Synthesis and xanthine oxidase inhibitory activity of 7-methyl-2-(phenoxymethyl)-5H-[1,3,4]thiadiazolo[3,2-a]pyrimidin-5-one derivatives

Sathisha, KR and Khanum, Shaukath A and Chandra, Narendra Sharath JN and Ayisha, F and Balaji, S (2011) Synthesis and xanthine oxidase inhibitory activity of 7-methyl-2-(phenoxymethyl)-5H-[1,3,4]thiadiazolo[3,2-a]pyrimidin-5-one derivatives. Bioorganic & Medicinal Chemistry, 19 (1). pp. 211-220.

[img] PDF
bomc_2011_11_211.pdf - Published Version
Restricted to Registered users only

Download (675kB) | Request a copy
Official URL: http://dx.doi.org/10.1016/j.bmc.2010.11.034 |

Abstract

An elevated level of blood uric acid (hyperuricemia) is the underlying cause of gout. Xanthine oxidase is the key enzyme that catalyzes the oxidation of hypoxanthine to xanthine and then to uric acid. Allopurinol, a widely used xanthine oxidase inhibitor is the most commonly used drug to treat gout. However, a small but significant portion of the population suffers from adverse effects of allopurinol that includes gastrointestinal upset, skin rashes and hypersensitivity reactions. Moreover, an elevated level of uric acid is considered as an independent risk factor for cardiovascular diseases. Therefore use of allopurinol-like drugs with minimum side effects is the ideal drug of choice against gout. In this study, we report the synthesis of a series of pyrimidin-5-one analogues as effective and a new class of xanthine oxidase inhibitors. All the synthesized pyrimidin-5-one analogues are characterized by spectroscopic techniques and elemental analysis. Four (6a, 6b, 6d and 6f) out of 20 synthesized molecules in this class showed good inhibition against three different sources of xanthine oxidase, which were more potent than allopurinol based on their respective IC50 values. Molecular modeling and docking studies revealed that the molecule 6a has very good interactions with the Molybdenum–Oxygen–Sulfur (MOS) complex a key component in xanthine oxidase. These results highlight the identification of a new class of xanthine oxidase inhibitors that have potential to be more efficacious, than allopurinol, to treat gout and possibly against cardiovascular diseases.

Item Type: Article
Additional Information: Copyright © 2010 Elsevier Ltd
Uncontrolled Keywords: Pyrimidin-5-ones;Xanthine oxidase;Xanthine;Allopurinol
Subjects: Engineering > MIT Manipal > Biotechnology
Depositing User: ePrints@MU Administrator
Date Deposited: 19 May 2011 08:40
Last Modified: 07 Jul 2011 08:55
URI: http://eprints.manipal.edu/id/eprint/23

Actions (login required)

View Item View Item