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Artigo de periodico
Differential specificity of SARS-CoV-2 main protease variants on peptide versus protein-based substrates (2023)
Rocho, Fernanda dos Reis ; Snipas, Scott J.; Shamim, Anwar ; Rut, Wioletta; Drag, Marcin; Montanari, Carlos Alberto
Source: The FEBS Journal. Unidade: IQSC
Subjects: COVID-19, PEPTÍDEOS, PROTEÍNAS
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ABNT
ROCHO, Fernanda dos Reis et al. Differential specificity of SARS-CoV-2 main protease variants on peptide versus protein-based substrates. The FEBS Journal, p. online, 2023Tradução . . Disponível em: https://doi.org/10.1111/febs.16970. Acesso em: 20 maio 2024.
APA
Rocho, F. dos R., Snipas, S. J., Shamim, A., Rut, W., Drag, M., & Montanari, C. A. (2023). Differential specificity of SARS-CoV-2 main protease variants on peptide versus protein-based substrates. The FEBS Journal, online. doi:10.1111/febs.16970
NLM
Rocho F dos R, Snipas SJ, Shamim A, Rut W, Drag M, Montanari CA. Differential specificity of SARS-CoV-2 main protease variants on peptide versus protein-based substrates [Internet]. The FEBS Journal. 2023 ;online.[citado 2024 maio 20 ] Available from: https://doi.org/10.1111/febs.16970
Vancouver
Rocho F dos R, Snipas SJ, Shamim A, Rut W, Drag M, Montanari CA. Differential specificity of SARS-CoV-2 main protease variants on peptide versus protein-based substrates [Internet]. The FEBS Journal. 2023 ;online.[citado 2024 maio 20 ] Available from: https://doi.org/10.1111/febs.16970
Trabalho de evento-resumo
Thiadiazole derived compounds as new Plasmodium falciparum inhibitors: synthesis and structure-activity relationships (2022)
Ahmad, Anees; Casal, Mariana Ferrer; Shamim, Anwar; Aguiar, Anna Caroline Campos ; Maluf, Sarah El Chamy; Guido, Rafael Victorio Carvalho ; Willis, Paul; Vongeldern, Tom Tom; Baudd, Delphine; Soldati-Favre, Dominique; Dias, Luiz Carlos
Source: Anais eletrônicos. Conference titles: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidade: IFSC
Subjects: PLASMODIUM FALCIPARUM, QUÍMICA MÉDICA
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ABNT
AHMAD, Anees et al. Thiadiazole derived compounds as new Plasmodium falciparum inhibitors: synthesis and structure-activity relationships. 2022, Anais.. Campinas: Galoá, 2022. Disponível em: https://proceedings.science/brazmedchem-2022/papers/thiadiazole-derived-compounds-as-new-plasmodium-falciparum-inhibitors--synthesis-and-structure---activity-relationships. Acesso em: 20 maio 2024.
APA
Ahmad, A., Casal, M. F., Shamim, A., Aguiar, A. C. C., Maluf, S. E. C., Guido, R. V. C., et al. (2022). Thiadiazole derived compounds as new Plasmodium falciparum inhibitors: synthesis and structure-activity relationships. In Anais eletrônicos. Campinas: Galoá. Recuperado de https://proceedings.science/brazmedchem-2022/papers/thiadiazole-derived-compounds-as-new-plasmodium-falciparum-inhibitors--synthesis-and-structure---activity-relationships.
NLM
Ahmad A, Casal MF, Shamim A, Aguiar ACC, Maluf SEC, Guido RVC, Willis P, Vongeldern TT, Baudd D, Soldati-Favre D, Dias LC. Thiadiazole derived compounds as new Plasmodium falciparum inhibitors: synthesis and structure-activity relationships [Internet]. Anais eletrônicos. 2022 ;[citado 2024 maio 20 ] Available from: https://proceedings.science/brazmedchem-2022/papers/thiadiazole-derived-compounds-as-new-plasmodium-falciparum-inhibitors--synthesis-and-structure---activity-relationships.
