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公开(公告)号:US6008351A
公开(公告)日:1999-12-28
申请号:US573775
申请日:1995-12-18
申请人: Susan Yoshiko Tamura , Joseph Edward Semple , William Charles Ripka , Robert John Ardecky , Yu Ge , Stephen H. Carpenter , Terence K. Brunck , Marguerita S. L. Lim-Wilby , Ruth F. Nutt , Matthew M. Abelman
发明人: Susan Yoshiko Tamura , Joseph Edward Semple , William Charles Ripka , Robert John Ardecky , Yu Ge , Stephen H. Carpenter , Terence K. Brunck , Marguerita S. L. Lim-Wilby , Ruth F. Nutt , Matthew M. Abelman
IPC分类号: A61K31/44 , A61K31/495 , A61K31/505 , A61K38/00 , A61P7/02 , A61P43/00 , C07C257/18 , C07C279/24 , C07C279/34 , C07C281/06 , C07C311/54 , C07C327/48 , C07D211/56 , C07D211/76 , C07D213/75 , C07D213/76 , C07D239/46 , C07D239/47 , C07D239/52 , C07D239/54 , C07D239/545 , C07D401/12 , C07F7/18 , C07K5/06 , C07K5/078 , C07D239/02
CPC分类号: C07K5/06191 , C07D211/56 , C07D211/76 , C07D213/75 , C07D239/47 , C07D239/545 , C07D401/12 , C07K5/06139 , A61K38/00
摘要: The present invention discloses peptide aldehydes which are potent and specific inhibitors of thrombin, their pharmaceutically acceptable salts, pharmaceutically acceptable compositions thereof, and methods of using them as therapeutic agents for disease states in mammals characterized by abnormal thrombosis.
摘要翻译: 本发明公开了肽醛,其是凝血酶的有效和特异性抑制剂,其药学上可接受的盐,药学上可接受的组合物,以及将其用作以异常血栓形成为特征的哺乳动物的疾病状态的治疗剂。
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公开(公告)号:US5714580A
公开(公告)日:1998-02-03
申请号:US455974
申请日:1995-05-31
IPC分类号: A61K38/55 , A61P1/00 , C07C251/76 , C07C281/10 , C07K1/113 , C07K5/072 , C07K5/078 , C07K5/093 , C07K14/81 , C07K5/00 , C07K7/00 , C07K17/00
CPC分类号: C07K5/06139 , C07C281/10 , C07K5/06104 , C07K5/06113
摘要: Novel compounds having activity against trypsin are disclosed. Specifically, novel peptide aldehyde analogues that have substantial potency and specificity as inhibitors of mammalian pancreatic trypsin are presented. The compounds are useful in the prevention and treatment of the tissue damage or destruction associated with pancreatitis.
摘要翻译: 公开了具有抗胰蛋白酶活性的新型化合物。 具体地说,具有作为哺乳动物胰腺胰蛋白酶抑制剂的实质效力和特异性的新型肽醛类似物。 该化合物可用于预防和治疗与胰腺炎相关的组织损伤或破坏。
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公开(公告)号:US5658930A
公开(公告)日:1997-08-19
申请号:US481660
申请日:1995-06-07
申请人: Susan Yoshiko Tamura , Joseph Edward Semple , William Charles Ripka , Robert John Ardecky , Yu Ge , Stephen H. Carpenter , Terence K. Brunck
发明人: Susan Yoshiko Tamura , Joseph Edward Semple , William Charles Ripka , Robert John Ardecky , Yu Ge , Stephen H. Carpenter , Terence K. Brunck
IPC分类号: A61K38/00 , C07D211/56 , C07D211/76 , C07D213/75 , C07D239/46 , C07D239/54 , C07D239/545 , C07D401/12 , C07K5/06 , C07K5/078 , A61K31/445 , A61K31/505 , C07D213/64 , C07D233/32 , C07D233/40
CPC分类号: C07D211/56 , C07D211/76 , C07D213/75 , C07D239/47 , C07D239/545 , C07D401/12 , C07K5/06139 , C07K5/06191 , A61K38/00
摘要: The present invention discloses peptide aldehydes which are potent and specific inhibitors of thrombin, their pharmaceutically acceptable salts, pharmaceutically acceptable compositions thereof, and methods of using them as therapeutic agents for disease states in mammals characterized by abnormal thrombosis.
