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Artigo de periodico
Synthesis, biochemical evaluation and molecular modeling studies of nonpeptidic nitrile-based fluorinated compounds (2021)
Lameiro, Rafael da Fonseca; Shamim, Anwar ; Rosini, Fabiana; Cendron, Rodrigo; Batista, Pedro Henrique Jatai ; Montanari, Carlos Alberto
Fonte: Future Medicinal Chemistry. Unidade: IQSC
Assuntos: DOENÇA DE CHAGAS, LEISHMANIA MEXICANA
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ABNT
LAMEIRO, Rafael da Fonseca et al. Synthesis, biochemical evaluation and molecular modeling studies of nonpeptidic nitrile-based fluorinated compounds. Future Medicinal Chemistry, v. 13, n. 1, p. 25–43, 2021Tradução . . Disponível em: https://doi.org/10.4155/fmc-2020-0057. Acesso em: 23 nov. 2025.
APA
Lameiro, R. da F., Shamim, A., Rosini, F., Cendron, R., Batista, P. H. J., & Montanari, C. A. (2021). Synthesis, biochemical evaluation and molecular modeling studies of nonpeptidic nitrile-based fluorinated compounds. Future Medicinal Chemistry, 13( 1), 25–43. doi:10.4155/fmc-2020-0057
NLM
Lameiro R da F, Shamim A, Rosini F, Cendron R, Batista PHJ, Montanari CA. Synthesis, biochemical evaluation and molecular modeling studies of nonpeptidic nitrile-based fluorinated compounds [Internet]. Future Medicinal Chemistry. 2021 ; 13( 1): 25–43.[citado 2025 nov. 23 ] Available from: https://doi.org/10.4155/fmc-2020-0057
Vancouver
Lameiro R da F, Shamim A, Rosini F, Cendron R, Batista PHJ, Montanari CA. Synthesis, biochemical evaluation and molecular modeling studies of nonpeptidic nitrile-based fluorinated compounds [Internet]. Future Medicinal Chemistry. 2021 ; 13( 1): 25–43.[citado 2025 nov. 23 ] Available from: https://doi.org/10.4155/fmc-2020-0057
Artigo de periodico
Design, synthesis and stepwise optimization of nitrile-based inhibitors of cathepsins B and L (2021)
Cianni, Lorenzo ; Rocho, Fernanda dos Reis ; Bonatto, Vinícius ; Martins, Felipe Cardoso Prado ; Lameira, Jerônimo ; Leitão, Andrei ; Montanari, Carlos Alberto ; Shamim, Anwar
Fonte: Bioorganic and Medicinal Chemistry. Unidade: IQSC
Assuntos: QUÍMICA MÉDICA, NEOPLASIAS, INIBIDORES DE ENZIMAS
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ABNT
CIANNI, Lorenzo et al. Design, synthesis and stepwise optimization of nitrile-based inhibitors of cathepsins B and L. Bioorganic and Medicinal Chemistry, v. 29, p. 115827, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2020.115827. Acesso em: 23 nov. 2025.
APA
Cianni, L., Rocho, F. dos R., Bonatto, V., Martins, F. C. P., Lameira, J., Leitão, A., et al. (2021). Design, synthesis and stepwise optimization of nitrile-based inhibitors of cathepsins B and L. Bioorganic and Medicinal Chemistry, 29, 115827. doi:10.1016/j.bmc.2020.115827
NLM
Cianni L, Rocho F dos R, Bonatto V, Martins FCP, Lameira J, Leitão A, Montanari CA, Shamim A. Design, synthesis and stepwise optimization of nitrile-based inhibitors of cathepsins B and L [Internet]. Bioorganic and Medicinal Chemistry. 2021 ; 29 115827.[citado 2025 nov. 23 ] Available from: https://doi.org/10.1016/j.bmc.2020.115827
Vancouver
Cianni L, Rocho F dos R, Bonatto V, Martins FCP, Lameira J, Leitão A, Montanari CA, Shamim A. Design, synthesis and stepwise optimization of nitrile-based inhibitors of cathepsins B and L [Internet]. Bioorganic and Medicinal Chemistry. 2021 ; 29 115827.[citado 2025 nov. 23 ] Available from: https://doi.org/10.1016/j.bmc.2020.115827
Artigo de periodico
Synthesis and matched molecular pair analysis of covalent reversible inhibitors of the cysteine protease CPB (2020)
Matos, Thiago Kelvin Brito ; Batista, Pedro Henrique Jatai ; Rocho, Fernanda dos Reis ; Vita, Daniela de ; Pearce, Nicholas; Kellam, Barrie ; Montanari, Carlos Alberto ; Leitão, Andrei
Fonte: Bioorganic & Medicinal Chemistry Letters. Unidade: IQSC
Assuntos: QUÍMICA ORGÂNICA, MEDICAMENTO, INIBIDORES DE ENZIMAS
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ABNT
MATOS, Thiago Kelvin Brito et al. Synthesis and matched molecular pair analysis of covalent reversible inhibitors of the cysteine protease CPB. Bioorganic & Medicinal Chemistry Letters, v. 30, n. 18, p. 127439, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.bmcl.2020.127439. Acesso em: 23 nov. 2025.
