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  • Source: European Journal of Pharmaceutical Sciences. Unidade: IFSC

    Subjects: PLANEJAMENTO DE FÁRMACOS, TUBERCULOSE, DIFRAÇÃO POR RAIOS X, ANÁLISE TÉRMICA, SOLUBILIDADE

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      MELO, Cristiane C. et al. Mechanochemistry applied to reformulation and scale-up production of ethionamide: salt selection and solubility enhancement. European Journal of Pharmaceutical Sciences, v. 81, n. Ja 2016, p. 149-156, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.ejps.2015.10.007. Acesso em: 21 maio 2024.
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      Melo, C. C., Silva, C. C. P., Pereira, C. C. S. S., Rosa, P. C. P., & Ellena, J. (2016). Mechanochemistry applied to reformulation and scale-up production of ethionamide: salt selection and solubility enhancement. European Journal of Pharmaceutical Sciences, 81( Ja 2016), 149-156. doi:10.1016/j.ejps.2015.10.007
    • NLM

      Melo CC, Silva CCP, Pereira CCSS, Rosa PCP, Ellena J. Mechanochemistry applied to reformulation and scale-up production of ethionamide: salt selection and solubility enhancement [Internet]. European Journal of Pharmaceutical Sciences. 2016 ; 81( Ja 2016): 149-156.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.ejps.2015.10.007
    • Vancouver

      Melo CC, Silva CCP, Pereira CCSS, Rosa PCP, Ellena J. Mechanochemistry applied to reformulation and scale-up production of ethionamide: salt selection and solubility enhancement [Internet]. European Journal of Pharmaceutical Sciences. 2016 ; 81( Ja 2016): 149-156.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.ejps.2015.10.007
  • Source: Journal of Coordination Chemistry. Unidade: IFSC

    Subjects: CITOTOXINAS, RUTÊNIO, AMINOÁCIDOS, COLÁGENO

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      SANTOS, Edjane R. et al. Ru(II)/bisphosphine/diimine/amino acid complexes: diastereoisomerism, cytotoxicity, and inhibition of tumor cell adhesion to collagen type I. Journal of Coordination Chemistry, v. 69, n. 23, p. 3518-3530, 2016Tradução . . Disponível em: https://doi.org/10.1080/00958972.2016.1244334. Acesso em: 21 maio 2024.
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      Santos, E. R., Corrêa, R. S., Ribeiro, J. U., Graminha, A. E., Ellena, J., Selistre-de-Araujo, H. S., & Batista, A. A. (2016). Ru(II)/bisphosphine/diimine/amino acid complexes: diastereoisomerism, cytotoxicity, and inhibition of tumor cell adhesion to collagen type I. Journal of Coordination Chemistry, 69( 23), 3518-3530. doi:10.1080/00958972.2016.1244334
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      Santos ER, Corrêa RS, Ribeiro JU, Graminha AE, Ellena J, Selistre-de-Araujo HS, Batista AA. Ru(II)/bisphosphine/diimine/amino acid complexes: diastereoisomerism, cytotoxicity, and inhibition of tumor cell adhesion to collagen type I [Internet]. Journal of Coordination Chemistry. 2016 ; 69( 23): 3518-3530.[citado 2024 maio 21 ] Available from: https://doi.org/10.1080/00958972.2016.1244334
    • Vancouver

      Santos ER, Corrêa RS, Ribeiro JU, Graminha AE, Ellena J, Selistre-de-Araujo HS, Batista AA. Ru(II)/bisphosphine/diimine/amino acid complexes: diastereoisomerism, cytotoxicity, and inhibition of tumor cell adhesion to collagen type I [Internet]. Journal of Coordination Chemistry. 2016 ; 69( 23): 3518-3530.[citado 2024 maio 21 ] Available from: https://doi.org/10.1080/00958972.2016.1244334
  • Source: Journal of Molecular Structure. Unidade: IFSC

    Subjects: ANTIFÚNGICOS (ATIVIDADE), PRAGAS DE PLANTAS, ESPECTROSCOPIA INFRAVERMELHA, DIFRAÇÃO POR RAIOS X

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      TAVARES, Eder C. et al. Tetraphenylphosphonium allyldithiocarbimates derived from Morita- Baylis-Hillman adducts: synthesis, characterization, crystal structure and antifungal activity. Journal of Molecular Structure, v. 1106, p. 130-140, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2015.10.097. Acesso em: 21 maio 2024.
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      Tavares, E. C., Rubinger, M. M. M., Filho, E. V., Oliveira, M. R. L., Piló-Veloso, D., Ellena, J., et al. (2016). Tetraphenylphosphonium allyldithiocarbimates derived from Morita- Baylis-Hillman adducts: synthesis, characterization, crystal structure and antifungal activity. Journal of Molecular Structure, 1106, 130-140. doi:10.1016/j.molstruc.2015.10.097
    • NLM

