Design ,synthesis and In-vitro antitumor evaluation of new 2, 3-diaryl-indenopyrazole and 2,3-diaryl-benzofuropyrazole derivatives as selective cyclooxygenase (COX-2) inhibitors

T. Zebardast; A. Zarghi; F. H.Shirazi

首页> 外文期刊>Research in Pharmaceutical Sciences >Design ,synthesis and In-vitro antitumor evaluation of new 2, 3-diaryl-indenopyrazole and 2,3-diaryl-benzofuropyrazole derivatives as selective cyclooxygenase (COX-2) inhibitors

【24h】

Design ,synthesis and In-vitro antitumor evaluation of new 2, 3-diaryl-indenopyrazole and 2,3-diaryl-benzofuropyrazole derivatives as selective cyclooxygenase (COX-2) inhibitors

机译：新的2,3-二芳基茚并吡唑和2,3-二芳基苯并呋喃吡唑衍生物作为选择性环加氧酶（COX-2）抑制剂的设计，合成和体外抗肿瘤评估

获取原文

掌桥外文数据库（机构版） >>

开具论文收录证明 >>

文献代查 >>

页面导航

著录项
相似文献
相关主题

著录项

来源
《Research in Pharmaceutical Sciences》 |2012年第5期|共页
作者
T. Zebardast; A. Zarghi; F. H.Shirazi;
展开▼
作者单位

展开▼
收录信息
原文格式 PDF
正文语种
中图分类药学;
关键词

相似文献

外文文献
中文文献
专利

1. Design, Synthesis and Biological Evaluation of4-(Imidazolylmethyl)-2-(4-methylsulfonyl phenyl)-Quinoline Derivatives as Selective COX-2 Inhibitors and In-vitro Anti-breast Cancer Agents [J] . Azizi Ebrahim, Ghodsi Razieh, Zarghi Afshin Iranian Journal of Pharmaceutical Research . 2016,第1期

机译：4-（咪唑基甲基）-2-（4-甲基磺酰基苯基）-喹啉衍生物作为选择性COX-2抑制剂和体外抗乳腺癌药物的设计，合成和生物学评价
2. Design, synthesis, and biological evaluation of new pyrazino[1,2-a]benzimidazole derivatives as selective cyclooxygenase (COX-2) inhibitors [J] . Movahed Mahsa Azami, Daraei Bahram, Shahosseini Soraya, Archiv der Pharmazie . 2019,第2期

机译：新吡唑啉[1,2-A]苯并咪唑衍生物作为选择性环氧酶（COX-2）抑制剂的设计，合成和生物学评价
3. Design and synthesis of new 1,3-benzdiazinan-4-one derivatives as selective cyclooxygenase (COX-2) inhibitors [J] . ZarghiA., ZebardastT., HajighasemaliF., Archiv der Pharmazie . 2012,第4期

机译：设计和合成作为选择性环氧合酶（COX-2）抑制剂的新的1,3-苯并二氮杂-4-酮衍生物
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. 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. Design Synthesis and Biological Evaluation of4-(Imidazolylmethyl)-2-(4-methylsulfonyl phenyl)-Quinoline Derivatives as Selective COX-2 Inhibitors and In-vitro Anti-breast Cancer Agents [O] . Razieh Ghodsi, Ebrahim Azizi, Afshin Zarghi 2016

机译：作为选择性COX-2抑制剂和体外抗乳腺癌药物的4-（咪唑基甲基）-2-（4-甲基磺酰基苯基）-喹啉衍生物的设计合成和生物学评价
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

Design ,synthesis and In-vitro antitumor evaluation of new 2, 3-diaryl-indenopyrazole and 2,3-diaryl-benzofuropyrazole derivatives as selective cyclooxygenase (COX-2) inhibitors

著录项

相似文献

相关主题

期刊订阅