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Novel chloroquinoline derivatives incorporating biologically active benzenesulfonamide moiety: synthesis, cytotoxic activity and molecular docking

机译：新型的具有生物活性苯磺酰胺部分的氯喹啉衍生物：合成，细胞毒活性和分子对接

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1. Novel chloroquinoline derivatives incorporating biologically active benzenesulfonamide moiety: synthesis, cytotoxic activity and molecular docking [J] . Mostafa M. Ghorab, Mansour S. Alsaid, Mohammed S. Al-Dosari, Chemistry central journal . 2016,第1期

机译：新型的具有生物活性苯磺酰胺部分的氯喹啉衍生物：合成，细胞毒活性和分子对接
2. Carbonic anhydrase inhibitors: Synthesis, molecular docking, cytotoxic and inhibition of the human carbonic anhydrase isoforms I, II, IX, XII with novel benzenesulfonamides incorporating pyrrole, pyrrolopyrimidine and fused pyrrolopyrimidine moieties [J] . GhorabM.M., AlsaidM.S., CerusoM., Bioorganic and medicinal chemistry . 2014,第14期

机译：碳酸酐酶抑制剂：具有吡咯，吡咯并嘧啶和稠合吡咯并嘧啶部分的新型苯磺酰胺的合成，分子对接，细胞毒性和对人类碳酸酐酶同工型I，II，IX，XII的抑制
3. Carbonic anhydrase inhibitors: Synthesis, molecular docking, cytotoxic and inhibition of the human carbonic anhydrase isoforms I, II, IX, XII with novel benzenesulfonamides incorporating pyrrole, pyrrolopyrimidine and fused pyrrolopyrimidine moieties [J] . GhorabM.M., AlsaidM.S., CerusoM., Bioorganic and medicinal chemistry . 2014,第14期

机译：碳酸酐酶抑制剂：合成，分子对接，细胞毒性和抑制人碳酸酐酶同种型I，II，IX，XII，具有掺入吡咯，吡咯基嘧啶和熔融吡咯嘧啶部分的新型苯磺胺酰胺
4. Molecular docking of asymmetric cinchona alkaloids derivatives as new spectrum biological activities antidiabetic agent [C] . Teni Ernawatia, Desita Triana, Galuh Widyarti, International Symposium on Applied Chemistry . 2018

机译：非对称Cinchona生物碱衍生物作为新型谱生物活性抗糖尿病药剂的分子对接
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. Novel chloroquinoline derivatives incorporating biologically active benzenesulfonamide moiety: synthesis cytotoxic activity and molecular docking [O] . Mostafa M. Ghorab, Mansour S. Alsaid, Mohammed S. Al-Dosari, 2016

机译：新型的具有生物活性苯磺酰胺部分的氯喹啉衍生物：合成细胞毒活性和分子对接
7. Antimicrobial and anticancer activity of some novel fluorinated thiourea derivatives carrying sulfonamide moieties: synthesis, biological evaluation and molecular docking [O] . 2017

机译：某些带有磺酰胺基团的新型氟化硫脲衍生物的抗菌和抗癌活性：合成，生物学评估和分子对接

Novel chloroquinoline derivatives incorporating biologically active benzenesulfonamide moiety: synthesis, cytotoxic activity and molecular docking

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