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Design, Synthesis, Antivirus Activity, and SARs of Phenanthroquinolizidine Alkaloid Derivatives

机译：设计，合成，抗病毒活性和SARS的菲喹丽氨氨酸生物碱衍生物

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Bo Su; Chunlong Cai; Yongqiang Li; Qingmin Wang;
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1. Target-Directed Design, Synthesis, Antiviral Activity, and SARs of 9-Substituted Phenanthroindolizidine Alkaloid Derivatives [J] . Yan Changcun, Dong Jianyang, Liu Yuxiu, Journal of Agricultural and Food Chemistry . 2021,第27期

机译：针对靶向的设计，合成，抗病毒活性和SARS的9-取代的菲甲烷醇类生物碱衍生物
2. Design, synthesis, antiviral activity, and SARs of 13a-substituted phenanthroindolizidine alkaloid derivatives [J] . SuB., CaiC., DengM., Bioorganic and Medicinal Chemistry Letters . 2014,第13期

机译：设计，合成，抗病毒活性和13a-取代的菲咯啉吲哚啶生物碱衍生物的SARs
3. Synthesis and SAR studies of phenanthroindolizidine and phenanthroquinolizidine alkaloids as potent anti-tumor agents [J] . WangZ., WuM., WangY., European Journal of Medicinal Chemistry: Chimie Therapeutique . 2012,第Null期

机译：菲咯啉吲哚并菲和邻喹喹啉嗪生物碱作为有效的抗肿瘤剂的合成与合成孔径雷达研究
4. Stereospecific Synthesis of Tryptamine Derivatives of Alkaloid Securinine and Their Potential Neuroprotective Activity [C] . S.G. Klochkov, M.E. Neganova, S.A. Pukhov, International Conference on Modern Synthetic Methodologies for Creating Drugs and Functional Materials . 2019

机译：生物碱SECURINININ衍生物的立体特异性合成及其潜在的神经保护活性
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. Design Synthesis and Structure-Activity Relationship (SAR) Studies of 24-Disubstituted Pyrimidine Derivatives: Dual Activity as Cholinesterase and Aβ-Aggregation Inhibitors [O] . Tarek Mohamed, Xiaobei Zhao, Lila K. Habib, -1

机译：24-二取代嘧啶衍生物的设计合成和结构 - 活性关系（SAR）研究：双活性作为胆碱酯酶和Aβ-聚集抑制剂
7. Design, synthesis and structure–activity relationship (SAR) studies of 2,4-disubstituted pyrimidine derivatives: Dual activity as cholinesterase and Aβ-aggregation inhibitors [O] . Tarek Mohamed, Xiaobei Zhao, Lila K. Habib, 2011

机译：2,4-二取代嘧啶衍生物的设计，合成和结构 - 活性关系（SAR）研究：双活性作为胆碱酯酶和Aβ-聚集抑制剂

Design, Synthesis, Antivirus Activity, and SARs of Phenanthroquinolizidine Alkaloid Derivatives

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