Tetrahydroquinoline alkaloid with anti-prostate cancer activity as well as preparation method and application thereof
An anti-prostate cancer, tetrahydroquinoline technology, applied in biochemical equipment and methods, microorganism-based methods, microorganisms, etc., can solve problems such as drug resistance and failure of clinical treatment of CRPC.
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Embodiment 1
[0025] Embodiment 1: Preparation and structure identification of compound 1
[0026] One, the preparation of compound 1 as shown in formula (I)
[0027] 1. Microbial culture conditions:
[0028] Each 1000mL medium is prepared as follows: Take 20g of glucose, 10g of yeast extract, 3g of beef extract, 3g of corn steep liquor, 10g of soluble starch, 0.5g of dipotassium hydrogen phosphate, 0.5g of magnesium sulfate, and 2g of calcium carbonate, and then dissolve them in an appropriate amount of In water, dilute to 1000mL with water, sterilize at 121°C for 20min, and set aside.
[0029] Streptomyces sp.HNM0561 was inoculated into the above-mentioned culture medium, and cultured on a shaker at 28°C for 3 days to obtain a seed culture solution, and then the seed culture solution was inoculated into the above-mentioned medium at a volume ratio of 1%, at 28°C The shaker culture was carried out under the conditions for 11 days, and the fermentation product of Streptomyces sp. HNM0561 ...
Embodiment 2
[0040] Example 2: Inhibitory activity of Malaymycin (1) on two human prostate cancer cell lines
[0041] Human prostate cancer cell C4-2B was ordered from UroCor Inc. Oklahoma City, OK, USA; human prostate cancer cell 22Rv1 was ordered from American Type Culture Collection (American Type Culture Collection, Manassas, VA, USA).
[0042] CCK-8 assay was used in the human prostate cancer cell inhibitory activity test. Culture in RPMI1640 medium, collect the cells in the logarithmic growth phase, count, resuspend the cells, adjust the cell concentration to an appropriate concentration, inoculate a 96-well plate (500–1000 cells per well), and add 100 μl of cell suspension to each well. Cells at 37°C, 100% relative humidity, 5% CO 2 Incubate for 24 hours in the incubator. Dilute the compound to be tested to an appropriate concentration with medium, and add 50 μl / well to the cells. For C4-2B and 22Rv1 cells, the final concentration of compound 1 (Malaymycin) and positive control ...
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