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Artigo de periodico
Discovery of novel inhibitors of Cruzain cysteine protease of Trypanosoma cruzi (2024)
Prates, João Lucas Bruno; Lopes, Juliana Romano ; Chin, Chung Man ; Ferreira, Elizabeth Igne ; Santos, Jean Leandro dos ; Scarim, Cauê Benito
Source: Current Medicinal Chemistry. Unidade: FCF
Subjects: TRYPANOSOMA CRUZI, DOENÇA DE CHAGAS, DESENVOLVIMENTO DE PRODUTOS, PRODUTOS NOVOS, FÁRMACOS
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ABNT
PRATES, João Lucas Bruno et al. Discovery of novel inhibitors of Cruzain cysteine protease of Trypanosoma cruzi. Current Medicinal Chemistry, v. 31, n. 16, p. 2285-2308, 2024Tradução . . Disponível em: https://dx.doi.org/10.2174/0109298673254864230921090. Acesso em: 27 ago. 2024.
APA
Prates, J. L. B., Lopes, J. R., Chin, C. M., Ferreira, E. I., Santos, J. L. dos, & Scarim, C. B. (2024). Discovery of novel inhibitors of Cruzain cysteine protease of Trypanosoma cruzi. Current Medicinal Chemistry, 31( 16), 2285-2308. doi:10.2174/0109298673254864230921090
NLM
Prates JLB, Lopes JR, Chin CM, Ferreira EI, Santos JL dos, Scarim CB. Discovery of novel inhibitors of Cruzain cysteine protease of Trypanosoma cruzi [Internet]. Current Medicinal Chemistry. 2024 ; 31( 16): 2285-2308.[citado 2024 ago. 27 ] Available from: https://dx.doi.org/10.2174/0109298673254864230921090
Vancouver
Prates JLB, Lopes JR, Chin CM, Ferreira EI, Santos JL dos, Scarim CB. Discovery of novel inhibitors of Cruzain cysteine protease of Trypanosoma cruzi [Internet]. Current Medicinal Chemistry. 2024 ; 31( 16): 2285-2308.[citado 2024 ago. 27 ] Available from: https://dx.doi.org/10.2174/0109298673254864230921090
Artigo de periodico
Aryl-isoquinoline as a potential scaffold for novel antitumor agents against glioblastoma cells (2024)
Fernandes, Thais Batista ; Yang, Rosania; Ferreira, Glaucio Monteiro ; Souza, Priscila Oliveira de ; Lopes, Vitor Galvão ; Toledo, Mônica Franco Zannini Junqueira ; Roliano, Gabriela Gonçalves ; Debom, Gabriela Nogueira ; Vassiliades, Sandra Valeria ; Hassimotto, Neuza Mariko Aymoto ; Hirata, Mario Hiroyuki ; Braganhol, Elizandra ; Parise Filho, Roberto
Source: Letters in Drug Design & Discovery. Unidade: FCF
Subjects: GLIOMA, SISTEMA NERVOSO CENTRAL
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ABNT
FERNANDES, Thais Batista et al. Aryl-isoquinoline as a potential scaffold for novel antitumor agents against glioblastoma cells. Letters in Drug Design & Discovery, v. 21, p. 948-960, 2024Tradução . . Disponível em: https://doi.org/10.2174/1570180820666230131111033. Acesso em: 27 ago. 2024.
