Filtros : "Não indexado na Web of Science" "Ellena, Javier" Removidos: " IFSC007" "FILOSOFIA E CIENCIA DA EDUCACAO" Limpar

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  • Source: International Research Journal of Pure and Applied Chemistry. Unidade: IFSC

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

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      SOW, Salif et al. Syntheses and X-ray structure of N-(benzothiazol-2-yl)-3-chlorobenzamide. International Research Journal of Pure and Applied Chemistry, v. 25, n. 4, p. 116999-1-116999-9 + supplementary materials, 2024Tradução . . Disponível em: https://doi.org/10.9734/irjpac/2024/v25i4861. Acesso em: 24 jun. 2024.
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      Sow, S., Odame, F., Diouf, N., Thiam, E. I., Diouf, O., Ellena, J., et al. (2024). Syntheses and X-ray structure of N-(benzothiazol-2-yl)-3-chlorobenzamide. International Research Journal of Pure and Applied Chemistry, 25( 4), 116999-1-116999-9 + supplementary materials. doi:10.9734/irjpac/2024/v25i4861
    • NLM

      Sow S, Odame F, Diouf N, Thiam EI, Diouf O, Ellena J, Tshentu ZR, Gaye M. Syntheses and X-ray structure of N-(benzothiazol-2-yl)-3-chlorobenzamide [Internet]. International Research Journal of Pure and Applied Chemistry. 2024 ; 25( 4): 116999-1-116999-9 + supplementary materials.[citado 2024 jun. 24 ] Available from: https://doi.org/10.9734/irjpac/2024/v25i4861
    • Vancouver

      Sow S, Odame F, Diouf N, Thiam EI, Diouf O, Ellena J, Tshentu ZR, Gaye M. Syntheses and X-ray structure of N-(benzothiazol-2-yl)-3-chlorobenzamide [Internet]. International Research Journal of Pure and Applied Chemistry. 2024 ; 25( 4): 116999-1-116999-9 + supplementary materials.[citado 2024 jun. 24 ] Available from: https://doi.org/10.9734/irjpac/2024/v25i4861
  • Unidade: IFSC

    Subjects: CIÊNCIA, CONHECIMENTO

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      Revista Latinoamericana de Difusión Científica. . Maracaibo: Fundación Difusión Científica. . Acesso em: 24 jun. 2024. , 2024
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      Revista Latinoamericana de Difusión Científica. (2024). Revista Latinoamericana de Difusión Científica. Maracaibo: Fundación Difusión Científica.
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      Revista Latinoamericana de Difusión Científica. 2024 ;[citado 2024 jun. 24 ]
    • Vancouver

      Revista Latinoamericana de Difusión Científica. 2024 ;[citado 2024 jun. 24 ]
  • Unidade: IFSC

    Subjects: CIÊNCIA, CONHECIMENTO

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      Revista Latinoamericana de Difusión Científica. . Maracaibo: Fundación Difusión Científica. . Acesso em: 24 jun. 2024. , 2023
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      Revista Latinoamericana de Difusión Científica. (2023). Revista Latinoamericana de Difusión Científica. Maracaibo: Fundación Difusión Científica.
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      Revista Latinoamericana de Difusión Científica. 2023 ;[citado 2024 jun. 24 ]
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      Revista Latinoamericana de Difusión Científica. 2023 ;[citado 2024 jun. 24 ]
  • Unidade: IFSC

    Subjects: CIÊNCIA, CONHECIMENTO

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      Revista Latinoamericana de Difusión Científica. . Maracaibo: Fundación Difusión Científica y Academia de Historia del Estado Zulia. . Acesso em: 24 jun. 2024. , 2022
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      Revista Latinoamericana de Difusión Científica. (2022). Revista Latinoamericana de Difusión Científica. Maracaibo: Fundación Difusión Científica y Academia de Historia del Estado Zulia.
    • NLM

      Revista Latinoamericana de Difusión Científica. 2022 ;[citado 2024 jun. 24 ]
    • Vancouver

      Revista Latinoamericana de Difusión Científica. 2022 ;[citado 2024 jun. 24 ]
  • Source: Biophysical Reviews. Conference titles: International Union for Pure and Applied Biophysics - IUPAB - Congress. Unidades: IFSC, FFCLRP

    Subjects: ANTINEOPLÁSICOS, COMPOSTOS DE COORDENAÇÃO, PLANEJAMENTO DE FÁRMACOS, CITOTOXINAS

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      FACHHIN, Gianella et al. Development of new copper coordination compounds as possible drugs to fight cancer. Biophysical Reviews. Heidelberg: Instituto de Física de São Carlos, Universidade de São Paulo. Disponível em: https://repositorio.usp.br/directbitstream/f3f8901e-f9cf-498c-a884-d575515a1bcc/3058463.pdf. Acesso em: 24 jun. 2024. , 2021
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      Fachhin, G., Yañez, C., Garcia, E., Rosa, B., Leite, C., Napoleone, A., et al. (2021). Development of new copper coordination compounds as possible drugs to fight cancer. Biophysical Reviews. Heidelberg: Instituto de Física de São Carlos, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/f3f8901e-f9cf-498c-a884-d575515a1bcc/3058463.pdf
    • NLM

