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    • 72. 发明公开
    • N1-(펜에틸)-N2-치환된 바이구아나이드 유도체, 이의 제조방법 및 이를 유효성분으로 함유하는 약학 조성물
    • N1-(苯乙烯)-N取代的双胍衍生物,其制备方法和包含该化合物的药物组合物
    • KR1020110053837A
    • 2011-05-24
    • KR1020090110521
    • 2009-11-16
    • 한올바이오파마주식회사한국화학연구원
    • 김성욱전성수오병규강민석천혜경김광록이상달정원훈이종철
    • C07C279/26C07C277/04A61K31/155A61P3/10
    • PURPOSE: An N1-(phenethyl)-N2-substituted biguanide derivative is provided to ensure excellent blood glucose drop action and lipid lowering action even with a little dosage compared existing drug and to enable use for the treatment of diabetes, obesity, hyperlipidemia, hypercholesterolemia, steatosis, coronary artery disease, osteoporosis, polycystic ovarian syndrome, metabolic syndrome, cancer etc. CONSTITUTION: A compound or pharmaceutically acceptable salts are represented by chemical formula 1. In chemical formula 1, R is C1-12 alkyl, C1-12 alkenyl or C1-12 alkynyl substituted or unsubstituted with one or more substituents selected from C3-8 cycloalkyl and C5-12 aryl; C3-8 cycloalkyl substituted or unsubstituted with one or more substituents selected from halogen, hydroxyl, C1-6 alkyl, C1-6 alkenyl, C1-6 alkynyl, C1-6 alkoxy and C5-12 aryl; and C5-12 aryl substituted or unsubstituted with one or more substituents selected from halogen, hydroxyl, C1-6 alkyl, C1-6 alkenyl, C1-6 alkynyl, C1-6 alkoxy and C3-8 cycloalkyl.
    • 目的:提供N1-(苯乙基)-N2-取代双胍衍生物,以确保优异的血糖降低作用和降脂作用,即使与现有药物相比,用量少,可用于治疗糖尿病,肥胖,高脂血症,高胆固醇血症 ,脂肪变性,冠状动脉疾病,骨质疏松症,多囊卵巢综合征,代谢综合征,癌症等。构成:化学式1表示化合物或其药学上可接受的盐。在化学式1中,R是C 1-12烷基,C 1-12链烯基 或被一个或多个选自C 3-8环烷基和C 5--12芳基的取代基取代或未取代的C1-12炔基; 羟基,C 1-6烷基,C 1-6烯基,C 1-6炔基,C 1-6烷氧基和C 5-12芳基的取代或未取代的C 3-8环烷基; 和被选自卤素,羟基,C 1-6烷基,C 1-6烯基,C 1-6炔基,C 1-6烷氧基和C 3-8环烷基的一个或多个取代基取代或未取代的C 5-12芳基。
    • 73. 发明公开
    • 변형된 인간 트롬보포이에틴 폴리펩타이드 절편 및 그의 제조방법
    • 改性人类血小板聚糖片段及其制备方法
    • KR1020100085879A
    • 2010-07-29
    • KR1020100005348
    • 2010-01-20
    • 한올바이오파마주식회사
    • 김성욱전성수박승국정재갑이성률송연정심원조
    • C07K14/505C12N15/12C12N15/63A61K38/17
    • C07K14/515A61K38/196Y02A50/473
    • PURPOSE: A mutated human thrombopoietin polypeptide fragment is provided to ensure platelet proliferation ability in vivo and in vitro and improved resistance to protease in vivo. CONSTITUTION: A human thrombopoietin polypeptide fragment contains mutated or substituted amino acid at 3rd, 6th, 8-12th, 14-18th, 20-23th, 25th, 26th, 31-34th, 39-41th, 43-46th, 48-52th, 55-57th, 56th, 60th, 62th, 64-67th, 69-79th, 81th, 86th, 89-91th, 93th, 95th, 97-104th, 107-109th, 112th, 116th, 117th, 120-123th, 126th, 128th, 129th, 131th, 133-147th, 150th, or 152th amino acid. A pharmaceutical formulation contains mutated TPO fragment having the mutated amino acid. A pharmaceutical composition for preventing or treating thrombocytopenia or diseases caused by thrombocytopenia contains the mutated TPO fragment.
