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Artigo de periodico
Lactic acid bacteria secreted proteins as potential Listeria monocytogenes quorum sensing inhibitors (2023)
Marques, Pedro Henrique; Jaiswal, Arun Kumar; Almeida, Felipe Alves de ; Pinto, Uelinton Manoel ; Machado, Alessandra Barbosa Ferreira; Tiwari, Sandeep; Soares, Siomar de Castro; Paiva, Aline Dias
Source: Molecular Diversity. Unidade: FCF
Subjects: BACTÉRIAS LÁTICAS, LISTERIA
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ABNT
MARQUES, Pedro Henrique et al. Lactic acid bacteria secreted proteins as potential Listeria monocytogenes quorum sensing inhibitors. Molecular Diversity, 2023Tradução . . Disponível em: https://doi.org/10.1007/s11030-023-10722-7. Acesso em: 03 jun. 2024.
APA
Marques, P. H., Jaiswal, A. K., Almeida, F. A. de, Pinto, U. M., Machado, A. B. F., Tiwari, S., et al. (2023). Lactic acid bacteria secreted proteins as potential Listeria monocytogenes quorum sensing inhibitors. Molecular Diversity. doi:10.1007/s11030-023-10722-7
NLM
Marques PH, Jaiswal AK, Almeida FA de, Pinto UM, Machado ABF, Tiwari S, Soares S de C, Paiva AD. Lactic acid bacteria secreted proteins as potential Listeria monocytogenes quorum sensing inhibitors [Internet]. Molecular Diversity. 2023 ;[citado 2024 jun. 03 ] Available from: https://doi.org/10.1007/s11030-023-10722-7
Vancouver
Marques PH, Jaiswal AK, Almeida FA de, Pinto UM, Machado ABF, Tiwari S, Soares S de C, Paiva AD. Lactic acid bacteria secreted proteins as potential Listeria monocytogenes quorum sensing inhibitors [Internet]. Molecular Diversity. 2023 ;[citado 2024 jun. 03 ] Available from: https://doi.org/10.1007/s11030-023-10722-7
Artigo de periodico
Synthesis of α-amino-1,3-dicarbonyl compounds via Ugi flow chemistry reaction: access to functionalized 1,2,3-triazoles (2017)
Vasconcelos, Stanley N. S; Fornari, Evelin; Caracelli, Ignez; Stefani, Hélio Alexandre
Source: Molecular Diversity. Unidade: FCF
Subjects: ALFA-AMINOÁCIDOS, SÍNTESE ORGÂNICA
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ABNT
VASCONCELOS, Stanley N. S et al. Synthesis of α-amino-1,3-dicarbonyl compounds via Ugi flow chemistry reaction: access to functionalized 1,2,3-triazoles. Molecular Diversity, v. 21, n. 4, p. 893-902, 2017Tradução . . Disponível em: https://doi.org/10.1007/s11030-017-9764-5. Acesso em: 03 jun. 2024.
APA
Vasconcelos, S. N. S., Fornari, E., Caracelli, I., & Stefani, H. A. (2017). Synthesis of α-amino-1,3-dicarbonyl compounds via Ugi flow chemistry reaction: access to functionalized 1,2,3-triazoles. Molecular Diversity, 21( 4), 893-902. doi:10.1007/s11030-017-9764-5
NLM
Vasconcelos SNS, Fornari E, Caracelli I, Stefani HA. Synthesis of α-amino-1,3-dicarbonyl compounds via Ugi flow chemistry reaction: access to functionalized 1,2,3-triazoles [Internet]. Molecular Diversity. 2017 ; 21( 4): 893-902.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1007/s11030-017-9764-5
Vancouver
Vasconcelos SNS, Fornari E, Caracelli I, Stefani HA. Synthesis of α-amino-1,3-dicarbonyl compounds via Ugi flow chemistry reaction: access to functionalized 1,2,3-triazoles [Internet]. Molecular Diversity. 2017 ; 21( 4): 893-902.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1007/s11030-017-9764-5
Artigo de periodico
Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine (2016)
Vasconcelos, Stanley Nunes Siqueira; Shamim, Anwar; Ali, Bakhat; Oliveira, Isadora M. de; Stefani, Hélio Alexandre
Source: Molecular Diversity. Unidade: FCF
Subjects: PEPTÍDEOS, TIROXINA
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ABNT
VASCONCELOS, Stanley Nunes Siqueira et al. Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine. Molecular Diversity, v. 20, n. 2, p. 469-481, 2016Tradução . . Disponível em: https://doi.org/10.1007/s11030-015-9642-y. Acesso em: 03 jun. 2024.