APA
Fernandes, T. B., Yang, R., Ferreira, G. M., Souza, P. O. de, Lopes, V. G., Toledo, M. F. Z. J., et al. (2024). Aryl-isoquinoline as a potential scaffold for novel antitumor agents against glioblastoma cells. Letters in Drug Design & Discovery, 21, 948-960. doi:10.2174/1570180820666230131111033
NLM
Fernandes TB, Yang R, Ferreira GM, Souza PO de, Lopes VG, Toledo MFZJ, Roliano GG, Debom GN, Vassiliades SV, Hassimotto NMA, Hirata MH, Braganhol E, Parise Filho R. Aryl-isoquinoline as a potential scaffold for novel antitumor agents against glioblastoma cells [Internet]. Letters in Drug Design & Discovery. 2024 ; 21 948-960.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/1570180820666230131111033
Vancouver
Fernandes TB, Yang R, Ferreira GM, Souza PO de, Lopes VG, Toledo MFZJ, Roliano GG, Debom GN, Vassiliades SV, Hassimotto NMA, Hirata MH, Braganhol E, Parise Filho R. Aryl-isoquinoline as a potential scaffold for novel antitumor agents against glioblastoma cells [Internet]. Letters in Drug Design & Discovery. 2024 ; 21 948-960.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/1570180820666230131111033
Artigo de periodico
Folate pathway inhibitors, an underestimated and underexplored molecular target for new anti-tuberculosis agents (2023)
Vassiliades, Sandra Valeria ; Borges, Lara Gimenez; Giarolla, Jeanine ; Parise Filho, Roberto
Source: Mini-Reviews in Medicinal Chemistry. Unidade: FCF
Subjects: HOMEOSTASE, TUBERCULOSE, ÁCIDO FÓLICO
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ABNT
VASSILIADES, Sandra Valeria et al. Folate pathway inhibitors, an underestimated and underexplored molecular target for new anti-tuberculosis agents. Mini-Reviews in Medicinal Chemistry, v. 23, n. 17, p. 1711-1732, 2023Tradução . . Disponível em: https://doi.org/10.2174/1389557523666230206163154. Acesso em: 27 ago. 2024.
APA
Vassiliades, S. V., Borges, L. G., Giarolla, J., & Parise Filho, R. (2023). Folate pathway inhibitors, an underestimated and underexplored molecular target for new anti-tuberculosis agents. Mini-Reviews in Medicinal Chemistry, 23( 17), 1711-1732. doi:10.2174/1389557523666230206163154
NLM
Vassiliades SV, Borges LG, Giarolla J, Parise Filho R. Folate pathway inhibitors, an underestimated and underexplored molecular target for new anti-tuberculosis agents [Internet]. Mini-Reviews in Medicinal Chemistry. 2023 ; 23( 17): 1711-1732.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/1389557523666230206163154
Vancouver
Vassiliades SV, Borges LG, Giarolla J, Parise Filho R. Folate pathway inhibitors, an underestimated and underexplored molecular target for new anti-tuberculosis agents [Internet]. Mini-Reviews in Medicinal Chemistry. 2023 ; 23( 17): 1711-1732.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/1389557523666230206163154
Artigo de periodico-carta/editorial
Therapeutic potential of flavonoid derivatives for certain neglected tropical diseases [Editorial] (2022)
Pone, Boniface Kamdem ; Ferreira, Elizabeth Igne
Source: Current Drug Targets. Unidade: FCF
Subjects: FLAVONOIDES, MEDICAMENTO, DOENÇAS NEGLIGENCIADAS
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ABNT
PONE, Boniface Kamdem e FERREIRA, Elizabeth Igne. Therapeutic potential of flavonoid derivatives for certain neglected tropical diseases [Editorial]. Current Drug Targets. Sharjah: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. Disponível em: https://doi.org/10.2174/1389450123666220309093827. Acesso em: 27 ago. 2024. , 2022
APA
Pone, B. K., & Ferreira, E. I. (2022). Therapeutic potential of flavonoid derivatives for certain neglected tropical diseases [Editorial]. Current Drug Targets. Sharjah: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. doi:10.2174/1389450123666220309093827
NLM
Pone BK, Ferreira EI. Therapeutic potential of flavonoid derivatives for certain neglected tropical diseases [Editorial] [Internet]. Current Drug Targets. 2022 ; 23( 7): 680-682.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/1389450123666220309093827
Vancouver
Pone BK, Ferreira EI. Therapeutic potential of flavonoid derivatives for certain neglected tropical diseases [Editorial] [Internet]. Current Drug Targets. 2022 ; 23( 7): 680-682.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/1389450123666220309093827
Artigo de periodico
Zika virus NS2B-NS3 protease: quantum chemical properties insights into designing inhibitory peptides (2022)
Silva, João Vitor da ; Savino, Débora Feliciano; Hirata, Mario Hiroyuki ; Ferreira, Glaucio Monteiro ; Giarolla, Jeanine
Source: Protein and Peptide Letters. Unidade: FCF
Subjects: ZIKA VÍRUS, PEPTÍDEOS, MODELAGEM MOLECULAR
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ABNT
SILVA, João Vitor da et al. Zika virus NS2B-NS3 protease: quantum chemical properties insights into designing inhibitory peptides. Protein and Peptide Letters, v. 29, p. 901-910, 2022Tradução . . Disponível em: https://doi.org/10.2174/0929866529666220919143316. Acesso em: 27 ago. 2024.
