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Comparative enzyme inhibition study of 1-deazapurines

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Abstract

A series of nitrogen heterocycles including the derivatives of 1-deazapurines, were studied for miscellaneous enzyme inhibition activities in search of the potent enzyme inhibitor. The hyperactive enzymes like carbonic anhydrase-II, phosphodiesterase-I, xanthine oxidase, α-glucosidase, and β-glucuronidase were selected for the study. The compounds 1, 2, 3, 6, 8, 1113 and 1517, showed significant and selective activities against different enzymes. The compounds 11 and 12 were found the most potent against carbonic anhydrase-II, α-glucosidase and β-glucuronidase in comparison to their standard compounds. These selective inhibitors can be used as lead compounds for development of drugs against various diseases associated with these enzymes.

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Acknowledgments

The authors thank Higher Education Commission Pakistan for the financial support (Grant No: PM-IPFP/HRD/HEC/2012/2794).

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Correspondence to Iftikhar Ali.

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Ali, I., Khan, A., Hussain, A. et al. Comparative enzyme inhibition study of 1-deazapurines. Med Chem Res 25, 2599–2606 (2016). https://doi.org/10.1007/s00044-016-1700-1

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