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Discovery of Novel Oral Protein Synthesis Inhibitors of Mycobacterium tuberculosis That Target Leucyl-tRNA Synthetase

机译：发现新型口腔蛋白质合成抑制剂的分枝杆菌结核菌靶幼虫 - TRNA合成酶

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Andrés Palencia; Xianfeng Li; Wei Bu; Wai Choi; Charles Z. Ding; Eric E. Easom; Lisa Feng; Vincent Hernandez; Paul Houston; Liang Liu; Maliwan Meewan; Manisha Mohan; Fernando L. Rock; Holly Sexton; Suoming Zhang; Yasheen Zhou; Baojie Wan; Yuehong Wang; Scott G. Franzblau; Lisa Woolhiser; Veronica Gruppo; Anne J. Lenaerts; Theresa OMalley; Tanya Parish; Christopher B. Cooper; M. Gerard Waters; Zhenkun Ma; Thomas R. Ioerger; James C. Sacchettini; Joaquín Rullas; Iñigo Angulo-Barturen; Esther Pérez-Herrán; Alfonso Mendoza; David Barros; Stephen Cusack; Jacob J. Plattner; M. R. K. Alley;
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1. Discovery of Novel Oral Protein Synthesis Inhibitors of Mycobacterium tuberculosis That Target Leucyl-tRNA Synthetase [J] . Palencia Andres, Li Xianfeng, Bu Wei, Antimicrobial agents and chemotherapy. . 2016,第10期

机译：发现新型结核分枝杆菌口服蛋白合成抑制剂靶向亮氨酰tRNA合成酶
2. Identification of Mycobacterium tuberculosis leucyl-tRNA synthetase (LeuRS) inhibitors among the derivatives of 5-phenylamino-2H-[1,2,4]triazin-3-one [J] . Gudzera Olga I., Golub Andriy G., Bdzhola Volodymyr G., Journal of enzyme inhibition and medicinal chemistry. . 2016,第Suppla2期

机译：鉴定分枝杆菌结核病白胶 - TRNA合成酶（Leurs）抑制剂在5-苯基氨基-2H- [1,2,4]三嗪-3-一度的衍生物中的抑制剂
3. Discovery of novel leucyladenylate sulfamate surrogates as leucyl-tRNA synthetase (LRS)-targeted mammalian target of rapamycin complex 1 (mTORC1) inhibitors [J] . Suyoung Yoon, Dongxu Zuo, Jong Hyun Kim, Bioorganic and medicinal chemistry . 2018,第14期

机译：将新型脱苯基磺酸盐蛋白酶替代品作为白胶-TRNA合成酶（LRS） - 雷帕霉素络合物1（MTORC1）抑制剂的哺乳动物靶标
4. Analytics for In Silico Development of Inhibitors from Neem (Azadirachta Indica) Against Pantothenate Synthetase of Mycobacterium Tuberculosis [C] . Saurov Mahanta, Bhaskarjyoti Gogoi, Bhaben Tanti International Conference on Data Management, Analytics and Innovation . 2020

机译：来自Neem（Azadirachta Thema）抑制剂的抑制剂的分析，对结核分枝杆菌的泛酸合成酶
5. Understanding primary and alternate functions of leucyl-tRNA synthetases from Escherichia coli, Saccharomyces cerevisiae and Mycobacterium tuberculosis. [D] . Poruri, Kiranmai. 2007

机译：了解大肠埃希氏菌，酿酒酵母和结核分枝杆菌的亮氨酰-tRNA合成酶的主要功能和替代功能。
6. Discovery of Novel Oral Protein Synthesis Inhibitors of Mycobacterium tuberculosis That Target Leucyl-tRNA Synthetase [O] . Andrés Palencia, Xianfeng Li, Wei Bu, 2016

机译：新型结核分枝杆菌口服蛋白合成抑制剂的靶向亮氨酰tRNA合成酶的发现。
7. Discovery of Leucyladenylate Sulfamates as Novel Leucyl-tRNA Synthetase (LRS)-Targeted Mammalian Target of Rapamycin Complex 1 (mTORC1) Inhibitors [O] . -1

机译：将脱苯基磺酸盐作为新型乳糖酰络合物1（MTORC1）抑制剂的新型乳糖-TRNA合成酶（LRS）的乳酰基氨基酯的发现

Discovery of Novel Oral Protein Synthesis Inhibitors of Mycobacterium tuberculosis That Target Leucyl-tRNA Synthetase

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