Synthesis and antiproliferative activity of novel aminoalkylated flavones
-
Published:2017-08
Issue:8
Volume:53
Page:871-875
-
ISSN:0009-3122
-
Container-title:Chemistry of Heterocyclic Compounds
-
language:en
-
Short-container-title:Chem Heterocycl Comp
Author:
Yan Lili,Liu Haoran,Wang Qiuan,Wang Gangqiang
Publisher
Springer Science and Business Media LLC
Subject
Organic Chemistry
Reference9 articles.
1. (a) Verma, A. K.; Pratap, R. Tetrahedron 2012, 68, 8523. (b) Li, S.; Pan, M. H.; Lai, C. S.; Lo, C. Y.; Dushenkov, S.; Ho, C. T. Bioorg. Med. Chem. 2007, 15, 3381. (c) Liu, H. R.; Huang, X. Q.; Lou, D. H.; Liu, X. J.; Liu, W. K.; Wang, Q. A. Bioorg. Med. Chem. Lett. 2014, 24, 4749. (d) Soltesova-Prnova, M.; Milackova, I.; Stefek, M. Chem. Pap. 2016, 70, 1439. 2. (a) Zhao, J.; Pawar, R. S.; Ali Z.; Kham, I. A. J. Nat. Prod. 2007, 70, 289. (b) Kou, L. Q.; Cheng, X. L. Zhang, Z. T. J. Chem. Crystallogr. 2008, 38, 21. 3. (a) Kuo, Y. J.; Hwang, S. Y.; Wu, M. D.; Liao, C. C.; Liang, Y. H.; Kuo, Y. H.; Ho, H. O. Chem. Pharm. Bull. 2008, 56, 585. (b) Mori, A.; Nishino, C.; Enoki, N.; Tawata, S. Phytochemistry 1988, 27, 1017. (c) Wongsrikaew, N.; Kim, H.; Vichitphan, K.; Cho, S. K.; Han, J. J. Korean Soc. Appl. Biol. Chem. 2012, 55, 813. 4. (d) Manthey, J. A.; Grohmann, K.; Guthrie, N. Curr. Med. Chem. 2001, 8, 135. (b) Kesarkar, S.; Bhandage, A.; Deshmukh, S.; Abhyankar, M. J. Pharm. Res. 2009, 2, 1148. (a) Li, X.; Chen, G. L.; Zhang, X. J.; Zhang, Q.; Zheng, S. L.; Wang, G. D.; Chen, Q. H. Bioorg. Med. Chem. Lett. 2016, 26, 4241. (b) Yuan, J.; Wong, I.; Jiang, T.; Wang, S. W.; Liu, T.; Wen, B. J.; Chow, L. M.; Wan, S. B. Eur. J. Med. Chem. 2012, 54, 413. (c) Amrutha, K.; Pandurangan, N. J.; Shaji, S. K.; Sunilkumar, D.; Subhalakshmi, K.; Rajakrishna, L.; Banerji, A. Bioorg. Med. Chem. Lett. 2014, 24, 4735. 5. (a) Kovaleva, K. S.; Yarovaya, O. I.; Shernyukov, A. V.; Zarubaev, V. V.; Shtro, A. A.; Orshanskaya, Y. R.; Salakhutdinov, N. F. Chem. Heterocycl. Compd. 2017, 53, 364. [Khim. Geterotsikl. Soedin. 2017, 53, 364.] (b) Zhang, S.; Ma, J.; Bao, Y.; Yang, P.; Zhou, L.; Li, K.; Sun, X. Bioorg. Med. Chem. 2008, 16, 7127. (c) Bonesi, M.; Tundis, R.; Deguin, B.; Loizzo, M. R.; Menichini, F.; Tillequin, F.; Menichini, F. Bioorg. Med. Chem. Lett. 2008, 18, 5431. (d) Lozinskii, O. A.; Shokol, T. V.; Khilya, V. P. Chem. Heterocycl. Compd. 2011, 47, 1055. [Khim. Geterotsikl. Soedin. 2011, 1283.] (e) Liu, C. Y.; Dong, L. P.; Wang, S. C.; Wang, Q. A. Mol. Diversity 2015, 19, 737. (f) Voskoboynik, O. Y.; Kolomoets, O. S.; Berest, G. G.; Nosulenko, I. S.; Martynenko, Y. V.; Kovalenko, S. I. Chem. Heterocycl. Compd. 2017, 53, 256. [Khim. Geterotsikl. Soedin. 2017, 53, 256.]
Cited by
4 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
|
|