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FEITOSA, Lívia Melo et al. Discovery of new piperaquine hybrid analogs linked by triazolopyrimidine and pyrazolopyrimidine scaffolds with antiplasmodial and transmission blocking activities. European Journal of Medicinal Chemistry, v. 267, p. 116163-1-116163-12, 2024Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2024.116163. Acesso em: 31 out. 2024.
APA
Feitosa, L. M., França, R. R. F., Ferreira, M. de L. G., Aguiar, A. C. C., Souza, G. E. de, Maluf, S. E. C., et al. (2024). Discovery of new piperaquine hybrid analogs linked by triazolopyrimidine and pyrazolopyrimidine scaffolds with antiplasmodial and transmission blocking activities. European Journal of Medicinal Chemistry, 267, 116163-1-116163-12. doi:10.1016/j.ejmech.2024.116163
NLM
Feitosa LM, França RRF, Ferreira M de LG, Aguiar ACC, Souza GE de, Maluf SEC, Souza JO de, Zapata LCC, Duarte DMFA, Morais I, Nogueira F, Nonato MC, Pinheiro LC da S, Guido RVC, Boechat N. Discovery of new piperaquine hybrid analogs linked by triazolopyrimidine and pyrazolopyrimidine scaffolds with antiplasmodial and transmission blocking activities [Internet]. European Journal of Medicinal Chemistry. 2024 ; 267 116163-1-116163-12.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.ejmech.2024.116163
Vancouver
Feitosa LM, França RRF, Ferreira M de LG, Aguiar ACC, Souza GE de, Maluf SEC, Souza JO de, Zapata LCC, Duarte DMFA, Morais I, Nogueira F, Nonato MC, Pinheiro LC da S, Guido RVC, Boechat N. Discovery of new piperaquine hybrid analogs linked by triazolopyrimidine and pyrazolopyrimidine scaffolds with antiplasmodial and transmission blocking activities [Internet]. European Journal of Medicinal Chemistry. 2024 ; 267 116163-1-116163-12.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.ejmech.2024.116163
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CAVINI, Ítalo Augusto et al. Novel lipid-interaction motifs within the c-terminal domain of septin10 from schistosoma mansoni. Biochimica et Biophysica Acta: Biomembranes, v. 1866, n. 7, p. 184371-1-184371-9 + supplementary data, 2024Tradução . . Disponível em: https://doi.org/10.1016/j.bbamem.2024.184371. Acesso em: 31 out. 2024.
APA
Cavini, Í. A., Fontes, M. G., Zeraik, A. E., Lopes, J. L. de S., & Araújo, A. P. U. de. (2024). Novel lipid-interaction motifs within the c-terminal domain of septin10 from schistosoma mansoni. Biochimica et Biophysica Acta: Biomembranes, 1866( 7), 184371-1-184371-9 + supplementary data. doi:10.1016/j.bbamem.2024.184371
NLM
Cavini ÍA, Fontes MG, Zeraik AE, Lopes JL de S, Araújo APU de. Novel lipid-interaction motifs within the c-terminal domain of septin10 from schistosoma mansoni [Internet]. Biochimica et Biophysica Acta: Biomembranes. 2024 ; 1866( 7): 184371-1-184371-9 + supplementary data.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.bbamem.2024.184371
Vancouver
Cavini ÍA, Fontes MG, Zeraik AE, Lopes JL de S, Araújo APU de. Novel lipid-interaction motifs within the c-terminal domain of septin10 from schistosoma mansoni [Internet]. Biochimica et Biophysica Acta: Biomembranes. 2024 ; 1866( 7): 184371-1-184371-9 + supplementary data.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.bbamem.2024.184371
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WALLACH, Izhar et al. AI is a viable alternative to high throughput screening: a 318-target study. Scientific Reports, v. 14, 2024Tradução . . Disponível em: https://doi.org/10.1038/s41598-024-54655-z. Acesso em: 31 out. 2024.
