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Artigo de periodico
Sustainable synthesis of benzylidenemalononitrile compounds under microwave irradiation (2022)
Jimenez, David Esteban Quintero ; Zanin, Lucas Lima ; Ferreira, Irlon Maciel ; Deflon, Victor Marcelo ; Diniz, Luan F. ; Ellena, Javier ; Haiduke, Roberto Luiz Andrade ; Porto, Andre Luiz Meleiro
Source: Current Organic Chemistry. Unidades: IQSC, IFSC
Subjects: DIFRAÇÃO POR RAIOS X, FOTOQUÍMICA, QUÍMICA VERDE
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ABNT
JIMENEZ, David Esteban Quintero et al. Sustainable synthesis of benzylidenemalononitrile compounds under microwave irradiation. Current Organic Chemistry, v. 26, n. 16, p. 1552-1564 + supplementary material, 2022Tradução . . Disponível em: https://doi.org/10.2174/1385272827666221125091631. Acesso em: 05 jun. 2024.
APA
Jimenez, D. E. Q., Zanin, L. L., Ferreira, I. M., Deflon, V. M., Diniz, L. F., Ellena, J., et al. (2022). Sustainable synthesis of benzylidenemalononitrile compounds under microwave irradiation. Current Organic Chemistry, 26( 16), 1552-1564 + supplementary material. doi:10.2174/1385272827666221125091631
NLM
Jimenez DEQ, Zanin LL, Ferreira IM, Deflon VM, Diniz LF, Ellena J, Haiduke RLA, Porto ALM. Sustainable synthesis of benzylidenemalononitrile compounds under microwave irradiation [Internet]. Current Organic Chemistry. 2022 ; 26( 16): 1552-1564 + supplementary material.[citado 2024 jun. 05 ] Available from: https://doi.org/10.2174/1385272827666221125091631
Vancouver
Jimenez DEQ, Zanin LL, Ferreira IM, Deflon VM, Diniz LF, Ellena J, Haiduke RLA, Porto ALM. Sustainable synthesis of benzylidenemalononitrile compounds under microwave irradiation [Internet]. Current Organic Chemistry. 2022 ; 26( 16): 1552-1564 + supplementary material.[citado 2024 jun. 05 ] Available from: https://doi.org/10.2174/1385272827666221125091631
Artigo de periodico
Overview of PCTK3/CDK18: A Cyclin-Dependent Kinase Involved in Specific Functions in Post-Mitotic Cells (2021)
Pepino, Rebeka de Oliveira ; Coelho, Fernanda; Janku, Tatiane Aparecida Buzanello ; Alencar, Diandra Pinheiro ; Azevedo Jr, Walter Figueira de ; Canduri, Fernanda
Source: Current Medicinal Chemistry. Unidade: IQSC
Subjects: BIOQUÍMICA, BIOLOGIA MOLECULAR, NEOPLASIAS, DOENÇA DE ALZHEIMER
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ABNT
PEPINO, Rebeka de Oliveira et al. Overview of PCTK3/CDK18: A Cyclin-Dependent Kinase Involved in Specific Functions in Post-Mitotic Cells. Current Medicinal Chemistry, v. 28, p. 6846-6865, 2021Tradução . . Disponível em: https://doi.org/10.2174/092986732866621032912214. Acesso em: 05 jun. 2024.
