4,7-benzofurandione derivatives
    31.
    发明授权
    4,7-benzofurandione derivatives 失效
    4,7-苯并呋喃二酮衍生物

    公开(公告)号:US4968821A

    公开(公告)日:1990-11-06

    申请号:US217264

    申请日:1988-07-11

    摘要: 4,7-Benzofurandione derivatives of Formula I, pharmaceutical compositions, and methods of treatment are disclosed. These compounds are useful as inhibitors of mammalian leukotriene biosynthesis. As such, these compounds are useful therapeutic agents for treating allergic conditions, asthma, cardiovascular disorders, inflammation, psoriasis and allergic conjunctivitis. The compounds are also useful as analgesics and as cytoprotective agents. Also disclosed are novel intermediates useful for the preparation of the 4,7-benzofurandiones of this invention. ##STR1##

    摘要翻译: 公开了式I的4,7-苯并呋喃二酮衍生物,药物组合物和治疗方法。 这些化合物可用作哺乳动物白细胞三烯生物合成的抑制剂。 因此,这些化合物是用于治疗过敏性疾病,哮喘,心血管疾病,炎症,牛皮癣和过敏性结膜炎的有用治疗剂。 该化合物也可用作止痛剂和细胞保护剂。 还公开了可用于制备本发明的4,7-苯并呋喃二酸的新型中间体。

    Nucleoside and nucleotide analogues with quaternary carbon centers and methods of use
    34.
    发明授权
    Nucleoside and nucleotide analogues with quaternary carbon centers and methods of use 有权
    具有季碳中心的核苷和核苷酸类似物及其使用方法

    公开(公告)号:US08361988B2

    公开(公告)日:2013-01-29

    申请号:US12523193

    申请日:2008-01-17

    申请人: Yvan Guindon

    发明人: Yvan Guindon

    摘要: The present invention comprises compounds useful as antiviral or antitumor agents. The compounds comprise nucleotide analogues that comprise tetrahydrofuranyl or tetrahydrothienyl moeities with quaternary centers at the 3′ position. The nucleotide analogues can be used to inhibit cancer or viruses. Accordingly, the compounds of the present invention are useful for treating, preventing, and/or inhibiting diseases or conditions associated with cancers and viruses. Thus, the present invention also comprising pharmaceutical formulations comprising the compounds and methods of using the compounds and formulations to inhibit viruses or tumors and treat, prevent, or inhibit the foregoing diseases.

    摘要翻译: 本发明包括可用作抗病毒剂或抗肿瘤剂的化合物。 这些化合物包含核苷酸类似物,其包含在3'位上具有四元中心的四氢呋喃基或四氢噻吩基。 核苷酸类似物可用于抑制癌症或病毒。 因此,本发明的化合物可用于治疗,预防和/或抑制与癌症和病毒相关的疾病或病症。 因此,本发明还包括包含该化合物的药物制剂和使用该化合物和制剂抑制病毒或肿瘤并治疗,预防或抑制前述疾病的方法。

    Treating herpes Viral infections
    35.
    发明授权
    Treating herpes Viral infections 失效
    治疗疱疹病毒感染

    公开(公告)号:US5242946A

    公开(公告)日:1993-09-07

    申请号:US830019

    申请日:1992-01-31

    申请人: Yvan Guindon

    发明人: Yvan Guindon

    IPC分类号: A61K31/22

    CPC分类号: A61K31/22 Y10S514/934

    摘要: A group of known naphthalene derivatives have been found to be useful for preventing or relieving herpes viral infections.

    摘要翻译: 已经发现一组已知的萘衍生物可用于预防或缓解疱疹病毒感染。

    4,7-diacetoxy-2-(4-methoxybenzyl)-3,5,6-trimethylbenzofuran
    36.
    发明授权
    4,7-diacetoxy-2-(4-methoxybenzyl)-3,5,6-trimethylbenzofuran 失效
    4,7-二乙酰氧基-2-(4-甲氧基苄基)-3,5,6-三甲基苯并呋喃

