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Artigo de periodico
Exploration the effect of selenophene moiety and benzothiophene based acceptors on optical nonlinearity of D–π–A based heterocyclic organic compounds in chloroform solvent: a DFT approach (2024)
Shafiq, Iqra ; Braga, Ataualpa Albert Carmo ; Tariq, Zara; Alhokbany, Norah ; Chen, Ke
Source: Journal of Molecular Liquids. Unidade: IQ
Subjects: FULERENO, COMPOSTOS ORGÂNICOS, COMPOSTOS HETEROCÍCLICOS
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SHAFIQ, Iqra et al. Exploration the effect of selenophene moiety and benzothiophene based acceptors on optical nonlinearity of D–π–A based heterocyclic organic compounds in chloroform solvent: a DFT approach. Journal of Molecular Liquids, v. 393, p. 1-17 art. 123569, 2024Tradução . . Disponível em: https://dx.doi.org/10.1016/j.molliq.2023.123569. Acesso em: 25 jun. 2024.
APA
Shafiq, I., Braga, A. A. C., Tariq, Z., Alhokbany, N., & Chen, K. (2024). Exploration the effect of selenophene moiety and benzothiophene based acceptors on optical nonlinearity of D–π–A based heterocyclic organic compounds in chloroform solvent: a DFT approach. Journal of Molecular Liquids, 393, 1-17 art. 123569. doi:10.1016/j.molliq.2023.123569
NLM
Shafiq I, Braga AAC, Tariq Z, Alhokbany N, Chen K. Exploration the effect of selenophene moiety and benzothiophene based acceptors on optical nonlinearity of D–π–A based heterocyclic organic compounds in chloroform solvent: a DFT approach [Internet]. Journal of Molecular Liquids. 2024 ; 393 1-17 art. 123569.[citado 2024 jun. 25 ] Available from: https://dx.doi.org/10.1016/j.molliq.2023.123569
Vancouver
Shafiq I, Braga AAC, Tariq Z, Alhokbany N, Chen K. Exploration the effect of selenophene moiety and benzothiophene based acceptors on optical nonlinearity of D–π–A based heterocyclic organic compounds in chloroform solvent: a DFT approach [Internet]. Journal of Molecular Liquids. 2024 ; 393 1-17 art. 123569.[citado 2024 jun. 25 ] Available from: https://dx.doi.org/10.1016/j.molliq.2023.123569
Artigo de periodico
Pharmacological inhibition of PIP4K2 potentiates venetoclax-induced apoptosis in Acute Myeloid Leukemia (2023)
Lima, Keli Cristina de ; Carvalho, Maria Fernanda Lopes ; Pereira-Martins, Diego Antonio ; Nogueira, Frederico Lisboa ; Miranda, Lívia Bassani Lins de ; Mariane Cristina do Nascimento ; Cavaglieri, Rita de Cássia ; Schuringa, Jan Jacob ; Rego, Eduardo Magalhães ; Machado Neto, João Agostinho
Source: International Journal of Molecular Sciences. Unidades: FM, ICB, FMRP
Subjects: FARMACOLOGIA, LEUCEMIA MIELOIDE AGUDA, NEOPLASIAS POR TIPO HISTOLÓGICO, ANTINEOPLÁSICOS, APOPTOSE, PROTEÍNAS PROTO-ONCOGÊNICAS, COMPOSTOS HETEROCÍCLICOS
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LIMA, Keli Cristina de et al. Pharmacological inhibition of PIP4K2 potentiates venetoclax-induced apoptosis in Acute Myeloid Leukemia. International Journal of Molecular Sciences, v. 24, n. 23, p. 12 , 2023Tradução . . Disponível em: https://doi.org/10.3390/ijms242316899. Acesso em: 25 jun. 2024.
APA
Lima, K. C. de, Carvalho, M. F. L., Pereira-Martins, D. A., Nogueira, F. L., Miranda, L. B. L. de, Mariane Cristina do Nascimento,, et al. (2023). Pharmacological inhibition of PIP4K2 potentiates venetoclax-induced apoptosis in Acute Myeloid Leukemia. International Journal of Molecular Sciences, 24( 23), 12 . doi:https://doi.org/10.3390/ijms242316899
NLM
Lima KC de, Carvalho MFL, Pereira-Martins DA, Nogueira FL, Miranda LBL de, Mariane Cristina do Nascimento, Cavaglieri R de C, Schuringa JJ, Rego EM, Machado Neto JA. Pharmacological inhibition of PIP4K2 potentiates venetoclax-induced apoptosis in Acute Myeloid Leukemia [Internet]. International Journal of Molecular Sciences. 2023 ; 24( 23): 12 .[citado 2024 jun. 25 ] Available from: https://doi.org/10.3390/ijms242316899
Vancouver
Lima KC de, Carvalho MFL, Pereira-Martins DA, Nogueira FL, Miranda LBL de, Mariane Cristina do Nascimento, Cavaglieri R de C, Schuringa JJ, Rego EM, Machado Neto JA. Pharmacological inhibition of PIP4K2 potentiates venetoclax-induced apoptosis in Acute Myeloid Leukemia [Internet]. International Journal of Molecular Sciences. 2023 ; 24( 23): 12 .[citado 2024 jun. 25 ] Available from: https://doi.org/10.3390/ijms242316899
Dissertação (Mestrado)
O derivado de ftalocianina é menos citotóxico e não influencia negativamente a cicatrização in vitro de feridas comparado à clorexidina (2022)
Santos, Caíque Andrade; Zangrando, Mariana Schutzer Ragghianti (Orientador)
Unidade: FOB
Subjects: COMPOSTOS HETEROCÍCLICOS, CLOREXIDINA, CICATRIZAÇÃO, SOBREVIVÊNCIA CELULAR, FIBROBLASTOS
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SANTOS, Caíque Andrade. O derivado de ftalocianina é menos citotóxico e não influencia negativamente a cicatrização in vitro de feridas comparado à clorexidina. 2022. Dissertação (Mestrado) – Universidade de São Paulo, Bauru, 2022. Disponível em: https://www.teses.usp.br/teses/disponiveis/25/25152/tde-25012023-184430/. Acesso em: 25 jun. 2024.
