发明名称 |
Compounds and methods of modulating angiogenesis |
摘要 |
A pharmaceutical composition includes a synthetic peptide consisting of about 10 to about 50 amino acids and having an amino acid sequence substantially homologous to consecutive amino acids of a portion of the cytoplasmic domain of at least one of αvβ3 integrin or VEGFR2 that includes a tyrosine residue, the amino acid sequence of the peptide including a phosphorylated tyrosine residue or a γ-carboxyglutamic acid residue that is substituted for a corresponding tyrosine residue of the portion of the cytoplasmic domain of αvβ3 integrin or VEGFR2. |
申请公布号 |
US9592269(B2) |
申请公布日期 |
2017.03.14 |
申请号 |
US201514937289 |
申请日期 |
2015.11.10 |
申请人 |
The Cleveland Clinic Foundation |
发明人 |
Byzova Tatiana;Mahabaleshwar Ganapati H.;Feng Weiyi |
分类号 |
A61K38/17;A61K38/18;A61K38/08;A61K38/10 |
主分类号 |
A61K38/17 |
代理机构 |
Tarolli, Sundheim, Covell & Tummino LLP |
代理人 |
Tarolli, Sundheim, Covell & Tummino LLP |
主权项 |
1. A pharmaceutical composition comprising a synthetic peptide, the peptide consisting of about 10 to about 50 amino acids and comprising an amino acid sequence substantially homologous to a portion of VEGFR2, wherein the amino acid sequence is selected from the group consisting of: SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO:23, and SEQ ID NO: 24, the peptide inhibits interaction of αvβ3 integrin with VEGFR2. |
地址 |
Cleveland OH US |