Guanidino derivatives as inhibitors of cell adhesion
    9.
    发明授权
    Guanidino derivatives as inhibitors of cell adhesion 有权
    胍基衍生物作为细胞粘附抑制剂

    公开(公告)号:US07259159B2

    公开(公告)日:2007-08-21

    申请号:US10343173

    申请日:2001-07-23

    CPC分类号: C07D473/00 C07D487/04

    摘要: The present invention relates to acylguanidino derivatives of formula (I), in which R1, R2, R3, A, B, X, Y and n have the meanings indicated in claim 1, their physiologically tolerable salts and their prodrugs. The compounds of the formula (I) are valuable pharmaceutically active compounds. They are vitronectin receptor antagonists and inhibitors of cell adhesion and bone resorption by osteoclasts. This renders them suitable, for example, for the therapy and prophylaxis of illness which are based on the interaction between vitronectin receptors and their ligands in cell-cell or cell-matrix interaction processes or which can be prevented, alleviated or cured by influencing such interactions. For example, they can be applied for treating and preventing osteoporosis, or for inhibiting undesired angiogenesis or proliferation of cells of the vascular smooth muscles. The invention furthermore relates to processes for the preparation of compounds of the formula (I), their use, in particular as pharmaceutical active ingredients, and pharmaceutical compositions comprising them

    摘要翻译: 本发明涉及式(I)的酰基胍基衍生物,其中R 1,R 2,R 3,A,B,X ,Y和n具有权利要求1所述的含义,其生理上可耐受的盐及其前药。 式(I)的化合物是有价值的药物活性化合物。 它们是玻连蛋白受体拮抗剂和破骨细胞的细胞粘附和骨吸收的抑制剂。 这使得它们适合于例如基于玻连蛋白受体及其配体在细胞 - 细胞或细胞 - 基质相互作用过程中的相互作用的疾病的治疗和预防,或通过影响这些相互作用可以预防,缓解或治愈 。 例如,它们可以用于治疗和预防骨质疏松症,或用于抑制血管平滑肌细胞的不期望的血管生成或增殖。 本发明还涉及制备式(I)化合物的方法,其用途,特别是作为药物活性成分,以及包含它们的药物组合物