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  • Source: Mini-Reviews in Medicinal Chemistry. Unidade: FCF

    Subjects: HOMEOSTASE, TUBERCULOSE, ÁCIDO FÓLICO

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      VASSILIADES, Sandra Valeria et al. Folate pathway inhibitors, an underestimated and underexplored molecular target for new anti-tuberculosis agents. Mini-Reviews in Medicinal Chemistry, v. 23, n. 17, p. 1711-1732, 2023Tradução . . Disponível em: https://doi.org/10.2174/1389557523666230206163154. Acesso em: 25 jun. 2024.
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      Vassiliades, S. V., Borges, L. G., Giarolla, J., & Parise Filho, R. (2023). Folate pathway inhibitors, an underestimated and underexplored molecular target for new anti-tuberculosis agents. Mini-Reviews in Medicinal Chemistry, 23( 17), 1711-1732. doi:10.2174/1389557523666230206163154
    • NLM

      Vassiliades SV, Borges LG, Giarolla J, Parise Filho R. Folate pathway inhibitors, an underestimated and underexplored molecular target for new anti-tuberculosis agents [Internet]. Mini-Reviews in Medicinal Chemistry. 2023 ; 23( 17): 1711-1732.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1389557523666230206163154
    • Vancouver

      Vassiliades SV, Borges LG, Giarolla J, Parise Filho R. Folate pathway inhibitors, an underestimated and underexplored molecular target for new anti-tuberculosis agents [Internet]. Mini-Reviews in Medicinal Chemistry. 2023 ; 23( 17): 1711-1732.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1389557523666230206163154
  • Source: Current Topics in Medicinal Chemistry. Unidade: FCF

    Subjects: MEDICAMENTO, METABOLISMO

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      CUPPOLONI, Andréa et al. 2,3-Diarylindoles as COX-2 Inhibitors: exploring the structure-activity relationship through molecular docking simulations. Current Topics in Medicinal Chemistry, v. 23, n. 12, p. 1081-1089, 2023Tradução . . Disponível em: https://doi.org/10.2174/1568026623666230207120752. Acesso em: 25 jun. 2024.
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      Cuppoloni, A., Silva, J. V. da, Snape, T. J., Lal, S., & Giarolla, J. (2023). 2,3-Diarylindoles as COX-2 Inhibitors: exploring the structure-activity relationship through molecular docking simulations. Current Topics in Medicinal Chemistry, 23( 12), 1081-1089. doi:10.2174/1568026623666230207120752
    • NLM

      Cuppoloni A, Silva JV da, Snape TJ, Lal S, Giarolla J. 2,3-Diarylindoles as COX-2 Inhibitors: exploring the structure-activity relationship through molecular docking simulations [Internet]. Current Topics in Medicinal Chemistry. 2023 ; 23( 12): 1081-1089.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1568026623666230207120752
    • Vancouver

      Cuppoloni A, Silva JV da, Snape TJ, Lal S, Giarolla J. 2,3-Diarylindoles as COX-2 Inhibitors: exploring the structure-activity relationship through molecular docking simulations [Internet]. Current Topics in Medicinal Chemistry. 2023 ; 23( 12): 1081-1089.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1568026623666230207120752
  • Source: Letters in Drug Design & Discovery. Unidade: FCF

    Subjects: NEOPLASIAS PULMONARES, NANOTECNOLOGIA, RESISTÊNCIA MICROBIANA ÀS DROGAS

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      AWASTHI, Rajendra et al. Diagnosis and clinical aspects of lung cancer: a special emphasis on drug targeting to cancer cells through nanoparticles. Letters in Drug Design & Discovery, v. 20, n. 5, p. 499-516, 2023Tradução . . Disponível em: https://doi.org/10.2174/1570180819666220510133408. Acesso em: 25 jun. 2024.
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      Awasthi, R., Singh, A. K., Mishra, G., Maurya, A., Dhiman, N., Kharkwal, H., et al. (2023). Diagnosis and clinical aspects of lung cancer: a special emphasis on drug targeting to cancer cells through nanoparticles. Letters in Drug Design & Discovery, 20( 5), 499-516. doi:10.2174/1570180819666220510133408
    • NLM

