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  • Source: Molecules. Unidade: FCF

    Subjects: ANTISSÉPTICOS BUCAIS, HIGIENE BUCAL

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    • ABNT

      NOGUEIRA, Cecília et al. Xylityl sesquicaprylate efficacy as an antiseptic ingredient for oral care products (Mouthwash): an in vitro screening investigation against eight microorganisms. Molecules, v. 28, p. 1-5 art. 28, 2023Tradução . . Disponível em: https://doi.org/10.3390/molecules28010028. Acesso em: 16 nov. 2024.
    • APA

      Nogueira, C., Mussi, L., Baby, A. R., Zupeli, R., & Magalhães, W. V. (2023). Xylityl sesquicaprylate efficacy as an antiseptic ingredient for oral care products (Mouthwash): an in vitro screening investigation against eight microorganisms. Molecules, 28, 1-5 art. 28. doi:10.3390/molecules28010028
    • NLM

      Nogueira C, Mussi L, Baby AR, Zupeli R, Magalhães WV. Xylityl sesquicaprylate efficacy as an antiseptic ingredient for oral care products (Mouthwash): an in vitro screening investigation against eight microorganisms [Internet]. Molecules. 2023 ; 28 1-5 art. 28.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/molecules28010028
    • Vancouver

      Nogueira C, Mussi L, Baby AR, Zupeli R, Magalhães WV. Xylityl sesquicaprylate efficacy as an antiseptic ingredient for oral care products (Mouthwash): an in vitro screening investigation against eight microorganisms [Internet]. Molecules. 2023 ; 28 1-5 art. 28.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/molecules28010028
  • Source: Molecules. Unidade: FCF

    Subjects: AEDES, PIMENTA, INSETICIDAS, CONTROLE DE VETORES

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      MORAIS, Lais Silva et al. Edible plant extracts against Aedes aegypti and validation of a Piper nigrum L. Ethanolic extract as a natural insecticide. Molecules, v. 58, n. 3 p. 1-17 art. 1264, 2023Tradução . . Disponível em: https://doi.org/10.3390/molecules28031264. Acesso em: 16 nov. 2024.
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      Morais, L. S., Sousa, J. P. B., Aguiar, C. M., Gomes, C. M., Demarque, D. P., Albernaz, L. C., & Espindola, L. S. (2023). Edible plant extracts against Aedes aegypti and validation of a Piper nigrum L. Ethanolic extract as a natural insecticide. Molecules, 58( 3 p. 1-17 art. 1264). doi:10.3390/molecules28031264
    • NLM

      Morais LS, Sousa JPB, Aguiar CM, Gomes CM, Demarque DP, Albernaz LC, Espindola LS. Edible plant extracts against Aedes aegypti and validation of a Piper nigrum L. Ethanolic extract as a natural insecticide [Internet]. Molecules. 2023 ; 58( 3 p. 1-17 art. 1264):[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/molecules28031264
    • Vancouver

      Morais LS, Sousa JPB, Aguiar CM, Gomes CM, Demarque DP, Albernaz LC, Espindola LS. Edible plant extracts against Aedes aegypti and validation of a Piper nigrum L. Ethanolic extract as a natural insecticide [Internet]. Molecules. 2023 ; 58( 3 p. 1-17 art. 1264):[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/molecules28031264
  • Source: Molecules. Unidade: FCF

    Subjects: COLÁGENO, TILÁPIA, COSMÉTICOS, PELE DE ANIMAL

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      PINEDO, Nataly Reátegui et al. Characterization of collagen from three genetic lines (Gray, Red and F1) of Oreochromis niloticus (Tilapia) skin in young and old adults. Molecules, v. 27, p. 1-15 art. 1123, 2022Tradução . . Disponível em: https://doi.org/10.3390/molecules27031123. Acesso em: 16 nov. 2024.
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      Pinedo, N. R., Salirrosas, D., Tuesta, L. S., Quiñones, C., Rosas, S. R. J., Barraza, G., et al. (2022). Characterization of collagen from three genetic lines (Gray, Red and F1) of Oreochromis niloticus (Tilapia) skin in young and old adults. Molecules, 27, 1-15 art. 1123. doi:10.3390/molecules27031123
    • NLM