APA
Vasconcelos, S. N. S., Shamim, A., Ali, B., Oliveira, I. M. de, & Stefani, H. A. (2016). Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine. Molecular Diversity, 20( 2), 469-481. doi:10.1007/s11030-015-9642-y
NLM
Vasconcelos SNS, Shamim A, Ali B, Oliveira IM de, Stefani HA. Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine [Internet]. Molecular Diversity. 2016 ; 20( 2): 469-481.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1007/s11030-015-9642-y
Vancouver
Vasconcelos SNS, Shamim A, Ali B, Oliveira IM de, Stefani HA. Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine [Internet]. Molecular Diversity. 2016 ; 20( 2): 469-481.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1007/s11030-015-9642-y
Artigo de periodico
Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement (2015)
Souza, Frederico B; Shamim, Anwar; Argomedo, Luiz M. Z; Pimenta, Daniel Carvalho; Stefani, Hélio Alexandre
Source: Molecular Diversity. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, REAGENTES ORGÂNICOS
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ABNT
SOUZA, Frederico B et al. Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement. Molecular Diversity, v. 19, n. 4, p. 773-785, 2015Tradução . . Disponível em: https://doi.org/10.1007/s11030-015-9619-x. Acesso em: 03 jun. 2024.
APA
Souza, F. B., Shamim, A., Argomedo, L. M. Z., Pimenta, D. C., & Stefani, H. A. (2015). Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement. Molecular Diversity, 19( 4), 773-785. doi:10.1007/s11030-015-9619-x
NLM
Souza FB, Shamim A, Argomedo LMZ, Pimenta DC, Stefani HA. Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement [Internet]. Molecular Diversity. 2015 ; 19( 4): 773-785.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1007/s11030-015-9619-x
Vancouver
Souza FB, Shamim A, Argomedo LMZ, Pimenta DC, Stefani HA. Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement [Internet]. Molecular Diversity. 2015 ; 19( 4): 773-785.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1007/s11030-015-9619-x
Artigo de periodico
Synthesis of C-glycosyl-bis-1,2,3-triazole derivatives from 3,4,6-tri-O-acetyl-D-glucal (2015)
Shamim, Anwar; Souza, Frederico Bernardes de; Trossini, Gustavo Henrique Goulart ; Gatti, Fernando de Moura; Stefani, Hélio Alexandre
Source: Molecular Diversity. Unidade: FCF
Subjects: ULTRASSOM, FLUORESCÊNCIA
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ABNT
SHAMIM, Anwar et al. Synthesis of C-glycosyl-bis-1,2,3-triazole derivatives from 3,4,6-tri-O-acetyl-D-glucal. Molecular Diversity, 2015Tradução . . Disponível em: https://doi.org/10.1007/s11030-014-9564-0. Acesso em: 03 jun. 2024.
APA
Shamim, A., Souza, F. B. de, Trossini, G. H. G., Gatti, F. de M., & Stefani, H. A. (2015). Synthesis of C-glycosyl-bis-1,2,3-triazole derivatives from 3,4,6-tri-O-acetyl-D-glucal. Molecular Diversity. doi:10.1007/s11030-014-9564-0
NLM
Shamim A, Souza FB de, Trossini GHG, Gatti F de M, Stefani HA. Synthesis of C-glycosyl-bis-1,2,3-triazole derivatives from 3,4,6-tri-O-acetyl-D-glucal [Internet]. Molecular Diversity. 2015 ;[citado 2024 jun. 03 ] Available from: https://doi.org/10.1007/s11030-014-9564-0
Vancouver
Shamim A, Souza FB de, Trossini GHG, Gatti F de M, Stefani HA. Synthesis of C-glycosyl-bis-1,2,3-triazole derivatives from 3,4,6-tri-O-acetyl-D-glucal [Internet]. Molecular Diversity. 2015 ;[citado 2024 jun. 03 ] Available from: https://doi.org/10.1007/s11030-014-9564-0
Artigo de periodico
Design and exploratory data analysis of a second generation of dendrimer prodrugs potentially antichagasic and leishmanicide (2013)
Giarolla, Jeanine ; Pasqualoto, Kerly Fernanda Mesquita; Ferreira, Elizabeth Igne
Source: Molecular Diversity. Unidade: FCF
Subjects: MODELAGEM MOLECULAR, DOENÇA DE CHAGAS, LEISHMANIA
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ABNT
GIAROLLA, Jeanine e PASQUALOTO, Kerly Fernanda Mesquita e FERREIRA, Elizabeth Igne. Design and exploratory data analysis of a second generation of dendrimer prodrugs potentially antichagasic and leishmanicide. Molecular Diversity, v. 17, n. 4, p. 711-720, 2013Tradução . . Disponível em: https://doi.org/10.1007/s11030-013-9467-5. Acesso em: 03 jun. 2024.