      Awasthi R, Singh AK, Mishra G, Maurya A, Dhiman N, Kharkwal H, Sharma B, Jha NK, Dua K, Pinto T de JA, Kulkarni GT. Diagnosis and clinical aspects of lung cancer: a special emphasis on drug targeting to cancer cells through nanoparticles [Internet]. Letters in Drug Design & Discovery. 2023 ; 20( 5): 499-516.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1570180819666220510133408
    • Vancouver

      Awasthi R, Singh AK, Mishra G, Maurya A, Dhiman N, Kharkwal H, Sharma B, Jha NK, Dua K, Pinto T de JA, Kulkarni GT. Diagnosis and clinical aspects of lung cancer: a special emphasis on drug targeting to cancer cells through nanoparticles [Internet]. Letters in Drug Design & Discovery. 2023 ; 20( 5): 499-516.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1570180819666220510133408
  • Source: Current Organic Chemistry. Unidade: FCF

    Subjects: DOENÇA DE CHAGAS, SÍNTESE ORGÂNICA

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      MORAIS, Pedro Alves Bezerra e TROSSINI, Gustavo Henrique Goulart. Cruzain inhibitors: state-of-art of novel synthetic strategies. Current Organic Chemistry, v. 27, n. 4, p. 243-247, 2023Tradução . . Disponível em: https://doi.org/10.2174/1385272827666230418100932. Acesso em: 25 jun. 2024.
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      Morais, P. A. B., & Trossini, G. H. G. (2023). Cruzain inhibitors: state-of-art of novel synthetic strategies. Current Organic Chemistry, 27( 4), 243-247. doi:10.2174/1385272827666230418100932
    • NLM

      Morais PAB, Trossini GHG. Cruzain inhibitors: state-of-art of novel synthetic strategies [Internet]. Current Organic Chemistry. 2023 ; 27( 4): 243-247.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1385272827666230418100932
    • Vancouver

      Morais PAB, Trossini GHG. Cruzain inhibitors: state-of-art of novel synthetic strategies [Internet]. Current Organic Chemistry. 2023 ; 27( 4): 243-247.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1385272827666230418100932
  • Source: Current Drug Targets. Unidade: FCF

    Subjects: FLAVONOIDES, MEDICAMENTO, DOENÇAS NEGLIGENCIADAS

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      PONE, Boniface Kamdem e FERREIRA, Elizabeth Igne. Therapeutic potential of flavonoid derivatives for certain neglected tropical diseases [Editorial]. Current Drug Targets. Sharjah: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. Disponível em: https://doi.org/10.2174/1389450123666220309093827. Acesso em: 25 jun. 2024. , 2022
    • APA

      Pone, B. K., & Ferreira, E. I. (2022). Therapeutic potential of flavonoid derivatives for certain neglected tropical diseases [Editorial]. Current Drug Targets. Sharjah: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. doi:10.2174/1389450123666220309093827
    • NLM

      Pone BK, Ferreira EI. Therapeutic potential of flavonoid derivatives for certain neglected tropical diseases [Editorial] [Internet]. Current Drug Targets. 2022 ; 23( 7): 680-682.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1389450123666220309093827
    • Vancouver

      Pone BK, Ferreira EI. Therapeutic potential of flavonoid derivatives for certain neglected tropical diseases [Editorial] [Internet]. Current Drug Targets. 2022 ; 23( 7): 680-682.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1389450123666220309093827
  • Source: Current Drug Targets. Unidade: FCF

    Subjects: TRYPANOSOMA CRUZI, COMPOSTOS HETEROCÍCLICOS, ANTIPROTOZOÁRIOS, DOENÇAS NEGLIGENCIADAS

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      PONE, Kamdem Boniface et al. Triazole-containing heterocycles: privileged scaffolds in anti-Trypanosoma cruzi drug development. Current Drug Targets, v. 23, n. 1, p. 33-59, 2022Tradução . . Disponível em: https://doi.org/10.2174/1389450122666210412125643. Acesso em: 25 jun. 2024.
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      Pone, K. B., Dalhatou, S., Paumo, H. K., Seru, L. M. K., & Ferreira, E. I. (2022). Triazole-containing heterocycles: privileged scaffolds in anti-Trypanosoma cruzi drug development. Current Drug Targets, 23( 1), 33-59. doi:10.2174/1389450122666210412125643
    • NLM

