ReP USP - Resultado da busca

Artigo de periodico
Synthesis, crystal structure and physicochemical characterization of two Ni(II)‑famotidine metal complexes (2021)
Russo, Marcos G. ; Clavijo, Juan Carlos Tenorio; Álvarez, Natalia; Baldoni, Hector A.; Brusau, Elena V.; Ellena, Javier ; Narda, Griselda E.
Source: Journal of Chemical Crystallography. Unidade: IFSC
Subjects: CRISTALOGRAFIA, PLANEJAMENTO DE FÁRMACOS
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ABNT
RUSSO, Marcos G. et al. Synthesis, crystal structure and physicochemical characterization of two Ni(II)‑famotidine metal complexes. Journal of Chemical Crystallography, v. 51, n. 3, p. 337-351, 2021Tradução . . Disponível em: https://doi.org/10.1007/s10870-020-00860-3. Acesso em: 18 out. 2024.
APA
Russo, M. G., Clavijo, J. C. T., Álvarez, N., Baldoni, H. A., Brusau, E. V., Ellena, J., & Narda, G. E. (2021). Synthesis, crystal structure and physicochemical characterization of two Ni(II)‑famotidine metal complexes. Journal of Chemical Crystallography, 51( 3), 337-351. doi:10.1007/s10870-020-00860-3
NLM
Russo MG, Clavijo JCT, Álvarez N, Baldoni HA, Brusau EV, Ellena J, Narda GE. Synthesis, crystal structure and physicochemical characterization of two Ni(II)‑famotidine metal complexes [Internet]. Journal of Chemical Crystallography. 2021 ; 51( 3): 337-351.[citado 2024 out. 18 ] Available from: https://doi.org/10.1007/s10870-020-00860-3
Vancouver
Russo MG, Clavijo JCT, Álvarez N, Baldoni HA, Brusau EV, Ellena J, Narda GE. Synthesis, crystal structure and physicochemical characterization of two Ni(II)‑famotidine metal complexes [Internet]. Journal of Chemical Crystallography. 2021 ; 51( 3): 337-351.[citado 2024 out. 18 ] Available from: https://doi.org/10.1007/s10870-020-00860-3
Artigo de periodico
Rational design, supramolecular synthesis and solid state characterization of two bicomponent solid forms of mebendazole (2020)
Gutiérrez, Eduardo L. ; Godoy, Agustín A. ; Narda, Griselda E. ; Ellena, Javier
Source: CrystEngComm. Unidade: IFSC
Subjects: CRISTALOGRAFIA, PLANEJAMENTO DE FÁRMACOS, ESTRUTURA MOLECULAR (QUÍMICA TEÓRICA)
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ABNT
GUTIÉRREZ, Eduardo L. et al. Rational design, supramolecular synthesis and solid state characterization of two bicomponent solid forms of mebendazole. CrystEngComm, v. 22, n. 39, p. 6559-6568, 2020Tradução . . Disponível em: https://doi.org/10.1039/D0CE00924E. Acesso em: 18 out. 2024.
APA
Gutiérrez, E. L., Godoy, A. A., Narda, G. E., & Ellena, J. (2020). Rational design, supramolecular synthesis and solid state characterization of two bicomponent solid forms of mebendazole. CrystEngComm, 22( 39), 6559-6568. doi:10.1039/D0CE00924E
NLM
Gutiérrez EL, Godoy AA, Narda GE, Ellena J. Rational design, supramolecular synthesis and solid state characterization of two bicomponent solid forms of mebendazole [Internet]. CrystEngComm. 2020 ; 22( 39): 6559-6568.[citado 2024 out. 18 ] Available from: https://doi.org/10.1039/D0CE00924E
Vancouver
Gutiérrez EL, Godoy AA, Narda GE, Ellena J. Rational design, supramolecular synthesis and solid state characterization of two bicomponent solid forms of mebendazole [Internet]. CrystEngComm. 2020 ; 22( 39): 6559-6568.[citado 2024 out. 18 ] Available from: https://doi.org/10.1039/D0CE00924E
Artigo de periodico
Rational design of a famotidine-ibuprofen coamorphous system: an experimental and theoretical study (2018)
Russo, Marcos G.; Baldoni, Hector A.; Dávila, Yamina A.; Brusau, Elena V.; Ellena, Javier ; Narda, Griselda E.
Source: Journal of Physical Chemistry B. Unidade: IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, CRISTALOGRAFIA
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ABNT
RUSSO, Marcos G. et al. Rational design of a famotidine-ibuprofen coamorphous system: an experimental and theoretical study. Journal of Physical Chemistry B, v. 122, n. 37, p. 8772-8782, 2018Tradução . . Disponível em: https://doi.org/10.1021/acs.jpcb.8b06105. Acesso em: 18 out. 2024.
