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    • 45. 发明申请
    • Method of forming molded resin semiconductor device
    • 成型树脂半导体器件的形成方法
    • US20070134845A1
    • 2007-06-14
    • US11702550
    • 2007-02-06
    • Tomoki Kato
    • Tomoki Kato
    • H01L21/00
    • H01L21/568H01L23/3107H01L2924/0002H01L2924/00
    • A semiconductor chip and a wiring strip are placed on a flat side of a base sheet. The semiconductor chip has parallel first and second surfaces. Electrodes are connected to the first surface. The electrodes all terminate in the plane of the flat side of the base sheet and adhesively connected to the flat side of the base sheet. The wiring strip has one end portion connected to the second surface of the semiconductor chip and the opposite end portion terminating in the plane of the flat side of the base sheet and adhesively connected to the flat side of the base sheet. A mold resin fills gaps between the semiconductor chip, the wiring strip, and the base sheet to lock the semiconductor chip and the wiring strip. The base sheet is removed.
    • 将半导体芯片和布线条放置在基片的平坦侧上。 半导体芯片具有平行的第一和第二表面。 电极连接到第一表面。 电极全部终止于基片的平坦面的平面中,并且粘合地连接到基片的平坦侧。 布线条具有连接到半导体芯片的第二表面的一个端部和终止于基片的平坦侧的平面中的相对端部,并且粘合地连接到基片的平坦侧。 模具树脂填充半导体芯片,布线条和基片之间的间隙,以锁定半导体芯片和布线条。 去除基片。
    • 47. 发明授权
    • Sulfonylbenzene compounds as anti-inflammatory/analgesic agents
    • 磺酰苯化合物作为抗炎/止痛剂
    • US06949536B2
    • 2005-09-27
    • US10771861
    • 2004-02-03
    • Kazuo AndoTomoki KatoAkiyoshi KawaiTomomi Nonomura
    • Kazuo AndoTomoki KatoAkiyoshi KawaiTomomi Nonomura
    • A61K31/33A61K31/4025A61K31/422A61K31/425A61K31/427A61K31/454C07D233/00C07D277/00C07D333/00
    • A61K31/422A61K31/427A61K31/454C07C311/39C07C317/36C07D207/325C07D207/333C07D401/10C07D403/10C07D405/10C07D409/10C07D413/10C07D417/10
    • This invention provides a compound of the formula: or its pharmaceutically acceptable salt thereof, wherein A is partially unsaturated or unsaturated five membered heterocyclic, or partially unsaturated or unsaturated five membered carbocyclic, wherein the 4-(sulfonyl)phenyl and the 4-substituted phenyl in the formula (I) are attached to ring atoms of Ring A, which are adjacent to each other; R1 is optionally substituted aryl or heteroaryl, with the proviso that when A is pyrazole, R1 is heteroaryl; R2 is C1-4 alkyl; halo-substituted C1-4 alkyl, C1-4 alkylamino, C1-4 dialkylamino or amino; R3, R4 and R5 are independently hydrogen, halo, C1-4 alkyl, halo-substituted C1-4 alkyl or the like; or two of R3, R4 and R5 are taken together with atoms to which they are attached and form a 4-7 membered ring. R6 and R7 are independently hydrogen, halo, C1-4 alkyl, halo-substituted C1-4 alkyl, C1-4 alkoxy, C1-4 alkylthio, C1-4 alkylamino or N,N-di C1-4 alkylamino; and m and n are independently 1, 2, 3 or 4. This invention also provides a pharmaceutical composition useful for the treatment of a medical condition in which prostaglandins are implicated as pathogens.
    • 本发明提供下式的化合物或其药学上可接受的盐,其中A是部分不饱和或不饱和的五元杂环或部分不饱和或不饱和的五元碳环,其中4-(磺酰基)苯基和4-取代的苯基 在式(I)中,与环A相邻的环原子相连; R 1是任选取代的芳基或杂芳基,条件是当A是吡唑时,R 1是杂芳基; R 2是C 1-4烷基; 卤素取代的C 1-4烷基,C 1-4烷基氨基,C 1-4烷基氨基或氨基; R 4,R 4和R 5独立地是氢,卤素,C 1-4烷基,卤代 - 取代的C 1-4烷基等; 或者R 3,R 4和R 5中的两个与它们所连接的原子一起形成4-7元环 。 R 6和R 7独立地是氢,卤素,C 1-4烷基,卤素取代的C 1-4烷基, C 1-4烷基,C 1-4烷氧基,C 1-4烷硫基,C 1-4烷基氨基或N,N-二C < 烷基氨基; m和n分别为1,2,3或4.本发明还提供了一种药物组合物,其用于治疗前列腺素涉及病原体的医疗状况。