首页> 外文OA文献 >New Pyrrolo2, 1-fpurine-2, 4-dione and Imidazo2, 1-fpurine-2, 4-dione Derivatives as Potent and Selective Human A3 Adenosine Receptor Antagonists

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New Pyrrolo2, 1-fpurine-2, 4-dione and Imidazo2, 1-fpurine-2, 4-dione Derivatives as Potent and Selective Human A3 Adenosine Receptor Antagonists

机译：新的Pyrrolo 2,1-F嘌呤-2,4-二酮和咪唑2,1-F嘌呤-2,4-二酮衍生物作为有效和选择性的人A3腺苷受体拮抗剂

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1. New pyrrolo[2,1-f]purine-2,4-dione and imidazo[2,1-f]purine-2,4-dione derivatives as potent and selective human A(3) adenosine receptor antagonists [J] . Baraldi PG, Preti D, Tabrizi MA, Journal of Medicinal Chemistry . 2005,第14期

机译：新的吡咯并[2,1-f]嘌呤-2,4-二酮和咪唑并[2,1-f]嘌呤-2,4-二酮衍生物作为有效的和选择性的人A（3）腺苷受体拮抗剂
2. New Pyrrolo[2,l-f]purine-2,4-dione and Imidazo[2,l-f]purine-2,4-dione Derivatives as Potent and Selective Human AS Adenosine Receptor Antagonists [J] . Pier Giovanni Baraldi, Delia Preti, Mojgan Aghazadeh Tabrizi, Journal of Medicinal Chemistry . 2005,第14期

机译：新型吡咯并[2,1-f]嘌呤-2,4-二酮和咪唑并[2,1-f]嘌呤-2,4-二酮衍生物作为有效的和选择性的人类AS腺苷受体拮抗剂
3. Pyrido[2,1-f]purine-2,4-dione Derivatives as a Novel Class of Highly Potent Human A_3 Adenosine Receptor Antagonists [J] . Eva-Maria Priego, Jacobien von Frijtag Drabbe Kuenzel, P. IJerman, Journal of Medicinal Chemistry . 2002,第16期

机译：Pyrido [2,1-f]嘌呤-2,4-二酮衍生物作为一类新型的高效人A_3腺苷受体拮抗剂
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. Design, synthesis and biological evaluation of human inosine 5'-monophosphate dehydrogenase inhibitors: 1,5-diazabicyclo(3.1.0)hexane-2,4-diones, as novel isozyme-selective cancer chemotherapeutic agents. [D] . Barnes, Betsy Jo. 1999

机译：人肌苷5'-单磷酸脱氢酶抑制剂的设计，合成和生物学评估：1,5-二氮杂双环（3.1.0）己烷-2,4-二酮，作为新型的同工酶选择性癌症化学治疗剂。
6. Structure-Activity Relationships of Truncated Adenosine Derivatives as Highly Potent and Selective Human A3 Adenosine Receptor Antagonists [O] . Shantanu Pal, Won Jun Choi, Seung Ah Choe, -1

机译：截断腺苷衍生物作为高效性和选择性人A3腺苷受体拮抗剂的结构 - 活性关系
7. Selective human adenosine A3 antagonists based on pyrido2,1-fpurine-2,4-diones: Novel features of hA3 antagonist binding [O] . Priego Eva María, Peréz-Pérez María-Jesús, Von Frijtag Drabbe Kuenzel J. K., 2013

机译：基于吡啶并2,1-f嘌呤-2,4-二酮的选择性人腺苷A3拮抗剂：hA3拮抗剂结合的新特征

New Pyrrolo2, 1-fpurine-2, 4-dione and Imidazo2, 1-fpurine-2, 4-dione Derivatives as Potent and Selective Human A3 Adenosine Receptor Antagonists

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