The present invention relates to novel imidazolidinone derivatives thereof, their synthesis, and their use as &agr;v integrin receptor antagonists. More particularly, the compounds of the present invention are antagonists of the integrin receptors &agr;v&bgr;3 and/or &agr;v&bgr;5 and are useful for inhibiting bone resorption, treating and preventing osteoporosis, and inhibiting vascular restenosis, diabetic retinopathy, macular degeneration, angiogenesis, atherosclerosis, inflammation, inflammatory arthritis, viral disease, cancer, and metastatic tumor growth.
本发明涉及新型
咪唑啉酮衍
生物及其合成方法和用作αv整合素受体拮抗剂的用途。更具体地说,本发明的化合物是αvβ3和/或αvβ5整合素受体的拮抗剂,可用于抑制骨吸收、治疗和预防骨质疏松症、抑制血管再狭窄、糖尿病视网膜病变、黄斑变性、血管生成、动脉粥样硬化、炎症、炎性关节炎、病毒性疾病、癌症和转移性肿瘤生长。