APA
Matos, T. K. B., Batista, P. H. J., Rocho, F. dos R., Vita, D. de, Pearce, N., Kellam, B., et al. (2020). Synthesis and matched molecular pair analysis of covalent reversible inhibitors of the cysteine protease CPB. Bioorganic & Medicinal Chemistry Letters, 30( 18), 127439. doi:10.1016/j.bmcl.2020.127439
NLM
Matos TKB, Batista PHJ, Rocho F dos R, Vita D de, Pearce N, Kellam B, Montanari CA, Leitão A. Synthesis and matched molecular pair analysis of covalent reversible inhibitors of the cysteine protease CPB [Internet]. Bioorganic & Medicinal Chemistry Letters. 2020 ; 30( 18): 127439.[citado 2025 nov. 23 ] Available from: https://doi.org/10.1016/j.bmcl.2020.127439
Vancouver
Matos TKB, Batista PHJ, Rocho F dos R, Vita D de, Pearce N, Kellam B, Montanari CA, Leitão A. Synthesis and matched molecular pair analysis of covalent reversible inhibitors of the cysteine protease CPB [Internet]. Bioorganic & Medicinal Chemistry Letters. 2020 ; 30( 18): 127439.[citado 2025 nov. 23 ] Available from: https://doi.org/10.1016/j.bmcl.2020.127439
Artigo de periodico
On the intrinsic reactivity of highly potent trypanocidal cruzain inhibitors (2020)
Bonatt, Vinicius; Batista, Pedro Henrique Jatai ; Cianni, Lorenzo ; Vita, Daniela de ; Silva, Daniel G da; Cedron, Rodrigo; Tezuka, Daiane Yukie; Albuquerque, Sérgio de ; Moraes, Carolina Borsoi ; Franco, Caio Haddad ; Lameira, Jerônimo ; Leitão, Andrei ; Montanari, Carlos Alberto
Fonte: RSC Medicinal Chemistry. Unidades: PUSP-RP, IQSC, Interunidades em Bioengenharia
Assunto: DOENÇA DE CHAGAS
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ABNT
BONATT, Vinicius et al. On the intrinsic reactivity of highly potent trypanocidal cruzain inhibitors. RSC Medicinal Chemistry, v. 11, n. 11, p. 1275-1284, 2020Tradução . . Disponível em: https://doi.org/10.1039/D0MD00097C. Acesso em: 23 nov. 2025.