APA
Santos, C. A. (2022). O derivado de ftalocianina é menos citotóxico e não influencia negativamente a cicatrização in vitro de feridas comparado à clorexidina (Dissertação (Mestrado). Universidade de São Paulo, Bauru. Recuperado de https://www.teses.usp.br/teses/disponiveis/25/25152/tde-25012023-184430/
NLM
Santos CA. O derivado de ftalocianina é menos citotóxico e não influencia negativamente a cicatrização in vitro de feridas comparado à clorexidina [Internet]. 2022 ;[citado 2024 jun. 25 ] Available from: https://www.teses.usp.br/teses/disponiveis/25/25152/tde-25012023-184430/
Vancouver
Santos CA. O derivado de ftalocianina é menos citotóxico e não influencia negativamente a cicatrização in vitro de feridas comparado à clorexidina [Internet]. 2022 ;[citado 2024 jun. 25 ] Available from: https://www.teses.usp.br/teses/disponiveis/25/25152/tde-25012023-184430/
Artigo de periodico
Pyrazolines as potential anti-Alzheimer's agents: DFT, molecular docking, enzyme inhibition and pharmacokinetic studies (2022)
Machado, Valkiria; Cenci, Arthur R. ; Teixeira, Kerolain F.; Sens, Larissa; Tizziani, Tiago ; Nunes, Ricardo J.; Ferreira, Leonardo Luiz Gomes ; Yunes, Rosendo A.; Sandjo, Louis P.; Andricopulo, Adriano Defini ; Oliveira, Aldo S.
Source: RSC Medicinal Chemistry. Unidade: IFSC
Subjects: DOENÇA DE ALZHEIMER, COMPOSTOS HETEROCÍCLICOS, FARMACOCINÉTICA
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MACHADO, Valkiria et al. Pyrazolines as potential anti-Alzheimer's agents: DFT, molecular docking, enzyme inhibition and pharmacokinetic studies. RSC Medicinal Chemistry, v. 13, n. 12, p. 1644-1656 + supplementary information, 2022Tradução . . Disponível em: https://doi.org/10.1039/D2MD00262K. Acesso em: 25 jun. 2024.
APA
Machado, V., Cenci, A. R., Teixeira, K. F., Sens, L., Tizziani, T., Nunes, R. J., et al. (2022). Pyrazolines as potential anti-Alzheimer's agents: DFT, molecular docking, enzyme inhibition and pharmacokinetic studies. RSC Medicinal Chemistry, 13( 12), 1644-1656 + supplementary information. doi:10.1039/D2MD00262K
NLM
Machado V, Cenci AR, Teixeira KF, Sens L, Tizziani T, Nunes RJ, Ferreira LLG, Yunes RA, Sandjo LP, Andricopulo AD, Oliveira AS. Pyrazolines as potential anti-Alzheimer's agents: DFT, molecular docking, enzyme inhibition and pharmacokinetic studies [Internet]. RSC Medicinal Chemistry. 2022 ; 13( 12): 1644-1656 + supplementary information.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1039/D2MD00262K
Vancouver
Machado V, Cenci AR, Teixeira KF, Sens L, Tizziani T, Nunes RJ, Ferreira LLG, Yunes RA, Sandjo LP, Andricopulo AD, Oliveira AS. Pyrazolines as potential anti-Alzheimer's agents: DFT, molecular docking, enzyme inhibition and pharmacokinetic studies [Internet]. RSC Medicinal Chemistry. 2022 ; 13( 12): 1644-1656 + supplementary information.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1039/D2MD00262K
Artigo de periodico
A DFT study on the formation of heterocycles via iodine(iii)-promoted ring expansion reactions (2022)
Lussari, Natália ; Khan, Ajmir ; Pilli, Ronaldo A ; Santos, Alcindo Aparecido dos ; Silva Junior, Luiz Fernando da; Braga, Ataualpa Albert Carmo
Source: New Journal of Chemistry. Unidade: IQ
Assunto: COMPOSTOS HETEROCÍCLICOS
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LUSSARI, Natália et al. A DFT study on the formation of heterocycles via iodine(iii)-promoted ring expansion reactions. New Journal of Chemistry, v. 46, n. 43, p. 20817-20827, 2022Tradução . . Disponível em: https://doi.org/10.1039/D2NJ04393A. Acesso em: 25 jun. 2024.
