Filtros : " FCF004" "COMPOSTOS HETEROCÍCLICOS" Removidos: "ALIMENTOS E NUTRICAO EXPERIMENTAL" "FAU-AUP" "1984" Limpar

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  • Fonte: Journal of Pharmaceutical Sciences. Unidade: FCF

    Assuntos: COMPOSTOS HETEROCÍCLICOS, SOLUBILIDADE

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    • ABNT

      COMPRI, Jéssica de Cássia Zaghi et al. Highly water-soluble orotic acid nanocrystals produced by high-energy milling. Journal of Pharmaceutical Sciences, v. 108, n. 5, p. 1848-1856, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.xphs.2018.12.015. Acesso em: 01 ago. 2024.
    • APA

      Compri, J. de C. Z., Felli, V. M. A., Lourenço, F. R., Takatsuka, T., Fotaki, N., Löbenberg, R., et al. (2019). Highly water-soluble orotic acid nanocrystals produced by high-energy milling. Journal of Pharmaceutical Sciences, 108( 5), 1848-1856. doi:10.1016/j.xphs.2018.12.015
    • NLM

      Compri J de CZ, Felli VMA, Lourenço FR, Takatsuka T, Fotaki N, Löbenberg R, Bou-Chacra NA, Araujo GLB de. Highly water-soluble orotic acid nanocrystals produced by high-energy milling [Internet]. Journal of Pharmaceutical Sciences. 2019 ; 108( 5): 1848-1856.[citado 2024 ago. 01 ] Available from: https://doi.org/10.1016/j.xphs.2018.12.015
    • Vancouver

      Compri J de CZ, Felli VMA, Lourenço FR, Takatsuka T, Fotaki N, Löbenberg R, Bou-Chacra NA, Araujo GLB de. Highly water-soluble orotic acid nanocrystals produced by high-energy milling [Internet]. Journal of Pharmaceutical Sciences. 2019 ; 108( 5): 1848-1856.[citado 2024 ago. 01 ] Available from: https://doi.org/10.1016/j.xphs.2018.12.015
  • Fonte: Advanced Synthesis and Catalysis. Unidade: FCF

    Assuntos: CALCOGÊNIOS, COMPOSTOS HETEROCÍCLICOS, FERRO

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    • ABNT

      OLIVEIRA, Isadora M. de et al. Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization. Advanced Synthesis and Catalysis, v. 361, n. 13, p. 3163-3172, 2019Tradução . . Disponível em: https://doi.org/10.1002/adsc.201900142. Acesso em: 01 ago. 2024.
    • APA

      Oliveira, I. M. de, Esteves, C. H. A., Darbem, M. P., Pimenta, D. C., Schpector, J. Z., Ferreira, A. G., et al. (2019). Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization. Advanced Synthesis and Catalysis, 361( 13), 3163-3172. doi:10.1002/adsc.201900142
    • NLM

      Oliveira IM de, Esteves CHA, Darbem MP, Pimenta DC, Schpector JZ, Ferreira AG, Stefani HA, Manarin F. Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization [Internet]. Advanced Synthesis and Catalysis. 2019 ; 361( 13): 3163-3172.[citado 2024 ago. 01 ] Available from: https://doi.org/10.1002/adsc.201900142
    • Vancouver

      Oliveira IM de, Esteves CHA, Darbem MP, Pimenta DC, Schpector JZ, Ferreira AG, Stefani HA, Manarin F. Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization [Internet]. Advanced Synthesis and Catalysis. 2019 ; 361( 13): 3163-3172.[citado 2024 ago. 01 ] Available from: https://doi.org/10.1002/adsc.201900142
  • Fonte: Journal of the Chemical Society of Pakistan. Unidades: IQ, FCF

    Assuntos: COMPOSTOS HETEROCÍCLICOS, ANTIOXIDANTES

    Acesso à fonteComo citar
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    • ABNT

      AHMED, Faiz et al. A Facile single pot synthesis of highly functionalized tricyclic heterocycle compounds via sequential Knoevenagel-Michael addition and their α-glucosidase inhibition, antioxidants and antibacterial studies. Journal of the Chemical Society of Pakistan, v. 40, n. 4, p. 761-772, 2018Tradução . . Disponível em: https://www.jcsp.org.pk/PublishedVersion/94e37a96-6278-4cec-bb45-0d63c32f069eManuscript%20no%2014,%20Final%20Gally%20Proof%20of%2011601%20(Ashfaq%20Mahmood%20Qureshi).pdf. Acesso em: 01 ago. 2024.
    • APA