APA
Bonatt, V., Batista, P. H. J., Cianni, L., Vita, D. de, Silva, D. G. da, Cedron, R., et al. (2020). On the intrinsic reactivity of highly potent trypanocidal cruzain inhibitors. RSC Medicinal Chemistry, 11( 11), 1275-1284. doi:10.1039/D0MD00097C
NLM
Bonatt V, Batista PHJ, Cianni L, Vita D de, Silva DG da, Cedron R, Tezuka DY, Albuquerque S de, Moraes CB, Franco CH, Lameira J, Leitão A, Montanari CA. On the intrinsic reactivity of highly potent trypanocidal cruzain inhibitors [Internet]. RSC Medicinal Chemistry. 2020 ; 11( 11): 1275-1284.[citado 2025 nov. 23 ] Available from: https://doi.org/10.1039/D0MD00097C
Vancouver
Bonatt V, Batista PHJ, Cianni L, Vita D de, Silva DG da, Cedron R, Tezuka DY, Albuquerque S de, Moraes CB, Franco CH, Lameira J, Leitão A, Montanari CA. On the intrinsic reactivity of highly potent trypanocidal cruzain inhibitors [Internet]. RSC Medicinal Chemistry. 2020 ; 11( 11): 1275-1284.[citado 2025 nov. 23 ] Available from: https://doi.org/10.1039/D0MD00097C
Artigo de periodico
Mapping the S1 and S1’ subsites of cysteine proteases with new dipeptidyl nitrile inhibitors as trypanocidal agents (2020)
Cianni, Lorenzo ; Lemke, Carina; Gilberg, Erik; Feldmann, Christian; Rosini, Fabiana; Rocho, Fernanda dos Reis ; Ribeiro, Jean Francisco Rosa; Tezuka, Daiane Yukie; Lopes, Carla Duque ; Albuquerque, Sérgio de ; Bajorath, Jürgen; Laufer, Stefan; Leitão, Andrei ; Gütschow Michaell; Montanari, Carlos Alberto
Fonte: PLoS Neglected Tropical Diseases. Unidades: IQSC, FCFRP, FMRP
Assunto: QUÍMICA MÉDICA
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ABNT
CIANNI, Lorenzo et al. Mapping the S1 and S1’ subsites of cysteine proteases with new dipeptidyl nitrile inhibitors as trypanocidal agents. PLoS Neglected Tropical Diseases, v. 14, n. 3, p. 1-36, 2020Tradução . . Disponível em: https://doi.org/10.1371/journal.pntd.0007755. Acesso em: 23 nov. 2025.
APA
Cianni, L., Lemke, C., Gilberg, E., Feldmann, C., Rosini, F., Rocho, F. dos R., et al. (2020). Mapping the S1 and S1’ subsites of cysteine proteases with new dipeptidyl nitrile inhibitors as trypanocidal agents. PLoS Neglected Tropical Diseases, 14( 3), 1-36. doi:10.1371/journal.pntd.0007755
NLM
Cianni L, Lemke C, Gilberg E, Feldmann C, Rosini F, Rocho F dos R, Ribeiro JFR, Tezuka DY, Lopes CD, Albuquerque S de, Bajorath J, Laufer S, Leitão A, Gütschow Michaell, Montanari CA. Mapping the S1 and S1’ subsites of cysteine proteases with new dipeptidyl nitrile inhibitors as trypanocidal agents [Internet]. PLoS Neglected Tropical Diseases. 2020 ; 14( 3): 1-36.[citado 2025 nov. 23 ] Available from: https://doi.org/10.1371/journal.pntd.0007755
Vancouver
Cianni L, Lemke C, Gilberg E, Feldmann C, Rosini F, Rocho F dos R, Ribeiro JFR, Tezuka DY, Lopes CD, Albuquerque S de, Bajorath J, Laufer S, Leitão A, Gütschow Michaell, Montanari CA. Mapping the S1 and S1’ subsites of cysteine proteases with new dipeptidyl nitrile inhibitors as trypanocidal agents [Internet]. PLoS Neglected Tropical Diseases. 2020 ; 14( 3): 1-36.[citado 2025 nov. 23 ] Available from: https://doi.org/10.1371/journal.pntd.0007755
Artigo de periodico
Discovery of small molecule inhibitors of Leishmania braziliensis Hsp90 chaperone (2020)
Batista, Fernanda A. H; Ramos Junior, Sergio Luiz; Tassone, Giusy; Leitão, Andrei ; Montanari, Carlos Alberto ; Botta, Maurizio; Mori, Mattia; Borges, Julio Cesar
Fonte: Journal of Enzyme Inhibition and Medicinal Chemistry. Unidade: IQSC
Assunto: LEISHMANIA BRASILIENSIS
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ABNT
BATISTA, Fernanda A. H et al. Discovery of small molecule inhibitors of Leishmania braziliensis Hsp90 chaperone. Journal of Enzyme Inhibition and Medicinal Chemistry, v. 35, n. 1, p. 639-649, 2020Tradução . . Disponível em: https://doi.org/10.1080/14756366.2020.1726342. Acesso em: 23 nov. 2025.
