Hurdles in the Drug Discovery of Cathepsin K Inhibitors

被引:16
|
作者
Kometani, Motohiko [1 ]
Nonomura, Kazuhiko [1 ]
Tomoo, Takashi [1 ]
Niwa, Satoru [1 ]
机构
[1] Novartis Inst BioMed Res Tsukuba, Tsukuba, Ibaraki 3002611, Japan
关键词
Cathepsin K inhibitors; Species differences; PK/PD; On- and Off-target Side Effects; Osteoporosis; Bone resorption; Osteoclasts; CONVERTING ENZYME-INHIBITION; LYSOSOMAL CYSTEINE PROTEASES; BONE-MINERAL DENSITY; IN-VIVO; MATRIX METALLOPROTEINASES; MOLECULAR-CLONING; DEFICIENT MICE; POSTMENOPAUSAL OSTEOPOROSIS; OSTEOCLASTIC RESORPTION; FUNCTIONAL EXPRESSION;
D O I
10.2174/156802610791113478
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
There were many hurdles in the drug discovery of cathepsin K inhibitors such as species differences not only in bone metabolism but also in amino acid sequences in the critical site of the target enzyme, discrepancies between PK/PD due to unique tissue distribution of the inhibitor affecting both efficacy and side effects originated from a characteristic intracellular or tissue distribution of some classes of compounds. The value of this new therapeutic approach over the launched indirect competitors should be further clarified from the efficacy and side effect point of view. The cathepsin K inhibitor drug discovery was initiated based on a strong and osteoclast-specific expression of this enzyme. However, the tissues and cells expressing cathepsin K have been expanding as the investigation on pathological conditions progressed with respect to side effects as well as new possible indications.
引用
收藏
页码:733 / 744
页数:12
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