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Artigo de periodico
Binding of fluorescent dansyl amino acids in albumin: when access to the protein cavity is more important than the strength of binding (2021)
Bertozo, Luiza Carvalho; Maszota-Zieleniak, Martyna; Bolean, Maytê ; Ciancaglini, Pietro ; Samsonov, Sergey A.; Ximenes, Valdecir Farias
Fonte: Dyes and Pigments. Unidade: FFCLRP
Assuntos: ALBUMINAS, FLUORESCÊNCIA, QUÍMICA FARMACÊUTICA, MODELAGEM MOLECULAR
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ABNT
BERTOZO, Luiza Carvalho et al. Binding of fluorescent dansyl amino acids in albumin: when access to the protein cavity is more important than the strength of binding. Dyes and Pigments, v. 188, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2021.109195. Acesso em: 11 set. 2024.
APA
Bertozo, L. C., Maszota-Zieleniak, M., Bolean, M., Ciancaglini, P., Samsonov, S. A., & Ximenes, V. F. (2021). Binding of fluorescent dansyl amino acids in albumin: when access to the protein cavity is more important than the strength of binding. Dyes and Pigments, 188. doi:10.1016/j.dyepig.2021.109195
NLM
Bertozo LC, Maszota-Zieleniak M, Bolean M, Ciancaglini P, Samsonov SA, Ximenes VF. Binding of fluorescent dansyl amino acids in albumin: when access to the protein cavity is more important than the strength of binding [Internet]. Dyes and Pigments. 2021 ; 188[citado 2024 set. 11 ] Available from: https://doi.org/10.1016/j.dyepig.2021.109195
Vancouver
Bertozo LC, Maszota-Zieleniak M, Bolean M, Ciancaglini P, Samsonov SA, Ximenes VF. Binding of fluorescent dansyl amino acids in albumin: when access to the protein cavity is more important than the strength of binding [Internet]. Dyes and Pigments. 2021 ; 188[citado 2024 set. 11 ] Available from: https://doi.org/10.1016/j.dyepig.2021.109195
Artigo de periodico
Semi-synthesis of β-keto-1,2,3-triazole derivatives from ethinylestradiol and evaluation of the cytotoxic activity (2019)
Queiroz, Thayane M; Orozco, Erika Vanessa Meñaca ; Silva, Valdenizia; Santos, Luciano S.; Soares, Milena B.P.; Bezerra, Daniel P.; Porto, Andre Luiz Meleiro
Fonte: Heliyon. Unidade: IQSC
Assuntos: QUÍMICA ORGÂNICA, QUÍMICA FARMACÊUTICA, TOXICOLOGIA, CARCINOMA HEPATOCELULAR, ADENOCARCINOMA, MAMA
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ABNT
QUEIROZ, Thayane M et al. Semi-synthesis of β-keto-1,2,3-triazole derivatives from ethinylestradiol and evaluation of the cytotoxic activity. Heliyon, v. 5, n. 9, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.heliyon.2019.e02408. Acesso em: 11 set. 2024.
APA
Queiroz, T. M., Orozco, E. V. M., Silva, V., Santos, L. S., Soares, M. B. P., Bezerra, D. P., & Porto, A. L. M. (2019). Semi-synthesis of β-keto-1,2,3-triazole derivatives from ethinylestradiol and evaluation of the cytotoxic activity. Heliyon, 5( 9). doi:10.1016/j.heliyon.2019.e02408
NLM
Queiroz TM, Orozco EVM, Silva V, Santos LS, Soares MBP, Bezerra DP, Porto ALM. Semi-synthesis of β-keto-1,2,3-triazole derivatives from ethinylestradiol and evaluation of the cytotoxic activity [Internet]. Heliyon. 2019 ; 5( 9):[citado 2024 set. 11 ] Available from: https://doi.org/10.1016/j.heliyon.2019.e02408
Vancouver
Queiroz TM, Orozco EVM, Silva V, Santos LS, Soares MBP, Bezerra DP, Porto ALM. Semi-synthesis of β-keto-1,2,3-triazole derivatives from ethinylestradiol and evaluation of the cytotoxic activity [Internet]. Heliyon. 2019 ; 5( 9):[citado 2024 set. 11 ] Available from: https://doi.org/10.1016/j.heliyon.2019.e02408
Artigo de periodico
Absolute configurations of griseorhodins A and C (2017)
Ortega, Humberto E.; Batista, João M.; Melo, Weilan G.P.; Clardy, Jon; Pupo, Mônica Tallarico
Fonte: Tetrahedron Letters. Unidade: FCFRP
Assuntos: STREPTOMYCES, ANTIBIÓTICOS, QUÍMICA FARMACÊUTICA
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ABNT
ORTEGA, Humberto E. et al. Absolute configurations of griseorhodins A and C. Tetrahedron Letters, v. 58, n. 50, p. 4721-4723, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2017.11.008. Acesso em: 11 set. 2024.