摘要翻译: 本发明公开了肽醛,其是凝血酶的有效和特异性抑制剂,其药学上可接受的盐,药学上可接受的组合物,以及将其用作以异常血栓形成为特征的哺乳动物的疾病状态的治疗剂。
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公开(公告)号:US5843442A
公开(公告)日:1998-12-01
申请号:US453047
申请日:1995-05-30
申请人: Howard R. Soule , Terence K. Brunck
发明人: Howard R. Soule , Terence K. Brunck
IPC分类号: A61K38/00 , C07K16/40 , A61K39/395 , C07K16/00 , C07K16/18
摘要: Coagulation protein antagonists are disclosed, which include monoclonal-type antibodies and related cell lines disclosed for the production of specific, neutralizing antibodies against factors VII and VIIa and the tissue factor/factor VIIa bimolecular complex, which antibodies are useful for the prevention or treatment of thrombotic and related diseases, for immunoaffinity isolation and purification of factors VII and VIIa and the tissue factor/factor VIIa complex, and for determination of factors VII or VIIa and the tissue factor/factors VII or VIIa complex in a biological sample.
摘要翻译: 公开了凝血蛋白拮抗剂,其包括公开用于产生针对因子VII和VIIa的特异性中和抗体和组织因子/因子VIIa双分子复合物的单克隆抗体和相关细胞系,所述抗体可用于预防或治疗 血栓形成和相关疾病,用于免疫亲和分离和纯化因子VII和VIIa和组织因子/因子VIIa复合物,以及用于测定生物样品中因子VII或VIIa和组织因子/因子VII或VIIa复合物。
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公开(公告)号:US4999421A
公开(公告)日:1991-03-12
申请号:US211749
申请日:1988-06-27
CPC分类号: C07K14/005 , A61K39/00 , C12N2740/14022 , Y10S530/806
摘要: The mRNA coded by the "anti-sense" strand of the complementary DNA produced by HTLV-I infection contains significant open reading frames. Cells infected by HTLV-I virus produce mRNA that is anti-sense to the viral RNA genome. Infected cells may produce proteins from the newly discovered mRNA. The production of the anti-sense in mRNA initiates from a newly discovered transcriptional promoter located within 1.8 kb from the 3' terminus of the viral genome. The mRNA, protein, and antibodies directed thereto can be used in the prevention, diagnosis, and treatment of HTLV-I infections.
摘要翻译: 由HTLV-I感染产生的互补DNA的“反义”链编码的mRNA含有显着的开放阅读框架。 感染HTLV-I病毒的细胞产生对病毒RNA基因组无害的mRNA。 受感染的细胞可能从新发现的mRNA产生蛋白质。 mRNA中反义词的产生从位于距病毒基因组3'末端1.8kb的新发现的转录启动子起始。 指向其的mRNA,蛋白质和抗体可用于预防,诊断和治疗HTLV-1感染。
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公开(公告)号:US06432922B1
公开(公告)日:2002-08-13
申请号:US09359929
申请日:1999-07-22
申请人: Terence K. Brunck , Susan Y. Tamura
发明人: Terence K. Brunck , Susan Y. Tamura
IPC分类号: C07K506
CPC分类号: C07K5/06069 , A61K38/00
摘要: Novel compounds having activity inhibitors of urokinase and in reducing or inhibiting blood vessel formation are provided. These compounds have an arginine or arginine mimic aldehyde or an arginine ketoamide group at P1. These compounds are useful in vitro for monitoring plasminogen activator levels and in vivo in treatment of conditions which are ameliorated by inhibition of or decreased activity of urokinase and in treating pathologic conditions wherein blood vessel formation is related to a pathologic condition.
摘要翻译: 提供了具有尿激酶活性抑制剂和减少或抑制血管形成的新型化合物。 这些化合物在P1处具有精氨酸或精氨酸模拟醛或精氨酸酮酰胺基团。 这些化合物在体外可用于监测纤溶酶原激活物水平和体内治疗通过抑制或降低尿激酶活性和改善血管形成与病理状况相关的病理状况而改善的病症。
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公开(公告)号:US06221659B1
公开(公告)日:2001-04-24
申请号:US09008121
申请日:1998-01-16
申请人: Howard R. Soule , Terence K. Brunck
发明人: Howard R. Soule , Terence K. Brunck
IPC分类号: C12N506
摘要: Coagulation protein antagonists are disclosed, which include monoclonal-type antibodies and related cell lines disclosed for the production of specific, neutralizing antibodies against factors VII and VIIa and the tissue factor/factor VIIa bimolecular complex, which antibodies are useful for the prevention or treatment of thrombotic and related diseases, for immunoaffinity isolation and purification of factors VII and VIIa and the tissue factor/factor VIIa complex, and for determination of factors VII or VIIa and the tissue factor/factors VII or VIIa complex in a biological sample.