APA
Batista, F. A. H., Ramos Junior, S. L., Tassone, G., Leitão, A., Montanari, C. A., Botta, M., et al. (2020). Discovery of small molecule inhibitors of Leishmania braziliensis Hsp90 chaperone. Journal of Enzyme Inhibition and Medicinal Chemistry, 35( 1), 639-649. doi:10.1080/14756366.2020.1726342
NLM
Batista FAH, Ramos Junior SL, Tassone G, Leitão A, Montanari CA, Botta M, Mori M, Borges JC. Discovery of small molecule inhibitors of Leishmania braziliensis Hsp90 chaperone [Internet]. Journal of Enzyme Inhibition and Medicinal Chemistry. 2020 ; 35( 1): 639-649.[citado 2025 nov. 23 ] Available from: https://doi.org/10.1080/14756366.2020.1726342
Vancouver
Batista FAH, Ramos Junior SL, Tassone G, Leitão A, Montanari CA, Botta M, Mori M, Borges JC. Discovery of small molecule inhibitors of Leishmania braziliensis Hsp90 chaperone [Internet]. Journal of Enzyme Inhibition and Medicinal Chemistry. 2020 ; 35( 1): 639-649.[citado 2025 nov. 23 ] Available from: https://doi.org/10.1080/14756366.2020.1726342
Artigo de periodico
Dipeptidyl nitrile derivatives suppress the Trypanosoma cruzi in vitro infection (2020)
Quilles Junior, José Carlos ; Shamim, Anwar ; Tezuka, Daiane Yukie; Batista, Pedro Henrique Jatai ; Lopes, Carla Duque ; Albuquerque, Sérgio de ; Montanari, Carlos Alberto ; Leitão, Andrei
Fonte: Experimental Parasitology. Unidades: FCFRP, IQSC, Interunidades em Bioengenharia, EESC
Assunto: DOENÇA DE CHAGAS
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ABNT
QUILLES JUNIOR, José Carlos et al. Dipeptidyl nitrile derivatives suppress the Trypanosoma cruzi in vitro infection. Experimental Parasitology, v. 219, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.exppara.2020.108032. Acesso em: 23 nov. 2025.
APA
Quilles Junior, J. C., Shamim, A., Tezuka, D. Y., Batista, P. H. J., Lopes, C. D., Albuquerque, S. de, et al. (2020). Dipeptidyl nitrile derivatives suppress the Trypanosoma cruzi in vitro infection. Experimental Parasitology, 219. doi:10.1016/j.exppara.2020.108032
NLM
Quilles Junior JC, Shamim A, Tezuka DY, Batista PHJ, Lopes CD, Albuquerque S de, Montanari CA, Leitão A. Dipeptidyl nitrile derivatives suppress the Trypanosoma cruzi in vitro infection [Internet]. Experimental Parasitology. 2020 ; 219[citado 2025 nov. 23 ] Available from: https://doi.org/10.1016/j.exppara.2020.108032
Vancouver
Quilles Junior JC, Shamim A, Tezuka DY, Batista PHJ, Lopes CD, Albuquerque S de, Montanari CA, Leitão A. Dipeptidyl nitrile derivatives suppress the Trypanosoma cruzi in vitro infection [Internet]. Experimental Parasitology. 2020 ; 219[citado 2025 nov. 23 ] Available from: https://doi.org/10.1016/j.exppara.2020.108032
Artigo de periodico
Discovery of 2-aminopyridine Derivatives with Antichagasic and Antileishmanial Activity Using Phenotypic Assays (2020)
Tezuka, Daiane Yukie; Albuquerque, Sérgio de ; Montanari, Carlos Alberto ; Leitão, Andrei
Fonte: Letters in Drug Design and Discovery. Unidades: IQSC, Interunidades em Bioengenharia, FCFRP
Assunto: LEISHMANIA
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ABNT
TEZUKA, Daiane Yukie et al. Discovery of 2-aminopyridine Derivatives with Antichagasic and Antileishmanial Activity Using Phenotypic Assays. Letters in Drug Design and Discovery, v. 17, n. 7, p. 867-872, 2020Tradução . . Disponível em: https://doi.org/10.2174/1570180816666191204105232. Acesso em: 23 nov. 2025.
