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Artigo de periodico
Solid-state NMR characterization of mefloquine resinate complexes designed for taste-masking pediatric formulations (2024)
Borré, Leandro Bandeira; Sousa, Eduardo Gomes Rodrigues de ; Gil, Rosane Aguiar da Silva San; Baptista, Mateus Marinho; Leitão, Alexandre Amaral ; Almeida, João Monnerat Araujo Ribeiro de ; Carr, Olivia; Oliveira Junior, Osvaldo Novais de ; Shimizu, Flávio Makoto ; Guimarães, Thiago Frances
Source: Pharmaceuticals. Unidade: IFSC
Subjects: MALÁRIA, FÁRMACOS, RESSONÂNCIA MAGNÉTICA NUCLEAR, APRENDIZADO COMPUTACIONAL
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BORRÉ, Leandro Bandeira et al. Solid-state NMR characterization of mefloquine resinate complexes designed for taste-masking pediatric formulations. Pharmaceuticals, v. 17, n. 7, p. 870-1-870-16 + supplementary materials, 2024Tradução . . Disponível em: https://doi.org/10.3390/ph17070870. Acesso em: 19 nov. 2024.
APA
Borré, L. B., Sousa, E. G. R. de, Gil, R. A. da S. S., Baptista, M. M., Leitão, A. A., Almeida, J. M. A. R. de, et al. (2024). Solid-state NMR characterization of mefloquine resinate complexes designed for taste-masking pediatric formulations. Pharmaceuticals, 17( 7), 870-1-870-16 + supplementary materials. doi:10.3390/ph17070870
NLM
Borré LB, Sousa EGR de, Gil RA da SS, Baptista MM, Leitão AA, Almeida JMAR de, Carr O, Oliveira Junior ON de, Shimizu FM, Guimarães TF. Solid-state NMR characterization of mefloquine resinate complexes designed for taste-masking pediatric formulations [Internet]. Pharmaceuticals. 2024 ; 17( 7): 870-1-870-16 + supplementary materials.[citado 2024 nov. 19 ] Available from: https://doi.org/10.3390/ph17070870
Vancouver
Borré LB, Sousa EGR de, Gil RA da SS, Baptista MM, Leitão AA, Almeida JMAR de, Carr O, Oliveira Junior ON de, Shimizu FM, Guimarães TF. Solid-state NMR characterization of mefloquine resinate complexes designed for taste-masking pediatric formulations [Internet]. Pharmaceuticals. 2024 ; 17( 7): 870-1-870-16 + supplementary materials.[citado 2024 nov. 19 ] Available from: https://doi.org/10.3390/ph17070870
Artigo de periodico
Cryo-EM structure of 1-deoxy-D-xylulose 5-phosphate synthase DXPS from plasmodium falciparum reveals a distinct N-terminal domain (2024)
Gawriljuk, Victor Oliveira; Godoy, Andre Schutzer de ; Oerlemans, Rick; Welker, Luise A. T.; Hirsch, Anna Katharina Herta ; Groves, Matthew R.
Source: Nature Communications. Unidade: IFSC
Subjects: MALÁRIA, PLASMODIUM FALCIPARUM, ENZIMAS
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ABNT
GAWRILJUK, Victor Oliveira et al. Cryo-EM structure of 1-deoxy-D-xylulose 5-phosphate synthase DXPS from plasmodium falciparum reveals a distinct N-terminal domain. Nature Communications, v. 15, p. 6642-1-6642-10 + supplementary information, 2024Tradução . . Disponível em: https://doi.org/10.1038/s41467-024-50671-9. Acesso em: 19 nov. 2024.
APA
Gawriljuk, V. O., Godoy, A. S. de, Oerlemans, R., Welker, L. A. T., Hirsch, A. K. H., & Groves, M. R. (2024). Cryo-EM structure of 1-deoxy-D-xylulose 5-phosphate synthase DXPS from plasmodium falciparum reveals a distinct N-terminal domain. Nature Communications, 15, 6642-1-6642-10 + supplementary information. doi:10.1038/s41467-024-50671-9
NLM
Gawriljuk VO, Godoy AS de, Oerlemans R, Welker LAT, Hirsch AKH, Groves MR. Cryo-EM structure of 1-deoxy-D-xylulose 5-phosphate synthase DXPS from plasmodium falciparum reveals a distinct N-terminal domain [Internet]. Nature Communications. 2024 ; 15 6642-1-6642-10 + supplementary information.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1038/s41467-024-50671-9
Vancouver
Gawriljuk VO, Godoy AS de, Oerlemans R, Welker LAT, Hirsch AKH, Groves MR. Cryo-EM structure of 1-deoxy-D-xylulose 5-phosphate synthase DXPS from plasmodium falciparum reveals a distinct N-terminal domain [Internet]. Nature Communications. 2024 ; 15 6642-1-6642-10 + supplementary information.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1038/s41467-024-50671-9
Trabalho de evento-resumo
Synthesis and antimalarial activity of 4-(m-piperazin-1-yl)phenyl marinoquinolines and thieno[2,3-c]quinolines: a structure-activity relationship study (2022)
Trajano, Bruna Inacio; Souza, Guilherme Eduardo de; Guido, Rafael Victorio Carvalho ; Correia, Carlos Roque
Source: Anais eletrônicos. Conference titles: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidade: IFSC
Subjects: MALÁRIA, ANTIMALÁRICOS, ANTIPARASITÁRIOS
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TRAJANO, Bruna Inacio et al. Synthesis and antimalarial activity of 4-(m-piperazin-1-yl)phenyl marinoquinolines and thieno[2,3-c]quinolines: a structure-activity relationship study. 2022, Anais.. Campinas: Galoá, 2022. Disponível em: https://proceedings.science/brazmedchem-2022/papers/synthesis-and-antimalarial-activity-of-4--m-piperazin-1-yl-phenyl-marinoquinolines-and-thieno-2-3-c-quinolines--a-struct. Acesso em: 19 nov. 2024.
