Citation: Liu Weiwei, Liu Xiujian, Yin long, Cheng Fengchang. Progress in Syntheses and Biological Activities of 1,3,4-Thiadiazole Derivatives[J]. Chemistry, 2016, 79(10): 929-935,941.
1,3,4-噻二唑衍生物合成及其生物活性研究进展
English
Progress in Syntheses and Biological Activities of 1,3,4-Thiadiazole Derivatives
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Key words:
- 1,3,4-Thiadiazole
- / Derivatives
- / Synthesis methods
- / Biological activity
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[1] Y Hu, C Y Li, X M Wang et al. Chem. Rev., 2014, 114:5572~5610.[1] Y Hu, C Y Li, X M Wang et al. Chem. Rev., 2014, 114:5572~5610.
-
[2] H M Kuo, S Y Li, H S Sheu et al. Tetrahedron, 2012, 68(36):7331~7337.[2] H M Kuo, S Y Li, H S Sheu et al. Tetrahedron, 2012, 68(36):7331~7337.
-
[3] D Kumar, N M Kumar, K H Chang et al. Eur. J. Med. Chem., 2010, 45(10):4664~4668.[3] D Kumar, N M Kumar, K H Chang et al. Eur. J. Med. Chem., 2010, 45(10):4664~4668.
-
[4] C T Liao, Y J Wang, C S Huang et al. Tetrahedron, 2007, 63(50):12437~12445.[4] C T Liao, Y J Wang, C S Huang et al. Tetrahedron, 2007, 63(50):12437~12445.
-
[5] J K Augustine, V Vairaperumal, S Narasimhan et al. Tetrahedron, 2009, 65(48):9989~9996.[5] J K Augustine, V Vairaperumal, S Narasimhan et al. Tetrahedron, 2009, 65(48):9989~9996.
-
[6] M X Wei, L Feng, X Q Li et al. Eur. J. Med. Chem., 2009, 44(8):3340~3344.[6] M X Wei, L Feng, X Q Li et al. Eur. J. Med. Chem., 2009, 44(8):3340~3344.
-
[7] A A Kadi, E S Al-Abdullah, I A Shehata et al. Eur. J. Med. Chem., 2010, 45(11):5006~5011,[7] A A Kadi, E S Al-Abdullah, I A Shehata et al. Eur. J. Med. Chem., 2010, 45(11):5006~5011,
-
[8] G Rai, V Kenyon, A Jadhav et al. J. Med. Chem., 2010, 53(20):7392~7404.[8] G Rai, V Kenyon, A Jadhav et al. J. Med. Chem., 2010, 53(20):7392~7404.
-
[9] Y Luo, S Zhang, Z J Liu et al. Eur. J. Med. Chem., 2013, 64:54~61.[9] Y Luo, S Zhang, Z J Liu et al. Eur. J. Med. Chem., 2013, 64:54~61.
-
[10] A T Mavrova, D Wesselinova, J A Tsenov et al. Eur. J. Med. Chem., 2014, 86:676~683.[10] A T Mavrova, D Wesselinova, J A Tsenov et al. Eur. J. Med. Chem., 2014, 86:676~683.
-
[11] K R Sathisha, S A Khanum, J N N S Chandra et al. Bioorg. Med. Chem., 2011, 19:211~220.[11] K R Sathisha, S A Khanum, J N N S Chandra et al. Bioorg. Med. Chem., 2011, 19:211~220.
-
[12] J K Jiang, J G McCoy, M Shen et al. Bioorg. Med. Chem., 2014, 24:1148~1153.[12] J K Jiang, J G McCoy, M Shen et al. Bioorg. Med. Chem., 2014, 24:1148~1153.
-
[13] M N Noolvi, H M Patel, N Singh et al. Eur. J. Med. Chem., 2011, 46(9):4411~4418.[13] M N Noolvi, H M Patel, N Singh et al. Eur. J. Med. Chem., 2011, 46(9):4411~4418.