APA
Ortega, H. E., Batista, J. M., Melo, W. G. P., Clardy, J., & Pupo, M. T. (2017). Absolute configurations of griseorhodins A and C. Tetrahedron Letters, 58( 50), 4721-4723. doi:10.1016/j.tetlet.2017.11.008
NLM
Ortega HE, Batista JM, Melo WGP, Clardy J, Pupo MT. Absolute configurations of griseorhodins A and C [Internet]. Tetrahedron Letters. 2017 ; 58( 50): 4721-4723.[citado 2024 set. 11 ] Available from: https://doi.org/10.1016/j.tetlet.2017.11.008
Vancouver
Ortega HE, Batista JM, Melo WGP, Clardy J, Pupo MT. Absolute configurations of griseorhodins A and C [Internet]. Tetrahedron Letters. 2017 ; 58( 50): 4721-4723.[citado 2024 set. 11 ] Available from: https://doi.org/10.1016/j.tetlet.2017.11.008
Trabalho de evento-resumo
Synthesis of (Z)-5-(4-hydroxybenzylidene)thiazolidine-2,4-dione in batch and capillary micro reactor: comparison of performance and new catalysts (2017)
Pinheiro, Danilo da Silva; Palma, Mauri Sérgio Alves
Fonte: Proceedings. Nome do evento: World Chemistry Congress. Unidade: FCF
Assunto: QUÍMICA FARMACÊUTICA
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ABNT
PINHEIRO, Danilo da Silva e PALMA, Mauri Sérgio Alves. Synthesis of (Z)-5-(4-hydroxybenzylidene)thiazolidine-2,4-dione in batch and capillary micro reactor: comparison of performance and new catalysts. 2017, Anais.. Durham: International Union of Pure and Applied Chemistry (IUPAC), 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 11 set. 2024.
APA
Pinheiro, D. da S., & Palma, M. S. A. (2017). Synthesis of (Z)-5-(4-hydroxybenzylidene)thiazolidine-2,4-dione in batch and capillary micro reactor: comparison of performance and new catalysts. In Proceedings. Durham: International Union of Pure and Applied Chemistry (IUPAC). Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/
NLM
Pinheiro D da S, Palma MSA. Synthesis of (Z)-5-(4-hydroxybenzylidene)thiazolidine-2,4-dione in batch and capillary micro reactor: comparison of performance and new catalysts [Internet]. Proceedings. 2017 ;[citado 2024 set. 11 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Vancouver
Pinheiro D da S, Palma MSA. Synthesis of (Z)-5-(4-hydroxybenzylidene)thiazolidine-2,4-dione in batch and capillary micro reactor: comparison of performance and new catalysts [Internet]. Proceedings. 2017 ;[citado 2024 set. 11 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Artigo de periodico
Synthesis of two 'heteroaromatic rings of the future' for applications in medicinal chemistry (2016)
Silva-Júnior, P. E; Rezende, L. C. D; Gimenes, Julia Possamai; Maltarollo, Vinícius Gonçalves; Dale, James; Trossini, Gustavo Henrique Goulart ; Emery, Flavio da Silva; Ganesan, A
Fonte: RSC Advances. Unidades: FCF, FCFRP
Assuntos: COMPOSTOS HETEROCÍCLICOS, QUÍMICA FARMACÊUTICA
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ABNT
SILVA-JÚNIOR, P. E et al. Synthesis of two 'heteroaromatic rings of the future' for applications in medicinal chemistry. RSC Advances, v. 6, n. 27, p. 22777-22780, 2016Tradução . . Disponível em: https://doi.org/10.1039/c6ra01099g. Acesso em: 11 set. 2024.
