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Synthesis and Biological Evaluation of Novel 1-Deoxy-1-6-((hetero)arylcarbonyl)hydrazino-9H-purin-9-yl-N-ethyl-b-d-ribofuranuronamide Derivatives as Useful Templates for the Development of A2B Adenosine Receptor Agonists

机译：新型1-脱氧-1- 6 - （杂氧羰基）肼 -9H-五林-9-基 -N-乙基-BD-核呋喃酰胺胺衍生物作为A2B发育的有用模板，其合成及生物学评价腺苷受体激动剂

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1. Synthesis and Biological Evaluation of Novel 1-Deoxy-1-[6-[((hetero)arylcarbonyl)hydrazino]-9H-purin-9-yl]-N-ethyl-beta-D-ribofuranuronamide Derivatives as Useful Templates for the Development of A_(2B) Adenosine Receptor Agonists [J] . Pier Giovanni Baraldi, Delia Preti, Mojgan Aghazadeh Tabrizi Journal of Medicinal Chemistry . 2007,第2期

机译：新型1-脱氧-1- [6-[（（（杂）芳基羰基）肼基] -9H-嘌呤-9-基] -N-乙基-β-D-呋喃呋喃核酰胺衍生物的合成和生物学评价作为开发有用的模板（2B）腺苷受体激动剂
2. A2B adenosine receptor agonists: synthesis and biological evaluation of 2-phenylhydroxypropynyl adenosine and NECA derivatives. [J] . Vittori S, Costanzi S, Lambertucci C, Nucleosides, nucleotides and nucleic acids . 2004,第1a2期

机译：A2B腺苷受体激动剂：2-苯基羟基丙炔基腺苷和NECA衍生物的合成和生物学评估。
3. 1,2,4-triazolo[1,5-a]quinoxaline as a versatile tool for the design of selective human A(3) adenosine receptor antagonists: Synthesis, biological evaluation, and molecular modeling studies of 2-(hetero)aryl- and 2-carboxy-substitued derivatives [J] . Catarzi D, Colotta V, Varano F, Journal of Medicinal Chemistry . 2005,第25期

机译：1,2,4-三唑并[1,5-a]喹喔啉可作为设计选择性人类A（3）腺苷受体拮抗剂的多功能工具：2-（杂）芳基-的合成，生物学评估和分子模型研究和2-羧基取代的衍生物
4. Design, synthesis and biological evaluation of novel fentanyl analogues as agonist of μ-opioid receptor [C] . LIU Ming, HU Wen-xiang International Conference on Advanced Design and Manufacturing Engineering . 2012

机译：新型芬太尼类似物作为μ-ApiOID受体激动剂的设计，合成和生物学评价
5. Synthesis and biological evaluation of conformationally constrained sphingosine-1-phosphate analogs as subtype selective S1P receptor agonist/antagonist. [D] . Zhu, Ran. 2008

机译：构象受限的鞘氨醇-1-磷酸类似物作为亚型选择性S1P受体激动剂/拮抗剂的合成和生物学评估。
6. Adenosine Receptor Prodrugs: Synthesis and Biological Activity of Derivatives of Potent A1-Selective Agonists [O] . Michel C. Maillrad, Olga Nikodijević, Kathryn F. LaNoue, -1

机译：腺苷受体前药：有力A1选择性激动剂的衍生物的合成和生物活性。
7. SYNTHESIS, BIOLOGICAL EVALUATION AND BINDING STUDIES OF NEW FLAVONE DERIVATIVES AS ADENOSINE A2B RECEPTOR ANTAGONISTS [O] . Farag Sherbiny 2016

机译：新黄酮衍生物作为腺苷A2B受体拮抗剂的合成，生物学评价和结合研究

Synthesis and Biological Evaluation of Novel 1-Deoxy-1-6-((hetero)arylcarbonyl)hydrazino-9H-purin-9-yl-N-ethyl-b-d-ribofuranuronamide Derivatives as Useful Templates for the Development of A2B Adenosine Receptor Agonists

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