Design and synthesis of 1-glycosyl-4-{N-[(2′-morpholinethoxy)- phenyl]aminomethyl}-1H-1,2,3-triazoles as calcium activators

Yuxin Li , Fengjuan Di , Duoyi Wang , Wei Chen , Yingying Wan , Zhengming Li

Chemical Research in Chinese Universities ›› 2015, Vol. 31 ›› Issue (6) : 952 -957.

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Chemical Research in Chinese Universities ›› 2015, Vol. 31 ›› Issue (6) : 952 -957. DOI: 10.1007/s40242-015-5134-y
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Design and synthesis of 1-glycosyl-4-{N-[(2′-morpholinethoxy)- phenyl]aminomethyl}-1H-1,2,3-triazoles as calcium activators

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Abstract

A series of novel 1-glycosyl-4-{N-[(2′-morpholinethoxy)phenyl]aminomethyl}-1H-1,2,3-triazoles was designed and synthesized through a simple and efficient multistep synthetic method in good yields. The 1,2,3-triazole moiety acted as a single disubstituted ring and a linker between carbohydrates(D-glucose, D-galactose, maltose and lactose) and morpholine. The compounds were characterized by 1H NMR, 13C NMR and mass spectra(MS). Two different deprotection methods were discussed. The effects of compounds 5a, 5c and 6e on the intracellular calcium ion concentration([Ca2+]i) in the central neurons of S. exigua were well investigated by calcium imaging technique. The results demonstrated that compound 6e could elevate the calcium concentration in the glial cells, not in the neurons.

Keywords

Calcium channel / Click chemistry / Glial cell / Glycosyl / Triazole

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Yuxin Li, Fengjuan Di, Duoyi Wang, Wei Chen, Yingying Wan, Zhengming Li. Design and synthesis of 1-glycosyl-4-{N-[(2′-morpholinethoxy)- phenyl]aminomethyl}-1H-1,2,3-triazoles as calcium activators. Chemical Research in Chinese Universities, 2015, 31(6): 952-957 DOI:10.1007/s40242-015-5134-y

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References

[1]

Kamal A., Shankaraiah N., Devaiah V., Laxma R. K., Juvekar A., Sen S., Kurian N., Zingde S. Bioorg. Med. Chem. Lett., 2008, 18: 1468.

[2]

Soltis M. J., Yeh H. J., Cole K. A., Whittaker N., Wersto R. P., Kohn E. C. Drug Metab. Dispos., 1996, 24: 799.

[3]

Dedola S., Hughes D. L., Nepogodiev S. A., Rejzek M., Field R. A. Carbohydr. Res., 2010, 345: 1123.

[4]

Wang Z. J., Gao Y., Hou Y. L., Zhang C., Yu S. J., Bian Q., Li Z. M., Zhao W. G. Eur. J. Med. Chem., 2014, 86: 87.

[5]

Chen Y. B., Xiao Y. X., Shao X. S., Xu X. Y., Li Z. Chin. J. Chem., 2014, 32: 592.

[6]

Yuki W., Sadayuki A., Preparation of Tetrazolinone Derivatives as Agrochemical Fungicides and Pesticides, WO 2015030217, 2015

[7]

Kolb H. C., Finn M. G., Sharpless K. B. Angew. Chem. Int. Ed., 2001, 40: 2004.

[8]

Kolb H. C., Sharpless K. B. Drug Discovery Today, 2003, 8: 1128.

[9]

Cai Q., Yan J. J., Ding K. Org. Lett., 2012, 14: 3332.

[10]

Dario P. Molecules, 2013, 18: 9512.

[11]

Sabrina B. F., Ana C. R. S., Mariana F. C. C., Emerson S. L., Carlos R. K., Floriano P. S., Vitor F. F. J. Med. Chem., 2010, 53: 2364.

[12]

Muthana S., Yu H., Cao H., Cheng J., Chen X. J. Org. Chem., 2009, 74: 2928.

[13]

Mao M. Z., Li Y. X., Zhou Y. Y., Yang X. P., Zhang X. L., Zhang X., Li Z. M. Chem. Res. Chinese Universities, 2013, 29(5): 900.

[14]

Mao M. Z., Li Y. X., Zhou Y. Y., Chen W., Liu T. W., Yu S. J., Wang S. H., Li Z. M. Chem. Biol. Drug Des., 2011, 78: 695.

[15]

Tropper F. D., Andersson F. O., Braun S., Roy R. Synth., 1992, 7: 618.

[16]

Cheryl A. G. J. Med. Chem., 2008, 51: 4150.

[17]

Muller G. W., Chen R. S. C., Man H. W., Ruchelman A. L., Preparation of Dioxopiperidinyl-isoindolone and -isoindolediones Derivatives as Antitumor Agents, US 20070049618, 2007

[18]

Maegawa T., Takahashi T., Yoshimur M., Suzuka H., Monguchi Y., Sajiki H. Adv. Synth. Catal., 2009, 351: 2091.

[19]

Abbott W. S. J. Econ. Entomol., 1925, 18: 265.

[20]

González-Gómez, Añorbe L., Poblador A., Domínguez G., Pérez-Castells J. Eur. J. Org. Chem., 2008, 8: 1370.

[21]

Mazitschek R., Patel V., Wirth D. F., Clardy J. Bioorg. Med. Chem. Lett., 2008, 18: 2809.

[22]

Zhou Y. Y., Li Y. M., Yang X. P., Mao M. Z., Li Z. M. Chem. Res. Chinese Universities, 2013, 29(2): 249.

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