ZACE1: A HUMAN METALLOENZYME
    65.
    发明授权
    ZACE1: A HUMAN METALLOENZYME 有权
    ZACE1:人类金属酶

    公开(公告)号:EP1133564B1

    公开(公告)日:2004-08-04

    申请号:EP99965810.7

    申请日:1999-11-15

    CPC分类号: C12N9/6489 C07K2319/00

    摘要: Angiotensin-converting enzyme is a zinc metallopeptidase that plays roles in blood pressure regulation and fertility. The catalytic activities of angiotensin converting enzymes include the production of the potent vasopressor angiotensin II from angiotensin I, and the inactivation of the vasodilatory peptide bradykinin. Zace1 is a form of human zinc metallopeptidas, which includes one zinc-dependent catalytic domain containing the motif 'HEXXH' and one downstream 'EX(I/V)X(D/S)' motif.

    4-(2-(N-2-CARBOXAMIDOINDOLE)AMINOETHYL)-BENZENESULFONAMIDES OR SULFONYLUREAS AS PDGF ANTAGONISTS
    70.
    发明授权
    4-(2-(N-2-CARBOXAMIDOINDOLE)AMINOETHYL)-BENZENESULFONAMIDES OR SULFONYLUREAS AS PDGF ANTAGONISTS 失效
    作为PDGF拮抗剂的4-(2-(N-2-羧基氨基吲哚)氨基乙基)苯磺酰胺或磺酰脲类

    公开(公告)号:EP0835115B1

    公开(公告)日:2004-05-06

    申请号:EP96916719.6

    申请日:1996-05-29

    摘要: Methods for inhibiting intimal hyperplasia in the vasculature of mammals, including primates, are disclosed. The methods comprise administering to the mammal a non-peptide PDGF antagonist such as 4-(2-(N-2-carboxamidoindole)aminoethyl)-benzenesulfonamides or sulfonylureas. The methods are useful in reducing intimal hyperplasia due to, for example, vascular injuries resulting from angioplasty, endarterectomy, reduction atherectomy or anastomosis of a vascular graft. The non-peptide PDGF antagonists may optionally be administered coordinately with heparin, whereby the coordinately administration of non-peptide PDGF antagonist and heparin are combinatorially effective in inhibiting intimal hyperplasia.

    摘要翻译: 公开了用于抑制包括灵长类在内的哺乳动物脉管系统内膜增生的方法。 所述方法包括对哺乳动物施用非肽PDGF拮抗剂例如4-(2-(N-2-甲酰氨基吲哚)氨基乙基)苯磺酰胺或磺酰脲。 该方法可用于减少由于例如血管成形术,内膜切除术,减动脉粥样硬化斑块切除术或血管移植物的吻合术引起的血管损伤引起的内膜增生。 非肽类PDGF拮抗剂可以任选地与肝素配位给药,由此非肽类PDGF拮抗剂和肝素的协调给药在抑制内膜增生方面是组合有效的。