2-(benzyl)-3-arylbenzofurans as antitumour and hypocholesterolemic agents
    3.
    发明授权
    2-(benzyl)-3-arylbenzofurans as antitumour and hypocholesterolemic agents 失效
    2-(苄基)-3-芳基苯并呋喃酮作为抗肿瘤和低胆固醇血症药

    公开(公告)号:US5354861A

    公开(公告)日:1994-10-11

    申请号:US971507

    申请日:1992-11-04

    CPC分类号: C07D307/80

    摘要: The synthesis and the biological evaluation of a series of basic ethers of 2-benzyl-3-arylbenzofurans as antitumor agents is described. These compounds bind significantly to the antiestrogen-binding sites but only poorly to the estrogen receptor sites and are cytotoxic to tumor cells. Some of these compounds also significantly inhibited de novo cholesterol biosynthesis in an estrogen receptor negative lymphoma cell line rich in antiestrogen-binding sites.

    摘要翻译: 描述了一系列作为抗肿瘤剂的2-苄基-3-芳基苯并呋喃的碱性醚的合成和生物学评价。 这些化合物显着地与抗雌激素结合位点结合,但仅与雌激素受体位点差,并且对肿瘤细胞具有细胞毒性。 这些化合物中的一些还显着抑制了含有抗雌激素结合位点的雌激素受体阴性淋巴瘤细胞系中的新生胆固醇生物合成。

    2-(benzyl)-3-arylbenzofurans as antitumour and hypocholesterolemic agents
    4.
    发明授权
    2-(benzyl)-3-arylbenzofurans as antitumour and hypocholesterolemic agents 失效
    2-(苄基)-3-芳基苯并呋喃酮作为抗肿瘤和低胆固醇血症药

    公开(公告)号:US5459139A

    公开(公告)日:1995-10-17

    申请号:US251998

    申请日:1994-06-01

    CPC分类号: C07D307/80

    摘要: The synthesis and the biological evaluation of a series of basic ethers of 2-benzyl-3-arylbenzofurans as antitumor agents is described. These compounds bind significantly to the antiestrogen-binding sites but only poorly to the estrogen receptor sites and are cytotoxic to tumor cells. Some of these compounds also significantly inhibited de novo cholesterol biosynthesis in an estrogen receptor negative lymphoma cell line rich in antiestrogen-binding sites.

    摘要翻译: 描述了一系列作为抗肿瘤剂的2-苄基-3-芳基苯并呋喃的碱性醚的合成和生物学评价。 这些化合物显着地与抗雌激素结合位点结合,但仅与雌激素受体位点差,并且对肿瘤细胞具有细胞毒性。 这些化合物中的一些还显着抑制了含有抗雌激素结合位点的雌激素受体阴性淋巴瘤细胞系中的新生胆固醇生物合成。