Name | 2-(3,4-dihydroxyphenyl)-7-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one |
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Synonyms |
Luteolin-5-O-b-D-glucopyranoside
2-(3,4-Dihydroxyphenyl)-5-(b-D-glucopyranosyloxy)-7-hydroxy-4H-1-benzopyran-4-one Luteolin-5-O-glucopyranoside 2-(3,4-Dihydroxyphenyl)-7-hydroxy-4-oxo-4H-chromen-5-yl β-D-glucopyranoside Luteolin-5-O-β-D-glucopyranoside Luteollin 5-glucoside 4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-5-(β-D-glucopyranosyloxy)-7-hydroxy- galuteolin luteolin 5-O-β-D-glucopyranosyl |
Description | Luteolin 5-O-glucoside, a major flavonoidfrom Cirsium maackii, possesses anti-inflammatory activity. Luteolin 5-O-glucoside inhibits LPS-induced NO production and t-BHP-induced ROS generation. Luteolin 5-O-glucoside suppresses the expression of iNOS and COX-2 in macrophages[1]. |
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Related Catalog | |
In Vitro | Luteolin 5-O-glucoside, at a non-toxic concentration, inhibits LPS-induced NO production and t-BHP-induced ROS generation in a dose-dependent manner in RAW 264.7 cells. Luteolin 5-O-glucoside also suppresses the expression of iNOS and COX-2 in LPS-stimulated macrophages[1]. |
References |
Density | 1.7±0.1 g/cm3 |
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Boiling Point | 864.2±65.0 °C at 760 mmHg |
Melting Point | 260-263℃ |
Molecular Formula | C21H20O11 |
Molecular Weight | 448.377 |
Flash Point | 305.8±27.8 °C |
Exact Mass | 448.100555 |
PSA | 190.28000 |
LogP | 0.13 |
Vapour Pressure | 0.0±0.3 mmHg at 25°C |
Index of Refraction | 1.740 |
HS Code | 2932999099 |
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Precursor 0 | |
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DownStream 1 | |
HS Code | 2932999099 |
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Summary | 2932999099. other heterocyclic compounds with oxygen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |