Design, synthesis, and biological evaluation of novel investigational nonapeptide KISS1R agonists with testosterone-suppressive activity

T Asami, N Nishizawa, H Matsui… - Journal of Medicinal …, 2013 - ACS Publications
T Asami, N Nishizawa, H Matsui, K Nishibori, Y Ishibashi, Y Horikoshi, M Nakayama…
Journal of Medicinal Chemistry, 2013ACS Publications
Metastin/kisspeptin is a 54 amino acid peptide ligand of the KISS1R receptor and is a critical
regulator of GnRH secretion. The N-terminally truncated peptide, metastin (45–54),
possesses a 10-fold higher receptor-binding affinity than full-length metastin and agonistic
KISS1R activity but is rapidly inactivated in rodent plasma. We have developed a
decapeptide analog [d-Tyr45, d-Trp47, azaGly51, Arg (Me) 53] metastin (45–54) with
improved serum stability compared with metastin (45–54) but with decreased KISS1R …
Metastin/kisspeptin is a 54 amino acid peptide ligand of the KISS1R receptor and is a critical regulator of GnRH secretion. The N-terminally truncated peptide, metastin(45–54), possesses a 10-fold higher receptor-binding affinity than full-length metastin and agonistic KISS1R activity but is rapidly inactivated in rodent plasma. We have developed a decapeptide analog [d-Tyr45,d-Trp47,azaGly51,Arg(Me)53]metastin(45–54) with improved serum stability compared with metastin(45–54) but with decreased KISS1R agonistic activity. Amino acid replacements at positions 45–47 led to an enhancement of KISS1R agonistic activity and metabolic stability. N-terminal truncation resulted in a stable nonapeptide, [d-Tyr46,d-Pya(4)47,azaGly51,Arg(Me)53]metastin(46–54), compound 26, which displayed KISS1R binding affinities comparable to metastin(45–54) and had improved serum stability. Compound 26 reduced plasma testosterone in male rats and is the first short-length metastin analog to possess testosterone suppressive activities. Compound 26 has led to the elucidation of investigational analogs TAK-683 and TAK-448, both of which have undergone clinical evaluation for hormone-dependent diseases such as prostate cancer.
ACS Publications