View source for 2-Isopropyl-5-methyl-1-(2,6-dihydroxy-4-nonylphenyl)cyclohex-1-ene

{{Drugbox|
|IUPAC_name = 2-Isopropyl-5-methyl-1-(2,6-dihydroxy-4-nonylphenyl)cyclohex-1-ene
| image = IPMDHNPC.png
| width= 240
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| C=25 | H=40 | O=2
| molecular_weight = 372.582 g/mol
| smiles = CC(C)C=2CCC(C)CC=2c1c(O)cc(cc1O)CCCCCCCCC
| bioavailability=
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'''2-Isopropyl-5-methyl-1-(2,6-dihydroxy-4-nonylphenyl)cyclohex-1-ene''' is an [[analgesic]] compound which 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 CB<sub>1</sub> agonist.<ref>Raj K. Razdan. The Total Synthesis of Cannabinoids. p245. Volume 4 of The Total Synthesis of Natural Products, edited by John Apsimon. Wiley Interscience. May 1981. ISBN 978-0-471-05460-3</ref>

It can be synthesized by [[Birch reduction]] from the nonyl-analog of [[cannabidiol]].<ref>{{cite journal| author = Razdan RK, Pars HG, Thompson WR, Granchelli FE | journal = Tetrahedron Letters | year = 1974 | pages=4315| doi = 10.1016/S0040-4039(01)92152-5| title = Lithium-ammonia reduction of tetrahydrocannabinols| volume = 15}}</ref>

==References==
<references/>

{{cannabinoids}}

{{DEFAULTSORT:Isopropyl-5-methyl-1-(2,6-dihydroxy-4-nonylphenyl)cyclohex-1-ene, 2-}}
[[Category:Cannabinoids]]
[[Category:Benzenediols]]

{{cannabinoid-stub}}
[[Category:2Fix]]