APA
Lussari, N., Khan, A., Pilli, R. A., Santos, A. A. dos, Silva Junior, L. F. da, & Braga, A. A. C. (2022). A DFT study on the formation of heterocycles via iodine(iii)-promoted ring expansion reactions. New Journal of Chemistry, 46( 43), 20817-20827. doi:10.1039/D2NJ04393A
NLM
Lussari N, Khan A, Pilli RA, Santos AA dos, Silva Junior LF da, Braga AAC. A DFT study on the formation of heterocycles via iodine(iii)-promoted ring expansion reactions [Internet]. New Journal of Chemistry. 2022 ; 46( 43): 20817-20827.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1039/D2NJ04393A
Vancouver
Lussari N, Khan A, Pilli RA, Santos AA dos, Silva Junior LF da, Braga AAC. A DFT study on the formation of heterocycles via iodine(iii)-promoted ring expansion reactions [Internet]. New Journal of Chemistry. 2022 ; 46( 43): 20817-20827.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1039/D2NJ04393A
Artigo de periodico
Structural, thermal, electronic, vibrational, magnetic, and cytotoxic properties of chloro(glycinato-N,O)(1,10-phenanthroline-N,N′)‑copper(II) trihydrate coordination complex (2022)
Oliveira Neto, J. G. de; Silva Filho, J. G.; Bittar, E. M.; Silva, L. M.; Sousa, F. F. de; Domingos, H. V.; Lotufo, Leticia Veras Costa ; Reis, A. S.; Santos, A. O. dos
Source: Journal of Inorganic Biochemistry. Unidade: ICB
Subjects: FARMACOLOGIA, NEOPLASIAS DO COLON, ANTINEOPLÁSICOS, CÉLULAS CULTIVADAS DE TUMOR, COMPOSTOS HETEROCÍCLICOS, COBRE
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OLIVEIRA NETO, J. G. de et al. Structural, thermal, electronic, vibrational, magnetic, and cytotoxic properties of chloro(glycinato-N,O)(1,10-phenanthroline-N,N′)‑copper(II) trihydrate coordination complex. Journal of Inorganic Biochemistry, v. 226, p. 1-9, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.jinorgbio.2021.111658. Acesso em: 25 jun. 2024.
APA
Oliveira Neto, J. G. de, Silva Filho, J. G., Bittar, E. M., Silva, L. M., Sousa, F. F. de, Domingos, H. V., et al. (2022). Structural, thermal, electronic, vibrational, magnetic, and cytotoxic properties of chloro(glycinato-N,O)(1,10-phenanthroline-N,N′)‑copper(II) trihydrate coordination complex. Journal of Inorganic Biochemistry, 226, 1-9. doi:10.1016/j.jinorgbio.2021.111658
NLM
Oliveira Neto JG de, Silva Filho JG, Bittar EM, Silva LM, Sousa FF de, Domingos HV, Lotufo LVC, Reis AS, Santos AO dos. Structural, thermal, electronic, vibrational, magnetic, and cytotoxic properties of chloro(glycinato-N,O)(1,10-phenanthroline-N,N′)‑copper(II) trihydrate coordination complex [Internet]. Journal of Inorganic Biochemistry. 2022 ; 226 1-9.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1016/j.jinorgbio.2021.111658
Vancouver
Oliveira Neto JG de, Silva Filho JG, Bittar EM, Silva LM, Sousa FF de, Domingos HV, Lotufo LVC, Reis AS, Santos AO dos. Structural, thermal, electronic, vibrational, magnetic, and cytotoxic properties of chloro(glycinato-N,O)(1,10-phenanthroline-N,N′)‑copper(II) trihydrate coordination complex [Internet]. Journal of Inorganic Biochemistry. 2022 ; 226 1-9.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1016/j.jinorgbio.2021.111658
Artigo de periodico
A highly sensitive molecularly imprinted polymer (MIP)-coated microwave glucose sensor (2022)
Omidvar, Amir Hossein; Shahri, Atena Amanati; Serrano, Ariana Lacorte Caniato ; Gruber, Jonas ; Rehder, Gustavo Pamplona
Source: Sensors. Unidades: IQ, EP
Subjects: SENSORES QUÍMICOS, COMPOSTOS HETEROCÍCLICOS
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OMIDVAR, Amir Hossein et al. A highly sensitive molecularly imprinted polymer (MIP)-coated microwave glucose sensor. Sensors, v. 22, n. 22, p. 1-15 art. 8648, 2022Tradução . . Disponível em: https://doi.org/10.3390/s22228648. Acesso em: 25 jun. 2024.
