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  • Source: Molecules. Unidade: FCF

    Subjects: ANTISSÉPTICOS BUCAIS, HIGIENE BUCAL

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      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: 17 jul. 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 jul. 17 ] 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 jul. 17 ] 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: 17 jul. 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 jul. 17 ] 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 jul. 17 ] Available from: https://doi.org/10.3390/molecules28031264
  • Source: Molecules. Unidade: FCF

    Subjects: MELANINAS, PELE

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      BRATHWAITE, Ana Clara Nogueira et al. Pouteria macrophylla fruit Extract Microemulsion for cutaneous depigmentation: evaluation using a 3D pigmented skin model. Molecules, v. 27, p. 1-16 art. 5982, 2022Tradução . . Disponível em: https://doi.org/10.3390/molecules27185982. Acesso em: 17 jul. 2024.
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      Brathwaite, A. C. N., Silva, T. A., Carvalho, L. A. da C., Branquinho, M. S. F., Nunes, R. F., Cunha-Filho, M., et al. (2022). Pouteria macrophylla fruit Extract Microemulsion for cutaneous depigmentation: evaluation using a 3D pigmented skin model. Molecules, 27, 1-16 art. 5982. doi:10.3390/molecules27185982
    • NLM

      Brathwaite ACN, Silva TA, Carvalho LA da C, Branquinho MSF, Nunes RF, Cunha-Filho M, Gelfuso GM, Maria-Engler SS, Carvalho JL, Silva JKR da, Gratieri T. Pouteria macrophylla fruit Extract Microemulsion for cutaneous depigmentation: evaluation using a 3D pigmented skin model [Internet]. Molecules. 2022 ; 27 1-16 art. 5982.[citado 2024 jul. 17 ] Available from: https://doi.org/10.3390/molecules27185982
    • Vancouver

      Brathwaite ACN, Silva TA, Carvalho LA da C, Branquinho MSF, Nunes RF, Cunha-Filho M, Gelfuso GM, Maria-Engler SS, Carvalho JL, Silva JKR da, Gratieri T. Pouteria macrophylla fruit Extract Microemulsion for cutaneous depigmentation: evaluation using a 3D pigmented skin model [Internet]. Molecules. 2022 ; 27 1-16 art. 5982.[citado 2024 jul. 17 ] Available from: https://doi.org/10.3390/molecules27185982
  • 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: 17 jul. 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 jul. 17 ] 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 jul. 17 ] 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: 17 jul. 2024.
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      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 jul. 17 ] 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 jul. 17 ] Available from: https://doi.org/10.3390/molecules26216704
  • Source: Molecules. Unidade: FCF

    Subjects: PIMENTA, APOPTOSE, METABÓLITOS SECUNDÁRIOS

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      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: 17 jul. 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 jul. 17 ] 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 jul. 17 ] Available from: https://doi.org/10.3390/molecules26061521
  • Source: Molecules. Unidades: IQ, FCF

    Subjects: ANTIPARASITÁRIOS, PORFIRINAS

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      DEDA, Daiana K et al. Porphyrin derivative nanoformulations for therapy and antiparasitic agents. Molecules, v. 25, n. 9, p. 1-31 art. 2080, 2020Tradução . . Disponível em: https://doi.org/10.3390/molecules25092080. Acesso em: 17 jul. 2024.
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      Deda, D. K., Iglesias, B. A., Alves, E., Araki, K., & Garcia, C. R. da S. (2020). Porphyrin derivative nanoformulations for therapy and antiparasitic agents. Molecules, 25( 9), 1-31 art. 2080. doi:10.3390/molecules25092080
    • NLM

      Deda DK, Iglesias BA, Alves E, Araki K, Garcia CR da S. Porphyrin derivative nanoformulations for therapy and antiparasitic agents [Internet]. Molecules. 2020 ; 25( 9): 1-31 art. 2080.[citado 2024 jul. 17 ] Available from: https://doi.org/10.3390/molecules25092080
    • Vancouver

      Deda DK, Iglesias BA, Alves E, Araki K, Garcia CR da S. Porphyrin derivative nanoformulations for therapy and antiparasitic agents [Internet]. Molecules. 2020 ; 25( 9): 1-31 art. 2080.[citado 2024 jul. 17 ] Available from: https://doi.org/10.3390/molecules25092080
  • Source: Molecules. Unidades: FCF, CENA