Vancouver
Ahmad A, Casal MF, Shamim A, Aguiar ACC, Maluf SEC, Guido RVC, Willis P, Vongeldern TT, Baudd D, Soldati-Favre D, Dias LC. Thiadiazole derived compounds as new Plasmodium falciparum inhibitors: synthesis and structure-activity relationships [Internet]. Anais eletrônicos. 2022 ;[citado 2024 maio 20 ] Available from: https://proceedings.science/brazmedchem-2022/papers/thiadiazole-derived-compounds-as-new-plasmodium-falciparum-inhibitors--synthesis-and-structure---activity-relationships.
Trabalho de evento-resumo
MMV's drug discovery project: test cascade towards the development of new antimalarials (2022)
Dias, Luiz Carlos; Soldati-Favre, Dominique; Casal, Mariana Ferrer; Ahmad, Anees; Shamim, Anwar; Aguiar, Anna Caroline Campos; Maluf, Sarah El Chamy; Souza, Guilherme Eduardo de; Guido, Rafael Victorio Carvalho ; Vongeldern, Tom Tom; Baudd, Delphine; Willis, Paul
Source: Anais eletrônicos. Conference titles: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidade: IFSC
Subjects: ANTIMALÁRICOS, PLANEJAMENTO DE FÁRMACOS
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ABNT
DIAS, Luiz Carlos et al. MMV's drug discovery project: test cascade towards the development of new antimalarials. 2022, Anais.. Campinas: Galoá, 2022. Disponível em: https://proceedings.science/brazmedchem-2022/papers/mmv-s-drug-discovery-project---test-cascade-towards-the-development-of-new-antimalarials-. Acesso em: 20 maio 2024.
APA
Dias, L. C., Soldati-Favre, D., Casal, M. F., Ahmad, A., Shamim, A., Aguiar, A. C. C., et al. (2022). MMV's drug discovery project: test cascade towards the development of new antimalarials. In Anais eletrônicos. Campinas: Galoá. Recuperado de https://proceedings.science/brazmedchem-2022/papers/mmv-s-drug-discovery-project---test-cascade-towards-the-development-of-new-antimalarials-.
NLM
Dias LC, Soldati-Favre D, Casal MF, Ahmad A, Shamim A, Aguiar ACC, Maluf SEC, Souza GE de, Guido RVC, Vongeldern TT, Baudd D, Willis P. MMV's drug discovery project: test cascade towards the development of new antimalarials [Internet]. Anais eletrônicos. 2022 ;[citado 2024 maio 20 ] Available from: https://proceedings.science/brazmedchem-2022/papers/mmv-s-drug-discovery-project---test-cascade-towards-the-development-of-new-antimalarials-.
Vancouver
Dias LC, Soldati-Favre D, Casal MF, Ahmad A, Shamim A, Aguiar ACC, Maluf SEC, Souza GE de, Guido RVC, Vongeldern TT, Baudd D, Willis P. MMV's drug discovery project: test cascade towards the development of new antimalarials [Internet]. Anais eletrônicos. 2022 ;[citado 2024 maio 20 ] Available from: https://proceedings.science/brazmedchem-2022/papers/mmv-s-drug-discovery-project---test-cascade-towards-the-development-of-new-antimalarials-.
Artigo de periodico
Synthesis, biochemical evaluation and molecular modeling studies of nonpeptidic nitrile-based fluorinated compounds (2021)
Lameiro, Rafael da Fonseca; Shamim, Anwar ; Rosini, Fabiana; Cendron, Rodrigo; Batista, Pedro Henrique Jatai ; Montanari, Carlos Alberto
Source: Future Medicinal Chemistry. Unidade: IQSC
Subjects: DOENÇA DE CHAGAS, LEISHMANIA MEXICANA
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ABNT
LAMEIRO, Rafael da Fonseca et al. Synthesis, biochemical evaluation and molecular modeling studies of nonpeptidic nitrile-based fluorinated compounds. Future Medicinal Chemistry, v. 13, n. 1, p. 25–43, 2021Tradução . . Disponível em: https://doi.org/10.4155/fmc-2020-0057. Acesso em: 20 maio 2024.