APA
Omidvar, A. H., Shahri, A. A., Serrano, A. L. C., Gruber, J., & Rehder, G. P. (2022). A highly sensitive molecularly imprinted polymer (MIP)-coated microwave glucose sensor. Sensors, 22( 22), 1-15 art. 8648. doi:10.3390/s22228648
NLM
Omidvar AH, Shahri AA, Serrano ALC, Gruber J, Rehder GP. A highly sensitive molecularly imprinted polymer (MIP)-coated microwave glucose sensor [Internet]. Sensors. 2022 ; 22( 22): 1-15 art. 8648.[citado 2024 jun. 25 ] Available from: https://doi.org/10.3390/s22228648
Vancouver
Omidvar AH, Shahri AA, Serrano ALC, Gruber J, Rehder GP. A highly sensitive molecularly imprinted polymer (MIP)-coated microwave glucose sensor [Internet]. Sensors. 2022 ; 22( 22): 1-15 art. 8648.[citado 2024 jun. 25 ] Available from: https://doi.org/10.3390/s22228648
Artigo de periodico
Synthesis of 1,2,3-triazole compounds by click chemistry in aqueous medium and evaluation of bactericidal and antitumoral properties (2022)
Zanin, Lucas Lima ; Jimenez, David Esteban Quintero ; Birolli, Willian Garcia ; Venâncio, Tiago ; Valdes, Talita Alvarenga; Leitão, Andrei ; Porto, Andre Luiz Meleiro
Source: Current Bioactive Compounds. Unidades: IQSC, BIOENGENHARIA
Subjects: QUÍMICA VERDE, COMPOSTOS HETEROCÍCLICOS, BACTERICIDAS, NEOPLASIAS, CATÁLISE
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ZANIN, Lucas Lima et al. Synthesis of 1,2,3-triazole compounds by click chemistry in aqueous medium and evaluation of bactericidal and antitumoral properties. Current Bioactive Compounds, v. 18, n. 4, p. e191121198117, 2022Tradução . . Disponível em: https://doi.org/10.2174/1573407217666211119092038. Acesso em: 25 jun. 2024.
APA
Zanin, L. L., Jimenez, D. E. Q., Birolli, W. G., Venâncio, T., Valdes, T. A., Leitão, A., & Porto, A. L. M. (2022). Synthesis of 1,2,3-triazole compounds by click chemistry in aqueous medium and evaluation of bactericidal and antitumoral properties. Current Bioactive Compounds, 18( 4), e191121198117. doi:10.2174/1573407217666211119092038
NLM
Zanin LL, Jimenez DEQ, Birolli WG, Venâncio T, Valdes TA, Leitão A, Porto ALM. Synthesis of 1,2,3-triazole compounds by click chemistry in aqueous medium and evaluation of bactericidal and antitumoral properties [Internet]. Current Bioactive Compounds. 2022 ; 18( 4): e191121198117.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1573407217666211119092038
Vancouver
Zanin LL, Jimenez DEQ, Birolli WG, Venâncio T, Valdes TA, Leitão A, Porto ALM. Synthesis of 1,2,3-triazole compounds by click chemistry in aqueous medium and evaluation of bactericidal and antitumoral properties [Internet]. Current Bioactive Compounds. 2022 ; 18( 4): e191121198117.[citado 2024 jun. 25 ] Available from: https://doi.org/10.2174/1573407217666211119092038
Dissertação (Mestrado)
Controle da ansiedade com benzodiazepínicos em cirurgias de terceiros molares inferior: revisão sistemática (2022)
Nuñez Tejada, Gerson Leonel; Faria, Flavio Augusto Cardoso de (Orientador)
Unidade: FOB
Subjects: ANSIEDADE AO TRATAMENTO ODONTOLÓGICO, EXTRAÇÃO DENTÁRIA, TERCEIRO MOLAR, COMPOSTOS HETEROCÍCLICOS, SEDATIVOS, REVISÃO SISTEMÁTICA
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NUÑEZ TEJADA, Gerson Leonel. Controle da ansiedade com benzodiazepínicos em cirurgias de terceiros molares inferior: revisão sistemática. 2022. Dissertação (Mestrado) – Universidade de São Paulo, Bauru, 2022. Disponível em: https://www.teses.usp.br/teses/disponiveis/25/25149/tde-25012023-185212/. Acesso em: 25 jun. 2024.
APA
Nuñez Tejada, G. L. (2022). Controle da ansiedade com benzodiazepínicos em cirurgias de terceiros molares inferior: revisão sistemática (Dissertação (Mestrado). Universidade de São Paulo, Bauru. Recuperado de https://www.teses.usp.br/teses/disponiveis/25/25149/tde-25012023-185212/
NLM
Nuñez Tejada GL. Controle da ansiedade com benzodiazepínicos em cirurgias de terceiros molares inferior: revisão sistemática [Internet]. 2022 ;[citado 2024 jun. 25 ] Available from: https://www.teses.usp.br/teses/disponiveis/25/25149/tde-25012023-185212/
Vancouver
Nuñez Tejada GL. Controle da ansiedade com benzodiazepínicos em cirurgias de terceiros molares inferior: revisão sistemática [Internet]. 2022 ;[citado 2024 jun. 25 ] Available from: https://www.teses.usp.br/teses/disponiveis/25/25149/tde-25012023-185212/
Dissertação (Mestrado)
Evaluation of the efficacy of an oral antiseptic containing an iron phthalocyanine derivative in improving the clinical picture, decreasing viral load and length of hospital stay in patients with COVID-19 (2022)
Orcina, Bernardo da Fonseca; Santos, Paulo Sergio da Silva (Orientador)
Unidade: FOB
Subjects: ANTISSÉPTICOS BUCAIS, FERRO, COMPOSTOS HETEROCÍCLICOS, COVID-19, CARGA VIRAL, TEMPO DE INTERNAÇÃO
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ORCINA, Bernardo da Fonseca. Evaluation of the efficacy of an oral antiseptic containing an iron phthalocyanine derivative in improving the clinical picture, decreasing viral load and length of hospital stay in patients with COVID-19. 2022. Dissertação (Mestrado) – Universidade de São Paulo, Bauru, 2022. Disponível em: https://www.teses.usp.br/teses/disponiveis/25/25149/tde-26012023-122706/. Acesso em: 25 jun. 2024.