      Ahmed, F., Rauf, A., Sharif, A., Ahmad, E., Arshad, M., Espósito, B. P., et al. (2018). A Facile single pot synthesis of highly functionalized tricyclic heterocycle compounds via sequential Knoevenagel-Michael addition and their α-glucosidase inhibition, antioxidants and antibacterial studies. Journal of the Chemical Society of Pakistan, 40( 4), 761-772. Recuperado de https://www.jcsp.org.pk/PublishedVersion/94e37a96-6278-4cec-bb45-0d63c32f069eManuscript%20no%2014,%20Final%20Gally%20Proof%20of%2011601%20(Ashfaq%20Mahmood%20Qureshi).pdf
    • NLM

      Ahmed F, Rauf A, Sharif A, Ahmad E, Arshad M, Espósito BP, Kaneko TM, Qureshi AM. A Facile single pot synthesis of highly functionalized tricyclic heterocycle compounds via sequential Knoevenagel-Michael addition and their α-glucosidase inhibition, antioxidants and antibacterial studies [Internet]. Journal of the Chemical Society of Pakistan. 2018 ; 40( 4): 761-772.[citado 2024 ago. 01 ] Available from: https://www.jcsp.org.pk/PublishedVersion/94e37a96-6278-4cec-bb45-0d63c32f069eManuscript%20no%2014,%20Final%20Gally%20Proof%20of%2011601%20(Ashfaq%20Mahmood%20Qureshi).pdf
    • Vancouver

      Ahmed F, Rauf A, Sharif A, Ahmad E, Arshad M, Espósito BP, Kaneko TM, Qureshi AM. A Facile single pot synthesis of highly functionalized tricyclic heterocycle compounds via sequential Knoevenagel-Michael addition and their α-glucosidase inhibition, antioxidants and antibacterial studies [Internet]. Journal of the Chemical Society of Pakistan. 2018 ; 40( 4): 761-772.[citado 2024 ago. 01 ] Available from: https://www.jcsp.org.pk/PublishedVersion/94e37a96-6278-4cec-bb45-0d63c32f069eManuscript%20no%2014,%20Final%20Gally%20Proof%20of%2011601%20(Ashfaq%20Mahmood%20Qureshi).pdf
  • Fonte: Toxicology in Vitro. Unidade: FCF

    Assuntos: COMPOSTOS HETEROCÍCLICOS, STAPHYLOCOCCUS

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    • ABNT

      FERNANDES, Mariane Ballerini et al. Caco-2 cells cytotoxicity of nifuroxazide derivatives with potential activity against Methicillin-resistant Staphylococcus aureus. Toxicology in Vitro, v. 28, n. 3, p. 535-540, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.tiv.2012.01.018. Acesso em: 01 ago. 2024.
    • APA

      Fernandes, M. B., Gonçalves, J. E., Scotti, M. T., Oliveira, A. A. de, Tavares, L. C., & Storpirtis, S. (2012). Caco-2 cells cytotoxicity of nifuroxazide derivatives with potential activity against Methicillin-resistant Staphylococcus aureus. Toxicology in Vitro, 28( 3), 535-540. doi:10.1016/j.tiv.2012.01.018
    • NLM

      Fernandes MB, Gonçalves JE, Scotti MT, Oliveira AA de, Tavares LC, Storpirtis S. Caco-2 cells cytotoxicity of nifuroxazide derivatives with potential activity against Methicillin-resistant Staphylococcus aureus [Internet]. Toxicology in Vitro. 2012 ; 28( 3): 535-540.[citado 2024 ago. 01 ] Available from: https://doi.org/10.1016/j.tiv.2012.01.018
    • Vancouver

      Fernandes MB, Gonçalves JE, Scotti MT, Oliveira AA de, Tavares LC, Storpirtis S. Caco-2 cells cytotoxicity of nifuroxazide derivatives with potential activity against Methicillin-resistant Staphylococcus aureus [Internet]. Toxicology in Vitro. 2012 ; 28( 3): 535-540.[citado 2024 ago. 01 ] Available from: https://doi.org/10.1016/j.tiv.2012.01.018

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