APA
Silva-Júnior, P. E., Rezende, L. C. D., Gimenes, J. P., Maltarollo, V. G., Dale, J., Trossini, G. H. G., et al. (2016). Synthesis of two 'heteroaromatic rings of the future' for applications in medicinal chemistry. RSC Advances, 6( 27), 22777-22780. doi:10.1039/c6ra01099g
NLM
Silva-Júnior PE, Rezende LCD, Gimenes JP, Maltarollo VG, Dale J, Trossini GHG, Emery F da S, Ganesan A. Synthesis of two 'heteroaromatic rings of the future' for applications in medicinal chemistry [Internet]. RSC Advances. 2016 ; 6( 27): 22777-22780.[citado 2024 set. 11 ] Available from: https://doi.org/10.1039/c6ra01099g
Vancouver
Silva-Júnior PE, Rezende LCD, Gimenes JP, Maltarollo VG, Dale J, Trossini GHG, Emery F da S, Ganesan A. Synthesis of two 'heteroaromatic rings of the future' for applications in medicinal chemistry [Internet]. RSC Advances. 2016 ; 6( 27): 22777-22780.[citado 2024 set. 11 ] Available from: https://doi.org/10.1039/c6ra01099g
Artigo de periodico
Homology modelling, virtual screening and molecular dynamics of the MARK3 KA1 domain for cancer drug design (2011)
Semighini, Evandro P.; Taft, Carlton A.; Silva, Carlos Henrique Tomich de Paula da
Fonte: Molecular Simulations. Unidade: FCFRP
Assuntos: NEOPLASIAS, QUÍMICA FARMACÊUTICA, PLANEJAMENTO DE FÁRMACOS, MODELAGEM MOLECULAR, HOMOLOGIA
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ABNT
SEMIGHINI, Evandro P. e TAFT, Carlton A. e SILVA, Carlos Henrique Tomich de Paula da. Homology modelling, virtual screening and molecular dynamics of the MARK3 KA1 domain for cancer drug design. Molecular Simulations, v. 37, n. 14, p. 1186-1206, 2011Tradução . . Disponível em: https://doi.org/10.1080/08927022.2011.589052. Acesso em: 11 set. 2024.
APA
Semighini, E. P., Taft, C. A., & Silva, C. H. T. de P. da. (2011). Homology modelling, virtual screening and molecular dynamics of the MARK3 KA1 domain for cancer drug design. Molecular Simulations, 37( 14), 1186-1206. doi:10.1080/08927022.2011.589052
NLM
Semighini EP, Taft CA, Silva CHT de P da. Homology modelling, virtual screening and molecular dynamics of the MARK3 KA1 domain for cancer drug design [Internet]. Molecular Simulations. 2011 ; 37( 14): 1186-1206.[citado 2024 set. 11 ] Available from: https://doi.org/10.1080/08927022.2011.589052
Vancouver
Semighini EP, Taft CA, Silva CHT de P da. Homology modelling, virtual screening and molecular dynamics of the MARK3 KA1 domain for cancer drug design [Internet]. Molecular Simulations. 2011 ; 37( 14): 1186-1206.[citado 2024 set. 11 ] Available from: https://doi.org/10.1080/08927022.2011.589052
Artigo de periodico
Cyclooligomerisation of azido-alkyne-functionalised sugars: synthesis of 1,6-linked cyclic pseudo-galactooligosaccharides and assessment of their sialylation by Trypanosoma cruzi trans-sialidase (2010)
Campo, Vanessa L.; Carvalho, Ivone; Silva, Carlos Henrique Tomich de Paula da; Schenkman, Sergio; Hill, Lionel; Nepogodiev, Sergey A.; Field, Robert A.