APA
Pepino, R. de O., Coelho, F., Janku, T. A. B., Alencar, D. P., Azevedo Jr, W. F. de, & Canduri, F. (2021). Overview of PCTK3/CDK18: A Cyclin-Dependent Kinase Involved in Specific Functions in Post-Mitotic Cells. Current Medicinal Chemistry, 28, 6846-6865. doi:10.2174/092986732866621032912214
NLM
Pepino R de O, Coelho F, Janku TAB, Alencar DP, Azevedo Jr WF de, Canduri F. Overview of PCTK3/CDK18: A Cyclin-Dependent Kinase Involved in Specific Functions in Post-Mitotic Cells [Internet]. Current Medicinal Chemistry. 2021 ; 28 6846-6865.[citado 2024 jun. 05 ] Available from: https://doi.org/10.2174/092986732866621032912214
Vancouver
Pepino R de O, Coelho F, Janku TAB, Alencar DP, Azevedo Jr WF de, Canduri F. Overview of PCTK3/CDK18: A Cyclin-Dependent Kinase Involved in Specific Functions in Post-Mitotic Cells [Internet]. Current Medicinal Chemistry. 2021 ; 28 6846-6865.[citado 2024 jun. 05 ] Available from: https://doi.org/10.2174/092986732866621032912214
Artigo de periodico
The Effect of Dipeptidyl Nitrile Derivatives on Pancreatic Ductal Adenocarcinoma Cells In Vitro (2021)
Botelho, Sabrina Mendes ; Rocho, Fernanda dos Reis ; Cianni, Lorenzo ; Montanari, Carlos Alberto ; Leitão, Andrei
Source: Current Chemical Biology. Unidade: IQSC
Subjects: CÉLULAS, ANTINEOPLÁSICOS, TERAPIA COMBINADA
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ABNT
BOTELHO, Sabrina Mendes et al. The Effect of Dipeptidyl Nitrile Derivatives on Pancreatic Ductal Adenocarcinoma Cells In Vitro. Current Chemical Biology, v. 15, n. 4, p. 278 - 286, 2021Tradução . . Disponível em: https://doi.org/10.2174/2212796815666211214111243. Acesso em: 05 jun. 2024.
APA
Botelho, S. M., Rocho, F. dos R., Cianni, L., Montanari, C. A., & Leitão, A. (2021). The Effect of Dipeptidyl Nitrile Derivatives on Pancreatic Ductal Adenocarcinoma Cells In Vitro. Current Chemical Biology, 15( 4), 278 - 286. doi:10.2174/2212796815666211214111243
NLM
Botelho SM, Rocho F dos R, Cianni L, Montanari CA, Leitão A. The Effect of Dipeptidyl Nitrile Derivatives on Pancreatic Ductal Adenocarcinoma Cells In Vitro [Internet]. Current Chemical Biology. 2021 ;15( 4): 278 - 286.[citado 2024 jun. 05 ] Available from: https://doi.org/10.2174/2212796815666211214111243
Vancouver
Botelho SM, Rocho F dos R, Cianni L, Montanari CA, Leitão A. The Effect of Dipeptidyl Nitrile Derivatives on Pancreatic Ductal Adenocarcinoma Cells In Vitro [Internet]. Current Chemical Biology. 2021 ;15( 4): 278 - 286.[citado 2024 jun. 05 ] Available from: https://doi.org/10.2174/2212796815666211214111243
Artigo de periodico
Antioxidant, Antitumor and Bactericidal Activities of Ethyl Gallate Quinoxalines (2020)
Lima, Rafaely Nascimento ; Gonçalves, Jaqueline R.; Silva, Valdenizia R; Santos, Luciano de S; Bezerra, Daniel P; Soares, Milena B. P; Leitão, Andrei ; Porto, Andre Luiz Meleiro
Source: Current Bioactive Compounds. Unidades: IQSC, INTER IFSC/IQSC/ICMC
Subjects: NEOPLASIAS, ANTIOXIDANTES, BACTERICIDAS
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ABNT
LIMA, Rafaely Nascimento et al. Antioxidant, Antitumor and Bactericidal Activities of Ethyl Gallate Quinoxalines. Current Bioactive Compounds, v. 16, n. 6, p. 900-910, 2020Tradução . . Disponível em: https://doi.org/10.2174/1573407215666190318144105. Acesso em: 05 jun. 2024.