APA
Wallach, I., Andricopulo, A. D., Souza, G. E. de, Valli, M., Guido, R. V. C., Debonsi, H. M., & Teixeira, T. R. (2024). AI is a viable alternative to high throughput screening: a 318-target study. Scientific Reports, 14. doi:10.1038/s41598-024-54655-z
NLM
Wallach I, Andricopulo AD, Souza GE de, Valli M, Guido RVC, Debonsi HM, Teixeira TR. AI is a viable alternative to high throughput screening: a 318-target study [Internet]. Scientific Reports. 2024 ; 14[citado 2024 out. 31 ] Available from: https://doi.org/10.1038/s41598-024-54655-z
Vancouver
Wallach I, Andricopulo AD, Souza GE de, Valli M, Guido RVC, Debonsi HM, Teixeira TR. AI is a viable alternative to high throughput screening: a 318-target study [Internet]. Scientific Reports. 2024 ; 14[citado 2024 out. 31 ] Available from: https://doi.org/10.1038/s41598-024-54655-z
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CAVINI, Ítalo Augusto et al. Deciphering lipid binding: unveiling novel interaction motifs in the Cterminal domain of Schistosoma mansoni septin10. FEBS Open Bio. Oxford: Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1002/2211-5463.13837. Acesso em: 31 out. 2024. , 2024
APA
Cavini, Í. A., Fontes, M. G., Zeraik, A. E., Lopes, J. L. de S., & Araújo, A. P. U. de. (2024). Deciphering lipid binding: unveiling novel interaction motifs in the Cterminal domain of Schistosoma mansoni septin10. FEBS Open Bio. Oxford: Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo. doi:10.1002/2211-5463.13837
NLM
Cavini ÍA, Fontes MG, Zeraik AE, Lopes JL de S, Araújo APU de. Deciphering lipid binding: unveiling novel interaction motifs in the Cterminal domain of Schistosoma mansoni septin10 [Internet]. FEBS Open Bio. 2024 ; 14 96.[citado 2024 out. 31 ] Available from: https://doi.org/10.1002/2211-5463.13837
Vancouver
Cavini ÍA, Fontes MG, Zeraik AE, Lopes JL de S, Araújo APU de. Deciphering lipid binding: unveiling novel interaction motifs in the Cterminal domain of Schistosoma mansoni septin10 [Internet]. FEBS Open Bio. 2024 ; 14 96.[citado 2024 out. 31 ] Available from: https://doi.org/10.1002/2211-5463.13837
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YUYAMA, Kamila Tomoko et al. Discovering the potential of the alkaloids from malouetia tamaquarina (Apocynaceae) and its endophytes against Neglected Tropical Diseases (NTDs). 2023, Anais.. Northbrook: American Society of Pharmacognosy - ASP, 2023. Disponível em: https://repositorio.usp.br/directbitstream/4317357f-e5fe-4a89-92b6-31fd09055f01/PROD034757_3149170.pdf. Acesso em: 31 out. 2024.
APA
Yuyama, K. T., Macedo, C. C. de, Melo, W. G. da P., Silva, M. H. da, Aguiar, J. P. L., Castello, A. C. D., et al. (2023). Discovering the potential of the alkaloids from malouetia tamaquarina (Apocynaceae) and its endophytes against Neglected Tropical Diseases (NTDs). In Abstracts Book. Northbrook: American Society of Pharmacognosy - ASP. Recuperado de https://repositorio.usp.br/directbitstream/4317357f-e5fe-4a89-92b6-31fd09055f01/PROD034757_3149170.pdf
NLM
Yuyama KT, Macedo CC de, Melo WG da P, Silva MH da, Aguiar JPL, Castello ACD, Ferreira LLG, Andricopulo AD, Silva GF da, Schmidt TJ, Pupo MT. Discovering the potential of the alkaloids from malouetia tamaquarina (Apocynaceae) and its endophytes against Neglected Tropical Diseases (NTDs) [Internet]. Abstracts Book. 2023 ;[citado 2024 out. 31 ] Available from: https://repositorio.usp.br/directbitstream/4317357f-e5fe-4a89-92b6-31fd09055f01/PROD034757_3149170.pdf
Vancouver
Yuyama KT, Macedo CC de, Melo WG da P, Silva MH da, Aguiar JPL, Castello ACD, Ferreira LLG, Andricopulo AD, Silva GF da, Schmidt TJ, Pupo MT. Discovering the potential of the alkaloids from malouetia tamaquarina (Apocynaceae) and its endophytes against Neglected Tropical Diseases (NTDs) [Internet]. Abstracts Book. 2023 ;[citado 2024 out. 31 ] Available from: https://repositorio.usp.br/directbitstream/4317357f-e5fe-4a89-92b6-31fd09055f01/PROD034757_3149170.pdf
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MENDES, Léia da Costa et al. Using molecular networking and docking to explore arginase inhibitors among Drimys brasiliensis chemical constituents. Medicinal Chemistry Research, v. 32, n. 10, p. 2208-2218, 2023Tradução . . Disponível em: https://doi.org/10.1007/s00044-023-03123-w. Acesso em: 31 out. 2024.
