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公开(公告)号:US5859284A
公开(公告)日:1999-01-12
申请号:US701942
申请日:1996-08-23
申请人: Kenneth M. Kent , Choung U. Kim , Lawrence R. McGee , John D. Munger, Jr. , Ernest J. Prisbe , Michael J. Postich , John C. Rohloff , Daphne E. St. John , Matthew A. Williams , Lijun Zhang
发明人: Kenneth M. Kent , Choung U. Kim , Lawrence R. McGee , John D. Munger, Jr. , Ernest J. Prisbe , Michael J. Postich , John C. Rohloff , Daphne E. St. John , Matthew A. Williams , Lijun Zhang
IPC分类号: B05B7/12 , C07C227/08 , C07D203/26 , C07D303/40 , C07D317/46 , C07C69/757 , C07D307/00
CPC分类号: C07D303/40 , B05B7/1209 , C07C227/08 , C07D203/26 , C07D317/46 , C07C2101/16 , Y02P20/55
摘要: The present invention provides new synthetic methods and compositions. In particular, new methods of preparing intermediates useful in the synthesis of neuraminidase inhibitors and compositions useful as intermediates that are themselves useful in the synthesis of neuraminidase inhibitors are provided.
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公开(公告)号:US6057459A
公开(公告)日:2000-05-02
申请号:US175744
申请日:1998-10-20
申请人: Kenneth M. Kent , Choung U. Kim , Lawrence R. McGee , John D. Munger, Jr. , Ernest J. Prisbe , Michael J. Postich , John C. Rohloff , Daphne E. St. John , Matthew A. Williams , Lijun Zhang
发明人: Kenneth M. Kent , Choung U. Kim , Lawrence R. McGee , John D. Munger, Jr. , Ernest J. Prisbe , Michael J. Postich , John C. Rohloff , Daphne E. St. John , Matthew A. Williams , Lijun Zhang
IPC分类号: B05B7/12 , C07C227/08 , C07D203/26 , C07D303/40 , C07D317/46 , C07D317/68
CPC分类号: C07D303/40 , B05B7/1209 , C07C227/08 , C07D203/26 , C07D317/46 , C07C2101/16 , Y02P20/55
摘要: The present invention provides new synthetic methods and compositions. In particular, new methods of preparing intermediates useful in the synthesis of neuraminidase inhibitors and compositions useful as intermediates that are themselves useful in the synthesis of neuraminidase inhibitors are provided.
摘要翻译: 本发明提供了新的合成方法和组合物。 特别地,提供了可用于合成神经氨酸酶抑制剂的中间体的新方法和可用作中间体的组合物,其本身可用于神经氨酸酶抑制剂的合成。
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公开(公告)号:US06204398B1
公开(公告)日:2001-03-20
申请号:US09242119
申请日:1999-04-28
申请人: Kenneth M. Kent , Choung U. Kim , Lawrence R. McGee , John D. Munger , Ernest J. Prisbe , Michael J. Postich , John C. Rohloff , Daphne E. Kelly , Matthew A. Williams , Lijun Zhang
发明人: Kenneth M. Kent , Choung U. Kim , Lawrence R. McGee , John D. Munger , Ernest J. Prisbe , Michael J. Postich , John C. Rohloff , Daphne E. Kelly , Matthew A. Williams , Lijun Zhang
IPC分类号: C07D31744
CPC分类号: C07D303/40 , B05B7/1209 , C07C227/08 , C07C2601/16 , C07D203/26 , C07D317/46 , Y02P20/55
摘要: The present invention provides new synthetic methods and compositions. In particular, new methods of preparing intermediates such as those having formulas (I)-(IV), useful in the synthesis of neuraminidase inhibitors and compositions useful as intermediates that are themselves useful in the synthesis of neuraminidase inhibitors are provided.
