会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 2. 发明申请
    • ANTIVIRAL AGENTS
    • 抗病毒剂
    • WO1995022330A1
    • 1995-08-24
    • PCT/AU1995000076
    • 1995-02-17
    • COMMONWEALTH SCIENTIFIC AND INDUSTRIAL RESEARCH ORGANISATIONMARCUCCIO, Sebastian, MarioHOLAN, GeorgeCOGHLAN, Phillip, AlbertJARVIS, Karen, ElizabethROBERTSON, Alan, DuncanTURNER, Kathleen, AnneWEIGOLD, Helmut
    • COMMONWEALTH SCIENTIFIC AND INDUSTRIAL RESEARCH ORGANISATION
    • A61K31/52
    • C07D473/00A61K31/52C07F9/65616C07F9/65742
    • The invention relates to a method for the treatment and/or prophylaxis of a Hepadnaviridae associated infection which comprises administration of an effective amount of a compound of Formula (1), wherein R1 is hydrogen, halogen, hydroxy, azide, optionally substituted alkyl, optionally substituted alkoxy, optionally substituted aryloxy, mercapto, optionally substituted alkylthio, optionally substituted amino, optionally substituted hydrazino or optionally substituted hydroxylamino; R2 is hydrogen, halogen, hydroxy, azide, optionally substituted alkoxy, optionally substituted aryloxy, mercapto, optionally substituted alkylthio or optionally substituted amino; R3 and R3' are the same or different and selected from hydrogen, optionally substituted alkyl, halogen, hydroxy, azide, optionally substituted alkoxy, optionally substituted aryloxy, mercapto, optionally substituted thio and optionally substituted amino; or R3 and R3' together form =O, =S, =NOH or =NOR, wherein R is optionally substituted alkyl; and R4, R5 and R6 are the same or different and selected from optionally substituted alkyl, optionally substituted aralkyl, halogen, hydroxy, azide, optionally substituted alkoxy, optionally substituted aryloxy, mercapto, optionally substituted alkylthio, optionally substituted amino, optionally substituted acyl, optionally substituted ester, cyano, carboxy and mono-, di- or tri- phosphate; two of R4, R5 and R6 are joined together to form a cyclic group; or R4, R5 and R6 are joined together to form a cyclic ortho ester group, salts thereof, pharmaceutically acceptable derivatives thereof, pro-drugs thereof, tautomers thereof and/or isomers thereof to a subject requiring said treatment and/or prophylaxis. The invention also relates to novel compounds of Formula (1), processes for their preparation and pharmaceutical or veterinary compositions containing them.
    • 本发明涉及一种治疗和/或预防肝炎病毒科相关感染的方法,其包括给予有效量的式(1)化合物,其中R 1是氢,卤素,羟基,叠氮化物,任选取代的烷基,任选地 取代的烷氧基,任选取代的芳氧基,巯基,任选取代的烷硫基,任选取代的氨基,任选取代的肼基或任选取代的羟基氨基; R 2是氢,卤素,羟基,叠氮化物,任选取代的烷氧基,任选取代的芳氧基,巯基,任选取代的烷硫基或任选取代的氨基; R 3和R 3'相同或不同,选自氢,任选取代的烷基,卤素,羟基,叠氮化物,任选取代的烷氧基,任选取代的芳氧基,巯基,任选取代的硫代和任选取代的氨基; 或R3和R3'一起形成= O,= S,= NOH或= NOR,其中R是任选取代的烷基; 卤素,羟基,叠氮化物,任选取代的烷氧基,任选取代的芳氧基,巯基,任选取代的烷硫基,任选取代的氨基,任选取代的酰基,任选取代的烷基, 任选取代的酯,氰基,羧基和一,二或三磷酸酯; R4,R5和R6中的两个连接在一起形成环状基团; 或R 4,R 5和R 6连接在一起以形成环状原酸酯基团,其盐,其药学上可接受的衍生物,其前药,其互变异构体和/或其异构体,用于需要所述治疗和/或预防的对象。 本发明还涉及式(1)的新化合物,其制备方法和含有它们的药物或兽药组合物。
    • 6. 发明申请
    • ANTIVIRAL AGENTS
    • 抗病毒剂
    • WO1994012192A1
    • 1994-06-09
    • PCT/AU1993000606
    • 1993-11-29
    • COMMONWEALTH SCIENTIFIC AND INDUSTRIAL RESEARCH ...WEIGOLD, HelmutBARTHOLOMEUSZ, Angeline, IngridMARCUCCIO, Sebastian, MarioHOLAN, George
    • COMMONWEALTH SCIENTIFIC AND INDUSTRIAL RESEARCH ...
    • A61K33/24
    • A61K33/24C01G41/006C01P2002/82C01P2006/80C01P2006/82Y02A50/385Y02A50/387Y02A50/389
    • Heteropolytungstates having anti-flaviviral activity having the general formulae (I) to (VII): (I) An[XW12O40] wherein X is selected from P , Si , Ge , Co , Co , Zn , Cu , B , H 2, Al , Fe , V , Ga , Mn , C . (II) An[X2W18O62] wherein X is P ; (III) An[XW11O39] wherein X is selected from P , Si , Ge , B , Al , Ga , Fe , Co ; (IV) An[XW9O34] wherein X is selected from P , Si , Ge ; (V) An[X2W17-mMmO61] wherein X is P , M is Mo , and m is 0, 1, 2, 4, or 5; (VI) An[X2W15-mMmO56] wherein X is P , M is V or Mo , and m is 0 or 1; (VII) An[XM2W9O39] wherein X is P, and M is Zr; and wherein in each of the general formulae (I) to (VII), A is a cation, and n is the number of cations necessary for electrical neutrality of the molecule; or dimers, hydrates or pharmaceutically acceptable derivatives thereof. Pharmaceutical compositions and methods for the treatment or prophylaxis of a flaviviral-associated infection which involve the use of these compounds are also disclosed.
    • 具有通式(I)至(VII)的抗黄病毒活性的异多钨酸盐:(I)An [XW12O40]其中X选自P v,Si IV,Ge IV,Co II, Co III,Zn II,Cu II,B III,H 2,Al III,Fe III,V V,Ga III,Mn IV, ,C 。 (II)An [X2W18O62]其中X为P;; (III)An [XW11O39]其中X选自PⅤ,Ⅳ,Ⅵ,Ⅵ,Ⅳ,Ⅳ,Ⅵa,Ⅳ,Ⅲ,Ⅳ >; (IV)[XW9O34]其中X选自PⅤ,SiⅣ,ⅣⅣ; (Ⅴ)An [X2W17-mMmO61]其中X为PⅤ,M为MoⅥ,m为0,1,2,4或5; (Ⅵ)[X2W15-mMmO56]其中X为PⅤ,M为VⅤ或MoⅥ,m为0或1; (Ⅶ)[XM2W9O39]其中X为P,M为Zr; 并且其中在每个通式(I)至(VII)中,A是阳离子,n是分子的电中性所必需的阳离子数; 或二聚体,水合物或其药学上可接受的衍生物。 还公开了用于治疗或预防涉及使用这些化合物的黄病毒相关感染的药物组合物和方法。