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    • 41. 发明授权
    • Authentication system managing method
    • 认证系统管理方法
    • US08079061B2
    • 2011-12-13
    • US11949159
    • 2007-12-03
    • Kazuhiko TaniguchiYoshiaki IsobeNariyasu HamadaHiroyuki Shimizu
    • Kazuhiko TaniguchiYoshiaki IsobeNariyasu HamadaHiroyuki Shimizu
    • G06F7/04G06F17/30
    • G07C9/00166G06F21/32G06K9/00926G06K9/00993G07C9/00158
    • Inputted information (such as biometric information) is compared to template information (including correlation or authentication) and the result is recorded as log information. According to log information for each of the types of the inputted information (such as information specifying the user who has inputted it and the template), analysis is executed for the inputted information for each of the types. This analysis includes the following aspects. That is, the following states are detected and an alarm is outputted for the accuracy of the corresponding type: when the ratio of negative comparison results (correlation failures) not smaller than a predetermined value is detected within a predetermined period of time; and when a negative result is detected within a predetermined time before an affirmative comparison result is obtained.
    • 将输入信息(如生物特征信息)与模板信息(包括相关或认证)进行比较,并将结果记录为日志信息。 根据输入信息的每种类型(诸如指定输入的用户的信息和模板)的日志信息,针对每种类型的输入信息执行分析。 该分析包括以下几个方面。 也就是说,检测到以下状态并为相应类型的精度输出报警:当在预定时间段内检测到不小于预定值的负比较结果(相关故障)的比率时; 并且当在获得肯定比较结果之前的预定时间内检测到否定结果时。
    • 43. 发明授权
    • Adenine compound and use thereof
    • 腺嘌呤化合物及其用途
    • US07754728B2
    • 2010-07-13
    • US10528343
    • 2003-09-26
    • Yoshiaki IsobeHaruo TakakuHaruhisa OgitaMasanori TobeAyumu KurimotoTetsuhiro OginoHitoshi Fujita
    • Yoshiaki IsobeHaruo TakakuHaruhisa OgitaMasanori TobeAyumu KurimotoTetsuhiro OginoHitoshi Fujita
    • C07D473/18C07D473/16A61K31/522A61P11/06A61P37/08
    • A61K31/5377A61K31/522A61K31/55
    • A drug for topically administration which is effective as an antiallergic agent. The drug for topically administration contains as an active ingredient an adenine compound represented by the general formula (1): [wherein ring A represents a 6 to 10 membered, mono or bicyclic, aromatic hydrocarbon or a 5 to 10 membered, mono or bicyclic, aromatic heterocycle containing one to three heteroatoms selected among 0 to 2 nitrogen atoms, 0 or 1 oxygen atom, and 0 or 1 sulfur atom; n is an integer of 0 to 2; m is an integer of 0 to 2; R represents halogeno, (un)substituted alkyl, etc.; X1 represents oxygen, sulfur, NR1 (R1 represents hydrogen or alkyl), or a single bond; Y1 represents a single bond, alkylene, etc.; Y2 represents a single bond, alkylene, etc.; Z represents alkylene; and at least one of Q1 and Q2 represents —COOR10 (wherein R10 represents (un)substituted alkyl, etc.), etc.] or a pharmaceutically acceptable salt of the compound.
    • 用作局部给药的药物,其作为抗过敏剂有效。 用于局部给药的药物含有作为活性成分的由通式(1)表示的腺嘌呤化合物:[其中环A表示6至10元,单或双环,芳族烃或5至10元,单或双环, 含有1至3个选自0至2个氮原子,0或1个氧原子和0或1个硫原子的杂原子的芳族杂环; n为0〜2的整数, m为0〜2的整数; R代表卤代,(取代)烷基等; X1代表氧,硫,NR1(R1代表氢或烷基)或单键; Y1表示单键,亚烷基等; Y2表示单键,亚烷基等; Z表示亚烷基; 并且Q1和Q2中的至少一个表示-COOR 10(其中R 10表示(un)取代的烷基等)等)或该化合物的药学上可接受的盐。
    • 46. 发明授权
    • Hydroquinone derivative and pharmaceutical use thereof
    • 对苯二酚衍生物及其药物用途
    • US5877318A
    • 1999-03-02
    • US113826
    • 1998-07-10
    • Yoshiaki IsobeYuso GotoMasanori TobeOsamu Takahashi
    • Yoshiaki IsobeYuso GotoMasanori TobeOsamu Takahashi
    • C07D239/54C07D239/545C07D405/12
    • C07D239/545C07D405/12
    • Disclosed is a hydroquinone derivative or a pharmaceutically acceptable salt thereof, the hydroquinone derivative being represented by formula (I): ##STR1## wherein R.sup.1 is a phenyl group which is unsubstituted or substituted with a substituent or substituents each independently selected from the group consisting of a halogen atom, a C1-4 alkyl group and a C1-4 alkoxy group;R.sup.2 is a hydrogen atom or a C1-4 alkyl group;each of R.sup.3 and R.sup.4 is independently a hydrogen atom or a C1-4 alkyl group;R.sup.5 is a hydrogen atom or a C1-4 alkyl group;each of R.sup.6, R.sup.7 and R.sup.8 is independently a hydrogen atom or a C1-4 alkyl group;P is a hydroxyl group;Q is a hydroxyl group, a C1-4 alkoxy group, a C1-18 acyloxy group or an oxo group;P may form together with Q an ether bond;R is a hydroxyl group, a C1-4 alkoxy group, a C1-18 acyloxy group or an oxo group, provided that when one of said Q and said R is an oxo group, the other is also an oxo group;X is a single bond, an --NR.sup.10 -- group or a --CH.sub.2 --NR.sup.10 -- group in which R.sup.10 is a hydrogen atom or a C1-4 alkyl group;Y is a methylene group or a carbonyl group; anddotted bonds in a six membered ring represent that said six membered ring has the maximum number of double bonds.
    • 公开了氢醌衍生物或其药学上可接受的盐,氢醌衍生物由式(I)表示:未取代或被各自独立地选自卤素原子,C 1-4烷基的取代基或取代基取代 和C 1-4烷氧基; R2是氢原子或C1-4烷基; R 3和R 4各自独立地为氢原子或C 1-4烷基; R5是氢原子或C1-4烷基; R6,R7和R8各自独立地为氢原子或C1-4烷基; P是羟基; Q是羟基,C 1-4烷氧基,C 1-18酰氧基或氧代基; P可与Q形成醚键; R是羟基,C 1-4烷氧基,C 1-18酰氧基或氧代基,条件是当所述Q和所述R中的一个是氧代基时,另一个也是氧代基; X是单键,-NR 10 - 基或-CH 2 -NR 10 - 基,其中R 10是氢原子或C 1-4烷基; Y是亚甲基或羰基; 六元环中的点状键表示所述六元环具有最大数量的双键。