    Subjects: ALCALOIDES, BIOMASSA

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      GONZÁLEZ-BLANCO, Carlos et al. Alternative isolation protocol for desulfo and zwitterionic cylindrospermopsin alkaloids and comparison of their toxicity in HepG2 cells. Molecules, v. 25, n. 13, p. 1-18 art. 3027, 2020Tradução . . Disponível em: https://doi.org/10.3390/molecules25133027. Acesso em: 17 jul. 2024.
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      González-Blanco, C., Dörr, F. A., Albuquerque, R. C., Onuki, J., & Pinto, E. (2020). Alternative isolation protocol for desulfo and zwitterionic cylindrospermopsin alkaloids and comparison of their toxicity in HepG2 cells. Molecules, 25( 13), 1-18 art. 3027. doi:10.3390/molecules25133027
    • NLM

      González-Blanco C, Dörr FA, Albuquerque RC, Onuki J, Pinto E. Alternative isolation protocol for desulfo and zwitterionic cylindrospermopsin alkaloids and comparison of their toxicity in HepG2 cells [Internet]. Molecules. 2020 ; 25( 13): 1-18 art. 3027.[citado 2024 jul. 17 ] Available from: https://doi.org/10.3390/molecules25133027
    • Vancouver

      González-Blanco C, Dörr FA, Albuquerque RC, Onuki J, Pinto E. Alternative isolation protocol for desulfo and zwitterionic cylindrospermopsin alkaloids and comparison of their toxicity in HepG2 cells [Internet]. Molecules. 2020 ; 25( 13): 1-18 art. 3027.[citado 2024 jul. 17 ] Available from: https://doi.org/10.3390/molecules25133027
  • Source: Molecules. Unidades: FCF, FMRP

    Subjects: ALCALOIDES, PLANTAS ALUCINÓGENAS

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      SILVEIRA, Gabriela de Oliveira et al. Stability evaluation of DMT and harmala alkaloids in ayahuasca tea samples. Molecules, v. 25, n. 9, p. 1-11 art. 2.072, 2020Tradução . . Disponível em: https://doi.org/10.3390/molecules25092072. Acesso em: 17 jul. 2024.
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      Silveira, G. de O., Santos, R. G. dos, Lourenço, F. R., Rossi, G. N., Hallak, J. E. C., & Yonamine, M. (2020). Stability evaluation of DMT and harmala alkaloids in ayahuasca tea samples. Molecules, 25( 9), 1-11 art. 2.072. doi:10.3390/molecules25092072
    • NLM

      Silveira G de O, Santos RG dos, Lourenço FR, Rossi GN, Hallak JEC, Yonamine M. Stability evaluation of DMT and harmala alkaloids in ayahuasca tea samples [Internet]. Molecules. 2020 ; 25( 9): 1-11 art. 2.072.[citado 2024 jul. 17 ] Available from: https://doi.org/10.3390/molecules25092072
    • Vancouver

      Silveira G de O, Santos RG dos, Lourenço FR, Rossi GN, Hallak JEC, Yonamine M. Stability evaluation of DMT and harmala alkaloids in ayahuasca tea samples [Internet]. Molecules. 2020 ; 25( 9): 1-11 art. 2.072.[citado 2024 jul. 17 ] Available from: https://doi.org/10.3390/molecules25092072
  • Source: Molecules. Unidades: FCF, FM, FCFRP

    Subjects: ANGIOTENSINA II, RECEPTORES DE ANGIOTENSINA, DOENÇAS CARDIOVASCULARES, INFLAMAÇÃO, NEOPLASIAS

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      ORTEGA PIJEIRA, Martha Sahylí et al. Synthesis and evaluation of [18F]FEtLos and [18F]AMBF3Los as novel 18F-Labelled Losartan derivatives for molecular imaging of Angiotensin II type 1 receptors. Molecules, v. 25, n. 8, p. 1-21, 2020Tradução . . Disponível em: https://doi.org/10.3390/molecules25081872. Acesso em: 17 jul. 2024.
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      Ortega Pijeira, M. S., Nunes, P. S. G., Santos, S. N. dos, Zhang, Z., Pérez Nario, A., Perini, E. A., et al. (2020). Synthesis and evaluation of [18F]FEtLos and [18F]AMBF3Los as novel 18F-Labelled Losartan derivatives for molecular imaging of Angiotensin II type 1 receptors. Molecules, 25( 8), 1-21. doi:10.3390/molecules25081872
    • NLM

