Filtros : "Emirados Árabes Unidos" "2014" Removido: "Financiamento FINEP" Limpar

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  • Source: Current Pharmaceutical Analysis. Unidade: FCF

    Assunto: ESTABILIDADE DOS MEDICAMENTOS

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    • ABNT

      GHISLENI, Daniela Dal Molim et al. Validation and measurement uncertainty of an UPLC-PDA stability indicating method applied to degradation kinetics of caspofungin. Current Pharmaceutical Analysis, v. 10, n. 3, p. 193-202, 2014Tradução . . Acesso em: 06 set. 2024.
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      Ghisleni, D. D. M., Okamoto, R. T., Lourenço, F. R., & Pinto, T. de J. A. (2014). Validation and measurement uncertainty of an UPLC-PDA stability indicating method applied to degradation kinetics of caspofungin. Current Pharmaceutical Analysis, 10( 3), 193-202.
    • NLM

      Ghisleni DDM, Okamoto RT, Lourenço FR, Pinto T de JA. Validation and measurement uncertainty of an UPLC-PDA stability indicating method applied to degradation kinetics of caspofungin. Current Pharmaceutical Analysis. 2014 ; 10( 3): 193-202.[citado 2024 set. 06 ]
    • Vancouver

      Ghisleni DDM, Okamoto RT, Lourenço FR, Pinto T de JA. Validation and measurement uncertainty of an UPLC-PDA stability indicating method applied to degradation kinetics of caspofungin. Current Pharmaceutical Analysis. 2014 ; 10( 3): 193-202.[citado 2024 set. 06 ]
  • Source: Current Analytical Chemistry. Unidades: FCF, IQ

    Subjects: ELETROFORESE (MÉTODO DE SEPARAÇÃO), ESTEROIDES

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      SILVA, Claudinei Alves da e AURORA-PRADO, Maria Segunda e TAVARES, Marina Franco Maggi. Determination of ethinylestradiol and levo-norgestrel using microemulsion electrokinetic chromatography. Current Analytical Chemistry, v. 10, n. 2, p. 216-224, 2014Tradução . . Disponível em: http://apps.webofknowledge.com/full_record.do?product=UA&search_mode=GeneralSearch&qid=5&SID=4Bj4Ns2BRnXmDjyUQki&page=1&doc=2. Acesso em: 06 set. 2024.
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      Silva, C. A. da, Aurora-Prado, M. S., & Tavares, M. F. M. (2014). Determination of ethinylestradiol and levo-norgestrel using microemulsion electrokinetic chromatography. Current Analytical Chemistry, 10( 2), 216-224. Recuperado de http://apps.webofknowledge.com/full_record.do?product=UA&search_mode=GeneralSearch&qid=5&SID=4Bj4Ns2BRnXmDjyUQki&page=1&doc=2
    • NLM

      Silva CA da, Aurora-Prado MS, Tavares MFM. Determination of ethinylestradiol and levo-norgestrel using microemulsion electrokinetic chromatography [Internet]. Current Analytical Chemistry. 2014 ; 10( 2): 216-224.[citado 2024 set. 06 ] Available from: http://apps.webofknowledge.com/full_record.do?product=UA&search_mode=GeneralSearch&qid=5&SID=4Bj4Ns2BRnXmDjyUQki&page=1&doc=2
    • Vancouver

      Silva CA da, Aurora-Prado MS, Tavares MFM. Determination of ethinylestradiol and levo-norgestrel using microemulsion electrokinetic chromatography [Internet]. Current Analytical Chemistry. 2014 ; 10( 2): 216-224.[citado 2024 set. 06 ] Available from: http://apps.webofknowledge.com/full_record.do?product=UA&search_mode=GeneralSearch&qid=5&SID=4Bj4Ns2BRnXmDjyUQki&page=1&doc=2
  • Source: Protein & Peptide Letters. Unidade: IQ

    Subjects: CARBOIDRATOS, HIDRÓLISE

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      GONÇALVES, Larissa Martins et al. Chimeric proteins combining phosphatase and cellulose binding activities: proof of concept and application in the hydrolysis of paraoxon. Protein & Peptide Letters, v. 21, n. 8, p. 488-475, 2014Tradução . . Acesso em: 06 set. 2024.
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      Gonçalves, L. M., Chaimovich Guralnik, H., Cuccovia, I. M., & Marana, S. R. (2014). Chimeric proteins combining phosphatase and cellulose binding activities: proof of concept and application in the hydrolysis of paraoxon. Protein & Peptide Letters, 21( 8), 488-475.
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      Gonçalves LM, Chaimovich Guralnik H, Cuccovia IM, Marana SR. Chimeric proteins combining phosphatase and cellulose binding activities: proof of concept and application in the hydrolysis of paraoxon. Protein & Peptide Letters. 2014 ; 21( 8): 488-475.[citado 2024 set. 06 ]
    • Vancouver

