| Literature DB >> 29724589 |
Hiroshi Miyazaki1, Yousuke Ikeda2, Osamu Sakurai2, Tsutomu Miyake2, Rie Tsubota2, Jyunko Okabe2, Masataka Kuroda2, Yutaka Hisada2, Tetsuya Yanagida2, Hikaru Yoneda2, Yukihito Tsukumo3, Shin Tokunaga3, Takehisa Kawata3, Rikiya Ohashi2, Hajime Fukuda2, Koki Kojima2, Ayako Kannami2, Takayuki Kifuji2, Naoya Sato2, Akiko Idei2, Taku Iguchi2, Tetsuya Sakairi2, Yasunori Moritani2.
Abstract
The calcium-sensing receptor (CaSR) plays an important role in sensing extracellular calcium ions and regulating parathyroid hormone secretion by parathyroid gland cells, and the receptor is a suitable target for the treatment of hyperparathyroidism. Cinacalcet hydrochloride is a representative CaSR agonist which widely used for the hyperparathyroidism. However, it has several issues to clinical use, such as nausea/vomiting and strong inhibition of CYP2D6. We tried to improve these issues of cinacalcet for a new pharmaceutical agent as a preferable CaSR agonist. Optimization from cinacalcet resulted in the identification of pyrrolidine compounds and successfully led to the discovery of evocalcet as an oral allosteric CaSR agonist. Evocalcet, which exhibited highly favorable profiles such as CaSR agonistic activity and good DMPK profiles, will provide a novel therapeutic option for secondary hyperparathyroidism.Entities:
Keywords: Allosteric calcium-sensing receptor agonist; Calcium-sensing receptor (CaSR); Cinacalcet; Evocalcet; Hyperparathyroidism
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Year: 2018 PMID: 29724589 DOI: 10.1016/j.bmcl.2018.04.055
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823