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China Olivetol Raw Material Factory Supply Olivetol Raw Material, High Quality Olivetol Powder Purity 99% Olivetol Raw Powder, Olivetol Powder is an important pharmaceutical intermediate, first obtained by degrading lichenic acid (also known as D-sonoric acid and amyllic acid) extracted from the lichen plant, Olivetol Powder is mainly used in laboratory research and development processes and in chemical production.
Manufactory Supply Olivetol Raw Material, High Purity Olivetol Powder, High Quality Olivetol Raw Powder.
Uses and functions of Olivetol Powder
3,5-Dihydroxyalkylbenzene has a wide range of biological activities and is effective against a wide range of pathogenic fungi and bacteria. In recent years, it has been found that high concentrations of 3,5-dihydroxyalkylbenzene can break DNA in the presence of copper chloride and oxygen.
Therefore, it is used to inhibit and treat human immune deficiency, cancer and other malignant tumours caused by reverse transcriptase virus with remarkable effect.
3,5-Dihydroxyalkylbenzene can also be used to synthesise cannabinoids, which is a generic term for a group of chemically similar substances in cannabis with physiological activity in the human body, numbering more than 60, and which can be used for analgesic, sedative, anti-inflammatory, digestive, and anti-hypertensive purposes. The first of these compounds is 3,5-dihydroxypentylbenzene (Olivetol).
Pharmacological Effects of Olivetol Raw Material
Olivetol Raw Material is an important pharmaceutical intermediate, first obtained by degrading lichenic acid (also known as D-sonoric acid, pentyl lichen condensate) extracted from the lichen plant, which is mainly used in the laboratory research and development process and in the chemical production process.
Production method of Olivetol Powder
3,5-Dihydroxypentylbenzene is used as a precursor for tetrahydrocannabinol-related synthesis. Biological Activity Olivetol is a naturally occurring polyphenolic compound found in lichens or produced by some insects.
Olivetol competitively inhibits cannabinoid receptors CB1 and CB2, and inhibits the activity of CYP2C19 and CYP2D6, with IC50 and Ki values of 15.3 μM,7.21 μM and 2.71 μM,2.87 μM, respectively.
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