Recent Advances of Hepsin-Targeted Inhibitors

Citations

WEB OF SCIENCE

8
Citations

SCOPUS

8

초록

Hepsin is a type II transmembrane serine protease (TTSP) that plays a crucial role in cell growth and development. Hepsin is highly expressed in prostate cancer (PCa) and associated with its progression and metastasis. Therefore, it has been considered as an attractive biomarker of PCa. Recently, low molecular weight inhibitors targeting hepsin have been developed. Based on the key chemical scaffold, they can be classified into four classes: Indolecarboxamidines, benzamidines, peptide-based analogs, and 2,3-dihydro-1H-perimidines. In this review, we discuss design strategy, structure-activity relationship (SAR), and binding mode of the four classes of hepsin inhibitors.

키워드

Hepsin; prostate cancer; type II transmembrane serine protease; structure-activity relationship (SAR); amidine; peptides; HEPATOCYTE GROWTH-FACTOR; MEMBRANE-ASSOCIATED PROTEASE; STRUCTURE-GUIDED DISCOVERY; ANCHORED SERINE PROTEASES; CYCLIC UREA INHIBITORS; DE-NOVO DESIGN; PROSTATE-CANCER; GENE-EXPRESSION; BIOLOGICAL EVALUATION; FACTOR XA
제목
Recent Advances of Hepsin-Targeted Inhibitors
저자
Kwon, Hongmok; Han, JooYeon; Lee, Ki-Yong; Son, Sang-Hyun; Byun, Youngjoo
DOI
10.2174/0929867324666170227115835
발행일
2017
유형
Review
저널명
Current Medicinal Chemistry
권
24
호
21
페이지
2294 ~ 2311