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A Synthesis of Novel Pyrazolylthienopyrimidine Derivatives as IL-6/STAT3 Inhibitors

机译：新型吡唑基吡啶并嘧啶衍生物作为IL-6 / STAT3抑制剂的合成

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《Bulletin of the Korean Chemical Society》 |2014年第9期|共页
作者
Seung Woong Lee; Sung Min Kim; Yang-Heon Song;
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中图分类化学;
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1. A Synthesis of Novel Pyrazolylthienopyrimidine Derivatives as IL-6/STAT3 Inhibitors [J] . Sung Min Kim, Seung Woong Lee, Yang-Heon Song Bulletin of the Korean Chemical Society . 2014,第9期

机译：新型吡唑基吡啶并嘧啶衍生物作为IL-6 / STAT3抑制剂的合成
2. Synthesis of Thienopyrimidine Derivatives as Inhibitors of STAT3 Activation Induced by IL-6 [J] . Jang Hyun-Jae, Kim Sung Min, Rho Mun-Chual, Journal of microbiology and biotechnology . 2019,第6期

机译：IL-6诱导的STAT3活化抑制剂的噻吩嘧啶衍生物的合成
3. BF211, a derivative of bufalin, enhances the cytocidal effects in multiple myeloma cells by inhibiting the IL-6/JAK2/STAT3 pathway [J] . Xiao-yu Wu, Fang Tian, Min-hui Su, International immunopharmacology . 2018,第期

机译：BF211是Bufalin的衍生物，通过抑制IL-6 / JAK2 / Stat3途径来增强多发性骨髓瘤细胞中的细胞癌效应
4. Synthesis of Oleic Imidazoline Derivative Using MAOS (Microwave Assisted Organic Synthesis) Method as Corrosion Inhibitor Towards Carbon Steel [C] . M. Mujahiduzzakka, D. U. C. Rahayu, D. A. Nurani, International Symposium on Current Progress in Mathematics and Sciences . 2020

机译：使用MAOS（微波辅助有机合成）法作为碳钢腐蚀抑制剂的油酸咪唑啉衍生物的合成
5. Part One. Synthesis of optically active tryptophan derivatives with potential activity as indoleamine 2,3-dioxygenase inhibitors: An approach via asymmetric catalytic hydrogenation. Part Two. Design, synthesis and pharmacology of selective ligands for alpha1-containing GABA(A)/benzodiazepine receptor subtypes: SAR studies of beta-carbolines at positions -3 and -6 and their corresponding bivalent ligands. Part Three. First enantiospecific total synthesis of the important biogenetic intermediates, (+)-polyneuridine and (+)-polyneuridine aldehyde, as well as 16-epi-vellosimine and macusine A. [D] . Yin, Wenyuan. 2007

机译：第一部分。具有吲哚胺2,3-二加氧酶抑制剂潜在活性的旋光色氨酸衍生物的合成：一种通过不对称催化氢化的方法。第二部分。含α1的GABA（A）/苯并二氮杂receptor受体亚型的选择性配体的设计，合成和药理作用：位于-3和-6位的β-咔啉及其相应的二价配体的SAR研究。第三部分。重要生物遗传中间体，（+）-聚神经氨酸和（+）-聚神经氨酸醛，以及16-表-维西辛和Macusine A的首次对映体全合成。
6. Homoharringtonine induces apoptosis and inhibits STAT3 via IL-6/JAK1/STAT3 signal pathway in Gefitinib-resistant lung cancer cells [O] . Wei Cao, Ying Liu, Ran Zhang, -1

机译：同型harringtonine诱导吉非替尼耐药的肺癌细胞凋亡并通过IL-6 / JAK1 / STAT3信号通路抑制STAT3
7. A Synthesis of Novel Pyrazolylthienopyrimidine Derivatives as IL-6/STAT3 Inhibitors [O] . Sung Min Kim, Seung Woong Lee, Yang-Heon Song 2014

机译：新型吡唑啉基嘧啶衍生物作为IL-6 / Stat3抑制剂的合成

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