      Tavares EC, Rubinger MMM, Filho EV, Oliveira MRL, Piló-Veloso D, Ellena J, Guilardi S, Souza RAC, Zambolim L. Tetraphenylphosphonium allyldithiocarbimates derived from Morita- Baylis-Hillman adducts: synthesis, characterization, crystal structure and antifungal activity [Internet]. Journal of Molecular Structure. 2016 ; 1106 130-140.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.molstruc.2015.10.097
    • Vancouver

      Tavares EC, Rubinger MMM, Filho EV, Oliveira MRL, Piló-Veloso D, Ellena J, Guilardi S, Souza RAC, Zambolim L. Tetraphenylphosphonium allyldithiocarbimates derived from Morita- Baylis-Hillman adducts: synthesis, characterization, crystal structure and antifungal activity [Internet]. Journal of Molecular Structure. 2016 ; 1106 130-140.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.molstruc.2015.10.097
  • Source: Spectrochimica Acta A. Unidade: IFSC

    Subjects: PLANEJAMENTO DE FÁRMACOS, DIFRAÇÃO POR RAIOS X, CRISTALOGRAFIA DE RAIOS X

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      FONSECA, Jéssica de Castro et al. Diffractaic acid: crystalline structure and physicochemical characterization. Spectrochimica Acta A, v. 165, p. 26-32, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.saa.2016.04.030. Acesso em: 21 maio 2024.
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      Fonseca, J. de C., Oliveira, Y. S. de, Bezerra, B. P., Ellena, J., Honda, N. K., Silva, C. V. N. S., et al. (2016). Diffractaic acid: crystalline structure and physicochemical characterization. Spectrochimica Acta A, 165, 26-32. doi:10.1016/j.saa.2016.04.030
    • NLM

      Fonseca J de C, Oliveira YS de, Bezerra BP, Ellena J, Honda NK, Silva CVNS, Santos NP da S, Magalhães NSS, Ayala AP. Diffractaic acid: crystalline structure and physicochemical characterization [Internet]. Spectrochimica Acta A. 2016 ; 165 26-32.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.saa.2016.04.030
    • Vancouver

      Fonseca J de C, Oliveira YS de, Bezerra BP, Ellena J, Honda NK, Silva CVNS, Santos NP da S, Magalhães NSS, Ayala AP. Diffractaic acid: crystalline structure and physicochemical characterization [Internet]. Spectrochimica Acta A. 2016 ; 165 26-32.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.saa.2016.04.030
  • Source: Dalton Transactions. Unidade: IFSC

    Subjects: LANTANÍDIOS, LUMINESCÊNCIA

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      D'VRIES, Richard D. et al. Tuning the structure, dimensionality and luminescent properties of lanthanide metal-organic frameworks under ancillary ligand influence. Dalton Transactions, v. 45, n. Ja 2016, p. 646-656 + supplementary information, 2016Tradução . . Disponível em: https://doi.org/10.1039/c5dt04033g. Acesso em: 21 maio 2024.
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      D'Vries, R. D., Gomez, G. E., Hodak, J. H., Soler-Illia, G. J. A. A., & Ellena, J. (2016). Tuning the structure, dimensionality and luminescent properties of lanthanide metal-organic frameworks under ancillary ligand influence. Dalton Transactions, 45( Ja 2016), 646-656 + supplementary information. doi:10.1039/c5dt04033g
    • NLM

      D'Vries RD, Gomez GE, Hodak JH, Soler-Illia GJAA, Ellena J. Tuning the structure, dimensionality and luminescent properties of lanthanide metal-organic frameworks under ancillary ligand influence [Internet]. Dalton Transactions. 2016 ; 45( Ja 2016): 646-656 + supplementary information.[citado 2024 maio 21 ] Available from: https://doi.org/10.1039/c5dt04033g
    • Vancouver

      D'Vries RD, Gomez GE, Hodak JH, Soler-Illia GJAA, Ellena J. Tuning the structure, dimensionality and luminescent properties of lanthanide metal-organic frameworks under ancillary ligand influence [Internet]. Dalton Transactions. 2016 ; 45( Ja 2016): 646-656 + supplementary information.[citado 2024 maio 21 ] Available from: https://doi.org/10.1039/c5dt04033g
  • Source: Journal of the Brazilian Chemical Society. Unidade: IFSC

