3-Hydroxy-6-methyl-...

3-Hydroxy-6-methyl-5-methoxy-2-pentyl-4H-pyran-4-one 125263-70-9 manufacturer
3-Hydroxy-6-methyl-5-methoxy-2-pentyl-4H-pyran-4-one 125263-70-9 manufacturer
3-Hydroxy-6-methyl-5-methoxy-2-pentyl-4H-pyran-4-one 125263-70-9 manufacturer
3-Hydroxy-6-methyl-5-methoxy-2-pentyl-4H-pyran-4-one 125263-70-9 manufacturer
3-Hydroxy-6-methyl-5-methoxy-2-pentyl-4H-pyran-4-one 125263-70-9 manufacturer

3-Hydroxy-6-methyl-5-methoxy-2-pentyl-4H-pyran-4-one 125263-70-9 manufacturer

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10 Metric Ton

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  • Min.Order :10 Metric Ton
  • Purity: 97%
  • Payment Terms : L/C,T/T,Other

Keywords

125263-70-9 manufacturer 3-Hydroxy-6-methyl-5-methoxy-2-pentyl-4H-pyran-4-one 125263-70-9 fast delivery

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  • Appearance:Powder or liquid
  • Application:Medicinal Chemistry Biomedicine Pharmaceutical intermediates Chemistry experiment Biological experiments Chemical reagent For R&D use only.
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  • ProductionCapacity:|Metric Ton|Day
  • Storage:Store in a tightly closed container, in a cool and dry place.
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Superiority:

Allixin is a phytoallexin found in garlic (Allium sativum) bulbs. Allixin has weak antimicrobial activity and exerts an anti-promoting activity against skin tumors induced by the chemical 12-O-tetradecanoylphorbol-13-acetate (TPA). Allixin also demonstrates an inhibitory effect on aflatoxin B1-induced mutagenesis.
 
Allixin is a phytoallexin found in garlic (Allium sativum) bulbs. It was first isolated and characterized in 1989. When garlic is stored for long periods of time, it can form visible accumulations of crystalline allixin on its surface, particularly in areas where tissue has become necrotic. After 2 years of storage, the amount of allixin accumulated can approach 1% of the dry weight of the cloves. Since allixin has weak antimicrobial activity,these high concentrations are thought to be produced by the garlic bulb to protect itself from further damage from microorganisms.
 

Details:

In in vitro studies, allixin demonstrates neurotrophic activity, but at high concentrations it has cytotoxic effects. Simple chemical analogs of allixin were found to have more potent neurotrophic activity, but without the cytotoxic effects.Allixin may therefore be a useful starting point for the development of pharmaceutical drugs for the treatment of neurodegenerative disorders or for neuronal regeneration in the brain.
 

 
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