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Artigo de periodico
Antioxidant and anti-sickling activity of glucal-based triazoles compounds – an in vitro and in silico study (2021)
Veloso, Rodolpho Rebello; Shamim, Anwar ; Lamarre, Yann Ives; Stefani, Hélio Alexandre ; Sciani, Juliana Mozer
Source: Bioorganic Chemistry. Unidades: FCF, IQSC, FMRP
Subjects: ANEMIA FALCIFORME, ANTIOXIDANTES
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ABNT
VELOSO, Rodolpho Rebello et al. Antioxidant and anti-sickling activity of glucal-based triazoles compounds – an in vitro and in silico study. Bioorganic Chemistry, v. 109, p. 104709, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2021.104709. Acesso em: 16 set. 2024.
APA
Veloso, R. R., Shamim, A., Lamarre, Y. I., Stefani, H. A., & Sciani, J. M. (2021). Antioxidant and anti-sickling activity of glucal-based triazoles compounds – an in vitro and in silico study. Bioorganic Chemistry, 109, 104709. doi:10.1016/j.bioorg.2021.104709
NLM
Veloso RR, Shamim A, Lamarre YI, Stefani HA, Sciani JM. Antioxidant and anti-sickling activity of glucal-based triazoles compounds – an in vitro and in silico study [Internet]. Bioorganic Chemistry. 2021 ;109 104709.[citado 2024 set. 16 ] Available from: https://doi.org/10.1016/j.bioorg.2021.104709
Vancouver
Veloso RR, Shamim A, Lamarre YI, Stefani HA, Sciani JM. Antioxidant and anti-sickling activity of glucal-based triazoles compounds – an in vitro and in silico study [Internet]. Bioorganic Chemistry. 2021 ;109 104709.[citado 2024 set. 16 ] Available from: https://doi.org/10.1016/j.bioorg.2021.104709
Artigo de periodico
Synthesis of chalcones derived from 1-naphthylacetophenone and evaluation of their cytotoxic and apoptotic effects in acute leukemia cell lines (2021)
Jacques, Amanda Virtuoso; Stefanes, Natália Marcéli; Walter, Laura Otto; Perondia, Daiane Mari; Efe, Fernanda da Luz; Souza, Luiz Felipe Schmitz de; Sens, Larissa; Syracuse, Stephanie Milis; Moraes, Ana Carolina Rabello de; Oliveira, Aldo Sena de ; Martins, Carolina Teixeira; Magalhães, Luma Godoy; Andricopulo, Adriano Defini ; Silva, Lisandra de Oliveira; Nunes, Ricardo José; Santos-Silva, Maria Cláudia
Source: Bioorganic Chemistry. Unidades: IFSC, IQSC
Subjects: CRISTALOGRAFIA, FARMACOLOGIA, LEUCEMIA MIELOIDE AGUDA, PROTEÍNAS, PROLIFERAÇÃO CELULAR
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ABNT
JACQUES, Amanda Virtuoso et al. Synthesis of chalcones derived from 1-naphthylacetophenone and evaluation of their cytotoxic and apoptotic effects in acute leukemia cell lines. Bioorganic Chemistry, v. No 2021, p. 105315-1-105315-11, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2021.105315. Acesso em: 16 set. 2024.
APA
Jacques, A. V., Stefanes, N. M., Walter, L. O., Perondia, D. M., Efe, F. da L., Souza, L. F. S. de, et al. (2021). Synthesis of chalcones derived from 1-naphthylacetophenone and evaluation of their cytotoxic and apoptotic effects in acute leukemia cell lines. Bioorganic Chemistry, No 2021, 105315-1-105315-11. doi:10.1016/j.bioorg.2021.105315
NLM
Jacques AV, Stefanes NM, Walter LO, Perondia DM, Efe F da L, Souza LFS de, Sens L, Syracuse SM, Moraes ACR de, Oliveira AS de, Martins CT, Magalhães LG, Andricopulo AD, Silva L de O, Nunes RJ, Santos-Silva MC. Synthesis of chalcones derived from 1-naphthylacetophenone and evaluation of their cytotoxic and apoptotic effects in acute leukemia cell lines [Internet]. Bioorganic Chemistry. 2021 ; No 2021 105315-1-105315-11.[citado 2024 set. 16 ] Available from: https://doi.org/10.1016/j.bioorg.2021.105315
Vancouver
Jacques AV, Stefanes NM, Walter LO, Perondia DM, Efe F da L, Souza LFS de, Sens L, Syracuse SM, Moraes ACR de, Oliveira AS de, Martins CT, Magalhães LG, Andricopulo AD, Silva L de O, Nunes RJ, Santos-Silva MC. Synthesis of chalcones derived from 1-naphthylacetophenone and evaluation of their cytotoxic and apoptotic effects in acute leukemia cell lines [Internet]. Bioorganic Chemistry. 2021 ; No 2021 105315-1-105315-11.[citado 2024 set. 16 ] Available from: https://doi.org/10.1016/j.bioorg.2021.105315
Artigo de periodico
Batzelladine D and norbatzelladine L purified from marine sponge Monanchora arbuscula induce the reversal of fluconazole (2020)
Domingos, Levy T.S.; Santos, Mario F. C; Moraes, Daniel C. de; Sá, Leandro Figueira Reis de; Silva, Vinicius A.D. da; Meuren, Lana M.; Berlinck, Roberto Gomes de Souza ; Pereira, Antonio Ferreira
Source: Bioorganic Chemistry. Unidade: IQSC
Assunto: PRODUTOS NATURAIS
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ABNT
DOMINGOS, Levy T.S. et al. Batzelladine D and norbatzelladine L purified from marine sponge Monanchora arbuscula induce the reversal of fluconazole. Bioorganic Chemistry, v. 105, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2020.104402. Acesso em: 16 set. 2024.
