Filtros : "MONTANARI, CARLOS ALBERTO" "2017" "IQSC" Removidos: "Prokopczyk, Igor Muccilo" "Committee of the International Congress of Pharmaceutical Sciences" Limpar

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  • Source: Chemical Biology and Drug Design. Unidade: IQSC

    Subjects: BIOQUÍMICA, BIOLOGIA

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      Chemical Biology and Drug Design. Chemical Biology and Drug Design. Hoboken: Wiley-Blackwell Publishing, Inc. Disponível em: https://repositorio.usp.br/directbitstream/7d5f144e-eeb7-48f5-b01d-9a5c9bacb874/P17700.pdf. Acesso em: 04 out. 2024. , 2017
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      Chemical Biology and Drug Design. (2017). Chemical Biology and Drug Design. Chemical Biology and Drug Design. Hoboken: Wiley-Blackwell Publishing, Inc. Recuperado de https://repositorio.usp.br/directbitstream/7d5f144e-eeb7-48f5-b01d-9a5c9bacb874/P17700.pdf
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      Chemical Biology and Drug Design [Internet]. Chemical Biology and Drug Design. 2017 ;[citado 2024 out. 04 ] Available from: https://repositorio.usp.br/directbitstream/7d5f144e-eeb7-48f5-b01d-9a5c9bacb874/P17700.pdf
    • Vancouver

      Chemical Biology and Drug Design [Internet]. Chemical Biology and Drug Design. 2017 ;[citado 2024 out. 04 ] Available from: https://repositorio.usp.br/directbitstream/7d5f144e-eeb7-48f5-b01d-9a5c9bacb874/P17700.pdf
  • Source: Plos Neglected Tropical Diseases. Unidades: IQSC, FCFRP

    Subjects: DOENÇA DE CHAGAS, TERAPÊUTICA MÉDICA

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      BURTOLOSO, Antonio Carlos Bender et al. Anti-trypanosomal activity of non-peptidic nitrile-based cysteine protease inhibitors. Plos Neglected Tropical Diseases, p. 1-16, 2017Tradução . . Disponível em: https://doi.org/10.1371/journal.pndt.0005343. Acesso em: 04 out. 2024.
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      Burtoloso, A. C. B., Albuquerque, S. de, Furker, M., Gomes, J. C., Gonçalez, C., Kenny, P. W., et al. (2017). Anti-trypanosomal activity of non-peptidic nitrile-based cysteine protease inhibitors. Plos Neglected Tropical Diseases, 1-16. doi:10.1371/journal.pndt.0005343
    • NLM

      Burtoloso ACB, Albuquerque S de, Furker M, Gomes JC, Gonçalez C, Kenny PW, Leitão A, Montanari CA, Guilles Junior JC, Ribeiro JFR, Rocha JR. Anti-trypanosomal activity of non-peptidic nitrile-based cysteine protease inhibitors [Internet]. Plos Neglected Tropical Diseases. 2017 ;1-16.[citado 2024 out. 04 ] Available from: https://doi.org/10.1371/journal.pndt.0005343
    • Vancouver

      Burtoloso ACB, Albuquerque S de, Furker M, Gomes JC, Gonçalez C, Kenny PW, Leitão A, Montanari CA, Guilles Junior JC, Ribeiro JFR, Rocha JR. Anti-trypanosomal activity of non-peptidic nitrile-based cysteine protease inhibitors [Internet]. Plos Neglected Tropical Diseases. 2017 ;1-16.[citado 2024 out. 04 ] Available from: https://doi.org/10.1371/journal.pndt.0005343
  • Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC

    Assunto: HALOGÊNIOS

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      CIANNI, Lorenzo et al. On the study of halogen bond interaction to increase cruzain affinity of covalently boundd reversible inhibitors. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/da742f21-6f52-4436-9709-ea8a58a5d735/P16976.pdf. Acesso em: 04 out. 2024.
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      Cianni, L., Sartori, G., Vita, D. de, Rosini, F., Leitão, A., & Montanari, C. A. (2017). On the study of halogen bond interaction to increase cruzain affinity of covalently boundd reversible inhibitors. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/da742f21-6f52-4436-9709-ea8a58a5d735/P16976.pdf
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      Cianni L, Sartori G, Vita D de, Rosini F, Leitão A, Montanari CA. On the study of halogen bond interaction to increase cruzain affinity of covalently boundd reversible inhibitors [Internet]. Proceedings. 2017 ;[citado 2024 out. 04 ] Available from: https://repositorio.usp.br/directbitstream/da742f21-6f52-4436-9709-ea8a58a5d735/P16976.pdf
    • Vancouver

      Cianni L, Sartori G, Vita D de, Rosini F, Leitão A, Montanari CA. On the study of halogen bond interaction to increase cruzain affinity of covalently boundd reversible inhibitors [Internet]. Proceedings. 2017 ;[citado 2024 out. 04 ] Available from: https://repositorio.usp.br/directbitstream/da742f21-6f52-4436-9709-ea8a58a5d735/P16976.pdf
  • Source: Anais. Conference titles: Simpósio Internacional de Iniciação Científica e Tecnológica da USP - SIICUSP. Unidade: IQSC

