Detalhe da pesquisa
1.
Evolution of Linoleic Acid Biosynthesis Paved the Way for Ecological Success of Termites.
Mol Biol Evol
; 40(4)2023 04 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37043525
2.
Diketo-Ketoenol Tautomers in Curcuminoids: Synthesis, Separation of Tautomers, and Kinetic and Structural Studies.
J Org Chem
; 87(15): 10309-10318, 2022 08 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35895908
3.
Putative ligand binding sites of two functionally characterized bark beetle odorant receptors.
BMC Biol
; 19(1): 16, 2021 01 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-33499862
4.
Synthesis and In Vitro Evaluation of C-7 and C-8 Luteolin Derivatives as Influenza Endonuclease Inhibitors.
Int J Mol Sci
; 22(14)2021 Jul 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-34299354
5.
Investigation of flexibility of neuraminidase 150-loop using tamiflu derivatives in influenza A viruses H1N1 and H5N1.
Bioorg Med Chem
; 27(13): 2935-2947, 2019 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31128993
6.
DNA-linked inhibitor antibody assay (DIANA) as a new method for screening influenza neuraminidase inhibitors.
Biochem J
; 475(23): 3847-3860, 2018 12 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30404922
7.
Identification and Enantiodivergent Synthesis of (5 Z,9 S)-Tetradec-5-en-9-olide, a Queen-Specific Volatile of the Termite Silvestritermes minutus.
J Nat Prod
; 81(10): 2266-2274, 2018 10 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-30299957
8.
Synthesis and evaluation of 2-pyridinylpyrimidines as inhibitors of HIV-1 structural protein assembly.
Bioorg Med Chem Lett
; 26(15): 3487-90, 2016 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27353536
9.
Characterization of Triacylglycerol Estolide Isomers Using High-Resolution Tandem Mass Spectrometry with Nanoelectrospray Ionization.
Biomolecules
; 13(3)2023 03 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36979410
10.
Understanding desaturation/hydroxylation activity of castor stearoyl Δ9-Desaturase through rational mutagenesis.
Comput Struct Biotechnol J
; 20: 1378-1388, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35386101
11.
Thermodynamic and structural characterization of an optimized peptide-based inhibitor of the influenza polymerase PA-PB1 subunit interaction.
Antiviral Res
; 208: 105449, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36265804
12.
Synthesis of buprenorphine from oripavine via N-demethylation of oripavine quaternary salts.
J Org Chem
; 76(11): 4628-34, 2011 Jun 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-21495679
13.
Several generations of chemoenzymatic synthesis of oseltamivir (Tamiflu): evolution of strategy, quest for a process-quality synthesis, and evaluation of efficiency metrics.
J Org Chem
; 76(24): 10050-67, 2011 Dec 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-22007598
14.
Binding of de novo synthesized radiolabeled juvenile hormone (JH III) by JH receptors from the Cuban subterranean termite Prorhinotermes simplex and the German cockroach Blattella germanica.
Insect Biochem Mol Biol
; 139: 103671, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34656795
15.
structural characterization of the interaction between the C-terminal domain of the influenza polymerase PA subunit and an optimized small peptide inhibitor.
Antiviral Res
; 185: 104971, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33166574
16.
Unraveling the anti-influenza effect of flavonoids: Experimental validation of luteolin and its congeners as potent influenza endonuclease inhibitors.
Eur J Med Chem
; 208: 112754, 2020 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-32883638
17.
Kinetic, Thermodynamic, and Structural Analysis of Drug Resistance Mutations in Neuraminidase from the 2009 Pandemic Influenza Virus.
Viruses
; 10(7)2018 06 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-29933553
18.
Kinetic, thermodynamic and structural analysis of tamiphosphor binding to neuraminidase of H1N1 (2009) pandemic influenza.
Eur J Med Chem
; 121: 100-109, 2016 Oct 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27236066
19.
Specific Inhibitors of HIV Capsid Assembly Binding to the C-Terminal Domain of the Capsid Protein: Evaluation of 2-Arylquinazolines as Potential Antiviral Compounds.
J Med Chem
; 59(2): 545-58, 2016 Jan 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-26685880