APA
Mendes, L. da C., Dantas, T. B. V., Severino, R. P., Silva, L. R. G. da, Souza, D. H. F. de, Cass, Q. B., et al. (2023). Using molecular networking and docking to explore arginase inhibitors among Drimys brasiliensis chemical constituents. Medicinal Chemistry Research, 32( 10), 2208-2218. doi:10.1007/s00044-023-03123-w
NLM
Mendes L da C, Dantas TBV, Severino RP, Silva LRG da, Souza DHF de, Cass QB, Ramalho SD, Vieira PC, Souza GE de, Guido RVC, Urschel M-K, Kersten C, Sousa LRF de. Using molecular networking and docking to explore arginase inhibitors among Drimys brasiliensis chemical constituents [Internet]. Medicinal Chemistry Research. 2023 ; 32( 10): 2208-2218.[citado 2024 out. 31 ] Available from: https://doi.org/10.1007/s00044-023-03123-w
Vancouver
Mendes L da C, Dantas TBV, Severino RP, Silva LRG da, Souza DHF de, Cass QB, Ramalho SD, Vieira PC, Souza GE de, Guido RVC, Urschel M-K, Kersten C, Sousa LRF de. Using molecular networking and docking to explore arginase inhibitors among Drimys brasiliensis chemical constituents [Internet]. Medicinal Chemistry Research. 2023 ; 32( 10): 2208-2218.[citado 2024 out. 31 ] Available from: https://doi.org/10.1007/s00044-023-03123-w
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AMORIM, Marcelo Rodrigues de et al. Polyketide- and terpenoid-derived metabolites produced by a marine-derived fungus, Peroneutypa sp. Journal of Natural Products, v. 86, n. 6, p. 1476-1486 + supporting information, 2023Tradução . . Disponível em: https://doi.org/10.1021/acs.jnatprod.3c00175. Acesso em: 31 out. 2024.
APA
Amorim, M. R. de, Barbosa, C. de S., Paz, T. A., Ióca, L. P., Nicácio, K. de J., Oliveira, L. F. P. de, et al. (2023). Polyketide- and terpenoid-derived metabolites produced by a marine-derived fungus, Peroneutypa sp. Journal of Natural Products, 86( 6), 1476-1486 + supporting information. doi:10.1021/acs.jnatprod.3c00175
NLM
Amorim MR de, Barbosa C de S, Paz TA, Ióca LP, Nicácio K de J, Oliveira LFP de, Goulart MO, Paulino JM, Cruz MO da, Ferreira AG, Furlan M, Lira SP de, Santos RA dos, Rodrigues A, Guido RVC, Berlinck RG de S. Polyketide- and terpenoid-derived metabolites produced by a marine-derived fungus, Peroneutypa sp [Internet]. Journal of Natural Products. 2023 ; 86( 6): 1476-1486 + supporting information.[citado 2024 out. 31 ] Available from: https://doi.org/10.1021/acs.jnatprod.3c00175
Vancouver
Amorim MR de, Barbosa C de S, Paz TA, Ióca LP, Nicácio K de J, Oliveira LFP de, Goulart MO, Paulino JM, Cruz MO da, Ferreira AG, Furlan M, Lira SP de, Santos RA dos, Rodrigues A, Guido RVC, Berlinck RG de S. Polyketide- and terpenoid-derived metabolites produced by a marine-derived fungus, Peroneutypa sp [Internet]. Journal of Natural Products. 2023 ; 86( 6): 1476-1486 + supporting information.[citado 2024 out. 31 ] Available from: https://doi.org/10.1021/acs.jnatprod.3c00175
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ARGENTIN, Marcela Nunes et al. Synthesis and antibacterial activity of polyalthic acid analogs. Antibiotics, v. 12, n. 7, p. 1202-1-1202-12 + supplementary materials, 2023Tradução . . Disponível em: https://doi.org/10.3390/antibiotics12071202. Acesso em: 31 out. 2024.
