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Conformationally restricted quinazolone derivatives as PI3Kδ-selective inhibitors: the design, synthesis and biological evaluation

机译：构象限制喹唑酮衍生物作为PI3Kδ - 选择性抑制剂：设计，合成和生物学评估

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Xiaodong Ma; Fang Fang; Qiangqiang Tao; Li Shen; Guochen Zhong; Tao Qiao; Xiaoqing Lv; Jiaming Li;
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年度 2019
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1. Conformationally restricted quinazolone derivatives as PI3Kδ-selective inhibitors: the design, synthesis and biological evaluation [J] . Xiaodong Ma, Fang Fang, Qiangqiang Tao, MedChemComm . 2019,第3期

机译：构象限制喹唑酮衍生物作为PI3Kδ选择性抑制剂：设计，合成和生物学评估
2. Design, synthesis and biological evaluation of novel benzothiadiazine derivatives as potent PI3K delta-selective inhibitors for treating B-cell-mediated malignancies [J] . Ma Xiaodong, Wei Jun, Wang Chang, European Journal of Medicinal Chemistry: Chimie Therapeutique . 2019,第期

机译：新型苯并噻嗪衍生物的设计，合成及生物学评价为有效的PI3Kδ选择性抑制剂治疗B细胞介导的恶性肿瘤
3. Design, Synthesis and Biological Evaluation of Novel Benzothiazole Derivatives as Selective PI3K beta Inhibitors [J] . Cao Shuang, Cao Ruiyuan, Liu Xialing, Molecules . 2016,第7期

机译：新型苯并噻唑衍生物作为选择性PI3Kβ抑制剂的设计，合成和生物学评价
4. Design, Synthesis, and Pharmacological Evaluation of Novel Tasiamide B Derivatives: Selective Inhibitors of BACE1 [C] . Jian Liu, SimingYang, Wei Zhang, Chinese International Peptide Symposium . 2013

机译：新型三胺B衍生物的设计，合成和药理评价：BACE1的选择性抑制剂
5. Structure-Based Drug Design in Medicinal Chemistry: I. Development of Translesion Synthesis Inhibitors II. Synthesis and Biological Evaluation of Sulfonyl Piperazine Derivatives for LpxH Inhibition [D] . Lee, Minhee 2017

机译：药物化学中基于结构的药物设计：I.跨病变合成抑制剂的开发II。磺酰哌嗪衍生物对LpxH的抑制作用及其合成及生物学评价
6. Conformationally restricted quinazolone derivatives as PI3Kδ-selective inhibitors: the design synthesis and biological evaluation [O] . Xiaodong Ma, Fang Fang, Qiangqiang Tao, 2019

机译：构象受限的喹唑酮衍生物作为PI3Kδ选择性抑制剂：设计合成和生物学评价
7. Design, Synthesis and Biological Evaluation of Novel Benzothiazole Derivatives as Selective PI3Kβ Inhibitors [O] . Shuang Cao, Ruiyuan Cao, Xialing Liu, 2016

机译：新型苯并噻唑衍生物作为选择性pI3Kβ抑制剂的设计，合成及生物学评价

Conformationally restricted quinazolone derivatives as PI3Kδ-selective inhibitors: the design, synthesis and biological evaluation

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