APA
Lameiro, R. da F., Shamim, A., Rosini, F., Cendron, R., Batista, P. H. J., & Montanari, C. A. (2021). Synthesis, biochemical evaluation and molecular modeling studies of nonpeptidic nitrile-based fluorinated compounds. Future Medicinal Chemistry, 13( 1), 25–43. doi:10.4155/fmc-2020-0057
NLM
Lameiro R da F, Shamim A, Rosini F, Cendron R, Batista PHJ, Montanari CA. Synthesis, biochemical evaluation and molecular modeling studies of nonpeptidic nitrile-based fluorinated compounds [Internet]. Future Medicinal Chemistry. 2021 ; 13( 1): 25–43.[citado 2024 maio 20 ] Available from: https://doi.org/10.4155/fmc-2020-0057
Vancouver
Lameiro R da F, Shamim A, Rosini F, Cendron R, Batista PHJ, Montanari CA. Synthesis, biochemical evaluation and molecular modeling studies of nonpeptidic nitrile-based fluorinated compounds [Internet]. Future Medicinal Chemistry. 2021 ; 13( 1): 25–43.[citado 2024 maio 20 ] Available from: https://doi.org/10.4155/fmc-2020-0057
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: 20 maio 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 maio 20 ] 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 maio 20 ] Available from: https://doi.org/10.1016/j.bioorg.2021.104709
Artigo de periodico
Design, synthesis and stepwise optimization of nitrile-based inhibitors of cathepsins B and L (2021)
Cianni, Lorenzo ; Rocho, Fernanda dos Reis ; Bonatto, Vinícius ; Martins, Felipe Cardoso Prado ; Lameira, Jerônimo ; Leitão, Andrei ; Montanari, Carlos Alberto ; Shamim, Anwar
Source: Bioorganic and Medicinal Chemistry. Unidade: IQSC
Subjects: QUÍMICA MÉDICA, NEOPLASIAS, INIBIDORES DE ENZIMAS
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ABNT
CIANNI, Lorenzo et al. Design, synthesis and stepwise optimization of nitrile-based inhibitors of cathepsins B and L. Bioorganic and Medicinal Chemistry, v. 29, p. 115827, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2020.115827. Acesso em: 20 maio 2024.
APA
Cianni, L., Rocho, F. dos R., Bonatto, V., Martins, F. C. P., Lameira, J., Leitão, A., et al. (2021). Design, synthesis and stepwise optimization of nitrile-based inhibitors of cathepsins B and L. Bioorganic and Medicinal Chemistry, 29, 115827. doi:10.1016/j.bmc.2020.115827
NLM
Cianni L, Rocho F dos R, Bonatto V, Martins FCP, Lameira J, Leitão A, Montanari CA, Shamim A. Design, synthesis and stepwise optimization of nitrile-based inhibitors of cathepsins B and L [Internet]. Bioorganic and Medicinal Chemistry. 2021 ; 29 115827.[citado 2024 maio 20 ] Available from: https://doi.org/10.1016/j.bmc.2020.115827
Vancouver
Cianni L, Rocho F dos R, Bonatto V, Martins FCP, Lameira J, Leitão A, Montanari CA, Shamim A. Design, synthesis and stepwise optimization of nitrile-based inhibitors of cathepsins B and L [Internet]. Bioorganic and Medicinal Chemistry. 2021 ; 29 115827.[citado 2024 maio 20 ] Available from: https://doi.org/10.1016/j.bmc.2020.115827
Artigo de periodico
Predicting the Relative Binding Affinity for Reversible Covalent Inhibitors by Free Energy Perturbation Calculations (2021)
Bonatto, Vinícius ; Shamim, Anwar ; Rocho, Fernanda dos Reis ; Leitão, Andrei ; Luque, F. Javier; Montanari, Carlos Alberto
Source: Journal of Chemical Information and Modeling. Unidade: IQSC
Subjects: MEDICAMENTO, ENZIMAS
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ABNT
BONATTO, Vinícius et al. Predicting the Relative Binding Affinity for Reversible Covalent Inhibitors by Free Energy Perturbation Calculations. Journal of Chemical Information and Modeling, v. 61, p. 4733−4744, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.jcim.1c00515. Acesso em: 20 maio 2024.