    Subjects: CITOTOXINAS, TUBERCULOSE, PLANEJAMENTO DE FÁRMACOS

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      LIMA, Benedicto A. V. et al. Anti-mycobacterium tuberculosis and cytotoxicity activities of ruthenium(II)/ bipyridine/diphosphine/pyrimidine-2-thiolate complexes: the role of the non-coordinated N-atom. Journal of the Brazilian Chemical Society, v. 27, n. Ja 2016, p. 30-40, 2016Tradução . . Disponível em: https://doi.org/10.5935/0103-5053.20150237. Acesso em: 21 maio 2024.
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      Lima, B. A. V., Corrêa, R. S., Graminha, A. E., Kuznetsov, A., Ellena, J., Pavan, F. R., et al. (2016). Anti-mycobacterium tuberculosis and cytotoxicity activities of ruthenium(II)/ bipyridine/diphosphine/pyrimidine-2-thiolate complexes: the role of the non-coordinated N-atom. Journal of the Brazilian Chemical Society, 27( Ja 2016), 30-40. doi:10.5935/0103-5053.20150237
    • NLM

      Lima BAV, Corrêa RS, Graminha AE, Kuznetsov A, Ellena J, Pavan FR, Leite CQF, Batista AA. Anti-mycobacterium tuberculosis and cytotoxicity activities of ruthenium(II)/ bipyridine/diphosphine/pyrimidine-2-thiolate complexes: the role of the non-coordinated N-atom [Internet]. Journal of the Brazilian Chemical Society. 2016 ; 27( Ja 2016): 30-40.[citado 2024 maio 21 ] Available from: https://doi.org/10.5935/0103-5053.20150237
    • Vancouver

      Lima BAV, Corrêa RS, Graminha AE, Kuznetsov A, Ellena J, Pavan FR, Leite CQF, Batista AA. Anti-mycobacterium tuberculosis and cytotoxicity activities of ruthenium(II)/ bipyridine/diphosphine/pyrimidine-2-thiolate complexes: the role of the non-coordinated N-atom [Internet]. Journal of the Brazilian Chemical Society. 2016 ; 27( Ja 2016): 30-40.[citado 2024 maio 21 ] Available from: https://doi.org/10.5935/0103-5053.20150237
  • Source: Journal of Molecular Structure. Unidade: IFSC

    Subjects: ANTIFÚNGICOS (ATIVIDADE), CRISTALOGRAFIA, NÍQUEL

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      VIDIGAL, Antonio E. C. et al. Syntheses, characterization and antifungal activity of heteroleptic nickel(II) complexes with N-alkylsulfonyldithiocarbimates and phosphines. Journal of Molecular Structure, v. 1114, p. 21-29, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2016.02.060. Acesso em: 21 maio 2024.
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      Vidigal, A. E. C., Rubinger, M. M. M., Oliveira, M. R. L., Guilardi, S., Souza, R. A. C., Ellena, J., & Zambolim, L. (2016). Syntheses, characterization and antifungal activity of heteroleptic nickel(II) complexes with N-alkylsulfonyldithiocarbimates and phosphines. Journal of Molecular Structure, 1114, 21-29. doi:10.1016/j.molstruc.2016.02.060
    • NLM

      Vidigal AEC, Rubinger MMM, Oliveira MRL, Guilardi S, Souza RAC, Ellena J, Zambolim L. Syntheses, characterization and antifungal activity of heteroleptic nickel(II) complexes with N-alkylsulfonyldithiocarbimates and phosphines [Internet]. Journal of Molecular Structure. 2016 ; 1114 21-29.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.molstruc.2016.02.060
    • Vancouver

      Vidigal AEC, Rubinger MMM, Oliveira MRL, Guilardi S, Souza RAC, Ellena J, Zambolim L. Syntheses, characterization and antifungal activity of heteroleptic nickel(II) complexes with N-alkylsulfonyldithiocarbimates and phosphines [Internet]. Journal of Molecular Structure. 2016 ; 1114 21-29.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.molstruc.2016.02.060
  • Source: Journal of Molecular Structure. Unidade: IFSC

