Stabilized compounds having secondary structure motifs
The present invention provides novel stabilized crosslinked compounds having secondary structure motifs, libraries of these novel compounds, and methods for the synthesis of these compounds libraries thereof. The synthesis of these novel stabilized compounds involves (1) synthesizing a peptide from a selected number of natural or non-natural amino acids, wherein said peptide comprises at least two moieties capable of undergoing reaction to promote carbon-carbon bond formation; and (2) contacting said peptide with a reagent to generate at least one crosslinker and to effect stabilization of a secondary structure motif. The present invention, in a preferred embodiment, provides stabilized p53 donor helical peptides. Additionally, the present invention provides methods for disrupting the p53/MDM2 binding interaction comprising (1) providing a crosslinked stabilized α-helical structure; and (2) contacting said crosslinked stabilized α-helical structure with MDM2.
1. A compound represented by formula A:
wherein:
R 1 , R 2 and R 4 are each independently —H or a protecting group suitable for peptide synthesis;
R 3 is methyl;
R 5 is an optionally substituted moiety of the formula —CH 2 CH 2 (CH 2 ) n CH═CH 2 , wherein n is 1, 2, 3 or 4; and
said compound is in a protected form suitable for peptide synthesis.
2. The compound of claim 1 , wherein n is 1.
3. The compound of claim 1 , wherein n is 4.
4. The compound of claim 1 , wherein the absolute stereochemistry at the α-position is R.
5. The compound of claim 1 , wherein the absolute stereochemistry at the α-position is S.
6. The compound of claim 1 , wherein R 4 is —H.
7. The compound of claim 1 , wherein R 1 or R 2 is an Fmoc or a Boc protecting group.
8. The compound of claim 1 , wherein the compound is selected from the group consisting of:
and said compound is in a protected form suitable for peptide synthesis.
9. A compound represented by formula B:
wherein:
R 1 , R 2 and R 4 are each independently —H or a protecting group suitable for peptide synthesis;
R 3 is methyl; and
n is 7 or 9.
10. The compound of claim 9 , wherein the absolute stereochemistry at the α-position is R.
11. The compound of claim 9 , wherein the absolute stereochemistry at the α-position is S.
12. The compound of claim 9 , wherein said compound is selected from the group consisting of:
and
said compound is in a protected form suitable for peptide synthesis.
13. A compound selected from the group consisting of:
wherein R 1 , R 2 and R 4 are each independently —H or a protecting group suitable for peptide synthesis.