      Ortega Pijeira MS, Nunes PSG, Santos SN dos, Zhang Z, Pérez Nario A, Perini EA, Turato WM, Rodríguez Riera Z, Chammas R, Elsinga PH, Lin K-S, Carvalho I, Bernardes ES. Synthesis and evaluation of [18F]FEtLos and [18F]AMBF3Los as novel 18F-Labelled Losartan derivatives for molecular imaging of Angiotensin II type 1 receptors [Internet]. Molecules. 2020 ; 25( 8): 1-21.[citado 2024 jul. 17 ] Available from: https://doi.org/10.3390/molecules25081872
    • Vancouver

      Ortega Pijeira MS, Nunes PSG, Santos SN dos, Zhang Z, Pérez Nario A, Perini EA, Turato WM, Rodríguez Riera Z, Chammas R, Elsinga PH, Lin K-S, Carvalho I, Bernardes ES. Synthesis and evaluation of [18F]FEtLos and [18F]AMBF3Los as novel 18F-Labelled Losartan derivatives for molecular imaging of Angiotensin II type 1 receptors [Internet]. Molecules. 2020 ; 25( 8): 1-21.[citado 2024 jul. 17 ] Available from: https://doi.org/10.3390/molecules25081872
  • Source: Molecules. Unidades: ESALQ, FCF

    Subjects: COMPOSTOS VOLÁTEIS, CROMATOGRAFIA A GÁS, ESPECTROMETRIA DE MASSAS, PÓS-COLHEITA, JABUTICABA, VARIEDADES VEGETAIS

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      FREITAS, Thais Padua de et al. Volatile compounds and physicochemical quality of four jabuticabas (Plinia sp.). Molecules, v. 25, p. 1-17, 2020Tradução . . Disponível em: https://doi.org/10.3390/molecules25194543. Acesso em: 17 jul. 2024.
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      Freitas, T. P. de, Taver, I. B., Spricigo, P. C., Amaral, L. B. do, Purgatto, E., & Jacomino, A. P. (2020). Volatile compounds and physicochemical quality of four jabuticabas (Plinia sp.). Molecules, 25, 1-17. doi:10.3390/molecules25194543
    • NLM

      Freitas TP de, Taver IB, Spricigo PC, Amaral LB do, Purgatto E, Jacomino AP. Volatile compounds and physicochemical quality of four jabuticabas (Plinia sp.) [Internet]. Molecules. 2020 ; 25 1-17.[citado 2024 jul. 17 ] Available from: https://doi.org/10.3390/molecules25194543
    • Vancouver

      Freitas TP de, Taver IB, Spricigo PC, Amaral LB do, Purgatto E, Jacomino AP. Volatile compounds and physicochemical quality of four jabuticabas (Plinia sp.) [Internet]. Molecules. 2020 ; 25 1-17.[citado 2024 jul. 17 ] Available from: https://doi.org/10.3390/molecules25194543
  • Source: Molecules. Unidades: IQ, FCF

    Subjects: MODELAGEM MOLECULAR, BACTÉRIAS

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      FERREIRA, Glaucio Monteiro et al. Inhibition of Porcine Aminopeptidase M (pAMP) by the Pentapeptide Microginins. Molecules, v. 24, p. 1-14 art. 4369, 2019Tradução . . Disponível em: https://doi.org/10.3390/molecules24234369. Acesso em: 17 jul. 2024.
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      Ferreira, G. M., Kronenberger, T., Almeida, É. C. de, Sampaio, J., Ferreira, C., Pinto, E., & Trossini, G. H. G. (2019). Inhibition of Porcine Aminopeptidase M (pAMP) by the Pentapeptide Microginins. Molecules, 24, 1-14 art. 4369. doi:10.3390/molecules24234369
    • NLM