APA
Tezuka, D. Y., Albuquerque, S. de, Montanari, C. A., & Leitão, A. (2020). Discovery of 2-aminopyridine Derivatives with Antichagasic and Antileishmanial Activity Using Phenotypic Assays. Letters in Drug Design and Discovery, 17( 7), 867-872. doi:10.2174/1570180816666191204105232
NLM
Tezuka DY, Albuquerque S de, Montanari CA, Leitão A. Discovery of 2-aminopyridine Derivatives with Antichagasic and Antileishmanial Activity Using Phenotypic Assays [Internet]. Letters in Drug Design and Discovery. 2020 ; 17( 7): 867-872.[citado 2025 nov. 23 ] Available from: https://doi.org/10.2174/1570180816666191204105232
Vancouver
Tezuka DY, Albuquerque S de, Montanari CA, Leitão A. Discovery of 2-aminopyridine Derivatives with Antichagasic and Antileishmanial Activity Using Phenotypic Assays [Internet]. Letters in Drug Design and Discovery. 2020 ; 17( 7): 867-872.[citado 2025 nov. 23 ] Available from: https://doi.org/10.2174/1570180816666191204105232
Artigo de periodico
Crystal structure of Leishmania mexicana cysteine protease B in complex with a high-affinity azadipeptide nitrile inhibitor (2020)
Ribeiro, Jean Francisco Rosa ; Cianni, Lorenzo ; Li, Chan; Warwick, Thomas G.; Vita, Daniela de ; Rosini, Fabiana; Rocho, Fernanda dos Reis ; Martins, Felipe Cardoso Prado ; Kenny, Peter W; Lameira, Jerônimo ; Leitão, Andrei ; Emsley, Jonas ; Montanari, Carlos Alberto
Fonte: Bioorganic and Medicinal Chemistry. Unidade: IQSC
Assuntos: LEISHMANIA MEXICANA, MEDICAMENTO
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ABNT
RIBEIRO, Jean Francisco Rosa et al. Crystal structure of Leishmania mexicana cysteine protease B in complex with a high-affinity azadipeptide nitrile inhibitor. Bioorganic and Medicinal Chemistry, v. 22, n. 22, p. 115743, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2020.115743. Acesso em: 23 nov. 2025.
APA
Ribeiro, J. F. R., Cianni, L., Li, C., Warwick, T. G., Vita, D. de, Rosini, F., et al. (2020). Crystal structure of Leishmania mexicana cysteine protease B in complex with a high-affinity azadipeptide nitrile inhibitor. Bioorganic and Medicinal Chemistry, 22( 22), 115743. doi:10.1016/j.bmc.2020.115743
NLM
Ribeiro JFR, Cianni L, Li C, Warwick TG, Vita D de, Rosini F, Rocho F dos R, Martins FCP, Kenny PW, Lameira J, Leitão A, Emsley J, Montanari CA. Crystal structure of Leishmania mexicana cysteine protease B in complex with a high-affinity azadipeptide nitrile inhibitor [Internet]. Bioorganic and Medicinal Chemistry. 2020 ; 22( 22): 115743.[citado 2025 nov. 23 ] Available from: https://doi.org/10.1016/j.bmc.2020.115743
Vancouver
Ribeiro JFR, Cianni L, Li C, Warwick TG, Vita D de, Rosini F, Rocho F dos R, Martins FCP, Kenny PW, Lameira J, Leitão A, Emsley J, Montanari CA. Crystal structure of Leishmania mexicana cysteine protease B in complex with a high-affinity azadipeptide nitrile inhibitor [Internet]. Bioorganic and Medicinal Chemistry. 2020 ; 22( 22): 115743.[citado 2025 nov. 23 ] Available from: https://doi.org/10.1016/j.bmc.2020.115743
Artigo de periodico
Optimization strategy of single-digit nanomolar cross-class inhibitors of mammalian and protozoa cysteine proteases (2020)
Cianni, Lorenzo ; Rocho, Fernanda dos Reis ; Rosini, Fabiana; Bonatto, Vinícius ; Ribeiro, Jean Francisco Rosa ; Lameira, Jerônimo ; Leitão, Andrei ; Shamim, Anwar ; Montanari, Carlos Alberto
Fonte: Bioorganic Chemistry. Unidade: IQSC
Assuntos: FÁRMACOS, BIOMARCADORES, PROTEÍNAS
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ABNT
CIANNI, Lorenzo et al. Optimization strategy of single-digit nanomolar cross-class inhibitors of mammalian and protozoa cysteine proteases. Bioorganic Chemistry, v. 101, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2020.104039. Acesso em: 23 nov. 2025.
