Abstract:
본 발명은 N,N-디메틸 이미도디카르본이미딕 디아미드의 신규한 디카르복실산염, 그의 제조방법 및 그의 약제학적 조성물에 관한 것이다. 더욱 상세하게는 N,N-디메틸 이미도디카르본이미딕 디아미드와 특정한 디카르복실산을 반응시켜 제조한 결정성 산부가염에 관한 것으로서 용해도, 안정성, 비흡습성, 부착방지특성 등의 물리화학적 성질이 더욱 개선될 뿐 아니라 독성이 낮아, 당뇨 및 당뇨병, 비만증, 고지혈증, 지방간, 관상 동맥 질환, 골다공증, 다낭성 난소증후군 등이 복합적으로 나타나는 이른바 대사성 증후군을 지닌 자들의 당뇨병 및 그의 합병증, p53 유전자가 결여된 암, 근육통, 근육세포독성 및 횡문근 융해 등의 예방 또는 치료에 필요한 N,N-디메틸 이미도디카르본이미딕 디아미드의 신규한 디카르복실산염, 그의 제조방법과 그의 약제학적 조성물에 관한 것이다. 메트포르민, 디카르복실산염, 아디핀산, 글루타르산, 말론산, 사과산, 당뇨병
Abstract:
PURPOSE: A pharmaceutical formulation containing simvastatin and olmesartan is provided to effectively treat hypertension and hyperlipidemia and prevent complication with less side effects. CONSTITUTION: A pharmaceutical formulation contains a immediate release compartment containing a simvastatin as a pharmacologically active ingredient, its isomer or its pharmaceutically acceptable salt, and a sustained release compartment containing olmesartan, its prodrug or its pharmaceutically acceptable salt. The olmesartan prodrug is olmesartan medoxomil. The sustained release compartment is coated containing osmotic regulator with semi-permeable film coating agent.
Abstract:
PURPOSE: A pharmaceutical formulation containing immediate release atorvastatin and sustained release olmesartan is provided to treat coronary artery disease and maximize body absorption of drug. CONSTITUTION: A pharmaceutical formulation contains immediate release compartment of atorvastatin and sustained release compartment of olmesartan. The olmesartan is its isomer, its pharmaceutically acceptable salt, or its prodrug. An olmesartan prodrug is olmesartan medoxomil.
Abstract:
PURPOSE: A pharmaceutical formulation for treating cardiovascular diseases is provided to uniformly maintain blood pressure and use for suppressing blood pressure when a hypertension patient sleeps. CONSTITUTION: A pharmaceutical formulation for treating cardiovascular disease contains immediate release compartment and sustained release compartment. The immediate release compartment contains an olmesartan as a pharmacologically active ingredient, its pharmaceutically acceptable salt or its prodrug. The sustained release compartment contains an amlodipine as a pharmacologically active ingredient, or its pharmaceutically acceptable salt.
Abstract:
A N,N-dimethyl imidodicarbonimidic diamide nicotinate is provided to improve manufacturing with low toxicity and prevent and treat diabetes and complication of diabetes. A metformin nicotinic acid salt is denoted by the chemical formula 1. In the chemical formula 1, n is 1 or 2. The metformin nicotinic acid salt is anhydrous or hydrous state. A method for manufacturing the metformin nicotinic acid salt comprises: a step of reacting 1-4 mole equivalent of inorganic base in sodium hydroxide or potassium hydroxide in water or organic solvent to produce metformin free base of the chemical formula 3; and a step of removing inorganic salt in the compound of the chemical formula 3 and reacting with 1-4 mole equivalent of nicotinic acid of the chemical formula 4. The organic solvent is methanole, ethanol, isopropanol, acetone, or acetonitrile. A pharmaceutical composition comprises the metformin nicotinic acid salt of the chemical formula 1 as an active ingredient.
Abstract:
Metformin dicarboxylate is provided to improve physical and chemical properties including solubility, stability, non-hygroscopicity and anti-adhesive properties, and low toxicity and to ensure effects in the prevention and treatment of not only diabetes and its complications in patients with so-called metabolic syndromes such as diabetes, obesity, hyperlipidemia, fatty liver, coronary artery disease, osteoporosis, and polycystic ovary syndromes. Metformin dicarboxylate is represented by the following formula 1, wherein X is -(CH2)n- (n = 1, 3 or 4) or -CH2-CH(OH)-. A method for preparing metformin dicarboxylate represented by the formula 1 comprises the steps of: allowing 2-4 molar equivalents of metformin hydrochloride of the following formula 2 to react with 2-4 molar equivalents of inorganic alkali in water, organic solvent or a mixture thereof to produce a metformin free-base of the following formula 3, and then allowing the metformin free-base to react with 1 molar equivalent of dicarboxylic acid of the following formula 4.
Abstract:
본 발명은 N,N-디메틸 이미도디카르본이미딕 디아미드의 니코틴산염, 그의 제조방법 및 그를 포함하는 약제학적 조성물에 관한 것으로서, 더욱 상세하게는 용해도, 안정성, 비흡습성, 정제 제형으로서의 가공성 등의 물리화학적 성질이 개선되었을 뿐 아니라, 독성이 낮고, N,N-디메틸 이미도디카르본이미딕 디아미드가 본질적으로 발휘하는 약화학적 특성인 당뇨 및 당뇨병, 비만증, 고지혈증, 지방간, 관상동맥질환, 골다공증, 다낭성 난소증후군 등이 복합적으로 나타나는 이른바 대사성 증후군을 지닌 자들의 당뇨병 치료, 당뇨병자의 합병증의 근본 핵심 원인 물질인 중성 지질 저하 작용에 의한 합병증 예방 및 치료 그리고 p53 유전자가 결여된 암, 근육통, 근육세포 독성 및 횡문근 융해의 예방 및 치료 효과를 더욱 증가시켜줄 수 있는 치료제로서 유� ��한 N,N-디메틸 이미도디카르본이미딕 디아미드의 니코틴산염, 그의 제조방법과 그의 약제학적 조성물에 관한 것이다. 메트포르민, 메트포르민 니코틴산염, 메트포르민 이니코틴산염, N,N-디메틸 이미도디카르본이미딕 디아미드, 니코틴산염, 결정성 산부가염, 당뇨병, 대사성증후군