APA
Silva, J. V. da, Savino, D. F., Hirata, M. H., Ferreira, G. M., & Giarolla, J. (2022). Zika virus NS2B-NS3 protease: quantum chemical properties insights into designing inhibitory peptides. Protein and Peptide Letters, 29, 901-910. doi:10.2174/0929866529666220919143316
NLM
Silva JV da, Savino DF, Hirata MH, Ferreira GM, Giarolla J. Zika virus NS2B-NS3 protease: quantum chemical properties insights into designing inhibitory peptides [Internet]. Protein and Peptide Letters. 2022 ; 29 901-910.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/0929866529666220919143316
Vancouver
Silva JV da, Savino DF, Hirata MH, Ferreira GM, Giarolla J. Zika virus NS2B-NS3 protease: quantum chemical properties insights into designing inhibitory peptides [Internet]. Protein and Peptide Letters. 2022 ; 29 901-910.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/0929866529666220919143316
Artigo de periodico
Insights into newly approved drugs from a medicinal chemistry perspective (2021)
Lima, Elys Juliane Cardoso ; Gomes, Renan Augusto ; Fornari, Evelin; Emery, Flavio da Silva ; Trossini, Gustavo Henrique Goulart
Source: Mini-Reviews in Medicinal Chemistry. Unidades: FCFRP, FCF
Assunto: FÁRMACOS
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ABNT
LIMA, Elys Juliane Cardoso et al. Insights into newly approved drugs from a medicinal chemistry perspective. Mini-Reviews in Medicinal Chemistry, v. 21, n. 16, p. 2227-2248, 2021Tradução . . Disponível em: https://doi.org/10.2174/1389557521666210226145328. Acesso em: 27 ago. 2024.
APA
Lima, E. J. C., Gomes, R. A., Fornari, E., Emery, F. da S., & Trossini, G. H. G. (2021). Insights into newly approved drugs from a medicinal chemistry perspective. Mini-Reviews in Medicinal Chemistry, 21( 16), 2227-2248. doi:10.2174/1389557521666210226145328
NLM
Lima EJC, Gomes RA, Fornari E, Emery F da S, Trossini GHG. Insights into newly approved drugs from a medicinal chemistry perspective [Internet]. Mini-Reviews in Medicinal Chemistry. 2021 ; 21( 16): 2227-2248.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/1389557521666210226145328
Vancouver
Lima EJC, Gomes RA, Fornari E, Emery F da S, Trossini GHG. Insights into newly approved drugs from a medicinal chemistry perspective [Internet]. Mini-Reviews in Medicinal Chemistry. 2021 ; 21( 16): 2227-2248.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/1389557521666210226145328
Artigo de periodico
Evidences of G-Coupled Protein Receptor (GPCR) signaling in the human malaria parasite Plasmodium falciparum for sensing its microenvironment and the role of purinergic signaling in malaria parasites (2021)
Pereira, Pedro Henrique Scarpelli; Pereira, Lucas Borges; Garcia, Célia Regina da Silva
Source: Current Topics in Medicinal Chemistry. Unidade: FCF
Subjects: PLASMODIUM FALCIPARUM, MALÁRIA
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ABNT
PEREIRA, Pedro Henrique Scarpelli e PEREIRA, Lucas Borges e GARCIA, Célia Regina da Silva. Evidences of G-Coupled Protein Receptor (GPCR) signaling in the human malaria parasite Plasmodium falciparum for sensing its microenvironment and the role of purinergic signaling in malaria parasites. Current Topics in Medicinal Chemistry, v. 21, p. 171-180, 2021Tradução . . Disponível em: https://doi.org/10.2174/1568026620666200826122716. Acesso em: 27 ago. 2024.
