Epoxy annona lactone compound with anti-tumor activity and its preparation method and application
A technology of anti-tumor activity and annua lactone, applied in the field of medicine, can solve the problems of large toxic and side effects, high price, limited anti-tumor activity, etc., and achieve the effect of strong anti-tumor activity and low toxicity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0034] The preparation of embodiment 1 epoxy-type annona lactone compound (diprotexinine B)
[0035] Take 10kg of dried custard apple seeds, percolate with chloroform after crushing, reclaim and combine the percolation liquid, filter, and reclaim the filtrate under reduced pressure to obtain 1 kg of concentrated solution, the concentrated solution is separated by column chromatography with normal phase silica gel, and separated by petroleum ether-ethyl acetate -Methanol gradient elution, a total of 500 fractions were collected and combined into twelve fractions (F1-F12) according to the thin-layer chromatography. F3 (178.8 g) was separated by normal phase silica gel column chromatography and eluted with petroleum ether-ethyl acetate (20:1-0:1) gradient to obtain diproticinine B (1). The purity was 98.3% by HPLC detection.
[0036] Structural analysis: white powder, molecular formula: C 35 h 60 o 4 ; Melting point: 60-62℃; Optical rotation: [α] 25 D +13.0(c 0.1,EtOH); UV:...
Embodiment 2
[0039] Example 2. Acute toxicity test of epoxy type annona lactone compound (diprotecinine B).
[0040] Calculate the half lethal dose LD of mice according to Bliss method 50 value, and the results are as follows:
[0041] Table 2. Acute toxicity test data
[0042]
[0043]
[0044] LD obtained from experiment 50 The value shows that the acute toxicity of diproticinine B is low. Among the three routes of administration, the toxicity of oral administration is the least. Because the drug reaches the various organs quickly by intravenous injection, it presents a more sensitive dose-effect (death) relationship. .
Embodiment 3
[0045] Example 3: Inhibitory effect on human tumor cells in vitro.
[0046] Drug-resistant tumor strains: human breast cancer (MCF-7 / ADR), human liver cancer (SMMC-7721 / T), human lung cancer (A549 / T) three tumor strains, using thiazolium blue reduction method (MTT) for in vitro anti- In the tumor experiment, 6 concentrations of diproticinine B prepared in Example 1 were set, cisplatin was used as the positive control group, and dimethyl sulfoxide, the solvent of the sample, was used as the negative control group. As can be seen from the experimental results in Table 3, diproticinin B shows different inhibitory effects on 3 strains of human tumor cells, and the anti-tumor experimental data in vitro shows that diproticinin B provided by the present invention has a higher inhibitory effect than the positive drug cisplatin. Stronger cell selective inhibitory activity.
[0047] Table 3 Inhibitory effect of diproticinine B on 3 strains of drug-resistant tumor cells.
[0048]
PUM
Property | Measurement | Unit |
---|---|---|
melting point | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com