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机译:新型哌啶衍生物作为高亲和力LS -ACHBP配体具有α7NACHR活动的新型哌啶衍生物的发现
School of Pharmacy Fudan University;
School of Pharmacy Fudan University;
School of Pharmacy Fudan University;
School of Pharmacy Fudan University;
School of Pharmacy Fudan University;
School of Pharmacy Fudan University;
School of Pharmacy Fudan University;
School of Pharmacy Fudan University;
School of Pharmacy Fudan University;
School of Pharmacy Fudan University;
School of Pharmacy Fudan University;
School of Pharmacy Fudan University;
School of Pharmacy Fudan University;
School of Pharmacy Fudan University;
School of Pharmacy Fudan University;
School of Pharmacy Fudan University;
School of Pharmacy Fudan University;
Piperidine derivatives; Ls-AChBP; Cocrystallization; α7 nAChR; Molecular docking;
机译:新型哌啶衍生物作为高亲和力LS -ACHBP配体具有α7NACHR活动的新型哌啶衍生物的发现
机译:6-芳基-6H-吡咯并(3,4-d)哒嗪衍生物的合成和生物学评估:电压门控钙通道的alpha2delta亚基的高亲和力配体。
机译:合成和生物学评估的6-芳基-6H-吡咯并(3,4-d)哒嗪衍生物作为电压门控钙通道的α(2)δ亚基的高亲和力配体。
机译:基于FKBP12结构的药物发现:作为神经免疫亲和素配体的L-1,4-噻嗪-3-羧酸衍生物的设计,合成和评估
机译:合成和评估新型N-烷基胺衍生物作为高亲和力sigma-1受体配体。
机译:新型哌啶衍生物作为乙酰胆碱结合蛋白配体的发现合成生物学评估和基于结构的优化
机译:新型嘧啶衍生物的合成与生物学评价,作为GALR2的亚微摩尔亲和配体