Detalles de la búsqueda
1.
Identification of novel non-toxic and anti-angiogenic α-fluorinated chalcones as potent colchicine binding site inhibitors.
J Enzyme Inhib Med Chem;
37(1): 339-354, 2022 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-34979843
2.
Synthesis and biological evaluation of halogenated phenoxychalcones and their corresponding pyrazolines as cytotoxic agents in human breast cancer.
J Enzyme Inhib Med Chem;
37(1): 189-201, 2022 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-34894967
3.
Total Synthesis of the Natural Chalcone Lophirone E, Synthetic Studies toward Benzofuran and Indole-Based Analogues, and Investigation of Anti-Leishmanial Activity.
Molecules;
27(2)2022 Jan 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-35056779
4.
EGFR and COX-2 Dual Inhibitor: The Design, Synthesis, and Biological Evaluation of Novel Chalcones.
Molecules;
27(4)2022 Feb 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-35208952
5.
A synthesized heterocyclic chalcone inhibits neutrophilic inflammation through K+ -dependent pH regulation.
FASEB J;
34(5): 7127-7143, 2020 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-32275103
6.
Leloir glycosyltransferases enabled to flow synthesis: Continuous production of the natural C-glycoside nothofagin.
Biotechnol Bioeng;
118(11): 4402-4413, 2021 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-34355386
7.
Synthesis of pyranochalcone derivatives and their inhibitory effect on NF-κB activation.
Bioorg Med Chem Lett;
42: 128042, 2021 06 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-33862226
8.
Design, synthesis, characterization, and anticancer activity of a novel series of O-substituted chalcone derivatives.
Bioorg Med Chem Lett;
35: 127827, 2021 03 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-33508467
9.
A multiple acetal chalcone-BODIPY-based fluorescence: synthesis, physical property, and biological studies.
Anal Bioanal Chem;
413(9): 2529-2541, 2021 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-33712915
10.
Chalcones and their B-aryl analogues as myeloperoxidase inhibitors: In silico, in vitro and ex vivo investigations.
Bioorg Chem;
110: 104773, 2021 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-33744807
11.
Combined 3D-QSAR and docking analysis for the design and synthesis of chalcones as potent and selective monoamine oxidase B inhibitors.
Bioorg Chem;
108: 104689, 2021 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-33571810
12.
Synthesis of azachalcones, their α-amylase, α-glucosidase inhibitory activities, kinetics, and molecular docking studies.
Bioorg Chem;
106: 104489, 2021 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-33272713
13.
Design, synthesis and antibacterial activity of chalcones against MSSA and MRSA planktonic cells and biofilms.
Bioorg Chem;
116: 105279, 2021 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-34509799
14.
Synthesis of chalcones derived from 1-naphthylacetophenone and evaluation of their cytotoxic and apoptotic effects in acute leukemia cell lines.
Bioorg Chem;
116: 105315, 2021 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-34496319
15.
Discovery of isoliquiritigenin analogues that reverse acute hepatitis by inhibiting macrophage polarization.
Bioorg Chem;
114: 105043, 2021 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-34120019
16.
Design, synthesis and biological evaluation of novel bischalcone derivatives as potential anticancer agents.
Bioorg Chem;
111: 104882, 2021 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-33839582
17.
Design, synthesis and drug resistance reversal potential of novel curcumin mimics Van D: Synergy potential of curcumin mimics.
Bioorg Chem;
106: 104454, 2021 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-33213895
18.
Structural exploration of multifunctional monoamine oxidase B inhibitors as potential drug candidates against Alzheimer's disease.
Bioorg Chem;
114: 105070, 2021 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-34126574
19.
The discovery of novel sanjuanolide derivatives as chemotherapeutic agents targeting castration-resistant prostate cancer.
Bioorg Chem;
111: 104880, 2021 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-33839585
20.
Novel urea linked ciprofloxacin-chalcone hybrids having antiproliferative topoisomerases I/II inhibitory activities and caspases-mediated apoptosis.
Bioorg Chem;
106: 104422, 2021 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-33248713