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Truncated (N)-Methanocarba Nucleosides as Partial Agonists at Mouse and Human A3 Adenosine Receptors: Affinity Enhancement by N6(2-Phenylethyl) Substitution

机译：截短的（n）-methanocarba核苷作为小鼠和人A3腺苷受体的局部激动剂：N6（2-苯基乙基）取代的亲和增强

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1. Truncated (N)-Methanocarba Nucleosides as Partial Agonists at Mouse and Human A(3) Adenosine Receptors: Affinity Enhancement by N-6-(2-Phenylethyl) Substitution [J] . Tosh Dilip K., Salmaso Veronica, Rao Harsha, Journal of Medicinal Chemistry . 2020 ,第8期

机译：截短（n）-methanocarba核苷作为小鼠和人A（3）腺苷受体的部分激动剂：N-6-（2-苯基乙基）取代的亲和增强
2. N6,5'-Disubstituted adenosine derivatives as partial agonists for the human adenosine A3 receptor. [J] . van Tilburg-EW, von Frijtag-Drabbe-Kunzel-J, de Groote-M, Journal of Medicinal Chemistry . 1999 ,第8期

机译：N6,5'-二取代的腺苷衍生物作为人腺苷A3受体的部分激动剂。
3. 2-Substituted N-ethylcarboxamidoadenosine derivatives as high-affinity agonists at human A3 adenosine receptors. [J] . Klotz KN, Camaioni E, Volpini R, Naunyn-Schmiedeberg's Archives of Pharmacology . 1999 ,第2期

机译：2-取代的N-乙基羧酰胺基腺苷衍生物作为对人A3腺苷受体的高亲和力激动剂。
4. QSAR Analysis of Human Adenosine A3 Receptor Antagonists [C] . QIAO Kang, ZENG Ling-Xiao, JIN Hong-Wei, International conference of molecular simulations and applied informatics technologies . 2012

机译：人腺苷A3受体拮抗剂的QSAR分析
5. A3 adenosine receptor-mediated suppression of pro-inflammatory functions of mouse bone marrow neutrophils through inhibition of Rac. [D] . van der Hoeven, Dharini. 2009

机译：通过抑制Rac，A3腺苷受体介导的小鼠骨髓中性粒细胞促炎功能的抑制。
6. Truncated (N)-Methanocarba Nucleosides as A1 Adenosine Receptor Agonists and Partial Agonists: Overcoming Lack of a Recognition Element [O] . Dilip K. Tosh, Khai Phan, Francesca Deflorian, 2011

机译：截短的（N）-甲氨基甲酸酯核苷作为A1腺苷受体激动剂和部分激动剂：克服缺乏识别元素的问题。
7. Synthesis and Anti-Renal Fibrosis Activity of Conformationally Locked Truncated 2-Hexynyl-N6-Substituted-(N)-Methanocarba-nucleosides as A3 Adenosine Receptor Antagonists and Partial Agonists [O] . Akshata Nayak, Girish Chandra, Inah Hwang, 2014

机译：组合锁定截短的2-己酰基-N6-取代 - （n） - 甲烷的纤维化活性为A3腺苷受体拮抗剂和部分激动剂的抗肾纤维化活性

Truncated (N)-Methanocarba Nucleosides as Partial Agonists at Mouse and Human A3 Adenosine Receptors: Affinity Enhancement by N6(2-Phenylethyl) Substitution

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