A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CUNHA, Micael Rodrigues et al. Peppers: a “hot” natural source for antitumor compounds. Molecules, v. 26, n. 6, p. 1-21 art. 1521, 2021Tradução . . Disponível em: https://doi.org/10.3390/molecules26061521. Acesso em: 04 ago. 2024.
APA
Cunha, M. R., Tavares, M. T., Fernandes, T. B., & Parise Filho, R. (2021). Peppers: a “hot” natural source for antitumor compounds. Molecules, 26( 6), 1-21 art. 1521. doi:10.3390/molecules26061521
NLM
Cunha MR, Tavares MT, Fernandes TB, Parise Filho R. Peppers: a “hot” natural source for antitumor compounds [Internet]. Molecules. 2021 ; 26( 6): 1-21 art. 1521.[citado 2024 ago. 04 ] Available from: https://doi.org/10.3390/molecules26061521
Vancouver
Cunha MR, Tavares MT, Fernandes TB, Parise Filho R. Peppers: a “hot” natural source for antitumor compounds [Internet]. Molecules. 2021 ; 26( 6): 1-21 art. 1521.[citado 2024 ago. 04 ] Available from: https://doi.org/10.3390/molecules26061521
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TAVARES, Maurício Temotheo et al. Structure-activity relationship and mechanistic studies for a series of cinnamyl hydroxamate histone deacetylase inhibitors. Bioorganic and Medicinal Chemistry, v. 35, p. 1-42 art. 116085, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2021.116085. Acesso em: 04 ago. 2024.
APA
Tavares, M. T., Almeida, L. C. de, Kronenberger, T., Ferreira, G. M., Divitiis, T. F. de, Toledo, M. F. Z. J., et al. (2021). Structure-activity relationship and mechanistic studies for a series of cinnamyl hydroxamate histone deacetylase inhibitors. Bioorganic and Medicinal Chemistry, 35, 1-42 art. 116085. doi:10.1016/j.bmc.2021.116085
NLM
Tavares MT, Almeida LC de, Kronenberger T, Ferreira GM, Divitiis TF de, Toledo MFZJ, Hassimotto NMA, Machado Neto JA, Costa-Lotufo LV, Parise Filho R. Structure-activity relationship and mechanistic studies for a series of cinnamyl hydroxamate histone deacetylase inhibitors [Internet]. Bioorganic and Medicinal Chemistry. 2021 ; 35 1-42 art. 116085.[citado 2024 ago. 04 ] Available from: https://doi.org/10.1016/j.bmc.2021.116085
Vancouver
Tavares MT, Almeida LC de, Kronenberger T, Ferreira GM, Divitiis TF de, Toledo MFZJ, Hassimotto NMA, Machado Neto JA, Costa-Lotufo LV, Parise Filho R. Structure-activity relationship and mechanistic studies for a series of cinnamyl hydroxamate histone deacetylase inhibitors [Internet]. Bioorganic and Medicinal Chemistry. 2021 ; 35 1-42 art. 116085.[citado 2024 ago. 04 ] Available from: https://doi.org/10.1016/j.bmc.2021.116085
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERNANDES, Thais Batista et al. Design of arylsulfonylhydrazones as potential FabH inhibitors: synthesis, antimicrobial evaluation and molecular docking. Medicinal Chemistry, v. 17, p. 474-484, 2021Tradução . . Disponível em: https://doi.org/10.2174/1573406415666191122111228. Acesso em: 04 ago. 2024.
APA
Fernandes, T. B., Segretti, N. D., Lourenço, F. R., Cândido, T. M., Baby, A. R., Barbosa, E. G., & Parise Filho, R. (2021). Design of arylsulfonylhydrazones as potential FabH inhibitors: synthesis, antimicrobial evaluation and molecular docking. Medicinal Chemistry, 17, 474-484. doi:10.2174/1573406415666191122111228
NLM
Fernandes TB, Segretti ND, Lourenço FR, Cândido TM, Baby AR, Barbosa EG, Parise Filho R. Design of arylsulfonylhydrazones as potential FabH inhibitors: synthesis, antimicrobial evaluation and molecular docking [Internet]. Medicinal Chemistry. 2021 ; 17 474-484.[citado 2024 ago. 04 ] Available from: https://doi.org/10.2174/1573406415666191122111228
Vancouver
Fernandes TB, Segretti ND, Lourenço FR, Cândido TM, Baby AR, Barbosa EG, Parise Filho R. Design of arylsulfonylhydrazones as potential FabH inhibitors: synthesis, antimicrobial evaluation and molecular docking [Internet]. Medicinal Chemistry. 2021 ; 17 474-484.[citado 2024 ago. 04 ] Available from: https://doi.org/10.2174/1573406415666191122111228