APA
Bonatto, V., Shamim, A., Rocho, F. dos R., Leitão, A., Luque, F. J., & Montanari, C. A. (2021). Predicting the Relative Binding Affinity for Reversible Covalent Inhibitors by Free Energy Perturbation Calculations. Journal of Chemical Information and Modeling, 61, 4733−4744. doi:10.1021/acs.jcim.1c00515
NLM
Bonatto V, Shamim A, Rocho F dos R, Leitão A, Luque FJ, Montanari CA. Predicting the Relative Binding Affinity for Reversible Covalent Inhibitors by Free Energy Perturbation Calculations [Internet]. Journal of Chemical Information and Modeling. 2021 ; 61 4733−4744.[citado 2024 maio 20 ] Available from: https://doi.org/10.1021/acs.jcim.1c00515
Vancouver
Bonatto V, Shamim A, Rocho F dos R, Leitão A, Luque FJ, Montanari CA. Predicting the Relative Binding Affinity for Reversible Covalent Inhibitors by Free Energy Perturbation Calculations [Internet]. Journal of Chemical Information and Modeling. 2021 ; 61 4733−4744.[citado 2024 maio 20 ] Available from: https://doi.org/10.1021/acs.jcim.1c00515
Artigo de periodico
Dipeptidyl nitrile derivatives suppress the Trypanosoma cruzi in vitro infection (2020)
Quilles Junior, José Carlos ; Shamim, Anwar ; Tezuka, Daiane Yukie; Batista, Pedro Henrique Jatai ; Lopes, Carla Duque ; Albuquerque, Sérgio de ; Montanari, Carlos Alberto ; Leitão, Andrei
Source: Experimental Parasitology. Unidades: FCFRP, IQSC, BIOENGENHARIA, EESC
Assunto: DOENÇA DE CHAGAS
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ABNT
QUILLES JUNIOR, José Carlos et al. Dipeptidyl nitrile derivatives suppress the Trypanosoma cruzi in vitro infection. Experimental Parasitology, v. 219, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.exppara.2020.108032. Acesso em: 20 maio 2024.
APA
Quilles Junior, J. C., Shamim, A., Tezuka, D. Y., Batista, P. H. J., Lopes, C. D., Albuquerque, S. de, et al. (2020). Dipeptidyl nitrile derivatives suppress the Trypanosoma cruzi in vitro infection. Experimental Parasitology, 219. doi:10.1016/j.exppara.2020.108032
NLM
Quilles Junior JC, Shamim A, Tezuka DY, Batista PHJ, Lopes CD, Albuquerque S de, Montanari CA, Leitão A. Dipeptidyl nitrile derivatives suppress the Trypanosoma cruzi in vitro infection [Internet]. Experimental Parasitology. 2020 ; 219[citado 2024 maio 20 ] Available from: https://doi.org/10.1016/j.exppara.2020.108032
Vancouver
Quilles Junior JC, Shamim A, Tezuka DY, Batista PHJ, Lopes CD, Albuquerque S de, Montanari CA, Leitão A. Dipeptidyl nitrile derivatives suppress the Trypanosoma cruzi in vitro infection [Internet]. Experimental Parasitology. 2020 ; 219[citado 2024 maio 20 ] Available from: https://doi.org/10.1016/j.exppara.2020.108032
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: 20 maio 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 maio 20 ] 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 maio 20 ] Available from: https://doi.org/10.1016/j.bioorg.2020.104039
Trabalho de evento-resumo
2,2,2-Trifluoroethylamine as a peptidic bond bioisostere in reversible covalent inhibitors of cysteine proteases (2019)
Lameiro, Rafael da Fonseca; Shamim, Anwar ; Montanari, Carlos Alberto
Source: Book of Abstracts. Conference titles: The São Carlos Special Medicinal Chemistry Meeting - SancaMedChem2019. Unidade: IQSC
Subjects: SÍNTESE ORGÂNICA, DOENÇAS PARASITÁRIAS, PEPTÍDEOS
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ABNT
LAMEIRO, Rafael da Fonseca e SHAMIM, Anwar e MONTANARI, Carlos Alberto. 2,2,2-Trifluoroethylamine as a peptidic bond bioisostere in reversible covalent inhibitors of cysteine proteases. 2019, Anais.. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP, 2019. Disponível em: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf. Acesso em: 20 maio 2024.
