Matches in DBpedia 2016-04 for { ?s ?p "2-Isopropyl-5-methyl-1-(2,6-dihydroxy-4-nonylphenyl)cyclohex-1-ene is an analgesic compound that is a cannabinoid agonist. It is a ring-opened cannabinoid derivative, an analogue of cannabidiol. However, unlike cannabidiol, this compound produces potent cannabis-like effects in animals, suggesting it acts as a CB1 agonist.It can be synthesized by Birch reduction from the nonyl-analog of cannabidiol."@en }
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- 2-Isopropyl-5-methyl-1-(2,6-dihydroxy-4-nonylphenyl)cyclohex-1-ene abstract "2-Isopropyl-5-methyl-1-(2,6-dihydroxy-4-nonylphenyl)cyclohex-1-ene is an analgesic compound that is a cannabinoid agonist. It is a ring-opened cannabinoid derivative, an analogue of cannabidiol. However, unlike cannabidiol, this compound produces potent cannabis-like effects in animals, suggesting it acts as a CB1 agonist.It can be synthesized by Birch reduction from the nonyl-analog of cannabidiol.".
- Q209414 abstract "2-Isopropyl-5-methyl-1-(2,6-dihydroxy-4-nonylphenyl)cyclohex-1-ene is an analgesic compound that is a cannabinoid agonist. It is a ring-opened cannabinoid derivative, an analogue of cannabidiol. However, unlike cannabidiol, this compound produces potent cannabis-like effects in animals, suggesting it acts as a CB1 agonist.It can be synthesized by Birch reduction from the nonyl-analog of cannabidiol.".
- 2-Isopropyl-5-methyl-1-(2,6-dihydroxy-4-nonylphenyl)cyclohex-1-ene comment "2-Isopropyl-5-methyl-1-(2,6-dihydroxy-4-nonylphenyl)cyclohex-1-ene is an analgesic compound that is a cannabinoid agonist. It is a ring-opened cannabinoid derivative, an analogue of cannabidiol. However, unlike cannabidiol, this compound produces potent cannabis-like effects in animals, suggesting it acts as a CB1 agonist.It can be synthesized by Birch reduction from the nonyl-analog of cannabidiol.".
- Q209414 comment "2-Isopropyl-5-methyl-1-(2,6-dihydroxy-4-nonylphenyl)cyclohex-1-ene is an analgesic compound that is a cannabinoid agonist. It is a ring-opened cannabinoid derivative, an analogue of cannabidiol. However, unlike cannabidiol, this compound produces potent cannabis-like effects in animals, suggesting it acts as a CB1 agonist.It can be synthesized by Birch reduction from the nonyl-analog of cannabidiol.".