APA
Argentin, M. N., Cruz, F. de P. N., Souza, A. B., D’Aurea, E. M. de O., Bastos, J. K., Ambrósio, S. R., et al. (2023). Synthesis and antibacterial activity of polyalthic acid analogs. Antibiotics, 12( 7), 1202-1-1202-12 + supplementary materials. doi:10.3390/antibiotics12071202
NLM
Argentin MN, Cruz F de PN, Souza AB, D’Aurea EM de O, Bastos JK, Ambrósio SR, Veneziani RCS, Camargo ILB da C, Mizuno CS. Synthesis and antibacterial activity of polyalthic acid analogs [Internet]. Antibiotics. 2023 ; 12( 7): 1202-1-1202-12 + supplementary materials.[citado 2024 out. 31 ] Available from: https://doi.org/10.3390/antibiotics12071202
Vancouver
Argentin MN, Cruz F de PN, Souza AB, D’Aurea EM de O, Bastos JK, Ambrósio SR, Veneziani RCS, Camargo ILB da C, Mizuno CS. Synthesis and antibacterial activity of polyalthic acid analogs [Internet]. Antibiotics. 2023 ; 12( 7): 1202-1-1202-12 + supplementary materials.[citado 2024 out. 31 ] Available from: https://doi.org/10.3390/antibiotics12071202
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SILVA, Airton Damasceno et al. Liquid fungal cocultivation as a strategy to access bioactive metabolites. Planta Medica, v. 87, n. 1/2, p. 187-195, 2021Tradução . . Disponível em: https://doi.org/10.1055/a-1200-2046. Acesso em: 31 out. 2024.
APA
Silva, A. D., Ambrozin, A. R. P., Camargo, A. F. S. de, Cruz, F. de P. N., Ferreira, L. L. G., Andricopulo, R. K., et al. (2021). Liquid fungal cocultivation as a strategy to access bioactive metabolites. Planta Medica, 87( 1/2), 187-195. doi:10.1055/a-1200-2046
NLM
Silva AD, Ambrozin ARP, Camargo AFS de, Cruz F de PN, Ferreira LLG, Andricopulo RK, Silva TL, Camargo ILB da C, Andricopulo AD, Vieira PC. Liquid fungal cocultivation as a strategy to access bioactive metabolites [Internet]. Planta Medica. 2021 ; 87( 1/2): 187-195.[citado 2024 out. 31 ] Available from: https://doi.org/10.1055/a-1200-2046
Vancouver
Silva AD, Ambrozin ARP, Camargo AFS de, Cruz F de PN, Ferreira LLG, Andricopulo RK, Silva TL, Camargo ILB da C, Andricopulo AD, Vieira PC. Liquid fungal cocultivation as a strategy to access bioactive metabolites [Internet]. Planta Medica. 2021 ; 87( 1/2): 187-195.[citado 2024 out. 31 ] Available from: https://doi.org/10.1055/a-1200-2046
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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YUYAMA, Kamila T. et al. Discovering the potential of the secondary metabolites from Malouetia tamaquarina (Apocynaceae) and its endophytes against neglected tropical diseases. 2021, Anais.. Münster: University of Münster, 2021. Disponível em: https://repositorio.usp.br/directbitstream/d150eb7a-918c-4fe4-a5f4-be8b2f266cf4/3062064.pdf. Acesso em: 31 out. 2024.
APA
Yuyama, K. T., Macedo, C. C., Melo, W. G. da P., Silva, M. H. da, Lima, I. N., Souza, T. M., et al. (2021). Discovering the potential of the secondary metabolites from Malouetia tamaquarina (Apocynaceae) and its endophytes against neglected tropical diseases. In Program and Book of Abstracts. Münster: University of Münster. Recuperado de https://repositorio.usp.br/directbitstream/d150eb7a-918c-4fe4-a5f4-be8b2f266cf4/3062064.pdf
NLM
Yuyama KT, Macedo CC, Melo WG da P, Silva MH da, Lima IN, Souza TM, Souza YB, Aguiar JPL, Castello ACD, Ferreira LLG, Andricopulo AD, Silva GF, Schmidt TJ, Pupo MT. Discovering the potential of the secondary metabolites from Malouetia tamaquarina (Apocynaceae) and its endophytes against neglected tropical diseases [Internet]. Program and Book of Abstracts. 2021 ;[citado 2024 out. 31 ] Available from: https://repositorio.usp.br/directbitstream/d150eb7a-918c-4fe4-a5f4-be8b2f266cf4/3062064.pdf
Vancouver
Yuyama KT, Macedo CC, Melo WG da P, Silva MH da, Lima IN, Souza TM, Souza YB, Aguiar JPL, Castello ACD, Ferreira LLG, Andricopulo AD, Silva GF, Schmidt TJ, Pupo MT. Discovering the potential of the secondary metabolites from Malouetia tamaquarina (Apocynaceae) and its endophytes against neglected tropical diseases [Internet]. Program and Book of Abstracts. 2021 ;[citado 2024 out. 31 ] Available from: https://repositorio.usp.br/directbitstream/d150eb7a-918c-4fe4-a5f4-be8b2f266cf4/3062064.pdf
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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DOMINGUEZ, Humberto Enrique Ortega et al. Antileishmanial macrolides from ant-associated Streptomyces sp. ISID311. Bioorganic and Medicinal Chemistry, v. 32, n. 2, p. 116016-1-116016-9 + supplementary data, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2021.116016. Acesso em: 31 out. 2024.