      Fachhin G, Yañez C, Garcia E, Rosa B, Leite C, Napoleone A, Alvarez N, Freddi P, Mendes LFS, Ellena J, Costa Filho AJ da, Batista AA. Development of new copper coordination compounds as possible drugs to fight cancer [Internet]. Biophysical Reviews. 2021 ; 13( 6): 1337.[citado 2024 jun. 24 ] Available from: https://repositorio.usp.br/directbitstream/f3f8901e-f9cf-498c-a884-d575515a1bcc/3058463.pdf
    • Vancouver

      Fachhin G, Yañez C, Garcia E, Rosa B, Leite C, Napoleone A, Alvarez N, Freddi P, Mendes LFS, Ellena J, Costa Filho AJ da, Batista AA. Development of new copper coordination compounds as possible drugs to fight cancer [Internet]. Biophysical Reviews. 2021 ; 13( 6): 1337.[citado 2024 jun. 24 ] Available from: https://repositorio.usp.br/directbitstream/f3f8901e-f9cf-498c-a884-d575515a1bcc/3058463.pdf
  • Source: Journal of Experimental Techniques and Instrumentation. Unidade: IFSC

    Subjects: PLANEJAMENTO DE FÁRMACOS, CRISTALOGRAFIA

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      ELLENA, Javier. Crystal engineering in the design of new solid pharmaceutical forms with enhanced pharmaceutical properties. Journal of Experimental Techniques and Instrumentation, v. 4, n. 3, p. 72-80, 2021Tradução . . Disponível em: https://doi.org/10.30609/jeti.v4i3.12950. Acesso em: 24 jun. 2024.
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      Ellena, J. (2021). Crystal engineering in the design of new solid pharmaceutical forms with enhanced pharmaceutical properties. Journal of Experimental Techniques and Instrumentation, 4( 3), 72-80. doi:10.30609/jeti.v4i3.12950
    • NLM

      Ellena J. Crystal engineering in the design of new solid pharmaceutical forms with enhanced pharmaceutical properties [Internet]. Journal of Experimental Techniques and Instrumentation. 2021 ; 4( 3): 72-80.[citado 2024 jun. 24 ] Available from: https://doi.org/10.30609/jeti.v4i3.12950
    • Vancouver

      Ellena J. Crystal engineering in the design of new solid pharmaceutical forms with enhanced pharmaceutical properties [Internet]. Journal of Experimental Techniques and Instrumentation. 2021 ; 4( 3): 72-80.[citado 2024 jun. 24 ] Available from: https://doi.org/10.30609/jeti.v4i3.12950
  • Source: IOSR Journal of Applied Chemistry. Unidade: IFSC

    Subjects: FERRO, ZINCO, CRISTALOGRAFIA ESTRUTURAL

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      HABA, Pokpa et al. Synthesis, structural study and X-ray structure determination of transition metal complexes of 4-phenyl-1-(1-(pyridin-2-yl) ethylidene)thiosemicarbazide. IOSR Journal of Applied Chemistry, v. 12, n. 8, p. 01-11, 2019Tradução . . Disponível em: https://doi.org/10.9790/5736-1208010111. Acesso em: 24 jun. 2024.
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      Haba, P., Tamboura, F. B., Sy, A., Sarr, M., Diallo Ba, M., Thiam, I. E., et al. (2019). Synthesis, structural study and X-ray structure determination of transition metal complexes of 4-phenyl-1-(1-(pyridin-2-yl) ethylidene)thiosemicarbazide. IOSR Journal of Applied Chemistry, 12( 8), 01-11. doi:10.9790/5736-1208010111
    • NLM

      Haba P, Tamboura FB, Sy A, Sarr M, Diallo Ba M, Thiam IE, Gaye M, Retailleau P, Ellena J. Synthesis, structural study and X-ray structure determination of transition metal complexes of 4-phenyl-1-(1-(pyridin-2-yl) ethylidene)thiosemicarbazide [Internet]. IOSR Journal of Applied Chemistry. 2019 ; 12( 8): 01-11.[citado 2024 jun. 24 ] Available from: https://doi.org/10.9790/5736-1208010111
    • Vancouver

