Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Triterpenoid saponins compound, and preparation method and uses thereof

A technology of triterpene saponins and compounds, which is applied in the field of medicine, can solve the problems that the structure of natural ginsenosides is not in the best state, has not been developed and utilized, and achieves obvious anti-tumor activity and good anti-tumor effect

Inactive Publication Date: 2016-04-13
CHANGCHUN UNIV OF CHINESE MEDICINE
View PDF1 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

But at the same time, Panax notoginseng is a traditional Chinese herbal medicine, and the uses of many components have not been developed and utilized.
Notoginseng saponin is its main active ingredient, but according to the metabolism of ginsenoside in the body and its structure-activity relationship, "ginsenoside" is absorbed by the gastrointestinal tract and then metabolized by intestinal bacteria into secondary saponins and glycosides. Absorbed into the blood circulation to play a pharmacological role, indicating that the structure of natural ginsenosides is not the best structure

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
  • Triterpenoid saponins compound, and preparation method and uses thereof
  • Triterpenoid saponins compound, and preparation method and uses thereof
  • Triterpenoid saponins compound, and preparation method and uses thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0043] One, a kind of triterpene saponin compound structural formula that the present invention relates to is as follows:

[0044]

[0045] Its chemical name is: 6-O-β-D-glucoside-Dama-22,(23)(Z)-ene-3β,6α,12β,20,25-pentaol-20-furan ring side chain. The triterpene saponins compound described in the present invention is a new compound isolated for the first time from the transformation product of Panax notoginseng, named pseudo-ginsenoside RT 7 .

[0046] The physicochemical constants of triterpene saponins compound described in the present invention are as follows:

[0047] White powder (methanol), ESI-MS: m / z675.40 ([M+Na] + ), m / z687.38 ([M+Cl] – ), combined with hydrogen spectrum and carbon spectrum, it is speculated that its molecular formula is C 36 h 60 o 10 . 10% sulfuric acid ethanol solution was purple, Molish reaction was positive, Liebermann-Burchard reaction was positive. 1 H and 13 See Table 1 for C-NMR data.

[0048] Table 1 of compounds 1 H-NMR, 1...

Embodiment 2

[0070] Embodiment 2: Antitumor activity test of the compound of the present invention

[0071] 1. Test materials

[0072] 1. Tumor strains tested in vitro:

[0073] Helas human cervical cancer cells were provided by the Pharmacology Laboratory of the R&D Center of Changchun University of Traditional Chinese Medicine.

[0074] 2. Reagents for in vitro tests:

[0075] Newborn bovine serum, dimethyl sulfoxide (DMSO) and MTT tetraoxalate (Sigma).

[0076] 3. In vitro test equipment:

[0077] Microplate reader: Multiskan Ascent, model: VL.23354-00541T.

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

No PUM Login to View More

Abstract

The invention belongs to the technical field of medicines, and discloses a triterpenoid saponins compound, and a preparation method and uses thereof. The triterpenoid saponins compound is 6-O-beta-D-glucoside-dammara-22,(23)(Z)-ene-3beta,6alpha,12beta,20,25-pentol-20-furyl side chain, and the structure formula is shown in the specification. The chemical structure of the triterpenoid saponins compound is determined by employing mass spectrum and one-dimension and two-dimension nuclear magnetic resonance spectrum technologies and chemical methods. In-vitro antitumor activity tests show that the triterpenoid saponins compound possesses obvious antitumor activity and provides a new source for preparing antitumor medicines.

Description

technical field [0001] The invention belongs to the technical field of medicines, and in particular relates to triterpene saponins and their preparation methods and applications. Background technique [0002] Panax notoginseng is the dry root and rhizome of Panax notoginseng of the Araliaceae plant. In my country's Yunnan, Guangxi and other places. This product is warm in nature, sweet in taste, slightly bitter, non-toxic. The raw product of Panax notoginseng can reduce swelling and relieve pain, dissipate blood stasis and stop bleeding, and the cooked product can enrich blood and activate blood circulation. Panax notoginseng has a long history of being used to treat diseases, and it is one of the traditional precious medicinal materials commonly used in my country. For thousands of years, it has made great contributions to the prosperity of the Chinese nation, and is deeply concerned and valued by people all over the world. [0003] Nowadays, the rapid development of mod...

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): C07J17/00A61K31/7048C12P33/20A61P35/00
Inventor 邱智东徐伟
Owner CHANGCHUN UNIV OF CHINESE MEDICINE
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products