      Pone KB, Dalhatou S, Paumo HK, Seru LMK, Ferreira EI. Triazole-containing heterocycles: privileged scaffolds in anti-Trypanosoma cruzi drug development [Internet]. Current Drug Targets. 2022 ; 23( 1): 33-59.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1389450122666210412125643
    • Vancouver

      Pone KB, Dalhatou S, Paumo HK, Seru LMK, Ferreira EI. Triazole-containing heterocycles: privileged scaffolds in anti-Trypanosoma cruzi drug development [Internet]. Current Drug Targets. 2022 ; 23( 1): 33-59.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1389450122666210412125643
  • Source: Current Drug Targets. Unidade: FCF

    Subjects: DOENÇAS NEGLIGENCIADAS, ANTIMALÁRICOS

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      BONIFACE, Pone Kamdem e FERREIRA, Elizabeth Igne. The role of nitro (NO 2-), Chloro (Cl), and Fluoro (F) substitution in the design of antileishmanial and antichagasic compounds. Current Drug Targets, v. 22, p. 379-398, 2021Tradução . . Disponível em: https://doi.org/10.2174/1389450121666201228122239. Acesso em: 25 jun. 2024.
    • APA

      Boniface, P. K., & Ferreira, E. I. (2021). The role of nitro (NO 2-), Chloro (Cl), and Fluoro (F) substitution in the design of antileishmanial and antichagasic compounds. Current Drug Targets, 22, 379-398. doi:10.2174/1389450121666201228122239
    • NLM

      Boniface PK, Ferreira EI. The role of nitro (NO 2-), Chloro (Cl), and Fluoro (F) substitution in the design of antileishmanial and antichagasic compounds [Internet]. Current Drug Targets. 2021 ; 22 379-398.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1389450121666201228122239
    • Vancouver

      Boniface PK, Ferreira EI. The role of nitro (NO 2-), Chloro (Cl), and Fluoro (F) substitution in the design of antileishmanial and antichagasic compounds [Internet]. Current Drug Targets. 2021 ; 22 379-398.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1389450121666201228122239
  • Source: Mini-Reviews in Medicinal Chemistry. Unidades: FCFRP, FCF

    Assunto: FÁRMACOS

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      LIMA, Elys Juliane Cardoso et al. Insights into newly approved drugs from a medicinal chemistry perspective. Mini-Reviews in Medicinal Chemistry, v. 21, n. 16, p. 2227-2248, 2021Tradução . . Disponível em: https://doi.org/10.2174/1389557521666210226145328. Acesso em: 25 jun. 2024.
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      Lima, E. J. C., Gomes, R. A., Fornari, E., Emery, F. da S., & Trossini, G. H. G. (2021). Insights into newly approved drugs from a medicinal chemistry perspective. Mini-Reviews in Medicinal Chemistry, 21( 16), 2227-2248. doi:10.2174/1389557521666210226145328
    • NLM

      Lima EJC, Gomes RA, Fornari E, Emery F da S, Trossini GHG. Insights into newly approved drugs from a medicinal chemistry perspective [Internet]. Mini-Reviews in Medicinal Chemistry. 2021 ; 21( 16): 2227-2248.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1389557521666210226145328
    • Vancouver

      Lima EJC, Gomes RA, Fornari E, Emery F da S, Trossini GHG. Insights into newly approved drugs from a medicinal chemistry perspective [Internet]. Mini-Reviews in Medicinal Chemistry. 2021 ; 21( 16): 2227-2248.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1389557521666210226145328
  • Source: Current Topics in Medicinal Chemistry. Unidade: FCF

    Subjects: TUBERCULOSE, ANTIBIÓTICOS, INIBIDORES DE ENZIMAS, QUIMIOTERAPIA

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      PRIMI, Marina Candido et al. Design of novel phosphopantetheine adenylyltransferase inhibitors: a potential new approach to tackle Mycobacterium tuberculosis. Current Topics in Medicinal Chemistry, v. 21, p. 1186-1197, 2021Tradução . . Disponível em: https://doi.org/10.2174/1568026621666210728094804. Acesso em: 25 jun. 2024.
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      Primi, M. C., Tavares, M. T., Klein, L. L., Izard, T., Sant'Anna, C. M. R., Franzblau, S. G., & Ferreira, E. I. (2021). Design of novel phosphopantetheine adenylyltransferase inhibitors: a potential new approach to tackle Mycobacterium tuberculosis. Current Topics in Medicinal Chemistry, 21, 1186-1197. doi:10.2174/1568026621666210728094804
    • NLM