APA
Giarolla, J., Pasqualoto, K. F. M., & Ferreira, E. I. (2013). Design and exploratory data analysis of a second generation of dendrimer prodrugs potentially antichagasic and leishmanicide. Molecular Diversity, 17( 4), 711-720. doi:10.1007/s11030-013-9467-5
NLM
Giarolla J, Pasqualoto KFM, Ferreira EI. Design and exploratory data analysis of a second generation of dendrimer prodrugs potentially antichagasic and leishmanicide [Internet]. Molecular Diversity. 2013 ; 17( 4): 711-720.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1007/s11030-013-9467-5
Vancouver
Giarolla J, Pasqualoto KFM, Ferreira EI. Design and exploratory data analysis of a second generation of dendrimer prodrugs potentially antichagasic and leishmanicide [Internet]. Molecular Diversity. 2013 ; 17( 4): 711-720.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1007/s11030-013-9467-5
Artigo de periodico
Expanding cyclitol structural diversity by biocatalysis and metalocatalysis: a click chemistry approach (2011)
Sovera, Victoria de la; Bellomo, Ana; Pena, Jesus Marcelo; Gonzalez, David; Stefani, Hélio Alexandre
Source: Molecular Diversity. Unidade: FCF
Subjects: PALÁDIO, SÍNTESE ORGÂNICA
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ABNT
SOVERA, Victoria de la et al. Expanding cyclitol structural diversity by biocatalysis and metalocatalysis: a click chemistry approach. Molecular Diversity, v. 15, n. 1, p. 163-172, 2011Tradução . . Disponível em: https://doi.org/10.1007/s11030-010-9237-6. Acesso em: 03 jun. 2024.
APA
Sovera, V. de la, Bellomo, A., Pena, J. M., Gonzalez, D., & Stefani, H. A. (2011). Expanding cyclitol structural diversity by biocatalysis and metalocatalysis: a click chemistry approach. Molecular Diversity, 15( 1), 163-172. doi:10.1007/s11030-010-9237-6
NLM
Sovera V de la, Bellomo A, Pena JM, Gonzalez D, Stefani HA. Expanding cyclitol structural diversity by biocatalysis and metalocatalysis: a click chemistry approach [Internet]. Molecular Diversity. 2011 ; 15( 1): 163-172.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1007/s11030-010-9237-6
Vancouver
Sovera V de la, Bellomo A, Pena JM, Gonzalez D, Stefani HA. Expanding cyclitol structural diversity by biocatalysis and metalocatalysis: a click chemistry approach [Internet]. Molecular Diversity. 2011 ; 15( 1): 163-172.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1007/s11030-010-9237-6
Artigo de periodico
Structural relationships in the solid state of the anti-chagas agent (E)-phenylethenylbenzofuroxam (2010)
Martins, Felipe Terra; Ayala, Alejandro Pedro; Porcal, Williams; Cerecetto, Hugo; González, Mercedes; Ellena, Javier
Source: Molecular Diversity. Unidade: IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, DOENÇA DE CHAGAS (TRATAMENTO), ESPECTROSCOPIA RAMAN, CRISTALOGRAFIA
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ABNT
MARTINS, Felipe Terra et al. Structural relationships in the solid state of the anti-chagas agent (E)-phenylethenylbenzofuroxam. Molecular Diversity, v. No 2010, n. 4, p. 643-652, 2010Tradução . . Disponível em: https://doi.org/10.1007/s11030-009-9202-4. Acesso em: 03 jun. 2024.
