칼슘이온 채널 조절제로서 유효한 피라졸릴메틸아민-피페라진 유도체와 이의 제조방법
    26.
    发明公开
    칼슘이온 채널 조절제로서 유효한 피라졸릴메틸아민-피페라진 유도체와 이의 제조방법 失效
    新型吡咯烷基胺化合物作为钙通道调节剂及其制备方法

    公开(公告)号:KR1020100042111A

    公开(公告)日:2010-04-23

    申请号:KR1020080101249

    申请日:2008-10-15

    Abstract: PURPOSE: A pyrazolylmethylamine-piperazine derivative which is effective as a calcium ion channel modulator is provided to ensure effective activation as an T-type calcium ion channel antagonist and to use as an agent for preventing and treating brain diseases, heart diseases and pain diseases. CONSTITUTION: A pyrazolylmethylamine-peperazine derivative is denoted by chemical formula 1. A pharmaceutical composition for preventing and treating brain diseases, heart diseases or pain diseases by T-type calcium ion channel antagonism contains the pyrazolylmethylamine-peperazine derivative of chemical formula 1 or its pharmaceutically acceptable salt an active ingredient. The brain disease is epilepsy, depression, Parkison's disease, dementia or somnipathy. The heart disease is hypertension, cardiac arrhythmia, myocardial infarction, or congestive failure. The pain disease is chronic pain, acute pain, or neurogenic pain. The pyrazolylmethylamine-peperazine derivative is prepared by binding pyrazolylmethylamine compound of chemical formula 3 with piperazine acetyl halide compound of chemical formula 2.

    Abstract translation: 目的:提供作为钙离子通道调节剂有效的吡唑基甲胺 - 哌嗪衍生物,以确保作为T型钙离子通道拮抗剂的有效活化,并用作预防和治疗脑疾病,心脏病和疼痛疾病的药剂。 构成:吡唑基甲胺 - 哌嗪衍生物由化学式1表示。用于通过T型钙离子通道拮抗作用预防和治疗脑疾病,心脏病或疼痛疾病的药物组合物含有化学式1的吡唑基甲基 - 哌嗪衍生物或其药学上可接受的盐 可接受的盐为活性成分。 脑疾病是癫痫,抑郁症,帕金森病,痴呆或嗜睡。 心脏病是高血压,心律失常,心肌梗死或充血性衰竭。 疼痛疾病是慢性疼痛,急性疼痛或神经源性疼痛。 通过将化学式3的吡唑基甲基胺化合物与化学式2的哌嗪乙酰卤化合物结合,制备吡唑基甲胺 - 哌嗪衍生物。

    PAC-1을 이용한 단백질 발현 조절 시스템과 방법 및 PAC-1을 유효성분 포함하는 독시사이클린 길항제
    28.
    发明授权
    PAC-1을 이용한 단백질 발현 조절 시스템과 방법 및 PAC-1을 유효성분 포함하는 독시사이클린 길항제 有权
    使用PAC-1调节蛋白质表达的系统和方法以及使用PAC-1作为毒物调节蛋白质表达的方法

    公开(公告)号:KR101712638B1

    公开(公告)日:2017-03-07

    申请号:KR1020150116566

    申请日:2015-08-19

    Abstract: 본발명은 PAC-1(프로카스파아제활성화화합물 1)을이용한단백질발현조절시스템과방법및 PAC-1을유효성분으로하는독시사이클린길항제에관한것으로, 보다상세하게는 TetR(테트라사이클린억제제)에의해조절되는표적단백질발현시스템에서, TetR과 PAC-1의결합에의해상기단백질발현을조절하는것을특징으로하는 PAC-1을이용한단백질발현제어시스템과방법및 PAC-1을유효성분으로하는독시사이클린길항제에관한것이다.

    Abstract translation: 本发明涉及使用PAC-1(前胱天蛋白酶活化化合物1)和包含PAC-1作为活性成分的多西环素拮抗剂调节蛋白质表达的系统和方法,更具体地说, 其中在本发明的靶蛋白表达系统中TetR和PAC-1的组合调控蛋白的表达,以及使用PAC-1控制蛋白表达的方法和控制PAC- 会的。

    4각 고리 질소 화합물, 이를 포함하는 우울증, 정신 질환, 조루증, 또는 신경병증성 통증의 예방 또는 치료용 약학 조성물, 및 상기 약학 조성물을 포함하는 제제
    30.
    发明授权
    4각 고리 질소 화합물, 이를 포함하는 우울증, 정신 질환, 조루증, 또는 신경병증성 통증의 예방 또는 치료용 약학 조성물, 및 상기 약학 조성물을 포함하는 제제 有权
    用于治疗或预防呕吐,精神疾病,预防性呕吐或包括其的神经病性疼痛的药物组合物和包含其的药物的四组分循环氮化合物

    公开(公告)号:KR101426408B1

    公开(公告)日:2014-08-07

    申请号:KR1020130017607

    申请日:2013-02-19

    CPC classification number: C07D205/04 C07D417/12

    Abstract: The present invention relates to a 4-membered cyclic nitrogen compound which can be used as a therapeutic agent or a preventive agent for depression, mental disease, premature ejaculation, or neuropathic pain by preventing re-uptake of certain neurotransmitters with high efficiency; a pharmaceutical composition which can inhibit serotonin and dopamine or norepinephrine re-uptake and has a high therapeutic or prophylactic effect against depression, mental disease, premature ejaculation, or neuropathic pain; and a pharmaceutical formulation comprising the same.

    Abstract translation: 本发明涉及一种4元环状氮化合物,其可以通过防止某些神经递质以高效率的再摄取而用作治疗剂或抑郁症,精神疾病,早泄或神经性疼痛的预防剂。 能够抑制5-羟色胺和多巴胺或去甲肾上腺素再吸收并对抑郁,精神疾病,早泄或神经性疼痛具有高治疗或预防作用的药物组合物; 和含有该制剂的药物制剂。

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