APA
Trajano, B. I., Souza, G. E. de, Guido, R. V. C., & Correia, C. R. (2022). Synthesis and antimalarial activity of 4-(m-piperazin-1-yl)phenyl marinoquinolines and thieno[2,3-c]quinolines: a structure-activity relationship study. In Anais eletrônicos. Campinas: Galoá. Recuperado de https://proceedings.science/brazmedchem-2022/papers/synthesis-and-antimalarial-activity-of-4--m-piperazin-1-yl-phenyl-marinoquinolines-and-thieno-2-3-c-quinolines--a-struct.
NLM
Trajano BI, Souza GE de, Guido RVC, Correia CR. Synthesis and antimalarial activity of 4-(m-piperazin-1-yl)phenyl marinoquinolines and thieno[2,3-c]quinolines: a structure-activity relationship study [Internet]. Anais eletrônicos. 2022 ;[citado 2024 nov. 19 ] Available from: https://proceedings.science/brazmedchem-2022/papers/synthesis-and-antimalarial-activity-of-4--m-piperazin-1-yl-phenyl-marinoquinolines-and-thieno-2-3-c-quinolines--a-struct.
Vancouver
Trajano BI, Souza GE de, Guido RVC, Correia CR. Synthesis and antimalarial activity of 4-(m-piperazin-1-yl)phenyl marinoquinolines and thieno[2,3-c]quinolines: a structure-activity relationship study [Internet]. Anais eletrônicos. 2022 ;[citado 2024 nov. 19 ] Available from: https://proceedings.science/brazmedchem-2022/papers/synthesis-and-antimalarial-activity-of-4--m-piperazin-1-yl-phenyl-marinoquinolines-and-thieno-2-3-c-quinolines--a-struct.
Artigo de periodico
Biodefensive based on Piper nigrum essential oil for controlling of Anopheles aquasalis larvae: influence of temperature (35 °C) and preservatives (2022)
Vieira, Ayná Caroline Marcião ; Azevedo, Sidney Gomes; Linhares, Ramon Andrade; Justiniano, Silvia Cássia Brandão; Pontes, Grafe Oliveira ; Lima, Alessandra Ramos ; Campelo, Pedro Henrique ; Bezerra, Jaqueline de Araújo ; Pinto, Camila da Costa; Fonseca Filho, Henrique Duarte da ; Matos, Robert Saraiva ; Ţălu, Ştefan ; Bagnato, Vanderlei Salvador ; Inada, Natalia Mayumi ; Sanches, Edgar Aparecido
Source: Biomolecules. Unidade: IFSC
Subjects: MALÁRIA, ANOPHELES, ÓLEOS ESSENCIAIS
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ABNT
VIEIRA, Ayná Caroline Marcião et al. Biodefensive based on Piper nigrum essential oil for controlling of Anopheles aquasalis larvae: influence of temperature (35 °C) and preservatives. Biomolecules, v. No 2022, n. 11, p. 1711-1-1711-19, 2022Tradução . . Disponível em: https://doi.org/10.3390/biom12111711. Acesso em: 19 nov. 2024.
APA
Vieira, A. C. M., Azevedo, S. G., Linhares, R. A., Justiniano, S. C. B., Pontes, G. O., Lima, A. R., et al. (2022). Biodefensive based on Piper nigrum essential oil for controlling of Anopheles aquasalis larvae: influence of temperature (35 °C) and preservatives. Biomolecules, No 2022( 11), 1711-1-1711-19. doi:10.3390/biom12111711
NLM
Vieira ACM, Azevedo SG, Linhares RA, Justiniano SCB, Pontes GO, Lima AR, Campelo PH, Bezerra J de A, Pinto C da C, Fonseca Filho HD da, Matos RS, Ţălu Ş, Bagnato VS, Inada NM, Sanches EA. Biodefensive based on Piper nigrum essential oil for controlling of Anopheles aquasalis larvae: influence of temperature (35 °C) and preservatives [Internet]. Biomolecules. 2022 ; No 2022( 11): 1711-1-1711-19.[citado 2024 nov. 19 ] Available from: https://doi.org/10.3390/biom12111711
Vancouver
Vieira ACM, Azevedo SG, Linhares RA, Justiniano SCB, Pontes GO, Lima AR, Campelo PH, Bezerra J de A, Pinto C da C, Fonseca Filho HD da, Matos RS, Ţălu Ş, Bagnato VS, Inada NM, Sanches EA. Biodefensive based on Piper nigrum essential oil for controlling of Anopheles aquasalis larvae: influence of temperature (35 °C) and preservatives [Internet]. Biomolecules. 2022 ; No 2022( 11): 1711-1-1711-19.[citado 2024 nov. 19 ] Available from: https://doi.org/10.3390/biom12111711
Artigo de periodico
Preclinical characterization and target validation of the antimalarial pantothenamide MMV693183 (2022)
Vries, Laura E. ; Aguiar, Anna Caroline Campos ; Guido, Rafael Victorio Carvalho
Source: Nature Communications. Unidade: IFSC
Subjects: PLASMODIUM FALCIPARUM, PLANEJAMENTO DE FÁRMACOS, ANTIPARASITÁRIOS, MALÁRIA
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ABNT
VRIES, Laura E. e AGUIAR, Anna Caroline Campos e GUIDO, Rafael Victorio Carvalho. Preclinical characterization and target validation of the antimalarial pantothenamide MMV693183. Nature Communications, v. 13, p. 2158-1-2158-16, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41467-022-29688-5. Acesso em: 19 nov. 2024.
