Arenobufagin space isomer compound and preparation and application thereof
A technology of spatial isomers and sandbuad toxin, which is applied in the field of new compounds of space isomers of sandbuad toxin and the preparation and separation of new compounds, which can solve the problem of few reports of space isomers
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Embodiment 1
[0027] Embodiment 1: Preparation of bufadienolactone extract
[0028] Get 10Kg of toad skin and extract 3 times with 95% ethanol, the amount of alcohol used is 10 times, and the extraction time is 120 minutes each time. %-50% ethanol for elution, and then 70%-100% ethanol for elution, collect the latter, recover the solvent under reduced pressure, and dry to obtain 125 g of bufadienolactone extract.
Embodiment 2
[0029] Embodiment 2: Preparation of bufadienolactone fraction
[0030] The bufadienolactone extract obtained in Example 1 was separated by preparative HPLC (XterraC18, A: 0.1% (v / v) formic acid in water; B: 0.1% (v / v) formic acid in acetonitrile, gradient conditions: 5% B to 95% B, 60 min;), during the separation process, an ultraviolet detector is used for detection, and the detection wavelength is 300 nm. Each fraction was collected according to the retention time of different sample peaks during the detection process; a total of 20 fractions (Fraction1-20) were collected.
Embodiment 3
[0031] Embodiment 3: the preparation of compound I
[0032] Fraction 8 recovered the solvent, separated by HPLC (cyclodextrin chromatographic column, A: water; B: acetonitrile, gradient condition: 5% B ~ 30% B, 55min), collected the main chromatographic peaks, recovered the solvent respectively, and analyzed by NMR The experiment confirmed that 4 mg of the fraction containing compound I (peak 5) was obtained, and the HPLC detection content was 98%. The rationale determination showed the following data: white powder, HR-MS, [M+H]+(m / z): 417.2273, UV: 298nm, 1 HNMR (CD 3 OD, 400MHz) δ: 7.81 (1H, dd, J=9.6, 2.4), 7.42 (1H, d, J=1.6), 6.21 (1H, d, J=9.2), 4.26 (1H, d, J=11.6 ), 4.04 (1H, dd, J=13.6, 7.6), 2.65 (1H, td, J=14, 3.2), 1.06 (1H, s), 0.81 (1H, s), etc.; 13 CNMR (CD 3 OD, 100MHz) δ: 213.4, 163.0, 150.2, 147.7, 121.7, 114.5, 84.7, 73.7, 71.0, 62.3, 43.5, 40.6, 39.5, 37.1, 36.0, 35.9, 31.8, 30.5, 27.7, 26.8, 22.0, 21.5, 16.7.
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