摘要翻译: 本发明提供了新的合成方法和组合物。 特别地,提供了可用于合成神经氨酸酶抑制剂的中间体如具有式(I) - (IV)的中间体的新方法和可用作中间体的组合物,其本身可用于合成神经氨酸酶抑制剂。
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公开(公告)号:US5886213A
公开(公告)日:1999-03-23
申请号:US917640
申请日:1997-08-22
申请人: Kenneth M. Kent , Choung U. Kim , Lawrence R. McGee , John D. Munger , Ernest J. Prisbe , Michael J. Postich , John C. Rohloff , Daphne E. Kelly , Matthew A. Williams , Lijun Zhang
发明人: Kenneth M. Kent , Choung U. Kim , Lawrence R. McGee , John D. Munger , Ernest J. Prisbe , Michael J. Postich , John C. Rohloff , Daphne E. Kelly , Matthew A. Williams , Lijun Zhang
IPC分类号: C07C233/52 , C07C247/14 , C07C205/04 , C07C229/08
CPC分类号: C07C247/14 , C07C233/52 , C07B2200/07 , C07C2101/16
摘要: The present invention provides new synthetic methods and compositions. In particular, new methods of preparing intermediates useful in the synthesis of neuraminidase inhibitors and compositions useful as intermediates that are themselves useful in the synthesis of neuraminidase inhibitors are provided.
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公开(公告)号:US06518438B2
公开(公告)日:2003-02-11
申请号:US09967368
申请日:2001-09-27
申请人: Kenneth M. Kent , Choung U. Kim , Lawrence R. McGee , John D. Munger , Ernest J. Prisbe , Michael J. Postich , John C. Rohloff , Daphne E. Kelly , Matthew A. Williams , Lijun Zhang
发明人: Kenneth M. Kent , Choung U. Kim , Lawrence R. McGee , John D. Munger , Ernest J. Prisbe , Michael J. Postich , John C. Rohloff , Daphne E. Kelly , Matthew A. Williams , Lijun Zhang
IPC分类号: C07D20326
CPC分类号: C07D317/46 , C07C227/08 , C07C2601/16 , C07D203/26 , C07D303/40
摘要: The present invention provides new synthetic methods and compositions. In particular, new methods of preparing intermediates useful in the synthesis of neuraminidase inhibitors and compositions useful as intermediates that are themselves useful in the synthesis of neuraminidase inhibitors are provided.
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公开(公告)号:US5811450A
公开(公告)日:1998-09-22
申请号:US740568
申请日:1996-10-31
申请人: Norbert W. Bischofberger , Choung U. Kim , Steven H. Krawczyk , Lawrence R. McGee , Michael J. Postich , Wenjin Yang
发明人: Norbert W. Bischofberger , Choung U. Kim , Steven H. Krawczyk , Lawrence R. McGee , Michael J. Postich , Wenjin Yang
IPC分类号: A61K31/38 , C07D337/00
CPC分类号: C07D337/04 , C07D417/06 , C07D495/04
摘要: Tri- and tetra substituted thiepane compositions having use as immunogens, therapeutics, diagnostics and for other industrial purposes are disclosed. The compositions inhibit proteolytic activity of viral enzymes and are useful for the inhibition of such enzymes as well as in assays for the detection of such enzymes. Embodiments in which antigenic polypeptides are bonded to the compositions are useful in raising antibodies against the thiepane haptens or the polypeptide. Labeled thiepanes of this invention are useful as diagnostic reagents.
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公开(公告)号:US6034118A
公开(公告)日:2000-03-07
申请号:US552429
申请日:1995-11-03
申请人: Norbert W. Bischofberger , Choung U. Kim , Steven H. Krawczyk , Lawrence R. McGee , Michael J. Postich , Wenjin Yang
发明人: Norbert W. Bischofberger , Choung U. Kim , Steven H. Krawczyk , Lawrence R. McGee , Michael J. Postich , Wenjin Yang
IPC分类号: C07D337/04 , C07D495/04 , A61K31/38 , C07D337/00
CPC分类号: C07D337/04 , C07D495/04
摘要: Tri- and tetra substituted thiepane compositions having use as immunogens, therapeutics, diagnostics and for other industrial purposes are disclosed. The compositions inhibit proteolytic activity of viral enzymes and are useful for the inhibition of such enzymes as well as in assays for the detection of such enzymes. Embodiments in which antigenic polypeptides are bonded to the compositions are useful in raising antibodies against the thiepane haptens or the polypeptide. Labeled thiepanes of this invention are useful as diagnostic reagents.
摘要翻译: 公开了用作免疫原,治疗学,诊断和用于其它工业目的的三取代和四取代的硫代吡喃组合物。 组合物抑制病毒酶的蛋白水解活性,并且可用于抑制这些酶以及用于检测这些酶的测定。 其中抗原性多肽与组合物结合的实施方案可用于产生针对硫替平半抗原或多肽的抗体。 本发明的标记的thiepane可用作诊断试剂。
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