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1.
公开(公告)号:US08119592B2
公开(公告)日:2012-02-21
申请号:US12089895
申请日:2006-10-10
IPC分类号: A61K38/12
CPC分类号: C07D487/04 , C07D471/04
摘要: Macrocyclic compounds having the structures described herein are useful for inhibiting replication of the hepatitis C virus (HCV). In preferred embodiments, the compounds are active against both the NS3 protease and the NS3 helicase of HCV.
摘要翻译: 具有本文所述结构的大环化合物可用于抑制丙型肝炎病毒(HCV)的复制。 在优选的实施方案中,所述化合物对NS3蛋白酶和HCV的NS3解旋酶均有活性。
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2.
公开(公告)号:US20090093533A1
公开(公告)日:2009-04-09
申请号:US12089895
申请日:2006-10-10
IPC分类号: A61K31/407 , C07D245/00 , A61P31/12
CPC分类号: C07D487/04 , C07D471/04
摘要: Macrocyclic compounds having the structures described herein are useful for inhibiting replication of the hepatitis C virus (HCV). In preferred embodiments, the compounds are active against both the NS3 protease and the NS3 helicase of HCV.
摘要翻译: 具有本文所述结构的大环化合物可用于抑制丙型肝炎病毒(HCV)的复制。 在优选的实施方案中,所述化合物对NS3蛋白酶和HCV的NS3解旋酶均有活性。
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3.
公开(公告)号:US20080019942A1
公开(公告)日:2008-01-24
申请号:US11773912
申请日:2007-07-05
申请人: Scott Seiwert , Leonid Beigelman , Lawrence Blatt , Timothy Kercher , April Kennedy , Steven Andrews
发明人: Scott Seiwert , Leonid Beigelman , Lawrence Blatt , Timothy Kercher , April Kennedy , Steven Andrews
IPC分类号: A61K38/21 , A61K31/4035 , A61K31/416 , A61K31/437 , C07D209/44 , C07D471/04 , C07D231/54 , A61P31/12 , A61K31/505 , A61K31/52
CPC分类号: C07D403/14 , C07D231/56 , C07D471/04
摘要: The embodiments provide compounds of the general Formula I, as well as compositions, including pharmaceutical compositions, comprising a subject compound. The embodiments provide compounds of the general Formula II, as well as compositions, including pharmaceutical compositions, comprising a subject compound. The embodiments provide compounds of the general Formula III, as well as compositions, including pharmaceutical compositions, comprising a subject compound. The embodiments further provide treatment methods, including methods of treating a hepatitis C virus infection and methods of treating liver fibrosis, the methods generally involving administering to an individual in need thereof an effective amount of a subject compound or composition.
摘要翻译: 实施方案提供了通式I的化合物,以及包含主题化合物的组合物,包括药物组合物。 实施方案提供了通式II的化合物,以及包含主题化合物的组合物,包括药物组合物。 实施方案提供了通式III的化合物,以及包含主题化合物的组合物,包括药物组合物。 实施方案还提供治疗方法,包括治疗丙型肝炎病毒感染的方法和治疗肝纤维化的方法,所述方法通常涉及向有需要的个体施用有效量的主题化合物或组合物。
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公开(公告)号:US20060270612A1
公开(公告)日:2006-11-30
申请号:US11431132
申请日:2006-05-09
IPC分类号: A61K31/7052 , A61K31/4704 , A61K31/4412
CPC分类号: A61K31/4412 , A61K31/44 , A61K31/444 , A61K31/45 , A61K31/4704 , A61K31/7052 , A61K47/56 , A61K47/58 , C07D213/16 , C07D213/26 , C07D213/63 , C07D213/64 , C07D213/69 , C07D215/227 , C07H15/26 , C07K1/1077 , C08F289/00 , Y02A50/401 , Y02A50/409 , Y02A50/411 , Y02A50/475
摘要: Disclosed are methods of modulating a stress activated protein kinase (SAPK) system with an active compound, wherein the active compound exhibits low potency for inhibition of at least one p38 MAPK; and wherein the contacting is conducted at a SAPK-modulating concentration that is at a low percentage inhibitory concentration for inhibition of the at least one p38 MAPK by the compound. Also disclosed are derivatives of pirfenidone. These derivatives can modulate a stress activated protein kinase (SAPK) system.