-
[14] G L Almajan, S F Barbuceanu, G Bancescu et al. Eur. J. Med. Chem., 2010, 45(12):6139~6146.[14] G L Almajan, S F Barbuceanu, G Bancescu et al. Eur. J. Med. Chem., 2010, 45(12):6139~6146.
-
[15] F Aryanasab, A Z Halimehjani, M R Saidi. Tetrahed. Lett., 2010, 51(5):790~792.[15] F Aryanasab, A Z Halimehjani, M R Saidi. Tetrahed. Lett., 2010, 51(5):790~792.
-
[16] U Salgm-Goksen, N Gokhan-Kelekci, O Goktas et al. Bioorg. Med. Chem., 2007, 15(17):5738~5751.[16] U Salgm-Goksen, N Gokhan-Kelekci, O Goktas et al. Bioorg. Med. Chem., 2007, 15(17):5738~5751.
-
[17] K Matsuno, Y Masuda, Y Uehara et al. ACS Med. Chem. Lett., 2010, 1(8):371~375.[17] K Matsuno, Y Masuda, Y Uehara et al. ACS Med. Chem. Lett., 2010, 1(8):371~375.
-
[18] T T Wang, W K Miao, S S Wu et al. Chin. J. Chem., 2011, 29(5):959~967.[18] T T Wang, W K Miao, S S Wu et al. Chin. J. Chem., 2011, 29(5):959~967.
-
[19] M D Hall, N K Salam, J L Hellawell et al. J. Med. Chem., 2009, 52(10):3191~3204.[19] M D Hall, N K Salam, J L Hellawell et al. J. Med. Chem., 2009, 52(10):3191~3204.
-
[20] A A Hassan, A F E Mourad, K M El-Shaieb et al. Molecules, 2005, 10(7):822~832.[20] A A Hassan, A F E Mourad, K M El-Shaieb et al. Molecules, 2005, 10(7):822~832.
-
[21] A A Hassan, A F E Mourad, K M El-Shaieb et al. Heteroatom Chem., 2003, 14(6):535~541.[21] A A Hassan, A F E Mourad, K M El-Shaieb et al. Heteroatom Chem., 2003, 14(6):535~541.
-
[22] J M Farrar, M K Patel, P Kaszynski et al. J. Org. Chem., 2000, 65(4):931~940.[22] J M Farrar, M K Patel, P Kaszynski et al. J. Org. Chem., 2000, 65(4):931~940.
-
[23] A R Sayed. Tetrahed. Lett., 2010, 51(34):4490~4493.[23] A R Sayed. Tetrahed. Lett., 2010, 51(34):4490~4493.
-
[24] A S Shawali, A R Sayed. J. Sulfur Chem., 2006, 27(3):233~244.[24] A S Shawali, A R Sayed. J. Sulfur Chem., 2006, 27(3):233~244.
-
[25] A S Shawali, A R Sayed. J. Sulfur Chem., 2007, 28:23~29.[25] A S Shawali, A R Sayed. J. Sulfur Chem., 2007, 28:23~29.
-
[26] M A Epishina, A S Kulikov, N V Ignat'ev et al. Mendeleev Commun., 2011, 21(6):331~333.[26] M A Epishina, A S Kulikov, N V Ignat'ev et al. Mendeleev Commun., 2011, 21(6):331~333.
-
[27] M E Layton, M J Kelly, K J Rodzinak et al. ACS Chem. Neurosci., 2011, 2(7):352~362.[27] M E Layton, M J Kelly, K J Rodzinak et al. ACS Chem. Neurosci., 2011, 2(7):352~362.
-
[28] J Matysiak, A Skrzypek, A Niewiadomy. Heteroatom Chem., 2010, 21(7):533~540.[28] J Matysiak, A Skrzypek, A Niewiadomy. Heteroatom Chem., 2010, 21(7):533~540.
-
[29] V Padmavathi, G D Reddy, S N Reddy et al. Eur. J. Med. Chem., 2011, 46(4):1367~1373.[29] V Padmavathi, G D Reddy, S N Reddy et al. Eur. J. Med. Chem., 2011, 46(4):1367~1373.