      Primi MC, Tavares MT, Klein LL, Izard T, Sant'Anna CMR, Franzblau SG, Ferreira EI. Design of novel phosphopantetheine adenylyltransferase inhibitors: a potential new approach to tackle Mycobacterium tuberculosis [Internet]. Current Topics in Medicinal Chemistry. 2021 ; 21 1186-1197.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1568026621666210728094804
    • Vancouver

      Primi MC, Tavares MT, Klein LL, Izard T, Sant'Anna CMR, Franzblau SG, Ferreira EI. Design of novel phosphopantetheine adenylyltransferase inhibitors: a potential new approach to tackle Mycobacterium tuberculosis [Internet]. Current Topics in Medicinal Chemistry. 2021 ; 21 1186-1197.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1568026621666210728094804
  • Source: Current Organic Chemistry. Unidade: FCF

    Subjects: QUIMIOTERÁPICOS, COMPOSTOS HETEROCÍCLICOS

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      PRASHER, Parteek et al. Synthesis and anticancer properties of ‘azole’ based chemotherapeutics as emerging chemical moieties: a comprehensive review. Current Organic Chemistry, v. 25, p. 654-668, 2021Tradução . . Disponível em: https://doi.org/10.2174/1385272824999200820152501. Acesso em: 25 jun. 2024.
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      Prasher, P., Sharma, M., Zacconi, F., Gupt, G., Aljabali, A. A., Mishra, V., et al. (2021). Synthesis and anticancer properties of ‘azole’ based chemotherapeutics as emerging chemical moieties: a comprehensive review. Current Organic Chemistry, 25, 654-668. doi:10.2174/1385272824999200820152501
    • NLM

      Prasher P, Sharma M, Zacconi F, Gupt G, Aljabali AA, Mishra V, Tambuwala MM, Kapoor DN, Negi P, Pinto T de JA, Singh I, Chellappan DK, Dua K. Synthesis and anticancer properties of ‘azole’ based chemotherapeutics as emerging chemical moieties: a comprehensive review [Internet]. Current Organic Chemistry. 2021 ; 25 654-668.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1385272824999200820152501
    • Vancouver

      Prasher P, Sharma M, Zacconi F, Gupt G, Aljabali AA, Mishra V, Tambuwala MM, Kapoor DN, Negi P, Pinto T de JA, Singh I, Chellappan DK, Dua K. Synthesis and anticancer properties of ‘azole’ based chemotherapeutics as emerging chemical moieties: a comprehensive review [Internet]. Current Organic Chemistry. 2021 ; 25 654-668.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1385272824999200820152501
  • Source: Medicinal Chemistry. Unidade: FCF

    Subjects: AGENTES ANTIMICROBIANOS, ANTIOXIDANTES, RESISTÊNCIA MICROBIANA ÀS DROGAS

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      FERNANDES, Thais Batista et al. Design of arylsulfonylhydrazones as potential FabH inhibitors: synthesis, antimicrobial evaluation and molecular docking. Medicinal Chemistry, v. 17, p. 474-484, 2021Tradução . . Disponível em: https://doi.org/10.2174/1573406415666191122111228. Acesso em: 25 jun. 2024.
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      Fernandes, T. B., Segretti, N. D., Lourenço, F. R., Cândido, T. M., Baby, A. R., Barbosa, E. G., & Parise Filho, R. (2021). Design of arylsulfonylhydrazones as potential FabH inhibitors: synthesis, antimicrobial evaluation and molecular docking. Medicinal Chemistry, 17, 474-484. doi:10.2174/1573406415666191122111228
    • NLM

      Fernandes TB, Segretti ND, Lourenço FR, Cândido TM, Baby AR, Barbosa EG, Parise Filho R. Design of arylsulfonylhydrazones as potential FabH inhibitors: synthesis, antimicrobial evaluation and molecular docking [Internet]. Medicinal Chemistry. 2021 ; 17 474-484.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1573406415666191122111228
    • Vancouver

