Catalogue number | C108542 |
Chemical name | Saikosaponin B2 |
CAS Number | 58316-41-9 |
Synonyms | (2S,3S,4S,5S,6R)-2-[[(2R,3R,4S,5S,6R)-2-[[(3S,4R,6aR,6bR,8R,8aS,14aR,14bS)-8-hydroxy-4,8a-bis(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,14a-dodecahydropicen-3-yl]oxy]-3,5-dihydroxy-6-methyl-4-oxanyl]oxy]-6-(hydroxymethyl)oxane-3 |
Molecular Weight | C42H68O13 |
Formula | 780.9 |
Purity | 98% |
Physical Description | Powder |
Solvent | Chloroform, Dichloromethane,DMSO |
Storage | Stored at 2-8°C, Protected from air and light, refrigerate or freeze |
Applications | Treatment with 5 microM of saikosaponin (SS) b2 for 30 days was found to induce differentiation of B16 melanoma cells, with potentiation of expressions of melanogenesis and tyrosinase. To explore the mechanism of this effect, we observed the cell growth, cell cycle and morphology, and found that SSb2 did not affect any of these parameters. That is, SSb2 induced the differentiation of B16 melanoma cells without growth inhibition or cytotoxicity under conditions of low dose and long-term treatment. Phorbol ester, a protein kinase C (PKC) activator, markedly inhibited the expressions of melanogenesis and tyrosinase in both the control B16 melanoma cells and the long-term treated B16 melanoma cells. Down-regulation of the PKC activity may be involved in the effects of SSb2. |
References | 1. Phytochemistry, 1996, 42(6), 1673–1675. 2. Phytochemistry, 1996, 41(3), 895-901. 3. J. Chem. Soc., Perkin Trans. 1, 1975, 2043-2048. 4. Cell Struct Funct., 1998, 23(5), 265-272. |
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