LENTIVIRAL VECTORS PSEUDOTYPED WITH A SINDBIS VIRUS ENVELOPE GLYCOPROTEIN
    1.
    发明申请
    LENTIVIRAL VECTORS PSEUDOTYPED WITH A SINDBIS VIRUS ENVELOPE GLYCOPROTEIN 审中-公开
    使用SINDBIS VIRUS ENVELOPE GLYCOPROTEIN的LENIVEIRAL VECTORS PSEUDOTYPED

    公开(公告)号:US20110064763A1

    公开(公告)日:2011-03-17

    申请号:US12842609

    申请日:2010-07-23

    摘要: Lentiviral vector particles comprising a Sindbis virus E2 glycoprotein variant and a lentiviral vector genome comprising a sequence of interest are provided. A lentiviral vector particle comprising: (a) an envelope comprising a Sindbis virus E2 glycoprotein variant; and (b) a lentiviral vector genome comprising a sequence of interest; wherein the E2 glycoprotein variant facilitates infection of dendritic cells by the lentiviral vector particle, and wherein the E2 glycoprotein variant has reduced binding to heparan sulfate compared to a reference sequence (HR strain).

    摘要翻译: 提供包含辛德毕斯病毒E2糖蛋白变体和包含感兴趣序列的慢病毒载体基因组的慢病毒载体颗粒。 一种慢病毒载体颗粒,包括:(a)包含辛德毕斯病毒E2糖蛋白变体的包膜; 和(b)包含感兴趣序列的慢病毒载体基因组; 其中E2糖蛋白变体便于慢病毒载体颗粒感染树突状细胞,并且其中E2糖蛋白变体与参考序列(HR应变)相比具有减少的与硫酸乙酰肝素的结合。

    Use of 9, 10-anthraquinone compounds
    8.
    发明授权
    Use of 9, 10-anthraquinone compounds 有权
    使用9,10-蒽醌化合物

    公开(公告)号:US08895725B2

    公开(公告)日:2014-11-25

    申请号:US13130130

    申请日:2009-11-23

    摘要: Use of 9,10-anthraquinone compounds of formula (I) or pharmaceutical salts thereof or plant extracts containing said compounds in the preparation of anti-HCV medicaments is disclosed, in which Y1 are Y2 are independently hydrogen, hydroxyl or groups of formula (II); and R1, R2, R3, R4, R5 and R6 are independently hydrogen, hydroxyl, carboxyl, cyano group, nitro group, groups of formula (III) or groups selected from those substituted or unsubstituted groups: amino, C1-C6 aliphatic hydrocarbon, C3-C7 cyclic aliphatic hydrocarbon, C1-C6 alkoxy, C2-C7 carbalkoxy, C1-C4 acyloxy, C6-C20 aryl, or 5 to 7 members heterocyclic or benzoheterocyclic thereof; or R5 and R6 form the group of formula (IV). The compounds of present invention are cheap, safe and effective because that they mostly come from traditional Chinese medicines and have better anti-HCV effects and lighter side effects.

    摘要翻译: 公开了在制备抗HCV药物中使用式(I)的9,10-蒽醌化合物或其药用盐或含有所述化合物的植物提取物,其中Y 1为Y 2独立地为氢,羟基或式(II ); 并且R 1,R 2,R 3,R 4,R 5和R 6独立地是氢,羟基,羧基,氰基,硝基,式(III)的基团或选自那些取代或未取代的基团的基团:氨基,C 1 -C 6脂族烃, C 3 -C 7环脂族烃,C 1 -C 6烷氧基,C 2 -C 7烷酰氧基,C 1 -C 4酰氧基,C 6 -C 20芳基或5至7元杂环或苯并杂环; 或R 5和R 6形成式(IV)的基团。 本发明化合物廉价,安全有效,因为它们主要来自中药,抗HCV效果更好,副作用更轻。

    USE OF 9, 10-ANTHRAQUINONE COMPOUNDS
    10.
    发明申请
    USE OF 9, 10-ANTHRAQUINONE COMPOUNDS 有权
    使用9,10-蒽醌化合物

    公开(公告)号:US20110224414A1

    公开(公告)日:2011-09-15

    申请号:US13130130

    申请日:2009-11-23

    摘要: Use of 9,10-anthraquinone compounds of formula (I) or pharmaceutical salts thereof or plant extracts containing said compounds in the preparation of anti-HCV medicaments is disclosed, in which Y1 are Y2 are independently hydrogen, hydroxyl or groups of formula (II); and R1, R2, R3, R4, R5 and R6 are independently hydrogen, hydroxyl, carboxyl, cyano group, nitro group, groups of formula (III) or groups selected from those substituted or unsubstituted groups: amino, C1-C6 aliphatic hydrocarbon, C3-C7 cyclic aliphatic hydrocarbon, C1-C6 alkoxy, C2-C7 carbalkoxy, C1-C4 acyloxy, C6-C20 aryl, or 5 to 7 members heterocyclic or benzoheterocyclic thereof; or R5 and R6 form the group of formula (IV). The compounds of present invention are cheap, safe and effective, because that they mostly conic from traditional Chinese medicines and have better anti-HCV effects and lighter side effects.

    摘要翻译: 公开了在制备抗HCV药物中使用式(I)的9,10-蒽醌化合物或其药用盐或含有所述化合物的植物提取物,其中Y 1为Y 2独立地为氢,羟基或式(II ); 并且R 1,R 2,R 3,R 4,R 5和R 6独立地是氢,羟基,羧基,氰基,硝基,式(III)的基团或选自那些取代或未取代的基团的基团:氨基,C 1 -C 6脂族烃, C 3 -C 7环脂族烃,C 1 -C 6烷氧基,C 2 -C 7烷酰氧基,C 1 -C 4酰氧基,C 6 -C 20芳基或5至7元杂环或苯并杂环; 或R 5和R 6形成式(IV)的基团。 本发明化合物廉价,安全有效,因为它们大多是中药复方,抗HCV效果更好,副作用更轻。