The application of the spider aromatic iridoid part in the preparation of n-type calcium channel inhibitors
A technology of aromatic iridoid and spider, which is applied to the application field of spider iridoid part in the preparation of N-type calcium channel inhibitor, can solve the problem that the research on spider incense is still insufficient, and achieves broad application prospects. Effect
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Embodiment 1
[0026] This example provides a method for preparing the iridoid part of Aranthus chinensis, the steps are as follows: Take 1000 grams of medicinal material powder of Arachnis alba, add 3500 ml of 95% ethanol and place it in the reflux device for reflux for 3 hours, filter out the ethanol liquid after cooling, and add the residue to 3000ml of ethanol was refluxed again for 2 hours, the ethanol extract was filtered out and combined into the first ethanol filtrate to obtain about 6000ml of ethanol extract, concentrated ethanol extract to water suspension, and ethyl acetate was added to extract the iridoid part of spider , the spider iridoid part can effectively inhibit N type calcium channel. The iridoid part of the spider fragrance is added with appropriate excipients, binders, and disintegrants and compressed into tablets to obtain 1000 tablets.
Embodiment 2
[0028] This example provides a method for obtaining the hydrolyzate of the iridoid part, and the specific steps are as follows: add 1000 ml of 0.01M hydrochloric acid aqueous solution to the part of the iridoid obtained in the above-mentioned Example 1, and then rotate and stir for 1 hour After the reaction is stopped, it is neutralized with 0.01M NaOH to pH=7, then extracted with ethyl acetate, and concentrated to obtain the hydrolyzate of the iridoid part, which can effectively inhibit the N type calcium channel.
Embodiment 3
[0030] Identification and verification of the active substance of the iridoid part of spider fragrance in Example 1
[0031] The spider iridoid part obtained in the above-mentioned embodiment 1, get 50g and use 100g silica gel (200-300 mesh) to mix the sample, put 10 times the amount of silica gel column (0.5kg, 200-300 mesh), mobile phase is petroleum ether: Acetone=50:1~0:1, 7 components (Fr1-7) were eluted. Fraction 4 (Fr.4, 2.8g) was further subjected to silica gel column chromatography (petroleum ether: acetone = 20:1~1:1 gradient elution) to obtain 4 fractions (sub Fr.4.1~4.4). Wherein the second subcomponent (sub Fr.4.2, 0.8 g) is subjected to MCI gel (60%~90% methanol gradient elution), gel sephadex LH-20 (methanol), reverse phase ODS (methanol: water=50 :50~90:10) was purified to obtain compound valeriandoid B8 (compound 1, as shown in formula II, 5 mg). Component 6 (Fr.6, 5.3 g) was obtained by an approximate method to obtain valtrate hydrine J (compound 2, represe...
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