Fonte: Chemical Science. Unidade: FCFRP
Assuntos: TRYPANOSOMA CRUZI, QUÍMICA FARMACÊUTICA
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ABNT
CAMPO, Vanessa L. et al. Cyclooligomerisation of azido-alkyne-functionalised sugars: synthesis of 1,6-linked cyclic pseudo-galactooligosaccharides and assessment of their sialylation by Trypanosoma cruzi trans-sialidase. Chemical Science, n. 4, p. 507-514, 2010Tradução . . Disponível em: https://doi.org/10.1039/c0sc00301h. Acesso em: 11 set. 2024.
APA
Campo, V. L., Carvalho, I., Silva, C. H. T. de P. da, Schenkman, S., Hill, L., Nepogodiev, S. A., & Field, R. A. (2010). Cyclooligomerisation of azido-alkyne-functionalised sugars: synthesis of 1,6-linked cyclic pseudo-galactooligosaccharides and assessment of their sialylation by Trypanosoma cruzi trans-sialidase. Chemical Science, ( 4), 507-514. doi:10.1039/c0sc00301h
NLM
Campo VL, Carvalho I, Silva CHT de P da, Schenkman S, Hill L, Nepogodiev SA, Field RA. Cyclooligomerisation of azido-alkyne-functionalised sugars: synthesis of 1,6-linked cyclic pseudo-galactooligosaccharides and assessment of their sialylation by Trypanosoma cruzi trans-sialidase [Internet]. Chemical Science. 2010 ;( 4): 507-514.[citado 2024 set. 11 ] Available from: https://doi.org/10.1039/c0sc00301h
Vancouver
Campo VL, Carvalho I, Silva CHT de P da, Schenkman S, Hill L, Nepogodiev SA, Field RA. Cyclooligomerisation of azido-alkyne-functionalised sugars: synthesis of 1,6-linked cyclic pseudo-galactooligosaccharides and assessment of their sialylation by Trypanosoma cruzi trans-sialidase [Internet]. Chemical Science. 2010 ;( 4): 507-514.[citado 2024 set. 11 ] Available from: https://doi.org/10.1039/c0sc00301h
Artigo de periodico
Synthesis, in vitro evaluation, and SAR studies of a potential antichagasic 1H-pyrazolo[3,4-b]pyridine series (2007)
Dias, Luiza R. S.; Santos, Marcelo B.; Albuquerque, Sérgio de; Castro, Helena C.; Souza, Alessandra M. T. de; Freitas, Antônio C. C.; DiVaio, Maria A. V.; Cabral, Lucio M.; Rodrigues, Carlos R.
Fonte: Bioorganic & Medicinal Chemistry. Unidade: FCFRP
Assuntos: QUÍMICA FARMACÊUTICA, DOENÇA DE CHAGAS (TRATAMENTO)
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ABNT
DIAS, Luiza R. S. et al. Synthesis, in vitro evaluation, and SAR studies of a potential antichagasic 1H-pyrazolo[3,4-b]pyridine series. Bioorganic & Medicinal Chemistry, v. 15, p. 211-219, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2006.09.067. Acesso em: 11 set. 2024.