    Assunto: DOENÇA DE CHAGAS

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      SANTOS, Juliana Jarussi dos et al. Planjemaneto, síntese e atividade tripanossomicida de inibidores covalentes reversíveis da enzima cruzaína. 2017, Anais.. São Paulo: Instituto de Química de São Carlos, Universidade de São Paulo, 2017. Disponível em: http://siicusp.prp.usp.br/pt/programacao/. Acesso em: 04 out. 2024.
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      Santos, J. J. dos, De Vita, D., Cianni, L., & Montanari, C. A. (2017). Planjemaneto, síntese e atividade tripanossomicida de inibidores covalentes reversíveis da enzima cruzaína. In Anais. São Paulo: Instituto de Química de São Carlos, Universidade de São Paulo. Recuperado de http://siicusp.prp.usp.br/pt/programacao/
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      Santos JJ dos, De Vita D, Cianni L, Montanari CA. Planjemaneto, síntese e atividade tripanossomicida de inibidores covalentes reversíveis da enzima cruzaína [Internet]. Anais. 2017 ;[citado 2024 out. 04 ] Available from: http://siicusp.prp.usp.br/pt/programacao/
    • Vancouver

      Santos JJ dos, De Vita D, Cianni L, Montanari CA. Planjemaneto, síntese e atividade tripanossomicida de inibidores covalentes reversíveis da enzima cruzaína [Internet]. Anais. 2017 ;[citado 2024 out. 04 ] Available from: http://siicusp.prp.usp.br/pt/programacao/
  • Source: ACS Medicinal Chemistry Letters. Unidade: IQSC

    Subjects: TRYPANOSOMA CRUZI, QUÍMICA MÉDICA

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      SILVA, Daniel G da et al. New class of antitrypanosomal agents based on imidazopyridines. ACS Medicinal Chemistry Letters, v. 8, n. 7, p. 686-689, 2017Tradução . . Disponível em: https://doi.org/10.1021/acsmedchemlett.7b00202. Acesso em: 04 out. 2024.
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      Silva, D. G. da, Gillespie, J. R., Radane, R. M., Herbst, Z. M., Nguyen, U. T. T., Buckner, F. S., et al. (2017). New class of antitrypanosomal agents based on imidazopyridines. ACS Medicinal Chemistry Letters, 8( 7), 686-689. doi:10.1021/acsmedchemlett.7b00202
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      Silva DG da, Gillespie JR, Radane RM, Herbst ZM, Nguyen UTT, Buckner FS, Montanari CA, Gelb MH. New class of antitrypanosomal agents based on imidazopyridines [Internet]. ACS Medicinal Chemistry Letters. 2017 ; 8( 7): 686-689.[citado 2024 out. 04 ] Available from: https://doi.org/10.1021/acsmedchemlett.7b00202
    • Vancouver

      Silva DG da, Gillespie JR, Radane RM, Herbst ZM, Nguyen UTT, Buckner FS, Montanari CA, Gelb MH. New class of antitrypanosomal agents based on imidazopyridines [Internet]. ACS Medicinal Chemistry Letters. 2017 ; 8( 7): 686-689.[citado 2024 out. 04 ] Available from: https://doi.org/10.1021/acsmedchemlett.7b00202
  • Source: Bioorganic & Medicinal Chemistry Letters. Unidade: IQSC

    Subjects: ONCOLOGIA, PRÓSTATA

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      SAIDEL, Marta Érica et al. Novel anti-prostate cancer scaffold identified by the combination of in silico and cell-based assays targeting the PI3K-AKT-mTOR pathway. Bioorganic & Medicinal Chemistry Letters, v. 27, p. 4001-4006, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.bmcl.2017.07.061. Acesso em: 04 out. 2024.
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      Saidel, M. É., Santos, K. C. dos, Nagano, L. F. P., Montanari, C. A., & Leitão, A. (2017). Novel anti-prostate cancer scaffold identified by the combination of in silico and cell-based assays targeting the PI3K-AKT-mTOR pathway. Bioorganic & Medicinal Chemistry Letters, 27, 4001-4006. doi:10.1016/j.bmcl.2017.07.061
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      Saidel MÉ, Santos KC dos, Nagano LFP, Montanari CA, Leitão A. Novel anti-prostate cancer scaffold identified by the combination of in silico and cell-based assays targeting the PI3K-AKT-mTOR pathway [Internet]. Bioorganic & Medicinal Chemistry Letters. 2017 ; 27 4001-4006.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.bmcl.2017.07.061
    • Vancouver

      Saidel MÉ, Santos KC dos, Nagano LFP, Montanari CA, Leitão A. Novel anti-prostate cancer scaffold identified by the combination of in silico and cell-based assays targeting the PI3K-AKT-mTOR pathway [Internet]. Bioorganic & Medicinal Chemistry Letters. 2017 ; 27 4001-4006.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.bmcl.2017.07.061
  • Source: Journal of Biomolecular Structure and Dynamics. Unidade: IQSC