APA
Lameiro, R. da F., Shamim, A., & Montanari, C. A. (2019). 2,2,2-Trifluoroethylamine as a peptidic bond bioisostere in reversible covalent inhibitors of cysteine proteases. In Book of Abstracts. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP. Recuperado de http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
NLM
Lameiro R da F, Shamim A, Montanari CA. 2,2,2-Trifluoroethylamine as a peptidic bond bioisostere in reversible covalent inhibitors of cysteine proteases [Internet]. Book of Abstracts. 2019 ;[citado 2024 maio 20 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Vancouver
Lameiro R da F, Shamim A, Montanari CA. 2,2,2-Trifluoroethylamine as a peptidic bond bioisostere in reversible covalent inhibitors of cysteine proteases [Internet]. Book of Abstracts. 2019 ;[citado 2024 maio 20 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Artigo de periodico
Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones (2019)
Vasconcelos, Stanley Nunes Siqueira ; Oliveira, Isadora Maria de ; Shamim, Anwar ; Zukerman-Schpector, Júlio ; Pimenta, Daniel Carvalho ; Stefani, Hélio Alexandre
Source: Advanced Synthesis & Catalysis. Unidades: FCF, IQSC
Subjects: ALDEÍDOS, ESTEREOQUÍMICA
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ABNT
VASCONCELOS, Stanley Nunes Siqueira et al. Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones. Advanced Synthesis & Catalysis, v. 361, p. 4243-4254, 2019Tradução . . Disponível em: https://doi.org/10.1002/adsc.201900564. Acesso em: 20 maio 2024.
APA
Vasconcelos, S. N. S., Oliveira, I. M. de, Shamim, A., Zukerman-Schpector, J., Pimenta, D. C., & Stefani, H. A. (2019). Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones. Advanced Synthesis & Catalysis, 361, 4243-4254. doi:10.1002/adsc.201900564
NLM
Vasconcelos SNS, Oliveira IM de, Shamim A, Zukerman-Schpector J, Pimenta DC, Stefani HA. Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones [Internet]. Advanced Synthesis & Catalysis. 2019 ; 361 4243-4254.[citado 2024 maio 20 ] Available from: https://doi.org/10.1002/adsc.201900564
Vancouver
Vasconcelos SNS, Oliveira IM de, Shamim A, Zukerman-Schpector J, Pimenta DC, Stefani HA. Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones [Internet]. Advanced Synthesis & Catalysis. 2019 ; 361 4243-4254.[citado 2024 maio 20 ] Available from: https://doi.org/10.1002/adsc.201900564
Trabalho de evento-resumo
Synthesis of Dipeptidyl and Peptidomimetic Nitriles as Cruzain, CPB and Related Human Cathepsins Inhibitors (2019)
Shamim, Anwar ; Montanari, Carlos Alberto
Source: Book of Abstracts. Conference titles: The São Carlos Special Medicinal Chemistry Meeting - SancaMedChem2019. Unidade: IQSC
Assunto: QUÍMICA MÉDICA
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ABNT
SHAMIM, Anwar e MONTANARI, Carlos Alberto. Synthesis of Dipeptidyl and Peptidomimetic Nitriles as Cruzain, CPB and Related Human Cathepsins Inhibitors. 2019, Anais.. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP, 2019. Disponível em: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf. Acesso em: 20 maio 2024.
APA
Shamim, A., & Montanari, C. A. (2019). Synthesis of Dipeptidyl and Peptidomimetic Nitriles as Cruzain, CPB and Related Human Cathepsins Inhibitors. In Book of Abstracts. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP. Recuperado de http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
NLM
Shamim A, Montanari CA. Synthesis of Dipeptidyl and Peptidomimetic Nitriles as Cruzain, CPB and Related Human Cathepsins Inhibitors [Internet]. Book of Abstracts. 2019 ;[citado 2024 maio 20 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Vancouver
Shamim A, Montanari CA. Synthesis of Dipeptidyl and Peptidomimetic Nitriles as Cruzain, CPB and Related Human Cathepsins Inhibitors [Internet]. Book of Abstracts. 2019 ;[citado 2024 maio 20 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Artigo de periodico
Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives (2017)
Shamim, Anwar; Vasconcelos, Stanley Nunes Siqueira; Oliveira, Isadora Maria de; Reis, Joel Savi dos; Pimenta, Daniel Carvalho; Zukerman-Schpector, Júlio; Stefani, Hélio Alexandre
Source: Synthesis. Unidade: FCF
Assunto: SÍNTESE ORGÂNICA
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ABNT
SHAMIM, Anwar et al. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives. Synthesis, v. 49, n. 23, p. 5183-5196, 2017Tradução . . Disponível em: https://doi.org/10.1055/s-0036-1589090. Acesso em: 20 maio 2024.