-
[30] V Padmavathi, G S Reddy, A V N Mohan et al. ARKIVOC, 2008:48~60.[30] V Padmavathi, G S Reddy, A V N Mohan et al. ARKIVOC, 2008:48~60.
-
[31] J C Kappel, T S Yokum, G Barany. J. Comb. Chem., 2004, 6:746~752[31] J C Kappel, T S Yokum, G Barany. J. Comb. Chem., 2004, 6:746~752
-
[32] J Y Hwang, H S Choi, D H Lee et al. J. Comb. Chem., 2005, 7:816~819.[32] J Y Hwang, H S Choi, D H Lee et al. J. Comb. Chem., 2005, 7:816~819.
-
[33] Y D Gong, T Lee. J. Comb. Chem., 2010, 12(4):393~409.[33] Y D Gong, T Lee. J. Comb. Chem., 2010, 12(4):393~409.
-
[34] V Polshettiwar, R S Varma. Tetrahed. Lett., 2008, 49(5):879~883.[34] V Polshettiwar, R S Varma. Tetrahed. Lett., 2008, 49(5):879~883.
-
[35] A A Kiryanov, P Sampson, A J Seed. J. Org. Chem., 2001, 66(23):7925~7929.[35] A A Kiryanov, P Sampson, A J Seed. J. Org. Chem., 2001, 66(23):7925~7929.
-
[36] 李政, 田国强, 赵彦龙. 西北师范大学学报(自然科学版), 2008, 44(3):46~49.[36] 李政, 田国强, 赵彦龙. 西北师范大学学报(自然科学版), 2008, 44(3):46~49.
-
[37] 刘玮炜, 霍云峰, 张强. 华侨大学学报(自然科学版), 2013, 34(5):539~541.[37] 刘玮炜, 霍云峰, 张强. 华侨大学学报(自然科学版), 2013, 34(5):539~541.
-
[38] V Mathew, J Keshavayya, V P Vaidya et al. Eur. J. Med. Chem., 2007, 42(6):823~840.[38] V Mathew, J Keshavayya, V P Vaidya et al. Eur. J. Med. Chem., 2007, 42(6):823~840.
-
[39] B Chandrakantha, A M Isloor, P Shetty et al. Eur. J. Med. Chem., 2014, 71:316~323.[39] B Chandrakantha, A M Isloor, P Shetty et al. Eur. J. Med. Chem., 2014, 71:316~323.
-
[40] M N Noolvi, H M Patel, S Kamboj et al. Arab. J. Chem., 2012, 2:003.[40] M N Noolvi, H M Patel, S Kamboj et al. Arab. J. Chem., 2012, 2:003.
-
[41] S Talath, A K Gadad, Eur. J. Med. Chem., 2006, 41(8):918~924.[41] S Talath, A K Gadad, Eur. J. Med. Chem., 2006, 41(8):918~924.
-
[42] 王美君, 卢俊瑞, 辛春伟等. 高等学校化学学报, 2015, 36:469~476.[42] 王美君, 卢俊瑞, 辛春伟等. 高等学校化学学报, 2015, 36:469~476.
-
[43] 李英俊, 孙亚珍, 靳焜等. 有机化学, 2008, 28:1074~1078.[43] 李英俊, 孙亚珍, 靳焜等. 有机化学, 2008, 28:1074~1078.
-
[44] Z Luo, B Chen, S Y He et al. Bioorg. Med. Chem. Lett., 2012, 22(9):3191~3193.[44] Z Luo, B Chen, S Y He et al. Bioorg. Med. Chem. Lett., 2012, 22(9):3191~3193.
-
[45] D A Ibrahim. Eur. J. Med. Chem., 2009, 44(7):2776~2781.[45] D A Ibrahim. Eur. J. Med. Chem., 2009, 44(7):2776~2781.
-
[46] W Rzeski, J Matysiakb, M K Szerszen et al. Bioorg. Med. Chem., 2007, 15(9):3201~3207.[46] W Rzeski, J Matysiakb, M K Szerszen et al. Bioorg. Med. Chem., 2007, 15(9):3201~3207.
-
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