Detalhe da pesquisa
1.
DFT/NMR Approach for the Configuration Assignment of Groups of Stereoisomers by the Combination and Comparison of Experimental and Predicted Sets of Data.
J Org Chem
; 85(5): 3297-3306, 2020 03 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31961156
2.
Elucidating heteroatom influence on homonuclear 4 J(H,H) coupling constants by DFT/NMR approach.
Magn Reson Chem
; 58(6): 566-575, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31883165
3.
Determining the Effect of Pterostilbene on Insulin Secretion Using Chemoproteomics.
Molecules
; 25(12)2020 Jun 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-32585851
4.
Protein Preparation Automatic Protocol for High-Throughput Inverse Virtual Screening: Accelerating the Target Identification by Computational Methods.
J Chem Inf Model
; 59(11): 4678-4690, 2019 11 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-31593460
5.
Garcinol and Related Polyisoprenylated Benzophenones as Topoisomerase II Inhibitors: Biochemical and Molecular Modeling Studies.
J Nat Prod
; 82(10): 2768-2779, 2019 10 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-31618025
6.
Immunomodulatory Biscembranoids and Assignment of Their Relative and Absolute Configurations: Data Set Modulation in the Density Functional Theory/Nuclear Magnetic Resonance Approach.
J Nat Prod
; 82(5): 1264-1273, 2019 05 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-30957492
7.
Identification by Inverse Virtual Screening of magnolol-based scaffold as new tankyrase-2 inhibitors.
Bioorg Med Chem
; 26(14): 3953-3957, 2018 08 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29934219
8.
Determination of Gymnemic Acid I as a Protein Biosynthesis Inhibitor Using Chemical Proteomics.
J Nat Prod
; 80(4): 909-915, 2017 04 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-28256837
9.
Discovering the Biological Target of 5-epi-Sinuleptolide Using a Combination of Proteomic Approaches.
Mar Drugs
; 15(10)2017 Oct 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-29027931
10.
Chemistry and Selective Tumor Cell Growth Inhibitory Activity of Polyketides from the South China Sea Sponge Plakortis sp.
Mar Drugs
; 15(5)2017 May 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28467388
11.
2,3-Dihydrobenzofuran privileged structures as new bioinspired lead compounds for the design of mPGES-1 inhibitors.
Bioorg Med Chem
; 24(4): 820-6, 2016 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26777299
12.
Bissubvilides A and B, Cembrane-Capnosane Heterodimers from the Soft Coral Sarcophyton subviride.
J Nat Prod
; 79(10): 2552-2558, 2016 10 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-27704808
13.
Mechanistic insights on petrosaspongiolide M inhibitory effects on immunoproteasome and autophagy.
Biochim Biophys Acta
; 1844(4): 713-21, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24530967
14.
Bio-inspired benzo[k,l]xanthene lignans: synthesis, DNA-interaction and antiproliferative properties.
Org Biomol Chem
; 12(17): 2686-701, 2014 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-24647864
15.
Structural basis for the design and synthesis of selective HDAC inhibitors.
Bioorg Med Chem
; 21(13): 3795-807, 2013 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23693069
16.
Differential in gel electrophoresis (DIGE) comparative proteomic analysis of macrophages cell cultures in response to perthamide C treatment.
Mar Drugs
; 11(4): 1288-99, 2013 Apr 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-23595056
17.
Plakilactones G and H from a marine sponge. Stereochemical determination of highly flexible systems by quantitative NMR-derived interproton distances combined with quantum mechanical calculations of (13)C chemical shifts.
Beilstein J Org Chem
; 9: 2940-9, 2013 Dec 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-24454574
18.
Chemical proteomics reveals heat shock protein 60 to be the main cellular target of the marine bioactive sesterterpene suvanine.
Chembiochem
; 13(13): 1953-8, 2012 Sep 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-22829539
19.
The inactivation mechanism of human group IIA phospholipase A(2) by Scalaradial.
Chembiochem
; 13(15): 2259-64, 2012 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23008213
20.
Modulation of proteasome machinery by natural and synthetic analogues of the marine bioactive compound petrosaspongiolide M.
Chembiochem
; 13(7): 982-6, 2012 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-22438326