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. Author manuscript; available in PMC: 2016 Dec 15.
Published in final edited form as: Eur J Pharmacol. 2015 Nov 10;769:100–109. doi: 10.1016/j.ejphar.2015.11.003

Table 2.

The effects of Honaucin A derivatives on cell viability, TRAP activity and IC50 in RANKL-induced Osteoclastogenesis.

Compound Cell viability (0.5 μg/ml)
TRAP (%) TRAP (%) IC50 (μg/ml)
Day 1 Day 3 0.1 μg/ml 0.5μg/ml
Honaucin A 106.20 93.40 69.03 ± 4 59.63 ± 1.1 0.63 ± 0.09
Hex-Honaucin A 102.41 91.81 64.01 ± 1.9 47.28 ± 1.8 0.68 ± 0.09
Br-Honaucin A 103.27 96.55 45.18 ± 2.6 40.58 ± 1.8 0.54 ± 0.06
I-Honaucin A 98.79 86.90 59.83 ± 3.4 46.02 ± 2.9 0.61± 0.09

Cell viability was measured by MTT assay in RAW 264.7 cells upon treatment with individual compounds at 0.5 μg/ml final concentrations for 1 day and 3 days. Cell viability represents the percentage of the control. Relative TRAP activity of individual compounds at 0.1 μg/ml and 0.5 μg/ml in the presence of 50 μg/ml RANKL. IC50 was calculated for TRAP activity. Values are expressed as means ± S.D. of triplicate experiments