Fibrinolytic protein and production method thereof
    1.
    发明授权
    Fibrinolytic protein and production method thereof 失效
    纤维蛋白溶解蛋白及其制备方法

    公开(公告)号:US5750650A

    公开(公告)日:1998-05-12

    申请号:US67180

    申请日:1993-05-24

    CPC分类号: C12N9/50 C12N9/54

    摘要: A novel peptide having molecular weight of 31,000 (SDS-PAGE) is obtained from aqueous extract of Natto or the culture of Bacillus natto by purification procedures including alcohol fractionation and/or salting out and hydrophobic chromatography, and the physicochemical properties, including the amino acid sequence, of the peptide are determined. The peptide is active in fibrinolysis, exhibits strong thrombolytic activity by oral administration and is useful as an oral thrombolytic agent.

    摘要翻译: 通过包括醇分馏和/或盐析和疏水色谱法的纯化方法从Natto的水提取物或纳豆芽孢杆菌的培养物获得分子量为31,000的新型肽(SDS-PAGE),并且包括氨基酸的物理化学性质 确定肽的序列。 该肽在纤维蛋白溶解中有活性,通过口服给药具有强烈的溶栓活性,可用作口服溶栓剂。

    Subtilisin as an oral thrombolytic agent
    2.
    发明授权
    Subtilisin as an oral thrombolytic agent 失效
    枯草杆菌蛋白酶作为口服溶栓剂

    公开(公告)号:US5296223A

    公开(公告)日:1994-03-22

    申请号:US960259

    申请日:1992-10-13

    CPC分类号: A61K38/482

    摘要: There are provided thrombolytic agents suited for oral administration. The agent comprises a proteolytic enzyme of subtilisin family, such as subtilisin BPN', subtilisin Carsberg, subtilisin amylosacchariticus, etc., produced by microorganisms belonging to genus Bacillus, such as Bacillus subtilis, Bacillus licheniformis, Bacillus amyloliquefaciens, etc. and, even when administered orally, exhibits thrombolytic activity.

    摘要翻译: 提供适合口服给药的溶栓剂。 该试剂包括枯草杆菌蛋白酶家族的蛋白水解酶,如枯草杆菌蛋白酶BPN',枯草杆菌蛋白酶Carsberg,枯草杆菌蛋白酶淀粉酵母等,由属于芽孢杆菌属的微生物如枯草芽孢杆菌,地衣芽孢杆菌,解淀粉芽孢杆菌等产生,并且即使 口服给药,具有溶栓活性。

    Process for concentrating and separating trypsin inhibitor and
kallidinogenase in human urine
    5.
    发明授权
    Process for concentrating and separating trypsin inhibitor and kallidinogenase in human urine 失效
    浓缩和分离人尿中胰蛋白酶抑制剂和杀鼠肽素酶的方法

    公开(公告)号:US4780209A

    公开(公告)日:1988-10-25

    申请号:US104634

    申请日:1987-10-02

    IPC分类号: C07K14/81 C12N9/64 B01D15/08

    摘要: Two components, trypsin and kallidinogenase, in human urine are concentrated simultaneously by allowing human urine at neutral pH, collecting bubbles thus formed to obtain the concentrate of the two components, adjusting the concentrate to weak acidity, contacting the acidified concentrate with chitosan to allow the two components to be adsorbed onto chitosan, eluting the components from the adsorbent with aqueous ammonia solution, and neutralizing and heating the eluate at about 60.degree. C. for about 10 hours to make the eluate virus-free, followed by separating the components from the eluate.

    摘要翻译: 将人尿中的两种成分,胰蛋白酶和杀鼠肽素酶同时浓缩,使人尿液处于中性pH值,收集形成的气泡,得到两种成分的浓缩物,将浓缩物调节至弱酸性,将酸化浓缩物与壳聚糖接触, 吸附在壳聚糖上的两种组分,用氨水溶液从吸附剂中洗脱组分,并在约60℃下中和并加热洗脱液约10小时,使洗脱液无病毒,然后将组分从 洗脱液

    Process for concentrating and purifying human urinary kallikrein
    6.
    发明授权
    Process for concentrating and purifying human urinary kallikrein 失效
    浓缩和净化人类尿激肽释放酶的方法

