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SYNTHESIS, INSILICO DOCKING AND ADMET STUDIES OF ARYL ACETIC ACID DERIVATIVES AS PROSTAGLANDIN ENDOPEROXIDE H SYNTHASE-2 INHIBITORS

机译：芳基乙酸衍生物作为前列腺素内转油氧化物H合酶-2抑制剂的合成，Insilico对接和呼吸探服和呼吸研究

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Abirami Kandhaswamy; Saravanan Rangan; Irshad Ahmed; Ks Meena Mohan;
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1. SYNTHESIS, INSILICO DOCKING AND ADMET STUDIES OF ARYL ACETIC ACID DERIVATIVES AS PROSTAGLANDIN ENDOPEROXIDE H SYNTHASE-2 INHIBITORS [J] . Abirami Kandhaswamy, Saravanan Rangan, Irshad Ahmed, Asian Journal of Pharmaceutical and Clinical Research . 2017,第4期

机译：内酯类内毒素H SYNTHase-2抑制剂前列腺素芳基乙酸衍生物的合成，硅酮对接和修饰研究
2. Molecular Docking Study of a Series of Substituted Xanthone Derivatives as Novel COX-2 Inhibitors Targeting Prostaglandin Endoperoxide Synthase -2 [J] . Aparoop Das, Urvashee Gogoi, Junmoni Kalita Satyasish Silya Current enzyme inhibition . 2016,第2期

机译：一系列靶向前列腺素内过氧化物合酶-2的新型COX-2抑制剂取代的蒽酮衍生物的分子对接研究
3. Aryl butenoic acid derivatives as a new class of histone deacetylase inhibitors: synthesis, in vitro evaluation, and molecular docking studies [J] . Peruze AYHAN ESJYOK, Ozlem SEVEN, Guluzar EYMUR Turkish journal of chemistry . 2014,第2期

机译：芳基丁烯酸衍生物作为一类新的组蛋白脱乙酰基酶抑制剂：合成，体外评估和分子对接研究
4. Synthesis, In Silico Molecular Docking Modeling and Pharmacophore Mapping of (E)-3-(4-Hydroxy-2,6-Dimethoxyphenyl)-1 -Phenylprop-2-en-1 - One as Potential New Inhibitor of Microsomal Prostaglandin E2 Synthase-1 [C] . Pitipat Sanphetchaloemchok, Mohd Fadhlizil Fasihi Mohd Aluwi, Kamal Rullah, Postgraduate Symposium on Industrial Science and Technology . 2020

机译：（E）-3-（4-羟基-2,6-二甲氧基苯基）-1-phenylprop-2-en-1的硅分子对接建模和药效线映射，作为微粒体前列腺素E2合酶的潜在新抑制剂 - 1
5. I. Synthesis of Aryl C-Nucleosides and Retinoid Analogs II. Investigation into Docking Studies of Bisabosqual Analogs [D] . Stolarzewicz, Erik 2010

机译：I.芳基C-核苷和类维生素A类似物的合成II。双等浮游生物类似物对接研究的研究
6. Novel chalcone/aryl carboximidamide hybrids as potent anti-inflammatory via inhibition of prostaglandin E2 and inducible NO synthase activities: design synthesis molecular docking studies and ADMET prediction [O] . Tarek S. Ibrahim, Amr H. Moustafa, Ahmad J. Almalki, 2021

机译：新型Chalcone /芳基羧酰亚胺酰胺杂交剂作为效力抗炎通过抑制前列腺素E2和诱导型无合成酶活性：设计合成分子对接研究和呼吸预测
7. Aryl butenoic acid derivatives as a new class of histone deacetylase inhibitors: synthesis, in vitro evaluation, and molecular docking studies [O] . Esiyok Ayhan Peruze, Seven Ozlem, Eymur Guluzar, 2014

机译：芳基丁烯酸衍生物作为新型组蛋白脱乙酰基酶抑制剂：合成，体外评估和分子对接研究

SYNTHESIS, INSILICO DOCKING AND ADMET STUDIES OF ARYL ACETIC ACID DERIVATIVES AS PROSTAGLANDIN ENDOPEROXIDE H SYNTHASE-2 INHIBITORS

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