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    • 3. 发明申请
    • 2-Amino-9-[(2-hydroxymethyl) cyclopropylidenemethyl] purines as antiviral agents
    • 2-氨基-9 - [(2-羟甲基)环丙基亚甲基]嘌呤作为抗病毒剂
    • US20070225302A1
    • 2007-09-27
    • US11707248
    • 2007-02-15
    • Jiri ZemlickaJohn DrachXinchao Chen
    • Jiri ZemlickaJohn DrachXinchao Chen
    • A61K31/52
    • C07D473/00C07F9/65616
    • Compounds which are active against viruses have the following Formulas: wherein B is 2-aminopurine-9-yl, which may be unsubstituted or substituted in the 6 position with NHR1, OR2, or SR3; R1 is selected from the group consisting of alkyl, alkenyl, alkynyl, and C4-18 cycloalkyl, any of which may be optionally substituted with one or more members of the group consisting of hydroxy, halo, amino, acyl, cycloalkyl, heterocyclyl and aryl; R2 is selected from the group consisting of C2-18 alkyl, alkenyl, alkynyl, and cycloalkyl, any of which may be branched or unbranched and optionally substituted with one or more members of the group consisting of hydroxy, halo, amino, acyl, cycloalkyl, heterocyclyl, and aryl; and R3 is selected from the group consisting of alkyl, alkenyl, alkynyl, and cycloalkyl, any of which may be branched or unbranched and optionally substituted with one or more members of the group consisting of hydroxy, halo, amino, acyl, cycloalkyl, heterocyclyl and aryl.
    • 对病毒有活性的化合物具有下式:其中B是2-氨基嘌呤-9-基,其可以是未取代的或在6位被NHR 1或OR 2取代, SUB>或SR 3; R 1选自烷基,烯基,炔基和C 4-18环烷基,其中任何一个可以任选地被一个或多个 由羟基,卤素,氨基,酰基,环烷基,杂环基和芳基组成的基团; R 2选自C 2-18烷基,烯基,炔基和环烷基,其中任何一个可以是支链或非支链的,并且任选地被一个或多个 由羟基,卤素,氨基,酰基,环烷基,杂环基和芳基组成的组中的更多成员; 和R 3 3选自烷基,烯基,炔基和环烷基,其中任何一个可以是支链或非支链的,并且任选被一个或多个由羟基,卤代 ,氨基,酰基,环烷基,杂环基和芳基。
    • 4. 发明申请
    • 2-amino-9-[(2-hydroxymethyl) cyclopropylidenemethyl] purine antiviral agents
    • 2-氨基-9 - [(2-羟甲基)环丙基亚甲基]嘌呤抗病毒剂
    • US20050124582A1
    • 2005-06-09
    • US10942314
    • 2004-09-15
    • Jiri ZemlickaJohn DrachXinchao Chen
    • Jiri ZemlickaJohn DrachXinchao Chen
    • C07D473/16A61K31/52A61P31/12A61P31/18A61P31/20A61P31/22C07D473/00C07D473/18C07D473/24C07D473/32C07F9/6561A61K31/675C07D473/12
    • C07D473/00C07F9/65616
    • Compounds which are active against viruses have the following Formulas: wherein B is 2-aminopurine-9-yl, which may be unsubstituted or substituted in the 6 position with NHR1, OR2, or SR3; R1 is selected from the group consisting of alkyl, alkenyl, alkynyl, and C4-18 cycloalkyl, any of which may be optionally substituted with one or more members of the group consisting of hydroxy, halo, amino, acyl, cycloalkyl, heterocyclyl and aryl; R2 is selected from the group consisting of C2-18 alkyl, alkenyl, alkynyl, and cycloalkyl, any of which may be branched or unbranched and optionally substituted with one or more members of the group consisting of hydroxy, halo, amino, acyl, cycloalkyl, heterocyclyl, and aryl; and R3 is selected from the group consisting of alkyl, alkenyl, alkynyl, and cycloalkyl, any of which may be branched or unbranched and optionally substituted with one or more members of the group consisting of hydroxy, halo, amino, acyl, cycloalkyl, heterocyclyl and aryl.
    • 对病毒有活性的化合物具有下式:其中B是2-氨基嘌呤-9-基,其可以是未取代的或在6位被NHR 1或OR 2取代, SUB>或SR 3; R 1选自烷基,烯基,炔基和C 4-18环烷基,其中任何一个可以任选地被一个或多个 由羟基,卤素,氨基,酰基,环烷基,杂环基和芳基组成的基团; R 2选自C 2-18烷基,烯基,炔基和环烷基,其中任何一个可以是支链或非支链的,并且任选地被一个或多个 由羟基,卤素,氨基,酰基,环烷基,杂环基和芳基组成的组中的更多成员; 和R 3 3选自烷基,烯基,炔基和环烷基,其中任何一个可以是支链或非支链的,并且任选被一个或多个由羟基,卤代 ,氨基,酰基,环烷基,杂环基和芳基。
    • 9. 发明授权
    • 2-amino-9-[(2-hydroxymethyl) cyclopropylidenemethyl] purines as antiviral agents
    • 2-氨基-9 - [(2-羟甲基)环丙基亚甲基]嘌呤作为抗病毒剂
    • US09174990B2
    • 2015-11-03
    • US11707248
    • 2007-02-15
    • Jiri ZemlickaJohn C. DrachXinchao Chen
    • Jiri ZemlickaJohn C. DrachXinchao Chen
    • C07D473/00C07F9/6561
    • C07D473/00C07F9/65616
    • Compounds which are active against viruses have the following Formulas: wherein B is 2-aminopurine-9-yl, which may be unsubstituted or substituted in the 6 position with NHR1, OR2, or SR3; R1 is selected from the group consisting of alkyl, alkenyl, alkynyl, and C4-18 cycloalkyl, any of which may be optionally substituted with one or more members of the group consisting of hydroxy, halo, amino, acyl, cycloalkyl, heterocyclyl and aryl; R2 is selected from the group consisting of C2-18 alkyl, alkenyl, alkynyl, and cycloalkyl, any of which may be branched or unbranched and optionally substituted with one or more members of the group consisting of hydroxy, halo, amino, acyl, cycloalkyl, heterocyclyl, and aryl; and R3 is selected from the group consisting of alkyl, alkenyl, alkynyl, and cycloalkyl, any of which may be branched or unbranched and optionally substituted with one or more members of the group consisting of hydroxy, halo, amino, acyl, cycloalkyl, heterocyclyl and aryl.
    • 对病毒有活性的化合物具有下式:其中B是2-氨基嘌呤-9-基,其可以是未被取代的或在6位被NHR1,OR2或SR3取代; R 1选自烷基,烯基,炔基和C 4-18环烷基,其中任何一个可以任选地被羟基,卤素,氨基,酰基,环烷基,杂环基和芳基中的一个或多个成员取代 ; R2选自C2-18烷基,烯基,炔基和环烷基,其中任何一个可以是支链或非支链的,并且任选被一个或多个由羟基,卤素,氨基,酰基,环烷基 ,杂环基和芳基; 并且R 3选自烷基,烯基,炔基和环烷基,其中任何一个可以是支链或非支链的,并且任选被一个或多个由羟基,卤素,氨基,酰基,环烷基,杂环基 和芳基。