    Subjects: ESPECTROSCOPIA INFRAVERMELHA, DIFRAÇÃO POR RAIOS X, PLANEJAMENTO DE FÁRMACOS, CRISTALOGRAFIA

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      CARVALHO JR., Paulo S. et al. X-Ray diffraction, spectroscopy and thermochemical characterization of the pharmaceutical paroxetine nitrate salt. Journal of Molecular Structure, v. 1118, p. 288-292, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2016.04.014. Acesso em: 21 maio 2024.
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      Carvalho Jr., P. S., Melo, C. C., Ayala, A. P., & Ellena, J. (2016). X-Ray diffraction, spectroscopy and thermochemical characterization of the pharmaceutical paroxetine nitrate salt. Journal of Molecular Structure, 1118, 288-292. doi:10.1016/j.molstruc.2016.04.014
    • NLM

      Carvalho Jr. PS, Melo CC, Ayala AP, Ellena J. X-Ray diffraction, spectroscopy and thermochemical characterization of the pharmaceutical paroxetine nitrate salt [Internet]. Journal of Molecular Structure. 2016 ; 1118 288-292.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.molstruc.2016.04.014
    • Vancouver

      Carvalho Jr. PS, Melo CC, Ayala AP, Ellena J. X-Ray diffraction, spectroscopy and thermochemical characterization of the pharmaceutical paroxetine nitrate salt [Internet]. Journal of Molecular Structure. 2016 ; 1118 288-292.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.molstruc.2016.04.014
  • Source: Spectrochimica Acta A. Unidade: IFSC

    Subjects: INTERAÇÃO DE MEDICAMENTOS, ESPECTROSCOPIA INFRAVERMELHA, RESSONÂNCIA MAGNÉTICA NUCLEAR

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      RUSSO, Marcos G. et al. Looking for the interactions between omeprazole and amoxicillin in a disordered phase: an experimental and theoretical study. Spectrochimica Acta A, v. 156, p. 70-77, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.saa.2015.11.021. Acesso em: 21 maio 2024.
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      Russo, M. G., Sancho, M. I., Silva, L. M. A., Baldoni, H. A., Venancio, T., Ellena, J., & Narda, G. E. (2016). Looking for the interactions between omeprazole and amoxicillin in a disordered phase: an experimental and theoretical study. Spectrochimica Acta A, 156, 70-77. doi:10.1016/j.saa.2015.11.021
    • NLM

      Russo MG, Sancho MI, Silva LMA, Baldoni HA, Venancio T, Ellena J, Narda GE. Looking for the interactions between omeprazole and amoxicillin in a disordered phase: an experimental and theoretical study [Internet]. Spectrochimica Acta A. 2016 ; 156 70-77.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.saa.2015.11.021
    • Vancouver

      Russo MG, Sancho MI, Silva LMA, Baldoni HA, Venancio T, Ellena J, Narda GE. Looking for the interactions between omeprazole and amoxicillin in a disordered phase: an experimental and theoretical study [Internet]. Spectrochimica Acta A. 2016 ; 156 70-77.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.saa.2015.11.021
  • Source: Crystal Growth and Design. Unidade: IFSC

    Subjects: PLANEJAMENTO DE FÁRMACOS, CRISTALOGRAFIA

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      CARVALHO JUNIOR, Paulo S. et al. Reversible solid-state hydration/dehydration of paroxetine HBr hemihydrate: structural and thermochemical studies. Crystal Growth and Design, v. 16, n. Ja 2016, p. 1543-1549, 2016Tradução . . Disponível em: https://doi.org/10.1021/acs.cgd.5b01672. Acesso em: 21 maio 2024.
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      Carvalho Junior, P. S., Melo, C. C., Ayala, A. P., Silva, C. C. P., & Ellena, J. (2016). Reversible solid-state hydration/dehydration of paroxetine HBr hemihydrate: structural and thermochemical studies. Crystal Growth and Design, 16( Ja 2016), 1543-1549. doi:10.1021/acs.cgd.5b01672
    • NLM

      Carvalho Junior PS, Melo CC, Ayala AP, Silva CCP, Ellena J. Reversible solid-state hydration/dehydration of paroxetine HBr hemihydrate: structural and thermochemical studies [Internet]. Crystal Growth and Design. 2016 ; 16( Ja 2016): 1543-1549.[citado 2024 maio 21 ] Available from: https://doi.org/10.1021/acs.cgd.5b01672
    • Vancouver

      Carvalho Junior PS, Melo CC, Ayala AP, Silva CCP, Ellena J. Reversible solid-state hydration/dehydration of paroxetine HBr hemihydrate: structural and thermochemical studies [Internet]. Crystal Growth and Design. 2016 ; 16( Ja 2016): 1543-1549.[citado 2024 maio 21 ] Available from: https://doi.org/10.1021/acs.cgd.5b01672
  • Source: Polyhedron. Unidade: IFSC

