세로토닌 6 수용체 리간드의 고효율 검색을 위한 HA-5-HT6R을 안정적으로 발현하는 세포주
    25.
    发明公开

    公开(公告)号:KR1020100035883A

    公开(公告)日:2010-04-07

    申请号:KR1020080095258

    申请日:2008-09-29

    Abstract: PURPOSE: A cell line expressing HA-5-HT6R and a method for detecting serotonin 6 receptor ligand are provided to enhance detection efficiency and to diagnose and treat brain diseases such as depression and Alzheimer. CONSTITUTION: A cell line which stably expresses HA-5-HT6R is prepared by transducing a vector containing a 5-HT6R gene construct connected with HA(hemagglutinin) to host cells. The cell line is deposited in a deposit number KCLRF-BP-00187. The host cells are HEK293, COS7, CHO-K1 or CHO-G5A. A method for detecting 5-HT6R ligand at high efficiency comprises: a step of treating a test compound to cell line which stably expressing HA-5-HT6R; a step of measuring 5-HT6R activity of treated cell line; and a step of selecting test compound which increases or decreases 5-HT6R activity in the cell line comparing to untreated cell line.

    Abstract translation: 目的:提供表达HA-5-HT6R的细胞系和检测血清素6受体配体的方法,以提高检测效率,诊断和治疗脑疾病如抑郁症和阿尔茨海默病。 构成:通过将含有与HA(血凝素)连接的5-HT6R基因构建体的载体转导到宿主细胞来制备稳定表达HA-5-HT6R的细胞系。 细胞系以保藏号KCLRF-BP-00187沉积。 宿主细胞是HEK293,COS7,CHO-K1或CHO-G5A。 一种以高效率检测5-HT6R配体的方法包括:将测试化合物处理稳定表达HA-5-HT6R的细胞系的步骤; 测定处理细胞系5-HT6R活性的步骤; 以及与未处理的细胞系相比,选择增加或减少细胞系中5-HT6R活性的试验化合物的步骤。

    CLC-Kb 염화 이온 채널 조절물질 도출을 위한 세포기반 형광 이미징 고효율 검색 및 광범위 특성 연구용 세포주
    26.
    发明公开
    CLC-Kb 염화 이온 채널 조절물질 도출을 위한 세포기반 형광 이미징 고효율 검색 및 광범위 특성 연구용 세포주 有权
    使用YFP荧光成像和CLC-KB通道的广谱分析研究CLC-KB通道调制器的基于细胞的高通量筛选的细胞系

    公开(公告)号:KR1020160017521A

    公开(公告)日:2016-02-16

    申请号:KR1020140101184

    申请日:2014-08-06

    CPC classification number: C12N5/16

    Abstract: 본발명은 CLC-Kb 채널을코딩하는유전자, Barttin(Y98A)를코딩하는유전자및 형광단백질을코딩하는유전자를포함하는플라스미드로형질전환시킨세포주에관한것으로서, 상기 CLC-Kb 채널및 Barttin(Y98A)는 N-말단또는 C-말단에에피토프태그되어있고, 상기형광단백질은할라이드이온에노란색으로반응하는것을특징으로하고, 상기 CLC-Kb 채널, Barttin(Y98A) 및형광단백질을안정적으로발현하는것을특징으로한다. 또한, 테트라사이클린유도에의해발현되는유도안정적발현시스템을가지며, 세포기반형광이미징을이용한고효율검색에활용할수 있으며, CLC-Kb 채널과 Barttin(Y98A)를안정적으로발현함으로써 CLC-Kb 채널과 Barttin이관여하고있는세포내 신호전달과정연구에이용이가능함은물론, 본발명에따른세포주를이용한 CLC-Kb 채널작용기작에대한분자수준의연구, 생리학적기능연구, 바터증후군, 고혈압등 CLC-Kb 채널과관련된신장및 심장질환의예방및 치료제개발에널리활용될수 있다.

    Abstract translation: 本发明涉及包含编码CLC-Kb通道的基因,编码Barttin(Y98A)的基因和通过转化成质粒来编码荧光蛋白的基因的细胞系。 CLC-Kb通道和Barttin(Y98A)被表位标记到N末端或C-末端,荧光蛋白与卤素离子反应为黄色。 细胞系稳定表达CLC-Kb通道,Barttin(Y98A)和荧光蛋白。 此外,细胞系具有由四环诱导表达的稳定的诱导表达系统,可用于使用基于细胞的荧光成像的高效搜索,可用于研究细胞内的信号传递过程,其中CLC -Kb通道和Barttin(Y98A)通过稳定表达CLC-Kb通道和Barttin(Y98A)而参与,并且可以广泛用于使用细胞系的CLC-Kb通道作用代码的分子水平研究 本发明的生理功能研究以及与CLC-Kb通道相关的肾脏和心脏疾病如面糊综合征,高血压等的预防和治疗剂发展。

    CLC-Ka 염화 이온 채널 조절물질 도출을 위한 세포기반 형광 이미징 고효율 검색 및 광범위 특성 연구용 세포주
    27.
    发明公开
    CLC-Ka 염화 이온 채널 조절물질 도출을 위한 세포기반 형광 이미징 고효율 검색 및 광범위 특성 연구용 세포주 有权
    使用YFP荧光成像和CLC-KA通道的广谱分析研究CLC-KA通道调制器的基于细胞的高通量筛选的细胞系

