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公开(公告)号:US20180147227A1
公开(公告)日:2018-05-31
申请号:US15877597
申请日:2018-01-23
申请人: Karl D. Normington , David A. Sinclair , David J. Livingston , James M. Mckearin , Bruce Szczpankiewicz , Jonathan N. Kremsky
发明人: Karl D. Normington , David A. Sinclair , David J. Livingston , James M. Mckearin , Bruce Szczpankiewicz , Jonathan N. Kremsky
IPC分类号: A61K31/706
CPC分类号: A61K31/706 , A61K31/443 , A61K31/661 , A61K31/665 , A61K31/7052 , C07F9/06 , C07F9/547 , C07F9/65586 , C07F9/6561 , C07F9/65742 , C07H11/04 , C07H19/04 , C07H19/048
摘要: The invention relates to compositions of nicotinamide mononucleotide derivatives and their methods of use. The invention also relates to methods of preparing nicotinamide mononucleotide derivatives. The invention relates to pharmaceutical compositions and nutritional supplements containing a nicotinamide mononucleotide derivative. The invention relates to methods of using nicotinamide mononucleotide derivatives that promote the increase of intracellular levels of nicotinamide adenine dinucleotide (NAD+) in cells and tissues for treating diseases and improving cell and tissue survival.
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公开(公告)号:US20170189434A1
公开(公告)日:2017-07-06
申请号:US15463683
申请日:2017-03-20
申请人: Karl D. Normington , David A. Sinclair , David J. Livingston , James M. McKearin , Bruce Szczpankiewicz , Jonathan N. Kremsky
发明人: Karl D. Normington , David A. Sinclair , David J. Livingston , James M. McKearin , Bruce Szczpankiewicz , Jonathan N. Kremsky
IPC分类号: A61K31/706
CPC分类号: A61K31/706 , A61K31/443 , A61K31/661 , A61K31/665 , A61K31/7052 , C07F9/06 , C07F9/547 , C07F9/65586 , C07F9/6561 , C07F9/65742 , C07H11/04 , C07H19/04 , C07H19/048
摘要: The invention relates to compositions of nicotinamide mononucleotide derivatives and their methods of use. The invention also relates to methods of preparing nicotinamide mononucleotide derivatives. The invention relates to pharmaceutical compositions and nutritional supplements containing a nicotinamide mononucleotide derivative. The invention relates to methods of using nicotinamide mononucleotide derivatives that promote the increase of intracellular levels of nicotinamide adenine dinucleotide (NAD+) in cells and tissues for treating diseases and improving cell and tissue survival.
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公开(公告)号:US20120165319A1
公开(公告)日:2012-06-28
申请号:US13293592
申请日:2011-11-10
申请人: Mark James Batchelor , David Bebbington , Guy W. Bemis , Wolf Herman Fridman , Roger John Gillespie , Julian M.C. Golec , Yong Gu , David J. Lauffer , David J. Livingston , Saroop Singh Matharu , Michael D. Mullican , Mark A. Murcko , Robert Murdoch , Philip Nyce , Andrea L.C. Robidoux , Michael Su , M. Woods Wannamaker , Keith P. Wilson , Robert E. Zelle
发明人: Mark James Batchelor , David Bebbington , Guy W. Bemis , Wolf Herman Fridman , Roger John Gillespie , Julian M.C. Golec , Yong Gu , David J. Lauffer , David J. Livingston , Saroop Singh Matharu , Michael D. Mullican , Mark A. Murcko , Robert Murdoch , Philip Nyce , Andrea L.C. Robidoux , Michael Su , M. Woods Wannamaker , Keith P. Wilson , Robert E. Zelle
IPC分类号: A61K31/551 , A61K31/55 , A61P19/02 , A61P1/18 , A61P29/00 , A61P35/02 , A61P1/04 , A61P37/00 , A61P1/16 , A61P25/00 , A61P17/06 , A61P37/06 , C07D487/04 , A61P1/00
CPC分类号: C07D243/12 , C07D401/06 , C07D401/12 , C07D403/12 , C07D405/12 , C07D405/14 , C07D409/12 , C07D413/12 , C07D417/12 , C07D471/04 , C07D487/04 , C07K5/06139 , C07K5/0821
摘要: The present invention relates to novel classes of compounds which are inhibitors of interleukin-1β converting enzyme. The ICE inhibitors of this invention are characterized by specific structural and physicochemical features. This invention also relates to pharmaceutical compositions comprising these compounds. The compounds and pharmaceutical compositions of this invention are particularly well suited for inhibiting ICE activity and consequently, may be advantageously used as agents against IL-1-, apoptosis-, IGIF-, and IFN-γ-mediated diseases, inflammatory diseases, autoimmune diseases, destructive bone disorders, proliferative disorders, infectious diseases, degenerative diseases, and necrotic diseases. This invention also relates to methods for inhibiting ICE activity, for treating interleukin-1-, apoptosis-, IGIF- and IFN-γ-mediated diseases and decreasing IGIF and IFN-γ production using the compounds and compositions of this invention. This invention also relates to methods for preparing N-acylamino compounds.