    Subjects: PLANEJAMENTO DE FÁRMACOS, TUBERCULOSE (ESTUDO;TRATAMENTO), RUTÊNIO, CITOTOXINAS

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      BARBOSA, Marília I. F. et al. Ruthenium(II) complexes with hydroxypyridinecarboxylates: screening potential metallodrugs against Mycobacterium tuberculosis. Polyhedron, v. 85, n. Ja 2015, p. 376-382, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.poly.2014.08.057. Acesso em: 21 maio 2024.
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      Barbosa, M. I. F., Corrêa, R. S., Pozzi, L. V., Lopes, É. O., Pavan, F. R., Leite, C. Q. F., et al. (2015). Ruthenium(II) complexes with hydroxypyridinecarboxylates: screening potential metallodrugs against Mycobacterium tuberculosis. Polyhedron, 85( Ja 2015), 376-382. doi:10.1016/j.poly.2014.08.057
    • NLM

      Barbosa MIF, Corrêa RS, Pozzi LV, Lopes ÉO, Pavan FR, Leite CQF, Ellena J, Machado SP, Poelhsitz GV, Batista AA. Ruthenium(II) complexes with hydroxypyridinecarboxylates: screening potential metallodrugs against Mycobacterium tuberculosis [Internet]. Polyhedron. 2015 ; 85( Ja 2015): 376-382.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.poly.2014.08.057
    • Vancouver

      Barbosa MIF, Corrêa RS, Pozzi LV, Lopes ÉO, Pavan FR, Leite CQF, Ellena J, Machado SP, Poelhsitz GV, Batista AA. Ruthenium(II) complexes with hydroxypyridinecarboxylates: screening potential metallodrugs against Mycobacterium tuberculosis [Internet]. Polyhedron. 2015 ; 85( Ja 2015): 376-382.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.poly.2014.08.057
  • Source: Crystal Growth and Design. Unidade: IFSC

    Subjects: CRISTALOGRAFIA, MOLÉCULA (ESTRUTURA)

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      VITTAL, Jagadese J. e ELLENA, Javier. Crystal Growth and Design celebrates the international year of Crystallography 2014. Crystal Growth and Design. Washington, DC: Instituto de Física de São Carlos, Universidade de São Paulo. Disponível em: https://doi.org/10.1021/cg501847a. Acesso em: 21 maio 2024. , 2015
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      Vittal, J. J., & Ellena, J. (2015). Crystal Growth and Design celebrates the international year of Crystallography 2014. Crystal Growth and Design. Washington, DC: Instituto de Física de São Carlos, Universidade de São Paulo. doi:10.1021/cg501847a
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      Vittal JJ, Ellena J. Crystal Growth and Design celebrates the international year of Crystallography 2014 [Internet]. Crystal Growth and Design. 2015 ; 15( Ja 2015): 2-4.[citado 2024 maio 21 ] Available from: https://doi.org/10.1021/cg501847a
    • Vancouver

      Vittal JJ, Ellena J. Crystal Growth and Design celebrates the international year of Crystallography 2014 [Internet]. Crystal Growth and Design. 2015 ; 15( Ja 2015): 2-4.[citado 2024 maio 21 ] Available from: https://doi.org/10.1021/cg501847a
  • Source: Polyhedron. Unidades: IFSC, FCFRP, IQ

    Subjects: CRISTALOGRAFIA, COBRE, RAIOS X

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      ALMEIDA, Janaina do Couto et al. Copper(II) complexes with b-diketones and N-donor heterocyclic ligands: Crystal structure, spectral properties, and cytotoxic activity. Polyhedron, v. 89, p. 1-8, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.poly.2014.12.026. Acesso em: 21 maio 2024.
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      Almeida, J. do C., Paixão, D. A., Marzano, I. M., Ellena, J., Pivatto, M., Lopes, N. P., et al. (2015). Copper(II) complexes with b-diketones and N-donor heterocyclic ligands: Crystal structure, spectral properties, and cytotoxic activity. Polyhedron, 89, 1-8. doi:10.1016/j.poly.2014.12.026
    • NLM

      Almeida J do C, Paixão DA, Marzano IM, Ellena J, Pivatto M, Lopes NP, Ferreira AM da C, Pereira-Maia EC, Guilardi S, Guerra W. Copper(II) complexes with b-diketones and N-donor heterocyclic ligands: Crystal structure, spectral properties, and cytotoxic activity [Internet]. Polyhedron. 2015 ; 89 1-8.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.poly.2014.12.026
    • Vancouver