APA
Pereira, P. H. S., Pereira, L. B., & Garcia, C. R. da S. (2021). Evidences of G-Coupled Protein Receptor (GPCR) signaling in the human malaria parasite Plasmodium falciparum for sensing its microenvironment and the role of purinergic signaling in malaria parasites. Current Topics in Medicinal Chemistry, 21, 171-180. doi:10.2174/1568026620666200826122716
NLM
Pereira PHS, Pereira LB, Garcia CR da S. Evidences of G-Coupled Protein Receptor (GPCR) signaling in the human malaria parasite Plasmodium falciparum for sensing its microenvironment and the role of purinergic signaling in malaria parasites [Internet]. Current Topics in Medicinal Chemistry. 2021 ; 21 171-180.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/1568026620666200826122716
Vancouver
Pereira PHS, Pereira LB, Garcia CR da S. Evidences of G-Coupled Protein Receptor (GPCR) signaling in the human malaria parasite Plasmodium falciparum for sensing its microenvironment and the role of purinergic signaling in malaria parasites [Internet]. Current Topics in Medicinal Chemistry. 2021 ; 21 171-180.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/1568026620666200826122716
Artigo de periodico
Design of novel phosphopantetheine adenylyltransferase inhibitors: a potential new approach to tackle Mycobacterium tuberculosis (2021)
Primi, Marina Candido ; Tavares, Maurício Temotheo ; Klein, Larry L; Izard, Tina; Sant'Anna, Carlos M. R; Franzblau, Scott Gary; Ferreira, Elizabeth Igne
Source: Current Topics in Medicinal Chemistry. Unidade: FCF
Subjects: TUBERCULOSE, ANTIBIÓTICOS, INIBIDORES DE ENZIMAS, QUIMIOTERAPIA
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ABNT
PRIMI, Marina Candido et al. Design of novel phosphopantetheine adenylyltransferase inhibitors: a potential new approach to tackle Mycobacterium tuberculosis. Current Topics in Medicinal Chemistry, v. 21, p. 1186-1197, 2021Tradução . . Disponível em: https://doi.org/10.2174/1568026621666210728094804. Acesso em: 27 ago. 2024.
APA
Primi, M. C., Tavares, M. T., Klein, L. L., Izard, T., Sant'Anna, C. M. R., Franzblau, S. G., & Ferreira, E. I. (2021). Design of novel phosphopantetheine adenylyltransferase inhibitors: a potential new approach to tackle Mycobacterium tuberculosis. Current Topics in Medicinal Chemistry, 21, 1186-1197. doi:10.2174/1568026621666210728094804
NLM
Primi MC, Tavares MT, Klein LL, Izard T, Sant'Anna CMR, Franzblau SG, Ferreira EI. Design of novel phosphopantetheine adenylyltransferase inhibitors: a potential new approach to tackle Mycobacterium tuberculosis [Internet]. Current Topics in Medicinal Chemistry. 2021 ; 21 1186-1197.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/1568026621666210728094804
Vancouver
Primi MC, Tavares MT, Klein LL, Izard T, Sant'Anna CMR, Franzblau SG, Ferreira EI. Design of novel phosphopantetheine adenylyltransferase inhibitors: a potential new approach to tackle Mycobacterium tuberculosis [Internet]. Current Topics in Medicinal Chemistry. 2021 ; 21 1186-1197.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/1568026621666210728094804
Artigo de periodico
Design of arylsulfonylhydrazones as potential FabH inhibitors: synthesis, antimicrobial evaluation and molecular docking (2021)
Fernandes, Thais Batista; Segretti, Natanael Dante; Lourenço, Felipe Rebello ; Cândido, Thalita Marcílio ; Baby, André Rolim ; Barbosa, Euzébio Guimarães ; Parise Filho, Roberto
Source: Medicinal Chemistry. Unidade: FCF
Subjects: AGENTES ANTIMICROBIANOS, ANTIOXIDANTES, RESISTÊNCIA MICROBIANA ÀS DROGAS
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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: 27 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. 27 ] 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. 27 ] Available from: https://doi.org/10.2174/1573406415666191122111228
Artigo de periodico
Metalloproteinases suppression driven by the curcumin analog dm-1 modulates invasion in braf-resistant melanomas (2020)
Souza, Nayane de; Oliveira, Erica Aparecida de; Flores, Fernanda Faião; Pimenta, Luciana de Araujo; Quincoces, José A. P; Sampaio, Sandra C; Maria-Engler, Silvya Stuchi
Source: Anti-Cancer Agents in Medicinal Chemistry. Unidade: FCF
Subjects: MELANOMA, AÇAFRÃO, METALOPROTEINASES
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ABNT
SOUZA, Nayane de et al. Metalloproteinases suppression driven by the curcumin analog dm-1 modulates invasion in braf-resistant melanomas. Anti-Cancer Agents in Medicinal Chemistry, v. 20, p. 1038-1050, 2020Tradução . . Disponível em: https://doi.org/10.2174/1871520620666200218111422. Acesso em: 27 ago. 2024.
