Product Information
- (2E)-[6-(hexopyranosyloxy)-4,5-dihydroxycyclohex-2-en-1-ylidene]ethanenitrile
- (2Z)-2-[(4R,5S,6S)-6-(β-<span class="text-smallcaps">D</span>-Glucopyranosyloxy)-4,5-dihydroxy-2-cyclohexen-1-ylidene]acetonitrile
- (2Z)-[(4R,5S,6S)-6-(beta-L-glucopyranosyloxy)-4,5-dihydroxycyclohex-2-en-1-ylidene]ethanenitrile
- Acetonitrile, 2-[(4R,5S,6S)-6-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-4,5-dihydroxy-2-cyclohexen-1-ylidene]-, (2Z)-
- Acetonitrile, [(4R,5S,6S)-6-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-4,5-dihydroxy-2-cyclohexen-1-ylidene]-, (2Z)-
- Acetonitrile, [6-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-4,5-dihydroxy-2-cyclohexen-1-ylidene]-, [4R-(1Z,4α,5β,6α)]-
- Griffonin
- NSC 290807
Lithospermoside possesses strong inhibitory effects onEpstein-Barr virus early antigen (EBV-EA) activation, the potencies of which were either comparable to or stronger than that of a green tea polyphenol, it also exerts anti-tumor promoting activity in two-stage mouse skin carcinogenesis using 7,12-dimethylbenz[a]anthracene (DMBA) and 12-O-tetradecanoylphorbol-13-acetate (TPA).
Chemical properties
Technical inquiry about: BP-BP0879 Lithospermoside
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