PHOTOSENSITIVE COMPOUND, PHOTOSENSITIVE RESIN, AND PHOTOSENSITIVE COMPOSITION
    3.
    发明申请
    PHOTOSENSITIVE COMPOUND, PHOTOSENSITIVE RESIN, AND PHOTOSENSITIVE COMPOSITION 有权
    感光性化合物,感光树脂和感光性组合物

    公开(公告)号:US20150079519A1

    公开(公告)日:2015-03-19

    申请号:US14391170

    申请日:2013-02-28

    Inventor: Toru Shibuya

    Abstract: A photosensitive compound represented by formula (1) or formula (2). (Chemical formula 1) (In formula (1) and formula (2), n is an integer of 1-3; R1 is a linear or branched alkyl group having 1-6 carbon atoms or an alkylene group having 2-6 carbon atoms formed from two R1 together; R2 is —NR3R4; R3 and R4 are each independently a linear or branched alkyl group or alkenyl group having 1-6 carbon atoms, a linear or branched alkylene group having 2-6 carbon atoms formed by R3 and R4 together, or a linear or branched alkylene group or alkenylene group having 3-8 carbon atoms optionally containing an oxygen atom or nitrogen atom.)

    Abstract translation: 由式(1)或式(2)表示的光敏化合物。 (化学式1)(式(1)和式(2)中,n为1〜3的整数,R 1为碳原子数1〜6的直链或支链烷基或碳原子数2〜6的亚烷基 由两个R 1一起形成; R 2是-NR 3 R 4; R 3和R 4各自独立地是具有1-6个碳原子的直链或支链烷基或烯基,由R3和R4形成的具有2-6个碳原子的直链或支链亚烷基 一起或具有任选含有氧原子或氮原子的具有3-8个碳原子的直链或支链亚烷基或亚烯基)

    IODINE RADIOLABELLING METHOD
    4.
    发明申请
    IODINE RADIOLABELLING METHOD 有权
    碘放射线法

    公开(公告)号:US20120237444A1

    公开(公告)日:2012-09-20

    申请号:US13510656

    申请日:2010-12-10

    Applicant: Michelle Avory

    Inventor: Michelle Avory

    Abstract: The present invention provides a novel method of labelling biological targeting molecules (BTMs) of interest with radioiodine. Also provided are novel radioiodinated BTMs prepared using the method, as well as radiopharmaceutical compositions comprising such radioiodinated BTMs. The invention also provides radioiodinated intermediates useful in the method, as well as in vivo imaging methods using the radioiodinated BTMs.

    Abstract translation: 本发明提供了用放射性碘标记生物靶向分子(BTM)的新方法。 还提供了使用该方法制备的新型放射性碘化BTM,以及包含这种放射性碘化BTM的放射性药物组合物。 本发明还提供了可用于该方法的放射性碘化中间体,以及使用放射性碘化BTM的体内成像方法。

    Cinnamaldehyde compound having an azido group
    7.
    发明授权
    Cinnamaldehyde compound having an azido group 失效
    具有叠氮基的肉桂醛化合物

    公开(公告)号:US06768027B2

    公开(公告)日:2004-07-27

    申请号:US10400838

    申请日:2003-03-27

    Applicant: Mineko Takeda

    Inventor: Mineko Takeda

    CPC classification number: C07C247/16

    Abstract: The invention provides a novel azidocinnamaldehyde compound which, when used as an intermediate for providing a photosensitive moiety of a photoresist, introduces a photosensitive moiety having high sensitivity and attaining high contrast between the exposed portion and the unexposed portion, and which per se can serve as a photosensitive moiety. The azidocinnamaldehyde compound is represented by formula(I): wherein R represents a lower alkyl group and Y represents hydrogen or a sulfonate salt group.

    Abstract translation: 本发明提供了一种新的叠氮肉桂醛化合物,当用作提供光致抗蚀剂的光敏部分的中间体时,引入具有高灵敏度并在曝光部分和未曝光部分之间获得高对比度的感光部分,其本身可以用作 感光部分。 叠氮肉桂醛化合物由式(I)表示:其中R表示低级烷基,Y表示氢或磺酸盐基团。

    Method of improving the effectiveness of a cytotoxic drug or radiotherapy using a quinazolinone compound
    9.
    发明授权
    Method of improving the effectiveness of a cytotoxic drug or radiotherapy using a quinazolinone compound 失效
    使用喹唑啉酮化合物改善细胞毒性药物或放射疗法的有效性的方法

    公开(公告)号:US06316455B1

    公开(公告)日:2001-11-13

    申请号:US09448485

    申请日:1999-11-24

    Abstract: A range of 3-oxybenzamide compounds and related quinazolinone compounds are disclosed which can act as potent inhibitors of the DNA repair enzyme poly(ADP-ribose) polymerase or PARP enzyme (EC 2.4.2.30), and which thereby can provide useful therapeutic compounds for use in conjunction with DNA-damaging cytotoxic drugs or radiotherapy to potentiate the effects of the latter. The coumpounds disclosed include 3-benzyloxybenzamides, 3-oxybenzamides in which a chain of 5 or more methylene groups terminate in a halogen atom or in a purin-9-yl moiety, certain benzoxazole-4-carboxamide compounds and certain quinazolinone compounds. In formula X and Y together may form a bride —X—Y— that represents the grouping (a), (b) or (c) wherein R5 is H, alkyl, aryl or aralkyl.

    Abstract translation: 公开了一系列3-氧基苯甲酰胺化合物和相关的喹唑啉酮化合物,其可以作为DNA修复酶聚(ADP-核糖)聚合酶或PARP酶(EC 2.4.2.30)的有效抑制剂,由此可以为 与DNA损伤性细胞毒性药物或放射治疗联合使用以增强后者的作用。 公开的专利文献包括3-苄氧基苯甲酰胺,其中5个或更多个亚甲基的链终止于卤素原子或嘌呤-9-基部分的某些苯并恶唑-4-甲酰胺化合物和某些喹唑啉酮化合物的3-氧代苯甲酰胺。 式X和Y一起可以形成代表(a),(b)或(c)的组合的新娘-X-Y-,其中R 5是H,烷基,芳基或芳烷基。

    Tetrafluoroazidoaniline and method of making and using the same
    10.
    发明授权
    Tetrafluoroazidoaniline and method of making and using the same 失效
    四氟代叠氮苯胺及其制备及使用方法

    公开(公告)号:US06252096B1

    公开(公告)日:2001-06-26

    申请号:US09525753

    申请日:2000-03-14

    CPC classification number: C07C247/16 C07C311/44

    Abstract: The invention is directed to a novel compounds comprising 4-azidotetrafluoroaniline and the alkyl, acyl and sulfonamide derivatives thereof and to methods of making and using the same. The novel compounds are useful as a photoaffinity probe to study protein structure and function. Two methods for preparing 4-azidotetrafluoroaniline are disclosed, each employing a stable carbamate intermediate from which the 4-azidotetrafluoroaniline is derived.

    Abstract translation: 本发明涉及包含4-叠氮四氟四苯胺及其烷基,酰基和磺酰胺衍生物的新化合物及其制备和使用方法。 新型化合物可用作光亲和性探针来研究蛋白质结构和功能。 公开了制备4-叠氮四氟苯胺的两种方法,每种方法使用得自4-叠氮四氟乙苯的稳定的氨基甲酸酯中间体。

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