APA
Martins, F. T., Ayala, A. P., Porcal, W., Cerecetto, H., González, M., & Ellena, J. (2010). Structural relationships in the solid state of the anti-chagas agent (E)-phenylethenylbenzofuroxam. Molecular Diversity, No 2010( 4), 643-652. doi:10.1007/s11030-009-9202-4
NLM
Martins FT, Ayala AP, Porcal W, Cerecetto H, González M, Ellena J. Structural relationships in the solid state of the anti-chagas agent (E)-phenylethenylbenzofuroxam [Internet]. Molecular Diversity. 2010 ; No 2010( 4): 643-652.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1007/s11030-009-9202-4
Vancouver
Martins FT, Ayala AP, Porcal W, Cerecetto H, González M, Ellena J. Structural relationships in the solid state of the anti-chagas agent (E)-phenylethenylbenzofuroxam [Internet]. Molecular Diversity. 2010 ; No 2010( 4): 643-652.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1007/s11030-009-9202-4
Artigo de periodico
Fragment-based QSAR: perspectives in drug design (2009)
Salum, Lívia B.; Andricopulo, Adriano Defini
Source: Molecular Diversity. Unidade: IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA, RECEPTORES, QUÍMICA MÉDICA
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ABNT
SALUM, Lívia B. e ANDRICOPULO, Adriano Defini. Fragment-based QSAR: perspectives in drug design. Molecular Diversity, v. 13, n. 3, p. 277-285, 2009Tradução . . Disponível em: https://doi.org/10.1007/s11030-009-9112-5. Acesso em: 03 jun. 2024.
APA
Salum, L. B., & Andricopulo, A. D. (2009). Fragment-based QSAR: perspectives in drug design. Molecular Diversity, 13( 3), 277-285. doi:10.1007/s11030-009-9112-5
NLM
Salum LB, Andricopulo AD. Fragment-based QSAR: perspectives in drug design [Internet]. Molecular Diversity. 2009 ; 13( 3): 277-285.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1007/s11030-009-9112-5
Vancouver
Salum LB, Andricopulo AD. Fragment-based QSAR: perspectives in drug design [Internet]. Molecular Diversity. 2009 ; 13( 3): 277-285.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1007/s11030-009-9112-5
Artigo de periodico
Fragment-based and classical quantitative structure-activity relationships for a series of hydrazides as antituberculosis agents (2008)
Andrade, Carolina H.; Salum, Lívia B.; Castilho, Marcelo S.; Pasqualoto, Kerly F. M.; Ferreira, Elizabeth Igne ; Andricopulo, Adriano Defini
Source: Molecular Diversity. Unidades: FCF, IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, PRODUTOS NATURAIS, RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA, DOENÇAS INFECCIOSAS, DOENÇAS (TRATAMENTO), TUBERCULOSE
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ABNT
ANDRADE, Carolina H. et al. Fragment-based and classical quantitative structure-activity relationships for a series of hydrazides as antituberculosis agents. Molecular Diversity, v. 12, n. 1, p. 47-59, 2008Tradução . . Disponível em: https://doi.org/10.1007/s11030-008-9074-z. Acesso em: 03 jun. 2024.
APA
Andrade, C. H., Salum, L. B., Castilho, M. S., Pasqualoto, K. F. M., Ferreira, E. I., & Andricopulo, A. D. (2008). Fragment-based and classical quantitative structure-activity relationships for a series of hydrazides as antituberculosis agents. Molecular Diversity, 12( 1), 47-59. doi:10.1007/s11030-008-9074-z
NLM
Andrade CH, Salum LB, Castilho MS, Pasqualoto KFM, Ferreira EI, Andricopulo AD. Fragment-based and classical quantitative structure-activity relationships for a series of hydrazides as antituberculosis agents [Internet]. Molecular Diversity. 2008 ; 12( 1): 47-59.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1007/s11030-008-9074-z
Vancouver
Andrade CH, Salum LB, Castilho MS, Pasqualoto KFM, Ferreira EI, Andricopulo AD. Fragment-based and classical quantitative structure-activity relationships for a series of hydrazides as antituberculosis agents [Internet]. Molecular Diversity. 2008 ; 12( 1): 47-59.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1007/s11030-008-9074-z

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