Detalles de la búsqueda
1.
Synthesis and Biological Evaluation of 2-Azolylmethylene-3-(2H)-benzofuranone Derivatives as Potent Monoamine Oxidases Inhibitors.
Chem Pharm Bull (Tokyo);
72(1): 109-120, 2024.
Artículo
en Inglés
| MEDLINE | ID: mdl-38267058
2.
Synthesis of 2,8-Dioxabicyclo[3.3.1]nonane Derivatives and Their Neuroprotective Activities.
Chem Pharm Bull (Tokyo);
72(1): 56-60, 2024.
Artículo
en Inglés
| MEDLINE | ID: mdl-38171905
3.
A Tricyclic Aromatic Polyketide Isolated from the Marine-Derived Fungus Curvularia aeria.
Chem Pharm Bull (Tokyo);
72(1): 98-101, 2024.
Artículo
en Inglés
| MEDLINE | ID: mdl-38233138
4.
Inhibition of Polyamine Catabolism Reduces Cellular Senescence.
Int J Mol Sci;
24(17)2023 Aug 29.
Artículo
en Inglés
| MEDLINE | ID: mdl-37686212
5.
A Dual Anti-Inflammatory and Anti-Proliferative 3-Styrylchromone Derivative Synergistically Enhances the Anti-Cancer Effects of DNA-Damaging Agents on Colon Cancer Cells by Targeting HMGB1-RAGE-ERK1/2 Signaling.
Int J Mol Sci;
23(7)2022 Mar 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-35408786
6.
A 3-styrylchromone converted from trimebutine 3D pharmacophore possesses dual suppressive effects on RAGE and TLR4 signaling pathways.
Biochem Biophys Res Commun;
566: 1-8, 2021 08 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-34111666
7.
Synthesis and antifungal activity of polycyclic pyridone derivatives with anti-hyphal and biofilm formation activity against Candida albicans.
Bioorg Med Chem Lett;
37: 127845, 2021 04 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-33571649
8.
Synthesis and biological evaluation of 3-styrylchromone derivatives as selective monoamine oxidase B inhibitors.
Bioorg Med Chem;
42: 116255, 2021 07 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-34119696
9.
Synthesis of natural product-like polyprenylated phenols and quinones: Evaluation of their neuroprotective activities.
Bioorg Med Chem;
28(1): 115156, 2020 01 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-31740200
10.
Syntheses and Evaluation of 2- or 3-(N-Cyclicamino)chromone Derivatives as Monoamine Oxidase Inhibitors.
Chem Pharm Bull (Tokyo);
68(11): 1082-1089, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-33132375
11.
Design, synthesis and evaluation of 2-(indolylmethylidene)-2,3-dihydro-1-benzofuran-3-one and 2-(indolyl)-4H-chromen-4-one derivatives as novel monoamine oxidases inhibitors.
Bioorg Chem;
87: 594-600, 2019 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-30933784
12.
Synthesis and biological evaluation of pyrano[4,3-b][1]benzopyranone derivatives as monoamine oxidase and cholinesterase inhibitors.
Bioorg Chem;
83: 432-437, 2019 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-30428433
13.
2-Styrylchromone derivatives as potent and selective monoamine oxidase B inhibitors.
Bioorg Chem;
92: 103285, 2019 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-31561103
14.
Extracellular Spermine Activates DNA Methyltransferase 3A and 3B.
Int J Mol Sci;
20(5)2019 Mar 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-30871110
15.
Protective Effects of Brain Infarction by N-Acetylcysteine Derivatives.
Stroke;
49(7): 1727-1733, 2018 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-29866754
16.
3-(E)-Styryl-2H-chromene derivatives as potent and selective monoamine oxidase B inhibitors.
Bioorg Chem;
77: 436-442, 2018 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-29448189
17.
Characterization of the Dissolution Behavior of Piperine/Cyclodextrins Inclusion Complexes.
AAPS PharmSciTech;
19(2): 923-933, 2018 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-29071656
18.
Synthesis of Amide and Ester Derivatives of Cinnamic Acid and Its Analogs: Evaluation of Their Free Radical Scavenging and Monoamine Oxidase and Cholinesterase Inhibitory Activities.
Chem Pharm Bull (Tokyo);
65(11): 1020-1027, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-29093288
19.
2-Azolylchromone Derivatives as Potent and Selective Inhibitors of Monoamine Oxidases A and B.
Chem Pharm Bull (Tokyo);
64(10): 1499-1504, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-27725503
20.
Synthesis and Biological Evaluation of 3-Benzylidene-4-chromanone Derivatives as Free Radical Scavengers and α-Glucosidase Inhibitors.
Chem Pharm Bull (Tokyo);
64(8): 1203-7, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-27477661