Schima superba extract and applications thereof
A technology of extract and lotus root, applied in the field of lotus root extract, can solve the problem of no antibacterial biological activity of the lotus root extract, and achieve the effect of good antibacterial effect
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Embodiment 1
[0018] Anti-Candida Albicans Activity of Schima Schiba Extract in Vitro
[0019] In this experiment, sensitive strains of Candida albicans and drug-resistant strains of Candida albicans were used as indicator bacteria, and the antibacterial activity of Schima superba extract was determined by disk method in vitro susceptibility test.
[0020] Schiba Water Extract
[0021] The root bark of Schima superba is properly crushed, sieved through a 40-mesh sieve, 200g is taken, and 500mL of water is added to heat and reflux to extract 3 times for 1 hour each time. The extracts are combined and concentrated under reduced pressure to obtain 18.6g of extract.
[0022] Xylitol Extract
[0023] The root bark of Schima superba was properly crushed, passed through a 40-mesh sieve, 200 g was taken, and 500 mL of 95% ethanol water was added to heat and reflux for extraction 3 times for 1 hour each time. The extracts were combined and concentrated under reduced pressure to obtain 12.3 g of ext...
Embodiment 2
[0031] Dry coarse powder 4.5kg of Schima superba stem, heat and reflux 3 times with 95% ethanol (8 times the amount of medicinal material), each time for 2 hours, combine the extracts for 3 times, and concentrate under reduced pressure to obtain 200g of total extract.
[0032] The total extract was dissolved and dispersed with 50% methanol water, extracted with petroleum ether, chloroform, ethyl acetate and n-butanol in sequence to obtain 50 g of petroleum ether layer, 35 g of chloroform layer, 22 g of ethyl acetate layer and 20 g of n-butanol And the water layer 45g. The ethyl acetate fraction was subjected to silica gel column chromatography in a chloroform-methanol system (100:0; 90:10; 80:20; 70:30; 60:40; 50:50; 30:70; 0:100) to obtain Fr.1 -20 fractions. Wherein fraction Fr.12 (3.3g) is subjected to ODS reverse column chromatography (180g, 3.5cm x 40cm) water-methanol system (80:20; 70:30; 60:40; 40:60; 20:80; 0 :100) to obtain fraction Fr.12-1~13. After preparative o...
Embodiment 3
[0037] 1. Structural identification of the compound sasanquasaponin III (SS-9)
[0038]
[0039] White amorphous powder, (c 0.30, MeOH). Both Liebermann-Burchard and Molish reactions were positive, and the color of concentrated sulfuric acid-vanillin was red (TLC), which was speculated to be triterpenoid saponins. ESI-MS m / z1241.6[M+Na] + , suggesting that the molecular weight may be 1218, combined with 1 H NMR and 13 C NMR spectrum speculates that the molecular formula of compound SS-9 is C 59 h 94 o 26 .
[0040] 1 H NMR spectrum shows 7 angular methyl hydrogen signals [δ H 0.81(3H,s,H-25),1.03(3H,s,H-26),1.08(3H,s,H-29),1.08(3H,s,H-24),1.30(3H,s, H-23), 1.43(3H,s,H-30), 1.85(3H,s,H-27)], 1 ene hydrogen signal (δ H 5.48,br.s), four terminal hydrogen signals [δ H 4.92 (d, J=7.1Hz, H-1′), 5.95 (d, J=7.6Hz, H-1″), 6.19 (d, J=7.0Hz, H-1″′) and 6.26 (br. s,H-1″’)], a set of characteristic angelica acyl hydrogen signals [δ H 1.88(s, H 3 -5″″′), 2.05(d, J=6.6H...
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