Name | Lobetyolin |
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Synonyms |
(4E,12E)-1,7-Dihydroxy-4,12-tetradecadiene-8,10-diyn-6-yl β-D-glucopyranoside
(4E,12E)-1,7-Dihydroxytetradeca-4,12-diene-8,10-diyn-6-yl β-D-glucopyranoside β-D-Glucopyranoside, (7E)-2-hydroxy-1-[(1E)-5-hydroxy-1-penten-1-yl]-7-nonene-3,5-diyn-1-yl (2R,3R,4S,5S,6R)-2-[(4E,12E)-1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol |
Description | Lobetyolin is derived from Codonopsis pilosula and has antioxidative effect. |
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Related Catalog | |
In Vitro | Lobetyolin is derived from Codonopsis pilosula and has antioxidative effect. MUC5AC gene expression induced by phorbol 12-myristate 13-acetate (PMA) from NCI-H292 cells is inhibited by pretreatment with Lobetyolin, lobetyol or methyl linoleate. Lobetyolin does not affect PMA-induced MUC5AC production from NCI-H292 cells. The amounts of mucin in the cells of Lobetyolin-treated cultures are 100±25%, 487±33%, 524±38%, 411±24%, and 402±45% for control, 10 ng/mL of PMA alone, PMA plus Lobetyolin 1 μM, PMA plus Lobetyolin 10 μM, and PMA plus Lobetyolin 100 μM, respectively[1]. |
Cell Assay | After 24 hours of serum deprivation, cells are pretreated with Lobetyolin, lobetyol or methyl linoleate (1, 10, and 100 µM), for 30 minutes and then treated with phorbol 12-myristate 13-acetate (PMA; 10 ng/mL) for 24 hours in serum-free RPMI 1640. After 24 hours, the spent media are collected to measure the secretion of MUC5AC protein and cells are lysed with buffer solution containing 20 mM Tris, 0.5% NP-40, 250 mM NaCl, 3 mM EDTA, 3 mM EGTA, and protease inhibitor cocktail and collected to measure the production of MUC5AC protein (in 24-well culture plate)[1]. |
References |
Density | 1.4±0.1 g/cm3 |
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Boiling Point | 698.5±55.0 °C at 760 mmHg |
Molecular Formula | C20H28O8 |
Molecular Weight | 396.431 |
Flash Point | 376.2±31.5 °C |
Exact Mass | 396.178406 |
PSA | 139.84000 |
LogP | 2.02 |
Vapour Pressure | 0.0±5.0 mmHg at 25°C |
Index of Refraction | 1.607 |