APA
Russo, M. G., Baldoni, H. A., Dávila, Y. A., Brusau, E. V., Ellena, J., & Narda, G. E. (2018). Rational design of a famotidine-ibuprofen coamorphous system: an experimental and theoretical study. Journal of Physical Chemistry B, 122( 37), 8772-8782. doi:10.1021/acs.jpcb.8b06105
NLM
Russo MG, Baldoni HA, Dávila YA, Brusau EV, Ellena J, Narda GE. Rational design of a famotidine-ibuprofen coamorphous system: an experimental and theoretical study [Internet]. Journal of Physical Chemistry B. 2018 ; 122( 37): 8772-8782.[citado 2024 out. 18 ] Available from: https://doi.org/10.1021/acs.jpcb.8b06105
Vancouver
Russo MG, Baldoni HA, Dávila YA, Brusau EV, Ellena J, Narda GE. Rational design of a famotidine-ibuprofen coamorphous system: an experimental and theoretical study [Internet]. Journal of Physical Chemistry B. 2018 ; 122( 37): 8772-8782.[citado 2024 out. 18 ] Available from: https://doi.org/10.1021/acs.jpcb.8b06105
Artigo de periodico
Solid-state supramolecular synthesis based on the N–H...O heterosynthon: an approach to solve the polymorphism problem in famotidine (2014)
Russo, Marcos G.; Brusau, Elena V.; Ellena, Javier ; Narda, Griselda E.
Source: Journal of Pharmaceutical Sciences. Unidade: IFSC
Subjects: CRISTALOGRAFIA, ESTADO SÓLIDO, ANÁLISE TÉRMICA, SOLUBILIDADE
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ABNT
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: 18 out. 2024.
APA
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 out. 18 ] 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 out. 18 ] Available from: https://doi.org/10.1002/jps.24196
Artigo de periodico
Mebendazole mesylate monohydrate: a new route to improve the solubility of mebendazole polymorphs (2013)
Paula, Karina de; Camí, Gerardo E.; Brusau, Elena V.; Narda, Griselda E.; Ellena, Javier
Source: Journal of Pharmaceutical Sciences. Unidade: IFSC
Subjects: ESPECTROSCOPIA RAMAN, POLIMORFISMO, CRISTALOGRAFIA
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ABNT
PAULA, Karina de et al. Mebendazole mesylate monohydrate: a new route to improve the solubility of mebendazole polymorphs. Journal of Pharmaceutical Sciences, v. 102, n. 10, p. 3528-3538, 2013Tradução . . Disponível em: https://doi.org/10.1002/jps.23658. Acesso em: 18 out. 2024.
APA
Paula, K. de, Camí, G. E., Brusau, E. V., Narda, G. E., & Ellena, J. (2013). Mebendazole mesylate monohydrate: a new route to improve the solubility of mebendazole polymorphs. Journal of Pharmaceutical Sciences, 102( 10), 3528-3538. doi:10.1002/jps.23658
NLM
Paula K de, Camí GE, Brusau EV, Narda GE, Ellena J. Mebendazole mesylate monohydrate: a new route to improve the solubility of mebendazole polymorphs [Internet]. Journal of Pharmaceutical Sciences. 2013 ; 102( 10): 3528-3538.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/jps.23658
Vancouver
Paula K de, Camí GE, Brusau EV, Narda GE, Ellena J. Mebendazole mesylate monohydrate: a new route to improve the solubility of mebendazole polymorphs [Internet]. Journal of Pharmaceutical Sciences. 2013 ; 102( 10): 3528-3538.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/jps.23658
Artigo de periodico
Intermolecular contacts influencing the conformational and geometric features of the pharmaceutically preferred mebendazole polymorph C (2009)
Martins, Felipe T.; Neves, Person P.; Ellena, Javier ; Camí, Gerardo E.; Brusau, Elena V.; Narda, Griselda E.
Source: Journal of Pharmaceutical Sciences. Unidade: IFSC
Subjects: CRISTALOGRAFIA, MOLÉCULA (ESTRUTURA;ESTUDO), POLIMORFISMO, DIFRAÇÃO POR RAIOS X
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ABNT
MARTINS, Felipe T. et al. Intermolecular contacts influencing the conformational and geometric features of the pharmaceutically preferred mebendazole polymorph C. Journal of Pharmaceutical Sciences, v. 98, n. 7, p. 2336-2344, 2009Tradução . . Disponível em: https://doi.org/10.1002/jps.21593. Acesso em: 18 out. 2024.
APA
Martins, F. T., Neves, P. P., Ellena, J., Camí, G. E., Brusau, E. V., & Narda, G. E. (2009). Intermolecular contacts influencing the conformational and geometric features of the pharmaceutically preferred mebendazole polymorph C. Journal of Pharmaceutical Sciences, 98( 7), 2336-2344. doi:10.1002/jps.21593
NLM
Martins FT, Neves PP, Ellena J, Camí GE, Brusau EV, Narda GE. Intermolecular contacts influencing the conformational and geometric features of the pharmaceutically preferred mebendazole polymorph C [Internet]. Journal of Pharmaceutical Sciences. 2009 ; 98( 7): 2336-2344.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/jps.21593
Vancouver
Martins FT, Neves PP, Ellena J, Camí GE, Brusau EV, Narda GE. Intermolecular contacts influencing the conformational and geometric features of the pharmaceutically preferred mebendazole polymorph C [Internet]. Journal of Pharmaceutical Sciences. 2009 ; 98( 7): 2336-2344.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/jps.21593

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