Benzofuran-based hybrid compounds for the inhibition of cholinesterase activity, beta amyloid aggregation, and abeta neurotoxicity.
about
Multifunctional receptor-directed drugs for disorders of the central nervous systemThe discovery of potential acetylcholinesterase inhibitors: a combination of pharmacophore modeling, virtual screening, and molecular docking studies.Neuroprotective and antioxidant effects of novel benzofuran-2-carboxamide derivatives.Anti-amyloidogenic properties of some phenolic compoundsDesign, synthesis and evaluation of genistein-polyamine conjugates as multi-functional anti-Alzheimer agents.Development of an in-vivo active reversible butyrylcholinesterase inhibitor.Multi-Target Directed Drugs: A Modern Approach for Design of New Drugs for the treatment of Alzheimer's Disease.New approaches in the design and development of cannabinoid receptor ligands: multifunctional and bivalent compounds.Hybrids: a new paradigm to treat Alzheimer's disease.Iodine-mediated synthesis of heterocycles via electrophilic cyclization of alkynes.Development of 3D-QSAR Model for Acetylcholinesterase Inhibitors Using a Combination of Fingerprint, Molecular Docking, and Structure-Based Pharmacophore Approaches.Design, synthesis and cytotoxic activities of novel hybrid compounds between dihydrobenzofuran and imidazole.New benzofuran derivatives as an antioxidant agent.Benzofuranone derivatives as effective small molecules related to insulin amyloid fibrillation: a structure-function study.Synthesis, characterization, molecular docking studies and biological evaluation of some novel hybrids based on quinazolinone, benzofuran and imidazolium moieties as potential cytotoxic and antimicrobial agents.Design, synthesis, biological evaluation, and docking study of 4-isochromanone hybrids bearing N-benzyl pyridinium moiety as dual binding site acetylcholinesterase inhibitors (part II).Molecular docking and receptor-specific 3D-QSAR studies of acetylcholinesterase inhibitors.Regioselective 5-exo-Trig Heterocyclization of 2-Allyl-1-naphthols under the Influence of N-Iodosuccinimide or Molecular Iodine in Aqueous MicelleBenzofuran-Chalcone Hybrids as Potential Multifunctional Agents against Alzheimer’s Disease: Synthesis and in vivo Studies with TransgenicCaenorhabditis elegans
P2860
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P2860
Benzofuran-based hybrid compounds for the inhibition of cholinesterase activity, beta amyloid aggregation, and abeta neurotoxicity.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh
2008年學術文章
@zh-hant
name
Benzofuran-based hybrid compou ...... tion, and abeta neurotoxicity.
@en
Benzofuran-based hybrid compou ...... tion, and abeta neurotoxicity.
@nl
type
label
Benzofuran-based hybrid compou ...... tion, and abeta neurotoxicity.
@en
Benzofuran-based hybrid compou ...... tion, and abeta neurotoxicity.
@nl
prefLabel
Benzofuran-based hybrid compou ...... tion, and abeta neurotoxicity.
@en
Benzofuran-based hybrid compou ...... tion, and abeta neurotoxicity.
@nl
P2093
P50
P356
P1476
Benzofuran-based hybrid compou ...... tion, and abeta neurotoxicity.
@en
P2093
Alessandra Bisi
Andrea Tarozzi
Angela Rampa
Céline Rivière
Jean-Pierre Monti
Lorna Piazzi
Silvia Gobbi
Stefano Rizzo
P304
P356
10.1021/JM8002747
P407
P577
2008-04-18T00:00:00Z