      Fernandes TB, Segretti ND, Lourenço FR, Cândido TM, Baby AR, Barbosa EG, Parise Filho R. Design of arylsulfonylhydrazones as potential FabH inhibitors: synthesis, antimicrobial evaluation and molecular docking [Internet]. Medicinal Chemistry. 2021 ; 17 474-484.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1573406415666191122111228
  • Source: Current Drug Targets. Unidade: FCF

    Subjects: FILARIOSE, DOENÇAS

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      BONIFACE, Pone Kamdem e FERREIRA, Elizabeth Igne. An insight into the discovery of potent Antifilarial leads against lymphatic filariasis. Current Drug Targets, v. 21, p. 657-680, 2020Tradução . . Disponível em: https://doi.org/10.2174/1389450120666191204152415. Acesso em: 25 jun. 2024.
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      Boniface, P. K., & Ferreira, E. I. (2020). An insight into the discovery of potent Antifilarial leads against lymphatic filariasis. Current Drug Targets, 21, 657-680. doi:10.2174/1389450120666191204152415
    • NLM

      Boniface PK, Ferreira EI. An insight into the discovery of potent Antifilarial leads against lymphatic filariasis [Internet]. Current Drug Targets. 2020 ; 21 657-680.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1389450120666191204152415
    • Vancouver

      Boniface PK, Ferreira EI. An insight into the discovery of potent Antifilarial leads against lymphatic filariasis [Internet]. Current Drug Targets. 2020 ; 21 657-680.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1389450120666191204152415
  • Source: Current Drug Targets. Unidade: FCF

    Subjects: LEISHMANIA, FARMACOLOGIA

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      BONIFACE, Pone Kamdem e SANO, Cinthya Miyuki e FERREIRA, Elizabeth Igne. Unveiling the targets involved in the quest of antileishmanial Leads using in silico methods. Current Drug Targets, v. 21, p. 681-712, 2020Tradução . . Disponível em: https://doi.org/10.2174/1389450121666200128112948. Acesso em: 25 jun. 2024.
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      Boniface, P. K., Sano, C. M., & Ferreira, E. I. (2020). Unveiling the targets involved in the quest of antileishmanial Leads using in silico methods. Current Drug Targets, 21, 681-712. doi:10.2174/1389450121666200128112948
    • NLM

      Boniface PK, Sano CM, Ferreira EI. Unveiling the targets involved in the quest of antileishmanial Leads using in silico methods [Internet]. Current Drug Targets. 2020 ; 21 681-712.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1389450121666200128112948
    • Vancouver

      Boniface PK, Sano CM, Ferreira EI. Unveiling the targets involved in the quest of antileishmanial Leads using in silico methods [Internet]. Current Drug Targets. 2020 ; 21 681-712.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1389450121666200128112948
  • Source: Mini-Reviews in Medicinal Chemistry. Unidade: FCF

    Subjects: ZIKA VÍRUS, SAÚDE PÚBLICA

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      RAMPINI, Denise et al. Future and perspectives of the Zika Virus: drug repurposing as a powerful tool for treatment insights. Mini-Reviews in Medicinal Chemistry, v. 20, p. 1917-1928, 2020Tradução . . Disponível em: https://doi.org/10.2174/1389557520666200711174007. Acesso em: 25 jun. 2024.
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      Rampini, D., Prieto, D. C., Colzi, A. L., Araujo, R. V. de, & Giarolla, J. (2020). Future and perspectives of the Zika Virus: drug repurposing as a powerful tool for treatment insights. Mini-Reviews in Medicinal Chemistry, 20, 1917-1928. doi:10.2174/1389557520666200711174007
    • NLM

      Rampini D, Prieto DC, Colzi AL, Araujo RV de, Giarolla J. Future and perspectives of the Zika Virus: drug repurposing as a powerful tool for treatment insights [Internet]. Mini-Reviews in Medicinal Chemistry. 2020 ; 20 1917-1928.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1389557520666200711174007
    • Vancouver

      Rampini D, Prieto DC, Colzi AL, Araujo RV de, Giarolla J. Future and perspectives of the Zika Virus: drug repurposing as a powerful tool for treatment insights [Internet]. Mini-Reviews in Medicinal Chemistry. 2020 ; 20 1917-1928.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1389557520666200711174007
  • Source: Current Medicinal Chemistry. Unidade: FCF

