Hainan YouYou Biotechnology Co., Ltd

 

Oleocanthal is a structure similar to oleorin, Was first reported in 1992, The following year, its cleft ring ether terdoid structure was determined by Montedoro, The scientific name is hydrohydroxyphenyl ethanol-dialdehyde (p-hydroxyphenylethanol-elenolic acid dialdehyde, p-HPEA-EDA), Also known as 2- (4-hydroxyphenyl) ethyl (E) -4-formyl-3- (2-oxyethyl) hexyl-4-enolate, deacetoxyoxal oligomeric xyloside, decarboxylated methyl oligomeric xyloside, etc., The molecular formula, C17H20O5, Molecular weight of 304, As an olive polyphenolic compound, It causes throat and nose irritation, Thus it gets the name of Oleocanthal.

 

 

Oleocanthal has a certain water soluble, and easily soluble in polar organic solvents such as formaldehyde. Stable in acid media, but are susceptible to degradation under alkaline conditions. Stimulation of aldehyde will produce irritation to the oral pharynx, because there is a sensory receptor specific to the stimulating aldehyde in the oropharyngeal region of the mouth. When the Oleocanthal passes through the pharynx, it will selectively activate these specific receptors, thus producing a bitter taste and irritation. It was found that the subject's perception of the Oleocanthal may be directly related to the number of transient receptor potential ion channel (TRPA 1) receptors.

 

 

Studies have shown that Oleocanthal has many health benefits for the human body, and is currently mainly used as medicinal or health care ingredients. Studies show that it may help prevent certain inflammation-related diseases, such as arthritis and cardiovascular disease. Such as antioxidant, anti-inflammatory, antibacterial, neuroprotective, and antiplatelet aggregation. It is a more potent NSAID with greater activity than ibuprofen.

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