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Discovery of 3,6-disubstituted pyridazines as a novel class of anticancer agents targeting cyclin-dependent kinase 2: synthesis, biological evaluation and in silico insights

机译：发现3,6二取代的哒嗪作为一种靶向细胞周期蛋白依赖性激酶2的新类抗癌剂：合成，生物学评估和硅洞察力

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Ahmed Sabt; Wagdy M. Eldehna; Tarfah Al-Warhi; Ohoud J. Alotaibi; Mahmoud M. Elaasser; Howayda Suliman; Hatem A. Abdel-Aziz;
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1. Discovery of 3,6-disubstituted pyridazines as a novel class of anticancer agents targeting cyclin-dependent kinase 2: synthesis, biological evaluation and in silico insights [J] . Sabt Ahmed, Eldehna Wagdy M., Al-Warhi Tarfah, Trends in Ecology & Evolution . 2020,第1期

机译：发现3,6二取代的哒嗪作为一种小型抗癌剂，靶向细胞周期蛋白依赖性激酶2：合成，生物学评估和Silico Insights
2. Discovery of 3,6-disubstituted pyridazines as a novel class of anticancer agents targeting cyclin-dependent kinase 2: synthesis, biological evaluation and in silico insights [J] . Ahmed Sabt, Wagdy M. Eldehna, Tarfah Al-Warhi, Journal of enzyme inhibition and medicinal chemistry. . 2020,第1期

机译：发现3,6二取代的哒嗪作为一种靶向细胞周期蛋白依赖性激酶2的新类抗癌剂：合成，生物学评估和硅洞察力
3. Synthesis and biological evaluation of 3,6-disubstituted (1,2,4)triazolo(3,4-b)(1,3,4)thiadiazole derivatives as a novel class of potential anti-tumor agents. [J] . Ibrahim DA European Journal of Medicinal Chemistry: Chimie Therapeutique . 2009,第7期

机译：3,6-二取代的（1,2,4）三唑并（3,4-b）（1,3,4）噻二唑衍生物作为一类潜在的抗肿瘤药物的合成及生物学评价。
4. DESIGN,SYNTHESIS AND BIOLOGICAL EVALUATION OF 3-PHENYLISOXAZOLO5,4-DPYRIMIDINE DERIVATIVES AS ANTICANCER AGENTS [C] . Nikhil Gaikwad, Y.V.Madhavi Conference on Drug Design and Discovery Technologies . 2020

机译：3-苯基异恶唑的设计，合成和生物学评价5,4-D嘧啶衍生物作为抗癌剂
5. The design, synthesis and biological evaluation of novel taxoid anticancer agents and their tumor-targeted drug conjugates. [D] . Seitz, Joshua. 2013

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6. Discovery of 36-disubstituted pyridazines as a novel class of anticancer agents targeting cyclin-dependent kinase 2: synthesis biological evaluation and in silico insights [O] . Ahmed Sabt, Wagdy M. Eldehna, Tarfah Al-Warhi, 2020

机译：发现36二取代的哒嗪作为一种靶向细胞周期蛋白依赖性激酶2的新类抗癌剂：合成生物学评估和硅洞察力
7. Synthesis and Biological Evaluation of New Antitubulin Agents Containing 2-(3′,4′,5′-trimethoxyanilino)-3,6-disubstituted-4,5,6,7-tetrahydrothieno2,3-cpyridine Scaffold [O] . Romeo Romagnoli, Filippo Prencipe, Paola Oliva, 2020

机译：含有2-（3'，4'，5'-三甲氧基硅基硅氧烷-3,6-二取代-4,5,6,5,6,7-四氢噻吩的新型抗胰酶剂的合成及生物学评价 - 3,6-二取代 - 4,5,6,7-四氢噻吩诺2,3-C吡啶支架

Discovery of 3,6-disubstituted pyridazines as a novel class of anticancer agents targeting cyclin-dependent kinase 2: synthesis, biological evaluation and in silico insights

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