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Truncated (N)-Methanocarba Nucleosides as A1 Adenosine Receptor Agonists and Partial Agonists: Overcoming Lack of a Recognition Element

机译：截短（n）-methanocarba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

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Dilip K. Tosh; Khai Phan; Francesca Deflorian; Qiang Wei; Zhan-Guo Gao; Kenneth A. Jacobson;
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年度 2011
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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. Thermodynamics of full agonist, partial agonist, and antagonist binding to wild-type and mutant adenosine A1 receptors. [J] . Dalpiaz A, Townsend-Nicholson A, Beukers MW, Biochemical Pharmacology . 1998,第11期

机译：完全激动剂，部分激动剂和拮抗剂与野生型和突变型腺苷A1受体结合的热力学。
3. 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。
4. Different Effects of Adenosine A1 Agonist Ribavirin on Amphetamine-Induced Total Locomotor and Stereotypic Activities in Rats [C] . BRANKA JANA?, VESNA PE?I?, SANJA PEKOVI?, International Biophysics Symposium . 2005

机译：腺苷A1激动剂利巴韦林对大鼠Amphetamine诱导的总运动和陈规定型活性的不同作用
5. The cardiovascular effects of CGS 21680, an adenosine A(2A) receptor agonist and 17beta-estradiol in rats with impaired cardiac function. [D] . Nekooeian, Ali Akbar. 1999

机译：CGS 21680，腺苷A（2A）受体激动剂和17β-雌二醇对心脏功能受损的大鼠的心血管作用。
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. Truncated (N)-Methanocarba Nucleosides as Partial Agonists at Mouse and Human A3 Adenosine Receptors: Affinity Enhancement by N6(2-Phenylethyl) Substitution [O] . -1

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

Truncated (N)-Methanocarba Nucleosides as A1 Adenosine Receptor Agonists and Partial Agonists: Overcoming Lack of a Recognition Element

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