Design of weakly basic thrombin inhibitors incorporating novel P1 binding functions: molecular and X-ray crystallographic studies.
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Design of weakly basic thrombin inhibitors incorporating novel P1 binding functions: molecular and X-ray crystallographic studies. Descriptor: 2-acetamido-2-deoxy-beta-D-glucopyranose, Alpha Thrombin, N4-(N,N-DIPHENYLCARBAMOYL)-AMINOGUANIDINE, ... Authors: De Simone, G, Menchise, V, Omaggio, S, Pedone, C, Scozzafava, A, Supuran, C.T. Deposit date: 2003-01-16 Release date: 2003-08-26 Last modified: 2024-11-13 Method: X-RAY DIFFRACTION (1.9 Å) Cite: DESIGN OF WEAKLY BASIC THROMBIN INHIBITORS INCORPORATING NOVEL P1 BINDING FUNCTIONS: MOLECULAR AND X-RAY CRYSTALLOGRAPHIC STUDIES Biochemistry, 42, 2003
含新型P1结合功能的弱碱性凝血酶抑制剂设计:分子与X射线晶体学研究。描述符:2-乙酰氨基-2-脱氧-β-D-吡喃葡萄糖、α-凝血酶(Alpha Thrombin)、N4-(N,N-二苯基氨基甲酰基)-氨基胍……。作者:德·西蒙尼(De Simone, G)、门奇塞(Menchise, V)、奥马焦(Omaggio, S)、佩多内(Pedone, C)、斯科扎法瓦(Scozzafava, A)、苏普兰(Supuran, C.T.)。提交日期:2003-01-16;发布日期:2003-08-26;最后修改日期:2024-11-13。实验方法:X射线衍射(分辨率1.9 Å)。引用文献:《含新型P1结合功能的弱碱性凝血酶抑制剂设计:分子与X射线晶体学研究》,《生物化学(Biochemistry)》,第42卷,2003年。
创建时间:
2003-01-16