APA
Vries, L. E., Aguiar, A. C. C., & Guido, R. V. C. (2022). Preclinical characterization and target validation of the antimalarial pantothenamide MMV693183. Nature Communications, 13, 2158-1-2158-16. doi:10.1038/s41467-022-29688-5
NLM
Vries LE, Aguiar ACC, Guido RVC. Preclinical characterization and target validation of the antimalarial pantothenamide MMV693183 [Internet]. Nature Communications. 2022 ; 13 2158-1-2158-16.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1038/s41467-022-29688-5
Vancouver
Vries LE, Aguiar ACC, Guido RVC. Preclinical characterization and target validation of the antimalarial pantothenamide MMV693183 [Internet]. Nature Communications. 2022 ; 13 2158-1-2158-16.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1038/s41467-022-29688-5
Artigo de periodico
In vitro assessment for cytotoxicity screening of new antimalarial candidates (2022)
Espíndola, Mariana Rodrigues; Varotti, Fernando de Pilla; Aguiar, Anna Caroline Campos ; Andrade, Silmara Nunes; Rocha, Eliana Maria Mauricio da
Source: Brazilian Journal of Pharmaceutical Sciences. Unidade: IFSC
Subjects: ANTIMALÁRICOS, PLASMODIUM FALCIPARUM, PLANEJAMENTO DE FÁRMACOS, ANTIPARASITÁRIOS, MALÁRIA, BIOQUÍMICA, QUÍMICA MÉDICA
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ESPÍNDOLA, Mariana Rodrigues et al. In vitro assessment for cytotoxicity screening of new antimalarial candidates. Brazilian Journal of Pharmaceutical Sciences, v. 58, p. e18308-1-e18308-11, 2022Tradução . . Disponível em: https://doi.org/10.1590/s2175-97902022e18308. Acesso em: 19 nov. 2024.
APA
Espíndola, M. R., Varotti, F. de P., Aguiar, A. C. C., Andrade, S. N., & Rocha, E. M. M. da. (2022). In vitro assessment for cytotoxicity screening of new antimalarial candidates. Brazilian Journal of Pharmaceutical Sciences, 58, e18308-1-e18308-11. doi:10.1590/s2175-97902022e18308
NLM
Espíndola MR, Varotti F de P, Aguiar ACC, Andrade SN, Rocha EMM da. In vitro assessment for cytotoxicity screening of new antimalarial candidates [Internet]. Brazilian Journal of Pharmaceutical Sciences. 2022 ; 58 e18308-1-e18308-11.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s2175-97902022e18308
Vancouver
Espíndola MR, Varotti F de P, Aguiar ACC, Andrade SN, Rocha EMM da. In vitro assessment for cytotoxicity screening of new antimalarial candidates [Internet]. Brazilian Journal of Pharmaceutical Sciences. 2022 ; 58 e18308-1-e18308-11.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s2175-97902022e18308
Trabalho de evento-resumo
Síntese de novos derivados de marinoquinolinas indólicas com potencial atividade antimalárica (2022)
Silva, Wellington da; Souza, Guilherme Eduardo de ; Guido, Rafael Victorio Carvalho ; Correia, Carlos Roque Duarte
Source: Anais. Conference titles: Reunião Anual da Sociedade Brasileira de Química - RASBQ. Unidade: IFSC
Subjects: MALÁRIA, PLANEJAMENTO DE FÁRMACOS, QUÍMICA MÉDICA, PLASMODIUM FALCIPARUM
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SILVA, Wellington da et al. Síntese de novos derivados de marinoquinolinas indólicas com potencial atividade antimalárica. 2022, Anais.. São Paulo: Sociedade Brasileira de Química - SBQ, 2022. Disponível em: https://www.eventweb.com.br/45rasbq/specific-files/manuscripts/45rasbq/962_1647717551.pdf. Acesso em: 19 nov. 2024.
APA
Silva, W. da, Souza, G. E. de, Guido, R. V. C., & Correia, C. R. D. (2022). Síntese de novos derivados de marinoquinolinas indólicas com potencial atividade antimalárica. In Anais. São Paulo: Sociedade Brasileira de Química - SBQ. Recuperado de https://www.eventweb.com.br/45rasbq/specific-files/manuscripts/45rasbq/962_1647717551.pdf
NLM
Silva W da, Souza GE de, Guido RVC, Correia CRD. Síntese de novos derivados de marinoquinolinas indólicas com potencial atividade antimalárica [Internet]. Anais. 2022 ;[citado 2024 nov. 19 ] Available from: https://www.eventweb.com.br/45rasbq/specific-files/manuscripts/45rasbq/962_1647717551.pdf
Vancouver
Silva W da, Souza GE de, Guido RVC, Correia CRD. Síntese de novos derivados de marinoquinolinas indólicas com potencial atividade antimalárica [Internet]. Anais. 2022 ;[citado 2024 nov. 19 ] Available from: https://www.eventweb.com.br/45rasbq/specific-files/manuscripts/45rasbq/962_1647717551.pdf
Trabalho de evento-resumo
Better medicines for children: development and evaluation of chloroquine diphosphate using ion exchange resins to overcome taste masking challenges (2022)
Guimarães, Thiago Frances ; Vital, Italo C. F.; Silva, Valéria G.; Fonseca, Laís B.; Carr, Olivia; Oliveira Junior, Osvaldo Novais de ; Shimizu, Flávio Makoto ; Boniatti, Janine; Viçosa, Alessandra L.
