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1.
公开(公告)号:US20070043045A1
公开(公告)日:2007-02-22
申请号:US11505263
申请日:2006-08-16
申请人: Yongqi Deng , Lianyun Zhao , Gerald Shipps , Patrick Curran , M. Siddiqui , Rumin Zhang , Charles McNemar , Todd Mayhood , William Windsor , Emma Lees , David Parry
发明人: Yongqi Deng , Lianyun Zhao , Gerald Shipps , Patrick Curran , M. Siddiqui , Rumin Zhang , Charles McNemar , Todd Mayhood , William Windsor , Emma Lees , David Parry
IPC分类号: A61K31/5377 , A61K31/497 , A61K31/496 , A61K31/4439 , A61K31/4709 , A61K31/428 , A61K31/42 , A61K31/4196 , A61K31/4178 , A61K31/4025 , A61K31/416 , C07D413/02 , C07D405/02 , C07D409/02 , C07D417/02
CPC分类号: C07D405/12 , C07D333/40 , C07D405/14 , C07D409/12 , C07D409/14 , C07D413/12 , C07D413/14 , C07D417/12 , C07D417/14
摘要: Inhibitors of cyclin dependent kinase 2, compositions including the inhibitors, and methods of using the inhibitors and inhibitor compositions are described. The inhibitors and compositions including them are useful for treating disease or disease symptoms. The invention also provides for methods of making CDK-2 inhibitor compounds, methods of inhibiting CDK-2, and methods for treating disease or disease symptoms.
摘要翻译: 描述了细胞周期蛋白依赖性激酶2的抑制剂,包括抑制剂的组合物,以及使用抑制剂和抑制剂组合物的方法。 包括它们的抑制剂和组合物可用于治疗疾病或疾病症状。 本发明还提供了制备CDK-2抑制剂化合物的方法,抑制CDK-2的方法以及治疗疾病或疾病症状的方法。
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公开(公告)号:US5441734A
公开(公告)日:1995-08-15
申请号:US24330
申请日:1993-02-25
申请人: Paul Reichert , Charles McNemar , Nagamani Nagabhushan , Tattanahalli L. Nagabhushan , Stephen Tindall , Alan Hruza
发明人: Paul Reichert , Charles McNemar , Nagamani Nagabhushan , Tattanahalli L. Nagabhushan , Stephen Tindall , Alan Hruza
IPC分类号: A61K38/00 , A61K38/21 , C07K14/56 , C30B7/00 , C30B28/04 , C30B29/58 , A61K37/66 , A61K9/14 , C07K15/26
CPC分类号: C07K14/56 , A61K38/212 , C30B29/58 , C30B7/00
摘要: The present invention provides for crystalline zinc-interferon alfa-2 (IFN .alpha.-2) having a monoclinic morphology. The present invention further provides for crystalline cobalt-IFN .alpha.-2, crystalline calcium-IFN .alpha.-2, and crystalline IFN .alpha.-2 having a serum half-life of at least about 12 hours when injected into a primate. The present invention further provides for a method for producing a crystalline IFN .alpha.-2 comprising forming a soluble metal-IFN .alpha.-2 complex, and equilibrating the soluble metal-IFN .alpha.-2 complex in solution with an acetate salt of the metal under conditions that will cause the metal-IFN .alpha.-2 solution to become supersaturated and form crystalline metal-IFN .alpha.-2. The present invention also includes crystalline metal-alfa interferon having monoclinic, plate and needle morphologies.
摘要翻译: 本发明提供具有单斜晶形的结晶性锌 - 干扰素α-2(IFNα-2)。 本发明还提供了当注射到灵长类动物中时,具有至少约12小时的血清半衰期的结晶钴-IFFα-2,结晶性钙-IFNα2和结晶IFNα-2。 本发明进一步提供了一种用于产生结晶IFNα-2的方法,包括形成可溶性金属-IFMα-2复合物,并在条件下用金属的乙酸盐平衡溶液中的可溶性金属-IFMα-2复合物 这将导致金属-IFNα-2溶液变得过饱和并形成结晶金属-IFNα-2。 本发明还包括具有单斜晶系,板和针形态的结晶金属-α干扰素。
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3.
公开(公告)号:US5985263A
公开(公告)日:1999-11-16
申请号:US994621
申请日:1997-12-19
申请人: Seoju Lee , Charles McNemar
发明人: Seoju Lee , Charles McNemar
IPC分类号: A61K47/34 , A61K38/00 , A61K38/21 , A61K38/22 , A61K47/48 , C07K1/113 , C07K14/54 , C07K14/56 , C07K14/565 , C07K17/08 , A61K38/20 , A61K38/02
CPC分类号: A61K47/48215 , C07K14/5428 , C07K14/565 , C07K17/08 , A61K38/00
摘要: Substantially pure histidine-linked protein-polymer conjugates and processes for their preparation are disclosed. The processes include contacting a protein with an activated polymer under conditions sufficient to facilitate covalent attachment of at least a portion of the polymer strands on histidine residues of the protein and thereafter substantially separating the histidine-linked conjugates from the remaining reactants.
摘要翻译: 公开了基本上纯的组氨酸连接的蛋白质 - 聚合物缀合物及其制备方法。 所述方法包括使蛋白质与活化的聚合物接触,所述条件足以促进聚合物链的至少一部分共价连接到蛋白质的组氨酸残基上,然后将组氨酸连接的缀合物与剩余的反应物基本上分离。
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公开(公告)号:US5602232A
公开(公告)日:1997-02-11
申请号:US356021
申请日:1994-12-14
申请人: Paul Reichert , Charles McNemar , Nagamani Nagahhushan , Tattanahalli L. Nagahhushan , Stephen Tindall , Alan Hruza
发明人: Paul Reichert , Charles McNemar , Nagamani Nagahhushan , Tattanahalli L. Nagahhushan , Stephen Tindall , Alan Hruza
CPC分类号: C07K14/56 , A61K38/212 , C30B29/58 , C30B7/00
摘要: A method for producing a crystalline zinc interferon (IFN) .alpha.-2 comprising forming a soluble solution of IFN .alpha.-2 and a metal acetate salt under condtions wherein supersaturation and metal alpha interferon crystals occur.
摘要翻译: 包括在其中发生过饱和和金属α干扰素晶体的条件下形成IFNα-2的可溶性溶液和金属乙酸盐的生产结晶性锌干扰素(IFN)α-2的方法。
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