APA
Domingos, L. T. S., Santos, M. F. C., Moraes, D. C. de, Sá, L. F. R. de, Silva, V. A. D. da, Meuren, L. M., et al. (2020). Batzelladine D and norbatzelladine L purified from marine sponge Monanchora arbuscula induce the reversal of fluconazole. Bioorganic Chemistry, 105. doi:10.1016/j.bioorg.2020.104402
NLM
Domingos LTS, Santos MFC, Moraes DC de, Sá LFR de, Silva VAD da, Meuren LM, Berlinck RG de S, Pereira AF. Batzelladine D and norbatzelladine L purified from marine sponge Monanchora arbuscula induce the reversal of fluconazole [Internet]. Bioorganic Chemistry. 2020 ; 105[citado 2024 set. 16 ] Available from: https://doi.org/10.1016/j.bioorg.2020.104402
Vancouver
Domingos LTS, Santos MFC, Moraes DC de, Sá LFR de, Silva VAD da, Meuren LM, Berlinck RG de S, Pereira AF. Batzelladine D and norbatzelladine L purified from marine sponge Monanchora arbuscula induce the reversal of fluconazole [Internet]. Bioorganic Chemistry. 2020 ; 105[citado 2024 set. 16 ] Available from: https://doi.org/10.1016/j.bioorg.2020.104402
Artigo de periodico
Optimization strategy of single-digit nanomolar cross-class inhibitors of mammalian and protozoa cysteine proteases (2020)
Cianni, Lorenzo ; Rocho, Fernanda dos Reis ; Rosini, Fabiana; Bonatto, Vinícius ; Ribeiro, Jean Francisco Rosa ; Lameira, Jerônimo ; Leitão, Andrei ; Shamim, Anwar ; Montanari, Carlos Alberto
Source: Bioorganic Chemistry. Unidade: IQSC
Subjects: FÁRMACOS, BIOMARCADORES, PROTEÍNAS
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ABNT
CIANNI, Lorenzo et al. Optimization strategy of single-digit nanomolar cross-class inhibitors of mammalian and protozoa cysteine proteases. Bioorganic Chemistry, v. 101, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2020.104039. Acesso em: 16 set. 2024.
APA
Cianni, L., Rocho, F. dos R., Rosini, F., Bonatto, V., Ribeiro, J. F. R., Lameira, J., et al. (2020). Optimization strategy of single-digit nanomolar cross-class inhibitors of mammalian and protozoa cysteine proteases. Bioorganic Chemistry, 101. doi:10.1016/j.bioorg.2020.104039
NLM
Cianni L, Rocho F dos R, Rosini F, Bonatto V, Ribeiro JFR, Lameira J, Leitão A, Shamim A, Montanari CA. Optimization strategy of single-digit nanomolar cross-class inhibitors of mammalian and protozoa cysteine proteases [Internet]. Bioorganic Chemistry. 2020 ; 101[citado 2024 set. 16 ] Available from: https://doi.org/10.1016/j.bioorg.2020.104039
Vancouver
Cianni L, Rocho F dos R, Rosini F, Bonatto V, Ribeiro JFR, Lameira J, Leitão A, Shamim A, Montanari CA. Optimization strategy of single-digit nanomolar cross-class inhibitors of mammalian and protozoa cysteine proteases [Internet]. Bioorganic Chemistry. 2020 ; 101[citado 2024 set. 16 ] Available from: https://doi.org/10.1016/j.bioorg.2020.104039
Artigo de periodico
Leveraging the cruzain S3 subsite to increase affinity for reversible covalent inhibitors (2018)
Cianni, Lorenzo; Satori, Geraldo R; Rosini, Fabiana; De Vitta, Daniela; Pires, Gabriel Lino de Paula; Lopes, Bianca Rebelo; Leitão, Andrei ; Burtoloso, Antonio Carlos Bender ; Montanari, Carlos Alberto
Source: Bioorganic Chemistry. Unidade: IQSC
Subjects: MOLÉCULA, QUÍMICA MÉDICA
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ABNT
CIANNI, Lorenzo et al. Leveraging the cruzain S3 subsite to increase affinity for reversible covalent inhibitors. Bioorganic Chemistry, p. 285-292, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2018.04.006. Acesso em: 16 set. 2024.
APA
Cianni, L., Satori, G. R., Rosini, F., De Vitta, D., Pires, G. L. de P., Lopes, B. R., et al. (2018). Leveraging the cruzain S3 subsite to increase affinity for reversible covalent inhibitors. Bioorganic Chemistry, 285-292. doi:10.1016/j.bioorg.2018.04.006
NLM
Cianni L, Satori GR, Rosini F, De Vitta D, Pires GL de P, Lopes BR, Leitão A, Burtoloso ACB, Montanari CA. Leveraging the cruzain S3 subsite to increase affinity for reversible covalent inhibitors [Internet]. Bioorganic Chemistry. 2018 ; 285-292.[citado 2024 set. 16 ] Available from: https://doi.org/10.1016/j.bioorg.2018.04.006
Vancouver
Cianni L, Satori GR, Rosini F, De Vitta D, Pires GL de P, Lopes BR, Leitão A, Burtoloso ACB, Montanari CA. Leveraging the cruzain S3 subsite to increase affinity for reversible covalent inhibitors [Internet]. Bioorganic Chemistry. 2018 ; 285-292.[citado 2024 set. 16 ] Available from: https://doi.org/10.1016/j.bioorg.2018.04.006

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