APA
Shamim, A., Vasconcelos, S. N. S., Oliveira, I. M. de, Reis, J. S. dos, Pimenta, D. C., Zukerman-Schpector, J., & Stefani, H. A. (2017). Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives. Synthesis, 49( 23), 5183-5196. doi:10.1055/s-0036-1589090
NLM
Shamim A, Vasconcelos SNS, Oliveira IM de, Reis JS dos, Pimenta DC, Zukerman-Schpector J, Stefani HA. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives [Internet]. Synthesis. 2017 ; 49( 23): 5183-5196.[citado 2024 maio 20 ] Available from: https://doi.org/10.1055/s-0036-1589090
Vancouver
Shamim A, Vasconcelos SNS, Oliveira IM de, Reis JS dos, Pimenta DC, Zukerman-Schpector J, Stefani HA. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives [Internet]. Synthesis. 2017 ; 49( 23): 5183-5196.[citado 2024 maio 20 ] Available from: https://doi.org/10.1055/s-0036-1589090
Artigo de periodico
Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization (2017)
Shamim, Anwar; Souza, Frederico Bernardes de; Vasconcelos, Stanley Nunes Siqueira; Stefani, Hélio Alexandre
Source: Tetrahedron Letters. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, COBRE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SHAMIM, Anwar et al. Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization. Tetrahedron Letters, v. 58, n. 9, p. 884-888, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2017.01.059. Acesso em: 20 maio 2024.
APA
Shamim, A., Souza, F. B. de, Vasconcelos, S. N. S., & Stefani, H. A. (2017). Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization. Tetrahedron Letters, 58( 9), 884-888. doi:10.1016/j.tetlet.2017.01.059
NLM
Shamim A, Souza FB de, Vasconcelos SNS, Stefani HA. Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization [Internet]. Tetrahedron Letters. 2017 ; 58( 9): 884-888.[citado 2024 maio 20 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.059
Vancouver
Shamim A, Souza FB de, Vasconcelos SNS, Stefani HA. Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization [Internet]. Tetrahedron Letters. 2017 ; 58( 9): 884-888.[citado 2024 maio 20 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.059
Tese (Doutorado)
Funcionalização de 3,4,6-tri-O-acetil-D-glucal via click chemistry e reações de acoplamento cruzado catalizado por paládio (2017)
Shamim, Anwar; Stefani, Hélio Alexandre (Orientador)
Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, PALÁDIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SHAMIM, Anwar. Funcionalização de 3,4,6-tri-O-acetil-D-glucal via click chemistry e reações de acoplamento cruzado catalizado por paládio. 2017. Tese (Doutorado) – Universidade de São Paulo, São Paulo, 2017. Disponível em: http://www.teses.usp.br/teses/disponiveis/46/46136/tde-22112017-143637/. Acesso em: 20 maio 2024.
