TY - JOUR
T1 - NN1213 - A Potent, Long-Acting, and Selective Analog of Human Amylin
AU - Dahl, Kirsten
AU - Raun, Kirsten
AU - Hansen, Jakob Lerche
AU - Poulsen, Christian
AU - de la Cour, Charlotta D.
AU - Clausen, Trine Ryberg
AU - Hansen, Ann Maria Kruse
AU - John, Linu M.
AU - Plesner, Annette
AU - Sun, Gao
AU - Schlein, Morten
AU - Skyggebjerg, Rikke Bjerring
AU - Kruse, Thomas
N1 - Publisher Copyright:
© 2024 The Authors. Published by American Chemical Society
PY - 2024
Y1 - 2024
N2 - Amylin, a member of the calcitonin family, acts via amylin receptors in the hindbrain and hypothalamus to suppress appetite. Native ligands of these receptors are peptides with short half-lives. Conjugating fatty acids to these peptides can increase their half-lives. The long-acting human amylin analog, NN1213, was generated from structure–activity efforts optimizing solubility, stability, receptor affinity, and selectivity, as well as in vivo potency and clearance. In both rats and dogs, a single dose of NN1213 reduced appetite in a dose-dependent manner and with a long duration of action. Consistent with the effect on appetite, studies in obese rats demonstrated that daily NN1213 dosing resulted in a dose-dependent reduction in body weight over a 21-day period. Magnetic resonance imaging indicated that this was primarily driven by loss of fat mass. Based on these data, NN1213 could be considered an attractive option for weight management in the clinical setting.
AB - Amylin, a member of the calcitonin family, acts via amylin receptors in the hindbrain and hypothalamus to suppress appetite. Native ligands of these receptors are peptides with short half-lives. Conjugating fatty acids to these peptides can increase their half-lives. The long-acting human amylin analog, NN1213, was generated from structure–activity efforts optimizing solubility, stability, receptor affinity, and selectivity, as well as in vivo potency and clearance. In both rats and dogs, a single dose of NN1213 reduced appetite in a dose-dependent manner and with a long duration of action. Consistent with the effect on appetite, studies in obese rats demonstrated that daily NN1213 dosing resulted in a dose-dependent reduction in body weight over a 21-day period. Magnetic resonance imaging indicated that this was primarily driven by loss of fat mass. Based on these data, NN1213 could be considered an attractive option for weight management in the clinical setting.
U2 - 10.1021/acs.jmedchem.4c00022
DO - 10.1021/acs.jmedchem.4c00022
M3 - Journal article
C2 - 38960379
AN - SCOPUS:85198210214
SN - 0022-2623
VL - 67
SP - 11688
EP - 11700
JO - Journal of Medicinal Chemistry
JF - Journal of Medicinal Chemistry
IS - 14
ER -