Nuezhenoside-rhoifolin-hyperin composite and application in medicinal preparation thereof
A technology of rhoside and hyperoside, which is applied in the field of privetin, rhoside, hyperoside composition and its preparation of medicines, can solve problems such as undiscovered, and achieve inhibition of replication, prevention and treatment Influenza and its complications, effects of overcoming side effects
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Embodiment 1
[0032] The composition of lutein, anacardin, and hyperoside provided by the present invention, the molecular formula of the lutein: C 33 H 40 O 18 , Molecular weight: 724.2, the structural formula of the ligustin is as follows:
[0033]
[0034] The molecular formula of anacardin: C 27 H 30 O 14 , Molecular weight: 578.52, and the structural formula of anacardin is as follows:
[0035]
[0036] The molecular formula of hyperoside: C 21 H 20 O 12 , Molecular weight: 464.38, the structural formula of hyperoside is as follows:
[0037]
[0038] Take 1000g of the leaves of Shanxiangyuan, add 12 times the amount of 70% ethanol to reflux extraction for 1.5 hours, filter, and add 10 times the amount of 70% ethanol to the filter residue for reflux extraction for 1.5 hours, filter, combine the two extracts, recover the ethanol, the aqueous solution has passed through The processed D101 macroporous resin column was eluted with water, 10% ethanol, 45% ethanol, 1% sodium hydroxide solution, and ...
Embodiment 2
[0041] Take 1000g of Ligustrum lucidum, add 10 times the amount of 65% ethanol to reflux extraction for 2 hours, filter, add 8 times the amount of 65% ethanol to the filter residue and reflux extraction for 1.5 hours, filter, combine the two extracts, recover the ethanol, and the aqueous solution has passed through The processed D101 macroporous resin column is eluted with water, 8% ethanol, 40% ethanol, 1% sodium hydroxide solution, and the 40% ethanol eluted fraction is collected, concentrated under reduced pressure, and dried to obtain more than 30% lutein The mixed total glycosides were separated by silica gel column chromatography and Sephadex LH-20 column chromatography, combined the fractions of Ligustrum lucidum, and crystallized to obtain the pure Ligustrum lucidum (19.2g, purity: 98.6%). UV, IR, ESI-MS, 1 H-NMR, 13 C-NMR comparison confirmed the structure of Ligustrum.
Embodiment 3
[0043] Take 1000g of orange red, add 10 times the amount of 65% ethanol and reflux for 2 hours, filter, add 8 times the amount of 65% ethanol to the filter residue and reflux for 1.5 hours, filter, combine the two extracts, recover the ethanol, and the aqueous solution has been processed A good D101 macroporous resin column is eluted with water, 10% ethanol, 45% ethanol, 1% sodium hydroxide solution, and the 45% ethanol eluted fraction is collected, concentrated under reduced pressure, and dried to obtain more than 30% anacardin The mixed total glycosides were separated by silica gel column chromatography and Sephadex LH-20 column chromatography, combined with the fractions of anacardin and crystallized to obtain the pure product of anacardin (4.6g, purity: 98.5%), which was compared with the standard UV, IR, ESI-MS, 1 H-NMR, 13 C-NMR comparison confirmed the structure of anacardin.
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