivatives. ACS Omega, v. 9, n. 20, p. 22360-22370 + supporting information, 2024Tradução . . Disponível em: https://doi.org/10.1021/acsomega.4c01919. Acesso em: 30 jul. 2025.
APA
Slafer, B. W., Dessoy, M. A., Oliveira, R. G. de, Mollo, M. C., Lee, E., Matheeussen, A., et al. (2024). Synthesis and anti-trypanosoma cruzi activity of 3-cyanopyridine derivatives. ACS Omega, 9( 20), 22360-22370 + supporting information. doi:10.1021/acsomega.4c01919
NLM
Slafer BW, Dessoy MA, Oliveira RG de, Mollo MC, Lee E, Matheeussen A, Maes L, Caljon G, Ferreira LLG, Krogh R, Andricopulo AD, Cruz L dos R, Mowbray CE, Kratz JM, Dias LC. Synthesis and anti-trypanosoma cruzi activity of 3-cyanopyridine derivatives [Internet]. ACS Omega. 2024 ; 9( 20): 22360-22370 + supporting information.[citado 2025 jul. 30 ] Available from: https://doi.org/10.1021/acsomega.4c01919
Vancouver
Slafer BW, Dessoy MA, Oliveira RG de, Mollo MC, Lee E, Matheeussen A, Maes L, Caljon G, Ferreira LLG, Krogh R, Andricopulo AD, Cruz L dos R, Mowbray CE, Kratz JM, Dias LC. Synthesis and anti-trypanosoma cruzi activity of 3-cyanopyridine derivatives [Internet]. ACS Omega. 2024 ; 9( 20): 22360-22370 + supporting information.[citado 2025 jul. 30 ] Available from: https://doi.org/10.1021/acsomega.4c01919
Trabalho de evento-resumo
Quinazoline-Chalcone hybrids as tubulin colchicine-binding site inhibitors for antimetastatic cancer drug discovery (2024)
Afonso, Maynara; Souza, Matheus da Silva ; Mass, Eduardo; Russowsky, Dennis; Andricopulo, Adriano Defini
Source: Anais. Conference titles: Reunião Anual da Sociedade Brasileira de Química - RASBQ. Unidade: IFSC
Subjects: CRISTALOGRAFIA, NEOPLASIAS MAMÁRIAS, METÁSTASE NEOPLÁSICA, FÁRMACOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
AFONSO, Maynara et al. Quinazoline-Chalcone hybrids as tubulin colchicine-binding site inhibitors for antimetastatic cancer drug discovery. 2024, Anais.. São Paulo: Sociedade Brasileira de Química - SBQ, 2024. Disponível em: https://www.eventweb.com.br/rasbq2024/specific-files/manuscripts/rasbq2024/585_1708142139.pdf. Acesso em: 30 jul. 2025.
APA
Afonso, M., Souza, M. da S., Mass, E., Russowsky, D., & Andricopulo, A. D. (2024). Quinazoline-Chalcone hybrids as tubulin colchicine-binding site inhibitors for antimetastatic cancer drug discovery. In Anais. São Paulo: Sociedade Brasileira de Química - SBQ. Recuperado de https://www.eventweb.com.br/rasbq2024/specific-files/manuscripts/rasbq2024/585_1708142139.pdf
NLM
Afonso M, Souza M da S, Mass E, Russowsky D, Andricopulo AD. Quinazoline-Chalcone hybrids as tubulin colchicine-binding site inhibitors for antimetastatic cancer drug discovery [Internet]. Anais. 2024 ;[citado 2025 jul. 30 ] Available from: https://www.eventweb.com.br/rasbq2024/specific-files/manuscripts/rasbq2024/585_1708142139.pdf
Vancouver
Afonso M, Souza M da S, Mass E, Russowsky D, Andricopulo AD. Quinazoline-Chalcone hybrids as tubulin colchicine-binding site inhibitors for antimetastatic cancer drug discovery [Internet]. Anais. 2024 ;[citado 2025 jul. 30 ] Available from: https://www.eventweb.com.br/rasbq2024/specific-files/manuscripts/rasbq2024/585_1708142139.pdf
Artigo de periodico
Neglected tropical diseases: a chemoinformatics approach for the use of biodiversity in anti-trypanosomatid drug discovery (2024)
Valli, Marilia ; Döring, Thiago Henrique ; Marx, Edgard ; Ferreira, Leonardo Luiz Gomes ; Franco, José L. Medina ; Andricopulo, Adriano Defini
Source: Biomolecules. Unidade: IFSC
Subjects: DOENÇAS NEGLIGENCIADAS, DOENÇAS TROPICAIS ANIMAL, FÁRMACOS, LEISHMANIA, DOENÇA DE CHAGAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VALLI, Marilia et al. Neglected tropical diseases: a chemoinformatics approach for the use of biodiversity in anti-trypanosomatid drug discovery. Biomolecules, v. 14, n. 8, p. 1033-1-1033-19 + supporting information, 2024Tradução . . Disponível em: https://doi.org/10.3390/biom14081033. Acesso em: 30 jul. 2025.
APA
Valli, M., Döring, T. H., Marx, E., Ferreira, L. L. G., Franco, J. L. M., & Andricopulo, A. D. (2024). Neglected tropical diseases: a chemoinformatics approach for the use of biodiversity in anti-trypanosomatid drug discovery. Biomolecules, 14( 8), 1033-1-1033-19 + supporting information. doi:10.3390/biom14081033
NLM
Valli M, Döring TH, Marx E, Ferreira LLG, Franco JLM, Andricopulo AD. Neglected tropical diseases: a chemoinformatics approach for the use of biodiversity in anti-trypanosomatid drug discovery [Internet]. Biomolecules. 2024 ; 14( 8): 1033-1-1033-19 + supporting information.[citado 2025 jul. 30 ] Available from: https://doi.org/10.3390/biom14081033
Vancouver
Valli M, Döring TH, Marx E, Ferreira LLG, Franco JLM, Andricopulo AD. Neglected tropical diseases: a chemoinformatics approach for the use of biodiversity in anti-trypanosomatid drug discovery [Internet]. Biomolecules. 2024 ; 14( 8): 1033-1-1033-19 + supporting information.[citado 2025 jul. 30 ] Available from: https://doi.org/10.3390/biom14081033

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