摘要翻译: 本发明涉及作为白介素-1和bgr的抑制剂的新型化合物。 转化酶。 本发明的ICE抑制剂的特征在于具体的结构和物理化学特征。 本发明还涉及包含这些化合物的药物组合物。 本发明的化合物和药物组合物特别适用于抑制ICE活性,因此可有利地用作抗IL-1,细胞凋亡,IGIF和IFN-γ介导的疾病,炎性疾病,自身免疫性疾病 破坏性骨病,增殖性疾病,感染性疾病,退行性疾病和坏死性疾病。 本发明还涉及使用本发明的化合物和组合物来抑制ICE活性,用于治疗白细胞介素-1,细胞凋亡,IGIF和IFN-γ介导的疾病以及减少IGIF和IFN-γ产生的方法。 本发明还涉及制备N-酰基氨基化合物的方法。
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公开(公告)号:US07790713B2
公开(公告)日:2010-09-07
申请号:US11655938
申请日:2007-01-18
申请人: Mark James Batchelor , David Bebbington , Guy W. Bemis , Wolf Herman Fridman , Roger John Gillespie , Julian M. C. Golec , Yong Gu , David J. Lauffer , David J. Livingston , Saroop Singh Matharu , Michael D. Mullican , Mark A. Murcko , Robert Murdoch , Philip Nyce , Andrea L. C. Robidoux , Michael Su , M. Woods Wannamaker , Keith P. Wilson , Robert E. Zelle
发明人: Mark James Batchelor , David Bebbington , Guy W. Bemis , Wolf Herman Fridman , Roger John Gillespie , Julian M. C. Golec , Yong Gu , David J. Lauffer , David J. Livingston , Saroop Singh Matharu , Michael D. Mullican , Mark A. Murcko , Robert Murdoch , Philip Nyce , Andrea L. C. Robidoux , Michael Su , M. Woods Wannamaker , Keith P. Wilson , Robert E. Zelle
IPC分类号: C07D243/12 , A61K31/55 , A61P29/00
CPC分类号: C07D243/12 , A61K38/00 , C07D401/06 , C07D401/12 , C07D403/12 , C07D405/12 , C07D405/14 , C07D409/12 , C07D413/12 , C07D417/12 , C07D471/04 , C07D487/04 , C07K5/0202 , C07K5/06139 , C07K5/0821
摘要: The present invention relates to novel classes of compounds which are inhibitors of interleukin-1β converting enzyme. The ICE inhibitors of this invention are characterized by specific structural and physicochemical features. This invention also relates to pharmaceutical compositions comprising these compounds. The compounds and pharmaceutical compositions of this invention are particularly well suited for inhibiting ICE activity and consequently, may be advantageously used as agents against IL-1-, apoptosis-, IGIF-, and IFN-γ-mediated diseases, inflammatory diseases, autoimmune diseases, destructive bone disorders, proliferative disorders, infectious diseases, degenerative diseases, and necrotic diseases. This invention also relates to methods for inhibiting ICE activity, for treating interleukin-1-, apoptosis-, IGIF- and IFN-γ-mediated diseases and decreasing IGIF and IFN-γ production using the compounds and compositions of this invention. This invention also relates to methods for preparing-N-acylamino compounds.
