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    • 1. 发明申请
    • Bipodal-Peptide Binder
    • 双峰肽粘合剂
    • US20110152500A1
    • 2011-06-23
    • US12999717
    • 2009-10-20
    • Sang Yong JonSung Hyun KimSe Ho Park
    • Sang Yong JonSung Hyun KimSe Ho Park
    • C07K14/00C40B30/04
    • C07K14/001A61K49/0032A61K49/0056
    • The present invention deals with a bipodal-peptide binder that specifically binds with a target including (a) a structure stabilizing region that includes parallel, antiparallel or parallel and antiparallel amino acid strands wherein interstrand non-covalent bonds are formed; and (b) a target binding region I and a target binding region II that are bonded at both terminals of said structure stabilizing region and respectively include n and m amino acids, and a method of preparing same; the bipodal-peptide binder of the present invention exhibits the KD value (dissociation constant) of a very low level (for example, nM level) and, therefore, exhibits very high affinity toward a target. The bipodal-peptide binder of the present invention has applications not only in pharmaceuticals but also in in-vivo imaging, in vitro cell imaging, and drug delivery targeting, and can be very usefully employed as an escort molecule.
    • 本发明涉及与靶标特异性结合的双齿肽粘合剂,包括(a)结构稳定区,其包含平行,反向平行或平行和反平行的氨基酸链,其中形成了链间非共价键; 和(b)在所述结构稳定区的两端键合并分别包含n和m个氨基酸的靶结合区I和靶结合区II及其制备方法。 本发明的双齿 - 肽结合物表现出非常低水平(例如,nM水平)的KD值(解离常数),因此对目标表现出非常高的亲和力。 本发明的双齿肽粘合剂不仅在药物中也具有体内成像,体外细胞成像和药物递送靶向的用途,并且可以非常有用地用作护送分子。
    • 3. 发明申请
    • BPB-BASED CARGO DELIVERY SYSTEM
    • 基于BPB的货物运输系统
    • US20120321697A1
    • 2012-12-20
    • US13515163
    • 2010-12-03
    • Sang Yong JonSung Hyun KimSeho ParkDongkyu KimJinho ParkPhei Er Saw
    • Sang Yong JonSung Hyun KimSeho ParkDongkyu KimJinho ParkPhei Er Saw
    • A61K38/02A61K9/127C07K19/00C07K17/10B82Y5/00
    • C07K19/00
    • Disclosed are bipodal peptide binder (BPB) based cargo delivery systems wherein cargo is linked to a BPB for delivery into cells or to cell surfaces using target binding ability and specificity of the BPB. The BPB has a structure stabilizing region of parallel or antiparallel amino acid strands or a combination of these strands to induce interstrand non-covalent bonds. The BPB also has target binding regions I and II, each binding to each of both termini of the structure stabilizing region. The number of amino acid residues of regions I and II, respectively, are n and m. The BPB exhibits the KD value (dissociation constant) of a very low level (for example, nM level) and, therefore, exhibits very high affinity toward a biological target molecule. The BPB based cargo delivery system has applications in drugs, in vivo molecular imaging, in vitro cell imaging, drug delivery targeting and escort molecules.
    • 公开了基于双齿肽粘合剂(BPB)的货物运输系统,其中货物与BPB连接以使用BPB的靶结合能力和特异性递送至细胞或细胞表面。 BPB具有平行或反平行氨基酸链的结构稳定区或这些链的组合以诱导链间非共价键。 BPB还具有靶结合区域I和II,其各自结合结构稳定区域的两个末端中的每一个。 区域I和II的氨基酸残基数分别为n和m。 BPB显示非常低水平(例如,nM水平)的KD值(解离常数),因此对生物靶分子表现出非常高的亲和力。 基于BPB的货物运输系统在药物,体内分子成像,体外细胞成像,药物递送靶向和护送分子中都有应用。
    • 4. 发明申请
    • INTRACELLUAR TARGETING BIPODAL PEPTIDE BINDER
    • 腹腔内定向双功能胶原蛋白BINDER BINDER
    • US20120309934A1
    • 2012-12-06
    • US13515026
    • 2010-12-03
    • Sang Yong JonSung Hyun KimDaejin Kim
    • Sang Yong JonSung Hyun KimDaejin Kim
    • C07K19/00
    • C07K19/00A61K38/00
    • An intracellular targeting bipodal-peptide binder specifically binding to an intracellular target molecule, comprising: (a) a structure-stabilizing region comprising a parallel amino acid strand, an antiparallel amino acid strand or parallel and antiparallel amino acid strands to induce interstrand non-covalent bonds; (b) target binding regions I and II each binding to each of both termini of the structure-stabilizing region, wherein the number of amino acid residues of the target binding region I is n and the number of amino acid residues of the target binding region II is m; and (c) a cell-penetrating peptide (CPP) linked to the structure-stabilizing region, the target binding region I or the target binding region II. Also contemplated is a method for preparing an intracellular targeting bipodal-peptide binder. The bipodal-peptide binder capable of binding to intracellular targets has applications to drugs, in vivo molecular imaging, in vitro cell imaging, drug delivery targeting and escort molecules.