      Haba P, Tamboura FB, Sy A, Sarr M, Diallo Ba M, Thiam IE, Gaye M, Retailleau P, Ellena J. Synthesis, structural study and X-ray structure determination of transition metal complexes of 4-phenyl-1-(1-(pyridin-2-yl) ethylidene)thiosemicarbazide [Internet]. IOSR Journal of Applied Chemistry. 2019 ; 12( 8): 01-11.[citado 2024 jun. 24 ] Available from: https://doi.org/10.9790/5736-1208010111
  • Source: Cancer Reports and Reviews. Unidades: IFSC, FFCLRP

    Subjects: PLANEJAMENTO DE FÁRMACOS, NEOPLASIAS, CITOTOXINAS

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      ALVAREZ, Natalia et al. Copper-diimine coordination compounds as potential new tools in the treatment of cancer. Cancer Reports and Reviews, v. 2, n. 4, p. 1-5, 2018Tradução . . Disponível em: https://doi.org/10.15761/CRR.1000160. Acesso em: 24 jun. 2024.
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      Alvarez, N., Kramer, M. G., Ellena, J., Costa Filho, A. J. da, Torre, M. H., & Facchin, G. (2018). Copper-diimine coordination compounds as potential new tools in the treatment of cancer. Cancer Reports and Reviews, 2( 4), 1-5. doi:10.15761/CRR.1000160
    • NLM

      Alvarez N, Kramer MG, Ellena J, Costa Filho AJ da, Torre MH, Facchin G. Copper-diimine coordination compounds as potential new tools in the treatment of cancer [Internet]. Cancer Reports and Reviews. 2018 ; 2( 4): 1-5.[citado 2024 jun. 24 ] Available from: https://doi.org/10.15761/CRR.1000160
    • Vancouver

      Alvarez N, Kramer MG, Ellena J, Costa Filho AJ da, Torre MH, Facchin G. Copper-diimine coordination compounds as potential new tools in the treatment of cancer [Internet]. Cancer Reports and Reviews. 2018 ; 2( 4): 1-5.[citado 2024 jun. 24 ] Available from: https://doi.org/10.15761/CRR.1000160
  • Source: Advancements in Bioequivalence and Bioavailability. Unidade: IFSC

    Subjects: CRISTALOGRAFIA, PLANEJAMENTO DE FÁRMACOS, BIODISPONIBILIDADE

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      DINIZ, Luan F. e SOUZA, Matheus S. e ELLENA, Javier. Crystal engineering applied to the development of novel pharmaceutical solid forms with improved bioavailability: the co crystals case. Advancements in Bioequivalence and Bioavailability, v. 1, n. 3, p. 1-3, 2018Tradução . . Disponível em: https://doi.org/10.31031/ABB.2018.01.000514. Acesso em: 24 jun. 2024.
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      Diniz, L. F., Souza, M. S., & Ellena, J. (2018). Crystal engineering applied to the development of novel pharmaceutical solid forms with improved bioavailability: the co crystals case. Advancements in Bioequivalence and Bioavailability, 1( 3), 1-3. doi:10.31031/ABB.2018.01.000514
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      Diniz LF, Souza MS, Ellena J. Crystal engineering applied to the development of novel pharmaceutical solid forms with improved bioavailability: the co crystals case [Internet]. Advancements in Bioequivalence and Bioavailability. 2018 ; 1( 3): 1-3.[citado 2024 jun. 24 ] Available from: https://doi.org/10.31031/ABB.2018.01.000514
    • Vancouver

      Diniz LF, Souza MS, Ellena J. Crystal engineering applied to the development of novel pharmaceutical solid forms with improved bioavailability: the co crystals case [Internet]. Advancements in Bioequivalence and Bioavailability. 2018 ; 1( 3): 1-3.[citado 2024 jun. 24 ] Available from: https://doi.org/10.31031/ABB.2018.01.000514
  • Source: European Journal of Chemistry. Unidade: IFSC

    Subjects: CRISTALOGRAFIA, PLANEJAMENTO DE FÁRMACOS, SAIS

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      SARR, Mamour et al. Co-crystal structure of a dinuclear (Zn-Y) and a trinuclear (Zn-Y-Zn) complexes derived from a Schiff base ligand. European Journal of Chemistry, v. 9, n. 2, p. 67-73, 2018Tradução . . Disponível em: https://doi.org/10.5155/eurjchem.9.2.67-73.1688. Acesso em: 24 jun. 2024.
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      Sarr, M., Diop, M., Thiam, I. E., Gaye, M., Barry, A. H., Alvarez, N., & Ellena, J. (2018). Co-crystal structure of a dinuclear (Zn-Y) and a trinuclear (Zn-Y-Zn) complexes derived from a Schiff base ligand. European Journal of Chemistry, 9( 2), 67-73. doi:10.5155/eurjchem.9.2.67-73.1688
    • NLM

