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Correction to Discovery of 3-Oxabicyclo4.1.0heptane, a Non-nitrogen Containing Morpholine Isostere, and Its Application in Novel Inhibitors of the PI3K-AKT-mTOR Pathway

机译：校正3-氧基双环4.1.0庚烷，一种含有的吗啉异蹄孔的校正及其在PI3K-AKT-MTOR途径的新抑制剂中的应用

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Heather Hobbs; Gianpaolo Bravi; Ian Campbell; Maire Convery; Hannah Davies; Graham Inglis; Sandeep Pal; Simon Peace; Joanna Redmond; Declan Summers;
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年度 2019
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1. Discovery of 3-Oxabicyclo[4.1.0]heptane, a Non-nitrogen Containing Morpholine Isostere, and Its Application in Novel Inhibitors of the PI3K-AKT-mTOR Pathway (vol 62, pg 6972, 2019) [J] . Hobbs Heather, Bravi Gianpaolo, Campbell Ian, Journal of Medicinal Chemistry . 2019,第19期

机译：发现3-氧基酰亚乙二醇[4.1.0]庚烷，含有非氮素的吗啉等甾酮，其在PI3K-AKT-MTOR途径新抑制剂中的应用（Vol 62，PG 6972，2019）
2. Discovery of 3-Oxabicyclo[4.1.0]heptane, a Non-nitrogen Containing Morpholine Isostere, and Its Application in Novel Inhibitors of the PI3K-AKT-mTOR Pathway [J] . Hobbs Heather, Bravi Gianpaolo, Campbell Ian, Journal of Medicinal Chemistry . 2019,第15期

机译：发现3-氧基酰亚乙二醇[4.1.0]庚烷，含有的含硫胺虫等渗，其在PI3K-AKT-MTOR途径新抑制剂中的应用
3. Erratum to:Discovery of Chrysoeriol,a PI3K-AKT-mTOR Pathway Inhibitor with Potent Antitumor Activity against Human Multiple Myeloma Cells In Vitro [J] . Yang YANG, Xiaoxi ZHOU, Min XIAO, 当代医学科学(英文) . 2020,第006期

机译：误解：发现克莱氏醇，PI3K-AKT-MTOR途径抑制剂，其具有抗体多发性骨髓瘤细胞的有效抗肿瘤活性
4. Synthesis of inhibitors of the heptose biosynthetic pathway for the discovery of Antivirulence and Antibacterial Agents [C] . Stephane P. VINCENT International Carbohydrate Symposium . 2013

机译：肽生物合成途径抑制剂的合成抗血管和抗菌剂的发现
5. Application of organocatalysis to the synthesis of chiral morpholines, piperazines, aziridines, azetidines, beta-fluoroamines, and gamma-fluoroamines; discovery of selective phospholipase D inhibitors with optimized in vivo properties. [D] . O'Reilly, Matthew C. 2014

机译：有机催化在合成手性吗啉，哌嗪，氮丙啶，氮杂环丁烷，β-氟胺和γ-氟胺中的应用；发现具有优化体内特性的选择性磷脂酶D抑制剂。
6. Fragment based discovery of Arginine isosteres through REPLACE: towards non-ATP competitive CDK inhibitors [O] . Padmavathy Nandha Premnath, Shu Liu, Tracy Perkins, -1

机译：通过REPLACE基于片段的精氨酸等位基因发现：针对非ATP竞争性CDK抑制剂
7. Discovery of 3Oxabicyclo4.1.0heptane a Non-nitrogen Containing Morpholine Isostere, and Its Application in Novel Inhibitors of the PI3K-AKT-mTOR Pathway [O] . -1

机译：3-氧基酰基4.1.0庚烷含有非氮的吗啉等甾酮，及其在PI3K-AKT-MTOR途径的新抑制剂中的应用

Correction to Discovery of 3-Oxabicyclo4.1.0heptane, a Non-nitrogen Containing Morpholine Isostere, and Its Application in Novel Inhibitors of the PI3K-AKT-mTOR Pathway

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