醋酸依替巴肽用途
Eptifibatide, also co-promoted by Schering-Plough/Essex, is an antiplatelet drug of the glycoprotein IIb/IIIa inhibitor class. Eptifibatide is a cyclic heptapeptide derived from a protein found in the venom of the southeastern pygmy rattlesnake (Sistrurus miliarius barbouri). It belongs to the class of the arginin-glycin-aspartat-mimetics and reversibly binds to platelets. Eptifibatide has a short half-life. The drug is the third inhibitor of GPIIb/IIIa that has found broad acceptance after the specific antibody abciximab and the non-peptide tirofiban entered the global market.
1、产品物理参数:
2、醋酸依替巴肽物理化学性质
密度
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1.6±0.1 g/cm3
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熔点
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92-98 °C
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分子式
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C35H49N11O9S2
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分子量
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831.962
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精*确质量
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831.315613
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PSA
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374.49000
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LogP
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-4.84
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折射率
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1.735
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分子结构
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1、摩尔折射率:208.03
2、摩尔体积(cm3/mol):518.4
3、等张比容(90.2K):1530.5
4、表面张力(dyne/cm):75.9
5、介电常数:无可用的
6、极化率(10-24cm3):82.47
7、单一同位素质量:831.315612 Da
8、标称质量:831 Da
9、平均质量:831.9619 Da
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计算化学
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1.疏水参数计算参考值(XlogP):-2.4
2.氢键供体数量:10
3.氢键受体数量:12
4.可旋转化学键数量:10
5.互变异构体数量:1000
6.拓扑分子极性表面积377
7.重原子数量:57
8.表面电荷:0
9.复杂度:1520
10.同位素原子数量:0
11.确定原子立构中心数量:0
12.不确定原子立构中心数量:5
13.确定化学键立构中心数量:0
14.不确定化学键立构中心数量:0
15.共价键单元数量:1
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3、醋酸依替巴肽英文别名
n6-(aminoiminomethyl)-n2-(3-mercapto-1-oxopropyl-l-lysylglycyl-l-a-aspartyl-l-tryptophyl-l-prolyl-l-cysteinamide
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7H-Pyrrolo[2,1-g][1,2,5,8,11,14,17,20]dithiahexaazacyclotricosine-17-acetic acid, 3-(aminocarbonyl)-11-[4-[(aminoiminomethyl)amino]butyl]docosahydro-20-(1H-indol-3-ylmethyl)-1,9,12,15,18,21-hexaoxo-
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Mpr-Harg-Gly-Asp-Trp-Pro-Cys-NH2,( Disulfide Bridge:1-7)
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EFTIFIBATIDE
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MAP-LYS-GLY-ASP-TRP-PRO-CYS-NH2
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MFCD05662245
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[11-(4-Carbamimidamidobutyl)-3-carbamoyl-20-(1H-indol-3-ylmethyl)-1,9,12,15,18,21-hexaoxodocosahydro-7H-pyrrolo[2,1-g][1,2,5,8,11,14,17,20]dithiahexaazacyclotricosin-17-yl]acetic acid
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Mpr-Harg-Gly-Asp-Trp-Pro-Cys-NH2,( Disulfide Bridg on Mpr and Cys)
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Eptifitide
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INTEGRELIN
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Eptifibatide Acetate
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7H-pyrrolo[2,1-g][1,2,5,8,11,14,17,20]dithiahexaazacyclotricosine-17-acetic acid, 3-(aminocarbonyl)-11-[4-[(diaminomethylene)amino]butyl]docosahydro-20-(1H-indol-3-ylmethyl)-1,9,12,15,18,21-hexaoxo-
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