      Gonçalves LM, Chaimovich Guralnik H, Cuccovia IM, Marana SR. Chimeric proteins combining phosphatase and cellulose binding activities: proof of concept and application in the hydrolysis of paraoxon. Protein & Peptide Letters. 2014 ; 21( 8): 488-475.[citado 2024 set. 06 ]
  • Source: Current Pharmaceutical Design. Unidade: FCF

    Subjects: TUBERCULOSE, ÁCIDOS NUCLEICOS

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      BUENO, Renata Vieria et al. New tuberculostatic agents targeting nucleic acid biosynthesis: drug design using QSAR approaches. Current Pharmaceutical Design, v. 20, n. 27, p. 4474-4485, 2014Tradução . . Acesso em: 06 set. 2024.
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      Bueno, R. V., Braga, R. de C., Segretti, N. D., Ferreira, E. I., Trossini, G. H. G., & Andrade, C. H. (2014). New tuberculostatic agents targeting nucleic acid biosynthesis: drug design using QSAR approaches. Current Pharmaceutical Design, 20( 27), 4474-4485.
    • NLM

      Bueno RV, Braga R de C, Segretti ND, Ferreira EI, Trossini GHG, Andrade CH. New tuberculostatic agents targeting nucleic acid biosynthesis: drug design using QSAR approaches. Current Pharmaceutical Design. 2014 ; 20( 27): 4474-4485.[citado 2024 set. 06 ]
    • Vancouver

      Bueno RV, Braga R de C, Segretti ND, Ferreira EI, Trossini GHG, Andrade CH. New tuberculostatic agents targeting nucleic acid biosynthesis: drug design using QSAR approaches. Current Pharmaceutical Design. 2014 ; 20( 27): 4474-4485.[citado 2024 set. 06 ]
  • Source: Current Pharmaceutical Design. Unidade: FMVZ

    Subjects: NEUROIMUNOMODULAÇÃO, ESTRESSE PSICOLÓGICO, TUMOR DE EHRLICH ANIMAL, SISTEMA NERVOSO SIMPÁTICO

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      PALERMO-NETO, João e ALVES, Glaucie Jussilane. Neuroimmune interactions and psychologycal stress induced by cohabitation with a sick partner: a review. Current Pharmaceutical Design, v. 20, n. 29, p. 4629-4641, 2014Tradução . . Disponível em: https://doi.org/10.2174/1381612820666140130204657. Acesso em: 06 set. 2024.
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      Palermo-Neto, J., & Alves, G. J. (2014). Neuroimmune interactions and psychologycal stress induced by cohabitation with a sick partner: a review. Current Pharmaceutical Design, 20( 29), 4629-4641. doi:10.2174/1381612820666140130204657
    • NLM

      Palermo-Neto J, Alves GJ. Neuroimmune interactions and psychologycal stress induced by cohabitation with a sick partner: a review [Internet]. Current Pharmaceutical Design. 2014 ; 20( 29): 4629-4641.[citado 2024 set. 06 ] Available from: https://doi.org/10.2174/1381612820666140130204657
    • Vancouver

      Palermo-Neto J, Alves GJ. Neuroimmune interactions and psychologycal stress induced by cohabitation with a sick partner: a review [Internet]. Current Pharmaceutical Design. 2014 ; 20( 29): 4629-4641.[citado 2024 set. 06 ] Available from: https://doi.org/10.2174/1381612820666140130204657
  • Source: Letters in Drug Design & Discovery. Unidade: FCF

    Subjects: MODELAGEM MOLECULAR, DOENÇA DE CHAGAS

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      VITAL, Drielli Gomes e ARRIBAS, Marco e TROSSINI, Gustavo Henrique Goulart. Molecular modeling and docking application to evaluate cruzain inhibitory activity by chalcones and hydrazides. Letters in Drug Design & Discovery, v. 11, n. 3, p. 249-255, 2014Tradução . . Acesso em: 06 set. 2024.
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      Vital, D. G., Arribas, M., & Trossini, G. H. G. (2014). Molecular modeling and docking application to evaluate cruzain inhibitory activity by chalcones and hydrazides. Letters in Drug Design & Discovery, 11( 3), 249-255.
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      Vital DG, Arribas M, Trossini GHG. Molecular modeling and docking application to evaluate cruzain inhibitory activity by chalcones and hydrazides. Letters in Drug Design & Discovery. 2014 ; 11( 3): 249-255.[citado 2024 set. 06 ]
    • Vancouver

      Vital DG, Arribas M, Trossini GHG. Molecular modeling and docking application to evaluate cruzain inhibitory activity by chalcones and hydrazides. Letters in Drug Design & Discovery. 2014 ; 11( 3): 249-255.[citado 2024 set. 06 ]
  • Source: Medicinal Chemistry. Unidade: FCF

    Subjects: BIODISPONIBILIDADE, RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA

