Synthesis of 2,3-diaryl-1,3-thiazolidine-4-one derivatives as selective cyclooxygenase (COX-2) inhibitors.

Zarghi A; Najafnia L; Daraee B; Dadrass OG; Hedayati M

首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Synthesis of 2,3-diaryl-1,3-thiazolidine-4-one derivatives as selective cyclooxygenase (COX-2) inhibitors.

【24h】

Synthesis of 2,3-diaryl-1,3-thiazolidine-4-one derivatives as selective cyclooxygenase (COX-2) inhibitors.

机译：合成2,3-二芳基-1,3-噻唑烷-4-one衍生物作为选择性环加氧酶（COX-2）抑制剂。

获取原文

获取原文并翻译 | 示例

获取外文期刊封面封底 >>

开具论文收录证明 >>

文献代查 >>

页面导航

摘要
著录项
相似文献
相关主题

摘要

A group of 2,3-diaryl-1,3-thiazolidine-4-ones, possessing a methylsulfonyl pharmacophore, were synthesized and their biological activities were evaluated for cyclooxygenase-2 (COX-2) inhibitory activity.

机译：合成一组具有甲基磺酰基药效基团的2,3-二芳基-1,3-噻唑烷-4-酮，并评估其生物活性对环氧合酶-2（COX-2）的抑制活性。

著录项

来源
《Bioorganic and Medicinal Chemistry Letters》 |2007年第20期|共4页
作者
Zarghi A; Najafnia L; Daraee B; Dadrass OG; Hedayati M;
展开▼
作者单位

展开▼
收录信息
原文格式 PDF
正文语种 eng
中图分类
关键词
Prostaglandin-Endoperoxide Synthase; Synthesis; inhibitors; derivatives; 前列腺素内过氧化物合酶;

机译：Prostaglandin-Endoperoxide Synthase;Synthesis;inhibitors;derivatives;前列腺素内过氧化物合酶;

相似文献

外文文献
中文文献
专利

1. Synthesis of 2,3-diaryl-1,3-thiazolidine-4-one derivatives as selective cyclooxygenase (COX-2) inhibitors. [J] . Zarghi A, Najafnia L, Daraee B, Bioorganic and Medicinal Chemistry Letters . 2007,第20期

机译：合成2,3-二芳基-1,3-噻唑烷-4-one衍生物作为选择性环加氧酶（COX-2）抑制剂。
2. Design and synthesis of new 1,3-benzthiazinan-4-one derivatives as selective cyclooxygenase (COX-2) inhibitors. [J] . Zarghi A, Zebardast T, Daraie B Bioorganic and medicinal chemistry . 2009,第15期

机译：设计和合成作为选择性环加氧酶（COX-2）抑制剂的新1,3-苯并噻唑烷-4-酮衍生物。
3. Design and synthesis of 3-alkyl-2-aryl-1,3-thiazinan-4-one derivatives as selective cyclooxygenase (COX-2) inhibitors. [J] . Zebardast T, Zarghi A, Daraie B Bioorganic and Medicinal Chemistry Letters . 2009,第12期

机译：设计和合成作为选择性环氧合酶（COX-2）抑制剂的3-烷基-2-芳基-1,3-噻嗪南-4-酮衍生物。
4. Molecular Docking Technique for selection of some naproxen derivatives as inhibitors of cyclooxygenase 2 (COX-2) [C] . Beteringhe Adrian, Symeonidis Flavia Corina Mitroi International Conference on Electronics, Computers and Artificial Intelligence . 2015

机译：用于选择一些萘普生衍生物作为环氧氧酶2的抑制剂的分子对接技术（COX-2）
5. Design, synthesis and biological evaluation of novel tricyclic cyclooxygenase-2 (COX-2) inhibitors. [D] . Perampalli Nekkar, Praveen Rao. 2004

机译：新型三环环氧合酶2（COX-2）抑制剂的设计，合成和生物学评估。
6. Synthesis Anti-Inflammatory and Anti- Nociceptive Activities and Cytotoxic Effect of Novel Thiazolidin-4-ones Derivatives as Selective Cyclooxygenase (COX-2) Inhibitors [O] . Seyed Adel Moallem, Mohsen Imenshahidi, Narges Shahini, 2013

机译：新型噻唑烷丁-4-酮衍生物作为选择性环加氧酶（COX-2）抑制剂的合成抗炎和抗伤害活性及细胞毒性作用
7. Design and Synthesis of Some 5-Substituted-2-(4-(azido or methylsulfonyl) phenyl)-1H-indole Derivatives as Selective Cyclooxygenase (COX-2) Inhibitors [O] . Afshin Zarghi 2008

机译：设计和合成一些5取代的-2-（4-（甲基磺酰基）苯基）-1H-吲哚衍生物作为选择性环氧酶（COX-2）抑制剂

Synthesis of 2,3-diaryl-1,3-thiazolidine-4-one derivatives as selective cyclooxygenase (COX-2) inhibitors.

摘要

著录项

相似文献

相关主题

期刊订阅