Literature DB >> 24219111

Angiotensin-converting enzyme inhibitory effects by plant phenolic compounds: a study of structure activity relationships.

Nadin Al Shukor1, John Van Camp, Gerard Bryan Gonzales, Dorien Staljanssens, Karin Struijs, Moises J Zotti, Katleen Raes, Guy Smagghe.   

Abstract

In this study, 22 phenolic compounds were investigated to inhibit the angiotensin-converting enzyme (ACE). Tannic acid showed the highest activity (IC50 = 230 μM). The IC50 values obtained for phenolic acids and flavonoids ranged between 0.41 and 9.3 mM. QSAR analysis confirmed that the numbers of hydroxyl groups on the benzene ring play an important role for activity of phenolic compounds and that substitution of hydroxyl groups by methoxy groups decreased activity. Docking studies indicated that phenolic acids and flavonoids inhibit ACE via interaction with the zinc ion and this interaction is stabilized by other interactions with amino acids in the active site. Other compounds, such as resveratrol and pyrogallol, may inhibit ACE via interactions with amino acids at the active site, thereby blocking the catalytic activity of ACE. These structure-function relationships are useful for designing new ACE inhibitors and potential blood-pressure-lowering compounds based on phenolic compounds.

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Year:  2013        PMID: 24219111     DOI: 10.1021/jf404641v

Source DB:  PubMed          Journal:  J Agric Food Chem        ISSN: 0021-8561            Impact factor:   5.279


  27 in total

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