一种愈创木烷型倍半萜苷单体化合物及其制备方法和用途

By extracting and purifying the sesquiterpene glycoside monomer compound atractylone A from Atractylodes lancea, the problem of the lack of effective drugs for treating type 2 diabetes and inflammation in the existing technology has been solved, and significant hypoglycemic and anti-inflammatory effects have been achieved.

CN117659105BActive Publication Date: 2026-07-17INST OF BOTANY JIANGSU PROVINCE & CHINESE ACADEMY OF SCI

Patent Information

Authority / Receiving Office
CN · China
Patent Type
Patents(China)
Current Assignee / Owner
INST OF BOTANY JIANGSU PROVINCE & CHINESE ACADEMY OF SCI
Filing Date
2022-08-25
Publication Date
2026-07-17

AI Technical Summary

Technical Problem

There is a lack of effective natural drug sources in the current technology for the treatment of type 2 diabetes and its associated inflammation, especially drugs that improve insulin sensitivity and lower blood sugar.

Method used

A novel sesquiterpene glycoside monomer compound, abilide A, was extracted, isolated, and purified from the fresh rhizomes of Atractylodes lancea for the preparation of hypoglycemic and anti-inflammatory drugs. The preparation was carried out by methods such as water or organic solvent extraction, petroleum ether and ethyl acetate extraction, column chromatography, and macroporous resin adsorption.

Benefits of technology

A novel natural drug, atractylodes lactone A, has been obtained, which has significant hypoglycemic and anti-inflammatory effects, expanding the drug sources for the treatment of type 2 diabetes and providing better treatment options.

✦ Generated by Eureka AI based on patent content.

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Abstract

本发明公开了一种新倍半萜苷单体化合物及其制备方法和用途,属于天然药物化学领域,其特征是通过水或有机溶剂的化学方法从茅苍术根茎中提取、分离、纯化得到,命名为次裂环苍术内酯A。以及该化合物的制备方法和在医药领域中的用途,尤其在制备降血糖药物方面的应用。
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