Abstract
A series of unsymmetrically disubstituted urea derivatives 1– 28 has been synthesized and screened for their antiglycation activity in vitro. Compounds 26 (IC 50 = 4.26 ± 0.25 μM), 1 (IC 50 = 5.8 ± 0.08 μM), 22 (IC 50 = 4.26 ± 0.25 μM), 6 (IC 50 = 6.4 ± 0.02 μM), 5 (IC 50 = 6.6 ± 0.26 μM), 2 (IC 50 = 7.02 ± 0.31 μM), 3 (IC 50 = 7.14 ± 0.84 μM), 27 (IC 50 = 7.27 ± 0.36 μM), 4 (IC 50 = 8.16 ± 1.04 μM), 21 (IC 50 = 8.4 ± 0.15 μM), 23 (IC 50 = 9.0 ± 0.35 μM) and 1 3 (IC 50 = 15.22 ± 6.7 μM) showed an excellent antiglycation activity far better than the standard (rutin, IC 50 = 41.9 ± 2.3 μM). This study thus provides a series of potential molecules for further studies of antiglycation agents.
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