摘要翻译: 本发明涉及作为白介素-1和bgr的抑制剂的新型化合物。 转化酶。 本发明的ICE抑制剂的特征在于具体的结构和物理化学特征。 本发明还涉及包含这些化合物的药物组合物。 本发明的化合物和药物组合物特别适用于抑制ICE活性,因此可有利地用作抗IL-1,细胞凋亡,IGIF和IFN-γ介导的疾病,炎性疾病,自身免疫性疾病 破坏性骨病,增殖性疾病,感染性疾病,退行性疾病和坏死性疾病。 本发明还涉及使用本发明的化合物和组合物来抑制ICE活性,用于治疗白细胞介素-1,细胞凋亡,IGIF和IFN-γ介导的疾病以及减少IGIF和IFN-γ产生的方法。 本发明还涉及N-酰基氨基化合物的制备方法。
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公开(公告)号:US20100159455A1
公开(公告)日:2010-06-24
申请号:US12441672
申请日:2007-09-18
申请人: Tanya Landsman , David J. Livingston , Richard A. Martinelli , Yumei Huang , Benjamin Adam Seigal , Dingxue Yan , James M. Coull , Andrew M. Stern
发明人: Tanya Landsman , David J. Livingston , Richard A. Martinelli , Yumei Huang , Benjamin Adam Seigal , Dingxue Yan , James M. Coull , Andrew M. Stern
IPC分类号: C12Q1/68
CPC分类号: G01N33/542 , C12Q1/6804 , G01N33/566 , G01N2333/71 , C12Q2565/101 , C12Q2563/179 , C12Q2563/131
摘要: The invention provides compositions and methods, e.g., assay technologies and their use in biodetection and diagnostics. More particularly, the invention provides compositions and methods based on nucleic acid-templated chemistry in biodetection and profiling of receptors (and their families) and proteins (and their families), and the use of same in diagnostics.
摘要翻译: 本发明提供组合物和方法,例如测定技术及其在生物检测和诊断中的应用。 更具体地,本发明提供了基于生物检测和受体(及其家族)和蛋白质(及其家族)的生物检测和分析的核酸模板化学的组合物和方法,以及其在诊断中的用途。
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公开(公告)号:US06350741B1
公开(公告)日:2002-02-26
申请号:US09326494
申请日:1999-06-04
申请人: Julian M. C. Golec , David J. Lauffer , David J. Livingston , Michael D. Mullican , Philip L. Nyce , Andrea L. C. Robidoux , Marion W. Wannamaker
发明人: Julian M. C. Golec , David J. Lauffer , David J. Livingston , Michael D. Mullican , Philip L. Nyce , Andrea L. C. Robidoux , Marion W. Wannamaker
IPC分类号: A61K3155
CPC分类号: C07K5/06139 , A61K38/00 , C07K5/0202 , Y02A50/385 , Y02A50/387 , Y02A50/389 , Y02A50/475
摘要: The present invention relates to novel classes of compounds which are inhibitors of interleukin-1&bgr; converting enzyme (“ICE”). This invention also relates to pharmaceutical compositions comprising these compounds. The compounds and pharmaceutical compositions of this invention are particularly well suited for inhibiting ICE activity and consequently, may be advantageously used as agents against interleukin-1-(“IL-1”), apoptosis-, interferon-&ggr; inducing factor-(IGIF), or interferon-&ggr;-(“IFN-&ggr;”) mediated diseases, including inflammatory diseases, autoimmune diseases, destructive bone disorders, proliferative disorders, infectious diseases, and degenerative diseases. This invention also relates to methods for inhibiting ICE activity and decreasing IGIF production and IFN-&ggr; production and methods for treating interleukin-1, apoptosis- and interferon-&ggr;-mediated diseases using the compounds and compositions of this invention. This invention also relates to methods of preparing the compounds of this invention.