Source: Anais. Conference titles: Reunião Nacional de Pesquisa em Malária - RNP. Unidade: IFSC
Subjects: MALÁRIA, MEDICAMENTO, FARMACOLOGIA, PEDIATRIA
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ABNT
GUIMARÃES, Thiago Frances et al. Better medicines for children: development and evaluation of chloroquine diphosphate using ion exchange resins to overcome taste masking challenges. 2022, Anais.. Rio de Janeiro: Fundação Oswaldo Cruz - FIOCRUZ, 2022. Disponível em: https://www.malaria2020.com.br/trabalhos. Acesso em: 19 nov. 2024.
APA
Guimarães, T. F., Vital, I. C. F., Silva, V. G., Fonseca, L. B., Carr, O., Oliveira Junior, O. N. de, et al. (2022). Better medicines for children: development and evaluation of chloroquine diphosphate using ion exchange resins to overcome taste masking challenges. In Anais. Rio de Janeiro: Fundação Oswaldo Cruz - FIOCRUZ. Recuperado de https://www.malaria2020.com.br/trabalhos
NLM
Guimarães TF, Vital ICF, Silva VG, Fonseca LB, Carr O, Oliveira Junior ON de, Shimizu FM, Boniatti J, Viçosa AL. Better medicines for children: development and evaluation of chloroquine diphosphate using ion exchange resins to overcome taste masking challenges [Internet]. Anais. 2022 ;[citado 2024 nov. 19 ] Available from: https://www.malaria2020.com.br/trabalhos
Vancouver
Guimarães TF, Vital ICF, Silva VG, Fonseca LB, Carr O, Oliveira Junior ON de, Shimizu FM, Boniatti J, Viçosa AL. Better medicines for children: development and evaluation of chloroquine diphosphate using ion exchange resins to overcome taste masking challenges [Internet]. Anais. 2022 ;[citado 2024 nov. 19 ] Available from: https://www.malaria2020.com.br/trabalhos
Artigo de periodico
Epidemiological characterization and sensitivity to traditional antimalarials of Plasmodium spp. isolates from Porto Velho, western Amazon, Brazil (2022)
Medeiros, Daniel Sol Sol de; Ferreira, Amália dos Santos; Almeida, Marcinete Latorre; Rossi, Norton Rubens Diunior Lucas Pejara; Barbosa, Raul Afonso Pommer; Santos, Ana Paula Azevedo dos; Aguiar, Anna Caroline Campos ; Tada, Mauro Shugiro; Pereira, Dhelio Batista; Teles, Carolina Bioni Garcia
Source: Revista Eletrônica Acervo Saúde. Unidade: IFSC
Subjects: ANTIMALÁRICOS, PLASMODIUM FALCIPARUM, PLANEJAMENTO DE FÁRMACOS, ANTIPARASITÁRIOS, MALÁRIA, BIOQUÍMICA, QUÍMICA MÉDICA
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ABNT
MEDEIROS, Daniel Sol Sol de et al. Epidemiological characterization and sensitivity to traditional antimalarials of Plasmodium spp. isolates from Porto Velho, western Amazon, Brazil. Revista Eletrônica Acervo Saúde, v. 15, n. 9, p. e10745-1-e10745-13, 2022Tradução . . Disponível em: https://doi.org/10.25248/REAS.e10745.2022. Acesso em: 19 nov. 2024.
APA
Medeiros, D. S. S. de, Ferreira, A. dos S., Almeida, M. L., Rossi, N. R. D. L. P., Barbosa, R. A. P., Santos, A. P. A. dos, et al. (2022). Epidemiological characterization and sensitivity to traditional antimalarials of Plasmodium spp. isolates from Porto Velho, western Amazon, Brazil. Revista Eletrônica Acervo Saúde, 15( 9), e10745-1-e10745-13. doi:10.25248/REAS.e10745.2022
NLM
Medeiros DSS de, Ferreira A dos S, Almeida ML, Rossi NRDLP, Barbosa RAP, Santos APA dos, Aguiar ACC, Tada MS, Pereira DB, Teles CBG. Epidemiological characterization and sensitivity to traditional antimalarials of Plasmodium spp. isolates from Porto Velho, western Amazon, Brazil [Internet]. Revista Eletrônica Acervo Saúde. 2022 ; 15( 9): e10745-1-e10745-13.[citado 2024 nov. 19 ] Available from: https://doi.org/10.25248/REAS.e10745.2022
Vancouver
Medeiros DSS de, Ferreira A dos S, Almeida ML, Rossi NRDLP, Barbosa RAP, Santos APA dos, Aguiar ACC, Tada MS, Pereira DB, Teles CBG. Epidemiological characterization and sensitivity to traditional antimalarials of Plasmodium spp. isolates from Porto Velho, western Amazon, Brazil [Internet]. Revista Eletrônica Acervo Saúde. 2022 ; 15( 9): e10745-1-e10745-13.[citado 2024 nov. 19 ] Available from: https://doi.org/10.25248/REAS.e10745.2022
Artigo de periodico
Discovery and preclinical pharmacology of INE963, a potent and fast-acting blood-stage antimalarial with a high barrier to resistance and potential for single-dose cures in uncomplicated malaria (2022)
Taft, Benjamin R.; Aguiar, Anna Caroline Campos
Source: Journal of Medicinal Chemistry. Unidade: IFSC
Subjects: ANTIMALÁRICOS, PLASMODIUM FALCIPARUM, PLANEJAMENTO DE FÁRMACOS, ANTIPARASITÁRIOS, MALÁRIA, BIOQUÍMICA, QUÍMICA MÉDICA
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ABNT
TAFT, Benjamin R. e AGUIAR, Anna Caroline Campos. Discovery and preclinical pharmacology of INE963, a potent and fast-acting blood-stage antimalarial with a high barrier to resistance and potential for single-dose cures in uncomplicated malaria. Journal of Medicinal Chemistry, v. 65, n. 5, p. 3798-3813, 2022Tradução . . Disponível em: https://doi.org/10.1021/acs.jmedchem.1c01995. Acesso em: 19 nov. 2024.
