申请人:——
公开号:US20030096841A1
公开(公告)日:2003-05-22
The invention relates to isoindole-imide compounds and pharmaceutically acceptable salts, hydrates, solvates, clathrates, enantiomers, diastereomers, racemates, or mixtures of stereoisomers thereof, pharmaceutical compositions comprising these isoindole-imide compounds, and methods for reducing the level of cytokines and their precursors in mammals. In particular, the invention pertains to isoindole-imide compounds that are potent inhibitors of the production of TNF-&agr; in mammals. The isoindole-imides described herein are useful for treating or preventing diseases or disorders in mammals, for example, cancers, such as solid tumors and blood-born tumors; heart disease, such as congestive heart failure; osteoporosis; and genetic, inflammatory; allergic; and autoimmune diseases.
该发明涉及异吲哚-亚鞣酰亚胺化合物及其药用可接受的盐、水合物、溶剂合物、包合物、对映体、二对映异构体、混合物,以及包含这些异吲哚-亚鞣酰亚胺化合物的药物组合物,以及用于降低哺乳动物体内细胞因子及其前体水平的方法。具体而言,该发明涉及对哺乳动物体内TNF-α的产生具有强效抑制作用的异吲哚-亚鞣酰亚胺化合物。这里描述的异吲哚-亚鞣酰亚胺化合物可用于治疗或预防哺乳动物体内的疾病或疾病,例如实体肿瘤和血液性肿瘤等癌症;心脏疾病,如充血性心力衰竭;骨质疏松症;以及遗传性、炎症性、过敏性和自身免疫性疾病。