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FIGURE 8 CM-272 ( 35 ) and CM-579 ( 36 ) are other dual-target quinolone inhibitors targeting G9a and DNMT based on a rational drug design

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for cytokine production and for inhibiting influenza virus infection as reported by in vivo studies.[27] It is required as coenzyme/cofactor with prostaglandin-synthetase system (cyclooxegenase) used for formation of endoperoxides from arachidonate in prostaglandin synthesis,[9] and for the conversion of prostaglandin H 2 into prostaglandin D 2 and E 2 by endoperoxide isomerase.[27] It is required as a coenzyme with maleylacetoacetate isomerase that catalyzes Cis-trans isomerization of the maleylacetoacetate to fumarylacetoacetate, and for the enzyme glyoxylase which converts methylglyxol to lactic acid through intramolecular oxidation-reduction.[9,27] It also takes part in γ-glutamyl cycle for absorption of amino acid from the gut.[9] It function as a coenzyme with formaldehyde dehydrogenase which catalyzes the oxidation of formaldehyde, a carcinogen, produced during metabolism of methionine, choline, methanol, sarcosine and xenobiotics (by the cytochrome P450-dependent monooxygenase system of the ER), to formic acid.[9,27] Glutathione-S-transferase (GST), a family of phase II detoxification enzymes, initiates reaction of glutathione with various electrophiles, physiological metabolites (e.g