    Subjects: MODELAGEM MOLECULAR, BIOQUÍMICA CELULAR

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      SILVA, Daniel Gedder et al. Highly predictive hologram QSAR models of nitrile-containing cruzain inhibitors. Journal of Biomolecular Structure and Dynamics, v. 35, n. 15, p. 3232-3249, 2017Tradução . . Disponível em: https://doi.org/10.1080/07391102.2016.1252282. Acesso em: 04 out. 2024.
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      Silva, D. G., Rocha, J. R., Sartori, G. R., & Montanari, C. A. (2017). Highly predictive hologram QSAR models of nitrile-containing cruzain inhibitors. Journal of Biomolecular Structure and Dynamics, 35( 15), 3232-3249. doi:10.1080/07391102.2016.1252282
    • NLM

      Silva DG, Rocha JR, Sartori GR, Montanari CA. Highly predictive hologram QSAR models of nitrile-containing cruzain inhibitors [Internet]. Journal of Biomolecular Structure and Dynamics. 2017 ; 35( 15): 3232-3249.[citado 2024 out. 04 ] Available from: https://doi.org/10.1080/07391102.2016.1252282
    • Vancouver

      Silva DG, Rocha JR, Sartori GR, Montanari CA. Highly predictive hologram QSAR models of nitrile-containing cruzain inhibitors [Internet]. Journal of Biomolecular Structure and Dynamics. 2017 ; 35( 15): 3232-3249.[citado 2024 out. 04 ] Available from: https://doi.org/10.1080/07391102.2016.1252282
  • Source: Bioorganic & Medicinal Chemistry Letters. Unidade: IQSC

    Assunto: ALDEÍDOS

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      SILVA, Daniel G da et al. A comparative study of warheads for design of cysteine protease inhibitors. Bioorganic & Medicinal Chemistry Letters, v. 27, n. 22, p. 5031-5035, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.bmcl.2017.10.002. Acesso em: 04 out. 2024.
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      Silva, D. G. da, Ribeiro, J. F. R., De Vita, D., Cianni, L., Franco, C. H., Freitas Junior, L. H., et al. (2017). A comparative study of warheads for design of cysteine protease inhibitors. Bioorganic & Medicinal Chemistry Letters, 27( 22), 5031-5035. doi:10.1016/j.bmcl.2017.10.002
    • NLM

      Silva DG da, Ribeiro JFR, De Vita D, Cianni L, Franco CH, Freitas Junior LH, Moraes CB, Rocha JR, Burtoloso ACB, Kenny PW, Leitão A, Montanari CA. A comparative study of warheads for design of cysteine protease inhibitors [Internet]. Bioorganic & Medicinal Chemistry Letters. 2017 ; 27( 22): 5031-5035.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.bmcl.2017.10.002
    • Vancouver

      Silva DG da, Ribeiro JFR, De Vita D, Cianni L, Franco CH, Freitas Junior LH, Moraes CB, Rocha JR, Burtoloso ACB, Kenny PW, Leitão A, Montanari CA. A comparative study of warheads for design of cysteine protease inhibitors [Internet]. Bioorganic & Medicinal Chemistry Letters. 2017 ; 27( 22): 5031-5035.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.bmcl.2017.10.002
  • Source: Bioorganic & Medicinal Chemistry Letters. Unidade: IQSC

    Assunto: NEOPLASIAS DOS GENITAIS MASCULINOS

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      SANTA CRUZ, Elisa C et al. In silico selection and cell-based characterization of selective and bioactive compounds for androgen-dependent prostate cancer cell. Bioorganic & Medicinal Chemistry Letters, v. 27, p. 546-550, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.bmcl.2016.12.022. Acesso em: 04 out. 2024.
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      Santa Cruz, E. C., Carecho, A. R., Saidel, M. É., Montanari, C. A., & Leitão, A. (2017). In silico selection and cell-based characterization of selective and bioactive compounds for androgen-dependent prostate cancer cell. Bioorganic & Medicinal Chemistry Letters, 27, 546-550. doi:10.1016/j.bmcl.2016.12.022
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      Santa Cruz EC, Carecho AR, Saidel MÉ, Montanari CA, Leitão A. In silico selection and cell-based characterization of selective and bioactive compounds for androgen-dependent prostate cancer cell [Internet]. Bioorganic & Medicinal Chemistry Letters. 2017 ; 27 546-550.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.bmcl.2016.12.022
    • Vancouver

      Santa Cruz EC, Carecho AR, Saidel MÉ, Montanari CA, Leitão A. In silico selection and cell-based characterization of selective and bioactive compounds for androgen-dependent prostate cancer cell [Internet]. Bioorganic & Medicinal Chemistry Letters. 2017 ; 27 546-550.[citado 2024 out. 04 ] Available from: https://doi.org/10.1016/j.bmcl.2016.12.022

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