APA
Lima, R. N., Gonçalves, J. R., Silva, V. R., Santos, L. de S., Bezerra, D. P., Soares, M. B. P., et al. (2020). Antioxidant, Antitumor and Bactericidal Activities of Ethyl Gallate Quinoxalines. Current Bioactive Compounds, 16( 6), 900-910. doi:10.2174/1573407215666190318144105
NLM
Lima RN, Gonçalves JR, Silva VR, Santos L de S, Bezerra DP, Soares MBP, Leitão A, Porto ALM. Antioxidant, Antitumor and Bactericidal Activities of Ethyl Gallate Quinoxalines [Internet]. Current Bioactive Compounds. 2020 ; 16( 6): 900-910.[citado 2024 jun. 05 ] Available from: https://doi.org/10.2174/1573407215666190318144105
Vancouver
Lima RN, Gonçalves JR, Silva VR, Santos L de S, Bezerra DP, Soares MBP, Leitão A, Porto ALM. Antioxidant, Antitumor and Bactericidal Activities of Ethyl Gallate Quinoxalines [Internet]. Current Bioactive Compounds. 2020 ; 16( 6): 900-910.[citado 2024 jun. 05 ] Available from: https://doi.org/10.2174/1573407215666190318144105
Artigo de periodico
Application of Amine-based Ru Compounds in the Olefin Metathesis of Methyl Eugenol: A Comparison with Grubbs Catalysts (2020)
Sousa, Denise A.; Meneses, Paulo S.; Gois, Patrik D. S ; Silva, Eliada Andrade da ; Carvalho Junior, Valdemiro Pereira de ; Lima Neto, Benedito dos Santos ; Sá, José L. Silva
Source: Letters in Organic Chemistry. Unidade: IQSC
Subjects: QUÍMICA INORGÂNICA, QUÍMICA ANALÍTICA, RUTÊNIO
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ABNT
SOUSA, Denise A. et al. Application of Amine-based Ru Compounds in the Olefin Metathesis of Methyl Eugenol: A Comparison with Grubbs Catalysts. Letters in Organic Chemistry, v. 17, n. 8, p. 596-602 2020, 2020Tradução . . Disponível em: https://doi.org/10.2174/1570178617666191127102552. Acesso em: 05 jun. 2024.
APA
Sousa, D. A., Meneses, P. S., Gois, P. D. S., Silva, E. A. da, Carvalho Junior, V. P. de, Lima Neto, B. dos S., & Sá, J. L. S. (2020). Application of Amine-based Ru Compounds in the Olefin Metathesis of Methyl Eugenol: A Comparison with Grubbs Catalysts. Letters in Organic Chemistry, 17( 8), 596-602 2020. doi:10.2174/1570178617666191127102552
NLM
Sousa DA, Meneses PS, Gois PDS, Silva EA da, Carvalho Junior VP de, Lima Neto B dos S, Sá JLS. Application of Amine-based Ru Compounds in the Olefin Metathesis of Methyl Eugenol: A Comparison with Grubbs Catalysts [Internet]. Letters in Organic Chemistry. 2020 ; 17( 8): 596-602 2020.[citado 2024 jun. 05 ] Available from: https://doi.org/10.2174/1570178617666191127102552
Vancouver
Sousa DA, Meneses PS, Gois PDS, Silva EA da, Carvalho Junior VP de, Lima Neto B dos S, Sá JLS. Application of Amine-based Ru Compounds in the Olefin Metathesis of Methyl Eugenol: A Comparison with Grubbs Catalysts [Internet]. Letters in Organic Chemistry. 2020 ; 17( 8): 596-602 2020.[citado 2024 jun. 05 ] Available from: https://doi.org/10.2174/1570178617666191127102552
Artigo de periodico
Discovery of 2-aminopyridine Derivatives with Antichagasic and Antileishmanial Activity Using Phenotypic Assays (2020)
Tezuka, Daiane Yukie; Albuquerque, Sérgio de ; Montanari, Carlos Alberto ; Leitão, Andrei
Source: Letters in Drug Design and Discovery. Unidades: IQSC, BIOENGENHARIA, FCFRP
Assunto: LEISHMANIA
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ABNT
TEZUKA, Daiane Yukie et al. Discovery of 2-aminopyridine Derivatives with Antichagasic and Antileishmanial Activity Using Phenotypic Assays. Letters in Drug Design and Discovery, v. 17, n. 7, p. 867-872, 2020Tradução . . Disponível em: https://doi.org/10.2174/1570180816666191204105232. Acesso em: 05 jun. 2024.