    公开(公告)号:KR1020160017520A

    公开(公告)日:2016-02-16

    申请号:KR1020140101183

    申请日:2014-08-06

    CPC classification number: C12N5/16

    Abstract: 본발명은 CLC-Ka 채널을코딩하는유전자, Barttin(Y98A)를코딩하는유전자및 형광단백질을코딩하는유전자를포함하는플라스미드로형질전환시킨세포주에관한것으로서, 상기 CLC-Ka 채널및 Barttin(Y98A)는 N-말단또는 C-말단에에피토프태그되어있고, 상기형광단백질은할라이드이온에노란색으로반응하는것을특징으로하고, 상기 CLC-Ka 채널, Barttin(Y98A) 및형광단백질을안정적으로발현하는것을특징으로한다. 또한, 테트라사이클린유도에의해발현되는유도안정적발현시스템을가지며, 세포기반형광이미징을이용한고효율검색에활용할수 있으며, CLC-Ka 채널과 Barttin(Y98A)를안정적으로발현함으로써 CLC-Ka 채널과 Barttin이관여하고있는세포내 신호전달과정연구에이용이가능함은물론, 본발명에따른세포주를이용한 CLC-Ka 채널작용기작에대한분자수준의연구, 생리학적기능연구, 저나트륨혈증등 CLC-Ka 채널과관련된신장및 심장질환의예방및 치료제개발에널리활용될수 있다.

    Abstract translation: 本发明涉及包含编码CLC-Ka通道的基因,编码Barttin(Y98A)的基因和通过转化为质粒来编码荧光蛋白的基因的细胞系。 CLC-Ka通道和Barttin(Y98A)被表位标记到N末端或C-末端,荧光蛋白与卤素离子反应为黄色。 细胞系稳定表达CLC-Ka通道,Barttin(Y98A)和荧光蛋白。 此外,细胞系具有由四环诱导表达的稳定的诱导表达系统,可用于使用基于细胞的荧光成像的高效搜索,可用于研究细胞内的信号传递过程,其中CLC -Ka通道和Barttin(Y98A)通过稳定表达CLC-Ka通道和Barttin(Y98A)而参与,并且可以广泛用于CLC-Ka通道作用的分子水平研究,使用细胞系 本发明涉及生理功能研究,与低钠血症等CLC-Ka通道相关的肾脏和心脏病的预防和治疗剂的发展。

    Τ-형 칼슘 채널에 활성을 지닌 신규 1,4-다이아제판 피라졸 화합물
    28.
    发明公开
    Τ-형 칼슘 채널에 활성을 지닌 신규 1,4-다이아제판 피라졸 화합물 有权
    作为T型钙通道拮抗剂的1,4-二氮杂双环衍生物

    公开(公告)号:KR1020120097288A

    公开(公告)日:2012-09-03

    申请号:KR1020110016788

    申请日:2011-02-24

    Abstract: PURPOSE: A pharmaceutical composition containing 1,4-diazepane pyrazole compound and a pharmaceutically acceptable salt thereof is provided to be used as an agent for preventing or treating brain diseases, heart diseases, cancer, epilepsy, and pain. CONSTITUTION: A 1,4-diazepane pyrazole compound is denoted by chemical formula 1. A pharmaceutical composition for preventing and treating brain diseases such as epilepsy, depression, Parkinson's diseases, dementia, sleep disorders, or heart diseases such as hypertension, cardiac arrhythmia, or myocardial infarction, or pain contains the compound of chemical formula 1 as an active ingredient. A method for preparing the compound of chemical formula 1 comprises a step of reacting pyrazolemethyl amine of chemical formula 2 with chloroacetyl chloride.

    Abstract translation: 目的:提供含有1,4-二氮杂环庚烷吡唑化合物及其药学上可接受的盐的药物组合物,用作预防或治疗脑疾病,心脏病,癌症,癫痫和疼痛的药剂。 构成:1,4-二氮杂环庚烷吡唑化合物由化学式1表示。用于预防和治疗脑疾病如癫痫,抑郁症,帕金森病,痴呆,睡眠障碍或心脏病如高血压,心律失常, 或心肌梗塞,或疼痛含有化学式1的化合物作为活性成分。 制备化学式1的化合物的方法包括使化学式2的吡唑甲胺与氯乙酰氯反应的步骤。

    T-형 칼슘 채널에 활성을 지닌 피라조일 피페리딘 화합물
    29.
    发明公开
    T-형 칼슘 채널에 활성을 지닌 피라조일 피페리딘 화합물 有权
    吡唑啉酮化合物作为T型钙通道拮抗剂

    公开(公告)号:KR1020120097287A

    公开(公告)日:2012-09-03

    申请号:KR1020110016787

    申请日:2011-02-24

    Abstract: PURPOSE: A pharmaceutical composition containing pyrazoyl piperidine compounds and pharmaceutically acceptable salt thereof is provided to prevent or treat brain diseases, heard diseases, cancer, and pain. CONSTITUTION: A pyrazoyl piperidine compound is denoted by chemical formula 1. A pharmaceutical composition for treating cerebral diseases, cardiac diseases, cancer, or pain contains the compound of chemical formula 1 as an active ingredient. A method for preparing the compound comprises: a step of reacting piperidine acetate of chemical formula 2 and pyrazole methyl amine of chemical formula 3 of a step of reacting piperidine compound of chemical formula 4 with an aldehyde compound of chemical formula 5 by reduction-amination. [Reference numerals] (AA) Reductive amination

    Abstract translation: 目的:提供含有吡唑基哌啶化合物及其药学上可接受的盐的药物组合物,以预防或治疗脑疾病,听到疾病,癌症和疼痛。 构成:化学式1表示吡唑基哌啶化合物。用于治疗脑疾病,心脏病,癌症或疼痛的药物组合物含有化学式1的化合物作为活性成分。 制备该化合物的方法包括:使化学式2的哌啶乙酸酯与化学式3的吡唑甲胺与化学式4的哌啶化合物与化学式5的醛化合物的还原胺化反应的步骤。 (参考号)(AA)还原胺化

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