摘要翻译: 公开了用活性化合物调节应激活化蛋白激酶(SAPK)系统的方法,其中活性化合物表现出低的抑制至少一种p38MAPK的能力; 并且其中所述接触以对所述化合物抑制至少一种p38MAPK的低百分比抑制浓度的SAPK-调节浓度进行。 还公开了吡非尼酮的衍生物。 这些衍生物可以调节应激活化蛋白激酶(SAPK)系统。
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公开(公告)号:US20100249068A1
公开(公告)日:2010-09-30
申请号:US12728128
申请日:2010-03-19
申请人: Leonid Beigelman , Lawrence Blatt , Guangyi Wang
发明人: Leonid Beigelman , Lawrence Blatt , Guangyi Wang
IPC分类号: A61K31/675 , C07D403/04 , A61K31/505 , C07D473/34 , A61K31/52 , C07F9/02 , A61P35/02 , A61P31/12 , A61P33/02
CPC分类号: A61K31/7042 , A61K31/7052 , A61K31/7064 , A61K31/7068 , A61K31/7076 , C07H19/06 , C07H19/067 , C07H19/073 , C07H19/10 , C07H19/16 , C07H19/167 , C07H19/173 , C07H19/20 , Y02A50/414 , Y02A50/465
摘要: Disclosed herein are nucleotide analogs with protected phosphates, methods of synthesizing nucleotide analogs with protected phosphates and methods of treating diseases and/or conditions such as viral infections, cancer, and/or parasitic diseases with the nucleotide analogs with protected phosphates.
摘要翻译: 本文公开了具有被保护的磷酸盐的核苷酸类似物,与被保护的磷酸盐合成核苷酸类似物的方法以及用被保护的磷酸盐的核苷酸类似物治疗疾病和/或病症如病毒感染,癌症和/或寄生虫病的方法。
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公开(公告)号:US20100240604A1
公开(公告)日:2010-09-23
申请号:US12728068
申请日:2010-03-19
申请人: Leonid Beigelman , Lawrence Blatt , Harri Lonnberg
发明人: Leonid Beigelman , Lawrence Blatt , Harri Lonnberg
IPC分类号: A61K31/7072 , C07H19/056 , A61K31/7056 , C07H19/10 , A61K31/7068 , A61P35/00 , A61P31/12 , A61P35/02 , A61P31/18 , A61P33/00 , A61P31/20 , A61P31/14 , A61P31/22
CPC分类号: C07H19/073 , C07F9/6512 , C07F9/65616 , C07H19/056 , C07H19/10 , C07H19/14 , C07H19/173 , C07H19/20
摘要: Disclosed herein are nucleotide analogs with protected phosphates, methods of synthesizing nucleotide analogs with protected phosphates and methods of treating diseases and/or conditions such as viral infections, cancer, and/or parasitic diseases with the nucleotide analogs with protected phosphates.
摘要翻译: 本文公开了具有被保护的磷酸盐的核苷酸类似物,与被保护的磷酸盐合成核苷酸类似物的方法以及用被保护的磷酸盐的核苷酸类似物治疗疾病和/或病症如病毒感染,癌症和/或寄生虫病的方法。
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公开(公告)号:US20090181921A1
公开(公告)日:2009-07-16
申请号:US12340507
申请日:2008-12-19
申请人: Lawrence Blatt , Leonid Beigelman , Harri Lonnberg
发明人: Lawrence Blatt , Leonid Beigelman , Harri Lonnberg
IPC分类号: A61K31/7064 , C07H19/20 , A61P31/12
CPC分类号: C07H21/02
摘要: Disclosed herein are compounds that activate RNaseL, methods of synthesizing compounds that activate RNaseL and the use of compounds that activate RNaseL for treating and/or ameliorating a disease or a condition, such as a viral infection, cancer and/or parasitic disease.