      Pinedo NR, Salirrosas D, Tuesta LS, Quiñones C, Rosas SRJ, Barraza G, Cabrera A, Jara CA, Martinez RM, Baby AR, Prieto ZA. Characterization of collagen from three genetic lines (Gray, Red and F1) of Oreochromis niloticus (Tilapia) skin in young and old adults [Internet]. Molecules. 2022 ; 27 1-15 art. 1123.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/molecules27031123
    • Vancouver

      Pinedo NR, Salirrosas D, Tuesta LS, Quiñones C, Rosas SRJ, Barraza G, Cabrera A, Jara CA, Martinez RM, Baby AR, Prieto ZA. Characterization of collagen from three genetic lines (Gray, Red and F1) of Oreochromis niloticus (Tilapia) skin in young and old adults [Internet]. Molecules. 2022 ; 27 1-15 art. 1123.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/molecules27031123
  • Source: Molecules. Unidade: FCF

    Subjects: ACNE VULGAR, PORFIRINAS, SEBO

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      MUSSI, Lilian et al. Propanediol (and) caprylic acid (and) xylitol as a new single topical active Ingredient against acne: in vitro and in vivo efficacy assays. Molecules, v. 26, p. 1-14 art. 6704, 2021Tradução . . Disponível em: https://doi.org/10.3390/molecules26216704. Acesso em: 16 nov. 2024.
    • APA

      Mussi, L., Baby, A. R., Camargo Júnior, F. B. de, Padovani, G., Sufi, B. da S., & Magalhães, W. V. (2021). Propanediol (and) caprylic acid (and) xylitol as a new single topical active Ingredient against acne: in vitro and in vivo efficacy assays. Molecules, 26, 1-14 art. 6704. doi:10.3390/molecules26216704
    • NLM

      Mussi L, Baby AR, Camargo Júnior FB de, Padovani G, Sufi B da S, Magalhães WV. Propanediol (and) caprylic acid (and) xylitol as a new single topical active Ingredient against acne: in vitro and in vivo efficacy assays [Internet]. Molecules. 2021 ; 26 1-14 art. 6704.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/molecules26216704
    • Vancouver

      Mussi L, Baby AR, Camargo Júnior FB de, Padovani G, Sufi B da S, Magalhães WV. Propanediol (and) caprylic acid (and) xylitol as a new single topical active Ingredient against acne: in vitro and in vivo efficacy assays [Internet]. Molecules. 2021 ; 26 1-14 art. 6704.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/molecules26216704
  • Source: Molecules. Unidade: FCF

    Subjects: PIMENTA, APOPTOSE, METABÓLITOS SECUNDÁRIOS

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    • ABNT

      CUNHA, Micael Rodrigues et al. Peppers: a “hot” natural source for antitumor compounds. Molecules, v. 26, n. 6, p. 1-21 art. 1521, 2021Tradução . . Disponível em: https://doi.org/10.3390/molecules26061521. Acesso em: 16 nov. 2024.
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      Cunha, M. R., Tavares, M. T., Fernandes, T. B., & Parise Filho, R. (2021). Peppers: a “hot” natural source for antitumor compounds. Molecules, 26( 6), 1-21 art. 1521. doi:10.3390/molecules26061521
    • NLM

      Cunha MR, Tavares MT, Fernandes TB, Parise Filho R. Peppers: a “hot” natural source for antitumor compounds [Internet]. Molecules. 2021 ; 26( 6): 1-21 art. 1521.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/molecules26061521
    • Vancouver

      Cunha MR, Tavares MT, Fernandes TB, Parise Filho R. Peppers: a “hot” natural source for antitumor compounds [Internet]. Molecules. 2021 ; 26( 6): 1-21 art. 1521.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/molecules26061521
  • Source: Molecules. Unidade: FCF

