Cl-IB-MECA 3'-氟类似物作为腺苷A3受体配体的合成。

Moon Woo Chun, Moo Hong Lim, Hyung Ryong Moon, Hea Ok Kim, Kenneth A Jacobson, Lak Shin Jeong
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引用次数: 0

摘要

选择性强效腺苷A3受体激动剂Cl-IB-MECA的3′-氟类似物1是由d -木糖通过高区域选择性的氟阴离子打开环氧乙烷4合成的。与Cl-IB-MECA对A3腺苷受体的高结合亲和力相比,相应的3′-氟衍生物的结合亲和力明显降低,说明3′-羟基与A3腺苷受体结合时是氢键供体,而不是氟原子那样的氢键受体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis of 3'-fluoro analogue of Cl-IB-MECA as adenosine A3 receptor ligand.

3'-Fluoro analogue 1 of selective and potent adenosine A3 receptor agonist, Cl-IB-MECA was synthesized from D-xylose via highly regioselective opening of lyxo-epoxide 4 with fluoride anion. Compared to the high binding affinity of Cl-IB-MECA to the A3 adenosine receptor, the corresponding 3'-fluoro derivative showed remarkably decreased binding affinity, indicating that 3'-hydroxyl group acts as hydrogen bonding donor, not hydrogen bonding acceptor like fluorine atom in binding to the A3 adenosine receptor.

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