CRFR1 selective ligands
View Patent ↗CRF peptide analogs that bind to CRFR1 with an affinity far greater than they bind to CRFR2. Some of these analogs exhibit CRF agonist activity. One exemplary analog that may be made by solid-phase synthesis is: (cyclo 31-34)[Ac-Pro 4 ,D-Phe 12 ,Nle 18,21 ,Glu 31 ,Lys 34 ]-sucker urotensin(4-41).
1. A 38-residue or 39-residue CRFR1 ligand cyclic peptide which binds to CRFR1 with an affinity substantially greater than it binds to CRFR2, which peptide has the following formula, or a nontoxic salt thereof:
wherein the side chains of Glu and Lys are covalently linked as indicated;
Y 1 is an acyl group having not more than 7 carbon atoms or is radioiodinated tyrosine;
R 14 is CML or Leu;
R 18 is Val or CML;
R 32 is His or D-His;
R 33 is Aib, Ser, D-Ser or D-Ala;
R 36 is Lys or CML;
R 37 is CML or Leu; and
R 40 is Ile or CML;
provided that D-β-(2-napthyl)alanine(D-2Nal) or D-Leu may be substituted for D-Phe.
2. The peptide of claim 1 wherein R 37 is CML.
3. The peptide of claim 2 having the formula:
4. The peptide of claim 1 wherein R 36 is CML.
5. The peptide of claim 4 wherein R 32 is His.
6. The peptide of claim 4 wherein R 32 is D-His.
7. The peptide of claim 4 having the formula:
8. The peptide of claim 1 wherein R 14 is CML.
9. The peptide of claim 8 having the formula:
10. The peptide of claim 1 wherein R 18 is CML.
11. The peptide of claim 10 having the formula:
12. The peptide of claim 1 wherein R 40 is CML.
13. The peptide of claim 12 having the formula:
14. The peptide of claim 13 wherein R 33 is Aib.
15. The peptide of claim 13 wherein R 33 is D-Ser.
16. The peptide of claim 13 wherein R 33 is D-Ala.