摘要翻译: 本发明涉及作为白细胞介素-1β转换酶(“ICE”)抑制剂的新型化合物。 本发明还涉及包含这些化合物的药物组合物。 本发明的化合物和药物组合物特别适用于抑制ICE活性,因此可有利地用作抗白细胞介素-1-(“IL-1”),细胞凋亡,干扰素-γ诱导因子(IGIF) 或“干扰素-γ”(“IFN-γ”)介导的疾病,包括炎性疾病,自身免疫性疾病,破坏性骨病,增殖性疾病,感染性疾病和退行性疾病。 本发明还涉及使用本发明的化合物和组合物来抑制ICE活性和降低IGIF产生和IFN-γ产生的方法以及用于治疗白细胞介素-1,凋亡和干扰素-γ介导的疾病的方法。 本发明还涉及制备本发明化合物的方法。
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公开(公告)号:US5847135A
公开(公告)日:1998-12-08
申请号:US440898
申请日:1995-05-25
申请人: Guy W. Bemis , Julian M. C. Golec , David J. Lauffer , Michael D. Mullican , Mark A. Murcko , David J. Livingston
发明人: Guy W. Bemis , Julian M. C. Golec , David J. Lauffer , Michael D. Mullican , Mark A. Murcko , David J. Livingston
IPC分类号: C07K5/023 , A61K38/00 , A61P29/00 , A61P37/00 , C07K5/02 , C07K5/04 , C07D225/00 , C07D237/00 , C07D295/00 , C07D487/00
CPC分类号: C07K5/0202 , A61K38/00
摘要: The present invention relates to novel classes of compounds which are inhibitors of interleukin-1.beta. converting enzyme. The ICE inhibitors of this invention are characterized by specific structural and physicochemical features. This invention also relates to pharmaceutical compositions comprising these compounds. The compounds and pharmaceutical compositions of this invention are particularly well suited for inhibiting ICE activity and consequently, may be advantageously used as agents against interleukin-1 mediated diseases, including inflammatory diseases, autoimmune diseases and neurodegenerative diseases. This invention also relates to methods for inhibiting ICE activity and methods for treating interleukin-1 mediated diseases using the compounds and compositions of this invention.
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公开(公告)号:US20120238749A1
公开(公告)日:2012-09-20
申请号:US13271474
申请日:2011-10-12
申请人: Guy W. Bemis , Julian M. C. Golec , David J. Lauffer , Michael D. Mullican , Mark A. Murcko , David J. Livingston
发明人: Guy W. Bemis , Julian M. C. Golec , David J. Lauffer , Michael D. Mullican , Mark A. Murcko , David J. Livingston
IPC分类号: C07D213/74 , G01N33/573 , C07D217/26 , C07D487/04 , C07D233/90 , C07D211/60
CPC分类号: C07D243/08 , A61K38/00 , C07D243/12 , C07D263/56 , C07D413/04 , C07D487/04 , C07K5/0202 , C07K5/06052 , C07K5/0812
摘要: The present invention relates to novel classes of compounds which are inhibitors of interleukin-1β converting enzyme. The ICE inhibitors of this invention are characterized by specific structural and physicochemical features. This invention also relates to pharmaceutical compositions comprising these compounds. The compounds and pharmaceutical compositions of this invention are particularly well suited for inhibiting ICE activity and consequently, may be advantageously used as agents against interleukin-1 mediated diseases, including inflammatory diseases, autoimmune diseases and neurodegenerative diseases. This invention also relates to methods for inhibiting ICE activity and methods for treating interleukin-1 mediated diseases using the compounds and compositions of this invention.
摘要翻译: 本发明涉及作为白介素-1和bgr的抑制剂的新型化合物。 转化酶。 本发明的ICE抑制剂的特征在于具体的结构和物理化学特征。 本发明还涉及包含这些化合物的药物组合物。 本发明的化合物和药物组合物特别适用于抑制ICE活性,因此可有利地用作抗白介素-1介导的疾病(包括炎性疾病,自身免疫性疾病和神经变性疾病)的药物。 本发明还涉及使用本发明的化合物和组合物来抑制ICE活性的方法和用于治疗白细胞介素-1介导的疾病的方法。
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公开(公告)号:US06573259B2
公开(公告)日:2003-06-03
申请号:US10035850
申请日:2001-10-23
申请人: Julian M. C. Golec , David J. Lauffer , David J. Livingston , Michael D. Mullican , Mark A. Murcko , Philip L. Nyce , Andrea L. C. Robidoux , Marion W. Wannamaker
发明人: Julian M. C. Golec , David J. Lauffer , David J. Livingston , Michael D. Mullican , Mark A. Murcko , Philip L. Nyce , Andrea L. C. Robidoux , Marion W. Wannamaker
IPC分类号: A61K3155
CPC分类号: C07K5/0821 , A61K38/00 , C07K5/0202 , Y02A50/385 , Y02A50/387 , Y02A50/389 , Y02A50/475
摘要: The present invention relates to novel classes of compounds which are inhibitors of interleukin-1&bgr; converting enzyme (“ICE”). This invention also relates to pharmaceutical compositions comprising these compounds. The compounds and pharmaceutical compositions of this invention are particularly well suited for inhibiting ICE activity and consequently, may be advantageously used as agents against interleukin-1-(“IL-1”), apoptosis-, interferon-&ggr; inducing factor-(IGIF), interferon-&ggr;-(“IFN-&ggr;”) mediated diseases, excess dietary alcohol intake diseases, or viral diseases, including inflammatory diseases, autoimmune diseases, destructive bone disorders, proliferative disorders, infectious diseases, and degenerative diseases. This invention also relates to methods for inhibiting ICE activity and decreasing IGIF production and IFN-&ggr; production and methods for treating interleukin-1, apoptosis- and interferon-&ggr;-mediated diseases using the compounds and compositions of this invention. This invention also relates to methods of preparing the compounds of this invention.
