(E)-2-[2-(2-Nitrophenyl)ethenyl]-8-quinolyl acetate

被引:0
作者
Zhang, Li-Yan [2 ]
Huo, Yan-Ping [1 ]
机构
[1] Guangdong Univ Technol, Fac Chem Technol & Light Ind, Guangzhou 510006, Guangdong, Peoples R China
[2] Huangshan Univ, Dept Chem, Huangshan 245041, Peoples R China
来源
ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE | 2009年 / 65卷
基金
中国国家自然科学基金;
关键词
STYRYLQUINOLINE DERIVATIVES; CELLS;
D O I
10.1107/S1600536809044158
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
The title compound, C19H14N2O4, crystallizes with two molecules with very similar conformations in the asymmetric unit; the angles between the two ring systems are 8.7 (1) and 4.2 (1)degrees. In the crystal, intermolecular pi-pi interactions [centroid-centroid distance 3.973 (1) angstrom] lead to a three-dimensional network.
引用
收藏
页码:O2960 / U2706
页数:14
相关论文
共 10 条
[1]  
*BRUK AXS INC, 2001, SMART SADABS
[2]  
Bruker, 2003, SAINT PLUS
[3]  
Chen Chien-Shu, 2002, Chinese Pharmaceutical Journal (Taipei), V54, P353
[4]   Synthesis and biological evaluation of substituted quinolines:: Potential treatment of protozoal and retroviral co-infections [J].
Fakhfakh, MA ;
Fournet, A ;
Prina, E ;
Mouscadet, JF ;
Franck, X ;
Hocquemiller, R ;
Figadère, B .
BIOORGANIC & MEDICINAL CHEMISTRY, 2003, 11 (23) :5013-5023
[5]   Styrylquinoline derivatives:: A new class of potent HIV-1 integrase inhibitors that block HIV-1 replication in CEM cells [J].
Mekouar, K ;
Mouscadet, JF ;
Desmaële, D ;
Subra, F ;
Leh, H ;
Savouré, D ;
Auclair, C ;
d'Angelo, J .
JOURNAL OF MEDICINAL CHEMISTRY, 1998, 41 (15) :2846-2857
[6]   Modeling of the inhibition of retroviral integrases by styrylquinoline derivatives [J].
Ouali, M ;
Laboulais, C ;
Leh, H ;
Gill, D ;
Desmaële, D ;
Mekouar, K ;
Zouhiri, F ;
d'Angelo, J ;
Auclair, C ;
Mouscadet, JF ;
Le Bret, M .
JOURNAL OF MEDICINAL CHEMISTRY, 2000, 43 (10) :1949-1957
[7]   A short history of SHELX [J].
Sheldrick, George M. .
ACTA CRYSTALLOGRAPHICA A-FOUNDATION AND ADVANCES, 2008, 64 :112-122
[8]   First safe and practical synthesis of 2-amino-8-hydroxyquinoline [J].
Storz, T .
ORGANIC PROCESS RESEARCH & DEVELOPMENT, 2004, 8 (04) :663-665
[9]   Synthesis, crystal structure, and prediction of hole mobilities of 2,7′-ethylenebis(8-hydroxyquinoline) [J].
Zeng, He-Ping ;
OuYang, Xin-Hua ;
Wang, Ting-Ting ;
Yuan, Guo-Zan ;
Zhang, Guang-Hui ;
Zhang, Xin-min .
CRYSTAL GROWTH & DESIGN, 2006, 6 (07) :1697-1702
[10]   8-hydroxyquinoline derivatives induce the proliferation of rat mesenchymal stem cells (rMSCs) [J].
Zeng, He-Ping ;
Wang, Ting-Ting ;
Ouyang, Xin-Hua ;
Zhou, Ya-Dong ;
Jing, Hui-Lian ;
Yuan, Guo-Zan ;
Chen, Dong-Feng ;
Du, Shao-Hui ;
Li, Hui ;
Zhou, Jian-Hong .
BIOORGANIC & MEDICINAL CHEMISTRY, 2006, 14 (16) :5446-5450