机译:通过有效的α-酮杂环衍生物从蒙特卡洛模拟中阐明脂肪酸酰胺水解酶的抑制作用
Contribution from the Department of Chemistry,Yale University,225 Prospect Street, New Haven,Connecticut 06520-8107,and Department of Chemistry and the Skaggs Institute for Chemical Biology,The Scripps Research Institute,10550 North Torrey Pines Road;
Contribution from the Department of Chemistry,Yale University,225 Prospect Street, New Haven,Connecticut 06520-8107,and Department of Chemistry and the Skaggs Institute for Chemical Biology,The Scripps Research Institute,10550 North Torrey Pines Road;
Contribution from the Department of Chemistry,Yale University,225 Prospect Street, New Haven,Connecticut 06520-8107,and Department of Chemistry and the Skaggs Institute for Chemical Biology,The Scripps Research Institute,10550 North Torrey Pines Road;
机译:探索α-酮杂环酶抑制剂的基本取代作用:脂肪酸酰胺水解酶的强效和选择性抑制剂。
机译:发现了一种有效,具有选择性和有效作用的可作为止痛剂的脂肪酸酰胺水解酶可逆性α-酮杂环化合物抑制剂。
机译:通过QM / MM模拟阐明脂肪酸酰胺水解酶及其Lys142Ala变体的水解机理
机译:酰胺交换反应的动力学研究:蒙特卡洛模拟
机译:I.脂肪酸酰胺水解酶的α-酮杂环抑制剂中心杂环的优化和分析。二。氯肽II(complestatin)的全合成,并向第二代氯肽I和II的全合成方向发展。
机译:发现尿嘧啶衍生物作为脂肪酸酰胺水解酶的强抑制剂
机译:来自蒙特卡罗模拟的有效的A-酮环衍生物阐明脂肪酸酰胺水解酶抑制作用