      Almeida J do C, Paixão DA, Marzano IM, Ellena J, Pivatto M, Lopes NP, Ferreira AM da C, Pereira-Maia EC, Guilardi S, Guerra W. Copper(II) complexes with b-diketones and N-donor heterocyclic ligands: Crystal structure, spectral properties, and cytotoxic activity [Internet]. Polyhedron. 2015 ; 89 1-8.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.poly.2014.12.026
  • Source: Crystal Growth and Design. Unidade: IFSC

    Subjects: LANTANÍDIOS, CRISTALOGRAFIA

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      D'VRIES, Richard F. e CAMPS, Ihosvany e ELLENA, Javier. Exploring the system lanthanide/succinate in the formation of porous metal-organic frameworks: experimental and theoretical study. Crystal Growth and Design, v. 15, n. 6, p. 3015-3023, 2015Tradução . . Disponível em: https://doi.org/10.1021/acs.cgd.5b00426. Acesso em: 21 maio 2024.
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      D'Vries, R. F., Camps, I., & Ellena, J. (2015). Exploring the system lanthanide/succinate in the formation of porous metal-organic frameworks: experimental and theoretical study. Crystal Growth and Design, 15( 6), 3015-3023. doi:10.1021/acs.cgd.5b00426
    • NLM

      D'Vries RF, Camps I, Ellena J. Exploring the system lanthanide/succinate in the formation of porous metal-organic frameworks: experimental and theoretical study [Internet]. Crystal Growth and Design. 2015 ; 15( 6): 3015-3023.[citado 2024 maio 21 ] Available from: https://doi.org/10.1021/acs.cgd.5b00426
    • Vancouver

      D'Vries RF, Camps I, Ellena J. Exploring the system lanthanide/succinate in the formation of porous metal-organic frameworks: experimental and theoretical study [Internet]. Crystal Growth and Design. 2015 ; 15( 6): 3015-3023.[citado 2024 maio 21 ] Available from: https://doi.org/10.1021/acs.cgd.5b00426
  • Source: CrystEngComm. Unidade: IFSC

    Subjects: CRISTALOGRAFIA, HALOGÊNIOS

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      CLAVIJO, Juan Carlos Tenorio et al. Isostructurality and the conformational role of the 2′,3′-moieties in the diversity of lamivudine crystal forms probed in halide salts. CrystEngComm, v. 17, n. 28, p. 5187-5194, 2015Tradução . . Disponível em: https://doi.org/10.1039/c4ce02373k. Acesso em: 21 maio 2024.
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      Clavijo, J. C. T., Guimarães, F. F., Ellena, J., & Martins, F. T. (2015). Isostructurality and the conformational role of the 2′,3′-moieties in the diversity of lamivudine crystal forms probed in halide salts. CrystEngComm, 17( 28), 5187-5194. doi:10.1039/c4ce02373k
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      Clavijo JCT, Guimarães FF, Ellena J, Martins FT. Isostructurality and the conformational role of the 2′,3′-moieties in the diversity of lamivudine crystal forms probed in halide salts [Internet]. CrystEngComm. 2015 ; 17( 28): 5187-5194.[citado 2024 maio 21 ] Available from: https://doi.org/10.1039/c4ce02373k
    • Vancouver

      Clavijo JCT, Guimarães FF, Ellena J, Martins FT. Isostructurality and the conformational role of the 2′,3′-moieties in the diversity of lamivudine crystal forms probed in halide salts [Internet]. CrystEngComm. 2015 ; 17( 28): 5187-5194.[citado 2024 maio 21 ] Available from: https://doi.org/10.1039/c4ce02373k
  • Source: Inorganica Chimica Acta. Unidades: IQSC, IFSC

    Subjects: QUÍMICA INORGÂNICA, RUTÊNIO, RAIOS X (ESTRUTURA)

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      SANTOS, Karina et al. Crystal structure and catalytic activity of ruthenium (II)/dithiocarbamate complexes in the epoxidation of cyclooctene. Inorganica Chimica Acta, v. 429, p. 237-242, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.ica.2015.02.014. Acesso em: 21 maio 2024.
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      Santos, K., Dinelli, L. R., Bogado, A. L., Ramos, L. A., Cavalheiro, E. T. G., Ellena, J., et al. (2015). Crystal structure and catalytic activity of ruthenium (II)/dithiocarbamate complexes in the epoxidation of cyclooctene. Inorganica Chimica Acta, 429, 237-242. doi:10.1016/j.ica.2015.02.014
    • NLM

