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    • 5. 发明授权
    • 오보바톨 및 그 합성 유도체들을 유효성분으로 함유하는 당뇨와 대사증후군 질환 예방 및 치료용 조성물
    • 用于治疗含有OBOVATOL及其合成衍生物的糖尿病和代谢综合征的组合物
    • KR100909572B1
    • 2009-07-24
    • KR1020080113991
    • 2008-11-17
    • 주식회사 티지 바이오텍한국생명공학연구원
    • 허태린송희복김지은권병목한동초김혜난
    • A61K31/085A61K31/05A61P3/10
    • A61K31/085A23L2/52A23L33/10A23L33/15A23L33/16A61K9/145A61K9/1623A61K9/2018A61K9/4858A61K31/215
    • A pharmaceutical composition containing obovatol and its derivatives is provided to enhance the activity of AMPK(AMP-activated protein kinase) which acts pivotal role in diabetes and metabolic diseases and treat diabetes and metabolic diseases. A pharmaceutical composition for preventing or treating diabetes comprises an obovatol of chemical formula 1 and its derivative as an active ingredient. In the chemical formula 1, R1 and R2 is hydrogen, straight or branched alkyl of C1-C7, acetyl or alkoxyacetyl of C1-C7; R3 is hydrogen, straight or branched alkyl of C1-C7, alkenyl of C2-C7 or aryl. R1 and R2 is independently or selectively methyl, ethyl, acetyl, methoxy, ethoxy, methoxyacetyl or ethoxyacetyl; and R3 is hydrogen, propyl, prophenyl or arlyl. The pharmaceutical composition further comprises a pharmaceutically allowable carrier, excipient, and diluents. The composition is used in a form of powder, granule, tablet, capsule, suspension, emulsion, syrup, oral formulation of aerosol, suppository or sterilization injection solution.
    • 提供含有obovatol及其衍生物的药物组合物,以增强在糖尿病和代谢疾病中发挥关键作用并治疗糖尿病和代谢疾病的AMPK(AMP活化蛋白激酶)的活性。 用于预防或治疗糖尿病的药物组合物包含化学式1的低聚异戊二醇及其衍生物作为活性成分。 在化学式1中,R 1和R 2是氢,C1-C7的直链或支链烷基,C1-C7的乙酰基或烷氧基乙酰基; R3是氢,C1-C7的直链或支链烷基,C2-C7或芳基的烯基。 乙烯基,乙酰基,甲氧基,乙氧基,甲氧基乙酰基或乙氧基乙酰基; 和R3是氢,丙基,苯基或芳基。 药物组合物还包含药学上可允许的载体,赋形剂和稀释剂。 该组合物以粉末,颗粒,片剂,胶囊,悬浮液,乳液,糖浆,气雾剂,栓剂或灭菌注射液的口服制剂的形式使用。
    • 6. 发明公开
    • HGF 활성을 가지는 c-Met에 대한 인간항체 및 이의 용도
    • C-MET定位具有HGF活性的全身激动人体抗体及其用途
    • KR1020120134938A
    • 2012-12-12
    • KR1020110054177
    • 2011-06-03
    • 한국생명공학연구원주식회사 와이바이오로직스
    • 박영우조기원박찬웅유석호장명희김혜난윤선하조규원박미라
    • C07K16/22C12N15/13A61K39/395A61P25/28
    • C07K16/2863A61K2039/505C07K2317/21C07K2317/622C07K2317/75C07K2317/92C07K2317/94
    • PURPOSE: A human antibody which is derived from human body and specifically binds to c-Met is provided to treat neuronal infarction, progressive nephropathy, liver cirrhosis, lung fibrosis, kidney, liver, lung injury, and ulcerative wound which are cured by HGF or c-Met activation. CONSTITUTION: A human antibody contains a complementarity determining region (CDR) and framework region(FR) which are derived from human and specifically binds to c-Met. The human antibody contains: a heavy chain variable region containing heavy chain CDR1 of sequence number 1, heavy chain CDR2 of sequence number 2, and heavy chain CDR3 of sequence number 3; and a light chain variable region containing light chain CDR1 of sequence number 4, light chain CDR2 of sequence number 5, and light chain CDR3 of sequence number 6. The antibody contains a heavy chain variable region amino acid of sequence number 7 and a light chain variable region amino acid of sequence number 8. The human antibody is glycosylated or/and PEGylated. A composition for wound healing contains the human antibody as an active ingredient and pharmaceutically acceptable carrier. A composition for treating neurodegenerative diseases contains the human antibody as an active ingredient and pharmaceutically acceptable carrier.
    • 目的:提供从人体衍生并特异性结合c-Met的人类抗体,用于治疗由HGF或其他物质固化的神经元梗死,进行性肾病,肝硬化,肺纤维化,肾脏,肝脏,肺损伤和溃疡性伤口 c-Met激活。 构成:人抗体含有衍生自人体并且特异性结合c-Met的互补决定区(CDR)和框架区(FR)。 人抗体包含:含有序列号1的重链CDR1,序列号2的重链CDR2和序列号3的重链CDR3的重链可变区; 和含有序列号4的轻链CDR1,序列号5的轻链CDR2和序列号6的轻链CDR3的轻链可变区。抗体含有序列号7的重链可变区氨基酸和轻链 可变区氨基酸序列号8.人抗体是糖基化的或/和聚乙二醇化的。 用于伤口愈合的组合物包含人抗体作为活性成分和药学上可接受的载体。 用于治疗神经变性疾病的组合物含有人抗体作为活性成分和药学上可接受的载体。