APA
Tezuka, D. Y., Albuquerque, S. de, Montanari, C. A., & Leitão, A. (2020). Discovery of 2-aminopyridine Derivatives with Antichagasic and Antileishmanial Activity Using Phenotypic Assays. Letters in Drug Design and Discovery, 17( 7), 867-872. doi:10.2174/1570180816666191204105232
NLM
Tezuka DY, Albuquerque S de, Montanari CA, Leitão A. Discovery of 2-aminopyridine Derivatives with Antichagasic and Antileishmanial Activity Using Phenotypic Assays [Internet]. Letters in Drug Design and Discovery. 2020 ; 17( 7): 867-872.[citado 2024 jun. 05 ] Available from: https://doi.org/10.2174/1570180816666191204105232
Vancouver
Tezuka DY, Albuquerque S de, Montanari CA, Leitão A. Discovery of 2-aminopyridine Derivatives with Antichagasic and Antileishmanial Activity Using Phenotypic Assays [Internet]. Letters in Drug Design and Discovery. 2020 ; 17( 7): 867-872.[citado 2024 jun. 05 ] Available from: https://doi.org/10.2174/1570180816666191204105232
Artigo de periodico
Molecular Chaperones Involved in Protein Recovery from Aggregates are Present in Protozoa Causative of Malaria and Leishmaniasis (2019)
Batista, Fernanda A. H; Dores-Silva, Paulo R; Borges, Julio Cesar
Source: Current Proteomics. Unidade: IQSC
Assunto: PROTEÍNAS
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ABNT
BATISTA, Fernanda A. H e DORES-SILVA, Paulo R e BORGES, Julio Cesar. Molecular Chaperones Involved in Protein Recovery from Aggregates are Present in Protozoa Causative of Malaria and Leishmaniasis. Current Proteomics, v. 16, p. 12-21, 2019Tradução . . Disponível em: https://doi.org/10.2174/1570164615666180626123823. Acesso em: 05 jun. 2024.
APA
Batista, F. A. H., Dores-Silva, P. R., & Borges, J. C. (2019). Molecular Chaperones Involved in Protein Recovery from Aggregates are Present in Protozoa Causative of Malaria and Leishmaniasis. Current Proteomics, 16, 12-21. doi:10.2174/1570164615666180626123823
NLM
Batista FAH, Dores-Silva PR, Borges JC. Molecular Chaperones Involved in Protein Recovery from Aggregates are Present in Protozoa Causative of Malaria and Leishmaniasis [Internet]. Current Proteomics. 2019 ;16 12-21.[citado 2024 jun. 05 ] Available from: https://doi.org/10.2174/1570164615666180626123823
Vancouver
Batista FAH, Dores-Silva PR, Borges JC. Molecular Chaperones Involved in Protein Recovery from Aggregates are Present in Protozoa Causative of Malaria and Leishmaniasis [Internet]. Current Proteomics. 2019 ;16 12-21.[citado 2024 jun. 05 ] Available from: https://doi.org/10.2174/1570164615666180626123823
Artigo de periodico
Biological activity and physicochemical properties of dipeptidyl nitrile derivatives against pancreatic ductal adenocarcinoma cells (2019)
Quilles Junior, José Carlos ; Bernardi, Murillo Dorileo Leite; Batista, Pedro Henrique J; Silva, Samelyn da Costa Martins ; Rocha, Camila M.R.; Montanari, Carlos Alberto ; Leitão, Andrei
Source: Anti-Cancer Agents in Medicinal Chemistry. Unidades: IQSC, BIOENGENHARIA
Subjects: NEOPLASIAS, PÂNCREAS, MEDICAMENTO, INIBIÇÃO
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ABNT
QUILLES JUNIOR, José Carlos et al. Biological activity and physicochemical properties of dipeptidyl nitrile derivatives against pancreatic ductal adenocarcinoma cells. Anti-Cancer Agents in Medicinal Chemistry, v. 19, p. 112-120, 2019Tradução . . Disponível em: https://doi.org/10.2174/1871520618666181029141649. Acesso em: 05 jun. 2024.