    • 目的:提供突变的人血小板生成素多肽片段,以确保体内和体外的血小板增殖能力,并提高体内对蛋白酶的抗性。 构成:人血小板生成素多肽片段在第3,6,6,8,12,14,18,20-23,25,26,31-34,49-41,43-46,48-52,含有突变或取代的氨基酸, 第55-57号,第56号,第六十六次,第六十六次,第六十六次,第六十六次,第六次,第六次,第六次,第六次,第六十六次,第六十七次,第六十六次, 第128位,第129位,第131位,第133-147位,第150位或第152位氨基酸。 药物制剂含有具有突变的氨基酸的突变的TPO片段。 用于预防或治疗由血小板减少症引起的血小板减少症或疾病的药物组合物含有突变的TPO片段。
    • 77. 发明公开
    • 약제학적 제제
    • 药物制剂
    • KR1020090114328A
    • 2009-11-03
    • KR1020090037380
    • 2009-04-29
    • 한올바이오파마주식회사
    • 김성욱전성수이아람최진원
    • A61K9/22A61K9/52A61K47/38A61P9/12
    • A61K45/06
    • PURPOSE: A pharmaceutical formulation containing atorvastatin and irbesartan is provided to effectively prevent and treat hypertension, hyperlipidemia and their complication. CONSTITUTION: A pharmaceutical formulation of which release is controlled comprises a immediate release compartment containing atorvastatin as a pharmacologically active ingredient, its pharmaceutically acceptable salt, or its isomer, and a sustained release compartment containing irbesartan as pharmacologically active ingredient, its pharmaceutically acceptable salt or its isomer. The sustained release compartment contains osmosis controlling agent and is coated with semi-permeable coating substrate. The pharmaceutical formulation is used in the form of matrix.
    • 目的:提供含阿托伐他汀和厄贝沙坦的药物制剂,以有效预防和治疗高血压,高脂血症及其并发症。 构成:释放被控制的药物制剂包括含有阿托伐他汀作为药理学活性成分的立即释放隔室,其药学上可接受的盐或其异构体,以及含有厄贝沙坦作为药理学活性成分的缓释隔室,其药学上可接受的盐或其 异构体。 持续释放隔间含有渗透控制剂,并涂有半透性涂层基材。 药物制剂以基质的形式使用。
    • 78. 发明公开
    • 심혈관계 질환 치료용 약제학적 제제
    • 用于治疗心血管疾病的药物制剂
    • KR1020090114321A
    • 2009-11-03
    • KR1020090037373
    • 2009-04-29
    • 한올바이오파마주식회사
    • 김성욱전성수구자성김진욱남태영
    • A61K9/22A61K9/28A61P9/12A61K47/38
    • A61K45/06
    • PURPOSE: A pharmaceutical formulation containing simvastatin and valsartan as pharmacologically active ingredient is provided to enhance drug efficiency with reduced side effects. CONSTITUTION: A pharmaceutical formulation contains an immediate release compartment containing simvastatin as a pharmacologically active ingredient, its isomer or its pharmaceutically acceptable salt and a sustained release compartment containing valsartan as a pharmacologically active ingredient, its isomer or its pharmaceutically acceptable salt. The valsartan is released two hour after releasing of simvastatin. The pharmaceutical formulation is used in the form of particle, granule, pellet, tablet of sustained release compartment and capsule containing particle, granule, pellet, or tablet of immediate release compartment.
    • 目的:提供含有辛伐他汀和缬沙坦作为药理活性成分的药物制剂,以提高药物效率,减少副作用。 构成:药物制剂包含含有辛伐他汀作为药理活性成分,其异构体或其药学上可接受的盐的缓释隔室和含有缬沙坦作为药理学活性成分,其异构体或其药学上可接受的盐的缓释隔室。 释放辛伐他汀后两小时释放缬沙坦。 药物制剂以颗粒,颗粒,丸剂,持续释放隔间的片剂和含有颗粒,颗粒,丸剂或立即释放隔间的片剂的形式使用。