APA
Orcina, B. da F. (2022). Evaluation of the efficacy of an oral antiseptic containing an iron phthalocyanine derivative in improving the clinical picture, decreasing viral load and length of hospital stay in patients with COVID-19 (Dissertação (Mestrado). Universidade de São Paulo, Bauru. Recuperado de https://www.teses.usp.br/teses/disponiveis/25/25149/tde-26012023-122706/
NLM
Orcina B da F. Evaluation of the efficacy of an oral antiseptic containing an iron phthalocyanine derivative in improving the clinical picture, decreasing viral load and length of hospital stay in patients with COVID-19 [Internet]. 2022 ;[citado 2024 jun. 25 ] Available from: https://www.teses.usp.br/teses/disponiveis/25/25149/tde-26012023-122706/
Vancouver
Orcina B da F. Evaluation of the efficacy of an oral antiseptic containing an iron phthalocyanine derivative in improving the clinical picture, decreasing viral load and length of hospital stay in patients with COVID-19 [Internet]. 2022 ;[citado 2024 jun. 25 ] Available from: https://www.teses.usp.br/teses/disponiveis/25/25149/tde-26012023-122706/
Artigo de periodico
Triazole-containing heterocycles: privileged scaffolds in anti-Trypanosoma cruzi drug development (2022)
Pone, Kamdem Boniface ; Dalhatou, Sadou; Paumo, Hugues Kamdem ; Seru, Lebogang Maureen Katata ; Ferreira, Elizabeth Igne
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.
APA
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
Artigo de periodico
Synthesis and structure−activity relationships of imidazopyridine/pyrimidine- and furopyridine‐based anti‐infective agents against Trypanosomiases (2021)
Silva, Daniel G.; Junker, Anna; Melo, Shaiani Maria Gil de ; Fumagalli, Fernando; Gillespie, J. Robert; Molasky, Nora; Buckner, Frederick S.; Matheeussen, An; Caljon, Guy; Maes, Louis; Emery, Flavio da Silva
Source: ChemMedChem. Unidade: FCFRP
Subjects: TRIPANOSSOMICIDAS, ANTI-INFECCIOSOS, COMPOSTOS HETEROCÍCLICOS, DOENÇAS NEGLIGENCIADAS
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SILVA, Daniel G. et al. Synthesis and structure−activity relationships of imidazopyridine/pyrimidine- and furopyridine‐based anti‐infective agents against Trypanosomiases. ChemMedChem, v. 16, n. 6, p. 966-975, 2021Tradução . . Disponível em: https://doi.org/10.1002/cmdc.202000616. Acesso em: 25 jun. 2024.
APA
Silva, D. G., Junker, A., Melo, S. M. G. de, Fumagalli, F., Gillespie, J. R., Molasky, N., et al. (2021). Synthesis and structure−activity relationships of imidazopyridine/pyrimidine- and furopyridine‐based anti‐infective agents against Trypanosomiases. ChemMedChem, 16( 6), 966-975. doi:10.1002/cmdc.202000616
NLM
Silva DG, Junker A, Melo SMG de, Fumagalli F, Gillespie JR, Molasky N, Buckner FS, Matheeussen A, Caljon G, Maes L, Emery F da S. Synthesis and structure−activity relationships of imidazopyridine/pyrimidine- and furopyridine‐based anti‐infective agents against Trypanosomiases [Internet]. ChemMedChem. 2021 ; 16( 6): 966-975.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1002/cmdc.202000616
Vancouver
Silva DG, Junker A, Melo SMG de, Fumagalli F, Gillespie JR, Molasky N, Buckner FS, Matheeussen A, Caljon G, Maes L, Emery F da S. Synthesis and structure−activity relationships of imidazopyridine/pyrimidine- and furopyridine‐based anti‐infective agents against Trypanosomiases [Internet]. ChemMedChem. 2021 ; 16( 6): 966-975.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1002/cmdc.202000616
Artigo de periodico
Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases (2021)
Santos, Thiago dos ; Orenha, Henrique Pereira; Murie, Valter Eduardo ; Vessecchi, Ricardo ; Clososki, Giuliano Cesar
Source: Organic Letters. Unidades: FFCLRP, FCFRP
Subjects: COMPOSTOS DE NITROGÊNIO, NITRILAS, QUÍMICA ORGÂNICA, COMPOSTOS HETEROCÍCLICOS
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ABNT
SANTOS, Thiago dos et al. Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases. Organic Letters, v. 23, n. 19, p. 7396-7400, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.1c02572. Acesso em: 25 jun. 2024.
