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1 - 11 (11 records)

  • 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

    Source: Bioorganic and Medicinal Chemistry. Unidade: IQSC

    Subjects: 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: 08 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. 08 ] 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. 08 ] 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

    Source: Bioorganic & Medicinal Chemistry Letters. Unidade: IQSC

    Subjects: QUÍMICA ORGÂNICA, MEDICAMENTO, INIBIDORES DE ENZIMAS

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      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: 08 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. 08 ] 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. 08 ] Available from: https://doi.org/10.1016/j.bmcl.2020.127439

  • 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

    Source: 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: 08 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. 08 ] 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. 08 ] Available from: https://doi.org/10.1371/journal.pntd.0007755

  • Artigo de periodico

    Evaluating QM/MM Free Energy Surfaces for Ranking Cysteine Protease Covalent Inhibitors (2020)

    Costa, Clauber H. S; Bonatto, Vinícius ; Santos, Alberto M. dos; Lameira, Jerônimo ; Leitão, Andrei ; Montanari, Carlos Alberto

    Source: Journal of Chemical Information and Modeling. Unidade: IQSC

    Assunto: QUÍMICA MÉDICA

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      COSTA, Clauber H. S et al. Evaluating QM/MM Free Energy Surfaces for Ranking Cysteine Protease Covalent Inhibitors. Journal of Chemical Information and Modeling, p. 880-889, 2020Tradução . . Disponível em: https://doi.org/10.1021/acs.jcim.9b00847. Acesso em: 08 nov. 2025.

    • APA

      Costa, C. H. S., Bonatto, V., Santos, A. M. dos, Lameira, J., Leitão, A., & Montanari, C. A. (2020). Evaluating QM/MM Free Energy Surfaces for Ranking Cysteine Protease Covalent Inhibitors. Journal of Chemical Information and Modeling, 880-889. doi:10.1021/acs.jcim.9b00847

    • NLM

      Costa CHS, Bonatto V, Santos AM dos, Lameira J, Leitão A, Montanari CA. Evaluating QM/MM Free Energy Surfaces for Ranking Cysteine Protease Covalent Inhibitors [Internet]. Journal of Chemical Information and Modeling. 2020 ; 880-889.[citado 2025 nov. 08 ] Available from: https://doi.org/10.1021/acs.jcim.9b00847

    • Vancouver

      Costa CHS, Bonatto V, Santos AM dos, Lameira J, Leitão A, Montanari CA. Evaluating QM/MM Free Energy Surfaces for Ranking Cysteine Protease Covalent Inhibitors [Internet]. Journal of Chemical Information and Modeling. 2020 ; 880-889.[citado 2025 nov. 08 ] Available from: https://doi.org/10.1021/acs.jcim.9b00847

  • 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

    Source: Journal of Enzyme Inhibition and Medicinal Chemistry. Unidade: IQSC

    Assunto: LEISHMANIA BRASILIENSIS

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      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: 08 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. 08 ] 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. 08 ] Available from: https://doi.org/10.1080/14756366.2020.1726342

  • 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

    Source: Letters in Drug Design and Discovery. Unidades: IQSC, Interunidades em Bioengenharia, FCFRP

    Assunto: LEISHMANIA

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      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: 08 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. 08 ] 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. 08 ] 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

    Source: Bioorganic and Medicinal Chemistry. Unidade: IQSC

    Subjects: 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: 08 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. 08 ] 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. 08 ] 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

    Source: Bioorganic Chemistry. Unidade: IQSC

    Subjects: 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: 08 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. 08 ] 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. 08 ] Available from: https://doi.org/10.1016/j.bioorg.2020.104039

  • 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.

    Source: RSC Advances. Unidade: IQSC

    Subjects: QUÍMICA MÉDICA, NEOPLASIAS, PÂNCREAS

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      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: 08 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. 08 ] 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. 08 ] Available from: https://doi.org/10.1039/c9ra07161j

  • 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

    Source: Experimental Parasitology. Unidades: IQSC, FCFRP

    Subjects: PROTOZOA, LEISHMANIA

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      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: 08 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. 08 ] 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. 08 ] 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

    Source: Book of Abstracts. Conference titles: The São Carlos Special Medicinal Chemistry Meeting - SancaMedChem2019. Unidade: IQSC

    Subjects: SÍNTESE QUÍMICA, QUÍMICA MÉDICA

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    • 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: 08 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. 08 ] 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. 08 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
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