APA
Souza, N. de, Oliveira, E. A. de, Flores, F. F., Pimenta, L. de A., Quincoces, J. A. P., Sampaio, S. C., & Maria-Engler, S. S. (2020). Metalloproteinases suppression driven by the curcumin analog dm-1 modulates invasion in braf-resistant melanomas. Anti-Cancer Agents in Medicinal Chemistry, 20, 1038-1050. doi:10.2174/1871520620666200218111422
NLM
Souza N de, Oliveira EA de, Flores FF, Pimenta L de A, Quincoces JAP, Sampaio SC, Maria-Engler SS. Metalloproteinases suppression driven by the curcumin analog dm-1 modulates invasion in braf-resistant melanomas [Internet]. Anti-Cancer Agents in Medicinal Chemistry. 2020 ; 20 1038-1050.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/1871520620666200218111422
Vancouver
Souza N de, Oliveira EA de, Flores FF, Pimenta L de A, Quincoces JAP, Sampaio SC, Maria-Engler SS. Metalloproteinases suppression driven by the curcumin analog dm-1 modulates invasion in braf-resistant melanomas [Internet]. Anti-Cancer Agents in Medicinal Chemistry. 2020 ; 20 1038-1050.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/1871520620666200218111422
Artigo de periodico
An insight into the discovery of potent Antifilarial leads against lymphatic filariasis (2020)
Boniface, Pone Kamdem ; Ferreira, Elizabeth Igne
Source: Current Drug Targets. Unidade: FCF
Subjects: FILARIOSE, DOENÇAS
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ABNT
BONIFACE, Pone Kamdem e FERREIRA, Elizabeth Igne. An insight into the discovery of potent Antifilarial leads against lymphatic filariasis. Current Drug Targets, v. 21, p. 657-680, 2020Tradução . . Disponível em: https://doi.org/10.2174/1389450120666191204152415. Acesso em: 27 ago. 2024.
APA
Boniface, P. K., & Ferreira, E. I. (2020). An insight into the discovery of potent Antifilarial leads against lymphatic filariasis. Current Drug Targets, 21, 657-680. doi:10.2174/1389450120666191204152415
NLM
Boniface PK, Ferreira EI. An insight into the discovery of potent Antifilarial leads against lymphatic filariasis [Internet]. Current Drug Targets. 2020 ; 21 657-680.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/1389450120666191204152415
Vancouver
Boniface PK, Ferreira EI. An insight into the discovery of potent Antifilarial leads against lymphatic filariasis [Internet]. Current Drug Targets. 2020 ; 21 657-680.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/1389450120666191204152415
Artigo de periodico
Unveiling the targets involved in the quest of antileishmanial Leads using in silico methods (2020)
Boniface, Pone Kamdem ; Sano, Cinthya Miyuki; Ferreira, Elizabeth Igne
Source: Current Drug Targets. Unidade: FCF
Subjects: LEISHMANIA, FARMACOLOGIA
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ABNT
BONIFACE, Pone Kamdem e SANO, Cinthya Miyuki e FERREIRA, Elizabeth Igne. Unveiling the targets involved in the quest of antileishmanial Leads using in silico methods. Current Drug Targets, v. 21, p. 681-712, 2020Tradução . . Disponível em: https://doi.org/10.2174/1389450121666200128112948. Acesso em: 27 ago. 2024.
APA
Boniface, P. K., Sano, C. M., & Ferreira, E. I. (2020). Unveiling the targets involved in the quest of antileishmanial Leads using in silico methods. Current Drug Targets, 21, 681-712. doi:10.2174/1389450121666200128112948
NLM
Boniface PK, Sano CM, Ferreira EI. Unveiling the targets involved in the quest of antileishmanial Leads using in silico methods [Internet]. Current Drug Targets. 2020 ; 21 681-712.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/1389450121666200128112948
Vancouver
Boniface PK, Sano CM, Ferreira EI. Unveiling the targets involved in the quest of antileishmanial Leads using in silico methods [Internet]. Current Drug Targets. 2020 ; 21 681-712.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/1389450121666200128112948
Artigo de periodico
Fat substitution by inulin in goat milk ice cream produced with cajá (Spondias mombin) pulp and probiotic cultures: influence on composition, texture, and acceptability among consumers of two Brazilian regions (2020)
Paula, Clara Mitia de; Santos, Karina Maria Obrich dos; Oliveira, Leandro Silva; Oliveira, Jacqueline da Silva; Buriti, Flávia Carolina Alonso; Saad, Susana Marta Isay
Source: Emirates Journal of Food and Agriculture. Unidade: FCF
Subjects: CAJÁ, SORVETE, PROBIÓTICOS
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ABNT
PAULA, Clara Mitia de et al. Fat substitution by inulin in goat milk ice cream produced with cajá (Spondias mombin) pulp and probiotic cultures: influence on composition, texture, and acceptability among consumers of two Brazilian regions. Emirates Journal of Food and Agriculture, v. 32 n. 2, p. 140-149, 2020Tradução . . Disponível em: https://doi.org/10.9755/ejfa.2020.v32.i2.2074. Acesso em: 27 ago. 2024.
