QUERCETIN DERIVATIVES DOCKING BASED ON STUDY OF FLAVONOIDS INTERACTION TO CYCLOOXYGENASE-2 | Kartasasmita | Indonesian Journal of Chemistry 21545 40631 1 PB

Indo. J. Chem., 2009, 9 (2), 297 - 302

297

QUERCETIN DERIVATIVES DOCKING BASED ON STUDY OF FLAVONOIDS INTERACTION
TO CYCLOOXYGENASE-2
Docking Turunan Kuersetin Berdasarkan Studi Interaksi Flavonoid Terhadap Enzim
Siklooksigenase-2
Rahmana Emran Kartasasmita1*, Rina Herowati1, Nuraini Harmastuti 2, and Tutus Gusdinar1
1

School of Pharmacy, Bandung Institute of Technology, Jl. Ganesha 10 Bandung 40132
2

Faculty of Pharmacy, Setia Budi University, Jl. Letjen Sutoyo Solo 57127
Received September 3, 2008; Accepted June 23, 2009

ABSTRACT
Due to their ability to inhibit cyclooxygenase-2 (COX-2), certain flavonoids show anti-inflammatory effects.
Quercetin is a flavonoid suitable to be chosen as the lead compound for development of safe anti-inflammatory
agent, because in addition to its anti-inflammatory effect, quercetin shows also protective effect in gastrointestinal

track. The objective of this research is to study the binding modes of certain flavonoids and predict the quercetin
derivatives inhibiton activity on COX-2 by means of docking method using ArgusLab 4.0.1 software. Some
flavonoids (7-hydroxyflavone, apigenin, galangin, kaempferol, quercetin, naringenin and daidzein) and quercetin
derivatives were used as ligands for docking study. The COX-2 structure was obtained from Brookhaven protein
databank. After assigning hydrogen atoms and charges, computational docking was performed. The docking results
were evaluated based on the binding energy and hydrogen bonding of the ligands on binding site of COX-2. A curve
constructed by plotting binding energy versus logarithm of IC50 of flavonoids shows a good correlation with a
regression equation of log IC50 = 0.8069 ΔGbind + 9.4456 (r = 0.9226; P

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