摘要翻译: 本文公开的是激活RNaseL的化合物,合成活化RNaseL的化合物的方法和使用激活RNaseL的化合物来治疗和/或改善疾病或病症如病毒感染,癌症和/或寄生虫病。
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公开(公告)号:US20120070411A1
公开(公告)日:2012-03-22
申请号:US13236450
申请日:2011-09-19
申请人: Leonid Beigelman , Lawrence Blatt , Guangyi Wang , Vivek Kumar Rajwanshi , Natalia Dyatkina , David Bernard Smith
发明人: Leonid Beigelman , Lawrence Blatt , Guangyi Wang , Vivek Kumar Rajwanshi , Natalia Dyatkina , David Bernard Smith
IPC分类号: A61K38/21 , C07H19/10 , A61K31/7076 , A61K31/708 , A61K31/7068 , A61P31/22 , C12N9/99 , C12N5/071 , A61P31/14 , A61P31/12 , A61P31/20 , C07H19/207 , A61K31/7072
CPC分类号: C07H19/067 , A61K31/7068 , A61K31/7072 , A61K31/7076 , A61K31/708 , A61K38/21 , A61K45/06 , C07H19/167 , Y02A50/465 , A61K2300/00
摘要: Disclosed herein are phosphoroamidate nucleotide analogs, methods of synthesizing phosphoroamidate nucleotide analogs and methods of treating diseases and/or conditions such as viral infections, cancer, and/or parasitic diseases with the phosphoroamidate nucleotide analogs.
摘要翻译: 本文公开了磷酰胺酸核苷酸类似物,合成氨基磷酸酯核苷酸类似物的方法和用氨基磷酸酯核苷酸类似物治疗疾病和/或病症如病毒感染,癌症和/或寄生虫病的方法。
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公开(公告)号:US20100331397A1
公开(公告)日:2010-12-30
申请号:US12822088
申请日:2010-06-23
申请人: Leonid Beigelman , Lawrence Blatt , Harri Lönnberg , Roopa Rai , Guangyi Wang , Thomas Horn , Julian Symons , Antitsa Simitrova Stoycheva , Dean Ng , Jerome Deval
发明人: Leonid Beigelman , Lawrence Blatt , Harri Lönnberg , Roopa Rai , Guangyi Wang , Thomas Horn , Julian Symons , Antitsa Simitrova Stoycheva , Dean Ng , Jerome Deval
IPC分类号: A61K31/7088 , C07H21/00 , A61P31/04 , A61P31/12 , A61P35/00
CPC分类号: A61K31/7088 , C07H21/02 , Y02A50/387 , Y02A50/414 , Y02A50/465
摘要: Disclosed herein are compounds that activate RNaseL, methods of synthesizing compounds that activate RNaseL and the use of compounds that activate RNaseL for treating and/or ameliorating a disease or a condition, such as a viral infection, a bacterial infection, cancer and/or parasitic disease.
摘要翻译: 本文公开的是激活RNaseL的化合物,合成活化RNaseL的化合物的方法和使用激活RNaseL的化合物来治疗和/或改善疾病或病症如病毒感染,细菌感染,癌症和/或寄生虫 疾病。
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公开(公告)号:US20090176732A1
公开(公告)日:2009-07-09
申请号:US12340408
申请日:2008-12-19
申请人: Leonid Beigelman , Lawrence Blatt , Harri Lonnberg
发明人: Leonid Beigelman , Lawrence Blatt , Harri Lonnberg
IPC分类号: A61K31/7056 , C07H19/10 , C07H19/056 , A61K31/7072 , C07C69/02
CPC分类号: C07H19/056 , Y02P20/55
摘要: Disclosed herein are nucleotide analogs with one or more protecting groups, methods of synthesizing nucleotide analogs with one or more protecting groups and methods of treating diseases and/or conditions such as viral infections, cancer, and/or parasitic diseases with the nucleotide analogs with one or more protecting groups.
摘要翻译: 本文公开了具有一个或多个保护基团的核苷酸类似物,与一个或多个保护基团合成核苷酸类似物的方法以及用一种或多种与核苷酸类似物一起治疗疾病和/或病症如病毒感染,癌症和/或寄生虫病的方法 或更多的保护基团。
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