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公开(公告)号：USD401592S
公开(公告)日：1998-11-24
申请号：US68016
申请日：1997-03-14
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公开(公告)号：USD401594S
公开(公告)日：1998-11-24
申请号：US68018
申请日：1997-03-14
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公开(公告)号：USD401593S
公开(公告)日：1998-11-24
申请号：US68017
申请日：1997-03-14
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公开(公告)号：US07985874B2
公开(公告)日：2011-07-26
申请号：US10594182
申请日：2005-03-18
IPC分类号： C01B21/14
CPC分类号： G01N33/543 , G01N2400/00
摘要： A support comprising functional groups supported therein that specifically react with an aldehyde group of a sugar chain, and a polymer particle and a glycochip to which the support is applied, and uses thereof.
摘要翻译： 其中包含与糖链的醛基特异性反应的官能团的载体，以及应用了载体的聚合物颗粒和糖芯片及其用途。
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5.发明申请Method for Preparing Analysis Sample, Analysis Sample and Sugar Chain Capture Agent 失效分析样品，分析样品和糖链捕获剂的制备方法公开(公告)号：US20090068752A1
公开(公告)日：2009-03-12
申请号：US12224953
申请日：2007-03-13
申请人： Hideyuki Shimaoka , Hiromitsu Kuramoto , Shinichiro Nishimura , Yasuro Shinohara , Yoshiaki Miura , Jun-ichi Furukawa
发明人： Hideyuki Shimaoka , Hiromitsu Kuramoto , Shinichiro Nishimura , Yasuro Shinohara , Yoshiaki Miura , Jun-ichi Furukawa
CPC分类号： C07K1/22 , C07B2200/05 , C07B2200/11 , C07C323/60 , C07K5/0806 , Y10T436/143333 , Y10T436/17 , Y10T436/18 , Y10T436/182 , Y10T436/25 , Y10T436/25125
摘要： A method for preparing an analysis sample which involves the sugar chain capture step comprising a reaction of capturing a sugar chain and/or a sugar derivative from a biological sample by using a sugar chain capture agent and the excision step comprising excising a compound containing a moiety capturing the sugar chain and/or the sugar derivative from the sugar chain capture agent after the completion of the sugar chain capture reaction and releasing the compound.
摘要翻译： 一种制备包含糖链捕获步骤的分析样品的方法，其包括通过使用糖链捕获剂从生物样品捕获糖链和/或糖衍生物的反应，并且所述切除步骤包括切除含有部分的化合物 在糖链捕获反应完成后从糖链捕获剂捕获糖链和/或糖衍生物并释放该化合物。
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6.发明申请Alkynyl-substituted azasugar derivative and drug containing the same as the active ingredient 审中-公开炔基取代的十八烷基衍生物和含有与活性成分相同的药物公开(公告)号：US20060058350A1
公开(公告)日：2006-03-16
申请号：US10540485
申请日：2003-08-01
IPC分类号： A61K31/445 , C07D211/54
CPC分类号： C07D211/96
摘要： An alkynyl-substituted azasugar derivative and a drug containing the same as an active ingredient are disclosed. This drug is useful as a preventive or remedy for insulin-independent diabetes, rheumatoid arthritis, osteoarthritis, sepsis, acquired immune deficiency syndrome (AIDS), graft-versus-host disease (GVHD), asthma, atopic dermatitis, and ulcerative colitis.
摘要翻译： 公开了炔基取代的十八烷基衍生物和含有它们的活性成分的药物。 这种药物可用作胰岛素不依赖性糖尿病，类风湿性关节炎，骨关节炎，败血症，获得性免疫缺陷综合征（AIDS），移植物抗宿主病（GVHD），哮喘，特应性皮炎和溃疡性结肠炎的预防或补救。
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公开(公告)号：US20050154017A1
公开(公告)日：2005-07-14
申请号：US10504777
申请日：2003-06-26
IPC分类号： A61K31/445 , A61P17/00 , A61P43/00 , C07D211/96 , C07D491/04 , C07D491/056 , C07D211/40
CPC分类号： C07D491/04 , A61K31/445 , C07D211/96
摘要： A novel azasugar derivative, and a drug containing the same as an active ingredient are disclosed. The drug is useful for treatment of keratinocyte-proliferative diseases.
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公开(公告)号：USD398546S
公开(公告)日：1998-09-22
申请号：US68005
申请日：1997-03-14
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9.发明授权公开(公告)号：US07598372B2
公开(公告)日：2009-10-06
申请号：US10584065
申请日：2004-12-24
摘要： It is intended to chemically synthesize the trisaccharide moiety at the reducing end in the core sugar chain structure of an asparagine-linked glycoprotein. By using a highly inexpensive natural polysaccharide having a mannoseβ-1,4-bond as the starting material, a β-1,4-glycoside bond of mannose is formed.
摘要翻译： 旨在在天冬酰胺连接的糖蛋白的核心糖链结构的还原端化学合成三糖部分。 通过使用具有甘露糖-b-1,4键的高度廉价的天然多糖作为起始原料，形成甘露糖的β-1,4-糖苷键。
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10.发明申请Novel galactosylceramide analogues, and beta-glucocerebrosidase activator, external skin preparations and method of activating beta-glucocerebrosidase using the same 审中-公开新型半乳糖神经酰胺类似物和β-葡糖脑苷脂酶活化剂，外用皮肤制剂和使用其的β-葡糖脑苷脂酶活化方法公开(公告)号：US20070111951A1
公开(公告)日：2007-05-17
申请号：US11651978
申请日：2007-01-11
申请人： Rie Uematsu , Fumio Nakajima , Masahiro Yoshida , Kyoko Fukunaga , Mariko Hara , Shintaro Inoue , Shinichiro Nishimura
发明人： Rie Uematsu , Fumio Nakajima , Masahiro Yoshida , Kyoko Fukunaga , Mariko Hara , Shintaro Inoue , Shinichiro Nishimura
IPC分类号： A61K31/70
摘要： Galactosylceramide analogues represented by the following formula (1) or (2). (wherein X and Y each represent S or O, R1 and R2 each represent an alkyl group or an alkenyl group each having 9 to 35 carbon atoms. R3 represents an alkyl group or an alkenyl group each having 2 to 30 carbon atoms.) It is provided a β-glucocerebrosidase activator which is easily available, and external skin preparations and a method of activating β-glucocerebrosidase, in which improvement in formation of horny layer transmission barrier is expected by activating β-glucocerebrosidase so that an improved effect in rough skin is also expected.
摘要翻译： 由下式（1）或（2）表示的半乳糖神经酰胺类似物。 （其中X和Y各自表示S或O，R 1和R 2各自表示各自具有9至35个碳原子的烷基或烯基，R SUP > 3 表示各自具有2〜30个碳原子的烷基或烯基。）提供易于获得的β-葡萄糖脑苷脂酶激活剂，以及外用皮肤制剂和β-葡萄糖脑苷脂酶活化方法 通过激活β-葡糖脑苷脂酶预期角质层传播屏障形成的改善，从而也预期在粗糙皮肤中的改善效果。
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