摘要 |
The invention relates to cyclised peptides corresponding to sequence SEQ ID N<SUP>o</SUP> 1: X<SUB>1</SUB>X<SUB>2</SUB>RGDX<SUB>3</SUB>FGX<SUB>4</SUB>X<SUB>5</SUB>LLFIHFX<SUB>6</SUB>IGSX<SUB>7</SUB>HSX<SUB>8</SUB>IX<SUB>9</SUB>, wherein: the letters without any numerical index correspond to amino acids defined by the single-letter international code; X<SUB>1 </SUB>is G or GG having an amino-terminal end which may or may not be free; X<SUB>2 </SUB>is either a C, in which case X<SUB>2</SUB>=X<SUB>4</SUB>, the two Cs being connected by a disulphide bridge, or X<SUB>2 </SUB>is capable of forming a lactam bridge with X<SUB>4</SUB>, either X<SUB>2 </SUB>or X<SUB>4 </SUB>being an amino acid bearing an acid group, such as A or D, and the other bearing an amino function such as Q, N; X<SUB>3 </SUB>is either an M pattern or a norleucine pattern; X<SUB>5 </SUB>is one or several di-, tri-, or tetra-peptide patterns comprising G or a combination of G and S, or X<SUB>5 </SUB>is a C pattern having a side-chain which serves as a covalent linkage point with a 3-nitro-2-pyridinesulphenyl group which is located at the N-terminal end of the next amino acid (L); X<SUB>6 </SUB>is either an R pattern or a K pattern; X<SUB>7 </SUB>is either an R pattern or a K pattern; X<SUB>8 </SUB>is either an R pattern or a K pattern; and X<SUB>9 </SUB>is an aliphatic amino acid (such as G or A) having an amide C-terminal end. The inventive peptides can be used as active ingredients in medicaments, for example, for the treatment of pathologies linked to hypervascularisation.
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