    公开(公告)号:US4510248A

    公开(公告)日:1985-04-09

    申请号:US509030

    申请日:1983-06-29

    IPC分类号: C12N9/64 C12N9/48 C12N9/50

    CPC分类号: C12N9/6445

    摘要: Human urinary kallikrein is concentrated and purified by the following procedures; (a) Human urine is contacted with chitosan, a high molecular agglutinant obtained from chitin, at a pH from 4.0 to 7.0, thereby kallikrein is adsorbed on the chitosan and (b) kallikrein is eluted from the chitosan with an aqueous alkaline solution having a pH from 8.0 to 12.0.

    摘要翻译: 人尿激肽释放酶通过以下程序浓缩和纯化; (a)将人尿与壳多糖(几丁质获得的高分子凝集素)在4.0至7.0的pH下接触,由此激肽释放酶被吸附在壳聚糖上,(b)激肽释放酶用含有碱性溶液的水溶性脱乙酰壳多糖 pH 8.0〜12.0。

    Process of producing modified superoxide dismutase
    8.
    发明授权
    Process of producing modified superoxide dismutase 失效
    生产改性超氧化物歧化酶的方法

    公开(公告)号:US5403731A

    公开(公告)日:1995-04-04

    申请号:US162382

    申请日:1993-12-03

    CPC分类号: C12N9/0089 C08G65/33396

    摘要: A modified superoxide dismutase represented by the formula: ##STR1## (wherein R is as defined below; SOD is a residue of superoxide dismutase) is produced, in a shortened period of reaction with a high and constant modification ratio, by reacting a polymeric carbonyldiimidazole derivative represented by the formula: ##STR2## (wherein R is a residue of a water soluble polymer having an average molecular weight of about 2,000 to 10,000) with superoxide dismutase in the presence of a buffer having a pH of 9.0 to 11.0 and a concentration of 0.1 M to 0.5 M, preferably 0.2 M to 0.4 M, at a temperature of 30.degree. to 70.degree. C., preferably 45.degree. to 60.degree. C. The modified superoxide dismutase thus produced exhibits a suitably prolonged blood half-life.

    摘要翻译: 通过使聚合羰基二咪唑(聚合羰基二咪唑)反应,以缩短的反应速度缩短而制备由下式表示的改性超氧化物歧化酶:其中R定义如下; SOD为超氧化物歧化酶的残基; 在pH为9.0〜11.0的缓冲液和浓度为9.0〜11.0的存在下,用下式表示的衍生物:其中R为平均分子量为约2,000〜10,000的水溶性聚合物的残基,具有超氧化物歧化酶 在30至70℃,优选45-60℃的温度下,0.1M至0.5M,优选0.2M至0.4M。由此制备的改性超氧化物歧化酶表现出适当延长的血液半衰期。

    Process of treating inflammation with human urinary thiol protease
inhibitor
    10.
    发明授权
    Process of treating inflammation with human urinary thiol protease inhibitor 失效
    用人尿硫醇蛋白酶抑制剂治疗炎症的过程

    公开(公告)号:US4479937A

    公开(公告)日:1984-10-30

    申请号:US524549

    申请日:1983-08-19

    CPC分类号: C07K14/8139

    摘要: An anti-inflammatory agent comprising as an active component an inhibitor specifically inhibiting a thiol protease, which is obtained from human urine by extraction and purification. This agent has an action of inhibiting a disease caused by a thiol protease. This anti-inflammatory agent is prepared by a process in which a thiol protease inhibitor is extracted and purified from human urine by adopting in combination at least two treatments selected from a treatment with a molecular filter, a treatment with an ion exchanger, a treatment with an adsorber and an affinity chromatographic treatment.

    摘要翻译: 一种抗炎剂,其包含通过提取和纯化从人尿获得的特异性抑制硫醇蛋白酶的抑制剂作为活性成分。 该药剂具有抑制由硫醇蛋白酶引起的疾病的作用。 该抗炎剂通过以下方法制备,其中通过组合使用选自以下的至少两种处理组合提取和纯化巯基蛋白酶抑制剂:选自用分子过滤器处理,用离子交换剂处理,用离子交换剂处理, 吸附剂和亲和色谱处理。