Rhizoma cimicifugae extractive, two kinds of rhizoma cimicifugae ketone alkali, preparation method and application
A technology of Cimicifugatine and Cimicidone B is applied in the field of medicine, and can solve the problems such as no reports on the antitumor cytotoxic activity of Cimicifuga alkaloids, and achieve the effect of expanding the effect of drugs
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Embodiment 1
[0030] 10kg of dried rhizomes of Cimicifuga yunnanensis, powdered, extracted twice at room temperature with 80L of 95% ethanol solution, each time for 5 days. Combine the extracts and steam until there is no alcohol smell to obtain 1000 g of the total extract. The total extract was dispersed with 2L of water, extracted successively with equal volumes of petroleum ether and ethyl acetate to obtain CRE (530 g) extracted with ethyl acetate. The ethyl acetate extraction part was eluted with ethanol gradient on a macroporous resin (D101) chromatographic column (30%-95%), and 85%-95% eluted part was collected and dried to obtain 20 g of Cimicifuga sativa extract.
Embodiment 2
[0032] Dry 5 kg of Cimicifuga rhizome, powder it, and extract it twice with 50 L of ethyl acetate solution at room temperature, each time for 3 days. Combine the extracts and steam until there is no alcohol smell to obtain 200 g of the total extract. The total extract was dispersed with 2L of water, and extracted successively with equal volumes of petroleum ether and ethyl acetate to obtain the CRE (100 g) extracted with ethyl acetate. The ethyl acetate extraction part is eluted with ethanol gradient on a macroporous resin (D101) chromatographic column (30%-95%), and the 80%-95% eluted part is collected to obtain Cimicifuga japonicus extract. Further separated by Sephadex LH-20 column chromatography, using dichloromethane / methanol as mobile phase, separated to obtain two fractions, which were crystallized in methanol respectively to obtain compound 1 (15 mg) and compound 2 (17 mg).
Embodiment 3
[0034]5 kg of dried North American black cohosh rhizomes were crushed and then added with 40 L of methanol for reflux extraction twice. The first time was 2 hours. After the extract was filtered, 40 L of methanol was added to continue the reflux extraction for 1 hour. The two extracts were combined and then concentrated under reduced pressure to obtain an extract, which was suspended and dissolved in 3 L of water, and extracted successively with equal volumes of dichloromethane to obtain 420 g of extract. After gradient elution with macroporous resin (AB-8) chromatographic column (30%-95%) ethanol, 75%-95% eluted fractions were collected. Further separation by Sephadex LH-20 column chromatography, with dichloromethane / methanol as mobile phase, separated into two fractions, which were crystallized in dichloromethane to obtain compound 1 (45 mg) and compound 2 (52 mg).
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