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Inhibitory and Activating Effects of Some Flavonoid Derivatives on Human Pyruvate Kinase Isoenzyme M2
Author(s) -
Adem Sevki,
Aslan Abdulselam,
Ahmed Ishtiaq,
Krohn Karsten,
Guler Caglar,
Comaklı Veysel,
Demirdag Ramazan,
Kuzu Muslum
Publication year - 2016
Publication title -
archiv der pharmazie
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.468
H-Index - 61
eISSN - 1521-4184
pISSN - 0365-6233
DOI - 10.1002/ardp.201500357
Subject(s) - flavonoid , pkm2 , chemistry , pyruvate kinase , ic50 , enzyme , isozyme , catechin , biochemistry , in vitro , kinase , stereochemistry , glycolysis , polyphenol , antioxidant
Pyruvate kinase isoenzyme M2 (PKM2) is expressed excessively in many different cancer types and it plays an important role in the control of glucose metabolism. Thus, it is evaluated as an important target in the development of medication for cancer. The flavonoids comprise a large group of natural products with variable phenolic structures and occur mainly in plants. They are of great interest due to their biological properties. In this study, the effects of various flavonoid derivatives on the PKM2 enzyme activity were analyzed in vitro . The flavonoid derivatives 1 and 2 showed inhibition effect with IC 50 values of <60 μM. IC 50 values of compounds 3–8 were calculated as 134, 415, 145, 163, 295 μM, and 3.5 mM, respectively. The molecules 9–12 showed an activation effect with values of AC 50 of less than 90 μM. The IC 50 values of the derivatives 13–17 were calculated as 115, 150, 200, 221, and 275 μM, respectively. The results show that catechin derivatives can be probably used as lead compounds for the design of PKM2 enzyme activators and inhibitors.