    公开(公告)号:US4800228A

    公开(公告)日:1989-01-24

    申请号:US064269

    申请日:1987-06-18

    IPC分类号: C07D307/86 C07D407/06

    CPC分类号: C07D407/06 C07D307/86

    摘要: 4,7-Diacyloxybenzofuran derivatives of Formula I, are disclosed. These compounds are useful as inhibitors of mammalian leukotriene biosynthesis. As such, these compounds are useful therapeutic agents for treating allergic conditions, asthma, cardiovascular disorders, inflammation, psoriasis and allergic conjunctivitis. The compounds are also useful as analgesics and as cytoprotective agents. ##STR1##

    摘要翻译: 公开了式I的4,7-二酰氧基苯并呋喃衍生物。 这些化合物可用作哺乳动物白细胞三烯生物合成的抑制剂。 因此,这些化合物是用于治疗过敏性疾病,哮喘,心血管疾病,炎症,牛皮癣和过敏性结膜炎的有用治疗剂。 该化合物也可用作止痛剂和细胞保护剂。

    NUCLEOTIDE ANALOGUES WITH QUATERNARY CARBON STEREOGENIC CENTERS AND METHODS OF USE
    39.
    发明申请
    NUCLEOTIDE ANALOGUES WITH QUATERNARY CARBON STEREOGENIC CENTERS AND METHODS OF USE 有权
    具有季碳异体中心的核苷类似物及其使用方法

    公开(公告)号:US20110092451A1

    公开(公告)日:2011-04-21

    申请号:US12933291

    申请日:2009-03-18

    申请人: Yvan Guindon

    发明人: Yvan Guindon

    摘要: The present invention comprises compounds useful as antiviral or antitumor agents. The compounds comprise nucleotide analogues that comprise tetrahydrofuranyl or tetrahydrothienyl moeities with quaternary centers at the 3′ position. The nucleotide analogues can be used to inhibit cancer or viruses. Accordingly, the compounds of the present invention are useful for treating, preventing, and/or inhibiting diseases or conditions associated with cancers and viruses. Thus, the present invention also comprising pharmaceutical formulations comprising the compounds and methods of using the compounds and formulations to inhibit viruses or tumors and treat, prevent, or inhibit the foregoing diseases.

    摘要翻译: 本发明包括可用作抗病毒剂或抗肿瘤剂的化合物。 这些化合物包含核苷酸类似物,其包含在3'位上具有四元中心的四氢呋喃基或四氢噻吩基。 核苷酸类似物可用于抑制癌症或病毒。 因此,本发明的化合物可用于治疗,预防和/或抑制与癌症和病毒相关的疾病或病症。 因此,本发明还包括包含该化合物的药物制剂和使用该化合物和制剂抑制病毒或肿瘤并治疗,预防或抑制前述疾病的方法。

    Nucleoside and Nucleotide Analogues with Quaternary Carbon Centers and Methods of Use
    40.
    发明申请
    Nucleoside and Nucleotide Analogues with Quaternary Carbon Centers and Methods of Use 有权
    具有第四纪碳中心的核苷和核苷酸类似物和使用方法

    公开(公告)号:US20100093737A1

    公开(公告)日:2010-04-15

    申请号:US12523193

    申请日:2008-01-17

    申请人: Yvan Guindon

    发明人: Yvan Guindon

    摘要: The present invention comprises compounds useful as antiviral or antitumor agents. The compounds comprise nucleotide analogues that comprise tetrahydrofuranyl or tetrahydrothienyl moeities with quaternary centers at the 3′ position. The nucleotide analogues can be used to inhibit cancer or viruses. Accordingly, the compounds of the present invention are useful for treating, preventing, and/or inhibiting diseases or conditions associated with cancers and viruses. Thus, the present invention also comprising pharmaceutical formulations comprising the compounds and methods of using the compounds and formulations to inhibit viruses or tumors and treat, prevent, or inhibit the foregoing diseases.

    摘要翻译: 本发明包括可用作抗病毒剂或抗肿瘤剂的化合物。 这些化合物包含核苷酸类似物,其包含在3'位上具有四元中心的四氢呋喃基或四氢噻吩基。 核苷酸类似物可以用于抑制癌症或病毒。 因此,本发明的化合物可用于治疗,预防和/或抑制与癌症和病毒相关的疾病或病症。 因此,本发明还包括包含该化合物的药物制剂和使用该化合物和制剂抑制病毒或肿瘤并治疗,预防或抑制前述疾病的方法。