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. 2013 May 14;18(5):5568–5579. doi: 10.3390/molecules18055568

Table 2.

Melanogenesis inhibitory activity and cytotoxicity in B16 mouse melanoma cells of multiflorane-type triterpenes isolated from Cucurbita maxima seeds a.

Compound mean ± S.D. (%) at 10 μM mean ± S.D. (%) at 30 μM mean ± S.D. (%) at 100 μM
Melanin content Cell viability Melanin content Cell viability Melanin content Cell viability
1 94.8 ± 0.5 92.7 ± 2.2 77.1 ± 3.8 84.4 ± 4.0 73.7 ± 3.6 84.3 ± 5.2
2 106.8 ±9.3 106.3 ± 8.0 92.2 ± 5.4 107.1 ± 7.4 28.1 ± 2.3 69.0 ± 4.5
3 91.2 ± 2.2 107.2 ± 5.1 81.8 ± 4.0 105.6 ± 3.1 51.8 ± 8.0 95.1 ± 4.3
4 98.4 ± 3.2 110.8 ± 4.3 102.2 ± 11.7 103.0 ± 8.2 95.4 ± 8.4 101.1 ± 5.9
5 76.9 ± 4.0 99.5 ± 3.3 70.9 ± 0.1 97.7 ± 3.1 67.4 ± 3.6 99.6 ± 2.0
6 107.8 ± 2.6 91.0 ± 1.6 111.8 ± 7.1 81.8 ± 2.1 82.0 ± 5.1 74.4 ± 3.2
arbutin b 88.9 ± 2.3 100.0 ± 2.7 72.3 ± 3.1 94.4 ± 1.2 55.3 ± 1.0 89.9 ± 0.3

a Melanin content (%) and cell viability (%) were determined based on the absorbance at 450 nm, and 540 nm, respectively, by comparison with values for DMSO (100%). Each value represents the mean ± standard deviation (S.D.) of three determinations. The concentration of DMSO in the sample solution was 2 μL/mL. b Reference compound.