APA
Shamim, A. (2017). Funcionalização de 3,4,6-tri-O-acetil-D-glucal via click chemistry e reações de acoplamento cruzado catalizado por paládio (Tese (Doutorado). Universidade de São Paulo, São Paulo. Recuperado de http://www.teses.usp.br/teses/disponiveis/46/46136/tde-22112017-143637/
NLM
Shamim A. Funcionalização de 3,4,6-tri-O-acetil-D-glucal via click chemistry e reações de acoplamento cruzado catalizado por paládio [Internet]. 2017 ;[citado 2024 maio 20 ] Available from: http://www.teses.usp.br/teses/disponiveis/46/46136/tde-22112017-143637/
Vancouver
Shamim A. Funcionalização de 3,4,6-tri-O-acetil-D-glucal via click chemistry e reações de acoplamento cruzado catalizado por paládio [Internet]. 2017 ;[citado 2024 maio 20 ] Available from: http://www.teses.usp.br/teses/disponiveis/46/46136/tde-22112017-143637/
Artigo de periodico
Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles (2017)
Ali, Bakhat; Vasconcelos, Stanley N. S; Shamim, Anwar; Schpector, Júlio Zukerman; Stefani, Hélio Alexandre
Source: Arabian Journal of Chemistry. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, REAÇÕES QUÍMICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALI, Bakhat et al. Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles. Arabian Journal of Chemistry, v. 10, n. 4, p. 500-508, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.arabjc.2016.06.003. Acesso em: 20 maio 2024.
APA
Ali, B., Vasconcelos, S. N. S., Shamim, A., Schpector, J. Z., & Stefani, H. A. (2017). Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles. Arabian Journal of Chemistry, 10( 4), 500-508. doi:10.1016/j.arabjc.2016.06.003
NLM
Ali B, Vasconcelos SNS, Shamim A, Schpector JZ, Stefani HA. Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles [Internet]. Arabian Journal of Chemistry. 2017 ; 10( 4): 500-508.[citado 2024 maio 20 ] Available from: https://doi.org/10.1016/j.arabjc.2016.06.003
Vancouver
Ali B, Vasconcelos SNS, Shamim A, Schpector JZ, Stefani HA. Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles [Internet]. Arabian Journal of Chemistry. 2017 ; 10( 4): 500-508.[citado 2024 maio 20 ] Available from: https://doi.org/10.1016/j.arabjc.2016.06.003
Artigo de periodico
3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions (2017)
Vasconcelos, Stanley N. S; Silva, Vitor Hugo Menezes da; Braga, Ataualpa Albert Carmo ; Shamim, Anwar; Souza, Frederico B; Pimenta, Daniel C; Stefani, Hélio Alexandre
Source: Asian Journal Organic of Chemistry. Unidades: IQ, FCF
Subjects: SÍNTESE ORGÂNICA, COMPOSTOS ORGÂNICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VASCONCELOS, Stanley N. S et al. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. Asian Journal Organic of Chemistry, v. 6, n. 7, p. 913-920, 2017Tradução . . Disponível em: https://doi.org/10.1002/ajoc.201700154. Acesso em: 20 maio 2024.
APA
Vasconcelos, S. N. S., Silva, V. H. M. da, Braga, A. A. C., Shamim, A., Souza, F. B., Pimenta, D. C., & Stefani, H. A. (2017). 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. Asian Journal Organic of Chemistry, 6( 7), 913-920. doi:10.1002/ajoc.201700154
NLM
Vasconcelos SNS, Silva VHM da, Braga AAC, Shamim A, Souza FB, Pimenta DC, Stefani HA. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions [Internet]. Asian Journal Organic of Chemistry. 2017 ; 6( 7): 913-920.[citado 2024 maio 20 ] Available from: https://doi.org/10.1002/ajoc.201700154
Vancouver
Vasconcelos SNS, Silva VHM da, Braga AAC, Shamim A, Souza FB, Pimenta DC, Stefani HA. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions [Internet]. Asian Journal Organic of Chemistry. 2017 ; 6( 7): 913-920.[citado 2024 maio 20 ] Available from: https://doi.org/10.1002/ajoc.201700154
Artigo de periodico
Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines (2017)
Oliveira, Isadora M. de; Vasconcelos, Stanley S. N; Barbeiro, Cristiane S; Correra, Thiago Carita ; Shamim, Anwar; Pimenta, Daniel Carvalho; Caracelli, Ignez; Schpector, Júlio Zukerman; Stefani, Hélio Alexandre ; Manarin, Flávia
Source: New Journal of Chemistry. Unidades: IQ, FCF
Subjects: SÍNTESE ORGÂNICA, REAÇÕES ORGÂNICAS
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ABNT
OLIVEIRA, Isadora M. de et al. Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines. New Journal of Chemistry, v. 41, p. 9884-9888, 2017Tradução . . Disponível em: https://doi.org/10.1039/c7nj01803g. Acesso em: 20 maio 2024.