APA
Cianni, L., Rocho, F. dos R., Rosini, F., Bonatto, V., Ribeiro, J. F. R., Lameira, J., et al. (2020). Optimization strategy of single-digit nanomolar cross-class inhibitors of mammalian and protozoa cysteine proteases. Bioorganic Chemistry, 101. doi:10.1016/j.bioorg.2020.104039
NLM
Cianni L, Rocho F dos R, Rosini F, Bonatto V, Ribeiro JFR, Lameira J, Leitão A, Shamim A, Montanari CA. Optimization strategy of single-digit nanomolar cross-class inhibitors of mammalian and protozoa cysteine proteases [Internet]. Bioorganic Chemistry. 2020 ; 101[citado 2025 nov. 23 ] Available from: https://doi.org/10.1016/j.bioorg.2020.104039
Vancouver
Cianni L, Rocho F dos R, Rosini F, Bonatto V, Ribeiro JFR, Lameira J, Leitão A, Shamim A, Montanari CA. Optimization strategy of single-digit nanomolar cross-class inhibitors of mammalian and protozoa cysteine proteases [Internet]. Bioorganic Chemistry. 2020 ; 101[citado 2025 nov. 23 ] Available from: https://doi.org/10.1016/j.bioorg.2020.104039
Artigo de periodico
Organometallic Gold(III) complex [Au(Hdamp)(L14)]+ (L1 = SNSDonating Thiosemicarbazone) as a candidate to new formulations against Chagas disease (2019)
Lopes, Carla Duque ; Possato, Bruna ; Gaspari, Ana Paula Segantin ; Oliveira, Ronaldo Junio ; Abram, Ulrich ; Almeida, José P. A; Rocho, Fernanda dos Reis ; Leitão, Andrei ; Montanari, Carlos Alberto ; Maia, Pedro Ivo da Silva ; Silva, João Santana da ; Albuquerque, Sérgio de ; Carneiro, Zumira Aparecida
Fonte: ACS Infectious Diseases. Unidades: IQSC, FMRP, FCFRP
Assuntos: BIOQUÍMICA, DOENÇA DE CHAGAS
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ABNT
LOPES, Carla Duque et al. Organometallic Gold(III) complex [Au(Hdamp)(L14)]+ (L1 = SNSDonating Thiosemicarbazone) as a candidate to new formulations against Chagas disease. ACS Infectious Diseases, v. 5, n. 10, p. 1698-1707, 2019Tradução . . Disponível em: https://doi.org/10.1021/acsinfecdis.8b00284. Acesso em: 23 nov. 2025.
