A NOVEL ANTI-ALZHEIMER'S DISEASE DRUG, LADOSTIGIL: NEUROPROTECTIVE, MULTIMODAL BRAIN-SELECTIVE MONOAMINE OXIDASE AND CHOLINESTERASE INHIBITOR

被引:15
|
作者
Weinreb, Orly [1 ,2 ]
Amit, Tamar [1 ,2 ]
Bar-Am, Orit [1 ,2 ]
Youdim, Moussa B. H. [1 ,2 ,3 ]
机构
[1] Technion Israel Inst Technol, Rappaport Fac Med, Eve Topf Ctr Excellence Neurodegenerat Dis, Haifa, Israel
[2] Technion Israel Inst Technol, Rappaport Fac Med, Dept Mol Pharmacol, Haifa, Israel
[3] Yonsei Univ, Dept Biol, Seoul 120749, South Korea
来源
MONOAMINE OXIDASES AND THEIR INHIBITORS | 2011年 / 100卷
关键词
AMYLOID PRECURSOR PROTEIN; RAT PHEOCHROMOCYTOMA CELLS; HYDROGEN-PEROXIDE; ACETYLCHOLINESTERASE INHIBITORS; OXIDATIVE STRESS; NEUROTROPHIC-FACTORS; NEUROBLASTOMA-CELLS; KINASE-C; NEURODEGENERATIVE DISEASES; PARKINSONS-DISEASE;
D O I
10.1016/B978-0-12-386467-3.00010-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The novel therapeutic strategy in which drug candidates are designed to possess diverse pharmacological properties and act on multiple targets has stimulated the development of the multimodal drug, ladostigil [(N-propargyl-(3R) aminoindan-5yl)-ethyl methyl carbamate]. Ladostigil combines neuroprotective effects with monoamine oxidase-A and -B and cholinesterase inhibitory activities in a single molecule, presently in a Phase IIb clinical trial and intended for the treatment of Alzheimer's disease, and dementia comorbid with extrapyramidal disorders and depression. This chapter will discuss the preclinical scientific evidence for the therapeutic potential use of ladostigil in the clinic and molecular signaling pathways that are considered to be involved in the molecular activities of the drug.
引用
收藏
页码:191 / 215
页数:25
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