Ailanthus altissima bark extract, quassin compound, and preparation method, application and pharmaceutical composition of ailanthus altissima bark extract and quassin compound

By extracting and isolating the quassin-like compound L1 from the bark of the tree as a JAK2 inhibitor, the lack of effective treatments for triple-negative breast cancer has been addressed, achieving inhibition and apoptosis induction of triple-negative breast cancer cells and providing a new treatment strategy.

CN120965710APending Publication Date: 2025-11-18CHENGDU UNIV OF TRADITIONAL CHINESE MEDICINE
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Patent Information

Application Number
CN202511490574.6
Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Filing Date
2025-10-17
Publication Date
2025-11-18

AI Technical Summary

Technical Problem

Current treatment options for triple-negative breast cancer are limited, especially the lack of safe and effective endocrine therapy and HER2-targeted therapy, which leads to poor prognosis and early metastasis. Therefore, new treatment strategies need to be found.

Method used

L1, a quassin-like compound, was extracted from the bark of *Toona sinensis*. The compound was prepared by reflux extraction, silica gel column chromatography, and thin-layer chromatography. L1, which has JAK2 inhibitor activity, can bind to JAK2 protein with high affinity, block JAK2 kinase activity and its downstream STAT3 signaling pathway, inhibit the proliferation of triple-negative breast cancer cells and induce apoptosis.

Benefits of technology

Compound L1, as a novel JAK2 inhibitor, can significantly inhibit the proliferation and colony formation of triple-negative breast cancer cells and induce cancer cell apoptosis, providing a new targeted therapy strategy for triple-negative breast cancer and showing good application prospects.

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Abstract

The invention belongs to the field of biological medicines, and particularly relates to a cortex ailanthi extract, a quassin compound, and a preparation method, application and a pharmaceutical composition thereof. The quassin compound shown in the formula I is extracted from cortex ailanthi, can be used as a novel JAK2 inhibitor, can be combined with JAK2 protein in a high affinity manner, and blocks JAK2 kinase activity and a downstream STAT3 signal channel, so that triple negative breast cancer cell proliferation and clone formation are inhibited, and cancer cell apoptosis is induced. Therefore, the quassin compound disclosed by the invention is expected to provide a new strategy for targeted therapy of the triple negative breast cancer, and has a good application prospect. Formula I
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