Abelmoschus manihot extract and novel application of chemical components thereof
A technology of hollyhock flower and extract, which is applied in the field of hollyhock flower extract to treat or prevent diseases or diseases related to oxidative damage, and can solve problems such as damage and DNA nucleic acid strand breaks
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Embodiment 1
[0052] Embodiment 1: the preparation of extract of the present invention and formula I compound
[0053] Step 1: Take the dried flowers (2.8kg) of hollyhock flowers, heat and reflux with 10, 8, and 8 times the amount of 95% EtOH solution for extraction for 3, 2, and 2 hours successively, combine the filtrates, recover the solvent under reduced pressure, and vacuum at 50°C Dry to obtain 95% ethanol extract (648 g, 23.14%), which can be used as the reagent in the following test examples.
[0054] Step 2: Take 500g of the 95% ethanol extract obtained in the above step 1, and process it with D101 macroporous adsorption resin (water → 70% EtOH → 95% EtOH) to obtain water eluate (220g, 10.2%), 70% ethanol Eluate (120 g, 5.55%) and 95% ethanol eluate (22 g, 1.02%). Each eluate can be used as the reagent in the test examples below, especially the 70% ethanol eluate can be used as the reagent in the test examples below.
[0055] Step 3: The 70% ethanol eluate (96 g) obtained in the a...
Embodiment 2
[0057] Example 2: Structural identification and physicochemical properties of marshmallow anthoside C
[0058] Marshmallow anthoside C obtained in step 4 of Example 1: amorphous yellow powder. Under the 254nm ultraviolet light, there is a yellow dark spot, and the color of 10% sulfuric acid ethanol solution is brownish yellow, which may be flavonoids. Its specific rotation is negative ([α] D 25 : +49.0°, MeOH). High-resolution Q-TOF-ESI-MS gives its quasi-molecular ion peak m / z 509.0554[M-H] - , determine its molecular formula as C 21 h 18 o 15 . The information provided by the infrared spectrum shows that there is a hydroxyl group in the structure (3342cm-1 ), unsaturated ketone group (1652cm -1 ), aromatic ring (1607, 1511, 1418cm -1 ). Ultraviolet spectrum further suggested the existence of flavonol skeleton (305, 255nm). exist 1 H-NMR (400MHz, DMSO-d 6 ) in the low-field area of the spectrum δ12.44 (1H, br.s) suggests that there is a phenolic hydroxyl group ...
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