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Design and Synthesis of High Affinity Inhibitors of Plasmodium falciparum and Plasmodium vivax N-Myristoyltransferases Directed by Ligand Efficiency Dependent Lipophilicity (LELP)

机译：恶性疟原虫和间日疟原虫N-肉豆蔻酰基转移酶的高亲和力抑制剂的设计和合成由配体效率依赖性亲脂性（LELp）指导

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Rackham MD; Brannigan JA; Rangachari K; Meister S; Wilkinson AJ; Holder AA; Leatherbarrow RJ; Tate EW;
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年度 2014
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1. Design and Synthesis of High Affinity Inhibitors of Plasmodium falciparum and Plasmodium vivax N-Myristoyltransferases Directed by Ligand Efficiency Dependent Lipophilicity (LELP) [J] . Mark D. Rackham, James A. Brannigan, Kaveri Rangachari, Journal of Medicinal Chemistry . 2014,第6期

机译：配体效率依赖性亲脂性（LELP）指导的恶性疟原虫和间日疟原虫间质N-肉豆蔻酰基转移酶的高亲和力抑制剂的设计与合成
2. Discovery of novel and ligand-efficient inhibitors of plasmodium falciparum and plasmodium vivax N-myristoyltransferase [J] . Rackham M.D., Brannigan J.A., Moss D.K., Journal of Medicinal Chemistry . 2013,第1期

机译：发现恶性疟原虫和间日疟原虫N-肉豆蔻酰基转移酶的新型且配体有效的抑制剂
3. i >Plasmodium vivax/i>Plasmodium vivax and i >Plasmodium?falciparum/i>Plasmodium?falciparum infection in Neotropical primates in the western Amazon, Brazil [J] . Silva Tatiene R. M., Barros Flávia N. L., Bahia Michele, Zoonoses and Public Health . 2019,第7期

机译：＆ i>疟原虫疟原虫疟原虫和脂肪脂肪脂肪脂肪脂肪脂肪脂肪脂肪脂肪菊酯疟原虫？疟原虫疟原虫？巴西西亚马逊西澳大省的狂热激发疟原虫感染
4. Impact of climate variability on Plasmodiurn vivax and Plasmodium falciparum malaria in the high risk area of Yunnan Province, China [C] . Yan Bi, Weiwei Yu, Wenbiao Hu, Annual conference of the International Society of Exposure Science . 2014

机译：气候变化对云南省高危地区间日疟原虫和恶性疟原虫疟疾的影响
5. Whole Genome Analysis of the Human Malaria Parasites Plasmodium vivax and P. falciparum. [D] . Bright, Andrew Taylor. 2013

机译：人类疟原虫间日疟原虫和恶性疟原虫的全基因组分析。
6. Design and Synthesis of HighAffinity Inhibitors of Plasmodium falciparum and Plasmodium vivax N-Myristoyltransferases Directed by Ligand Efficiency Dependent Lipophilicity (LELP) [O] . Mark D. Rackham, James A. Brannigan, Kaveri Rangachari, -1

机译：高的设计与综合配体效率依赖性亲脂性（LELP）指导的恶性疟原虫和间日疟原虫N-肉豆蔻酰基转移酶的亲和抑制剂
7. Design and Synthesis of Inhibitors of Plasmodium falciparum N-Myristoyltransferase, A Promising Target for Antimalarial Drug Discovery [O] . Yu Z, Brannigan JA, Moss DK, 2012

机译：恶性疟原虫N-肉豆蔻酰基转移酶抑制剂的设计与合成，是抗疟药物发现的有希望的靶点

Design and Synthesis of High Affinity Inhibitors of Plasmodium falciparum and Plasmodium vivax N-Myristoyltransferases Directed by Ligand Efficiency Dependent Lipophilicity (LELP)

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