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    • 4. 发明申请
    • Window assembly-producing method and window plate
    • 窗组装生产方法和窗板
    • US20060157890A1
    • 2006-07-20
    • US10563374
    • 2004-06-14
    • Katsuyuki AmanoAkihiro SuzukiTatsuya TamuraHisao Kondo
    • Katsuyuki AmanoAkihiro SuzukiTatsuya TamuraHisao Kondo
    • B29C45/14
    • B29C45/14377B29C45/14311B29C45/14434B29C45/14778B29C2045/0093B29K2709/08B29L2031/7782B60J1/004
    • An adhesive agent is uniformly applied to a back surface of a window pane, the application made to an area where a covering member is planned to be adhered and to an area where a positioning fixture and a holding portion are planned to be adhered, the application is also made continuously such that adhesive agent layers of both planned adhesion areas being continuous with an adhesive agent continuous area in between. After that, the window pane and the positioning fixture are set in an injection mold and a polymer material is injected in the mold. This results that the covering member and the holding portion are formed into a shape where they are connected by a connection portion for material flow, which connection portion is formed at a position other than the adhesive agent continuous area. The forming results that the covering member and the holding portion are adhered and fixed to the back surface of the window pane with the adhesive agent layers in between. After the forming process above, the connection portion for material flow is removed.
    • 将粘合剂均匀地施加到窗玻璃的后表面上,将涂布物制成覆盖部件被计划粘附的区域和计划粘贴定位夹具和保持部分的区域,该应用 也使得两个计划的粘合区域的粘合剂层与其间的粘合剂连续区域连续地连续地制成。 之后,将窗玻璃和定位夹具放置在注射模具中,并将聚合物材料注入模具中。 因此,覆盖部件和保持部形成为通过用于材料流动的连接部连接的形状,该连接部形成在粘接剂连续区域以外的位置。 形成结果是,覆盖构件和保持部分粘合并固定到窗玻璃的后表面,其间具有粘合剂层。 在上述成形过程之后,物料流的连接部分被去除。
    • 8. 发明授权
    • Indolopyrrolocarbazole derivatives and antitumor agents
    • 吲哚吡咯咔唑衍生物和抗肿瘤剂
    • US06703373B1
    • 2004-03-09
    • US10070825
    • 2002-03-11
    • Katsuhisa KojiriHisao KondoHiroharu ArakawaMitsuru OhkuboHiroyuki Suda
    • Katsuhisa KojiriHisao KondoHiroharu ArakawaMitsuru OhkuboHiroyuki Suda
    • A01N4304
    • C07H19/00C07H15/00C07H19/22
    • A compound represented by the formula or a pharmaceutically acceptable salt thereof wherein R represents an unsubstituted pyridyl, furyl or thienyl group, or a pyridyl, furyl or thienyl group each of which has one or more substituents selected from the group consisting of a hydroxyl group, a lower alkoxy group, a hydroxy lower alkyl group and a hydroxy lower alkenyl group except that when the pyridyl, furyl or thienyl group has a lower alkoxy group as a substituent, each of which simultaneously has another substituent selected from the group consisting of a hydroxyl group, a lower alkoxy group, a hydroxy lower alkyl group and a hydroxy lower alkenyl group, m represents an integer of 1 to 3, and G represents a &bgr;-D-glucopyranosyl group, and the positions of substitution of the hydroxyl groups on the indolopyrrolocarbazole ring are the 1- and 11-positions, or the 2- and 10-positions, and an antitumore agent containing it as an effective ingredient. The compounds have a better antitumor action than known compounds having a similar structure.
    • 由下式表示的化合物或其药学上可接受的盐,其中R表示未取代的吡啶基,呋喃基或噻吩基,或吡啶基,呋喃基或噻吩基,其各自具有一个或多个选自羟基, 低级烷氧基,羟基低级烷基和羟基低级烯基,不同之处在于当吡啶基,呋喃基或噻吩基具有低级烷氧基作为取代基时,其各自同时具有选自羟基的另一取代基 ,低级烷氧基,羟基低级烷基和羟基低级烯基,m表示1〜3的整数,G表示β-D-吡喃葡萄糖基,吲哚并吡咯并唑的羟基取代位置 环是1-和11位,或2-和10-位,以及含有它作为有效成分的抗肿瘤剂。化合物具有更好的抗肿瘤 比已知具有相似结构的化合物。
    • 9. 发明授权
    • Process for producing 3-methyl-2-oxoindoline
    • 3-甲基-2-氧代二氢吲哚的制备方法
    • US06268512B1
    • 2001-07-31
    • US09600019
    • 2000-07-11
    • Hisao KondoTetsuro Higashikawa
    • Hisao KondoTetsuro Higashikawa
    • C07D20712
    • C07D209/34
    • The present invention is a process for producing 3-methyl-2-oxoindoline as defined by the following chemical formula (2), including heating of propionylphenylhydrazide as defined by the following chemical formula (1) in the presence of at least one kind of basic calcium compound, characterized in that an organic solvent withstanding at least at a temperature of 180° C. in the presence of the basic calcium compound is employed by at least an amount of equal weight to that of the propionylphenylhydrazide. With the construction mentioned above, even when the amount of calcium oxide is reduced down to as little as 15% of a conventionally used amount, at least 75% of a corresponding yield attained conventionally has been achieved. That is, not only control of the reaction and easy after treatment but also a high yield has been achieved;
    • 本发明是由以下化学式(2)定义的3-甲基-2-氧代二氢吲哚的制造方法,其中包括如下化学式(1)所定义的丙酰基苯基酰肼在至少一种碱性 钙化合物,其特征在于,在碱性钙化合物的存在下,至少在180℃的温度下耐受的有机溶剂的使用量至少与丙酰基苯肼的重量相同。 通过上述结构,即使氧化钙的量减少到常规使用量的少至15%,也达到了通常达到相应产率的至少75%。 也就是说,不仅控制反应,而且处理容易,而且成品率高;