4.6 Article

Inhibition of catechol-O-methyltransferase by natural pentacyclic triterpenes: structure-activity relationships and kinetic mechanism

Journal

JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY
Volume 36, Issue 1, Pages 1079-1087

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/14756366.2021.1928112

Keywords

catechol-O-methyltransferase (COMT); pentacyclic triterpenes; enzymatic activity inhibition; mitochondrial membrane potential (MMP)

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In this study, oleanic acid, betulinic acid, and celastrol were identified as potent inhibitors of COMT with the ability to specifically recognize and bind with the enzyme, while reducing the risk of liver toxicity. These findings could lead to the development of new lead compounds and derivatives for further testing.
Inhibitors of COMT are clinically used for the treatment of Parkinson's disease. Here, we report the first natural pentacyclic triterpenoid-type COMT inhibitors and their structure-activity relationships and inhibition mechanism. The most potent compounds were found to be oleanic acid, betulinic acid and celastrol with IC50 values of 3.89-5.07 mu M, that acted as mixed (uncompetitive plus non-competitive) inhibitors of COMT, representing a new skeleton of COMT inhibitor. Molecular docking suggested that they can specifically recognise and bind with the unique hydrophobic residues surrounding the catechol pocket. Furthermore, oleanic acid and betulinic acid proved to be less disruptive of mitochondrial membrane potential (MMP) compared to tolcapone, thus reducing the risk of liver toxicity. These findings could be used to produce an ideal lead compound and to guide synthetic efforts in generating related derivatives for further preclinical testing.

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