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C3 amino-substituted chalcone derivative with selective adenosine rA1 receptor affinity in the micromolar range

机译：C3氨基取代的醌衍生物，具有在微摩尔范围内的选择性腺苷Ra1受体亲和力

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Helena D. Janse van Rensburg; Lesetja J. Legoabe; Gisella Terre’Blanche;
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1. 5'-Carbamoyl derivatives of 2'-C-methyl-purine nucleosides as selective A1 adenosine receptor agonists: affinity, efficacy, and selectivity for A1 receptor from different species. [J] . Cappellacci L, Franchetti P, Vita P, Bioorganic and medicinal chemistry . 2008,第1期

机译：2'-C-甲基-嘌呤核苷的5'-氨基甲酰基衍生物作为选择性的A1腺苷受体激动剂：对来自不同物种的A1受体的亲和力，功效和选择性。
2. N~6-Cycloalkyl- and N6-Bicycloalkyl-C5'(C2')-modified Adenosine Derivatives as High-Affinity and Selective Agonists at the Human A_1 Adenosine Receptor with Antinociceptive Effects in Mice [J] . Palmarisa Franchetti, Loredana Capellacci, Patrizia Vita, Journal of Medicinal Chemistry . 2009,第8期

机译：N〜6-环烷基-和N6-双环烷基-C5'（C2'）修饰的腺苷衍生物作为高亲和力和选择性激动剂在人A_1腺苷受体上具有抗伤害感受性的小鼠。
3. N-6-Cycloalkyl- and N-6-Bicycloalkyl-C5 '(C2 ')-modified Adenosine Derivatives as High-Affinity and Selective Agonists at the Human A(1) Adenosine Receptor with Antinociceptive Effects in Mice (vol 52, pg 2393, 2009) [J] . Franchetti P, Cappellacci L, Vita P, Journal of Medicinal Chemistry . 2009,第10期

机译：N-6-环烷基-和N-6-双环烷基-C5'（C2'）修饰的腺苷衍生物作为高亲和力和选择性激动剂在人A（1）腺苷受体上对小鼠具有镇痛作用（第52卷，第2393页），2009）
4. The selective antagonism of A2A adenosine receptors prevents synaptic failure induced by oxygen and glucose deprivation in rat dentate gyrus [C] . Maraulaa G., Trainia C., Mellob T., European Congress of Pharmacology . 2012

机译：A2A腺苷受体的选择性拮抗剂可防止氧气牙齿诱导的氧气失败和葡萄糖剥夺的突触失败
5. The structural basis of chemokine binding affinity and receptor selectivity: Role of receptor N-terminal domain [D] . Ravindran, Aishwarya 2010

机译：趋化因子结合亲和力和受体选择性的结构基础：受体N末端结构域的作用
6. 2-Substituted adenosine derivatives: affinity and efficacy at four subtypes of human adenosine receptors [O] . Zhan-Guo Gao, Liaman K. Mamedova, Peiran Chen, -1

机译：2-取代的腺苷衍生物：对人类腺苷受体的四种亚型的亲和力和功效
7. N6-Cycloalkyl- andN6-Bicycloalkyl-C5′(C2′)-modified Adenosine Derivatives as High-Affinity and Selective Agonists at the Human A1Adenosine Receptor with Antinociceptive Effects in Mice [O] . Palmarisa Franchetti, Loredana Cappellacci, Patrizia Vita, 2009

机译：N6-环烷基-NANDN6-双环烷基-C5'（C2'） - 改性腺苷衍生物作为人A1腺苷受体的高亲和力和选择性激动剂，在小鼠中具有抗肤质作用
8. Short-Term Desensitization of Muscarinic Cholinergic Receptors in Mouse Neuroblastoma Cells: Selective Loss of Agonist Low-Affinity and Pirenzepine High-Affinity Binding Sites [R] . Cioffi, C. L., El-Fakahany, E. E. 1986

机译：小鼠神经母细胞瘤细胞中毒蕈碱胆碱能受体的短期脱敏：激动剂低亲和力和哌仑西平高亲和力结合位点的选择性丧失

C3 amino-substituted chalcone derivative with selective adenosine rA1 receptor affinity in the micromolar range

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