APA
Quilles Junior, J. C., Bernardi, M. D. L., Batista, P. H. J., Silva, S. da C. M., Rocha, C. M. R., Montanari, C. A., & Leitão, A. (2019). Biological activity and physicochemical properties of dipeptidyl nitrile derivatives against pancreatic ductal adenocarcinoma cells. Anti-Cancer Agents in Medicinal Chemistry, 19, 112-120. doi:10.2174/1871520618666181029141649
NLM
Quilles Junior JC, Bernardi MDL, Batista PHJ, Silva S da CM, Rocha CMR, Montanari CA, Leitão A. Biological activity and physicochemical properties of dipeptidyl nitrile derivatives against pancreatic ductal adenocarcinoma cells [Internet]. Anti-Cancer Agents in Medicinal Chemistry. 2019 ; 19 112-120.[citado 2024 jun. 05 ] Available from: https://doi.org/10.2174/1871520618666181029141649
Vancouver
Quilles Junior JC, Bernardi MDL, Batista PHJ, Silva S da CM, Rocha CMR, Montanari CA, Leitão A. Biological activity and physicochemical properties of dipeptidyl nitrile derivatives against pancreatic ductal adenocarcinoma cells [Internet]. Anti-Cancer Agents in Medicinal Chemistry. 2019 ; 19 112-120.[citado 2024 jun. 05 ] Available from: https://doi.org/10.2174/1871520618666181029141649
Artigo de periodico-carta/editorial
Chaperones & Co:: roles in Protein/Nucleic Acid Homeostasis. [Editorial] (2019)
Borges, Julio Cesar
Source: Current Proteomics. Unidade: IQSC
Assunto: PROTEÍNAS
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ABNT
BORGES, Julio Cesar. Chaperones & Co:: roles in Protein/Nucleic Acid Homeostasis. [Editorial]. Current Proteomics. Sharjah, United Arab Emirates: Instituto de Química de São Carlos, Universidade de São Paulo. Disponível em: http://www.eurekaselect.com/166739/article. Acesso em: 05 jun. 2024. , 2019
APA
Borges, J. C. (2019). Chaperones & Co:: roles in Protein/Nucleic Acid Homeostasis. [Editorial]. Current Proteomics. Sharjah, United Arab Emirates: Instituto de Química de São Carlos, Universidade de São Paulo. doi:10.2174/157016461601181029143029
NLM
Borges JC. Chaperones & Co:: roles in Protein/Nucleic Acid Homeostasis. [Editorial] [Internet]. Current Proteomics. 2019 ;16( 1):3-4.[citado 2024 jun. 05 ] Available from: http://www.eurekaselect.com/166739/article
Vancouver
Borges JC. Chaperones & Co:: roles in Protein/Nucleic Acid Homeostasis. [Editorial] [Internet]. Current Proteomics. 2019 ;16( 1):3-4.[citado 2024 jun. 05 ] Available from: http://www.eurekaselect.com/166739/article
Artigo de periodico
Structure based design, synthesis, and evaluation of potential inhibitors of steroid sulfatase (2014)
Costa, E. V.; Sousa, E.; Choosang, K.; Singh, S.; Rocha, J.; Lima, R. T.; Pakkong, P.; Ahmed, S.; Vasconcelos, M. H.; Montanari, Carlos Alberto ; Pinto, M. M.
Source: Current Topics in Medicinal Chemistry. Unidade: IQSC
Assunto: QUÍMICA MÉDICA
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ABNT
COSTA, E. V. et al. Structure based design, synthesis, and evaluation of potential inhibitors of steroid sulfatase. Current Topics in Medicinal Chemistry, v. 14, n. 8, p. 1033-1044, 2014Tradução . . Disponível em: https://repositorio.usp.br/directbitstream/9681e089-d632-4260-8666-e505cc746359/P15026.pdf. Acesso em: 05 jun. 2024.
