Detalles de la búsqueda
1.
Resveratrol Analogs and Prodrugs Differently Affect the Survival of Breast Cancer Cells Impairing Estrogen/Estrogen Receptor α/Neuroglobin Pathway.
Int J Mol Sci
; 24(3)2023 Jan 21.
Artículo
Inglés
| MEDLINE | ID: mdl-36768470
2.
Pterostilbene fluorescent probes as potential tools for targeting neurodegeneration in biological applications.
J Enzyme Inhib Med Chem
; 37(1): 1812-1820, 2022 Dec.
Artículo
Inglés
| MEDLINE | ID: mdl-35758192
3.
Resveratrol-like Compounds as SIRT1 Activators.
Int J Mol Sci
; 23(23)2022 Dec 01.
Artículo
Inglés
| MEDLINE | ID: mdl-36499460
4.
Activation of carbonic anhydrases from human brain by amino alcohol oxime ethers: towards human carbonic anhydrase VII selective activators.
J Enzyme Inhib Med Chem
; 36(1): 48-57, 2021 Dec.
Artículo
Inglés
| MEDLINE | ID: mdl-33103482
5.
Identification of histone deacetylase inhibitors with (arylidene)aminoxy scaffold active in uveal melanoma cell lines.
J Enzyme Inhib Med Chem
; 36(1): 34-47, 2021 Dec.
Artículo
Inglés
| MEDLINE | ID: mdl-33100043
6.
Carbonic Anhydrase Inhibitors and Epilepsy: State of the Art and Future Perspectives.
Molecules
; 26(21)2021 Oct 22.
Artículo
Inglés
| MEDLINE | ID: mdl-34770789
7.
Multifunctional Small Molecules as Potential Anti-Alzheimer's Disease Agents.
Molecules
; 26(19)2021 Oct 03.
Artículo
Inglés
| MEDLINE | ID: mdl-34641559
8.
Monoaryl derivatives as transthyretin fibril formation inhibitors: Design, synthesis, biological evaluation and structural analysis.
Bioorg Med Chem
; 28(18): 115673, 2020 09 15.
Artículo
Inglés
| MEDLINE | ID: mdl-32828431
9.
Natural compounds as inhibitors of transthyretin amyloidosis and neuroprotective agents: analysis of structural data for future drug design.
J Enzyme Inhib Med Chem
; 35(1): 1145-1162, 2020 Dec.
Artículo
Inglés
| MEDLINE | ID: mdl-32419519
10.
Novel tacrine-benzofuran hybrids as potential multi-target drug candidates for the treatment of Alzheimer's Disease.
J Enzyme Inhib Med Chem
; 35(1): 211-226, 2020 Dec.
Artículo
Inglés
| MEDLINE | ID: mdl-31760822
11.
Oxy-imino saccharidic derivatives as a new structural class of aldose reductase inhibitors endowed with anti-oxidant activity.
J Enzyme Inhib Med Chem
; 35(1): 1194-1205, 2020 Dec.
Artículo
Inglés
| MEDLINE | ID: mdl-32396745
12.
Design, synthesis and biological evaluation of bifunctional inhibitors of membrane type 1 matrix metalloproteinase (MT1-MMP).
Bioorg Med Chem
; 27(1): 196-207, 2019 01 01.
Artículo
Inglés
| MEDLINE | ID: mdl-30522899
13.
Synthesis and investigation of polyhydroxylated pyrrolidine derivatives as novel chemotypes showing dual activity as glucosidase and aldose reductase inhibitors.
Bioorg Chem
; 92: 103298, 2019 11.
Artículo
Inglés
| MEDLINE | ID: mdl-31557624
14.
Matrix metalloproteinase-12 inhibitors: synthesis, structure-activity relationships and intestinal absorption of novel sugar-based biphenylsulfonamide carboxylates.
Bioorg Med Chem
; 26(22): 5804-5815, 2018 12 01.
Artículo
Inglés
| MEDLINE | ID: mdl-30429099
15.
Comparison of helical scan and standard rotation methods in single-crystal X-ray data collection strategies.
J Synchrotron Radiat
; 24(Pt 1): 42-52, 2017 01 01.
Artículo
Inglés
| MEDLINE | ID: mdl-28009545
16.
N-(Aroyl)-N-(arylmethyloxy)-α-alanines: Selective inhibitors of aldose reductase.
Bioorg Med Chem
; 25(12): 3068-3076, 2017 06 15.
Artículo
Inglés
| MEDLINE | ID: mdl-28392277
17.
A new crystal form of human transthyretin obtained with a curcumin derived ligand.
J Struct Biol
; 194(1): 8-17, 2016 Apr.
Artículo
Inglés
| MEDLINE | ID: mdl-26796656
18.
Synthesis and structural analysis of halogen substituted fibril formation inhibitors of Human Transthyretin (TTR).
J Enzyme Inhib Med Chem
; 31(sup1): 40-51, 2016.
Artículo
Inglés
| MEDLINE | ID: mdl-27067161
19.
X-ray crystal structure and activity of fluorenyl-based compounds as transthyretin fibrillogenesis inhibitors.
J Enzyme Inhib Med Chem
; 31(5): 824-33, 2016 Oct.
Artículo
Inglés
| MEDLINE | ID: mdl-26235916
20.
Synthesis and cycloxygenase inhibitory properties of new naphthalene-methylsulfonamido, naphthalene-methylsulfonyl and tetrahydronaphthalen-methylsulfonamido compounds.
J Enzyme Inhib Med Chem
; 30(3): 406-12, 2015 Jun.
Artículo
Inglés
| MEDLINE | ID: mdl-25089708