APA
Taft, B. R., & Aguiar, A. C. C. (2022). Discovery and preclinical pharmacology of INE963, a potent and fast-acting blood-stage antimalarial with a high barrier to resistance and potential for single-dose cures in uncomplicated malaria. Journal of Medicinal Chemistry, 65( 5), 3798-3813. doi:10.1021/acs.jmedchem.1c01995
NLM
Taft BR, Aguiar ACC. Discovery and preclinical pharmacology of INE963, a potent and fast-acting blood-stage antimalarial with a high barrier to resistance and potential for single-dose cures in uncomplicated malaria [Internet]. Journal of Medicinal Chemistry. 2022 ; 65( 5): 3798-3813.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1021/acs.jmedchem.1c01995
Vancouver
Taft BR, Aguiar ACC. Discovery and preclinical pharmacology of INE963, a potent and fast-acting blood-stage antimalarial with a high barrier to resistance and potential for single-dose cures in uncomplicated malaria [Internet]. Journal of Medicinal Chemistry. 2022 ; 65( 5): 3798-3813.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1021/acs.jmedchem.1c01995
Artigo de periodico
Potent antimalarials with development potential identified by structure-guided computational optimization of a pyrrole-based dihydroorotate dehydrogenase inhibitor series (2021)
Palmer, Michael J.; Aguiar, Anna Caroline Campos; Guido, Rafael Victorio Carvalho
Source: Journal of Medicinal Chemistry. Unidade: IFSC
Subjects: ANTIMALÁRICOS, PLASMODIUM FALCIPARUM, PLANEJAMENTO DE FÁRMACOS, ANTIPARASITÁRIOS, MALÁRIA, BIOQUÍMICA, QUÍMICA MÉDICA
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ABNT
PALMER, Michael J. e AGUIAR, Anna Caroline Campos e GUIDO, Rafael Victorio Carvalho. Potent antimalarials with development potential identified by structure-guided computational optimization of a pyrrole-based dihydroorotate dehydrogenase inhibitor series. Journal of Medicinal Chemistry, v. 64, n. 9, p. 6085-6136, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.jmedchem.1c00173. Acesso em: 19 nov. 2024.
APA
Palmer, M. J., Aguiar, A. C. C., & Guido, R. V. C. (2021). Potent antimalarials with development potential identified by structure-guided computational optimization of a pyrrole-based dihydroorotate dehydrogenase inhibitor series. Journal of Medicinal Chemistry, 64( 9), 6085-6136. doi:10.1021/acs.jmedchem.1c00173
NLM
Palmer MJ, Aguiar ACC, Guido RVC. Potent antimalarials with development potential identified by structure-guided computational optimization of a pyrrole-based dihydroorotate dehydrogenase inhibitor series [Internet]. Journal of Medicinal Chemistry. 2021 ; 64( 9): 6085-6136.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1021/acs.jmedchem.1c00173
Vancouver
Palmer MJ, Aguiar ACC, Guido RVC. Potent antimalarials with development potential identified by structure-guided computational optimization of a pyrrole-based dihydroorotate dehydrogenase inhibitor series [Internet]. Journal of Medicinal Chemistry. 2021 ; 64( 9): 6085-6136.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1021/acs.jmedchem.1c00173
Artigo de periodico
Design of proteasome inhibitors with oral efficacy in vivo against Plasmodium falciparum and selectivity over the human proteasome (2021)
Xie, Stanley C. ; Aguiar, Anna Caroline Campos ; Guido, Rafael Victorio Carvalho
Source: Proceedings of the National Academy of Sciences of the United States of America - PNAS. Unidade: IFSC
Subjects: PLASMODIUM FALCIPARUM, PLANEJAMENTO DE FÁRMACOS, MALÁRIA, QUÍMICA MÉDICA
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ABNT
XIE, Stanley C. e AGUIAR, Anna Caroline Campos e GUIDO, Rafael Victorio Carvalho. Design of proteasome inhibitors with oral efficacy in vivo against Plasmodium falciparum and selectivity over the human proteasome. Proceedings of the National Academy of Sciences of the United States of America - PNAS, v. 118, n. 39, p. e2107213118-1-e2107213118-9, 2021Tradução . . Disponível em: https://doi.org/10.1073/pnas.2107213118. Acesso em: 19 nov. 2024.