      Sarr M, Diop M, Thiam IE, Gaye M, Barry AH, Alvarez N, Ellena J. Co-crystal structure of a dinuclear (Zn-Y) and a trinuclear (Zn-Y-Zn) complexes derived from a Schiff base ligand [Internet]. European Journal of Chemistry. 2018 ; 9( 2): 67-73.[citado 2024 jun. 24 ] Available from: https://doi.org/10.5155/eurjchem.9.2.67-73.1688
    • Vancouver

      Sarr M, Diop M, Thiam IE, Gaye M, Barry AH, Alvarez N, Ellena J. Co-crystal structure of a dinuclear (Zn-Y) and a trinuclear (Zn-Y-Zn) complexes derived from a Schiff base ligand [Internet]. European Journal of Chemistry. 2018 ; 9( 2): 67-73.[citado 2024 jun. 24 ] Available from: https://doi.org/10.5155/eurjchem.9.2.67-73.1688
  • Source: Blucher Material Science Proceedings. Conference titles: Reunião da Associação Brasileira de Cristalografia - ABCr. Unidades: FFCLRP, IFSC

    Subjects: QUÍMICA MÉDICA, NEOPLASIAS

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      ALVAREZ, N. et al. Structural characterization of [Cu(iminodiacetate)(diimine)] coordination complexes with in vitro antiproliferative activity. Blucher Material Science Proceedings. São Paulo: Edgard Blucher. Disponível em: https://doi.org/10.5151/23abcr-16. Acesso em: 24 jun. 2024. , 2017
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      Alvarez, N., Costa Filho, A. J. da, Torre, M. H., Kramer, M. G., Ellena, J., & Facchin, G. (2017). Structural characterization of [Cu(iminodiacetate)(diimine)] coordination complexes with in vitro antiproliferative activity. Blucher Material Science Proceedings. São Paulo: Edgard Blucher. doi:10.5151/23abcr-16
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      Alvarez N, Costa Filho AJ da, Torre MH, Kramer MG, Ellena J, Facchin G. Structural characterization of [Cu(iminodiacetate)(diimine)] coordination complexes with in vitro antiproliferative activity [Internet]. Blucher Material Science Proceedings. 2017 ; 2( 2): 29.[citado 2024 jun. 24 ] Available from: https://doi.org/10.5151/23abcr-16
    • Vancouver

      Alvarez N, Costa Filho AJ da, Torre MH, Kramer MG, Ellena J, Facchin G. Structural characterization of [Cu(iminodiacetate)(diimine)] coordination complexes with in vitro antiproliferative activity [Internet]. Blucher Material Science Proceedings. 2017 ; 2( 2): 29.[citado 2024 jun. 24 ] Available from: https://doi.org/10.5151/23abcr-16
  • Source: IUCrData. Unidade: IFSC

    Subjects: CRISTALOGRAFIA, MOLÉCULA, CRISTALOGRAFIA ESTRUTURAL

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      MORENO-FUQUEN, Rodolfo et al. 3-tert-Butyl-4-(4-chlorophenyl)-1-phenyl-1Hpyrazolo[ 3,4-e][1,4]thiazepin-7(4H,6H,8H)-one. IUCrData, v. 1, n. 4, p. x160608-1-x160608-2+full crystallographic data: data-1-data-6, 2016Tradução . . Disponível em: https://doi.org/10.1107/S2414314616006088. Acesso em: 24 jun. 2024.
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      Moreno-Fuquen, R., Castillo, J. C., Abonia, R., Clavijo, J. C. T., & Ellena, J. (2016). 3-tert-Butyl-4-(4-chlorophenyl)-1-phenyl-1Hpyrazolo[ 3,4-e][1,4]thiazepin-7(4H,6H,8H)-one. IUCrData, 1( 4), x160608-1-x160608-2+full crystallographic data: data-1-data-6. doi:10.1107/S2414314616006088
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      Moreno-Fuquen R, Castillo JC, Abonia R, Clavijo JCT, Ellena J. 3-tert-Butyl-4-(4-chlorophenyl)-1-phenyl-1Hpyrazolo[ 3,4-e][1,4]thiazepin-7(4H,6H,8H)-one [Internet]. IUCrData. 2016 ; 1( 4): x160608-1-x160608-2+full crystallographic data: data-1-data-6.[citado 2024 jun. 24 ] Available from: https://doi.org/10.1107/S2414314616006088
    • Vancouver

      Moreno-Fuquen R, Castillo JC, Abonia R, Clavijo JCT, Ellena J. 3-tert-Butyl-4-(4-chlorophenyl)-1-phenyl-1Hpyrazolo[ 3,4-e][1,4]thiazepin-7(4H,6H,8H)-one [Internet]. IUCrData. 2016 ; 1( 4): x160608-1-x160608-2+full crystallographic data: data-1-data-6.[citado 2024 jun. 24 ] Available from: https://doi.org/10.1107/S2414314616006088

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