APA
Dias, L. R. S., Santos, M. B., Albuquerque, S. de, Castro, H. C., Souza, A. M. T. de, Freitas, A. C. C., et al. (2007). Synthesis, in vitro evaluation, and SAR studies of a potential antichagasic 1H-pyrazolo[3,4-b]pyridine series. Bioorganic & Medicinal Chemistry, 15, 211-219. doi:10.1016/j.bmc.2006.09.067
NLM
Dias LRS, Santos MB, Albuquerque S de, Castro HC, Souza AMT de, Freitas ACC, DiVaio MAV, Cabral LM, Rodrigues CR. Synthesis, in vitro evaluation, and SAR studies of a potential antichagasic 1H-pyrazolo[3,4-b]pyridine series [Internet]. Bioorganic & Medicinal Chemistry. 2007 ; 15 211-219.[citado 2024 set. 11 ] Available from: https://doi.org/10.1016/j.bmc.2006.09.067
Vancouver
Dias LRS, Santos MB, Albuquerque S de, Castro HC, Souza AMT de, Freitas ACC, DiVaio MAV, Cabral LM, Rodrigues CR. Synthesis, in vitro evaluation, and SAR studies of a potential antichagasic 1H-pyrazolo[3,4-b]pyridine series [Internet]. Bioorganic & Medicinal Chemistry. 2007 ; 15 211-219.[citado 2024 set. 11 ] Available from: https://doi.org/10.1016/j.bmc.2006.09.067
Artigo de periodico
Synthesis of (+)-(2R,3S,4R)-2,3,4-trihydroxycyclohehanone from D-glucose (2004)
Carvalho, Ivone; Melo, Eduardo Borges de
Fonte: Carbohydrate Research. Unidade: FCFRP
Assunto: QUÍMICA FARMACÊUTICA
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ABNT
CARVALHO, Ivone e MELO, Eduardo Borges de. Synthesis of (+)-(2R,3S,4R)-2,3,4-trihydroxycyclohehanone from D-glucose. Carbohydrate Research, v. 339, p. 361-365, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.carres.2003.10.010. Acesso em: 11 set. 2024.
APA
Carvalho, I., & Melo, E. B. de. (2004). Synthesis of (+)-(2R,3S,4R)-2,3,4-trihydroxycyclohehanone from D-glucose. Carbohydrate Research, 339, 361-365. doi:10.1016/j.carres.2003.10.010
NLM
Carvalho I, Melo EB de. Synthesis of (+)-(2R,3S,4R)-2,3,4-trihydroxycyclohehanone from D-glucose [Internet]. Carbohydrate Research. 2004 ; 339 361-365.[citado 2024 set. 11 ] Available from: https://doi.org/10.1016/j.carres.2003.10.010
Vancouver
Carvalho I, Melo EB de. Synthesis of (+)-(2R,3S,4R)-2,3,4-trihydroxycyclohehanone from D-glucose [Internet]. Carbohydrate Research. 2004 ; 339 361-365.[citado 2024 set. 11 ] Available from: https://doi.org/10.1016/j.carres.2003.10.010
Artigo de periodico
Practical synthesis of the 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-'beta'-D-glucosides of Fmoc-serine and Fmoc-threonine and their benzyl esters (2003)
Carvalho, Ivone; Scheuerl, Shona L.; Kartha, K. P. Ravindranathan; Field, Robert A.
Fonte: Carbohydrate Research. Unidade: FCFRP
Assunto: QUÍMICA FARMACÊUTICA
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ABNT
CARVALHO, Ivone et al. Practical synthesis of the 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-'beta'-D-glucosides of Fmoc-serine and Fmoc-threonine and their benzyl esters. Carbohydrate Research, v. 338, n. 10, p. 1039-1043, 2003Tradução . . Disponível em: https://doi.org/10.1016/s0008-6215(03)00071-5. Acesso em: 11 set. 2024.
APA
Carvalho, I., Scheuerl, S. L., Kartha, K. P. R., & Field, R. A. (2003). Practical synthesis of the 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-'beta'-D-glucosides of Fmoc-serine and Fmoc-threonine and their benzyl esters. Carbohydrate Research, 338( 10), 1039-1043. doi:10.1016/s0008-6215(03)00071-5
NLM
Carvalho I, Scheuerl SL, Kartha KPR, Field RA. Practical synthesis of the 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-'beta'-D-glucosides of Fmoc-serine and Fmoc-threonine and their benzyl esters [Internet]. Carbohydrate Research. 2003 ; 338( 10): 1039-1043.[citado 2024 set. 11 ] Available from: https://doi.org/10.1016/s0008-6215(03)00071-5
Vancouver
Carvalho I, Scheuerl SL, Kartha KPR, Field RA. Practical synthesis of the 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-'beta'-D-glucosides of Fmoc-serine and Fmoc-threonine and their benzyl esters [Internet]. Carbohydrate Research. 2003 ; 338( 10): 1039-1043.[citado 2024 set. 11 ] Available from: https://doi.org/10.1016/s0008-6215(03)00071-5
Artigo de periodico
'gama'-Lactones from trichilia claussenii (1998)
Pupo, Mônica Tallarico; Vieira, Paulo C; Fernandes, João B; Silva, M Fátima G F da
Fonte: Phytochemistry. Unidade: FCFRP
Assunto: QUÍMICA FARMACÊUTICA
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ABNT
PUPO, Mônica Tallarico et al. 'gama'-Lactones from trichilia claussenii. Phytochemistry, v. 48, n. 2, p. 307-310, 1998Tradução . . Acesso em: 11 set. 2024.