APA
Lopes, C. D., Possato, B., Gaspari, A. P. S., Oliveira, R. J., Abram, U., Almeida, J. P. A., et al. (2019). Organometallic Gold(III) complex [Au(Hdamp)(L14)]+ (L1 = SNSDonating Thiosemicarbazone) as a candidate to new formulations against Chagas disease. ACS Infectious Diseases, 5( 10), 1698-1707. doi:10.1021/acsinfecdis.8b00284
NLM
Lopes CD, Possato B, Gaspari APS, Oliveira RJ, Abram U, Almeida JPA, Rocho F dos R, Leitão A, Montanari CA, Maia PI da S, Silva JS da, Albuquerque S de, Carneiro ZA. Organometallic Gold(III) complex [Au(Hdamp)(L14)]+ (L1 = SNSDonating Thiosemicarbazone) as a candidate to new formulations against Chagas disease [Internet]. ACS Infectious Diseases. 2019 ; 5( 10): 1698-1707.[citado 2025 nov. 23 ] Available from: https://doi.org/10.1021/acsinfecdis.8b00284
Vancouver
Lopes CD, Possato B, Gaspari APS, Oliveira RJ, Abram U, Almeida JPA, Rocho F dos R, Leitão A, Montanari CA, Maia PI da S, Silva JS da, Albuquerque S de, Carneiro ZA. Organometallic Gold(III) complex [Au(Hdamp)(L14)]+ (L1 = SNSDonating Thiosemicarbazone) as a candidate to new formulations against Chagas disease [Internet]. ACS Infectious Diseases. 2019 ; 5( 10): 1698-1707.[citado 2025 nov. 23 ] Available from: https://doi.org/10.1021/acsinfecdis.8b00284
Artigo de periodico
Apoferritin encapsulation of cysteine protease inhibitors for cathepsin L inhibition in cancer cells (2019)
Quilles Junior, José Carlos ; Rocho, Fernanda dos Reis ; Montanari, Carlos Alberto ; Leitão, Andrei ; Mignone, Viviane W.; Arruda, Maria Augusta; Turyanska, Lyudmila ; Bradshaw, Tracey D.
Fonte: RSC Advances. Unidade: IQSC
Assuntos: QUÍMICA MÉDICA, NEOPLASIAS, PÂNCREAS
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ABNT
QUILLES JUNIOR, José Carlos et al. Apoferritin encapsulation of cysteine protease inhibitors for cathepsin L inhibition in cancer cells. RSC Advances, v. 9, n. 45, p. 36699-36706, 2019Tradução . . Disponível em: https://doi.org/10.1039/c9ra07161j. Acesso em: 23 nov. 2025.
APA
Quilles Junior, J. C., Rocho, F. dos R., Montanari, C. A., Leitão, A., Mignone, V. W., Arruda, M. A., et al. (2019). Apoferritin encapsulation of cysteine protease inhibitors for cathepsin L inhibition in cancer cells. RSC Advances, 9( 45), 36699-36706. doi:10.1039/c9ra07161j
NLM
Quilles Junior JC, Rocho F dos R, Montanari CA, Leitão A, Mignone VW, Arruda MA, Turyanska L, Bradshaw TD. Apoferritin encapsulation of cysteine protease inhibitors for cathepsin L inhibition in cancer cells [Internet]. RSC Advances. 2019 ; 9( 45): 36699-36706.[citado 2025 nov. 23 ] Available from: https://doi.org/10.1039/c9ra07161j
Vancouver
Quilles Junior JC, Rocho F dos R, Montanari CA, Leitão A, Mignone VW, Arruda MA, Turyanska L, Bradshaw TD. Apoferritin encapsulation of cysteine protease inhibitors for cathepsin L inhibition in cancer cells [Internet]. RSC Advances. 2019 ; 9( 45): 36699-36706.[citado 2025 nov. 23 ] Available from: https://doi.org/10.1039/c9ra07161j
Trabalho de evento-resumo
Synthesis of peptoids of nitriles as cruzain inhibitors (2019)
Souza, Luana Alves Galvão de; Santos, Deborah Araujo dos; Montanari, Carlos Alberto ; Leitão, Andrei
Fonte: Book of Abstracts. Nome do evento: The São Carlos Special Medicinal Chemistry Meeting - SancaMedChem2019. Unidade: IQSC
Assuntos: DOENÇA DE CHAGAS, QUÍMICA MÉDICA
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ABNT
SOUZA, Luana Alves Galvão de et al. Synthesis of peptoids of nitriles as cruzain inhibitors. 2019, Anais.. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP, 2019. Disponível em: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf. Acesso em: 23 nov. 2025.
