5-HT7 수용체 조절제로 작용하는 아제핀 유도체

    公开(公告)号:WO2018117406A1

    公开(公告)日:2018-06-28

    申请号:PCT/KR2017/012493

    申请日:2017-11-06

    Abstract: 본 발명은 5-HT 7 수용체에 작용하는 아제핀 유도체 및 이의 약제학적으로 허용 가능한 염에 관한 것으로, 5-HT 7 세로토닌 수용체에 대하여 우수한 결합친화력과 우수한 길항 활성을 가져 5-HT 7 길항 활성이 요구되는 우울증, 편두통, 불안, 통증, 염증성 통증, 신경병성 통증, 체온조절 장애, 생체리듬조절 장애, 수면 장애 및 평활근 관련 질환 등의 중추신경계 질환의 치료 또는 예방제로 유용하게 적용할 수 있다.

    3,6-이치환-4,5,6,7-테트라하이드로-1H-피라졸로[3,4-c]피리딘-7-온 화합물과 이 화합물의 제조방법
    3.
    发明公开
    3,6-이치환-4,5,6,7-테트라하이드로-1H-피라졸로[3,4-c]피리딘-7-온 화합물과 이 화합물의 제조방법 有权
    新的3,6-取代-4,5,6,7-四氢-1H-吡唑并[3,4-C]吡啶-7-酮化合物及其制备方法

    公开(公告)号:KR1020110121868A

    公开(公告)日:2011-11-09

    申请号:KR1020100041360

    申请日:2010-05-03

    Abstract: PURPOSE: A novel 3,6-disubstituted-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridin-7-one compound is provided to suppress cancer cell and to be used as an anticancer agent. CONSTITUTION: A 3,6-disubstituted-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridin-7-one is denoted by chemical formula 1. A pharmaceutical composition for anticancer 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 performing acrylation of 3-amino compound of chemical formula 2 with acyl halide compound of chemical formula 3 to prepare 3-haloacylcarbamoyl compound of chemical formula 4; and a step of substituting 3-haloacylcarbamoyl compound of chemical formula 4 with amine compounds of chemical formula 5.

    Abstract translation: 目的:提供新的3,6-二取代-4,5,6,7-四氢-1H-吡唑并[3,4-c]吡啶-7-酮化合物以抑制癌细胞并用作抗癌剂 。 构成:3,6-二取代-4,5,6,7-四氢-1H-吡唑并[3,4-c]吡啶-7-酮由化学式1表示。用于抗癌的药物组合物含有 化学式1为活性成分。 制备化学式1化合物的方法包括:用化学式3的酰卤化合物进行化学式2的3-氨基化合物的丙烯酸化以制备化学式4的3-卤代酰基氨基甲酰基化合物的步骤; 和用化学式5的胺化合物代替化学式4的3-卤代酰基氨基甲酰基化合物的步骤。

    GSK-3 억제활성을 보이는 1H-인다졸 화합물
    7.
    发明公开
    GSK-3 억제활성을 보이는 1H-인다졸 화합물 有权
    具有GSK-3抑制活性的1H-吲唑化合物

    公开(公告)号:KR1020120038033A

    公开(公告)日:2012-04-23

    申请号:KR1020100097910

    申请日:2010-10-07

    Abstract: PURPOSE: A 1H-indazole compound with GSK3 inhibition and pharmaceutically acceptable salt thereof are provided to be used as a therapeutic agent for treating diseases caused by GSK-3 activation. CONSTITUTION: A 1H-indazole compounds is denoted by chemical formula 1. A method for preparing the compound comprises: a step of performing amidation of 3-amino-1H-indazole compounds of chemical formula 2 and a substituted carboxylic acid compound of chemical formula 3 under the presence of pyridine base and 1-ethyl-3-(3'-dimethyl aminopropyl)carbodiimide hydrochloride(EDCI).

    Abstract translation: 目的:提供具有GSK3抑制的1H-吲唑化合物及其药学上可接受的盐作为治疗由GSK-3激活引起的疾病的治疗剂。 构成:1H-吲唑化合物由化学式1表示。一种制备化合物的方法包括:进行化学式2的3-氨基-1H-吲唑化合物和化学式3的取代的羧酸化合物的酰胺化步骤 在吡啶碱和1-乙基-3-(3'-二甲基氨基丙基)碳二亚胺盐酸盐(EDCI)的存在下。

    항암활성을 가지는 2,4-다이아미노퀴나졸린 화합물
    8.
    发明公开
    항암활성을 가지는 2,4-다이아미노퀴나졸린 화합물 有权
    具有抗病毒活性的2,4-二氨基喹唑啉化合物

    公开(公告)号:KR1020120038034A

    公开(公告)日:2012-04-23

    申请号:KR1020100097911

    申请日:2010-10-07

    Abstract: PURPOSE: A 2,4-diaminoquinazoline compound with anticancer activity is provided to be used as an anticancer agent. CONSTITUTION: A 2,4-diaminoquinazoline compound is denoted by chemical formula 1. A pharmaceutical composition for anticancer contains 2,4-diaminoquinazoline compound of chemical formula 1. A method for preparing the compound of chemical formula 1 comprises: a step of binding 2-chloro-N-(furnylmethyl)quinazoliine-4-amine compounds of chemical formula 2 with an amine compound of chemical formula 3.

    Abstract translation: 目的:提供具有抗癌活性的2,4-二氨基喹唑啉化合物作为抗癌剂。 构成:2,4-二氨基喹唑啉化合物由化学式1表示。抗癌用药物组合物含有化学式1的2,4-二氨基喹唑啉化合物。化学式1化合物的制备方法包括:将2 - 氯-N-(苄基甲基)喹唑啉-4-胺化合物与化学式3的胺化合物。

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