    • 特异性结合细胞内靶分子的细胞内靶向双齿肽结合物,其包含:(a)包含平行氨基酸链,反平行氨基酸链或平行和反平行氨基酸链的结构稳定区,以诱导链间非共价键 债券 (b)靶结合区域I和II各自与结构稳定区域的两个末端各自结合,其中靶结合区域I的氨基酸残基数目为n,靶结合区域的氨基酸残基数 二是m 和(c)与结构稳定区域连接的细胞穿透肽(CPP),靶结合区域I或靶结合区域II。 还考虑了制备细胞内靶向双齿肽粘合剂的方法。 能够结合细胞内靶标的双峰肽结合物可用于药物,体内分子成像,体外细胞成像,药物递送靶向和护送分子。
    • 5. 发明授权
    • Display panel including patterned spacer
    • 显示面板包括图案间隔
    • US09152041B2
    • 2015-10-06
    • US11629476
    • 2005-07-05
    • Sung Hyun KimJin Suek KimKyung Jun KimSeung Hee LeeIl Eok KwonJeong Ae Yoon
    • Sung Hyun KimJin Suek KimKyung Jun KimSeung Hee LeeIl Eok KwonJeong Ae Yoon
    • C09K19/00G03F7/00G03F7/029
    • G03F7/0007G03F7/0295Y10T428/10Y10T428/1073
    • Disclosed is a display panel including a lower substrate, upper substrate, and a patterned spacer that causes the lower substrate and upper substrate to be spaced apart from each other by a predetermined distance, wherein the patterned spacer is obtained from a photosensitive resin composition comprising: (a) a triazine-based photopolymerization initiator represented by the following formula 1; (b) an alkali-soluble photo polymerizable reactive resin binder; and (c) a polymerizable compound: (wherein each of R1-R5 has the same meaning as defined herein). A photosensitive resin composition for use in a patterned spacer is also disclosed, the composition comprising: (a) a triazine-based photopolymerization initiator represented by the following formula 1; (b) an alkali-soluble photopolymerizable reactive resin binder; (c) a polymerizable compound; and (d) a solvent. The photosensitive resin composition shows high sensitivity and excellent properties related with development, and provides a patterned spacer having excellent strength, sensitivity, residue characteristics, film uniformity, residual film ratio, etc.
    • 公开了一种显示面板,其包括下基板,上基板和图案化间隔件,其使得下基板和上基板彼此间隔开预定距离,其中图案化间隔件由感光树脂组合物获得,包括: (a)由下式1表示的三嗪系光聚合引发剂; (b)碱溶性光聚合反应性树脂粘合剂; 和(c)可聚合化合物:(其中R 1 -R 5各自具有与本文所定义的相同的含义)。 还公开了用于图案化间隔物的感光性树脂组合物,该组合物包含:(a)由下式1表示的三嗪系光聚合引发剂; (b)碱溶性光聚合反应性树脂粘合剂; (c)可聚合化合物; 和(d)溶剂。 感光性树脂组合物显示出高的敏感性和与显影相关的优异性能,并且提供了具有优异的强度,灵敏度,残留特性,膜均匀性,残留膜比等的图案化间隔物。
    • 6. 发明授权
    • Apparatus, system, and method for preventing infection by malicious code
    • 用于防止恶意代码感染的装置,系统和方法
    • US08813229B2
    • 2014-08-19
    • US13574346
    • 2011-01-20
    • Jae Han LeeJeong Hun KimSung Hyun Kim
    • Jae Han LeeJeong Hun KimSung Hyun Kim
    • G08B23/00
    • G06F21/564G06F21/567
    • The invention relates to an apparatus for preventing infection by malicious code, comprising: a database in which files installed in an agent system, DNA values for each part of the files, and index information for indicating whether each file is normal or malicious are stored; a calculation unit which calculates a DNA value for a part of a file for which an execution is requested in the agent system; and a file inspection unit which searches the database to extract, in a group, files having the DNA value calculated by the calculation unit, inspects whether an object file is normal or malicious on the basis of the index information on the files extracted in a group, and allows the execution of the object file or makes a request for the calculation of DNA values of other parts which selectively include one part of the object file.
    • 本发明涉及一种防止恶意代码感染的装置,包括:数据库,其中安装在代理系统中的文件,文件的每个部分的DNA值,以及用于指示每个文件是正常还是恶意的索引信息; 计算单元,其计算在代理系统中请求执行的文件的一部分的DNA值; 以及文件检查单元,其搜索数据库以提取具有由计算单元计算出的DNA值的文件,根据关于在组中提取的文件的索引信息来检查对象文件是正常还是恶意的 ,并且允许执行目标文件或者请求计算选择性地包括目标文件的一部分的其他部分的DNA值。