The present invention relates to N,N-dimethyl imidodicarbonimidic diamide acetate, a method of preparing the same and a pharmaceutical composition comprising the same, and more particularly, to N,N-dimethyl imidodicarbonimidic diamide acetate which is a crystalline acid addition salt prepared by reacting N,N-dimethyl imidodicarbonimidic diamide with acetic acid, and which is very effective as a therapeutic agent for treating metabolic syndromes that glycosuria and diabetes mellitus, obesity, hyperlipidemia, fatty liver, coronary heart disease, osteoporosis, polycystic ovarian syndrome, a cancer depleted of gene P53, etc. are complexly occurred; treating diabetes mellitus and preventing its complication; and treating a cancer and preventing myalgia, muscle cell cytotoxicity and rhabdomyolysis, etc. since the acid addition salt is excellent in physicochemical properties such as solubility, stability, non-hygroscopicity, anti-adhering property, etc., and low toxicity, a method of preparing the same and a pharmaceutical composition comprising the same.
本发明涉及N,N-二甲基
咪唑二
羧酸二
脲乙酸盐及其制备方法和包含其的药物组合物,更具体地,涉及一种通过将N,N-二甲基
咪唑二
羧酸二
脲与
乙酸反应制备的结晶酸加盐体,该加盐体在物理
化学性质如溶解度、稳定性、不吸湿性、抗粘附性等方面表现出色,毒性低,非常有效地治疗代谢综合症,如糖尿病、肥胖症、高脂血症、脂肪肝、冠心病、骨质疏松症、多囊卵巢综合症、缺乏P53
基因的癌症等复杂情况;治疗糖尿病及预防其并发症;以及治疗癌症和预防肌肉疼痛、肌细胞细胞毒性和横纹肌溶解等,因为该酸加盐体具有良好的物理
化学性质和低毒性,因此提供了一种制备该酸加盐体的方法和包含其的药物组合物。