APA
Paula, C. M. de, Santos, K. M. O. dos, Oliveira, L. S., Oliveira, J. da S., Buriti, F. C. A., & Saad, S. M. I. (2020). Fat substitution by inulin in goat milk ice cream produced with cajá (Spondias mombin) pulp and probiotic cultures: influence on composition, texture, and acceptability among consumers of two Brazilian regions. Emirates Journal of Food and Agriculture, 32 n. 2, 140-149. doi:10.9755/ejfa.2020.v32.i2.2074
NLM
Paula CM de, Santos KMO dos, Oliveira LS, Oliveira J da S, Buriti FCA, Saad SMI. Fat substitution by inulin in goat milk ice cream produced with cajá (Spondias mombin) pulp and probiotic cultures: influence on composition, texture, and acceptability among consumers of two Brazilian regions [Internet]. Emirates Journal of Food and Agriculture. 2020 ; 32 n. 2 140-149.[citado 2024 ago. 27 ] Available from: https://doi.org/10.9755/ejfa.2020.v32.i2.2074
Vancouver
Paula CM de, Santos KMO dos, Oliveira LS, Oliveira J da S, Buriti FCA, Saad SMI. Fat substitution by inulin in goat milk ice cream produced with cajá (Spondias mombin) pulp and probiotic cultures: influence on composition, texture, and acceptability among consumers of two Brazilian regions [Internet]. Emirates Journal of Food and Agriculture. 2020 ; 32 n. 2 140-149.[citado 2024 ago. 27 ] Available from: https://doi.org/10.9755/ejfa.2020.v32.i2.2074
Artigo de periodico
Future and perspectives of the Zika Virus: drug repurposing as a powerful tool for treatment insights (2020)
Rampini, Denise ; Prieto, Diego Campos ; Colzi, Ana Luisa; Araujo, Renan Vinicius de ; Giarolla, Jeanine
Source: Mini-Reviews in Medicinal Chemistry. Unidade: FCF
Subjects: ZIKA VÍRUS, SAÚDE PÚBLICA
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ABNT
RAMPINI, Denise et al. Future and perspectives of the Zika Virus: drug repurposing as a powerful tool for treatment insights. Mini-Reviews in Medicinal Chemistry, v. 20, p. 1917-1928, 2020Tradução . . Disponível em: https://doi.org/10.2174/1389557520666200711174007. Acesso em: 27 ago. 2024.
APA
Rampini, D., Prieto, D. C., Colzi, A. L., Araujo, R. V. de, & Giarolla, J. (2020). Future and perspectives of the Zika Virus: drug repurposing as a powerful tool for treatment insights. Mini-Reviews in Medicinal Chemistry, 20, 1917-1928. doi:10.2174/1389557520666200711174007
NLM
Rampini D, Prieto DC, Colzi AL, Araujo RV de, Giarolla J. Future and perspectives of the Zika Virus: drug repurposing as a powerful tool for treatment insights [Internet]. Mini-Reviews in Medicinal Chemistry. 2020 ; 20 1917-1928.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/1389557520666200711174007
Vancouver
Rampini D, Prieto DC, Colzi AL, Araujo RV de, Giarolla J. Future and perspectives of the Zika Virus: drug repurposing as a powerful tool for treatment insights [Internet]. Mini-Reviews in Medicinal Chemistry. 2020 ; 20 1917-1928.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/1389557520666200711174007
Artigo de periodico
Arylsulfonylhydrazone induced apoptosis in MDA-MB-231 breast cancer cells (2018)
Fernandes, Thais Batista; Azevedo, Ricardo Alexandre de; Yang, Rosania; Teixeira, Sarah Fernandes; Trossini, Gustavo Henrique Goulart ; Barbuto, José Alexandre Marzagão ; Ferreira, Adilson Kleber; Parise Filho, Roberto
Source: Letters in Drug Design and Discovery. Unidades: FCF, ICB
Subjects: APOPTOSE, NEOPLASIAS MAMÁRIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERNANDES, Thais Batista et al. Arylsulfonylhydrazone induced apoptosis in MDA-MB-231 breast cancer cells. Letters in Drug Design and Discovery, v. 15, n. 12, p. 1288-1298, 2018Tradução . . Disponível em: https://doi.org/10.2174/1570180815666180321161513. Acesso em: 27 ago. 2024.
