首页> 外文OA文献 >Thiazolo4,5-dPyrimidines. Part II. Synthesis and Anti-Human Cytomegalovirus Activity in Vitro of Certain Acyclonucleosides and Acyclonucleotides Derived from the Guanine Analogue 5-Aminothiazolo4,5-dPyrimidine-2,7(3H,6H)-Dione

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Thiazolo4,5-dPyrimidines. Part II. Synthesis and Anti-Human Cytomegalovirus Activity in Vitro of Certain Acyclonucleosides and Acyclonucleotides Derived from the Guanine Analogue 5-Aminothiazolo4,5-dPyrimidine-2,7(3H,6H)-Dione

机译：噻唑洛4,5-D嘧啶。第二部分。某些酰核苷核苷的体外合成和抗人巨细胞病毒活性和衍生自鸟嘌呤类似物5-氨噻唑的酰核核苷酸4,5-D嘧啶-2,7（3h，6h） - 二硫酮

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GR Revankar; JO Ojwang; SD Mustain; RF Rando; E De Clercq; JH Huffman; JC Drach; J-P Sommadossi; AF Lewis;
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1. Thiazolo(4,5-d)pyrimidines. Part II. Synthesis and anti-human cytomegalovirus activity in vitro of certain acyclonucleosides and acyclonucleotides derived from the guanine analogue 5-aminothiazolo(4,5-d)pyrimidine-2,7(3H,6H)-dione. [J] . Revankar GR, Ojwang JO, Mustain SD, Antiviral chemistry & chemotherapy . 1998 ,第1期

机译：噻唑（4,5-d）嘧啶。第二部分某些鸟嘌呤类似物5-氨基噻唑（4,5-d）嘧啶-2,7（3H，6H）-二酮衍生的无环核苷和无环核苷酸的合成及体外抗人巨细胞病毒活性。
2. Synthesis and structure-activity relationships of N-6 substituted analogues of 9-hydroxy-4-phenylpyrrolo(3,4-c)carbazole-1,3(2H,6H)-diones as inhibitors of Wee1 and Chk1 checkpoint kinases. [J] . Smaill JB, Baker EN, Booth RJ, European Journal of Medicinal Chemistry: Chimie Therapeutique . 2008 ,第6期

机译：N-6取代的9-羟基-4-苯基吡咯并（3,4-c）咔唑-1,3（2H，6H）-二酮作为Wee1和Chk1检查点激酶的抑制剂的合成与构效关系。
3. SYNTHESIS AND IN VITRO ANTI-HUMAN CYTOMEGALOVIRUS (HCMV) ACTIVITY OF CERTAIN ALKENYL SUBSTITUTED CYTOSINES AND 5-HALOCYTOSINES [J] . Lewis AF., Rando RF., Revankar GR. Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry . 1995 ,第5期

机译：某些烯基取代的胞嘧啶和5-卤代胞嘧啶的合成及体外抗人巨细胞病毒（HCMV）活性
4. Part one. Synthesis of phosphorus-containing amino acid analogues derived from trans-4-hydroxyproline and the study of their bioactivity in the glutamate excitatory neurotransmitter system. Part two. Synthesis, structural modifications and in vitro pharmacology of quinoline-2,4-dicarboxylic acids as proposed inhibitors of the glutamate vesicular transporter. [D] . Carrigan, Christina Nicole. 2000

机译：第一部分。反式-4-羟基脯氨酸衍生的含磷氨基酸类似物的合成及其在谷氨酸兴奋性神经递质系统中的生物活性的研究。第二部分。喹啉-2,4-二羧酸作为谷氨酸囊泡转运蛋白的抑制剂的合成，结构修饰和体外药理作用。
5. Synthesis in vitro antitumour activity and molecular docking study of novel 2-substituted mercapto-3-(345-trimethoxybenzyl)-4(3H)-quinazolinone analogues [O] . Adel S. El-Azab, Alaa A.-M. Abdel-Aziz, Hazem A. Ghabbour, 2017

机译：新型2-取代巯基-3-（345-三甲氧基苄基）-4（3H）-喹唑啉酮类似物的合成体外抗肿瘤活性和分子对接研究
6. Chemical modifications of androsta-1,4-diene-3,17-dione. II. Synthesis of 17-nor-vitamin D analogues having a hydroxy group at 1.ALPHA.- or 2.BETA.-position and biological activity of 1.ALPHA.-hydroxy-17- nor-17,17-ethylenedioxyvitamin D. [O] . HARUO SAKAMOTO, AKIKO SUGIMOTO, CHIKARA KANEKO, 1975

机译：Androsta-1,4-二烯-3,17-Dione的化学修饰。 II。合成在α-或2.β-或2.beta.-或2.beta.-羟基-17- NOR-17,17-乙二氧二维素D.的17-或2.β-或2.β-或2.乙烯 - 17,17,17-乙二氧基氧氨苄蛋白D.

Thiazolo4,5-dPyrimidines. Part II. Synthesis and Anti-Human Cytomegalovirus Activity in Vitro of Certain Acyclonucleosides and Acyclonucleotides Derived from the Guanine Analogue 5-Aminothiazolo4,5-dPyrimidine-2,7(3H,6H)-Dione

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