发明名称 |
Combination therapy with interferon and andrographolides for Multiple Sclerosis |
摘要 |
The effectiveness of interferon for treating multiple sclerosis and other demyelinating diseases is synergistically potentiated by concomitant administration of a compound of Formula (I): wherein R1 is H, alkyl or OH, R2 is hydroxyalkyl or alkyl-O-L1, R3 is H or OH, X is C(═CH2), CH(OH), or spirooxirane-2, Z is CH2CH(OH) or C(=0), and R4 is an optionally substituted L2-alkyl or L2-alkenyl, wherein L2 is an optionally substituted 3-furanyl or 3-fur-3-enyl moiety.; |
申请公布号 |
US9060994(B2) |
申请公布日期 |
2015.06.23 |
申请号 |
US201213984124 |
申请日期 |
2012.12.19 |
申请人 |
Inno Biosciences, S.p.A. |
发明人 |
Hancke Orozco Juan L;Burgos Rafael |
分类号 |
A61K31/341;A61K38/21;A61P37/00 |
主分类号 |
A61K31/341 |
代理机构 |
Pharmaceutical Patent Atty's LLC |
代理人 |
Pharmaceutical Patent Atty's LLC |
主权项 |
1. A method for treating multiple sclerosis in a human patient by providing beta interferon to said a human patient, the improvement comprising administering to said human patient a compound of Formula I: wherein
R1 is selected from the group consisting of hydrogen, alkyl or hydroxyl,R2 is selected from the group consisting of hydroxyalkyl or alkyl-O-L1, wherein L1 is a carbohydrate moiety,R3 is selected from the group consisting of hydrogen or hydroxyl,X is selected from the group consisting of C(═CH2), CH(OH), or a spirooxirane-2 moiety,Z is selected from the group consisting of CH2, CH(OH) or C(═O), andR4 is selected from the group consisting of an optionally substituted L2-alkyl or L2-alkenyl, wherein L2 is an optionally substituted 3-furanyl or 3-fur-3-enyl moiety, or a pharmaceutically acceptable salt, ester, ether or prodrug thereof. |
地址 |
Santiago CL |