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      SILVA, Fredson Torres e TROSSINI, Gustavo Henrique Goulart. The survey of the use of QSAR methods to determine intestinal absorption and oral bioavailability during drug design. Medicinal Chemistry, v. 10, n. 5, p. 441-448, 2014Tradução . . Acesso em: 06 set. 2024.
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      Silva, F. T., & Trossini, G. H. G. (2014). The survey of the use of QSAR methods to determine intestinal absorption and oral bioavailability during drug design. Medicinal Chemistry, 10( 5), 441-448.
    • NLM

      Silva FT, Trossini GHG. The survey of the use of QSAR methods to determine intestinal absorption and oral bioavailability during drug design. Medicinal Chemistry. 2014 ; 10( 5): 441-448.[citado 2024 set. 06 ]
    • Vancouver

      Silva FT, Trossini GHG. The survey of the use of QSAR methods to determine intestinal absorption and oral bioavailability during drug design. Medicinal Chemistry. 2014 ; 10( 5): 441-448.[citado 2024 set. 06 ]
  • Source: Current Topics in Medicinal Chemistry. Unidade: IQSC

    Assunto: QUÍMICA MÉDICA

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      COSTA, E. V. et al. Structure based design, synthesis, and evaluation of potential inhibitors of steroid sulfatase. Current Topics in Medicinal Chemistry, v. 14, n. 8, p. 1033-1044, 2014Tradução . . Disponível em: https://repositorio.usp.br/directbitstream/9681e089-d632-4260-8666-e505cc746359/P15026.pdf. Acesso em: 06 set. 2024.
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      Costa, E. V., Sousa, E., Choosang, K., Singh, S., Rocha, J., Lima, R. T., et al. (2014). Structure based design, synthesis, and evaluation of potential inhibitors of steroid sulfatase. Current Topics in Medicinal Chemistry, 14( 8), 1033-1044. Recuperado de https://repositorio.usp.br/directbitstream/9681e089-d632-4260-8666-e505cc746359/P15026.pdf
    • NLM

      Costa EV, Sousa E, Choosang K, Singh S, Rocha J, Lima RT, Pakkong P, Ahmed S, Vasconcelos MH, Montanari CA, Pinto MM. Structure based design, synthesis, and evaluation of potential inhibitors of steroid sulfatase [Internet]. Current Topics in Medicinal Chemistry. 2014 ; 14( 8): 1033-1044.[citado 2024 set. 06 ] Available from: https://repositorio.usp.br/directbitstream/9681e089-d632-4260-8666-e505cc746359/P15026.pdf
    • Vancouver

      Costa EV, Sousa E, Choosang K, Singh S, Rocha J, Lima RT, Pakkong P, Ahmed S, Vasconcelos MH, Montanari CA, Pinto MM. Structure based design, synthesis, and evaluation of potential inhibitors of steroid sulfatase [Internet]. Current Topics in Medicinal Chemistry. 2014 ; 14( 8): 1033-1044.[citado 2024 set. 06 ] Available from: https://repositorio.usp.br/directbitstream/9681e089-d632-4260-8666-e505cc746359/P15026.pdf
  • Source: Letters in Drug Design & Discovery. Unidade: FCF

    Subjects: ANTIFÚNGICOS, AMINOÁCIDOS

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      BELLOMO, Ana et al. Antifungal activity of a library of cyclitols and related compounds. Letters in Drug Design & Discovery, v. 11, n. 1, p. 67-75, 2014Tradução . . Disponível em: http://www.ingentaconnect.com/content/ben/lddd/2013/00000011/00000001/art00011. Acesso em: 06 set. 2024.
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      Bellomo, A., Bertucci, A., Sovera, V. de la, Carrau, G., Raimondi, M., Zacchino, S., et al. (2014). Antifungal activity of a library of cyclitols and related compounds. Letters in Drug Design & Discovery, 11( 1), 67-75. Recuperado de http://www.ingentaconnect.com/content/ben/lddd/2013/00000011/00000001/art00011
    • NLM

      Bellomo A, Bertucci A, Sovera V de la, Carrau G, Raimondi M, Zacchino S, Stefani HA, Gonzalez D. Antifungal activity of a library of cyclitols and related compounds [Internet]. Letters in Drug Design & Discovery. 2014 ; 11( 1): 67-75.[citado 2024 set. 06 ] Available from: http://www.ingentaconnect.com/content/ben/lddd/2013/00000011/00000001/art00011
    • Vancouver

      Bellomo A, Bertucci A, Sovera V de la, Carrau G, Raimondi M, Zacchino S, Stefani HA, Gonzalez D. Antifungal activity of a library of cyclitols and related compounds [Internet]. Letters in Drug Design & Discovery. 2014 ; 11( 1): 67-75.[citado 2024 set. 06 ] Available from: http://www.ingentaconnect.com/content/ben/lddd/2013/00000011/00000001/art00011

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