发明名称 Peptide inhibitors of HK2 and their use
摘要 <p>Isolated peptide comprising an amino acid sequence selected from SRFKVWWAAG (SEQ ID NO:55), ARFKVWWAAG (SEQ ID NO:56), SAFKVWWAAG (SEQ ID NO:57), SRFKAWWAAG (SEQ ID NO:60), SRFKVAWAAG (SEQ ID NO:61), SRFKVWAAAG (SEQ ID NO:62), SRFKVWWAAG (SEQ ID NO:63), SRFKVWWAAG (SEQ ID NO:64), RFKVWWAAG (SEQ ID NO:65), SRFKVWWAG (SEQ ID NO:68), SRFKVWWG (SEQ ID NO:69), or from SRFKVWWG (SEQ ID NO:73), SRFKVWWG (SEQ ID NO:74), ARFKVWWG (SEQ ID NO:75), ARFKVWWG (SEQ ID NO:76), ARFKVWWGG (SEQ ID NO:77), ARFKVWWGG (SEQ ID NO:78), ARFKVWWA (SEQ ID NO:79), ARFKVWWA (SEQ ID NO:80), ARFKVWWAA (SEQ ID NO:81) and ARFKVWWA(CONH 2 ) (SEQ ID NO:82), or an amino acid sequence, which is SRFKVWWAAG (SEQ ID NO:1. The novel peptides are capable of binding to human kallikrein 2 and of inhibiting the proteolytic activity of human kallikrein 2. They can be used in prostate cancer treatment as such or in combination with other ligands modulating the activity of factors mediating tumor growth.</p>
申请公布号 EP2343311(A2) 申请公布日期 2011.07.13
申请号 EP20100185606 申请日期 2005.09.05
申请人 LICENTIA OY 发明人 STENMAN, ULF-HAAKAN;LEINONEN, JARI;NAERVAENEN, ALE
分类号 C07K7/06;A61K38/08;A61K38/10;A61K48/00;C07K;C07K7/08;G01N33/574;G01N33/68 主分类号 C07K7/06
代理机构 代理人
主权项
地址