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Refinado por: materia: Biochemistry & Molecular Biology eliminar
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1
1‐[(2,3‐Dihydro‐1‐benzofuran‐2‐yl) methyl]piperazines as novel anti‐inflammatory compounds: Synthesis and evaluation on H3R/H4R
1‐[(2,3‐Dihydro‐1‐benzofuran‐2‐yl) methyl]piperazines as novel anti‐inflammatory compounds: Synthesis and evaluation on H3R/H4R
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1‐[(2,3‐Dihydro‐1‐benzofuran‐2‐yl) methyl]piperazines as novel anti‐inflammatory compounds: Synthesis and evaluation on H3R/H4R

Corrêa, Michelle Fidelis ; Varela, Marina Themoteo ; Balbino, Aleksandro Martins ; Torrecilhas, Ana Claudia ; Landgraf, Richardt Gama ; Troncone, Lanfranco Ranieri Paolo ; Fernandes, João Paulo dos Santos

Chemical biology & drug design, 2017-08, Vol.90 (2), p.317-322 [Revista revisada por pares]

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2
1,1'-[ethenylidenebis(sulfonyl)]bis-benzene : A useful pre-chromatographic derivatization reagent for HPLC analyses of thiol drugs
1,1'-[ethenylidenebis(sulfonyl)]bis-benzene : A useful pre-chromatographic derivatization reagent for HPLC analyses of thiol drugs
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1,1'-[ethenylidenebis(sulfonyl)]bis-benzene : A useful pre-chromatographic derivatization reagent for HPLC analyses of thiol drugs

CAVRINI, V ; GOTTI, R ; ANDRISANO, V ; GATTI, R

Chromatographia, 1996-05, Vol.42 (9-10), p.515-520 [Revista revisada por pares]

Oxford: Springer

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3
1,10-phenanthroline inhibits sumoylation and reveals that yeast SUMO modifications are highly transient
1,10-phenanthroline inhibits sumoylation and reveals that yeast SUMO modifications are highly transient
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1,10-phenanthroline inhibits sumoylation and reveals that yeast SUMO modifications are highly transient

McNeil, J Bryan ; Lee, Su-Kyong ; Oliinyk, Anna ; Raina, Sehaj ; Garg, Jyoti ; Moallem, Marjan ; Urquhart-Cox, Verne ; Fillingham, Jeffrey ; Cheung, Peter ; Rosonina, Emanuel

EMBO reports, 2024-01, Vol.25 (1), p.68-81 [Revista revisada por pares]

London: Nature Publishing Group UK

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4
1,2,3-Triazole-based analogue of benznidazole displays remarkable activity against Trypanosoma cruzi
1,2,3-Triazole-based analogue of benznidazole displays remarkable activity against Trypanosoma cruzi
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1,2,3-Triazole-based analogue of benznidazole displays remarkable activity against Trypanosoma cruzi

de Andrade, Peterson ; Galo, Oswaldo A. ; Carvalho, Marcelo R. ; Lopes, Carla D. ; Carneiro, Zumira A. ; Sesti-Costa, Renata ; de Melo, Eduardo Borges ; Silva, João S. ; Carvalho, Ivone

Bioorganic & medicinal chemistry, 2015-11, Vol.23 (21), p.6815-6826 [Revista revisada por pares]

England: Elsevier Ltd

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5
1,2,3-Triazole derivatives: synthesis, docking, cytotoxicity analysis and in vivo antimalarial activity
1,2,3-Triazole derivatives: synthesis, docking, cytotoxicity analysis and in vivo antimalarial activity
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1,2,3-Triazole derivatives: synthesis, docking, cytotoxicity analysis and in vivo antimalarial activity

Valério Lopes, Fernanda ; Fazza Stroppa, Pedro Henrique ; Marinho, Juliane Aparecida ; Reis Soares, Roberta ; de Azevedo Alves, Lara ; Capriles Goliatt, Priscila Vanessa Zabala ; Abramo, Clarice ; David da Silva, Adilson

