Application of iridoid compound to preparation of medicaments for curing benign prostatoplasia
A technology for iridoids and benign prostatic hyperplasia, which can be used in drug combinations, pharmaceutical formulations, organic active ingredients, etc., can solve problems such as toxic side effects, high prices, and influence on clinical and market promotion.
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Embodiment 1
[0068] Preparation and structural identification of the compound of the present invention in embodiment 1
[0069] 1. Extraction and separation
[0070] The rhizome coarse powder (6kg) of S. chinensis was extracted by percolation with 95% ethanol as solvent, and 30 L of percolation liquid was collected, concentrated under reduced pressure to obtain 1500 g of total extract. The total extract was dispersed in 500ml of water, extracted successively with petroleum ether (60-90°C), ethyl acetate and n-butanol, and the solvent was recovered under reduced pressure to obtain 290g of petroleum ether (60-90°C) extract, extracted with ethyl acetate Product 130g, n-butanol extract 200g.
[0071] (1) further separation of petroleum ether extract
[0072] Petroleum ether (60-90°C) extract 100g was roughly divided into 204 parts by silica gel column chromatography (petroleum ether→petroleum ether / ethyl acetate→ethyl acetate→acetone gradient elution).
[0073] PE51 # ~65 # After the samp...
Embodiment 2
[0100] Embodiment 2 A preparation of capsules for resisting benign prostatic hyperplasia:
[0101] Take 1kg of compound A and 6kg of compound B, add an appropriate amount of starch, mix evenly, dry granulate, granulate and pack into capsules to obtain the product.
[0102] Prove the beneficial effect of the present invention by activity test below.
experiment example 2
[0106] Experimental Example 2 Compound B of the present invention (PE116 # ) inhibitory effect on 5α-reductase activity
[0107] The experimental method is the same as that of Experimental Example 1.
[0108]
[0109] The results show that sample PE116 # Shows positive with definite activity.
[0110] The above results showed that the petroleum ether part, the ethyl acetate part and the two monomer structures (compound A and compound B) significantly inhibited the formation of DHT.
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