Retraction notice to “Design, synthesis, structure–activity relationship and kinase inhibitory activity of substituted 3-methyl-1-phenyl-1 H -pyrazolo[3,4- d ]pyrimidin-4-ones” [Bioorg. Med. Chem. Lett. 26 (2016) 3093–3097]

Phoebe F. Lamie

首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Retraction notice to “Design, synthesis, structure–activity relationship and kinase inhibitory activity of substituted 3-methyl-1-phenyl-1 H -pyrazolo[3,4- d ]pyrimidin-4-ones” [Bioorg. Med. Chem. Lett. 26 (2016) 3093–3097]

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Retraction notice to “Design, synthesis, structure–activity relationship and kinase inhibitory activity of substituted 3-methyl-1-phenyl-1 H -pyrazolo[3,4- d ]pyrimidin-4-ones” [Bioorg. Med. Chem. Lett. 26 (2016) 3093–3097]

机译：缩回通知“取代的3-甲基-1-苯基-1H-Pyrazolo [3,4- D]吡啶蛋白-4-吡啶蛋白-4-吡啶蛋白-4-吡啶蛋白-4-α的设计，合成，结构 - 活性关系和激酶抑制活性”[Bioorg。医学。化学。吧。 26（2016）3093-3097]

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《Bioorganic and Medicinal Chemistry Letters》 |2017年第17期|共1页
作者
Phoebe F. Lamie;
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Department of Pharmaceutical Organic Chemistry Faculty of Pharmacy Beni-Suef University;

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正文语种 eng
中图分类药学;
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1. Retraction notice to “Design, synthesis, structure–activity relationship and kinase inhibitory activity of substituted 3-methyl-1-phenyl-1 H -pyrazolo[3,4- d ]pyrimidin-4-ones” [Bioorg. Med. Chem. Lett. 26 (2016) 3093–3097] [J] . Phoebe F. Lamie Bioorganic and Medicinal Chemistry Letters . 2017,第17期

机译：缩回通知“取代的3-甲基-1-苯基-1H-Pyrazolo [3,4- D]吡啶蛋白-4-吡啶蛋白-4-吡啶蛋白-4-吡啶蛋白-4-α的设计，合成，结构 - 活性关系和激酶抑制活性”[Bioorg。医学。化学。吧。 26（2016）3093-3097]
2. Corrigendum to “Synthesis and carbonic anhydrase inhibitory properties of novel chalcone substituted benzenesulfonamides” [Bioorg. Med. Chem. Lett. 26 (2016) 5867–5870] [J] . Tayfun Arslan, Emir Alper Türko?lu, Murat ?entürk, Bioorganic and Medicinal Chemistry Letters . 2017,第16期

机译：“新型醌取代苯并磺胺酰胺的”合成和碳酸酐“抑制性能的静脉静脉化”Bioorg。医学。化学。吧。 26（2016）5867-5870]
3. Corrigendum to “A cascade synthesis, in vitro cholinesterases inhibitory activity and docking studies of novel Tacrine-pyranopyrazole derivatives” [Bioorg. Med. Chem. Lett. 28 (14) (2018) 2481–2484] [J] . Chamseddine Derabli, Imen Boualia, Ahmed B. Abdelwahab, Bioorganic and Medicinal Chemistry Letters . 2018,第18期

机译：“级联合成，体外胆碱酯酶抑制活性和对接研究新型甲苯吡喃吡唑衍生物”的勘察[Bioorg。医学。化学。吧。 28（14）（2018）2481-2484]
4. Methyl(11aS)-1,2,3,5,11,11a-Hexahydro-3,3-dimethyl-1-oxo-6H-imidazo-3',4':1,2pyridin3,4-b-indol-2-Substituted Acetates: Synthesis and Three-Dimensional Quantitative Structure-Activity Relationship Investigation as a Class of Novel Vasodilator [C] . Jiawang Liu, Ming Zhao, Guohui Cui, 第四届国际分子模拟与信息技术应用学术会议（The 4th International Conference of Molecular Simulations and Applied Informatics Technologies）论文集 . 2008

机译：甲基（11aS）-1,2,3,5,11,11a-六氢-3,3-二甲基-1-氧代-6H-咪唑-3'，4'：1,2吡啶3,4- b-吲哚-2-取代的乙酸酯：一类新型血管扩张剂的合成与三维定量构效关系研究
5. I. Comparison of translesion bypass of guanine-N2 monoadducts of mitomycin C and guanine -N7 monoadducts of 2,7-diaminomitosene by T7 exo-, Klenow exo-, eta and Klenow exo+ DNA polymerases. II. Structure-based design, synthesis, structure-conformation and structure -activity relationships studies of D-Phe-Pro-D-Arg-P1'-CONH2 tetrapeptides with inhibitory activity for thrombin. [D] . Clement, Cristina C. 2006

机译：I.通过T7 exo-，Klenow exo-，eta和Klenow exo + DNA聚合酶比较丝裂霉素C的鸟嘌呤-N2单加合物和2,7-二氨基光油的鸟嘌呤-N7单加合物的跨病变旁路。二。具有凝血酶抑制活性的D-Phe-Pro-D-Arg-P1'-CONH2四肽的基于结构的设计，合成，结构构象和结构-活性关系研究。
6. Erratum to Synthesis biological evaluation andphysicochemical property assessment of 4-substituted 2-phenylaminoquinazolinesas Mer tyrosine kinase inhibitors Bioorg. Med. Chem. 24 (2016)3083–3092 [O] . Sheng-Biao Wang, Mu-Tian Cui, Xiao-Feng Wang, -1

机译：勘误至合成生物学评估和4-取代的2-苯基氨基喹唑啉的理化性质评估作为Mer酪氨酸激酶抑制剂 Bioorg。中化学24（2016）3083–3092
7. Erratum to “Synthesis, biological evaluation, and physicochemical property assessment of 4-substituted 2-phenylaminoquinazolines as Mer tyrosine kinase inhibitors” Bioorg. Med. Chem. 24 (2016) 3083–3092 [O] . Sheng-Biao Wang, Mu-Tian Cui, Xiao-Feng Wang, 2017

机译：误解“4-取代的2-苯基氨基喹唑啉的”合成，生物学评价和物理化学性能评估为MER酪氨酸激酶抑制剂“Bioorg。 Med。化学。 24（2016）3083-3092

Retraction notice to “Design, synthesis, structure–activity relationship and kinase inhibitory activity of substituted 3-methyl-1-phenyl-1 H -pyrazolo[3,4- d ]pyrimidin-4-ones” [Bioorg. Med. Chem. Lett. 26 (2016) 3093–3097]

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