APA
Costa, E. V., Sousa, E., Choosang, K., Singh, S., Rocha, J., Lima, R. T., et al. (2014). Structure based design, synthesis, and evaluation of potential inhibitors of steroid sulfatase. Current Topics in Medicinal Chemistry, 14( 8), 1033-1044. Recuperado de https://repositorio.usp.br/directbitstream/9681e089-d632-4260-8666-e505cc746359/P15026.pdf
NLM
Costa EV, Sousa E, Choosang K, Singh S, Rocha J, Lima RT, Pakkong P, Ahmed S, Vasconcelos MH, Montanari CA, Pinto MM. Structure based design, synthesis, and evaluation of potential inhibitors of steroid sulfatase [Internet]. Current Topics in Medicinal Chemistry. 2014 ; 14( 8): 1033-1044.[citado 2024 jun. 05 ] Available from: https://repositorio.usp.br/directbitstream/9681e089-d632-4260-8666-e505cc746359/P15026.pdf
Vancouver
Costa EV, Sousa E, Choosang K, Singh S, Rocha J, Lima RT, Pakkong P, Ahmed S, Vasconcelos MH, Montanari CA, Pinto MM. Structure based design, synthesis, and evaluation of potential inhibitors of steroid sulfatase [Internet]. Current Topics in Medicinal Chemistry. 2014 ; 14( 8): 1033-1044.[citado 2024 jun. 05 ] Available from: https://repositorio.usp.br/directbitstream/9681e089-d632-4260-8666-e505cc746359/P15026.pdf
Artigo de periodico
Machine learning techniques and drug design (2012)
Gertrudes, J. C; Maltarollo, Vinícius Gonçalves; Silva, R. A.; Oliveira, Patricia Rufino; Honório, Kathia Maria; Silva, Alberico Borges Ferreira da
Source: Current Medicinal Chemistry. Unidades: IQSC, EACH
Assunto: ESTRUTURA MOLECULAR (QUÍMICA TEÓRICA)
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ABNT
GERTRUDES, J. C et al. Machine learning techniques and drug design. Current Medicinal Chemistry, v. 19, n. 25, p. 4289-4297, 2012Tradução . . Disponível em: http://www.ingentaconnect-com.ez67.periodicos.capes.gov.br/content/ben/cmc/2012/00000019/00000025/art00007. Acesso em: 05 jun. 2024.
APA
Gertrudes, J. C., Maltarollo, V. G., Silva, R. A., Oliveira, P. R., Honório, K. M., & Silva, A. B. F. da. (2012). Machine learning techniques and drug design. Current Medicinal Chemistry, 19( 25), 4289-4297. Recuperado de http://www.ingentaconnect-com.ez67.periodicos.capes.gov.br/content/ben/cmc/2012/00000019/00000025/art00007
NLM
Gertrudes JC, Maltarollo VG, Silva RA, Oliveira PR, Honório KM, Silva ABF da. Machine learning techniques and drug design [Internet]. Current Medicinal Chemistry. 2012 ; 19( 25): 4289-4297.[citado 2024 jun. 05 ] Available from: http://www.ingentaconnect-com.ez67.periodicos.capes.gov.br/content/ben/cmc/2012/00000019/00000025/art00007
Vancouver
Gertrudes JC, Maltarollo VG, Silva RA, Oliveira PR, Honório KM, Silva ABF da. Machine learning techniques and drug design [Internet]. Current Medicinal Chemistry. 2012 ; 19( 25): 4289-4297.[citado 2024 jun. 05 ] Available from: http://www.ingentaconnect-com.ez67.periodicos.capes.gov.br/content/ben/cmc/2012/00000019/00000025/art00007
Artigo de periodico
Analysis of molecular targets of mycobacterium tuberculosis by analytical ultrcentrifugation (2011)
Borges, Julio Cesar ; Ramos, C H I
Source: Current Medicinal Chemistry. Unidade: IQSC
Subjects: BIOLOGIA MOLECULAR, BIOQUÍMICA
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ABNT
BORGES, Julio Cesar e RAMOS, C H I. Analysis of molecular targets of mycobacterium tuberculosis by analytical ultrcentrifugation. Current Medicinal Chemistry, v. 18, n. 9, p. 1276-1285, 2011Tradução . . Acesso em: 05 jun. 2024.