Chemico-biological interactions, 2021-12, Vol.350, p.109688-109688, Article 109688 [Revista revisada por pares]

Elsevier B.V

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6
1,2,3-Triazole Hybrids Containing Isatins and Phenolic Moieties: Regioselective Synthesis and Molecular Docking Studies
1,2,3-Triazole Hybrids Containing Isatins and Phenolic Moieties: Regioselective Synthesis and Molecular Docking Studies
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1,2,3-Triazole Hybrids Containing Isatins and Phenolic Moieties: Regioselective Synthesis and Molecular Docking Studies

Maiuolo, Loredana ; Tallarida, Matteo Antonio ; Meduri, Angelo ; Fiorani, Giulia ; Jiritano, Antonio ; De Nino, Antonio ; Algieri, Vincenzo ; Costanzo, Paola

Molecules (Basel, Switzerland), 2024-04, Vol.29 (7), p.1556 [Revista revisada por pares]

Switzerland: MDPI AG

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7
1,2,3-Triazolo[4,5-b]aminoquinolines: Design, synthesis, structure, acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibitory activity, and molecular docking of novel modified tacrines
1,2,3-Triazolo[4,5-b]aminoquinolines: Design, synthesis, structure, acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibitory activity, and molecular docking of novel modified tacrines
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1,2,3-Triazolo[4,5-b]aminoquinolines: Design, synthesis, structure, acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibitory activity, and molecular docking of novel modified tacrines

Kappenberg, Yuri G. ; Nogara, Pablo A. ; Stefanello, Felipe S. ; Delgado, Cássia P. ; Rocha, João B.T. ; Zanatta, Nilo ; Martins, Marcos A.P. ; Bonacorso, Helio G.

Bioorganic chemistry, 2023-10, Vol.139, p.106704-106704, Article 106704 [Revista revisada por pares]

United States: Elsevier Inc

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8
1,2,3,4-tetrahydro-2-methyl-β-carboline and solavetivone from Solanum jabrense
1,2,3,4-tetrahydro-2-methyl-β-carboline and solavetivone from Solanum jabrense
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1,2,3,4-tetrahydro-2-methyl-β-carboline and solavetivone from Solanum jabrense

da Silva, Tania Maria Sarmento ; Braz-Filho, Raimundo ; de Carvalho, Mário Geraldo ; de Fátima Agra, Maria

Biochemical systematics and ecology, 2002-12, Vol.30 (11), p.1083-1085 [Revista revisada por pares]

Elsevier Ltd

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9
1,2,4-Oxadiazole/2-Imidazoline Hybrids: Multi-target-directed Compounds for the Treatment of Infectious Diseases and Cancer
1,2,4-Oxadiazole/2-Imidazoline Hybrids: Multi-target-directed Compounds for the Treatment of Infectious Diseases and Cancer
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1,2,4-Oxadiazole/2-Imidazoline Hybrids: Multi-target-directed Compounds for the Treatment of Infectious Diseases and Cancer

Shetnev, Anton ; Baykov, Sergey ; Kalinin, Stanislav ; Belova, Alexandra ; Sharoyko, Vladimir ; Rozhkov, Anton ; Zelenkov, Lev ; Tarasenko, Marina ; Sadykov, Evgeny ; Korsakov, Mikhail ; Krasavin, Mikhail

International journal of molecular sciences, 2019-04, Vol.20 (7), p.1699 [Revista revisada por pares]

Switzerland: MDPI AG

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10
1,3‐Bis(aryloxy)propan‐2‐ols as potential antileishmanial agents
1,3‐Bis(aryloxy)propan‐2‐ols as potential antileishmanial agents
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1,3‐Bis(aryloxy)propan‐2‐ols as potential antileishmanial agents

Lavorato, Stefânia N. ; Duarte, Mariana C. ; Lage, Daniela P. ; Tavares, Carlos A. P. ; Coelho, Eduardo A. F. ; Alves, Ricardo J.

Chemical biology & drug design, 2017-11, Vol.90 (5), p.981-986 [Revista revisada por pares]

England: John Wiley and Sons Inc

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