APA
Dominguez, H. E. O., Lourenzon, V. B., Chevrette, M. G., Ferreira, L. L. G., Alvarenga, R. F. R., Melo, W. G. da P., et al. (2021). Antileishmanial macrolides from ant-associated Streptomyces sp. ISID311. Bioorganic and Medicinal Chemistry, 32( 2), 116016-1-116016-9 + supplementary data. doi:10.1016/j.bmc.2021.116016
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SILVEIRA, Flávia F. et al. Comparative study between the anti-P. falciparum activity of triazolopyrimidine, pyrazolopyrimidine and quinoline derivatives and the identification of new PfDHODH inhibitors. European Journal of Medicinal Chemistry, v. 209, n. Ja 2021, p. 112941-1-112941-16, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2020.112941. Acesso em: 31 out. 2024.
APA
Silveira, F. F., Souza, J. O. de, Hoelz, L. V. B., Campos, V. R., Jabor, V. A. P., Aguiar, A. C. C., et al. (2021). Comparative study between the anti-P. falciparum activity of triazolopyrimidine, pyrazolopyrimidine and quinoline derivatives and the identification of new PfDHODH inhibitors. European Journal of Medicinal Chemistry, 209( Ja 2021), 112941-1-112941-16. doi:10.1016/j.ejmech.2020.112941
NLM
Silveira FF, Souza JO de, Hoelz LVB, Campos VR, Jabor VAP, Aguiar ACC, Nonato MC, Albuquerque MG, Guido RVC, Boechat N, Pinheiro LCS. Comparative study between the anti-P. falciparum activity of triazolopyrimidine, pyrazolopyrimidine and quinoline derivatives and the identification of new PfDHODH inhibitors [Internet]. European Journal of Medicinal Chemistry. 2021 ; 209( Ja 2021): 112941-1-112941-16.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.ejmech.2020.112941
Vancouver
Silveira FF, Souza JO de, Hoelz LVB, Campos VR, Jabor VAP, Aguiar ACC, Nonato MC, Albuquerque MG, Guido RVC, Boechat N, Pinheiro LCS. Comparative study between the anti-P. falciparum activity of triazolopyrimidine, pyrazolopyrimidine and quinoline derivatives and the identification of new PfDHODH inhibitors [Internet]. European Journal of Medicinal Chemistry. 2021 ; 209( Ja 2021): 112941-1-112941-16.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.ejmech.2020.112941
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MENEGATTI, Carla et al. Meliponamycins: antimicrobials from stingless bee-associated Streptomyces sp. Journal of Natural Products, v. 83, n. 3, p. 610-616, 2020Tradução . . Disponível em: https://doi.org/10.1021/acs.jnatprod.9b01011. Acesso em: 31 out. 2024.
