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. Author manuscript; available in PMC: 2010 Mar 26.
Published in final edited form as: J Med Chem. 2009 Mar 26;52(6):1701–1711. doi: 10.1021/jm801449a

Table 3.

In Vitro Growth Inhibitory Effects of Compounds 8a-8j with Different “C” Rings against the Proliferation of Melanoma (A 375, B16-F1) and Prostate Cancer Cells (DU145, PC-3, LNCaP, PPC-1).

Compounds 8 C Ring IC50 ± SEM (μM)
B16-F1 A375 DU 145 PC-3 LNCaP PPC-1
graphic file with name nihms118359t2.jpg 8a Ph >100 >100 >20 >20 >20 >20
8b 4-Methoxy-Ph >100 >100 >20 >20 >20 >20
8c 3-Methoxy-Ph >100 >100 >20 >20 >20 >20
8d 2-Methoxy-Ph 59.4 ± 21.2 70.3 ± 32.5 >20 >20 >20 >20
8e 3, 4-Dimethoxy-Ph >100 >100 >20 >20 >20 >20
8f 3,4,5-Trimethoxy-Ph 0.055 ± 0.005 0.028 ± 0.005 0.071 ± 0.004 0.021 ± 0.001 0.028 ± 0.004 0.043 ± 0.005
8g 3, 5-Dimethoxy-Ph 0.350 ± 0.2 0.170 ± 0.1 0.424 ± 0.098 0.301 ± 0.030 0.323 ± 0.041 0.242 ± 0.014
8h 2-Fluoro-Ph >100 >100 >20 >20 >20 >20
8j Hexadecyla 18.6±17.5 16.0 ± 15.2 >20 >20 >20 >20
a

Compound 8j has a lipid chain at “C” ring position.