APA
Xie, S. C., Aguiar, A. C. C., & Guido, R. V. C. (2021). Design of proteasome inhibitors with oral efficacy in vivo against Plasmodium falciparum and selectivity over the human proteasome. Proceedings of the National Academy of Sciences of the United States of America - PNAS, 118( 39), e2107213118-1-e2107213118-9. doi:10.1073/pnas.2107213118
NLM
Xie SC, Aguiar ACC, Guido RVC. Design of proteasome inhibitors with oral efficacy in vivo against Plasmodium falciparum and selectivity over the human proteasome [Internet]. Proceedings of the National Academy of Sciences of the United States of America - PNAS. 2021 ; 118( 39): e2107213118-1-e2107213118-9.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1073/pnas.2107213118
Vancouver
Xie SC, Aguiar ACC, Guido RVC. Design of proteasome inhibitors with oral efficacy in vivo against Plasmodium falciparum and selectivity over the human proteasome [Internet]. Proceedings of the National Academy of Sciences of the United States of America - PNAS. 2021 ; 118( 39): e2107213118-1-e2107213118-9.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1073/pnas.2107213118
Artigo de periodico
Repositioning and characterization of 1‑(Pyridin-4-yl)pyrrolidin-2- one derivatives as plasmodium cytoplasmic prolyl-tRNA synthetase inhibitors (2021)
Okaniwa, Masanori; Aguiar, Anna Caroline Campos; Guido, Rafael Victorio Carvalho
Source: ACS Infectious Diseases. Unidade: IFSC
Subjects: PLASMODIUM, MALÁRIA, ANTIMALÁRICOS, ANTIPARASITÁRIOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OKANIWA, Masanori e AGUIAR, Anna Caroline Campos e GUIDO, Rafael Victorio Carvalho. Repositioning and characterization of 1‑(Pyridin-4-yl)pyrrolidin-2- one derivatives as plasmodium cytoplasmic prolyl-tRNA synthetase inhibitors. ACS Infectious Diseases, v. 7, n. 6, p. 1680-1689, 2021Tradução . . Disponível em: https://doi.org/10.1021/acsinfecdis.1c00020. Acesso em: 19 nov. 2024.
APA
Okaniwa, M., Aguiar, A. C. C., & Guido, R. V. C. (2021). Repositioning and characterization of 1‑(Pyridin-4-yl)pyrrolidin-2- one derivatives as plasmodium cytoplasmic prolyl-tRNA synthetase inhibitors. ACS Infectious Diseases, 7( 6), 1680-1689. doi:10.1021/acsinfecdis.1c00020
NLM
Okaniwa M, Aguiar ACC, Guido RVC. Repositioning and characterization of 1‑(Pyridin-4-yl)pyrrolidin-2- one derivatives as plasmodium cytoplasmic prolyl-tRNA synthetase inhibitors [Internet]. ACS Infectious Diseases. 2021 ; 7( 6): 1680-1689.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1021/acsinfecdis.1c00020
Vancouver
Okaniwa M, Aguiar ACC, Guido RVC. Repositioning and characterization of 1‑(Pyridin-4-yl)pyrrolidin-2- one derivatives as plasmodium cytoplasmic prolyl-tRNA synthetase inhibitors [Internet]. ACS Infectious Diseases. 2021 ; 7( 6): 1680-1689.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1021/acsinfecdis.1c00020
Artigo de periodico
Comparative study between the anti-P. falciparum activity of triazolopyrimidine, pyrazolopyrimidine and quinoline derivatives and the identification of new PfDHODH inhibitors (2021)
Silveira, Flávia F.; Souza, Juliana Oliveira de; Hoelz, Lucas V. B.; Campos, Vinícius R.; Jabor, Valquíria Aparecida Polisel; Aguiar, Anna Caroline Campos; Nonato, Maria Cristina ; Albuquerque, Magaly G. ; Guido, Rafael Victorio Carvalho ; Boechat, Nubia; Pinheiro, Luiz C. S.
Source: European Journal of Medicinal Chemistry. Unidades: IFSC, FCFRP
Subjects: ANTIMALÁRICOS, ANTIPARASITÁRIOS, MALÁRIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVEIRA, Flávia F. et al. Comparative study between the anti-P. falciparum activity of triazolopyrimidine, pyrazolopyrimidine and quinoline derivatives and the identification of new PfDHODH inhibitors. European Journal of Medicinal Chemistry, v. 209, n. Ja 2021, p. 112941-1-112941-16, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2020.112941. Acesso em: 19 nov. 2024.