APA
Fernandes, T. B., Azevedo, R. A. de, Yang, R., Teixeira, S. F., Trossini, G. H. G., Barbuto, J. A. M., et al. (2018). Arylsulfonylhydrazone induced apoptosis in MDA-MB-231 breast cancer cells. Letters in Drug Design and Discovery, 15( 12), 1288-1298. doi:10.2174/1570180815666180321161513
NLM
Fernandes TB, Azevedo RA de, Yang R, Teixeira SF, Trossini GHG, Barbuto JAM, Ferreira AK, Parise Filho R. Arylsulfonylhydrazone induced apoptosis in MDA-MB-231 breast cancer cells [Internet]. Letters in Drug Design and Discovery. 2018 ; 15( 12): 1288-1298.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/1570180815666180321161513
Vancouver
Fernandes TB, Azevedo RA de, Yang R, Teixeira SF, Trossini GHG, Barbuto JAM, Ferreira AK, Parise Filho R. Arylsulfonylhydrazone induced apoptosis in MDA-MB-231 breast cancer cells [Internet]. Letters in Drug Design and Discovery. 2018 ; 15( 12): 1288-1298.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/1570180815666180321161513
Artigo de periodico
Edelfosine: an antitumor drug prototype (2018)
Teixeira, Sarah Fernandes ; Rodrigues, Cecília Pessoa ; Costa, Cícero Júlio Silva ; Pettinati, Thais Narimatsu; Azevedo, Ricardo Alexandre de ; Mambelli, Lisley Inata; Jorge, Salomão Dória; Ramos, Rodrigo Nalio; Ferro, Emer Suavinho ; Barbuto, José Alexandre Marzagão ; Ferreira, Adilson Kleber
Source: Anti-Cancer Agents in Medicinal Chemistry. Unidades: ICB, FCF
Subjects: FARMACOLOGIA, IMUNOLOGIA, QUIMIOTERÁPICOS, NEOPLASIAS PULMONARES, SISTEMA IMUNE, FOSFOLIPÍDEOS, PACIENTES, CITOMETRIA DE FLUXO, CITOTOXICIDADE IMUNOLÓGICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TEIXEIRA, Sarah Fernandes et al. Edelfosine: an antitumor drug prototype. Anti-Cancer Agents in Medicinal Chemistry, v. 18, n. 6, p. 865-874, 2018Tradução . . Disponível em: https://doi.org/10.2174/1871520618666180105165431. Acesso em: 27 ago. 2024.
APA
Teixeira, S. F., Rodrigues, C. P., Costa, C. J. S., Pettinati, T. N., Azevedo, R. A. de, Mambelli, L. I., et al. (2018). Edelfosine: an antitumor drug prototype. Anti-Cancer Agents in Medicinal Chemistry, 18( 6), 865-874. doi:10.2174/1871520618666180105165431
NLM
Teixeira SF, Rodrigues CP, Costa CJS, Pettinati TN, Azevedo RA de, Mambelli LI, Jorge SD, Ramos RN, Ferro ES, Barbuto JAM, Ferreira AK. Edelfosine: an antitumor drug prototype [Internet]. Anti-Cancer Agents in Medicinal Chemistry. 2018 ; 18( 6): 865-874.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/1871520618666180105165431
Vancouver
Teixeira SF, Rodrigues CP, Costa CJS, Pettinati TN, Azevedo RA de, Mambelli LI, Jorge SD, Ramos RN, Ferro ES, Barbuto JAM, Ferreira AK. Edelfosine: an antitumor drug prototype [Internet]. Anti-Cancer Agents in Medicinal Chemistry. 2018 ; 18( 6): 865-874.[citado 2024 ago. 27 ] Available from: https://doi.org/10.2174/1871520618666180105165431

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