      Santos K, Dinelli LR, Bogado AL, Ramos LA, Cavalheiro ETG, Ellena J, Castellano EE, Batista AA. Crystal structure and catalytic activity of ruthenium (II)/dithiocarbamate complexes in the epoxidation of cyclooctene [Internet]. Inorganica Chimica Acta. 2015 ; 429 237-242.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.ica.2015.02.014
    • Vancouver

      Santos K, Dinelli LR, Bogado AL, Ramos LA, Cavalheiro ETG, Ellena J, Castellano EE, Batista AA. Crystal structure and catalytic activity of ruthenium (II)/dithiocarbamate complexes in the epoxidation of cyclooctene [Internet]. Inorganica Chimica Acta. 2015 ; 429 237-242.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.ica.2015.02.014
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: IFSC

    Subjects: CRISTALOGRAFIA, HIV (MEDICAMENTOS), TERMOANÁLISE

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      MARTINS, Felipe T. et al. Vibrational and thermal analyses of multicomponent crystal forms of the anti-HIV drugs lamivudine and zalcitabine. Journal of Pharmaceutical and Biomedical Analysis, v. 110, n. Ju 2015, p. 76-82, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2015.03.004. Acesso em: 21 maio 2024.
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      Martins, F. T., Guimarães, F. F., Honorato, S. B., Ayala, A. P., & Ellena, J. (2015). Vibrational and thermal analyses of multicomponent crystal forms of the anti-HIV drugs lamivudine and zalcitabine. Journal of Pharmaceutical and Biomedical Analysis, 110( Ju 2015), 76-82. doi:10.1016/j.jpba.2015.03.004
    • NLM

      Martins FT, Guimarães FF, Honorato SB, Ayala AP, Ellena J. Vibrational and thermal analyses of multicomponent crystal forms of the anti-HIV drugs lamivudine and zalcitabine [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2015 ; 110( Ju 2015): 76-82.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.jpba.2015.03.004
    • Vancouver

      Martins FT, Guimarães FF, Honorato SB, Ayala AP, Ellena J. Vibrational and thermal analyses of multicomponent crystal forms of the anti-HIV drugs lamivudine and zalcitabine [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2015 ; 110( Ju 2015): 76-82.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.jpba.2015.03.004
  • Source: Inorganic Chemistry. Unidade: IFSC

    Subjects: PLANEJAMENTO DE FÁRMACOS, CITOTOXINAS, NEOPLASIAS

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      VILLARREAL, Wilmer et al. Chiral platinum(II) complexes featuring phosphine and chloroquine ligands as cytotoxic and monofunctional DNA-binding agents. Inorganic Chemistry, v. 54, n. 24, p. 11709-11720, 2015Tradução . . Disponível em: https://doi.org/10.1021/acs.inorgchem.5b01647. Acesso em: 21 maio 2024.
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      Villarreal, W., Colina-Vegas, L., Oliveira, C. R. de, Tenorio, J. C., Ellena, J., Gozzo, F. C., et al. (2015). Chiral platinum(II) complexes featuring phosphine and chloroquine ligands as cytotoxic and monofunctional DNA-binding agents. Inorganic Chemistry, 54( 24), 11709-11720. doi:10.1021/acs.inorgchem.5b01647
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      Villarreal W, Colina-Vegas L, Oliveira CR de, Tenorio JC, Ellena J, Gozzo FC, Cominetti MR, Ferreira AG, Ferreira MAB, Navarro M, Batista AA. Chiral platinum(II) complexes featuring phosphine and chloroquine ligands as cytotoxic and monofunctional DNA-binding agents [Internet]. Inorganic Chemistry. 2015 ; 54( 24): 11709-11720.[citado 2024 maio 21 ] Available from: https://doi.org/10.1021/acs.inorgchem.5b01647
    • Vancouver

      Villarreal W, Colina-Vegas L, Oliveira CR de, Tenorio JC, Ellena J, Gozzo FC, Cominetti MR, Ferreira AG, Ferreira MAB, Navarro M, Batista AA. Chiral platinum(II) complexes featuring phosphine and chloroquine ligands as cytotoxic and monofunctional DNA-binding agents [Internet]. Inorganic Chemistry. 2015 ; 54( 24): 11709-11720.[citado 2024 maio 21 ] Available from: https://doi.org/10.1021/acs.inorgchem.5b01647
  • Source: Journal of Inorganic Biochemistry. Unidade: IFSC