APA
Pupo, M. T., Vieira, P. C., Fernandes, J. B., & Silva, M. F. G. F. da. (1998). 'gama'-Lactones from trichilia claussenii. Phytochemistry, 48( 2), 307-310.
NLM
Pupo MT, Vieira PC, Fernandes JB, Silva MFGF da. 'gama'-Lactones from trichilia claussenii. Phytochemistry. 1998 ; 48( 2): 307-310.[citado 2024 set. 11 ]
Vancouver
Pupo MT, Vieira PC, Fernandes JB, Silva MFGF da. 'gama'-Lactones from trichilia claussenii. Phytochemistry. 1998 ; 48( 2): 307-310.[citado 2024 set. 11 ]
Artigo de periodico
Synthesis of a novel pseudodisaccharide glycoside as a potential glycosidase inhibitor (1998)
Haines, Alan H.; Carvalho, Ivone
Fonte: Chemical Communications. Unidade: FCFRP
Assuntos: SÍNTESE ORGÂNICA (QUÍMICA), QUÍMICA FARMACÊUTICA
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ABNT
HAINES, Alan H. e CARVALHO, Ivone. Synthesis of a novel pseudodisaccharide glycoside as a potential glycosidase inhibitor. Chemical Communications, p. 817-818, 1998Tradução . . Disponível em: https://doi.org/10.1039/a800279g. Acesso em: 11 set. 2024.
APA
Haines, A. H., & Carvalho, I. (1998). Synthesis of a novel pseudodisaccharide glycoside as a potential glycosidase inhibitor. Chemical Communications, 817-818. doi:10.1039/a800279g
NLM
Haines AH, Carvalho I. Synthesis of a novel pseudodisaccharide glycoside as a potential glycosidase inhibitor [Internet]. Chemical Communications. 1998 ; 817-818.[citado 2024 set. 11 ] Available from: https://doi.org/10.1039/a800279g
Vancouver
Haines AH, Carvalho I. Synthesis of a novel pseudodisaccharide glycoside as a potential glycosidase inhibitor [Internet]. Chemical Communications. 1998 ; 817-818.[citado 2024 set. 11 ] Available from: https://doi.org/10.1039/a800279g
Artigo de periodico
Oxidative activity of primaquine metabolites on rat erythrocytes in vitro and in vivo (1994)
Vasquez-Vivar, J M; Augusto, Ohara
Fonte: Biochemical Pharmacolgy. Unidade: IQ
Assunto: QUÍMICA FARMACÊUTICA
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ABNT
VASQUEZ-VIVAR, J M e AUGUSTO, Ohara. Oxidative activity of primaquine metabolites on rat erythrocytes in vitro and in vivo. Biochemical Pharmacolgy, v. 47, p. 309-16, 1994Tradução . . Disponível em: https://doi.org/10.1016/0006-2952(94)90022-1. Acesso em: 11 set. 2024.
