发明名称 EGFR-BASED INHIBITOR PEPTIDES FOR COMBINATORIAL INACTIVATION OF ERBB1, ERBB2, AND ERBB3
摘要 Inhibitor peptides for combinatorial inactivation of ErbB1, ErbB2, and ErbB3 featuring an EGFR-based peptide and a cell penetrating component such as a protein transduction domain (e.g., PTD4) for enhancing penetration of the EGFR-based peptide info a cell The EGFR peptide may be from 8 to 30 amino acids in length. The inhibitor peptides can inhibit tumor growth, reduce metastasis, activate apoptosis, activate necrosis, disrupt calcium signaling, and/or increase ROS. In some embodiments, the EGFR-based peptide is at least 50% identical to at least 8 consecutive residues of SEQ ID NO: 1.
申请公布号 WO2016161440(A2) 申请公布日期 2016.10.06
申请号 WO2016US25905 申请日期 2016.04.04
申请人 ARIZONA CANCER THERAPEUTICS, LLC 发明人 SCHROEDER, Joyce, A.
分类号 C07K14/71;C07K14/47 主分类号 C07K14/71
代理机构 代理人
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