    Subjects: RUTÊNIO, SARCOMA, CRISTALOGRAFIA

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      PEREIRA, Flávia de C. et al. Cis-[RuCl(BzCN)(N–N)(P–P)]PF6 complexes: synthesis and in vitro antitumor activity (BzCN = benzonitrile; N–N = 2,2′-bipyridine; 1,10-phenanthroline; P–P = 1,4-bis(diphenylphosphino) butane, 1,2-bis(diphenylphosphino)ethane, or 1,1′-(diphenylphosphino)ferrocene). Journal of Inorganic Biochemistry, v. 149, p. 91-101, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.jinorgbio.2015.03.011. Acesso em: 21 maio 2024.
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      Pereira, F. de C., Lima, B. A. V., Lima, A. P., Pires, W. C., Monteiro, T., Magalhães, L. F., et al. (2015). Cis-[RuCl(BzCN)(N–N)(P–P)]PF6 complexes: synthesis and in vitro antitumor activity (BzCN = benzonitrile; N–N = 2,2′-bipyridine; 1,10-phenanthroline; P–P = 1,4-bis(diphenylphosphino) butane, 1,2-bis(diphenylphosphino)ethane, or 1,1′-(diphenylphosphino)ferrocene). Journal of Inorganic Biochemistry, 149, 91-101. doi:10.1016/j.jinorgbio.2015.03.011
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      Pereira F de C, Lima BAV, Lima AP, Pires WC, Monteiro T, Magalhães LF, Costa W, Graminha AE, Batista AA, Ellena J, Lacerda E de PS. Cis-[RuCl(BzCN)(N–N)(P–P)]PF6 complexes: synthesis and in vitro antitumor activity (BzCN = benzonitrile; N–N = 2,2′-bipyridine; 1,10-phenanthroline; P–P = 1,4-bis(diphenylphosphino) butane, 1,2-bis(diphenylphosphino)ethane, or 1,1′-(diphenylphosphino)ferrocene) [Internet]. Journal of Inorganic Biochemistry. 2015 ; 149 91-101.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.jinorgbio.2015.03.011
    • Vancouver

      Pereira F de C, Lima BAV, Lima AP, Pires WC, Monteiro T, Magalhães LF, Costa W, Graminha AE, Batista AA, Ellena J, Lacerda E de PS. Cis-[RuCl(BzCN)(N–N)(P–P)]PF6 complexes: synthesis and in vitro antitumor activity (BzCN = benzonitrile; N–N = 2,2′-bipyridine; 1,10-phenanthroline; P–P = 1,4-bis(diphenylphosphino) butane, 1,2-bis(diphenylphosphino)ethane, or 1,1′-(diphenylphosphino)ferrocene) [Internet]. Journal of Inorganic Biochemistry. 2015 ; 149 91-101.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.jinorgbio.2015.03.011
  • Source: Journal of Pharmaceutical Sciences. Unidade: IFSC

    Subjects: CRISTALOGRAFIA, ESTADO SÓLIDO, ANÁLISE TÉRMICA, SOLUBILIDADE

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      RUSSO, Marcos G. et al. Solid-state supramolecular synthesis based on the N–H..O heterosynthon: an approach to solve the polymorphism problem in famotidine. Journal of Pharmaceutical Sciences, v. No 2014, n. 11, p. 3754-3763, 2014Tradução . . Disponível em: https://doi.org/10.1002/jps.24196. Acesso em: 21 maio 2024.
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      Russo, M. G., Brusau, E. V., Ellena, J., & Narda, G. E. (2014). Solid-state supramolecular synthesis based on the N–H..O heterosynthon: an approach to solve the polymorphism problem in famotidine. Journal of Pharmaceutical Sciences, No 2014( 11), 3754-3763. doi:10.1002/jps.24196
    • NLM

      Russo MG, Brusau EV, Ellena J, Narda GE. Solid-state supramolecular synthesis based on the N–H..O heterosynthon: an approach to solve the polymorphism problem in famotidine [Internet]. Journal of Pharmaceutical Sciences. 2014 ; No 2014( 11): 3754-3763.[citado 2024 maio 21 ] Available from: https://doi.org/10.1002/jps.24196
    • Vancouver

      Russo MG, Brusau EV, Ellena J, Narda GE. Solid-state supramolecular synthesis based on the N–H..O heterosynthon: an approach to solve the polymorphism problem in famotidine [Internet]. Journal of Pharmaceutical Sciences. 2014 ; No 2014( 11): 3754-3763.[citado 2024 maio 21 ] Available from: https://doi.org/10.1002/jps.24196

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