4(5)-腈甲基咪唑置于盐酸,水体系中,化学反应 44.0H,以59%的收率获得产物4-咪唑乙酸盐酸盐 参考文献:发现α-取代的咪唑-4-乙酸类似物作为新型一类对视网膜血管音有影响的ρ1γ-氨基丁酸a型受体拮抗剂 标题:发现α-取代的咪唑-4-乙酸类似物作为新型一类对视网膜血管音有影响的ρ1γ-氨基丁酸a型受体拮抗剂 摘要:含ρ的γ-氨基丁酸a型受体(gaba A Rs)在控制视觉信号中起重要作用.因此,选择性靶向这些gaba A R的配体是令人关注的.在这项研究中,我们证明了部分gaba A R激动剂咪唑-4-乙酸(iaa)能够在体内穿透血脑屏障.我们制备了一系列的α-和n-烷基化以及iaa的双环类似物,以研究该支架的结构-活性关系,重点是iaa的乙酸侧链.通过iaa制备从化合物升通过有效最小步合成组氨酸,以及它们的药理学性质进行了表征在天然大鼠gaba甲rs In A [3H]Muscimol Binding Assay And At Recombinant Human α1β2γ2S And ρ1 Gabaars Using The Flipr™ Membrane Potential Assay. The (+)‐α‐methyl‐ And α‐cyclopropyl‐substituted Iaa Analogues DOI:10.1002/cmdc.201600356
专利号:CN-1472215-A 优先权日:2002-07-30 标 题 :Synthesis of product prepared from imidazole acted with halogenated acetate ethyl ester
专利号:EA-014940-B1 优先权日:2005-08-25 标题 :Condensed Derivatives of Imidazole to Inhibit Aldosterone Synthesis and Aromatics
专利号:RU-2179975-C1 优先权日:1997-11-28 标题 :Derivatives of imidazole eliciting inhibitory activity with respect to farnesyltransferase, method of their synthesis, intermediate compounds, pharmaceutical composition
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合成参考文献
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