摘要翻译: 公开了凝血蛋白拮抗剂,其包括公开用于产生针对因子VII和VIIa的特异性中和抗体和组织因子/因子VIIa双分子复合物的单克隆抗体和相关细胞系,所述抗体可用于预防或治疗 血栓形成和相关疾病,用于免疫亲和分离和纯化因子VII和VIIa和组织因子/因子VIIa复合物,以及用于测定生物样品中因子VII或VIIa和组织因子/因子VII或VIIa复合物。
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公开(公告)号:US6011158A
公开(公告)日:2000-01-04
申请号:US659983
申请日:1996-06-07
申请人: Susan Yoshiko Tamura , Joseph Edward Semple , William Charles Ripka , Robert John Ardecky , Yu Ge , Stephen H. Carpenter , Terence K. Brunck , Marguerita S. L. Lim-Wilby , Ruth F. Nutt , Matthew M. Abelman
发明人: Susan Yoshiko Tamura , Joseph Edward Semple , William Charles Ripka , Robert John Ardecky , Yu Ge , Stephen H. Carpenter , Terence K. Brunck , Marguerita S. L. Lim-Wilby , Ruth F. Nutt , Matthew M. Abelman
IPC分类号: A61K38/00 , C07D211/56 , C07D211/76 , C07D213/75 , C07D239/46 , C07D239/54 , C07D239/545 , C07D401/12 , C07K5/06 , C07K5/078 , C07D211/72
CPC分类号: C07D211/56 , C07D211/76 , C07D213/75 , C07D239/47 , C07D239/545 , C07D401/12 , C07K5/06139 , C07K5/06191 , A61K38/00
摘要: The present invention discloses peptide aldehydes which are potent and specific inhibitors of thrombin, their pharmaceutically acceptable salts, pharmaceutically acceptable compositions thereof, and methods of using them as therapeutic agents for disease states in mammals characterized by abnormal thrombosis.
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公开(公告)号:US5534498A
公开(公告)日:1996-07-09
申请号:US11666
申请日:1993-01-29
IPC分类号: A61K38/55 , A61P1/00 , C07C251/76 , C07C281/10 , C07K1/113 , C07K5/072 , C07K5/078 , C07K5/093 , C07K14/81 , A61K38/00 , C07K5/06 , C07K5/08
CPC分类号: C07K5/06139 , C07C281/10 , C07K5/06104 , C07K5/06113
摘要: Novel compounds having activity against trypsin are disclosed. Specifically, novel peptide aldehyde analogues that have substantial potency and specificity as inhibitors of mammalian pancreatic trypsin are presented. The compounds are useful in the prevention and treatment of the tissue damage or destruction associated with pancreatitis.
摘要翻译: 公开了具有抗胰蛋白酶活性的新型化合物。 具体地说,具有作为哺乳动物胰腺胰蛋白酶抑制剂的实质效力和特异性的新型肽醛类似物。 该化合物可用于预防和治疗与胰腺炎相关的组织损伤或破坏。
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10.
公开(公告)号:US06800434B2
公开(公告)日:2004-10-05
申请号:US09909062
申请日:2001-07-19
申请人: Anil K. Saksena , Viyyoor Moopil Girijavallabhan , Raymond G. Lovey , Edwin Jao , Frank Bennett , Jinping L. McCormick , Haiyan Wang , Russell E. Pike , Stephane L. Bogen , Yi-Tsung Liu , Ashok Arasappan , Tejal Parekh , Patrick A. Pinto , F. George Njoroge , Ashit K. Ganguly , Terence K. Brunck , Scott Jeffrey Kemp , Odile Esther Levy , Marguerita Lim-Wilby
发明人: Anil K. Saksena , Viyyoor Moopil Girijavallabhan , Raymond G. Lovey , Edwin Jao , Frank Bennett , Jinping L. McCormick , Haiyan Wang , Russell E. Pike , Stephane L. Bogen , Yi-Tsung Liu , Ashok Arasappan , Tejal Parekh , Patrick A. Pinto , F. George Njoroge , Ashit K. Ganguly , Terence K. Brunck , Scott Jeffrey Kemp , Odile Esther Levy , Marguerita Lim-Wilby
IPC分类号: A61K3800
摘要: The present invention discloses novel peptide compounds which have HCV protease inhibitory activity as well as methods for preparing such compounds. In another embodiment, the invention discloses pharmaceutical compositions comprising such peptides as well as methods of using them to treat disorders associated with the HCV protease.
摘要翻译: 本发明公开了具有HCV蛋白酶抑制活性的新型肽化合物及其制备方法。 在另一个实施方案中,本发明公开了包含这些肽的药物组合物以及使用它们来治疗与HCV蛋白酶相关的病症的方法。
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