    Assunto: DOENÇAS NEGLIGENCIADAS

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      FERREIRA, Elizabeth Igne. Drug design and development for neglected diseases [Editorial]. Current Medicinal Chemistry. Sharjah: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. Disponível em: https://doi.org/10.2174/092986732623190927101548. Acesso em: 25 jun. 2024. , 2019
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      Ferreira, E. I. (2019). Drug design and development for neglected diseases [Editorial]. Current Medicinal Chemistry. Sharjah: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. doi:10.2174/092986732623190927101548
    • NLM

      Ferreira EI. Drug design and development for neglected diseases [Editorial] [Internet]. Current Medicinal Chemistry. 2019 ; 26( 23): 4298-4300.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/092986732623190927101548
    • Vancouver

      Ferreira EI. Drug design and development for neglected diseases [Editorial] [Internet]. Current Medicinal Chemistry. 2019 ; 26( 23): 4298-4300.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/092986732623190927101548
  • Source: Current Topics in Medicinal Chemistry. Unidade: FCF

    Subjects: MODELAGEM MOLECULAR, SCHISTOSOMA MANSONI

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      TELES, Andre Lacerda Braga et al. Identification, characterization and molecular modelling studies of schistosoma mansoni dihydrofolate reductase inhibitors: From assay development to hit identification. Current Topics in Medicinal Chemistry, v. 18, p. 406-417, 2018Tradução . . Disponível em: https://doi.org/10.2174/1568026618666180509150134. Acesso em: 25 jun. 2024.
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      Teles, A. L. B., Silva, R. R., Ko, M., Ferreira, G. M., Pita, S. da R., Trossini, G. H. G., et al. (2018). Identification, characterization and molecular modelling studies of schistosoma mansoni dihydrofolate reductase inhibitors: From assay development to hit identification. Current Topics in Medicinal Chemistry, 18, 406-417. doi:10.2174/1568026618666180509150134
    • NLM

      Teles ALB, Silva RR, Ko M, Ferreira GM, Pita S da R, Trossini GHG, Carvalho P, Castilho MS. Identification, characterization and molecular modelling studies of schistosoma mansoni dihydrofolate reductase inhibitors: From assay development to hit identification [Internet]. Current Topics in Medicinal Chemistry. 2018 ; 18 406-417.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1568026618666180509150134
    • Vancouver

      Teles ALB, Silva RR, Ko M, Ferreira GM, Pita S da R, Trossini GHG, Carvalho P, Castilho MS. Identification, characterization and molecular modelling studies of schistosoma mansoni dihydrofolate reductase inhibitors: From assay development to hit identification [Internet]. Current Topics in Medicinal Chemistry. 2018 ; 18 406-417.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1568026618666180509150134
  • Source: Letters in Drug Design and Discovery. Unidades: FCF, ICB

    Subjects: APOPTOSE, NEOPLASIAS MAMÁRIAS

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      FERNANDES, Thais Batista et al. Arylsulfonylhydrazone induced apoptosis in MDA-MB-231 breast cancer cells. Letters in Drug Design and Discovery, v. 15, n. 12, p. 1288-1298, 2018Tradução . . Disponível em: https://doi.org/10.2174/1570180815666180321161513. Acesso em: 25 jun. 2024.
    • APA

      Fernandes, T. B., Azevedo, R. A. de, Yang, R., Teixeira, S. F., Trossini, G. H. G., Barbuto, J. A. M., et al. (2018). Arylsulfonylhydrazone induced apoptosis in MDA-MB-231 breast cancer cells. Letters in Drug Design and Discovery, 15( 12), 1288-1298. doi:10.2174/1570180815666180321161513
    • NLM

      Fernandes TB, Azevedo RA de, Yang R, Teixeira SF, Trossini GHG, Barbuto JAM, Ferreira AK, Parise Filho R. Arylsulfonylhydrazone induced apoptosis in MDA-MB-231 breast cancer cells [Internet]. Letters in Drug Design and Discovery. 2018 ; 15( 12): 1288-1298.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1570180815666180321161513
    • Vancouver

      Fernandes TB, Azevedo RA de, Yang R, Teixeira SF, Trossini GHG, Barbuto JAM, Ferreira AK, Parise Filho R. Arylsulfonylhydrazone induced apoptosis in MDA-MB-231 breast cancer cells [Internet]. Letters in Drug Design and Discovery. 2018 ; 15( 12): 1288-1298.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1570180815666180321161513
  • Source: Current Drug Targets. Unidades: ICB, FCF, EACH

