Detalhe da pesquisa
1.
Phenoxy- and Phenylamino-Heterocyclic Quinones: Synthesis and Preliminary Anti-Pancreatic Cancer Activity.
Chem Biodivers
; 19(6): e202101036, 2022 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-35581163
2.
New benzimidazolequinones as trypanosomicidal agents.
Bioorg Chem
; 111: 104823, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33798844
3.
Microwave-assisted nucleophilic degradation of organophosphorus pesticides in propylene carbonate.
Org Biomol Chem
; 18(39): 7868-7875, 2020 10 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-32985641
4.
Promising 2,6,9-Trisubstituted Purine Derivatives for Anticancer Compounds: Synthesis, 3D-QSAR, and Preliminary Biological Assays.
Int J Mol Sci
; 21(1)2019 Dec 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-31881717
5.
Dual function of amino acid ionic liquids (Bmim[AA]) on the degradation of the organophosphorus pesticide, Paraoxon®.
Org Biomol Chem
; 16(40): 7446-7453, 2018 10 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-30264845
6.
Gutmann's Donor Numbers Correctly Assess the Effect of the Solvent on the Kinetics of SN Ar Reactions in Ionic Liquids.
Chemistry
; 22(37): 13347-51, 2016 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27506894
7.
Design, synthesis, biological evaluation and binding mode modeling of benzimidazole derivatives targeting the cannabinoid receptor type 1.
Arch Pharm (Weinheim)
; 348(2): 81-8, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25641513
8.
Synthesis and pharmacophore modelling of 2,6,9-trisubstituted purine derivatives and their potential role as apoptosis-inducing agents in cancer cell lines.
Molecules
; 20(4): 6808-26, 2015 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25884555
9.
Synthesis and biological characterization of new aryloxyindole-4,9-diones as potent trypanosomicidal agents.
Bioorg Med Chem Lett
; 24(16): 3919-22, 2014 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25008454
10.
2-Phenylaminonaphthoquinones and related compounds: synthesis, trypanocidal and cytotoxic activities.
Bioorg Med Chem
; 22(17): 4609-20, 2014 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25127463
11.
Specific nucleophile-electrophile interactions in nucleophilic aromatic substitutions.
Org Biomol Chem
; 11(14): 2302-9, 2013 Apr 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-23423183
12.
Theoretical study on the molecular mechanism of the [5 + 2] vs. [4 + 2] cyclization mediated by Lewis acid in the quinone system.
Org Biomol Chem
; 11(48): 8357-65, 2013 Dec 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-24170110
13.
New short strategy for the synthesis of the dibenz[b,f]oxepin scaffold.
Molecules
; 18(12): 14797-806, 2013 Nov 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-24352054
14.
A ternary eutectic solvent for cellulose nanocrystal production: exploring the recyclability and pre-pilot scale-up.
Front Chem
; 11: 1233889, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37693168
15.
Mode of action of p-quinone derivatives with trypanocidal activity studied by experimental and in silico models.
Eur J Med Chem
; 246: 114926, 2023 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36508970
16.
Adsorption behavior of hydrophobically modified polyelectrolytes onto amino- or methyl-terminated surfaces.
Langmuir
; 27(22): 13524-32, 2011 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21962212
17.
NL MIND-BEST: a web server for ligands and proteins discovery--theoretic-experimental study of proteins of Giardia lamblia and new compounds active against Plasmodium falciparum.
J Theor Biol
; 276(1): 229-49, 2011 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-21277861
18.
6,9-Dimeth-oxy-3,4-dihydro-1H-1,4-oxazino[4,3-a]indol-1-one.
Acta Crystallogr Sect E Struct Rep Online
; 67(Pt 2): o318, 2011 Jan 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-21523004
19.
7-(tert-Butyl-diphenyl-sil-yloxy)-2,2-dimethyl-1-benzofuran-3(2H)-one.
Acta Crystallogr Sect E Struct Rep Online
; 67(Pt 2): o375, 2011 Jan 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-21523052
20.
How the Nature of an Alpha-Nucleophile Determines a Brønsted Type-Plot and Its Reaction Pathways. An Experimental Study.
Front Chem
; 9: 740161, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-35186890