APA
Souza, L. A. G. de, Santos, D. A. dos, Montanari, C. A., & Leitão, A. (2019). Synthesis of peptoids of nitriles as cruzain inhibitors. In Book of Abstracts. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP. Recuperado de http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
NLM
Souza LAG de, Santos DA dos, Montanari CA, Leitão A. Synthesis of peptoids of nitriles as cruzain inhibitors [Internet]. Book of Abstracts. 2019 ;[citado 2025 nov. 23 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Vancouver
Souza LAG de, Santos DA dos, Montanari CA, Leitão A. Synthesis of peptoids of nitriles as cruzain inhibitors [Internet]. Book of Abstracts. 2019 ;[citado 2025 nov. 23 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Artigo de periodico
Dipeptidyl nitrile derivatives have cytostatic effects against Leishmania spp. promastigotes (2019)
Quilles Junior, José C.; Tezuka, Daiane Yukie; Lopes, Carla D; Ribeiro, Fernanda L; Laughton, Charles A; Albuquerque, Sérgio de ; Montanari, Carlos Alberto ; Leitão, Andrei
Fonte: Experimental Parasitology. Unidades: IQSC, FCFRP
Assuntos: PROTOZOA, LEISHMANIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
QUILLES JUNIOR, José C. et al. Dipeptidyl nitrile derivatives have cytostatic effects against Leishmania spp. promastigotes. Experimental Parasitology, v. 200, p. 84-91, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.exppara.2019.04.001. Acesso em: 23 nov. 2025.
APA
Quilles Junior, J. C., Tezuka, D. Y., Lopes, C. D., Ribeiro, F. L., Laughton, C. A., Albuquerque, S. de, et al. (2019). Dipeptidyl nitrile derivatives have cytostatic effects against Leishmania spp. promastigotes. Experimental Parasitology, 200, 84-91. doi:10.1016/j.exppara.2019.04.001
NLM
Quilles Junior JC, Tezuka DY, Lopes CD, Ribeiro FL, Laughton CA, Albuquerque S de, Montanari CA, Leitão A. Dipeptidyl nitrile derivatives have cytostatic effects against Leishmania spp. promastigotes [Internet]. Experimental Parasitology. 2019 ;200 84-91.[citado 2025 nov. 23 ] Available from: https://doi.org/10.1016/j.exppara.2019.04.001
Vancouver
Quilles Junior JC, Tezuka DY, Lopes CD, Ribeiro FL, Laughton CA, Albuquerque S de, Montanari CA, Leitão A. Dipeptidyl nitrile derivatives have cytostatic effects against Leishmania spp. promastigotes [Internet]. Experimental Parasitology. 2019 ;200 84-91.[citado 2025 nov. 23 ] Available from: https://doi.org/10.1016/j.exppara.2019.04.001
Trabalho de evento-resumo
Synthesis of non-peptide nitrile cysteine protease inhibitors with bioisostere sulfonamides at position P3 (2019)
Santos, Deborah Araujo dos; Montanari, Carlos Alberto
Fonte: Book of Abstracts. Nome do evento: The São Carlos Special Medicinal Chemistry Meeting - SancaMedChem2019. Unidade: IQSC
Assuntos: SÍNTESE QUÍMICA, QUÍMICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Deborah Araujo dos e MONTANARI, Carlos Alberto. Synthesis of non-peptide nitrile cysteine protease inhibitors with bioisostere sulfonamides at position P3. 2019, Anais.. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP, 2019. Disponível em: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf. Acesso em: 23 nov. 2025.
APA
Santos, D. A. dos, & Montanari, C. A. (2019). Synthesis of non-peptide nitrile cysteine protease inhibitors with bioisostere sulfonamides at position P3. In Book of Abstracts. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP. Recuperado de http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
NLM
Santos DA dos, Montanari CA. Synthesis of non-peptide nitrile cysteine protease inhibitors with bioisostere sulfonamides at position P3 [Internet]. Book of Abstracts. 2019 ;[citado 2025 nov. 23 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Vancouver
Santos DA dos, Montanari CA. Synthesis of non-peptide nitrile cysteine protease inhibitors with bioisostere sulfonamides at position P3 [Internet]. Book of Abstracts. 2019 ;[citado 2025 nov. 23 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf

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