    Subjects: DIABETES MELLITUS NÃO INSULINO-DEPENDENTE, SÍNDROME X METABÓLICA, ÁCIDOS GRAXOS, DOENÇAS METABÓLICAS, PARASITOLOGIA

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      MALTAROLLO, Vinícius Gonçalves et al. Advances and challenges in drug design of PPARδ ligands. Current Drug Targets, v. 19, n. 2, p. 144-154, 2018Tradução . . Disponível em: https://doi.org/10.2174/1389450118666170414113159. Acesso em: 25 jun. 2024.
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      Maltarollo, V. G., Kronenberger, T., Windshuegel, B., Wrenger, C., Trossini, G. H. G., & Honório, K. M. (2018). Advances and challenges in drug design of PPARδ ligands. Current Drug Targets, 19( 2), 144-154. doi:10.2174/1389450118666170414113159
    • NLM

      Maltarollo VG, Kronenberger T, Windshuegel B, Wrenger C, Trossini GHG, Honório KM. Advances and challenges in drug design of PPARδ ligands [Internet]. Current Drug Targets. 2018 ; 19( 2): 144-154.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1389450118666170414113159
    • Vancouver

      Maltarollo VG, Kronenberger T, Windshuegel B, Wrenger C, Trossini GHG, Honório KM. Advances and challenges in drug design of PPARδ ligands [Internet]. Current Drug Targets. 2018 ; 19( 2): 144-154.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1389450118666170414113159
  • Source: Medicinal Chemistry. Unidade: FCF

    Subjects: MOLÉCULA, ANTINEOPLÁSICOS

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      VASCONCELOS, Stanley Nunes Siqueira et al. Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells. Medicinal Chemistry, v. 14, n. 7, p. 709-714, 2018Tradução . . Disponível em: https://doi.org/10.2174/1573406414666180309153142. Acesso em: 25 jun. 2024.
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      Vasconcelos, S. N. S., Sciani, J. M., Lisboa, N. M., & Stefani, H. A. (2018). Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells. Medicinal Chemistry, 14( 7), 709-714. doi:10.2174/1573406414666180309153142
    • NLM

      Vasconcelos SNS, Sciani JM, Lisboa NM, Stefani HA. Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells [Internet]. Medicinal Chemistry. 2018 ; 14( 7): 709-714.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1573406414666180309153142
    • Vancouver

      Vasconcelos SNS, Sciani JM, Lisboa NM, Stefani HA. Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells [Internet]. Medicinal Chemistry. 2018 ; 14( 7): 709-714.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1573406414666180309153142
  • Source: Current Drug Delivery. Unidade: FCF

    Subjects: BIOMATERIAIS, ESTERILIZAÇÃO

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      KIKUCHI, Irene Satiko et al. Hydrogel based drug delivery systems: a review with special emphasis on challenges associated with decontamination of hydrogels and biomaterials. Current Drug Delivery, v. 14, n. 7, p. 917-925, 2017Tradução . . Acesso em: 25 jun. 2024.
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      Kikuchi, I. S., Galante, R. S. C., Dua, K., Malipeddi, V. R., Ghisleni, D. D. M., & Pinto, T. de J. A. (2017). Hydrogel based drug delivery systems: a review with special emphasis on challenges associated with decontamination of hydrogels and biomaterials. Current Drug Delivery, 14( 7), 917-925.
    • NLM

      Kikuchi IS, Galante RSC, Dua K, Malipeddi VR, Ghisleni DDM, Pinto T de JA. Hydrogel based drug delivery systems: a review with special emphasis on challenges associated with decontamination of hydrogels and biomaterials. Current Drug Delivery. 2017 ; 14( 7): 917-925.[citado 2024 jun. 25 ]
    • Vancouver

      Kikuchi IS, Galante RSC, Dua K, Malipeddi VR, Ghisleni DDM, Pinto T de JA. Hydrogel based drug delivery systems: a review with special emphasis on challenges associated with decontamination of hydrogels and biomaterials. Current Drug Delivery. 2017 ; 14( 7): 917-925.[citado 2024 jun. 25 ]

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