Insulin derivatives with increased zinc binding
    3.
    发明授权
    Insulin derivatives with increased zinc binding 失效
    具有增加的锌结合的胰岛素衍生物

    公开(公告)号:US06221837B1

    公开(公告)日:2001-04-24

    申请号:US08900574

    申请日:1997-07-25

    IPC分类号: C07K1462

    摘要: Insulin derivatives with increased zinc binding where Z is a histidine residue or a peptide having 2 to 35 genetically encodable amino acid residues, having 1 to 5 histidine residues, are suitable for the production of pharmaceutical preparations for the treatment of diabetes. Insulins of the formula I form complexes with zinc++, comprising an insulin hexamer and approximately 5 to 9 mol of zinc++ per hexamer.

    摘要翻译: 具有增加的锌结合的胰岛素衍生物,其中Z是组氨酸残基或具有2至35个具有1至5个组氨酸残基的2至35个遗传编码氨基酸残基的肽,适用于制备用于治疗糖尿病的药物制剂。 式I的胰岛素与锌++形成复合物,其包含胰岛素六聚体和约5至9摩尔锌++每六聚体。

    Pulmonary insulin crystals
    4.
    发明授权
    Pulmonary insulin crystals 有权
    肺胰岛素晶体

    公开(公告)号:US06818738B2

    公开(公告)日:2004-11-16

    申请号:US10152535

    申请日:2002-05-20

    申请人: Svend Havelund

    发明人: Svend Havelund

    IPC分类号: C07K1462

    摘要: Disclosed is a method of preparing zinc free rapid acting insulin analogue. In one embodiment insulin crystals are prepared by providing a solution of an analogue having a pH between 7 and 9.5. The solution is mixed with a salt of an alkali metal or salt and formed crystals are recovered.

    摘要翻译: 公开了一种制备无锌快速作用胰岛素类似物的方法。 在一个实施方案中,通过提供pH在7和9.5之间的类似物的溶液来制备胰岛素晶体。 将该溶液与碱金属或盐的盐混合并回收形成的晶体。

    Method for making insulin precursors and insulin precursor analogues having improved fermentation yield in yeast
    5.
    发明授权
    Method for making insulin precursors and insulin precursor analogues having improved fermentation yield in yeast 有权
    制备酵母中发酵产量提高的胰岛素前体和胰岛素前体类似物的方法

    公开(公告)号:US06777207B2

    公开(公告)日:2004-08-17

    申请号:US09894711

    申请日:2001-06-28

    IPC分类号: C07K1462

    CPC分类号: C07K14/62

    摘要: Novel insulin precursors and insulin precursor analogs comprising a connecting peptide (mini C-peptide) of preferably up to 15 amino acid residues and comprising at least one Gly are provided. The precursors can be converted into human insulin or a human insulin analog. The precursors will typically have a distance between B27 (atom CG2) and A1 (atom CA) of less than 5 Å.

    摘要翻译: 提供了包含优选至多15个氨基酸残基并且包含至少一个Gly的连接肽(小C肽)的新型胰岛素前体和胰岛素前体类似物。 前体可转化为人胰岛素或人胰岛素类似物。 前体通常具有小于5埃的B27(原子CG2)和A1(原子CA)之间的距离。

    Seeding crystals for the preparation of peptides or proteins
    6.
    发明授权
    Seeding crystals for the preparation of peptides or proteins 有权
    种子晶体用于制备肽或蛋白质

    公开(公告)号:US06566490B1

    公开(公告)日:2003-05-20

    申请号:US09742193

    申请日:2000-12-20

    IPC分类号: C07K1462

    CPC分类号: C07K14/62 C30B7/00 C30B29/58

    摘要: Disclosed is a method for producing seeding microcrystals for the production of human insulin, the microcrystals being free of non-human pancreatic insulin, the method comprising providing an unseeded suspension of human insulin, the suspension being free of non-human pancreatic insulin, and homogenizing the insulin suspension under pressure to result in human insulin microcrystals suitable for use as seeding microcrystals for the production of zinc insulin products. The method of homogenization under pressure may also be used for the production of seeding mnicrocrystals for other peptides and proteins, in particular pharmaceutical peptides or proteins such as insulin, GLP-1, glucagon and growth hormones.

    摘要翻译: 公开了一种用于生产人胰岛素的接种微晶的方法,所述微晶不含非人胰岛素,所述方法包括提供人胰岛素的未密封悬浮液,所述悬浮液不含非人胰岛素,并均化 胰岛素悬浮液在压力下导致人胰岛素微晶适合用作接种微晶体,用于生产锌胰岛素产品。 在压力下均质化的方法也可用于制备用于其它肽和蛋白质,特别是药物肽或蛋白质如胰岛素,GLP-1,胰高血糖素和生长激素的接种微晶。

    Methods for treatment of diabetes using peptide analogues of insulin
    8.
    发明授权
    Methods for treatment of diabetes using peptide analogues of insulin 失效
    使用胰岛素的肽类似物治疗糖尿病的方法

    公开(公告)号:US06197926B1

    公开(公告)日:2001-03-06

    申请号:US09255668

    申请日:1999-02-23

    IPC分类号: C07K1462

    CPC分类号: C07K14/62 A61K38/00

    摘要: The present invention is directed toward peptide analogues of insulin B chain that are generally derived from peptides comprising residues 9 to 23 of the native B chain sequence. The analogues are altered from the native sequence at position 12, 13, 15 and/or 16, and may be additionally be altered at position 19 and/or other positions. Pharmaceutical compositions containing these peptide analogues arc provided. The peptide analogues are useful for treating and inhibiting the development of diabetes.

    摘要翻译: 本发明涉及胰岛素B链的肽类似物,其通常衍生自包含天然B链序列的残基9至23的肽。 类似物从位置12,13,15和/或16处的天然序列改变,并且可以另外在位置19和/或其他位置改变。 提供了含有这些肽类似物的药物组合物。 肽类似物可用于治疗和抑制糖尿病的发展。