APA
Oliveira, I. M. de, Vasconcelos, S. S. N., Barbeiro, C. S., Correra, T. C., Shamim, A., Pimenta, D. C., et al. (2017). Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines. New Journal of Chemistry, 41, 9884-9888. doi:10.1039/c7nj01803g
NLM
Oliveira IM de, Vasconcelos SSN, Barbeiro CS, Correra TC, Shamim A, Pimenta DC, Caracelli I, Schpector JZ, Stefani HA, Manarin F. Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines [Internet]. New Journal of Chemistry. 2017 ; 41 9884-9888.[citado 2024 maio 20 ] Available from: https://doi.org/10.1039/c7nj01803g
Vancouver
Oliveira IM de, Vasconcelos SSN, Barbeiro CS, Correra TC, Shamim A, Pimenta DC, Caracelli I, Schpector JZ, Stefani HA, Manarin F. Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines [Internet]. New Journal of Chemistry. 2017 ; 41 9884-9888.[citado 2024 maio 20 ] Available from: https://doi.org/10.1039/c7nj01803g
Artigo de periodico
Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine (2016)
Vasconcelos, Stanley Nunes Siqueira; Shamim, Anwar; Ali, Bakhat; Oliveira, Isadora M. de; Stefani, Hélio Alexandre
Source: Molecular Diversity. Unidade: FCF
Subjects: PEPTÍDEOS, TIROXINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VASCONCELOS, Stanley Nunes Siqueira et al. Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine. Molecular Diversity, v. 20, n. 2, p. 469-481, 2016Tradução . . Disponível em: https://doi.org/10.1007/s11030-015-9642-y. Acesso em: 20 maio 2024.
APA
Vasconcelos, S. N. S., Shamim, A., Ali, B., Oliveira, I. M. de, & Stefani, H. A. (2016). Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine. Molecular Diversity, 20( 2), 469-481. doi:10.1007/s11030-015-9642-y
NLM
Vasconcelos SNS, Shamim A, Ali B, Oliveira IM de, Stefani HA. Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine [Internet]. Molecular Diversity. 2016 ; 20( 2): 469-481.[citado 2024 maio 20 ] Available from: https://doi.org/10.1007/s11030-015-9642-y
Vancouver
Vasconcelos SNS, Shamim A, Ali B, Oliveira IM de, Stefani HA. Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine [Internet]. Molecular Diversity. 2016 ; 20( 2): 469-481.[citado 2024 maio 20 ] Available from: https://doi.org/10.1007/s11030-015-9642-y
Artigo de periodico
Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization (2015)
Shamim, Anwar; Vasconcelos, Stanley Nunes Siqueira; Ali, Bakhat; Madureira, Lucas Sousa; Zukerman-Schpector, Júlio; Stefani, Hélio Alexandre
Source: Tetrahedron Letters. Unidade: FCF
Subjects: COMPOSTOS HETEROCÍCLICOS, PALÁDIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SHAMIM, Anwar et al. Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization. Tetrahedron Letters, v. 56, n. 43, p. 5836-5842, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.08.052. Acesso em: 20 maio 2024.
APA
Shamim, A., Vasconcelos, S. N. S., Ali, B., Madureira, L. S., Zukerman-Schpector, J., & Stefani, H. A. (2015). Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization. Tetrahedron Letters, 56( 43), 5836-5842. doi:10.1016/j.tetlet.2015.08.052
NLM
Shamim A, Vasconcelos SNS, Ali B, Madureira LS, Zukerman-Schpector J, Stefani HA. Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization [Internet]. Tetrahedron Letters. 2015 ; 56( 43): 5836-5842.[citado 2024 maio 20 ] Available from: https://doi.org/10.1016/j.tetlet.2015.08.052
Vancouver
Shamim A, Vasconcelos SNS, Ali B, Madureira LS, Zukerman-Schpector J, Stefani HA. Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization [Internet]. Tetrahedron Letters. 2015 ; 56( 43): 5836-5842.[citado 2024 maio 20 ] Available from: https://doi.org/10.1016/j.tetlet.2015.08.052

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