APA
Santos, T. dos, Orenha, H. P., Murie, V. E., Vessecchi, R., & Clososki, G. C. (2021). Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases. Organic Letters, 23( 19), 7396-7400. doi:10.1021/acs.orglett.1c02572
NLM
Santos T dos, Orenha HP, Murie VE, Vessecchi R, Clososki GC. Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases [Internet]. Organic Letters. 2021 ; 23( 19): 7396-7400.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1021/acs.orglett.1c02572
Vancouver
Santos T dos, Orenha HP, Murie VE, Vessecchi R, Clososki GC. Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases [Internet]. Organic Letters. 2021 ; 23( 19): 7396-7400.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1021/acs.orglett.1c02572
Artigo de periodico
A comprehensive study of structural, non-covalent interactions and electronic insights into N-aryl substituted thiosemicarbazones via SC-XRD and first-principles DFT approach (2021)
Pasha, Anam Rubbab; Khalid, Muhammad; Shafiq, Zahid; Khan, Muhammad Usman; Naseer, Muhammad Moazzam; Tahir, Muhammad Nawaz; Hussain, Riaz; Braga, Ataualpa Albert Carmo ; Jawaria, Rifat
Source: Journal of Molecular Structure. Unidade: IQ
Assunto: COMPOSTOS HETEROCÍCLICOS
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ABNT
PASHA, Anam Rubbab et al. A comprehensive study of structural, non-covalent interactions and electronic insights into N-aryl substituted thiosemicarbazones via SC-XRD and first-principles DFT approach. Journal of Molecular Structure, v. 1230, p. 1-11 art. 129852, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2020.129852. Acesso em: 25 jun. 2024.
APA
Pasha, A. R., Khalid, M., Shafiq, Z., Khan, M. U., Naseer, M. M., Tahir, M. N., et al. (2021). A comprehensive study of structural, non-covalent interactions and electronic insights into N-aryl substituted thiosemicarbazones via SC-XRD and first-principles DFT approach. Journal of Molecular Structure, 1230, 1-11 art. 129852. doi:10.1016/j.molstruc.2020.129852
NLM
Pasha AR, Khalid M, Shafiq Z, Khan MU, Naseer MM, Tahir MN, Hussain R, Braga AAC, Jawaria R. A comprehensive study of structural, non-covalent interactions and electronic insights into N-aryl substituted thiosemicarbazones via SC-XRD and first-principles DFT approach [Internet]. Journal of Molecular Structure. 2021 ; 1230 1-11 art. 129852.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1016/j.molstruc.2020.129852
Vancouver
Pasha AR, Khalid M, Shafiq Z, Khan MU, Naseer MM, Tahir MN, Hussain R, Braga AAC, Jawaria R. A comprehensive study of structural, non-covalent interactions and electronic insights into N-aryl substituted thiosemicarbazones via SC-XRD and first-principles DFT approach [Internet]. Journal of Molecular Structure. 2021 ; 1230 1-11 art. 129852.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1016/j.molstruc.2020.129852
Artigo de periodico
Trypanocidal activity of new 1,6-diphenyl-1H-pyrazolo[3,4-b]pyridine derivatives: synthesis, in vitro and in vivo studies (2021)
Ribeiro, Joana Lucius de Sousa; Soares, Júlio César de Araujo Vanelis; Portapilla, Gisele Bulhões; Providello, Maiara Voltarelli ; Lima, Camilo Henrique da Silva; Muri, Estela Maris Freitas; Albuquerque, Sérgio de ; Dias, Luiza Rosaria Sousa
Source: Bioorganic & Medicinal Chemistry. Unidade: FCFRP
Subjects: DOENÇA DE CHAGAS, ANIMAIS PARASITOS, CIRCULAÇÃO SANGUÍNEA, COMPOSTOS HETEROCÍCLICOS
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ABNT
RIBEIRO, Joana Lucius de Sousa et al. Trypanocidal activity of new 1,6-diphenyl-1H-pyrazolo[3,4-b]pyridine derivatives: synthesis, in vitro and in vivo studies. Bioorganic & Medicinal Chemistry, v. 29, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2020.115855. Acesso em: 25 jun. 2024.
