Medical use of triacetyl andrographolide as proinflammatory cytokine inhibitor

An inflammatory cytokine and andrographolide technology is applied in the field of medical use of triacetylandrographolide as an inflammatory cytokine inhibitor, and can solve the problem that the inhibitory effect and activity of triacetylandrographolide cannot be predicted. How to wait for the problem to achieve the effect of improving the inhibitory activity

Active Publication Date: 2009-02-25
SUZHOU LEINA PHARMA RES DEV
View PDF3 Cites 9 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0011] In summary, it can be seen that even if all the above-mentioned published contents about andrographolide and triacetylandrographolide are

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Medical use of triacetyl andrographolide as proinflammatory cytokine inhibitor
  • Medical use of triacetyl andrographolide as proinflammatory cytokine inhibitor
  • Medical use of triacetyl andrographolide as proinflammatory cytokine inhibitor

Examples

Experimental program
Comparison scheme
Effect test

Example Embodiment

[0028] Preparation Example 1 Preparation of Andrographolide

[0029] Take 20 g of crude andrographolide, dissolve it in 450 mL of methanol at 72°C, let it stand for 24 hours and obtain white crystals by suction filtration, and dry it to obtain andrographolide.

Example Embodiment

[0030] Preparation Example 2 Preparation of triacetylandrographolide

[0031] 1g andrographolide dissolved in 10mLAc 2 O, heated to reflux for 2 hours, the reaction mixture was extracted with ethyl acetate, the organic layer was sequentially water, saturated NaHCO 3 Wash with saturated brine, anhydrous MgSO 4 dry. The white solid of triacetylandrographolide was obtained by silica gel column chromatography. The molecular formula is: C 26 H 36 O 8 .

[0032] The compound confirmation data is as follows:

[0033] (cm -1 ): 3454, 3080, 2954, 1731, 1683, 1375, 1250, 1191, 1075, 1026, 895, 606.

[0034] 1 H(400MHz, CDCl 3 ):δ

[0035] 7.00 (td, J = 6.84, 1.48 Hz, 1H, H-12), 5.92 (d, J = 5.96 Hz, 1H, H-14), 4.90 (bs, 1H, H-17a), 4.60 (dd, J = 11.68, 4.26 Hz, 1H, H-15a), 4.55 (dd, J = 11.24, 6.08 Hz, 1H, H-15b), 4.53 (bs, 1H, H-17b), 4.36 (d, J = 11.80 Hz , 1H, H-19a), 4.25 (dd, J = 11.24, 1.80 Hz, 1H, H-3), 4.12 (d, J = 11.80 Hz, 1H, H-19b), 2.52~2.37 (m, 3H) , 2.12 (s, 3H), 2.05 (s, 6...

Example Embodiment

[0039] Preparation Example 3 Preparation of 3,19-diacetylandrographolide, 14-acetylandrographolide, and 14,19-diacetylandrographolide

[0040] Add 5 g of andrographolide to 30 mL of acetic acid and stir and heat to 80° C., and react overnight. Extracted with ethyl acetate, the organic layer was washed with water and saturated brine successively, anhydrous MgSO 4 dry. Column chromatography obtained 3,19-diacetylandrographolide (AP11), 14,19-diacetylandrographolide (AP12), and 14-acetylandrographolide (AP13).

[0041]

[0042] The AP11 compound confirmation data is as follows:

[0043] Molecular formula: C 24 H 34 O 7 (434)

[0044] 1 H(400MHz, CDCl 3 ): 6.97 (1H, m, H-12), 5.03 (1H, d, J=5.6 Hz, H-14), 4.92 (1H, s, H-17), 4.62 (1H, s, H-17) , 4.59 (1H, dd, J = 11.2, 4.8 Hz, H-3), 4.47 (1H, dd, J = 10.4, 6.0 Hz, H-15), 4.38 (1H, d, J = 11.6 Hz, H- 19), 4.26 (1H, dd, J = 10.4, 2.0 Hz, H-15), 4.11 (1H, d, J = 12.0 Hz, H-19), 2.05 (6H, s, CH 3 CO-), 1.04 (3H, s, H-18), 0.78 (3H, s, H...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
The average particle sizeaaaaaaaaaa
The average particle sizeaaaaaaaaaa
Login to view more

Abstract

The invention relates to an application of 3,14,9-acetyl andrographolide in the preparation of an proinflammatory cytokine, wherein, the proinflammatory cytokine comprises any one of TNF-Alpha, IL-1Alpha, IL-1Beta, IL-2, IL-4, IL-6, IL-8, IL-10, IFN-Gamma and NO.

Description

technical field [0001] The invention relates to the application of triacetylandrographolide in the preparation of inflammatory cytokine inhibitors. Background technique [0002] Inflammatory cytokines are mainly secreted by macrophages, including TNF-α, IL-1α, IL-1β, IL-2, IL-4, IL-6, IL-8, IL-10, IFN-γ and other pro-inflammatory cytokines Cytokines and nitric oxide (NO) with the characteristics of inflammatory factors, etc. The most studied ones are TNF-α, IL-1β, IL-6, and NO. Excessive secretion of inflammatory cytokines plays an important role in the occurrence and development of many diseases. Such as: systemic inflammatory response syndrome (SIRS), sepsis, septic shock, septic shock, multiple organ dysfunction syndrome, rheumatoid arthritis, osteoarthritis, spondyloarthropathy, rheumatoid arthritis Inflammation, hypertension, coronary heart disease, myocardial infarction, heart failure, diabetes, systemic lupus erythematosus, lupus nephritis, scleroderma, sarcoidosis...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
IPC IPC(8): A61K31/365A61P29/00A61P31/00A61P25/00A61P35/00A61P11/00
Inventor 刘珂邵萌赵烽关玉昆滕厚雷吴巍徐卉翟大伟韩飞冯妍
Owner SUZHOU LEINA PHARMA RES DEV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products