Technische Universitat Munchen

Florian Reichart

Horst Kessler

Tobias Kapp

Oleg Maltsev

Disclosed are compounds represented by the following general formula (I): Cyclo-(Arg-Gly-Asp-X-X-X-X-X) (I) wherein the variables groups Xto Xhave the following meanings X: Leu, Ile, Nle, Val, Tyr, Phe; X: D-amino acid such as D-Pro, N-Me-D-Phe; X: Pro, N-Me-amino acid such as N-Me-Lys, N-Me-Lys(Ac); Pro-Rx3, N-Me-Lys-Rx4; X: Gly, Ala, Ser, Thr; X: Leu, Ala, Tyr, His, Ile, Nle, Val, Phe wherein Pro-Rx3 represents a proline residue that carries at the C-3, C-4 or C-5 carbon atom and preferably the C-4 carbon atom a functional group selected from &#x2014;NH2, &#x2014;OH, &#x2014;NH&#x2014;Ac, &#x2014;NH-hexyne, and wherein Lys-Rrepresents a lysine residue, wherein the &#x3c9;-amino nitrogen atom carries a group of the formula -L4-R4, wherein L4 is selected from the group consisting of covalent bond, &#x2014;C(O)&#x2014;, and &#x2014;C(O)&#x2014;O&#x2014;, . . . , and wherein R4 is selected from the group consisting of &#x2014;(CH2)n-C&#x2261;CH with n=0, 1, 2, 3, 4, 5, 6, 7 or 8, or wherein the sub-sequence -X-X- represents a &#x3b2;-turn mimetic diffe&#x3c9;&#x3c9;ring from the meanings above, or pharmaceutically acceptable salts, esters, solvates, polymorphs or modified forms thereof represented by the following general formula (II): (X)L(X)wherein X0 represents the compound of the general formula (I) as specified above (excluding one hydrogen atom to allow bonding to the linker), L represents a linker, Xrepresents the effector moiety and wherein n1 and n2 are each independently selected from the range of 1 to 5, preferably such that each of n1 and n2 represents 1, wherein n1+n2 represents the number of valencies of the linker and is preferably in the range of from 2 to 6, more preferably 2-5, with the proviso that each of n1 and n2 is at least 1, as well as uses therefore in therapy and imaging.

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Munich, Germany

Florian Reichart