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olivetol

Known as: 5-pentyl-1,3- benzenediol, 5-pentyl-1,3-dihydroxybenzene 
National Institutes of Health

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Broader (1)

Resorcinols

Papers overview

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2019
2019
Lactoperoxidase inhibition of some natural phenolic compounds: Kinetics and molecular docking studies.
The inhibition effects of some phenolic compounds from natural products such as taxifolin, resveratrol, olivetol, cynarine, and… 
2017
2017
Square wave and differential pulse voltammetric methods for the analysis of olivetol at gold electrode
Few electrochemical techniques have been employed for the determination of the powerful antitumor agent olivetol (OLV) in real… 
2013
2013
Structural requirements for potent direct inhibition of human cytochrome P450 1A1 by cannabidiol: role of pentylresorcinol moiety.
Our recent work has shown that cannabidiol (CBD) exhibits the most potent direct inhibition of human cytochrome P450 1A1 (CYP1A1… 
2008
2008
Activities of 2,4-Dihydroxy-6-n-pentylbenzoic Acid Derivatives
Esters of 2-hydroxy-4-methoxy-6-n-pentylbenzoic acid (2−8) (methyl, ethyl, butyl, pentyl, isopropyl, sec-butyl and benzyl… 
Highly Cited
1997
Highly Cited
1997
Simple Synthesis of 5-Substituted Resorcinols: A Revisited Family of Interesting Bioactive Molecules.
The reaction of 3,5-dimethoxybenzyl trimethylsilyl ether (3) with different aldehydes (n-PrCHO, n-C(11)H(23)CHO, MeCHO, PhCHO) in… 
1984
1984
Biotransformation of olivetol by Syncephalastrum racemosum.
A study of the biotransformation of olivetol by Syncephalastrum racemosum ATCC 18192 has led to the isolation of three… 
1982
1982
Intraocular pressure following systemic administration of cannabinoids.
Various cannabinoids have been tested for activity compared to delta 9-THC in reducing intraocular pressure after intravenous… 
1978
1978
Inhibition of prostaglandin biosynthesis by derivatives of olivetol formed under pyrolysis of cannabidiol.
1976
1976
Cannabinols and the rosette forming properties of lymphocytes in vitro.
1968
1968
Constituents of hashish. A novel reaction of olivetol with citral in the presence of pyridine. Total synthesis of dl-cannabicyclol and dl-cannabichromene.
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