首页> 外文会议>Chinese international peptide symposium >Evaluation of the Bioequivalence of the 20 mg /10 ml Doses of Two Injectable Preparations of Eptifibatide: A Randomized, Open-Label, Two-Period Crossover Study in Healthy Adult Male Chinese Volunteers
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Evaluation of the Bioequivalence of the 20 mg /10 ml Doses of Two Injectable Preparations of Eptifibatide: A Randomized, Open-Label, Two-Period Crossover Study in Healthy Adult Male Chinese Volunteers

机译:评价20mg / 10ml的两种可注射制剂的20mg / 10ml剂量的两种可注射制剂:在健康成年男性志愿者中随机,开放标签,双周交叉研究

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@@ Eptifibatide is a small, synthetic, cyclic heptapeptide, containing six amino acids and one mercaptopropionyl (des-amino cysteinyl) residue. Chemically it is N6-(aminoiminomethyl)-N2-(3-mercapto-1 -oxopropyl-L-lysylglycyl-L-a-aspartyl-L-tryptophyl-L-prolyl-L-cysteinamide, cyclic disulfide). It inhibits platelet function in a dose-specific fashion by reversibly binding the platelet GP Hb/Ⅲa receptor,[1] which is the aim target for the treatment of patients with coronary syndrome[1,2].
机译:@@ ePtifibatide是一种小,合成的环状肽,含有六个氨基酸和一个巯基丙基(DES-氨基胱烯基)残基。化学上是N6-(氨基氨基甲基)-N2-(3-巯基-1-氧丙基-L-溶甘氨酸-1-α-甘氨酸-L-L-溶氨基-1-吡啶基-1-胱氨酸甲酰胺,环二硫化物)。它通过可逆地结合血小板GP HB /ⅢA受体来抑制血小板函数以剂量特异性的方式,[1],[1]是治疗冠状动脉综合征患者的目标靶标[1,2]。

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