APA
Borges, J. C., & Ramos, C. H. I. (2011). Analysis of molecular targets of mycobacterium tuberculosis by analytical ultrcentrifugation. Current Medicinal Chemistry, 18( 9), 1276-1285.
NLM
Borges JC, Ramos CHI. Analysis of molecular targets of mycobacterium tuberculosis by analytical ultrcentrifugation. Current Medicinal Chemistry. 2011 ; 18( 9): 1276-1285.[citado 2024 jun. 05 ]
Vancouver
Borges JC, Ramos CHI. Analysis of molecular targets of mycobacterium tuberculosis by analytical ultrcentrifugation. Current Medicinal Chemistry. 2011 ; 18( 9): 1276-1285.[citado 2024 jun. 05 ]
Artigo de periodico
Tailoring NO donors metallopharmaceuticals: ruthenium nitrosyl ammines and aliphatic teraazamacrocycles (2010)
Tfouni, Elia; Doro, Fábio Gorzoni; Figueiredo, L E; Pereira, J CM; Metzker, Gustavo; Franco, Douglas Wagner
Source: Current Medicinal Chemistry. Unidades: FFCLRP, IQSC
Subjects: QUÍMICA INORGÂNICA, RUTÊNIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TFOUNI, Elia et al. Tailoring NO donors metallopharmaceuticals: ruthenium nitrosyl ammines and aliphatic teraazamacrocycles. Current Medicinal Chemistry, v. 17, p. 3643-3657, 2010Tradução . . Acesso em: 05 jun. 2024.
APA
Tfouni, E., Doro, F. G., Figueiredo, L. E., Pereira, J. C. M., Metzker, G., & Franco, D. W. (2010). Tailoring NO donors metallopharmaceuticals: ruthenium nitrosyl ammines and aliphatic teraazamacrocycles. Current Medicinal Chemistry, 17, 3643-3657.
NLM
Tfouni E, Doro FG, Figueiredo LE, Pereira JCM, Metzker G, Franco DW. Tailoring NO donors metallopharmaceuticals: ruthenium nitrosyl ammines and aliphatic teraazamacrocycles. Current Medicinal Chemistry. 2010 ; 17 3643-3657.[citado 2024 jun. 05 ]
Vancouver
Tfouni E, Doro FG, Figueiredo LE, Pereira JCM, Metzker G, Franco DW. Tailoring NO donors metallopharmaceuticals: ruthenium nitrosyl ammines and aliphatic teraazamacrocycles. Current Medicinal Chemistry. 2010 ; 17 3643-3657.[citado 2024 jun. 05 ]
Artigo de periodico
Two-dimensional QSAR studies on arylpiperazines as high-affinity 5-HT1A receptor ligands (2008)
Weber, Karen C.; Honoria, Kathia M.; Andricopulo, Adriano Defini; Silva, Alberico Borges Ferreira da
Source: Medicinal Chemistry. Unidades: IFSC, IQSC
Subjects: RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA, PLANEJAMENTO DE FÁRMACOS, SEROTONINA, PLACEBOS, PROTEÍNAS, LIGANTES, ANTIDEPRESSIVOS
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ABNT
WEBER, Karen C. et al. Two-dimensional QSAR studies on arylpiperazines as high-affinity 5-HT1A receptor ligands. Medicinal Chemistry, v. 4, n. 4, p. 328-335, 2008Tradução . . Disponível em: https://doi.org/10.2174/157340608784872325. Acesso em: 05 jun. 2024.
