摘要
均三唑并噻二唑是一类重要的稠杂环化合物,其衍生物具有抗菌、消炎、抗肿瘤、抗结核、酶抑制作用、调节植物生长等多种生物活性。本文按照均三唑并噻二唑类化合物呈现的不同生物活性进行分类,综述了近年来该类化合物在上述领域的研究进展。
s-Triazolothiadiazoles compounds are a kind of important fused heterocyclic compounds,which have extensive biological activity such as anti-bacterial, anti-inflammatory, anti-tumor, anti-tuberculosis, enzyme inhibition,regulating plant growth activity and so on. According to the different biological activities of striazolothiadiazoles compounds,the research progress of biological activities for the titled compounds in recent years are reviewed.
引文
[1]王艳,周成合.中国科学:化学,2011,41(9):1429~1456.
[2] J Sahu,S Ganguly,A Kaushik. Chin. J. Nat. Med. 2013,11(5):456~465.
[3] S Haider,M S A Hamid. Eur. J. Med. Chem.,2015,92:156~177.
[4] A Ayati,S Emami,A Foroumadi. Eur. J. Med. Chem.,2016,109:380~392.
[5]肖立伟,任萍,景学敏等.有机化学,2017,37:3085~3095.
[6] V Mathew,J Keshavayya,V P Vaidya. Eur. J. Med. Chem.,2006,41:1048~1058.
[7] V Mathew,J Keshavayya,V P Vaidya et al. Eur. J. Med.Chem.,2007,42:823~840.
[8] T Karabasanagouda,A V Adhikari,N S Shetty. Eur. J. Med.Chem.,2007,42:521~529.
[9]胡国强,侯莉莉,谢松强等.化学学报,2008,66(8):980~984.
[10] S N Swamy,P B S Basappa,B Prabhuswamy et al. Eur. J.Med. Chem.,2006,41:531~538.
[11] N S A M Khalil. Eur. J. Med. Chem.,2007,42:1193~1199.
[12]王美君,卢俊瑞,辛春伟等.高等学校化学学报,2015,36(3):469~476.
[13] P Karegoudar,D J Prasad,M Ashok et al. Eur. J. Med.Chem.,2008,43:808~815.
[14] D J Prasad,M Ashok,P Karegoudar et al. Eur. J. Med.Chem.,2009,44:551~557.
[15] M Amir,H Kumar,S A Javed. Eur. J. Med. Chem.,2008,43:2056~2066.
[16] G L Almajan,S F Barbuceanu,G Bancescu et al. Eur. J.Med. Chem.,2010,45:6139~6146.
[17] Z J Fan,Z K Yang,H K Zhang et al. J. Agric. Food Chem.,2010,58(5):2631~2636.
[18] A M Isloor,B Kalluraya,K S Pai. Eur. J. Med. Chem.,2010,45:825~830.
[19] A Cansz,A Cetin,C Orek et al. Spectrochim. Acta A,2012,97:606~615.
[20]姚明星,安悦,闫杰等.有机化学,2013,33:1015~1021.
[21]安悦,姚明星,周晓霞等.应用化学,2014,31(8):928~935.
[22] Y Kotaiah,K Nagaraju,N Harikrishna et al. Eur. J. Med.Chem.,2014,75:195~202.
[23]张欣,覃章兰.有机化学,2006,26(6):870~873.
[24]覃章兰,张欣.有机化学,2008,28(8):1483~1486.
[25]杜海棠,杜海军.有机化学,2010,30(1):137~141.
[26]孙晓红,白燕,刘源发.高等学校化学学报,2011,32(6):1312~1317.
[27] V Mathew,D Giles,J Keshavayya et al. Arch. Pharm. Chem.Life Sci. 2009,342:210~222.
[28]蔡志娟,薛思佳,柴安.有机化学,2007,27(11):1401~1403.
[29]薛思佳,柴安,蔡志娟等.有机化学,2008,28(3):494~497.
[30] D A Ibrahim. Eur. J. Med. Chem.,2009,44:2776~2781.
[31] S M I Badr,R M Barwa. Bioorg. Med. Chem.,2011,19:4506~4512.
[32] G Q Hu,Y Yang,L Yi et al. Acta Pharm. Sin. B,2011,1(3):172~177.
[33]吴书敏,闫强,倪礼礼等.中国药学杂志,2016,51(5):353~357.
[34] M M Kamel,N Y M Abdo. Eur. J. Med. Chem.,2014,86:75~80.
[35] A Husain,M Rashid,R Mishra et al. Eur. J. Med. Chem.,2013,62:785~798.
[36] S A F Rostom,M H Badr,H A A El Razik et al. Eur. J.Med. Chem.,2017,139:263~279.
[37] D Sunil,A M Isloor,P Shetty et al. Arab. J. Chem.,2010,3:211~217.
[38] W S I Abou-Elmagd,A I Hashem. J. Heterocycl. Chem.,2016,53:202~208.
[39] D Chowrasia, C Karthikeyan, L Choure et al. Arab. J.Chem.,2017,10:2424~2428.
[40] P R Kamath,D Sunil,S Das et al. Chem. Biol. Interact.,2017,268:53~67.
[41] H A Ibrahim,F M Awadallah,H M Refaat et al. Bioorg.Chem.,2018,77:457~470.
[42] S Ram,G Celik,P Khloya et al. Bioorg. Med. Chem.,2014,22:1873~1882.
[43]张成路,国阳,吴一非等.应用化学,2014,31(12):1419~1427.
[44]张成路,王雪,胡雪等.高等学校化学学报,2015,36(3):463~468.
[45]张成路,李传银,杨蒙等.应用化学,2017,34(4):385~393.
[46]张成路,李传银,顾耀东等.有机化学,2018,38:1223~1232.
[47]李英俊,李继阳,彭立娜等.有机化学,2017,37:485~495.
[48] I Khan,A Ibrar,S Zaib et al. Bioorg. Med. Chem.,2014,22:6163~6173.
[49] I Khan,S Zaib,A Ibrar et al. Eur. J. Med. Chem.,2014,78:167~177.
[50] I Khan,S M Bakht,A Ibrar et al. RSC Adv.,2015,5:21249~21267.
[51] S Llona-Minguez,A Hoglund,E Wiita et al. J. Med. Chem.,2017,60:2148~2154.
[52] P Cui,X Li,M Zhu et al. Eur. J. Med. Chem.,2017,127:159~165.
[53] G V S Kumar,Y R Prasad,B P Mallikarjuna et al. Eur. J.Med. Chem.,2010,45:5120~5129.
[54] M Himaja,K J Prathap,S V Mali. J. Heterocycl. Chem.,2012,49:823~828.
[55] Z Li,Y Liu,X Bai et al. RSC Adv.,2015,5:97089~97101.
[56] M Amir,H Kumar,S A Javed. Bioorg. Med. Chem. Lett.,2007,17:4504~4508.
[57] M W Akhter,M Z Hassan,M Amir. Arab. J. Chem.,2014,7:955~963.
[58] S J Gilani,S A Khan,N Siddiqui. Bioorg. Med. Chem. Lett.,2010,20:4762~4765.
[59] N Chidananda,B Poojary,V Sumangala et al. Eur. J. Med.Chem.,2012,51:124~136.
[60] M F El-Shehry,A A Abu-Hashem,E M El-Telbani. Eur. J.Med. Chem.,2010,45:1906~1911.
[61] X Q Deng,Z Q Dong,M X Song et al. Arch. Pharm. Chem.Life Sci.,2012,345:565~573.