Dryopteris fragrans phloroglucinol derivatives, separation and preparation method for isomers thereof and application thereof

A technology of Phloroglucinol and isomers of Phloroglucinol, applied in the field of chemistry and medicine, to achieve the effect of mild conditions, simple method and good medicinal activity

Active Publication Date: 2015-11-18
GUANGDONG PHARMA UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

However, there is no technical report on how to efficiently separate and prepare

Method used

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  • Dryopteris fragrans phloroglucinol derivatives, separation and preparation method for isomers thereof and application thereof
  • Dryopteris fragrans phloroglucinol derivatives, separation and preparation method for isomers thereof and application thereof
  • Dryopteris fragrans phloroglucinol derivatives, separation and preparation method for isomers thereof and application thereof

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Experimental program
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Embodiment 1

[0053] The separation and preparation of embodiment 1 phloroglucinol derivatives

[0054] The schematic diagram of the separation and preparation is shown in the appendix figure 1 And attached figure 2 shown.

[0055] S1. Extraction of the total phloroglucinol derivatives of Trichomonas chinensis: extract 10 kg dry coarse powder of Trichomonas 10 times by cold immersion in 50% edible ethanol twice, each time for 24 hours, concentrate and recover under reduced pressure Ethanol to alcohol-free sample aqueous solution;

[0056] S2. Adjust the pH to 1.5-4.5 with hydrochloric acid, let stand for 12-18 hours, and centrifuge to obtain 1.2 kg of precipitated extract.

[0057] S3. After dissolving the precipitated extract sample obtained in S2, mix the sample with silica gel, perform preliminary separation on the silica gel column, and successively use different proportions of petroleum ether: acetone to elute (100:1-1:1) to obtain the corresponding components Fr.A~E.

[0058] Th...

Embodiment 2

[0062] The separation and preparation of embodiment 2 phloroglucinol derivatives

[0063] The schematic diagram of the separation and preparation is shown in the appendix figure 1 And attached figure 2 shown.

[0064] S1. Extraction of the total phloroglucinol derivatives of Trichomonas chinensis: extract 10 kg dry coarse powder of Trichomonas 10 times by cold immersion in 50% edible ethanol twice, each time for 24 hours, concentrate and recover under reduced pressure Ethanol to alcohol-free sample aqueous solution;

[0065] S2. Adjust the pH to 1.5-4.5 with hydrochloric acid, let stand for 12-18 hours, and centrifuge to obtain 1.2 kg of precipitated extract.

[0066] S3. After dissolving the precipitated extract sample obtained in S2, mix the sample with silica gel, perform preliminary separation on the silica gel column, and successively use different proportions of petroleum ether: acetone to elute (100:1-1:1) to obtain the corresponding components Fr. A-E.

[0067] S...

Embodiment 3

[0069] Example 3 In vitro anti-superficial fungus effect of Phloroglucinol 4 pairs of isomer compounds

[0070] (1) Trichophyton rubrum (CMCC(f)T1b) and Microsporum gypsumoidus (CMCC(F)M2C), provided by the Institute of Dermatology, Chinese Academy of Medical Sciences. The microdilution method of dermatophytes was carried out according to the M38-A2 protocol formulated by CLSI in the United States, which is briefly described as follows. Gently scrape the colonies on the surface of the SDA medium with an inoculation loop and grind the mycelium with a sterile grinder, suspend the dermatophyte in sterile saline, adjust the turbidity to 0.5 McFarland turbidity, and count the number of spores with a hemocytometer and short mycelia. Make the bacterial concentration 1×10 3 CFU / ml to 3×10 3 CFU / ml. That is, the 0.5 McFarland turbidity bacteria solution was diluted 1000 times with RPMI-1640 liquid medium, and counted by the hemocytometer to obtain the inoculum solution. Use RPMI-1...

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Abstract

The present invention relates to the technical field of medicines and discloses dryopteris fragrans phloroglucinol derivatives, a separation and preparation method for isomers thereof and an application thereof Phloroglucinol compounds are separated and prepared from dryopteris fragrans(L.)Schott, which belongs to dryopteridaceae dryopteris plants, for the first time, and 4 pairs of isomers are discovered, wherein the 4 pairs of isomeric compounds have relatively strong effect of resisting skin superficial fungi. According to the in-vitro bacteriostatic experiment, the compounds provided by the present invention have good bacteriostatic effect on two skin pathogenic fungi, namely trichophyton rubrum and microsporum gypseum, and have characteristics of being low in side effect and being not liable to become resistant to the drug, and the like, thereby providing a novel natural compound for the treatment of skin superficial fungi infection and providing powerful technical support for preparing anti skin superficial fungi infection drugs or pharmaceutical compositions.

Description

technical field [0001] The invention relates to the technical fields of chemistry and medicine, and more specifically, to a separation and preparation method and application of Phloroglucinol derivatives of Phrylloglucinol and isomers thereof. Background technique [0002] The superficial fungi that parasitize the skin keratin tissue are dermatophytes, which can be divided into three genera: Trichophyton, Microsporum, and Epidermophyton. Dermatophyte infection is relatively common in my country, and the most common pathogenic bacteria are Trichophyton rubrum, Trichophyton mentagrophytes and Microsporum canis, which often cause diseases such as dermatophyte, tinea capitis, jock itch, and onychomycosis, accompanied by Redness, itching and other symptoms. Trichophyton rubrum is the main pathogenic bacterium that causes skin fungus, accounts for 69.5% of dermatophyte infections, can cause tinea manuum, tinea pedis, tinea capitis, etc. [0003] With the widespread use of antibio...

Claims

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Application Information

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IPC IPC(8): C07C49/84C07C49/83C07C49/723C07C45/78A61P31/10A61P17/00
CPCC07C45/78C07C49/723C07C49/83C07C49/84
Inventor 沈志滨唐春萍
Owner GUANGDONG PHARMA UNIV
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