APA
Ribeiro, J. L. de S., Soares, J. C. de A. V., Portapilla, G. B., Providello, M. V., Lima, C. H. da S., Muri, E. M. F., et al. (2021). Trypanocidal activity of new 1,6-diphenyl-1H-pyrazolo[3,4-b]pyridine derivatives: synthesis, in vitro and in vivo studies. Bioorganic & Medicinal Chemistry, 29. doi:10.1016/j.bmc.2020.115855
NLM
Ribeiro JL de S, Soares JC de AV, Portapilla GB, Providello MV, Lima CH da S, Muri EMF, Albuquerque S de, Dias LRS. Trypanocidal activity of new 1,6-diphenyl-1H-pyrazolo[3,4-b]pyridine derivatives: synthesis, in vitro and in vivo studies [Internet]. Bioorganic & Medicinal Chemistry. 2021 ; 29[citado 2024 jun. 25 ] Available from: https://doi.org/10.1016/j.bmc.2020.115855
Vancouver
Ribeiro JL de S, Soares JC de AV, Portapilla GB, Providello MV, Lima CH da S, Muri EMF, Albuquerque S de, Dias LRS. Trypanocidal activity of new 1,6-diphenyl-1H-pyrazolo[3,4-b]pyridine derivatives: synthesis, in vitro and in vivo studies [Internet]. Bioorganic & Medicinal Chemistry. 2021 ; 29[citado 2024 jun. 25 ] Available from: https://doi.org/10.1016/j.bmc.2020.115855
Artigo de periodico
Synthesis of cardanol-based 1,2,3-triazoles as potential green agents against neoplastic cells (2021)
Braga, Felipe C.; Ojeda, Mariah; Perdomo, Renata T.; Albuquerque, Sérgio de ; Rafique, Jamal; Lima, Dênis P. de; Beatriz, Adilson
Source: Sustainable Chemistry and Pharmacy. Unidade: FCFRP
Subjects: CARCINOMA, COMPOSTOS HETEROCÍCLICOS, LIPÍDEOS
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ABNT
BRAGA, Felipe C. et al. Synthesis of cardanol-based 1,2,3-triazoles as potential green agents against neoplastic cells. Sustainable Chemistry and Pharmacy, v. 20, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.scp.2021.100408. Acesso em: 25 jun. 2024.
APA
Braga, F. C., Ojeda, M., Perdomo, R. T., Albuquerque, S. de, Rafique, J., Lima, D. P. de, & Beatriz, A. (2021). Synthesis of cardanol-based 1,2,3-triazoles as potential green agents against neoplastic cells. Sustainable Chemistry and Pharmacy, 20. doi:10.1016/j.scp.2021.100408
NLM
Braga FC, Ojeda M, Perdomo RT, Albuquerque S de, Rafique J, Lima DP de, Beatriz A. Synthesis of cardanol-based 1,2,3-triazoles as potential green agents against neoplastic cells [Internet]. Sustainable Chemistry and Pharmacy. 2021 ; 20[citado 2024 jun. 25 ] Available from: https://doi.org/10.1016/j.scp.2021.100408
Vancouver
Braga FC, Ojeda M, Perdomo RT, Albuquerque S de, Rafique J, Lima DP de, Beatriz A. Synthesis of cardanol-based 1,2,3-triazoles as potential green agents against neoplastic cells [Internet]. Sustainable Chemistry and Pharmacy. 2021 ; 20[citado 2024 jun. 25 ] Available from: https://doi.org/10.1016/j.scp.2021.100408
Artigo de periodico
Regioselective functionalization of ester-, amide-, carbonate-, and carbamate-substituted 2-phenyl-2-oxazolines with mixed lithium–magnesium amides (2021)
Bozzini, Leandro Alves; Santos, Thiago dos ; Murie, Valter Eduardo ; Mello, Murilo B. M.; Vessecchi, Ricardo ; Clososki, Giuliano Cesar
Source: The Journal of Organic Chemistry. Unidades: FFCLRP, FCFRP
Subjects: COMPOSTOS HETEROCÍCLICOS, QUÍMICA MÉDICA, PRODUTOS NATURAIS, MEDICAMENTO
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ABNT
BOZZINI, Leandro Alves et al. Regioselective functionalization of ester-, amide-, carbonate-, and carbamate-substituted 2-phenyl-2-oxazolines with mixed lithium–magnesium amides. The Journal of Organic Chemistry, v. 86, n. 1, p. 1204-1215, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.0c02369. Acesso em: 25 jun. 2024.
APA
Bozzini, L. A., Santos, T. dos, Murie, V. E., Mello, M. B. M., Vessecchi, R., & Clososki, G. C. (2021). Regioselective functionalization of ester-, amide-, carbonate-, and carbamate-substituted 2-phenyl-2-oxazolines with mixed lithium–magnesium amides. The Journal of Organic Chemistry, 86( 1), 1204-1215. doi:10.1021/acs.joc.0c02369
NLM
Bozzini LA, Santos T dos, Murie VE, Mello MBM, Vessecchi R, Clososki GC. Regioselective functionalization of ester-, amide-, carbonate-, and carbamate-substituted 2-phenyl-2-oxazolines with mixed lithium–magnesium amides [Internet]. The Journal of Organic Chemistry. 2021 ; 86( 1): 1204-1215.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1021/acs.joc.0c02369
Vancouver
Bozzini LA, Santos T dos, Murie VE, Mello MBM, Vessecchi R, Clososki GC. Regioselective functionalization of ester-, amide-, carbonate-, and carbamate-substituted 2-phenyl-2-oxazolines with mixed lithium–magnesium amides [Internet]. The Journal of Organic Chemistry. 2021 ; 86( 1): 1204-1215.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1021/acs.joc.0c02369
Tese (Doutorado)
Novos métodos de pós funcionalização de BODIPYs e suas aplicações como sondas fluorescentes (2021)
Melo, Shaiani Maria Gil de ; Emery, Flavio da Silva
Unidade: FCFRP
Subjects: FLUORESCÊNCIA, AMÔNIA, COMPOSTOS ORGÂNICOS, COMPOSTOS HETEROCÍCLICOS
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ABNT
MELO, Shaiani Maria Gil de e EMERY, Flavio da Silva. Novos métodos de pós funcionalização de BODIPYs e suas aplicações como sondas fluorescentes. 2021. Tese (Doutorado) – Universidade de São Paulo, Ribeirão Preto, 2021. Disponível em: https://www.teses.usp.br/teses/disponiveis/60/60138/tde-22032022-090935/. Acesso em: 25 jun. 2024.