APA
Vasquez-Vivar, J. M., & Augusto, O. (1994). Oxidative activity of primaquine metabolites on rat erythrocytes in vitro and in vivo. Biochemical Pharmacolgy, 47, 309-16. doi:10.1016/0006-2952(94)90022-1
NLM
Vasquez-Vivar JM, Augusto O. Oxidative activity of primaquine metabolites on rat erythrocytes in vitro and in vivo [Internet]. Biochemical Pharmacolgy. 1994 ;47 309-16.[citado 2024 set. 11 ] Available from: https://doi.org/10.1016/0006-2952(94)90022-1
Vancouver
Vasquez-Vivar JM, Augusto O. Oxidative activity of primaquine metabolites on rat erythrocytes in vitro and in vivo [Internet]. Biochemical Pharmacolgy. 1994 ;47 309-16.[citado 2024 set. 11 ] Available from: https://doi.org/10.1016/0006-2952(94)90022-1
Artigo de periodico
Peroxidation of the antimalarial drug primaquine -characterization of a benzidine -like metabolite with methaemoglobin - forming activity (1993)
Morais, M S; Augusto, Ohara
Fonte: Xenobiotica. Unidade: IQ
Assuntos: BIOQUÍMICA, QUÍMICA FARMACÊUTICA
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ABNT
MORAIS, M S e AUGUSTO, Ohara. Peroxidation of the antimalarial drug primaquine -characterization of a benzidine -like metabolite with methaemoglobin - forming activity. Xenobiotica, v. 23, n. 2 , p. 133-9, 1993Tradução . . Disponível em: https://doi.org/10.3109/00498259309059369. Acesso em: 11 set. 2024.
APA
Morais, M. S., & Augusto, O. (1993). Peroxidation of the antimalarial drug primaquine -characterization of a benzidine -like metabolite with methaemoglobin - forming activity. Xenobiotica, 23( 2 ), 133-9. doi:10.3109/00498259309059369
NLM
Morais MS, Augusto O. Peroxidation of the antimalarial drug primaquine -characterization of a benzidine -like metabolite with methaemoglobin - forming activity [Internet]. Xenobiotica. 1993 ;23( 2 ): 133-9.[citado 2024 set. 11 ] Available from: https://doi.org/10.3109/00498259309059369
Vancouver
Morais MS, Augusto O. Peroxidation of the antimalarial drug primaquine -characterization of a benzidine -like metabolite with methaemoglobin - forming activity [Internet]. Xenobiotica. 1993 ;23( 2 ): 133-9.[citado 2024 set. 11 ] Available from: https://doi.org/10.3109/00498259309059369
Artigo de periodico
Micellar catalysis of the intramolecular aminolysis of a beta-lactam antibiotic cephaclor (1991)
Oliveira, A. G.; Nothenberg, Michael Simon; Cuccovia, Iolanda Midea ; Chaimovich Guralnik, Hernan
Fonte: Journal of Physical Organic Chemistry. Unidades: IQ, FCF
Assuntos: BIOQUÍMICA, ANTIBIÓTICOS (QUIMIOTERAPIA;FARMACOLOGIA), QUÍMICA FARMACÊUTICA
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ABNT
OLIVEIRA, A. G. et al. Micellar catalysis of the intramolecular aminolysis of a beta-lactam antibiotic cephaclor. Journal of Physical Organic Chemistry, v. 4 , n. 1 , p. 19-24, 1991Tradução . . Acesso em: 11 set. 2024.
APA
Oliveira, A. G., Nothenberg, M. S., Cuccovia, I. M., & Chaimovich Guralnik, H. (1991). Micellar catalysis of the intramolecular aminolysis of a beta-lactam antibiotic cephaclor. Journal of Physical Organic Chemistry, 4 ( 1 ), 19-24.
NLM
Oliveira AG, Nothenberg MS, Cuccovia IM, Chaimovich Guralnik H. Micellar catalysis of the intramolecular aminolysis of a beta-lactam antibiotic cephaclor. Journal of Physical Organic Chemistry. 1991 ;4 ( 1 ): 19-24.[citado 2024 set. 11 ]
Vancouver
Oliveira AG, Nothenberg MS, Cuccovia IM, Chaimovich Guralnik H. Micellar catalysis of the intramolecular aminolysis of a beta-lactam antibiotic cephaclor. Journal of Physical Organic Chemistry. 1991 ;4 ( 1 ): 19-24.[citado 2024 set. 11 ]

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