APA
Silveira, F. F., Souza, J. O. de, Hoelz, L. V. B., Campos, V. R., Jabor, V. A. P., Aguiar, A. C. C., et al. (2021). Comparative study between the anti-P. falciparum activity of triazolopyrimidine, pyrazolopyrimidine and quinoline derivatives and the identification of new PfDHODH inhibitors. European Journal of Medicinal Chemistry, 209( Ja 2021), 112941-1-112941-16. doi:10.1016/j.ejmech.2020.112941
NLM
Silveira FF, Souza JO de, Hoelz LVB, Campos VR, Jabor VAP, Aguiar ACC, Nonato MC, Albuquerque MG, Guido RVC, Boechat N, Pinheiro LCS. Comparative study between the anti-P. falciparum activity of triazolopyrimidine, pyrazolopyrimidine and quinoline derivatives and the identification of new PfDHODH inhibitors [Internet]. European Journal of Medicinal Chemistry. 2021 ; 209( Ja 2021): 112941-1-112941-16.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.ejmech.2020.112941
Vancouver
Silveira FF, Souza JO de, Hoelz LVB, Campos VR, Jabor VAP, Aguiar ACC, Nonato MC, Albuquerque MG, Guido RVC, Boechat N, Pinheiro LCS. Comparative study between the anti-P. falciparum activity of triazolopyrimidine, pyrazolopyrimidine and quinoline derivatives and the identification of new PfDHODH inhibitors [Internet]. European Journal of Medicinal Chemistry. 2021 ; 209( Ja 2021): 112941-1-112941-16.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.ejmech.2020.112941
Artigo de periodico
A multistage formulation based on full-length csp and AMA-1 ectodomain of plasmodium vivax induces high antibody titers and T-cells and partially protects mice challenged with a transgenic plasmodium berghei parasite (2020)
Lima, Luciana ; Marques, Rodolfo Ferreira ; Gimenez, Alba Marina; Françoso, Katia Sanches; Aliprandini, Eduardo ; Camargo, Tarsila Mendes de; Aguiar, Anna Caroline Campos; Pereira, Dhelio Batista ; Renia, Laurent ; Amino, Rogerio ; Soares, Irene da Silva
Source: Microorganisms. Unidades: FCF, FM, IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, DOENÇAS NEGLIGENCIADAS, MALÁRIA, ANTIMALÁRICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LIMA, Luciana et al. A multistage formulation based on full-length csp and AMA-1 ectodomain of plasmodium vivax induces high antibody titers and T-cells and partially protects mice challenged with a transgenic plasmodium berghei parasite. Microorganisms, v. 8, n. 6, p. 916-1-916-17, 2020Tradução . . Disponível em: https://doi.org/10.3390/microorganisms8060916. Acesso em: 19 nov. 2024.
APA
Lima, L., Marques, R. F., Gimenez, A. M., Françoso, K. S., Aliprandini, E., Camargo, T. M. de, et al. (2020). A multistage formulation based on full-length csp and AMA-1 ectodomain of plasmodium vivax induces high antibody titers and T-cells and partially protects mice challenged with a transgenic plasmodium berghei parasite. Microorganisms, 8( 6), 916-1-916-17. doi:10.3390/microorganisms8060916
NLM
Lima L, Marques RF, Gimenez AM, Françoso KS, Aliprandini E, Camargo TM de, Aguiar ACC, Pereira DB, Renia L, Amino R, Soares I da S. A multistage formulation based on full-length csp and AMA-1 ectodomain of plasmodium vivax induces high antibody titers and T-cells and partially protects mice challenged with a transgenic plasmodium berghei parasite [Internet]. Microorganisms. 2020 ; 8( 6): 916-1-916-17.[citado 2024 nov. 19 ] Available from: https://doi.org/10.3390/microorganisms8060916
Vancouver
Lima L, Marques RF, Gimenez AM, Françoso KS, Aliprandini E, Camargo TM de, Aguiar ACC, Pereira DB, Renia L, Amino R, Soares I da S. A multistage formulation based on full-length csp and AMA-1 ectodomain of plasmodium vivax induces high antibody titers and T-cells and partially protects mice challenged with a transgenic plasmodium berghei parasite [Internet]. Microorganisms. 2020 ; 8( 6): 916-1-916-17.[citado 2024 nov. 19 ] Available from: https://doi.org/10.3390/microorganisms8060916
Parte de monografia/livro
Fármacos antimaláricos (2020)
Souza, Guilherme Eduardo de; Aguiar, Anna Caroline Campos
Source: Livro Texto de Farmacologia: casos clínicos e atividades didáticas. Unidade: IFSC
Subjects: ANTIMALÁRICOS, MALÁRIA, DOENÇAS TROPICAIS ANIMAL, PLANEJAMENTO DE FÁRMACOS, FARMACOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SOUZA, Guilherme Eduardo de e AGUIAR, Anna Caroline Campos. Fármacos antimaláricos. Livro Texto de Farmacologia: casos clínicos e atividades didáticas. Tradução . Rio de Janeiro: Atheneu, 2020. p. 1148 . . Acesso em: 19 nov. 2024.
APA
Souza, G. E. de, & Aguiar, A. C. C. (2020). Fármacos antimaláricos. In Livro Texto de Farmacologia: casos clínicos e atividades didáticas (p. 1148 ). Rio de Janeiro: Atheneu.
NLM
Souza GE de, Aguiar ACC. Fármacos antimaláricos. In: Livro Texto de Farmacologia: casos clínicos e atividades didáticas. Rio de Janeiro: Atheneu; 2020. p. 1148 .[citado 2024 nov. 19 ]
Vancouver
Souza GE de, Aguiar ACC. Fármacos antimaláricos. In: Livro Texto de Farmacologia: casos clínicos e atividades didáticas. Rio de Janeiro: Atheneu; 2020. p. 1148 .[citado 2024 nov. 19 ]
Artigo de periodico
New molecular targets and strategies for antimalarial discovery (2019)
Aguiar, Anna Caroline Campos; Sousa, Lorena R. F.; Garcia, Célia Regina da Silva ; Oliva, Glaucius ; Guido, Rafael Victorio Carvalho
Source: Current Medicinal Chemistry. Unidades: IFSC, IB
Subjects: DOENÇAS TROPICAIS ANIMAL, MALÁRIA, PLANEJAMENTO DE FÁRMACOS, ANTIMALÁRICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
AGUIAR, Anna Caroline Campos et al. New molecular targets and strategies for antimalarial discovery. Current Medicinal Chemistry, v. 26, n. 23, p. 4380-4402, 2019Tradução . . Disponível em: https://doi.org/10.2174/0929867324666170830103003. Acesso em: 19 nov. 2024.
