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
    • 5. 发明授权
    • Ballistic fishing lure
    • 弹道钓鱼诱惑
    • US5787633A
    • 1998-08-04
    • US807708
    • 1997-02-28
    • John B. Taylor
    • John B. Taylor
    • A01K85/16
    • A01K85/16
    • A fishing lure includes a tubular main body member having a longitudinal central axis. A cap is sealingly fixed to a rearward end of the main body member. A cylindrical guide tube is connected to the cap. A cylindrical inner tube is telescopingly engaged with the guide tube and extends forwardly out of the guide tube to terminate at a forward end. A cylindrical coil spring within the inner tube extends between the cap and inner tube forward end, which creates a jumping motion for the lure, when extended and then released.
    • 钓鱼诱饵包括具有纵向中心轴线的管状主体构件。 密封地固定在主体部件的后端。 圆柱形导管连接到盖上。 圆柱形内管与引导管可伸缩地接合并向前延伸出导管,以在前端终止。 内管中的圆柱形螺旋弹簧在盖和内管前端之间延伸,当延伸并释放时,该弹簧产生用于诱惑的跳跃运动。
    • 6. 发明授权
    • Pyrroloquinoxalines
    • 吡咯喹喔啉
    • US4151280A
    • 1979-04-24
    • US895264
    • 1978-04-10
    • David A. RowlandsJohn B. Taylor
    • David A. RowlandsJohn B. Taylor
    • A61K31/495A61P37/08C07D235/06C07D487/04
    • C07D235/06C07D487/04Y10S514/826
    • Novel pyrroloquinoxalines of the formula ##STR1## wherein X and Y are individually selected from the group consisting of hydrogen, halogen, alkyl and alkoxy of 1 to 5 carbon atoms and --NO.sub.2, Z is selected from the group consisting of alkyl of 1 to 8 carbon atoms, cycloalkyl of 3 to 8 carbon atoms, alkenyl of 2 to 6 carbon atoms and phenyl and R is selected from the group consisting of hydrogen, alkyl of 1 to 5 carbon atoms, ##STR2## and non-toxic, pharmaceutically acceptable cations, n is an integer from 1 to 6 and R.sub.1 and R.sub.2 are individually alkyl of 1 to 5 carbon atoms and the non-toxic, pharmaceutically acceptable acid addition salts thereof having antiallergic activity and to a novel process for their preparation.
    • 新颖的式(I)的吡咯并喹啉,其中X和Y分别选自氢,卤素,1至5个碳原子的烷基和烷氧基和-NO 2,Z选自1至 3-8个碳原子的环烷基,2-6个碳原子的链烯基和苯基,R选自氢,1至5个碳原子的烷基,无毒的,药物上可接受的 阳离子,n为1〜6的整数,R1和R2分别为1〜5个碳原子的烷基和具有抗过敏活性的无毒的药学上可接受的酸加成盐及其制备方法。
    • 10. 发明授权
    • 1,2-Dihydro-6-phenyl-1H,4H-imidazobenzodiazepin-1-ones
    • 1,2-二氢-6-苯基-1H-,4H-咪唑并二氮杂-1-酮
    • US4185102A
    • 1980-01-22
    • US952494
    • 1978-10-18
    • John B. TaylorDerek R. Harrison
    • John B. TaylorDerek R. Harrison
    • C07D243/20C07F9/6558A61K31/55C07D471/04
    • C07F9/65583C07D243/20Y10S514/923
    • Novel 1,2-dihydro-6-phenyl-1H,4H-imidazo[1,2-a][1,4]-benzodiazepin-1-ones of the formula ##STR1## wherein R is selected from the group consisting of hydrogen, halogen, nitro and trifluoromethyl, R.sub.1 is selected from the group consisting of hydrogen and halogen, R.sub.2 is selected from the group consisting of hydrogen and methyl and R.sub.3 and R.sub.4 are individually selected from the group consisting of hydrogen, alkyl of 1 to 5 carbon atoms, hydroxyalkyl of 1 to 5 carbon atoms, aminoalkyl of 1 to 5 carbon atoms, mono-and di-alkylaminoalkyl with each alkyl having 1 to 5 carbon atoms, cycloalkyl of 3 to 8 carbon atoms and mono and di-nuclear aryl or R.sub.3 and R.sub.4 taken together with the nitrogen atom to which they are attached form a saturated heterocycle which may contain a second heteroatom optionally substituted with at least one member of the group consisting of alkyl of 1 to 5 carbon atoms, hydroxyalkyl of 1 to 5 carbon atoms, dialkylphosphinylalkyl with 1 to 5 carbon atoms in the alkyl groups, cycloalkylalkyl with 3 to 6 carbon atoms in the ring and 1 to 5 alkyl carbon atoms, alkenyl of 2 to 5 carbon atoms, phenyl and nitrogen heterocycles and their non-toxic, pharmaceutically acceptable acid addition salts having sedative, hypnotic, anxiolytic, tranquilizing, anticonvulsive and myorelaxant properties and their preparation.
    • 新的1,2-二氢-6-苯基-1H-,4H-咪唑并[1,2-a] [1,4] - 苯并二氮杂-1,其中R选自 氢,卤素,硝基和三氟甲基,R 1选自氢和卤素,R 2选自氢和甲基,R 3和R 4分别选自氢,1至5的烷基 碳原子数为1〜5的羟基烷基,1〜5个碳原子的氨基烷基,碳原子数1〜5的烷基的单烷基氨基烷基和二烷基氨基烷基,碳原子数为3〜8的环烷基,单 - 和二 - 核芳基或 R3和R4与它们所连接的氮原子一起形成饱和杂环,其可以含有任选被至少一个由1至5个碳原子的烷基取代的第二杂原子,1至5个碳原子的羟烷基 烷基中具有1至5个碳原子的二烷基氧膦基烷基, 在环中具有3至6个碳原子的烷基烷基和1至5个烷基碳原子,2至5个碳原子的烯基,苯基和氮杂环及其无毒的药学上可接受的酸加成盐,其具有镇静,催眠,抗焦虑,镇静, 抗惊厥和脱毛的性质及其制备。