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Artigo de periodico
The synthesized plant metabolite 3,4,5-tri-o-galloylquinic acid methyl ester inhibits calcium oxalate crystal growth in a drosophila model, downregulates renal cell surface annexin A1 expression, and decreases crystal adhesion to cells (2018)
Abd El-Salam, Mohamed ; Bastos, Jairo Kenupp; Han, Jing Jing; Previdi, Daniel ; Coelho, Eduardo Barbosa ; Donate, Paulo Marcos ; Romero, Michael F.; Lieske, John
Fonte: Journal of Medicinal Chemistry. Unidades: FCFRP, FMRP, FFCLRP
Assuntos: FRAÇÕES SUBCELULARES, CÉLULAS, RIM, ANTIOXIDANTES, DROSOPHILA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ABD EL-SALAM, Mohamed et al. The synthesized plant metabolite 3,4,5-tri-o-galloylquinic acid methyl ester inhibits calcium oxalate crystal growth in a drosophila model, downregulates renal cell surface annexin A1 expression, and decreases crystal adhesion to cells. Journal of Medicinal Chemistry, v. 61, n. 4, p. 1609-1621, 2018Tradução . . Disponível em: https://doi.org/10.1021/acs.jmedchem.7b01566. Acesso em: 04 dez. 2025.
APA
Abd El-Salam, M., Bastos, J. K., Han, J. J., Previdi, D., Coelho, E. B., Donate, P. M., et al. (2018). The synthesized plant metabolite 3,4,5-tri-o-galloylquinic acid methyl ester inhibits calcium oxalate crystal growth in a drosophila model, downregulates renal cell surface annexin A1 expression, and decreases crystal adhesion to cells. Journal of Medicinal Chemistry, 61( 4), 1609-1621. doi:10.1021/acs.jmedchem.7b01566
NLM
Abd El-Salam M, Bastos JK, Han JJ, Previdi D, Coelho EB, Donate PM, Romero MF, Lieske J. The synthesized plant metabolite 3,4,5-tri-o-galloylquinic acid methyl ester inhibits calcium oxalate crystal growth in a drosophila model, downregulates renal cell surface annexin A1 expression, and decreases crystal adhesion to cells [Internet]. Journal of Medicinal Chemistry. 2018 ; 61( 4): 1609-1621.[citado 2025 dez. 04 ] Available from: https://doi.org/10.1021/acs.jmedchem.7b01566
Vancouver
Abd El-Salam M, Bastos JK, Han JJ, Previdi D, Coelho EB, Donate PM, Romero MF, Lieske J. The synthesized plant metabolite 3,4,5-tri-o-galloylquinic acid methyl ester inhibits calcium oxalate crystal growth in a drosophila model, downregulates renal cell surface annexin A1 expression, and decreases crystal adhesion to cells [Internet]. Journal of Medicinal Chemistry. 2018 ; 61( 4): 1609-1621.[citado 2025 dez. 04 ] Available from: https://doi.org/10.1021/acs.jmedchem.7b01566
Artigo de periodico
Total synthesis of (3S, 5R, 3'S, 5'S)-capsorubin (2009)
Frederico, Daniel; Constantino, Maurício Gomes; Donate, Paulo Marcos
Fonte: Journal of the Brazilian Chemical Society. Unidade: FFCLRP
Assuntos: ANTIOXIDANTES, VITAMINA A
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FREDERICO, Daniel e CONSTANTINO, Maurício Gomes e DONATE, Paulo Marcos. Total synthesis of (3S, 5R, 3'S, 5'S)-capsorubin. Journal of the Brazilian Chemical Society, v. 20, n. 5, p. 888-894, 2009Tradução . . Disponível em: https://doi.org/10.1590/s0103-50532009000500013. Acesso em: 04 dez. 2025.
APA
Frederico, D., Constantino, M. G., & Donate, P. M. (2009). Total synthesis of (3S, 5R, 3'S, 5'S)-capsorubin. Journal of the Brazilian Chemical Society, 20( 5), 888-894. doi:10.1590/s0103-50532009000500013
NLM
Frederico D, Constantino MG, Donate PM. Total synthesis of (3S, 5R, 3'S, 5'S)-capsorubin [Internet]. Journal of the Brazilian Chemical Society. 2009 ; 20( 5): 888-894.[citado 2025 dez. 04 ] Available from: https://doi.org/10.1590/s0103-50532009000500013
Vancouver
Frederico D, Constantino MG, Donate PM. Total synthesis of (3S, 5R, 3'S, 5'S)-capsorubin [Internet]. Journal of the Brazilian Chemical Society. 2009 ; 20( 5): 888-894.[citado 2025 dez. 04 ] Available from: https://doi.org/10.1590/s0103-50532009000500013
Artigo de periodico
Trypanocidal structure-activity relationship for cis- and trans-methylpluviatolide (2008)
Silva, R. da; Saraiva, J.; Albuquerque, Sérgio de; Curti, Carlos; Donate, Paulo Marcos; Bianco, T. N. C.; Bastos, Jairo Kenupp; Silva, M. L. A.
Fonte: Phytochemistry. Unidades: FCFRP, FFCLRP
Assuntos: ANTIOXIDANTES, TRYPANOSOMA CRUZI
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, R. da et al. Trypanocidal structure-activity relationship for cis- and trans-methylpluviatolide. Phytochemistry, v. 69, n. 10, p. 1890-1894, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.phytochem.2008.04.002. Acesso em: 04 dez. 2025.
APA
Silva, R. da, Saraiva, J., Albuquerque, S. de, Curti, C., Donate, P. M., Bianco, T. N. C., et al. (2008). Trypanocidal structure-activity relationship for cis- and trans-methylpluviatolide. Phytochemistry, 69( 10), 1890-1894. doi:10.1016/j.phytochem.2008.04.002
NLM
Silva R da, Saraiva J, Albuquerque S de, Curti C, Donate PM, Bianco TNC, Bastos JK, Silva MLA. Trypanocidal structure-activity relationship for cis- and trans-methylpluviatolide [Internet]. Phytochemistry. 2008 ; 69( 10): 1890-1894.[citado 2025 dez. 04 ] Available from: https://doi.org/10.1016/j.phytochem.2008.04.002
Vancouver
Silva R da, Saraiva J, Albuquerque S de, Curti C, Donate PM, Bianco TNC, Bastos JK, Silva MLA. Trypanocidal structure-activity relationship for cis- and trans-methylpluviatolide [Internet]. Phytochemistry. 2008 ; 69( 10): 1890-1894.[citado 2025 dez. 04 ] Available from: https://doi.org/10.1016/j.phytochem.2008.04.002

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