Improved antiproliferative activities of a new series of 1,3,4-thiadiazole derivatives against human leukemia and breast cancer cell lines

Tingting Liu , Yichao Wan , Renshuai Liu , Lin Ma , Minyong Li , Hao Fang

Chemical Research in Chinese Universities ›› 2016, Vol. 32 ›› Issue (5) : 768 -774.

PDF
Chemical Research in Chinese Universities ›› 2016, Vol. 32 ›› Issue (5) : 768 -774. DOI: 10.1007/s40242-016-6159-6
Article

Improved antiproliferative activities of a new series of 1,3,4-thiadiazole derivatives against human leukemia and breast cancer cell lines

Author information +
History +
PDF

Abstract

Twenty-two novel 1,3,4-thiadiazole derivatives were synthesized using different aromatic acids as starting materials, followed by cyclization, coupling and deprotection reaction. The structures of all the target compounds were identified by means of 1H nuclear magnetic resonance(NMR), 13C NMR and high resolution mass spectrometer(HRMS). Further biological evaluations were performed for chronic myelogenous leukemia cell and breast cancer cell. The results suggest that most of the target compounds exhibit potent anti-proliferative activities. Especially, compound 5b shows better antiproliferative activities against MDA-MB-231 and K562 cell lines compared with gossypol.

Keywords

Thiadiazole / Anti-tumor activity / Antiproliferative activity

Cite this article

Download citation ▾
Tingting Liu, Yichao Wan, Renshuai Liu, Lin Ma, Minyong Li, Hao Fang. Improved antiproliferative activities of a new series of 1,3,4-thiadiazole derivatives against human leukemia and breast cancer cell lines. Chemical Research in Chinese Universities, 2016, 32(5): 768-774 DOI:10.1007/s40242-016-6159-6

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Sun W., Kimura H., Hattori N., Tanaka S., Matsuyama S., Shiota K. Biophys. Res. Commun., 2006, 342(3): 817.

[2]

Bange J., Zwick E., Ullrich A. Nat. Chem., 2001, 7(5): 548.

[3]

Park J. H., Oh C. H. Bull. Korean. Chem. Soc., 2010, 31(10): 2854.

[4]

Chern J. W., Liaw Y. C., Chen C. S., Rong J. G., Huang C. L., Chan C. H., Wang H. J. Heterocycles, 1993, 36(5): 1091.

[5]

Andreani A., Rambaldi M., Leoni A., Locatelli A., Bossa R., Fraccari A., Galatulas I., Salvatore G. J. Med. Chem., 1996, 39(14): 2852.

[6]

Yoo H., Suh M., Park S. J. Med. Chem., 1998, 41(24): 4716.

[7]

Andreani A., Granaiola M., Leoni A., Locatelli A., Morigi R., Rambaldi M., Giorgi G., Salvini L. V. G. Drug. Des., 2001, 16(2/3): 167.

[8]

Oleson J. J., Sloboda A., Troy W. P., Halliday S. L., Landes M. J., Angier R. B., Semb J., Cyr K., Williams J. H. J. Am. Chem. Soc., 1955, 77(24): 6713.

[9]

Haider S., Alam M. S., Hamid H. Eur. J. Med. Chem., 2014, 92(92): 156.

[10]

Guan P., Sun F. E., Hou X., Wang F., Yi F., Xu W., Fang H. Bioorg. Med. Chem., 2012, 20(12): 3865.

[11]

Guan P., Wang L., Hou X., Wan Y., Xu W., Tang W., Fang H. Bioorg. Med. Chem., 2014, 22(21): 5766.

[12]

Liu T., Wan Y., Fang H. Chin. J. Org. Chem., 2016, 36(2): 417.

AI Summary AI Mindmap
PDF

160

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/