APA
Weber, K. C., Honoria, K. M., Andricopulo, A. D., & Silva, A. B. F. da. (2008). Two-dimensional QSAR studies on arylpiperazines as high-affinity 5-HT1A receptor ligands. Medicinal Chemistry, 4( 4), 328-335. doi:10.2174/157340608784872325
NLM
Weber KC, Honoria KM, Andricopulo AD, Silva ABF da. Two-dimensional QSAR studies on arylpiperazines as high-affinity 5-HT1A receptor ligands [Internet]. Medicinal Chemistry. 2008 ; 4( 4): 328-335.[citado 2024 jun. 05 ] Available from: https://doi.org/10.2174/157340608784872325
Vancouver
Weber KC, Honoria KM, Andricopulo AD, Silva ABF da. Two-dimensional QSAR studies on arylpiperazines as high-affinity 5-HT1A receptor ligands [Internet]. Medicinal Chemistry. 2008 ; 4( 4): 328-335.[citado 2024 jun. 05 ] Available from: https://doi.org/10.2174/157340608784872325
Artigo de periodico
In silico prediction of human plasma protein binding using hologram QSAR (2007)
Moda, Tiago L.; Montanari, Carlos Alberto ; Andricopulo, Adriano Defini
Source: Letters in Drug Design and Discovery. Unidades: IQSC, IFSC
Subjects: RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA, PLASMA, FÁRMACOS, HOLOGRAMAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MODA, Tiago L. e MONTANARI, Carlos Alberto e ANDRICOPULO, Adriano Defini. In silico prediction of human plasma protein binding using hologram QSAR. Letters in Drug Design and Discovery, v. 4, n. 7, p. 502-509, 2007Tradução . . Acesso em: 05 jun. 2024.
APA
Moda, T. L., Montanari, C. A., & Andricopulo, A. D. (2007). In silico prediction of human plasma protein binding using hologram QSAR. Letters in Drug Design and Discovery, 4( 7), 502-509.
NLM
Moda TL, Montanari CA, Andricopulo AD. In silico prediction of human plasma protein binding using hologram QSAR. Letters in Drug Design and Discovery. 2007 ; 4( 7): 502-509.[citado 2024 jun. 05 ]
Vancouver
Moda TL, Montanari CA, Andricopulo AD. In silico prediction of human plasma protein binding using hologram QSAR. Letters in Drug Design and Discovery. 2007 ; 4( 7): 502-509.[citado 2024 jun. 05 ]
Artigo de periodico
Hologram quantitative structure-activity relationships for a class of inhibitors of HIV-1 protease (2007)
Ferreira, Leonardo G.; Leitão, Andrei ; Montanari, Carlos Alberto ; Andricopulo, Adriano Defini
Source: Letters in Drug Design and Discovery. Unidades: IQSC, IFSC
Subjects: HIV, SÍNDROME DE IMUNODEFICIÊNCIA ADQUIRIDA, INIBIDORES DE ENZIMAS, RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA, HOLOGRAMAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERREIRA, Leonardo G. et al. Hologram quantitative structure-activity relationships for a class of inhibitors of HIV-1 protease. Letters in Drug Design and Discovery, v. 4, n. 5, p. 356-364, 2007Tradução . . Acesso em: 05 jun. 2024.
APA
Ferreira, L. G., Leitão, A., Montanari, C. A., & Andricopulo, A. D. (2007). Hologram quantitative structure-activity relationships for a class of inhibitors of HIV-1 protease. Letters in Drug Design and Discovery, 4( 5), 356-364.
NLM
Ferreira LG, Leitão A, Montanari CA, Andricopulo AD. Hologram quantitative structure-activity relationships for a class of inhibitors of HIV-1 protease. Letters in Drug Design and Discovery. 2007 ; 4( 5): 356-364.[citado 2024 jun. 05 ]
Vancouver
Ferreira LG, Leitão A, Montanari CA, Andricopulo AD. Hologram quantitative structure-activity relationships for a class of inhibitors of HIV-1 protease. Letters in Drug Design and Discovery. 2007 ; 4( 5): 356-364.[citado 2024 jun. 05 ]

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