      Ferreira GM, Kronenberger T, Almeida ÉC de, Sampaio J, Ferreira C, Pinto E, Trossini GHG. Inhibition of Porcine Aminopeptidase M (pAMP) by the Pentapeptide Microginins [Internet]. Molecules. 2019 ; 24 1-14 art. 4369.[citado 2024 jul. 17 ] Available from: https://doi.org/10.3390/molecules24234369
    • Vancouver

      Ferreira GM, Kronenberger T, Almeida ÉC de, Sampaio J, Ferreira C, Pinto E, Trossini GHG. Inhibition of Porcine Aminopeptidase M (pAMP) by the Pentapeptide Microginins [Internet]. Molecules. 2019 ; 24 1-14 art. 4369.[citado 2024 jul. 17 ] Available from: https://doi.org/10.3390/molecules24234369
  • Source: Molecules. Unidade: FCF

    Subjects: NANOTECNOLOGIA, GENES

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      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: 17 jul. 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 jul. 17 ] 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 jul. 17 ] 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: 17 jul. 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 jul. 17 ] 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 jul. 17 ] 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: 17 jul. 2024.
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      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 jul. 17 ] 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 jul. 17 ] 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: 17 jul. 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 jul. 17 ] 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 jul. 17 ] 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: 17 jul. 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 jul. 17 ] 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 jul. 17 ] 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: 17 jul. 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
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      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 jul. 17 ] Available from: https://doi.org/10.3390/molecules1621070
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      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 jul. 17 ] Available from: https://doi.org/10.3390/molecules1621070
  • Source: Molecules. Unidade: FCF

    Subjects: RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA, FÁRMACOS

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      ANDRADE, Carolina Horta et al. 4D-QSAR: Perspectives in drug design. Molecules, v. 15, n. 5, p. 3281-3294, 2010Tradução . . Disponível em: https://doi.org/10.3390/molecules15053281. Acesso em: 17 jul. 2024.
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      Andrade, C. H., Pasqualoto, K. F. M., Ferreira, E. I., & Hopfinger, A. J. (2010). 4D-QSAR: Perspectives in drug design. Molecules, 15( 5), 3281-3294. doi:10.3390/molecules15053281
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      Andrade CH, Pasqualoto KFM, Ferreira EI, Hopfinger AJ. 4D-QSAR: Perspectives in drug design [Internet]. Molecules. 2010 ; 15( 5): 3281-3294.[citado 2024 jul. 17 ] Available from: https://doi.org/10.3390/molecules15053281
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      Andrade CH, Pasqualoto KFM, Ferreira EI, Hopfinger AJ. 4D-QSAR: Perspectives in drug design [Internet]. Molecules. 2010 ; 15( 5): 3281-3294.[citado 2024 jul. 17 ] Available from: https://doi.org/10.3390/molecules15053281
  • Source: Molecules. Unidade: FCF

    Subjects: ANTIPROTOZOÁRIOS, PRODUTOS NATURAIS, TRYPANOSOMA CRUZI

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      SCOTTI, Luciana et al. Chemometric studies on natural products as potential inhibitors of the NADH oxidase from Trypanosoma cruzi using VolSurf approach. Molecules, v. 15, n. 10, p. 7363-7377, 2010Tradução . . Disponível em: https://doi.org/10.3390/molecules15107363. Acesso em: 17 jul. 2024.
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      Scotti, L., Ferreira, E. I., Silva, M. S. da, & Scotti, M. T. (2010). Chemometric studies on natural products as potential inhibitors of the NADH oxidase from Trypanosoma cruzi using VolSurf approach. Molecules, 15( 10), 7363-7377. doi:10.3390/molecules15107363
    • NLM

      Scotti L, Ferreira EI, Silva MS da, Scotti MT. Chemometric studies on natural products as potential inhibitors of the NADH oxidase from Trypanosoma cruzi using VolSurf approach [Internet]. Molecules. 2010 ; 15( 10): 7363-7377.[citado 2024 jul. 17 ] Available from: https://doi.org/10.3390/molecules15107363
    • Vancouver

      Scotti L, Ferreira EI, Silva MS da, Scotti MT. Chemometric studies on natural products as potential inhibitors of the NADH oxidase from Trypanosoma cruzi using VolSurf approach [Internet]. Molecules. 2010 ; 15( 10): 7363-7377.[citado 2024 jul. 17 ] Available from: https://doi.org/10.3390/molecules15107363

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