Detalhe da pesquisa
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.
Artigo
em Inglês
| 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.
Artigo
em Inglês
| 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.
Artigo
em Inglês
| MEDLINE | ID: mdl-38233138
4.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-35408786
5.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-34111666
6.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-33571649
7.
Synthesis and biological evaluation of 3-styrylchromone derivatives as selective monoamine oxidase B inhibitors.
Bioorg Med Chem
; 42: 116255, 2021 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34119696
8.
Synthesis of natural product-like polyprenylated phenols and quinones: Evaluation of their neuroprotective activities.
Bioorg Med Chem
; 28(1): 115156, 2020 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31740200
9.
Syntheses and Evaluation of 2- or 3-(N-Cyclicamino)chromone Derivatives as Monoamine Oxidase Inhibitors.
Chem Pharm Bull (Tokyo)
; 68(11): 1082-1089, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33132375
10.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-30933784
11.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-30428433
12.
2-Styrylchromone derivatives as potent and selective monoamine oxidase B inhibitors.
Bioorg Chem
; 92: 103285, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31561103
13.
Protective Effects of Brain Infarction by N-Acetylcysteine Derivatives.
Stroke
; 49(7): 1727-1733, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29866754
14.
3-(E)-Styryl-2H-chromene derivatives as potent and selective monoamine oxidase B inhibitors.
Bioorg Chem
; 77: 436-442, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29448189
15.
Characterization of the Dissolution Behavior of Piperine/Cyclodextrins Inclusion Complexes.
AAPS PharmSciTech
; 19(2): 923-933, 2018 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-29071656
16.
p-Coumaroyl Malate Derivatives of the Pandanus amaryllifolius Leaf and Their Isomerization.
Chem Pharm Bull (Tokyo)
; 65(12): 1191-1194, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29199224
17.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-29093288
18.
2-Azolylchromone Derivatives as Potent and Selective Inhibitors of Monoamine Oxidases A and B.
Chem Pharm Bull (Tokyo)
; 64(10): 1499-1504, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27725503
19.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-27477661
20.
Synthesis and biological evaluation of piperic acid amides as free radical scavengers and α-glucosidase inhibitors.
Chem Pharm Bull (Tokyo)
; 63(5): 326-33, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25948326