Application of ferulamide compound in preparation of anticomplementary drugs
A ferulic acid amide and compound technology, applied in the separation/purification of carboxylic acid amide, drug combination, antipyretic, etc., can solve problems such as excessive activation of the autoimmune system
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Embodiment 1
[0031] Embodiment 1. Preparation of ferulic acid amides compound
[0032] Take Polygonum chinense Linn. 10kg medicinal material, pulverize it, and extract it by cold immersion in 95% ethanol for 3 times. After the extract is concentrated, it is suspended in water, and extracted with petroleum ether, ethyl acetate, and n-butanol respectively to obtain the active part positive Butanol 300g, get the extractant 250g and wet the macroporous resin D101 with H 2 O / EtOH (30,60,95%, v / v) obtained three fractions Fr.B1-Fr.B3; 18 Medium pressure flash preparative column with CH 3 OH-H 2 O (25:75to 100:0) was eluted to obtain 7 Fr.B2fractions (A-G).; all fractions were purified by semi-preparative column, and compound n-tans-feruloyl tyramine (1) and compound lyciumamide were obtained from Fr.B2fraction C D(2) and compound lyciumamide B(3), (CH 3 CN-H 2 O-CH 3 COOH37:63:0.05).
[0033] After further identification, the NMR data of the obtained compound 1-3 are shown in Table 1-3. ...
Embodiment 2
[0034] Example 2. Anti-complement classical pathway experiment in vitro
[0035]Take 0.1 mL of complement (guinea pig serum), add barbiturate buffer solution (BBS) to prepare a 1:10 solution, and double-dilute with BBS to 1:20, 1:40, 1:80, 1:160, 1:10 320, 1:640 and 1:1280 solutions; take 1:1000 hemolysin, each concentration of complement and 2% sheep red blood cell (SRBC) each 0.1mL dissolved in 0.3mL BBS, mix well, 37 ℃ water bath for 30min, put into Centrifuge in a low-temperature high-speed centrifuge at 5000rpm and 4°C for 10min; take 0.2mL of the supernatant from each tube and place it in a 96-well plate, and measure its absorbance at 405nm; set up a complete hemolysis group (0.1mL 2% SRBC dissolved in 0.5mL three distilled water); the absorbance of three-distilled water lysed blood vessels was used as the standard of total hemolysis to calculate the hemolysis rate. Take the complement dilution as the x-axis and the hemolysis percentage as the y-axis to draw a graph; se...
Embodiment 3
[0036] Example 3. Anti-complement alternative pathway experiment in vitro
[0037] Take complement (human serum) 0.2mL, add AP diluent (barbital buffer, pH 7.4, containing 5mM Mg 2+ , 8mMEGTA) was double-diluted into 8 concentration gradients (1:2, 1:4, 1:8, 1:16, 1:32, 1:64, 1:128, 1:256), and then hemolyzed In the reaction system, 0.15mL of various concentrations of complement and 0.2mL of 0.5% RRBC were dissolved in 0.35mL of AP diluent, mixed evenly, placed in a low-temperature high-speed centrifuge at 37°C for 30 minutes, centrifuged at 5000rpm, 4°C for 10 minutes; Put 0.2 mL of the supernatant in a 96-well plate, and measure the absorbance at 405 nm. At the same time, a total hemolysis group (0.5% RRBC 0.2mL dissolved in 0.5mL triple distilled water) was set up in the experiment; the absorbance of triple distilled water lysed blood vessels was used as the standard of total hemolysis, and the hemolysis rate was calculated. Take the dilution factor of complement as the x...
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