    Subjects: NANOTECNOLOGIA, GENES

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    • ABNT

      ARAUJO, Renan Vinicius de et al. New advances in general biomedical applications of PAMAM dendrimers. Molecules, v. 23, n. 11, p. 1-27 art. 2849, 2018Tradução . . Disponível em: https://doi.org/10.3390/molecules23112849. Acesso em: 16 nov. 2024.
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      Araujo, R. V. de, Santos, S. da S., Ferreira, E. I., & Giarolla, J. (2018). New advances in general biomedical applications of PAMAM dendrimers. Molecules, 23( 11), 1-27 art. 2849. doi:10.3390/molecules23112849
    • NLM

      Araujo RV de, Santos S da S, Ferreira EI, Giarolla J. New advances in general biomedical applications of PAMAM dendrimers [Internet]. Molecules. 2018 ; 23( 11): 1-27 art. 2849.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/molecules23112849
    • Vancouver

      Araujo RV de, Santos S da S, Ferreira EI, Giarolla J. New advances in general biomedical applications of PAMAM dendrimers [Internet]. Molecules. 2018 ; 23( 11): 1-27 art. 2849.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/molecules23112849
  • Source: Molecules. Unidade: FCF

    Subjects: ANGIOTENSINAS, CYANOPHYTA

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      PAIVA, Fernanda C. R et al. Identification, in vitro testing and molecular docking studies of microginins’ mechanism of angiotensin-converting enzyme inhibition. Molecules, v. 22, p. 1-10 art. 1884, 2017Tradução . . Disponível em: https://doi.org/10.3390/molecules22121884. Acesso em: 16 nov. 2024.
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      Paiva, F. C. R., Ferreira, G. M., Trossini, G. H. G., & Pinto, E. (2017). Identification, in vitro testing and molecular docking studies of microginins’ mechanism of angiotensin-converting enzyme inhibition. Molecules, 22, 1-10 art. 1884. doi:10.3390/molecules22121884
    • NLM

      Paiva FCR, Ferreira GM, Trossini GHG, Pinto E. Identification, in vitro testing and molecular docking studies of microginins’ mechanism of angiotensin-converting enzyme inhibition [Internet]. Molecules. 2017 ; 22 1-10 art. 1884.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/molecules22121884
    • Vancouver

      Paiva FCR, Ferreira GM, Trossini GHG, Pinto E. Identification, in vitro testing and molecular docking studies of microginins’ mechanism of angiotensin-converting enzyme inhibition [Internet]. Molecules. 2017 ; 22 1-10 art. 1884.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/molecules22121884
  • Source: Molecules. Unidade: FCF

    Subjects: NANOCOMPOSITOS, FÁRMACOS, BIOTRANSFORMAÇÃO

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      SANTOS, Soraya da Silva e FERREIRA, Elizabeth Igne e GIAROLLA, Jeanine. Dendrimer Prodrugs. Molecules, v. 21, n. 6 , p. 1-22 art. 686, 2016Tradução . . Disponível em: https://doi.org/10.3390/molecules21060686. Acesso em: 16 nov. 2024.
    • APA

      Santos, S. da S., Ferreira, E. I., & Giarolla, J. (2016). Dendrimer Prodrugs. Molecules, 21( 6 ), 1-22 art. 686. doi:10.3390/molecules21060686
    • NLM

      Santos S da S, Ferreira EI, Giarolla J. Dendrimer Prodrugs [Internet]. Molecules. 2016 ; 21( 6 ): 1-22 art. 686.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/molecules21060686
    • Vancouver

      Santos S da S, Ferreira EI, Giarolla J. Dendrimer Prodrugs [Internet]. Molecules. 2016 ; 21( 6 ): 1-22 art. 686.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/molecules21060686
  • Source: Molecules. Unidade: FCF

    Subjects: RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA, SESQUITERPENOS, ANTIPROTOZOÁRIOS

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      TROSSINI, Gustavo Henrique Goulart e MALTAROLLO, Vinícius Gonçalves e SCHMIDT, Thomas J. Hologram QSAR studies of antiprotozoal activities of sesquiterpene lactones. Molecules, v. 19, n. 7, p. 10546-10562, 2014Tradução . . Disponível em: https://doi.org/10.3390/molecules190710546. Acesso em: 16 nov. 2024.
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      Trossini, G. H. G., Maltarollo, V. G., & Schmidt, T. J. (2014). Hologram QSAR studies of antiprotozoal activities of sesquiterpene lactones. Molecules, 19( 7), 10546-10562. doi:10.3390/molecules190710546
    • NLM

