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    신경보호제로서의 유레아 유도체
    5.
    发明公开
    신경보호제로서의 유레아 유도체 有权
    尿素类似物作为神经保护剂

    公开(公告)号：KR1020130115696A

    公开(公告)日：2013-10-22

    申请号：KR1020120038239

    申请日：2012-04-13

    Applicant: 한국과학기술연구원

    Inventor： 추현아 ,  배애님 ,  김지윤 ,  박병건 ,  이지연 ,  노은주 ,  박정은 ,  라현화

    IPC: C07D211/42 ,  C07D241/28 ,  A61K31/44 ,  A61P25/00

    Abstract: PURPOSE: A urea derivative is provided to selectively suppress the action of mPTP in the brain, thereby being used as a neuroprotective agent which improves the action of the mitochondria. CONSTITUTION: A urea derivative is denoted by chemical formula 1. A method for preparing the urea derivative comprises the steps of making a compound of chemical formula 2 react with isocyanate compounds or isothiocyanate compounds. The compound of chemical formula 2 is prepared by making a compound of chemical formula 3 react with benzyl halide compounds. A pharmaceutical composition for suppressing the action of mPTP contains the urea derivative or a pharmaceutically acceptable salt thereof as an active ingredient. A pharmaceutical composition for treating nervous diseases contains the urea derivative or a pharmaceutically acceptable salt thereof as an active ingredient.

    Abstract translation: 目的：提供尿素衍生物以选择性抑制脑中mPTP的作用，从而用作改善线粒体作用的神经保护剂。 构成：以化学式1表示脲衍生物。制备尿素衍生物的方法包括使化学式2的化合物与异氰酸酯化合物或异硫氰酸酯化合物反应的步骤。 通过使化学式3的化合物与苄基卤化合物反应来制备化学式2的化合物。 用于抑制mPTP作用的药物组合物含有尿素衍生物或其药学上可接受的盐作为活性成分。 用于治疗神经疾病的药物组合物含有尿素衍生物或其药学上可接受的盐作为活性成分。

    뇌암 예방 또는 치료용 조성물
    6.
    发明公开
    뇌암 예방 또는 치료용 조성물 无效
    用于预防或治疗脑癌的组合物

    公开(公告)号：KR1020090084149A

    公开(公告)日：2009-08-05

    申请号：KR1020080010155

    申请日：2008-01-31

    Applicant: 한국과학기술연구원

    Inventor： 이창준 ,  노은주 ,  최진규 ,  한경석 ,  박정은 ,  강상수

    IPC: A61K31/522 ,  A61K31/52 ,  A61P35/00

    CPC classification number: A61K31/522

    Abstract: A composition which contains caffeine, its analog, or its pharmaceutically allowable salt is provided to suppress infiltration, metastasis, and proliferation and prevent and/or treat brain cancer. A composition for preventing and treating brain cancer comprises caffeine, caffeine anaolog, or its pharmaceutically allowable salt as an active ingredient. The caffeine, caffeine analog or its pharmaceutically allowable salt has the content of 0.3-30 mM. The daily dose of the composition is 1-5 mg/kg and the composition is administered at one time or several times. The brain cancer is glioma, exothelioma, pituitary adenoma, schwannoma, craniopharyngioma or the congenital brain tumor. The composition selectively block the subtype 3 of activation of inositol-1,4,5-triphosphate receptoer(IP3R).

    Abstract translation: 提供含有咖啡因，其类似物或其药学上可允许的盐的组合物以抑制浸润，转移和增殖，并预防和/或治疗脑癌。 用于预防和治疗脑癌的组合物包括咖啡因，咖啡因厌氧菌或其药学上可允许的盐作为活性成分。 咖啡因，咖啡因类似物或其药学上允许的盐的含量为0.3-30mM。 组合物的日剂量为1-5mg / kg，组合物一次或多次施用。 脑癌是神经胶质瘤，外皮瘤，垂体腺瘤，神经鞘瘤，颅咽管瘤或先天性脑瘤。 组合物选择性阻断肌醇-1,4,5-三磷酸盐受体（IP3R）的活化亚型3。

    Ｔ형 칼슘 채널 저해작용을 가지는 신규 1-(4-할로페닐 옥소 또는 싸이오)-3-(4-치환피페라진-1-일)프로판-2올 유도체 또는 이의 약학적으로 허용 가능한 염, 이의 제조방법 및 이를 유효성분으로 하는 약학적 조성물
    9.
    发明公开
    Ｔ형 칼슘 채널 저해작용을 가지는 신규 1-(4-할로페닐 옥소 또는 싸이오)-3-(4-치환피페라진-1-일)프로판-2올 유도체 또는 이의 약학적으로 허용 가능한 염, 이의 제조방법 및 이를 유효성분으로 하는 약학적 조성물 无效
    新型1-（4-戊烯基氧基或硫代）-3-（4-取代的哌嗪-1-基）丙烷-2-醇衍生物，其具有T型钙通道抑制活性或药物可接受的盐，其制备方法和药物组合物包含 同样作为活跃成分

    公开(公告)号：KR1020120066699A

    公开(公告)日：2012-06-25

    申请号：KR1020100093304

    申请日：2010-09-27

    Applicant: 한국과학기술연구원

    Inventor： 노은주 ,  박정은 ,  지완근 ,  신계정 ,  배애님 ,  최경일 ,  김동진 ,  금교창

    IPC: C07D295/033 ,  A61K31/495 ,  A61P25/08 ,  A61P9/12

    Abstract: PURPOSE: A pharmaceutical composition containing a novel 1-(4-halophenyl oxo or thio)-3-(4-substituted piperazine-1-yl)propane-2-ol derivative is provided to effectively suppress T type calcium channel activation and to prevent or treat hypertension, cancer, epilepsy, and neurogenic pain. CONSTITUTION: A novel 1-(4-halophenyl oxo or thio)-3-(4-substituted piperazine-1-yl)propan-2-ol derivative is denoted by chemical formula 1. A method for preparing the compound of chemical formula 1 comprises: a step of reacting a compound of chemical formula 2 with chiral epichlorohydrin under the presence of a base and solvent to prepare an epoxy compound of chemical formula 3; and a step of reacting the epoxy compound of chemical formula 3 with piperazine derivative of chemical formula 4. The base is potassium carbonate, sodium carbonate or pyridine. A pharmaceutical composition for preventing or treating diseases caused by overactivation of T type calcium channel contains the derivative or pharmaceutically acceptable salt thereof as an active ingredient.

    Abstract translation: 目的：提供含有新型1-（4-卤代苯基氧代或硫代）-3-（4-取代哌嗪-1-基）丙-2-醇衍生物的药物组合物，以有效抑制T型钙通道激活和预防 或治疗高血压，癌症，癫痫和神经源性疼痛。 构成：化学式1表示新的1-（4-卤代苯基氧代或硫代）-3-（4-取代哌嗪-1-基）丙-2-醇衍生物。一种制备化学式1化合物的方法 包括：在碱和溶剂的存在下使化学式2的化合物与手性表氯醇反应以制备化学式3的环氧化合物的步骤; 和使化学式3的环氧化合物与化学式4的哌嗪衍生物反应的步骤。碱是碳酸钾，碳酸钠或吡啶。 用于预防或治疗由T型钙通道过度活化引起的疾病的药物组合物含有其衍生物或药学上可接受的盐作为活性成分。

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