Citation: Xiao Liwei, Xiao Shuqiang, Li Zheng, Jing Xuemin, Dai Fucai. s-Triazolothiadiazoles: A Class of Important Structural Unit for Potential Drugs[J]. Chemistry, ;2019, 82(2): 120-127. shu

s-Triazolothiadiazoles: A Class of Important Structural Unit for Potential Drugs

  • Received Date: 6 August 2018
    Accepted Date: 12 October 2018

  • 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 s-triazolothiadiazoles compounds, the research progress of biological activities for the titled compounds in recent years are reviewed.
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    1. [1]

       

    2. [2]

      J Sahu, S Ganguly, A Kaushik. Chin. J. Nat. Med. 2013, 11(5): 456~465.

    3. [3]

      S Haider, M S A Hamid. Eur. J. Med. Chem., 2015, 92: 156~177. 

    4. [4]

      A Ayati, S Emami, A Foroumadi. Eur. J. Med. Chem., 2016, 109: 380~392. 

    5. [5]

       

    6. [6]

      V Mathew, J Keshavayya, V P Vaidya. Eur. J. Med. Chem., 2006, 41: 1048~1058. 

    7. [7]

      V Mathew, J Keshavayya, V P Vaidya et al. Eur. J. Med. Chem., 2007, 42: 823~840. 

    8. [8]

      T Karabasanagouda, A V Adhikari, N S Shetty. Eur. J. Med. Chem., 2007, 42: 521~529. 

    9. [9]

       

    10. [10]

      S N Swamy, P B S Basappa, B Prabhuswamy et al. Eur. J. Med. Chem., 2006, 41: 531~538. 

    11. [11]

      N S A M Khalil. Eur. J. Med. Chem., 2007, 42: 1193~1199. 

    12. [12]

       

    13. [13]

      P Karegoudar, D J Prasad, M Ashok et al. Eur. J. Med. Chem., 2008, 43: 808~815. 

    14. [14]

      D J Prasad, M Ashok, P Karegoudar et al. Eur. J. Med. Chem., 2009, 44: 551~557. 

    15. [15]

      M Amir, H Kumar, S A Javed. Eur. J. Med. Chem., 2008, 43: 2056~2066. 

    16. [16]

      G L Almajan, S F Barbuceanu, G Bancescu et al. Eur. J. Med. Chem., 2010, 45: 6139~6146. 

    17. [17]

      Z J Fan, Z K Yang, H K Zhang et al. J. Agric. Food Chem., 2010, 58(5): 2631~2636.

    18. [18]

      A M Isloor, B Kalluraya, K S Pai. Eur. J. Med. Chem., 2010, 45: 825~830. 

    19. [19]

      A Cansız, A Cetin, C Orek et al. Spectrochim. Acta A, 2012, 97: 606~615. 

    20. [20]

       

    21. [21]

       

    22. [22]

      Y Kotaiah, K Nagaraju, N Harikrishna et al. Eur. J. Med. Chem., 2014, 75: 195~202. 

    23. [23]

    24. [24]

       

    25. [25]

    26. [26]

    27. [27]

      V Mathew, D Giles, J Keshavayya et al. Arch. Pharm. Chem. Life Sci. 2009, 342: 210~222.

    28. [28]

    29. [29]

    30. [30]

      D A Ibrahim. Eur. J. Med. Chem., 2009, 44: 2776~2781. 

    31. [31]

      S M I Badr, R M Barwa. Bioorg. Med. Chem., 2011, 19: 4506~4512. 

    32. [32]

      G Q Hu, Y Yang, L Yi et al. Acta Pharm. Sin. B, 2011, 1(3): 172~177. 

    33. [33]

    34. [34]

      M M Kamel, N Y M Abdo. Eur. J. Med. Chem., 2014, 86: 75~80. 

    35. [35]

      A Husain, M Rashid, R Mishra et al. Eur. J. Med. Chem., 2013, 62: 785~798. 

    36. [36]

      S A F Rostom, M H Badr, H A A El Razik et al. Eur. J. Med. Chem., 2017, 139: 263~279. 

    37. [37]

      D Sunil, A M Isloor, P Shetty et al. Arab. J. Chem., 2010, 3: 211~217. 

    38. [38]

      W S I Abou-Elmagd, A I Hashem. J. Heterocycl. Chem., 2016, 53: 202~208. 

    39. [39]

      D Chowrasia, C Karthikeyan, L Choure et al. Arab. J. Chem., 2017, 10: 2424~2428. 

    40. [40]

      P R Kamath, D Sunil, S Das et al. Chem. Biol. Interact., 2017, 268: 53~67. 

    41. [41]

      H A Ibrahim, F M Awadallah, H M Refaat et al. Bioorg. Chem., 2018, 77: 457~470. 

    42. [42]

      S Ram, G Celik, P Khloya et al. Bioorg. Med. Chem., 2014, 22: 1873~1882. 

    43. [43]

    44. [44]

    45. [45]

    46. [46]

    47. [47]

    48. [48]

      I Khan, A Ibrar, S Zaib et al. Bioorg. Med. Chem., 2014, 22: 6163~6173. 

    49. [49]

      I Khan, S Zaib, A Ibrar et al. Eur. J. Med. Chem., 2014, 78: 167~177. 

    50. [50]

      I Khan, S M Bakht, A Ibrar et al. RSC Adv., 2015, 5: 21249~21267. 

    51. [51]

      S Llona-Minguez, A Hoglund, E Wiita et al. J. Med. Chem., 2017, 60: 2148~2154. 

    52. [52]

      P Cui, X Li, M Zhu et al. Eur. J. Med. Chem., 2017, 127: 159~165. 

    53. [53]

      G V S Kumar, Y R Prasad, B P Mallikarjuna et al. Eur. J. Med. Chem., 2010, 45: 5120~5129. 

    54. [54]

      M Himaja, K J Prathap, S V Mali. J. Heterocycl. Chem., 2012, 49: 823~828. 

    55. [55]

      Z Li, Y Liu, X Bai et al. RSC Adv., 2015, 5: 97089~97101. 

    56. [56]

      M Amir, H Kumar, S A Javed. Bioorg. Med. Chem. Lett., 2007, 17: 4504~4508. 

    57. [57]

      M W Akhter, M Z Hassan, M Amir. Arab. J. Chem., 2014, 7: 955~963. 

    58. [58]

      S J Gilani, S A Khan, N Siddiqui. Bioorg. Med. Chem. Lett., 2010, 20: 4762~4765. 

    59. [59]

      N Chidananda, B Poojary, V Sumangala et al. Eur. J. Med. Chem., 2012, 51: 124~136. 

    60. [60]

      M F El-Shehry, A A Abu-Hashem, E M El-Telbani. Eur. J. Med. Chem., 2010, 45: 1906~1911. 

    61. [61]

      X Q Deng, Z Q Dong, M X Song et al. Arch. Pharm. Chem. Life Sci., 2012, 345: 565~573. 

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