Application of ainsliaidimer A in preparing nucleolus transcription factor inhibitor medicament
A technology of dimerizing rabbit ears and transcription factors, which is applied in the field of medicine, can solve the problem of lack of chemical components in big-headed rabbit ears, and achieve the effect of great clinical application value
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Embodiment 1
[0018] Example 1 Preparation of compound dimeric terpene A
[0019] Ainsliaea macrocephala (Ainsliaea macrocephala) whole herb 5kg, reflux extraction 2 times with 80% ethanol 50L each time, 2 hours each time, the extract was concentrated under reduced pressure into liquid extract, diluted with water, extracted with 5L of petroleum ether, and then Extract with 5 L of ethyl acetate to obtain 320 g of the ethyl acetate fraction; mix the above ethyl acetate fraction with 300 g of silica gel to mix the sample, apply silica gel column chromatography, and use a chloroform-methanol system gradient with a volume ratio of 20:0 to 4:1 Elution, thin-layer chromatography detection, collect the fraction containing dimeric terpene A, then go through Sephadex column chromatography, elute with chloroform-methanol with a volume ratio of 1:1, and finally pass through C18 Reverse-phase column chromatography, eluting with methanol-water with a volume ratio of 4:6 to 6:4, and detection by thin-laye...
Embodiment 2
[0021] Example 2 Gel Retardation Electrophoresis Analysis (EMSA) Detects the Activity of NF-κB
[0022] Experiment set up control group and medicine group, control group does not add any medicine, medicine group adds 0.75ug / ml (concentration of dimeric rabbit auricine A drug) dimeric rabbit auricine A (add 0.5ml of medicine to 1× 10 7 HL-60 cells), under aseptic conditions, the cells of each group were put into culture flasks containing RPMI1640 medium containing 15% calf serum, and cultured in an incubator containing 5% carbon dioxide for 3, 6, and 12 days respectively. And 24h, collect each group of HL-60 cells. Each group is about 1×10 7 The cells were washed three times with PBS (phosphate buffered saline), and the nuclear protein was extracted using the NE-PER Nuclear and Cytoplasmic Extraction Reagents Kit (Cell Nucleus and Cell Protein Extraction Kit, Pierce Company, Cat. No.: 78833), and operated according to the instructions. The Lightshift EMSA Kit (Pierce Company...
Embodiment 3
[0023] Example 3 Detection of NF-κB in Cells by Immunoluminescence
[0024] Collect the control group and HL-60 cells treated with 0.75ug / ml dimeric auricine A for 3, 6, 12 and 24 hours respectively, and wash with PBS (as in Example 2). Add 10% buffered formalin fixative, fix for 15 minutes, and use NF-κB activation-nuclear translocation detection kit (beytotime company) (cy3-labeled secondary antibody) to detect changes in the distribution of NF-Kbp65 in cells. According to the instructions, the primary antibody was kept at 4°C for two nights, observed under a fluorescence microscope, and the site of p65 showed red fluorescence. Results The treatment of dimeric rabbit auris terpene A greatly decreased the amount of NF-κB p65 in the nucleus, and the amount of NF-κB p65 in the cytoplasm also decreased.
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