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Refinado por: Nome da Publicação: European Journal Of Medicinal Chemistry remover assunto: Medical Sciences remover
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1
Heteroarylaminoethyl and heteroarylthioethyl imidazoles. Synthesis and H3-receptor affinity
Heteroarylaminoethyl and heteroarylthioethyl imidazoles. Synthesis and H3-receptor affinity
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Heteroarylaminoethyl and heteroarylthioethyl imidazoles. Synthesis and H3-receptor affinity

PLAZZI, P. V ; BORDI, F ; MOR, M ; SILVA, C ; MORINI, G ; CARETTA, A ; BAROCELLI, E ; VITALI, T

European journal of medicinal chemistry, 1995, Vol.30 (11), p.881-889 [Periódico revisado por pares]

Oxford: Elsevier

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2
Synthesis and antinociceptive properties of new structurally planned imidazo[1,2- a]pyridine 3-acylarylhydrazone derivatives
Synthesis and antinociceptive properties of new structurally planned imidazo[1,2- a]pyridine 3-acylarylhydrazone derivatives
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Synthesis and antinociceptive properties of new structurally planned imidazo[1,2- a]pyridine 3-acylarylhydrazone derivatives

Ribeiro, Izabella G. ; da Silva, Kelly Christine M. ; Parrini, Sergio C. ; de Miranda, Ana Luisa P. ; Fraga, Carlos A.M. ; Barreiro, Eliezer J.

European journal of medicinal chemistry, 1998-03, Vol.33 (3), p.225-235 [Periódico revisado por pares]

Oxford: Elsevier Masson SAS

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3
Synthesis and evaluation of analgesic, antiinflammatory and antiplatelet properties of new 2-pyridylarylhydrazone derivatives
Synthesis and evaluation of analgesic, antiinflammatory and antiplatelet properties of new 2-pyridylarylhydrazone derivatives
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Synthesis and evaluation of analgesic, antiinflammatory and antiplatelet properties of new 2-pyridylarylhydrazone derivatives

Todeschini, Adriane R. ; de Miranda, Ana Luisa P. ; da Silva, Kelly Christine M. ; Parrini, Sergio C. ; Barreiro, Eliezer J.

European journal of medicinal chemistry, 1998-03, Vol.33 (3), p.189-199 [Periódico revisado por pares]

Oxford: Elsevier Masson SAS

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4
Synthesis and analgesic activity of novel N-acylarylhydrazones and isosters, derived from natural safrole
Synthesis and analgesic activity of novel N-acylarylhydrazones and isosters, derived from natural safrole
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Synthesis and analgesic activity of novel N-acylarylhydrazones and isosters, derived from natural safrole

Lima, Patrícia C. ; Lima, Lídia M. ; da Silva, Kelli Cristine M. ; Léda, Paulo Henrique O. ; de Miranda, Ana Luisa P. ; Fraga, Carlos A.M. ; Barreiro, Eliezer J.

European journal of medicinal chemistry, 2000-02, Vol.35 (2), p.187-203 [Periódico revisado por pares]

Oxford: Elsevier Masson SAS

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5
Synthesis, anticonvulsant properties and pharmacokinetic profile of novel 10,11-dihydro-10-oxo-5H-dibenz/b,f/azepine-5-carboxamide derivatives
Synthesis, anticonvulsant properties and pharmacokinetic profile of novel 10,11-dihydro-10-oxo-5H-dibenz/b,f/azepine-5-carboxamide derivatives
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Synthesis, anticonvulsant properties and pharmacokinetic profile of novel 10,11-dihydro-10-oxo-5H-dibenz/b,f/azepine-5-carboxamide derivatives

Learmonth, David A ; Benes, Jan ; Parada, António ; Hainzl, Dominik ; Beliaev, Alexander ; Bonifácio, Maria João ; Matias, Pedro M ; Carrondo, Maria A ; Garrett, José ; Soares-da-Silva, Patrı́cio

European journal of medicinal chemistry, 2001-03, Vol.36 (3), p.227-236 [Periódico revisado por pares]

Oxford: Elsevier Masson SAS

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6
New isoxazole derivatives designed as nicotinic acetylcholine receptor ligand candidates
New isoxazole derivatives designed as nicotinic acetylcholine receptor ligand candidates
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New isoxazole derivatives designed as nicotinic acetylcholine receptor ligand candidates

Silva, Nilda M ; Tributino, Jorge L.M ; Miranda, Ana L.P ; Barreiro, Eliezer J ; Fraga, Carlos A.M

European journal of medicinal chemistry, 2002-02, Vol.37 (2), p.163-170 [Periódico revisado por pares]

Oxford: Elsevier Masson SAS

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7
Synthesis, and biological evaluation of new 1,3,4-thiadiazolium-2-phenylamine derivatives against Leishmania amazonensis promastigotes and amastigotes
Synthesis, and biological evaluation of new 1,3,4-thiadiazolium-2-phenylamine derivatives against Leishmania amazonensis promastigotes and amastigotes
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Synthesis, and biological evaluation of new 1,3,4-thiadiazolium-2-phenylamine derivatives against Leishmania amazonensis promastigotes and amastigotes

da Silva, Edson F ; Canto-Cavalheiro, Marilene M ; Braz, Viviane R ; Cysne-Finkelstein, Léa ; Leon, Leonor L ; Echevarria, Aurea

European journal of medicinal chemistry, 2002-12, Vol.37 (12), p.979-984 [Periódico revisado por pares]

Oxford: Elsevier Masson SAS

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8
A quantum chemical and statistical study of flavonoid compounds (flavones) with anti-HIV activity
A quantum chemical and statistical study of flavonoid compounds (flavones) with anti-HIV activity
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A quantum chemical and statistical study of flavonoid compounds (flavones) with anti-HIV activity

Souza, Jaime ; de Almeida Santos, Regina Helena ; Ferreira, Márcia Miguel Castro ; Molfetta, Fábio Alberto ; Camargo, Ademir João ; Maria Honório, Káthia ; da Silva, Albérico Borges Ferreira

European journal of medicinal chemistry, 2003-11, Vol.38 (11), p.929-938 [Periódico revisado por pares]

Oxford: Elsevier Masson SAS

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9
Synthesis, antitumour and antimicrobial activities of new peptidyl derivatives containing the 1,3-benzodioxole system
Synthesis, antitumour and antimicrobial activities of new peptidyl derivatives containing the 1,3-benzodioxole system
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Synthesis, antitumour and antimicrobial activities of new peptidyl derivatives containing the 1,3-benzodioxole system

Leite, Ana Cristina Lima ; Peixoto da Silva, Kezia ; de Souza, Ivone A. ; Magali de Araújo, Janete ; Brondani, Dalci José

European journal of medicinal chemistry, 2004-12, Vol.39 (12), p.1059-1065 [Periódico revisado por pares]

Oxford: Elsevier Masson SAS

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10
A structure–activity relationship study of quinone compounds with trypanocidal activity
A structure–activity relationship study of quinone compounds with trypanocidal activity
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A structure–activity relationship study of quinone compounds with trypanocidal activity

Molfetta, F.A. ; Bruni, A.T. ; Honório, K.M. ; da Silva, A.B.F.

European journal of medicinal chemistry, 2005-04, Vol.40 (4), p.329-338 [Periódico revisado por pares]

Oxford: Elsevier Masson SAS

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