Discovery of Novel Selective Estrogen Receptor β (SERβ) Agonist ( S )-STO021 as an Antiosteoporosis Candidate with Dual Functions of Inhibiting Osteoclastogenesis and Activating Osteoblastogenesis

作者：Cheng Peng, Zixiang Geng, Zhe Jiang, Jin-Feng Ning, Nan Wang, Chen Zhong, Yongfang Zhao, Xun Sun, Mei‐Lin Tang · 发表于：Journal of Medicinal Chemistry · 年份：2025 · DOI：10.1021/acs.jmedchem.5c01697 · 被引用次数：1 · 研究领域：Bone Metabolism and Diseases、Estrogen and related hormone effects、Bone health and treatments

Abstract Osteoporosis is a systemic and chronic metabolic bone disease of high fracture and mortality. Simultaneous regulation of osteoblast-mediated bone formation and osteoclast-mediated bone resorption has become a potentially effective therapeutic strategy to overcome osteoporosis. Recently, selective activation of estrogen receptor β (SERβ) was demonstrated to promote osteoblast formation and inhibit osteoclast absorption, suggesting that SERβ agonists may be another promising therapeutic approach for treating osteoporosis. Herein, we reported the discovery of a bisphosphonate indanone compound (S)-STO021 as a novel SERβ agonist, which exhibited excellent dual functional effects of inhibiting osteoclast resorption and promoting osteoblast formation. Mechanically, the antiosteoporosis efficacy of (S)-STO021 was achieved through inhibiting the TAK1/MKK6/p38 signal and promoting the ERβ/BMP4/SMAD signal. Furthermore, (S)-STO021 could not only effectively improve the zebrafish osteoporosis model induced by glucocorticoids but also greatly restore the bone microstructure in ovariectomized rat models. Collectively, our SERβ agonist (S)-STO021 could regulate osteoblast and osteoclast differentiation, showing the potential to treat osteoporosis.