      Trossini GHG, Maltarollo VG, Schmidt TJ. Hologram QSAR studies of antiprotozoal activities of sesquiterpene lactones [Internet]. Molecules. 2014 ; 19( 7): 10546-10562.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/molecules190710546
    • Vancouver

      Trossini GHG, Maltarollo VG, Schmidt TJ. Hologram QSAR studies of antiprotozoal activities of sesquiterpene lactones [Internet]. Molecules. 2014 ; 19( 7): 10546-10562.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/molecules190710546
  • Source: Molecules. Unidade: FCF

    Subjects: DIFRAÇÃO POR RAIOS X, SÍNTESE ORGÂNICA

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      SCHPECTOR, Julio Zukermann et al. Synthesis, molecular and crystal structure analysis of 1-(4-Methylbenzenesulfonyl)indole-3-carbaldehyde and DFT investigation of its rotational conformers. Molecules, v. 19, n. 2, p. 1990-2003, 2014Tradução . . Disponível em: https://doi.org/10.3390/molecules19021990. Acesso em: 16 nov. 2024.
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      Schpector, J. Z., Madureira, L. S., Wulf, G. D., Stefani, H. A., Vasconcelos, S. N. S., Ng, S. W., & Tiekink, E. R. T. (2014). Synthesis, molecular and crystal structure analysis of 1-(4-Methylbenzenesulfonyl)indole-3-carbaldehyde and DFT investigation of its rotational conformers. Molecules, 19( 2), 1990-2003. doi:10.3390/molecules19021990
    • NLM

      Schpector JZ, Madureira LS, Wulf GD, Stefani HA, Vasconcelos SNS, Ng SW, Tiekink ERT. Synthesis, molecular and crystal structure analysis of 1-(4-Methylbenzenesulfonyl)indole-3-carbaldehyde and DFT investigation of its rotational conformers [Internet]. Molecules. 2014 ; 19( 2): 1990-2003.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/molecules19021990
    • Vancouver

      Schpector JZ, Madureira LS, Wulf GD, Stefani HA, Vasconcelos SNS, Ng SW, Tiekink ERT. Synthesis, molecular and crystal structure analysis of 1-(4-Methylbenzenesulfonyl)indole-3-carbaldehyde and DFT investigation of its rotational conformers [Internet]. Molecules. 2014 ; 19( 2): 1990-2003.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/molecules19021990
  • Source: Molecules. Unidade: FCF

    Subjects: PRODUTOS NATURAIS, FLAVONÓIDES, COMPOSITAE

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      SILVA, Fabiana Lima et al. Compilation of secondary metabolites from Bidens pilosa L. Molecules, v. 16, n. 2, p. 1070-1102, 2011Tradução . . Disponível em: https://doi.org/10.3390/molecules1621070. Acesso em: 16 nov. 2024.
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      Silva, F. L., Fischer, D. C. H., Tavares, J. F., Silva, M. S., Athayde-Filho, P. F. de, & Barbosa-Filho, J. M. (2011). Compilation of secondary metabolites from Bidens pilosa L. Molecules, 16( 2), 1070-1102. doi:10.3390/molecules1621070
    • NLM

      Silva FL, Fischer DCH, Tavares JF, Silva MS, Athayde-Filho PF de, Barbosa-Filho JM. Compilation of secondary metabolites from Bidens pilosa L. [Internet]. Molecules. 2011 ; 16( 2): 1070-1102.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/molecules1621070
    • Vancouver

      Silva FL, Fischer DCH, Tavares JF, Silva MS, Athayde-Filho PF de, Barbosa-Filho JM. Compilation of secondary metabolites from Bidens pilosa L. [Internet]. Molecules. 2011 ; 16( 2): 1070-1102.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/molecules1621070

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