APA
Menegatti, C., Lourenzon, V. B., Rodríguez-Hernández, D. C., Melo, W. G. da P., Ferreira, L. L. G., Andricopulo, A. D., et al. (2020). Meliponamycins: antimicrobials from stingless bee-associated Streptomyces sp. Journal of Natural Products, 83( 3), 610-616. doi:10.1021/acs.jnatprod.9b01011
NLM
Menegatti C, Lourenzon VB, Rodríguez-Hernández DC, Melo WG da P, Ferreira LLG, Andricopulo AD, Nascimento FS do, Pupo MT. Meliponamycins: antimicrobials from stingless bee-associated Streptomyces sp. [Internet]. Journal of Natural Products. 2020 ; 83( 3): 610-616.[citado 2024 out. 31 ] Available from: https://doi.org/10.1021/acs.jnatprod.9b01011
Vancouver
Menegatti C, Lourenzon VB, Rodríguez-Hernández DC, Melo WG da P, Ferreira LLG, Andricopulo AD, Nascimento FS do, Pupo MT. Meliponamycins: antimicrobials from stingless bee-associated Streptomyces sp. [Internet]. Journal of Natural Products. 2020 ; 83( 3): 610-616.[citado 2024 out. 31 ] Available from: https://doi.org/10.1021/acs.jnatprod.9b01011
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MINARINI, Luciene Andrade Da Rocha et al. Antimicrobial resistance as a global public health problem: how can we address it? [Editorial]. Frontiers in Public Health. Lausanne: Instituto de Física de São Carlos, Universidade de São Paulo. Disponível em: https://doi.org/10.3389/fpubh.2020.612844. Acesso em: 31 out. 2024. , 2020
APA
Minarini, L. A. D. R., Andrade, L. N. de, De Gregorio, E., Grosso, F., Naas, T., Zarrilli, R., & Camargo, I. L. B. da C. (2020). Antimicrobial resistance as a global public health problem: how can we address it? [Editorial]. Frontiers in Public Health. Lausanne: Instituto de Física de São Carlos, Universidade de São Paulo. doi:10.3389/fpubh.2020.612844
NLM
Minarini LADR, Andrade LN de, De Gregorio E, Grosso F, Naas T, Zarrilli R, Camargo ILB da C. Antimicrobial resistance as a global public health problem: how can we address it? [Editorial] [Internet]. Frontiers in Public Health. 2020 ; No 2020 612844-1-612844-6.[citado 2024 out. 31 ] Available from: https://doi.org/10.3389/fpubh.2020.612844
Vancouver
Minarini LADR, Andrade LN de, De Gregorio E, Grosso F, Naas T, Zarrilli R, Camargo ILB da C. Antimicrobial resistance as a global public health problem: how can we address it? [Editorial] [Internet]. Frontiers in Public Health. 2020 ; No 2020 612844-1-612844-6.[citado 2024 out. 31 ] Available from: https://doi.org/10.3389/fpubh.2020.612844
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PAIXÃO, Drielly A. et al. Crystal structure, anti-Trypanosoma cruzi and cytotoxic activities of Cu(II) complexes bearing β-diketone and α-diimine ligands. Inorganica Chimica Acta, v. 499, n. Ja 2020, p. 119164-1- 119164-8, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.ica.2019.119164. Acesso em: 31 out. 2024.
APA
Paixão, D. A., Oliveira, B. C. A., Almeida, J. do C., Sousa, L. M., Lopes, C. D., Carneiro, Z. A., et al. (2020). Crystal structure, anti-Trypanosoma cruzi and cytotoxic activities of Cu(II) complexes bearing β-diketone and α-diimine ligands. Inorganica Chimica Acta, 499( Ja 2020), 119164-1- 119164-8. doi:10.1016/j.ica.2019.119164
NLM
Paixão DA, Oliveira BCA, Almeida J do C, Sousa LM, Lopes CD, Carneiro ZA, Tezuka DY, Clavijo JCT, Ellena J, Polloni L, Machado PHA, Albuquerque S de, Oliveira Junior RJ, Guilardi S, Guerra W. Crystal structure, anti-Trypanosoma cruzi and cytotoxic activities of Cu(II) complexes bearing β-diketone and α-diimine ligands [Internet]. Inorganica Chimica Acta. 2020 ; 499( Ja 2020): 119164-1- 119164-8.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.ica.2019.119164
Vancouver
Paixão DA, Oliveira BCA, Almeida J do C, Sousa LM, Lopes CD, Carneiro ZA, Tezuka DY, Clavijo JCT, Ellena J, Polloni L, Machado PHA, Albuquerque S de, Oliveira Junior RJ, Guilardi S, Guerra W. Crystal structure, anti-Trypanosoma cruzi and cytotoxic activities of Cu(II) complexes bearing β-diketone and α-diimine ligands [Internet]. Inorganica Chimica Acta. 2020 ; 499( Ja 2020): 119164-1- 119164-8.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.ica.2019.119164
; Santos, Júlio Cesar dos (Editor); Guimarães, Luis Henrique Souza (Editor) 