APA
Aguiar, A. C. C., Sousa, L. R. F., Garcia, C. R. da S., Oliva, G., & Guido, R. V. C. (2019). New molecular targets and strategies for antimalarial discovery. Current Medicinal Chemistry, 26( 23), 4380-4402. doi:10.2174/0929867324666170830103003
NLM
Aguiar ACC, Sousa LRF, Garcia CR da S, Oliva G, Guido RVC. New molecular targets and strategies for antimalarial discovery [Internet]. Current Medicinal Chemistry. 2019 ; 26( 23): 4380-4402.[citado 2024 nov. 19 ] Available from: https://doi.org/10.2174/0929867324666170830103003
Vancouver
Aguiar ACC, Sousa LRF, Garcia CR da S, Oliva G, Guido RVC. New molecular targets and strategies for antimalarial discovery [Internet]. Current Medicinal Chemistry. 2019 ; 26( 23): 4380-4402.[citado 2024 nov. 19 ] Available from: https://doi.org/10.2174/0929867324666170830103003
Trabalho de evento-resumo
Aryl benzimidazoles: a new lead in malaria drug discovery (2019)
Kumar, Malkeet; Salas, Yuvixza Lizarme; Dias, Luiz Carlos; Aguiar, Anna Caroline Campos; Guido, Rafael Victorio Carvalho ; Jones, Barry; Willis, Paul; Fuchs, Aline; Campbell, Simon; Vongeldern, Tom
Source: Anais eletrônicos. Conference titles: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidade: IFSC
Subjects: MALÁRIA, PLASMODIUM, PLANEJAMENTO DE FÁRMACOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KUMAR, Malkeet et al. Aryl benzimidazoles: a new lead in malaria drug discovery. 2019, Anais.. Campinas: Galoá, 2019. Disponível em: https://proceedings.science/p/107216. Acesso em: 19 nov. 2024.
APA
Kumar, M., Salas, Y. L., Dias, L. C., Aguiar, A. C. C., Guido, R. V. C., Jones, B., et al. (2019). Aryl benzimidazoles: a new lead in malaria drug discovery. In Anais eletrônicos. Campinas: Galoá. Recuperado de https://proceedings.science/p/107216
NLM
Kumar M, Salas YL, Dias LC, Aguiar ACC, Guido RVC, Jones B, Willis P, Fuchs A, Campbell S, Vongeldern T. Aryl benzimidazoles: a new lead in malaria drug discovery [Internet]. Anais eletrônicos. 2019 ;[citado 2024 nov. 19 ] Available from: https://proceedings.science/p/107216
Vancouver
Kumar M, Salas YL, Dias LC, Aguiar ACC, Guido RVC, Jones B, Willis P, Fuchs A, Campbell S, Vongeldern T. Aryl benzimidazoles: a new lead in malaria drug discovery [Internet]. Anais eletrônicos. 2019 ;[citado 2024 nov. 19 ] Available from: https://proceedings.science/p/107216
Artigo de periodico
Antiplasmodial profile of selected compounds from Malaria Box: in vitro evaluation, speed of action and drug combination studies (2019)
Souza, Guilherme Eduardo de; Bueno, Renata Vieira; Souza, Juliana Oliveira de; Zanini, Camila Lima; Cruz, Fábio Cardoso; Oliva, Glaucius ; Guido, Rafael Victorio Carvalho ; Aguiar, Anna Caroline Campos
Source: Malaria Journal. Unidade: IFSC
Subjects: DOENÇAS TROPICAIS ANIMAL, MALÁRIA, PLANEJAMENTO DE FÁRMACOS, ANTIMALÁRICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SOUZA, Guilherme Eduardo de et al. Antiplasmodial profile of selected compounds from Malaria Box: in vitro evaluation, speed of action and drug combination studies. Malaria Journal, v. 18, n. 23, p. 447-1-447-13, 2019Tradução . . Disponível em: https://doi.org/10.1186/s12936-019-3069-3. Acesso em: 19 nov. 2024.
APA
Souza, G. E. de, Bueno, R. V., Souza, J. O. de, Zanini, C. L., Cruz, F. C., Oliva, G., et al. (2019). Antiplasmodial profile of selected compounds from Malaria Box: in vitro evaluation, speed of action and drug combination studies. Malaria Journal, 18( 23), 447-1-447-13. doi:10.1186/s12936-019-3069-3
NLM
Souza GE de, Bueno RV, Souza JO de, Zanini CL, Cruz FC, Oliva G, Guido RVC, Aguiar ACC. Antiplasmodial profile of selected compounds from Malaria Box: in vitro evaluation, speed of action and drug combination studies [Internet]. Malaria Journal. 2019 ; 18( 23): 447-1-447-13.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1186/s12936-019-3069-3
Vancouver
Souza GE de, Bueno RV, Souza JO de, Zanini CL, Cruz FC, Oliva G, Guido RVC, Aguiar ACC. Antiplasmodial profile of selected compounds from Malaria Box: in vitro evaluation, speed of action and drug combination studies [Internet]. Malaria Journal. 2019 ; 18( 23): 447-1-447-13.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1186/s12936-019-3069-3

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