Advances in the discovery of cathepsin K inhibitors on bone resorption

被引:71
作者
Lu, Jun [1 ,2 ]
Wang, Maolin [1 ,2 ]
Wang, Ziyue [1 ]
Fu, Zhongqi [1 ]
Lu, Aiping [1 ,2 ]
Zhang, Ge [1 ,2 ]
机构
[1] Hong Kong Baptist Univ, Sch Chinese Med, Law Sau Fai Inst Adv Translat Med Bone & Joint Di, Hong Kong, Hong Kong, Peoples R China
[2] Hong Kong Baptist Univ, Sch Chinese Med, Inst Integrated Bioinfomed & Translat Sci IBTS, Hong Kong, Hong Kong, Peoples R China
关键词
Cathepsin K; osteoclast; bone resorption; osteoporosis; cathepsin K inhibitors; BETA-SUBSTITUTED CYCLOHEXANECARBOXAMIDE; CHINESE HERBAL MEDICINE; CYSTEINE PROTEASE; POSTMENOPAUSAL WOMEN; SELECTIVE INHIBITORS; MINERAL DENSITY; 3,4-DISUBSTITUTED AZETIDINONES; ARYLAMINOETHYL AMIDES; OSTEOPOROSIS THERAPY; BIOCHEMICAL MARKERS;
D O I
10.1080/14756366.2018.1465417
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Cathepsin K (Cat K), highly expressed in osteoclasts, is a cysteine protease member of the cathepsin lysosomal protease family and has been of increasing interest as a target of medicinal chemistry efforts for its role in bone matrix degradation. Inhibition of the Cat K enzyme reduces bone resorption and thus, has rendered the enzyme as an attractive target for anti-resorptive osteoporosis therapy. Over the past decades, considerable efforts have been made to design and develop highly potent, excellently selective and orally applicable Cat K inhibitors. These inhibitors are derived from synthetic compounds or natural products, some of which have passed preclinical studies and are presently in clinical trials at different stages of advancement. In this review, we briefly summarised the historic development of Cat K inhibitors and discussed the relationship between structures of inhibitors and active sites in Cat K for the purpose of guiding future development of inhibitors.
引用
收藏
页码:890 / 904
页数:15
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