Novel diepoxy lignan compound and preparation method thereof
A technology of diepoxide and compound, applied in the field of medicine, can solve the problems of unclear material basis, unstable variety sources, and difficulty in formulating quality standards.
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Embodiment 1
[0040] Embodiment 1: the extraction and separation method of diepoxy lignan compound fresh bamboo bitumin B in fresh bamboo leek:
[0041] The moso bamboo was collected from Tonggu County, Yichun City, Jiangxi Province, and was identified as the fresh stem of Phyllostachys edulis (Carr.) H. de Lehaie, a plant of the genus Phyllostachys edulis (Carr.) H. de Lehaie, which was identified by Wu Ziping, a senior experimenter of Tonggu County Weisheng Industrial Co., Ltd. The specimens are kept in the herbarium of the Jiangxi Provincial Institute for Drug Inspection and Testing.
[0042] The preparation steps of fresh bamboo pitchin B are as follows:
[0043] (1) Extraction of fresh bamboo leek: after the moso bamboo is cut off, fresh bamboo leek is obtained through dry distillation;
[0044] (2) Concentrating fresh bamboo lek: concentrating the fresh bamboo lek under reduced pressure to obtain extract;
[0045] (3) Extraction: take fresh bamboo leek extract (37.8kg), add 40L of p...
Embodiment 2
[0049] Example 2: Structural identification of the diepoxy lignan compound fresh bamboo bitin B
[0050] The physical and chemical properties of fresh bamboo bitin B are as follows: white powder, easily soluble in organic reagents such as acetone, propylene glycol, pyridine, methanol, etc., with a melting point of 166-168 ° C, UV (CH 3 OH)λ max 240nm and 268nm. UHPLC-quadrupole-time-of-flight mass spectrometry gave the quasi-molecular ion peak m / z 401.1214[M+Na] + (calcd for C 18 h 18 o 6 Na, 401.0849), bound 1 H-NMR and 13 C-NMR spectrum confirms that its molecular formula is C 18 h 18 o 9 . 1 H and 13 The C NMR data are shown in Table 1. At the same time, by measuring two-dimensional H-C correlation spectrum (HSQC), H-C long-distance correlation spectrum (HMBC), CD spectrum, etc., the signal assignments of all carbon atoms and hydrogen atoms and the chemical structure of the compound were determined. The chemical structural formula is as follows:
[0051]
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Embodiment 3
[0055] Example 3: In vitro anti-tumor activity test of the diepoxylignan compound basalin B
[0056] Tumor cell growth inhibition rate (%)=(1-measured value of experimental well / measured value of control well)×100%
[0057] Test principle: MTT method: There is a dehydrogenase related to NAAP (nicotinamide adenine dinucleotide phosphate, coenzyme II) in the mitochondria of living cells, which can convert yellow thiazolyl blue MTT (3-(4, 5- Aimethylthiazo-2-yl)-2,5-Aiphenyl tetrazolium bromiAe) is reduced to insoluble blue-purple formazan (Formanzan), this enzyme disappears in dead cells, and MTT is not reduced. After dissolving formazan with AMSO (dimethyl sulfoxide), the optical density (OA) can be detected at 570 nm with a microplate reader, and the optical density value is proportional to the number of living cells.
[0058] The cell lines used are: HT-1376 (human bladder cancer cells) and HCT-8 (human colon cancer cells).
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