期刊
CURRENT OPINION IN PHARMACOLOGY
卷 7, 期 1, 页码 112-118出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.coph.2006.10.002
关键词
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Data accumulated during the past two decades place amyloid beta-peptide (A beta) at center stage as the main perpetrator in initiating the pathological cascade that eventually leads to Alzheimer's disease. Consequently, significant resources have been allocated to identify and develop treatment strategies that alter the metabolism of A beta. The gamma-secretase protease has deservedly received attention as an attractive drug target, as it is directly involved in A beta biogenesis and determines the pathogenic potential of A beta by its heterogeneous catalytic action, generating peptiedes of various lengths. Despite the complexity of the multi-subunit gamma-secretase and the lack of structural information, drug discovery research has identified small-molecule compounds that inhibit or modulate activity of this enzyme and some of these have already entered clinical trials.
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