APA
Melo, S. M. G. de, & Emery, F. da S. (2021). Novos métodos de pós funcionalização de BODIPYs e suas aplicações como sondas fluorescentes (Tese (Doutorado). Universidade de São Paulo, Ribeirão Preto. Recuperado de https://www.teses.usp.br/teses/disponiveis/60/60138/tde-22032022-090935/
NLM
Melo SMG de, Emery F da S. Novos métodos de pós funcionalização de BODIPYs e suas aplicações como sondas fluorescentes [Internet]. 2021 ;[citado 2024 jun. 25 ] Available from: https://www.teses.usp.br/teses/disponiveis/60/60138/tde-22032022-090935/
Vancouver
Melo SMG de, Emery F da S. Novos métodos de pós funcionalização de BODIPYs e suas aplicações como sondas fluorescentes [Internet]. 2021 ;[citado 2024 jun. 25 ] Available from: https://www.teses.usp.br/teses/disponiveis/60/60138/tde-22032022-090935/
Artigo de periodico
Conformational analysis and electronic interactions of some 2- [2 -(4 -sustituted-phenylsulfanyl)-acetyl]-5-substituted furans and 2- [2 -(phenylselanyl)-acetyl]-5-methylfuran (2021)
Valença, Jéssica; Olivato, Paulo Roberto ; Rodrigues, Daniel Nopper Silva ; Batista, Patrick Rodrigues ; Ducati, Lucas Colucci ; Colle, Maurizio Dal
Source: Journal of Molecular Structure. Unidade: IQ
Subjects: ESPECTROSCOPIA INFRAVERMELHA, COMPOSTOS HETEROCÍCLICOS, SOLVENTE
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ABNT
VALENÇA, Jéssica et al. Conformational analysis and electronic interactions of some 2- [2 -(4 -sustituted-phenylsulfanyl)-acetyl]-5-substituted furans and 2- [2 -(phenylselanyl)-acetyl]-5-methylfuran. Journal of Molecular Structure, v. 1225, p. 1-15 art. 129088, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2020.129088. Acesso em: 25 jun. 2024.
APA
Valença, J., Olivato, P. R., Rodrigues, D. N. S., Batista, P. R., Ducati, L. C., & Colle, M. D. (2021). Conformational analysis and electronic interactions of some 2- [2 -(4 -sustituted-phenylsulfanyl)-acetyl]-5-substituted furans and 2- [2 -(phenylselanyl)-acetyl]-5-methylfuran. Journal of Molecular Structure, 1225, 1-15 art. 129088. doi:10.1016/j.molstruc.2020.129088
NLM
Valença J, Olivato PR, Rodrigues DNS, Batista PR, Ducati LC, Colle MD. Conformational analysis and electronic interactions of some 2- [2 -(4 -sustituted-phenylsulfanyl)-acetyl]-5-substituted furans and 2- [2 -(phenylselanyl)-acetyl]-5-methylfuran [Internet]. Journal of Molecular Structure. 2021 ; 1225 1-15 art. 129088.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1016/j.molstruc.2020.129088
Vancouver
Valença J, Olivato PR, Rodrigues DNS, Batista PR, Ducati LC, Colle MD. Conformational analysis and electronic interactions of some 2- [2 -(4 -sustituted-phenylsulfanyl)-acetyl]-5-substituted furans and 2- [2 -(phenylselanyl)-acetyl]-5-methylfuran [Internet]. Journal of Molecular Structure. 2021 ; 1225 1-15 art. 129088.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1016/j.molstruc.2020.129088
Artigo de periodico
Synthesis and anticancer properties of ‘azole’ based chemotherapeutics as emerging chemical moieties: a comprehensive review (2021)
Prasher, Parteek ; Sharma, Mousmee ; Zacconi, Flavia ; Gupt, Gaurav ; Aljabali, Alaa A ; Mishra, Vijay ; Tambuwala, Murtaza M ; Kapoor, Deepak N ; Negi, Poonam ; Pinto, Terezinha de Jesus Andreoli ; Singh, Inderbir ; Chellappan, Dinesh Kumar ; Dua, Kamal
Source: Current Organic Chemistry. Unidade: FCF
Subjects: QUIMIOTERÁPICOS, COMPOSTOS HETEROCÍCLICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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.
APA
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

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