摘要翻译: 本发明涉及作为白细胞介素-1β转换酶(“ICE”)抑制剂的新型化合物。 本发明还涉及包含这些化合物的药物组合物。 本发明的化合物和药物组合物特别适用于抑制ICE活性,因此可有利地用作抗白细胞介素-1-(“IL-1”),细胞凋亡,干扰素-γ诱导因子(IGIF) 干扰素-γ-(“IFN-γ”)介导的疾病,过度饮食酒精摄入疾病或病毒性疾病,包括炎性疾病,自身免疫疾病,破坏性骨病,增殖性疾病,感染性疾病和退行性疾病。 本发明还涉及使用本发明的化合物和组合物来抑制ICE活性和降低IGIF产生和IFN-γ产生的方法以及用于治疗白细胞介素-1,凋亡和干扰素-γ介导的疾病的方法。 本发明还涉及制备本发明化合物的方法。
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公开(公告)号:US6162790A
公开(公告)日:2000-12-19
申请号:US24537
申请日:1998-02-17
申请人: Guy W. Bemis , John P. Duffy , Wolf Herman Fridman , Julian M. C. Golec , David J. Livingston , Michael D. Mullican , Mark A. Murcko , Robert E. Zelle
发明人: Guy W. Bemis , John P. Duffy , Wolf Herman Fridman , Julian M. C. Golec , David J. Livingston , Michael D. Mullican , Mark A. Murcko , Robert E. Zelle
IPC分类号: A61K38/00 , A61K38/55 , A61P1/00 , A61P1/04 , A61P1/16 , A61P1/18 , A61P3/10 , A61P5/14 , A61P7/00 , A61P7/06 , A61P9/10 , A61P11/00 , A61P11/06 , A61P13/12 , A61P17/00 , A61P17/06 , A61P17/14 , A61P19/02 , A61P19/08 , A61P19/10 , A61P21/00 , A61P21/04 , A61P25/00 , A61P25/16 , A61P25/28 , A61P29/00 , A61P31/00 , A61P35/00 , A61P35/02 , A61P37/02 , A61P43/00 , C07K5/00 , C07K5/02 , C07K5/08 , C07K5/083
CPC分类号: C07K5/0205 , A61K38/00 , C07K5/0202 , Y02A50/475
摘要: The present invention relates to novel classes of compounds which are inhibitors of interleukin-1 .beta. converting enzyme. This invention also relates to pharmaceutical compositions comprising these compounds. The compounds and pharmaceutical compositions of this invention are particularly well suited for inhibiting ICE activity and consequently, may be advantageously used as agents against interleukin-1 and apoptosis-mediated diseases, including inflammatory diseases, autoimmune diseases, proliferative, infectious, and degenerative diseases. This invention also relates to methods for inhibiting ICE activity and methods for treating interleukin-1 mediated diseases using the compounds and compositions of this invention.
摘要翻译: 本发明涉及作为白细胞介素-1β转换酶抑制剂的新型化合物。 本发明还涉及包含这些化合物的药物组合物。 本发明的化合物和药物组合物特别适用于抑制ICE活性,因此可有利地用作抗白介素-1和细胞凋亡介导的疾病(包括炎性疾病,自身免疫性疾病,增殖性,感染性和退行性疾病)的药物。 本发明还涉及使用本发明的化合物和组合物来抑制ICE活性的方法和用于治疗白细胞介素-1介导的疾病的方法。
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