发明名称 Novel peptides
摘要 Isolated peptides comprising an amino acid sequence having Formula I <?in-line-formulae description="In-line Formulae" end="lead"?>X1X2X3X4, I<?in-line-formulae description="In-line Formulae" end="tail"?> wherein X1 is an optional residue of an amino acid selected from the group of R, F, Y, S and conservative substitutes thereof; X2 stands for a residue of an amino acid selected from the group of R and A and conservative substitutes thereof; X3 is a residue of an amino acid selected from the group of F, P, G, Q, M and conservative substitutes thereof; and X4 is a residue of an amino acid selected from the group of K, F, G, P and conservative substitutes thereof. 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.
申请公布号 US2009214427(A1) 申请公布日期 2009.08.27
申请号 US20050661691 申请日期 2005.09.05
申请人 LICENTIA OY 发明人 STENMAN ULF-HAKAN;LEINONEN JARI;NARVANEN ALE
分类号 A61K49/00;A61K9/127;A61K31/7088;A61K38/07;A61K38/08;A61K38/10;A61K38/16;A61P35/00;C07H21/00;C07K;C07K5/00;C07K7/00;C07K14/00;C12N5/00 主分类号 A61K49/00
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