Anticancer application of sterols derivative
A use, cancer technology, applied in the field of medicine and chemical industry, can solve the problem of unknown anti-cancer ingredients and so on
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Embodiment 1
[0120] Embodiment 1: the preparation of formula II compound (1)
[0121] Steps:
[0122] 1) Take Xuezhikang Capsules (manufactured by Peking University Weixin) about 1 kg dry powder content, use 2-6 times the volume of dichloromethane as a solvent to ultrasonically extract 3 times, each time for 20-40 minutes, combine the extracts, concentrate under reduced pressure and The solvent was recovered to obtain 91 g of dichloromethane fine extract.
[0123] 2) 50 g of dichloromethane fine extract was taken, separated by silica gel column chromatography, and carried out gradient elution with petroleum ether and ethyl acetate. The volume ratio of petroleum ether-ethyl acetate is 75:25, 50:50, 25:75, 0:100 in sequence.
[0124] 3) Take 5.0 g of petroleum ether-ethyl acetate at a ratio of 25:75, separate it by C18 reverse-phase column chromatography, and obtain 4 fractions (methanol-water 10 :90, 50:50, 75:25, 100:0), wherein 1.3 g of methanol-water (75:25) eluting fraction was pur...
Embodiment 2
[0125] Embodiment 2: the preparation of formula II compound (2)
[0126] Steps:
[0127] 1) Take 5 kg of red yeast rice, use 2-6 times the volume of dichloromethane as a solvent for ultrasonic extraction 3 times, each time for 20-40 minutes, combine the extracts, concentrate under reduced pressure and recover the solvent to obtain 78 g of dichloromethane fine extract .
[0128] 2) Take 30 g of dichloromethane fine extract, and separate it by silica gel column chromatography, and carry out gradient elution with petroleum ether and ethyl acetate. The volume ratio of petroleum ether-ethyl acetate is 75:25, 50:50, 25:75, 0:100 in sequence.
[0129] 3) Take 3.0 g of petroleum ether-ethyl acetate at 25:75, separate by C18 reverse-phase column chromatography, and obtain 4 parts (methanol-water 10 :90, 50:50, 75:25, 100:0), wherein 0.8 g of methanol-water (75:25) eluting fraction was purified by semi-preparative high performance liquid chromatography and purified with acetonitril...
Embodiment 3
[0130] Embodiment 3: the structural identification of compound
[0131] The samples used were the compounds prepared in Examples 1 and 2.
[0132] 1. Physicochemical data of the compound
[0133] White powder, optical rotation: [α] 25 D -50.00 (c 0.118, CH 2 Cl 2 :MeOH=1:1);
[0134]There are three maximum absorption peaks in the UV spectrum, which are λ max (CH 2 Cl 2 : MeOH) = 271.6 nm, 282.2 nm, 293.8 nm.
[0135] FT-IR (KBr, cm -1 ) Spectrum: 3392 (-OH), 2969, 2933 (saturated hydrocarbon), 1652, 1647 (C=C), 1456, 1378 (gem dimethyl).
[0136] 2. Determination of molecular formula
[0137] m / z 483.3104[M+Na] given by HR-ESI-MS + (calcd.483.3081, err2.3), it is deduced that the molecular weight of the compound is 460.32. exist 1 H-NMR and 13 C-NMR shows that there are 40 hydrogen signals and 28 carbon signals in total. From DEPT shows that there are 6 quaternary carbons, 10 CH, 6 CH 2 and 6 CH 3 . exist 13 In C-NMR, there are 4 olefinic carbon signals a...
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