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Cannabielsoin

From Wikipedia, the free encyclopedia
Cannabielsoin
Names
IUPAC name
(5aS,6S,9R,9aR)-6-methyl-3-pentyl-9-prop-1-en-2-yl-7,8,9,9a-tetrahydro-5aH-dibenzofuran-1,6-diol
Other names
  • Cannabielsoin A
  • CBE
  • Cannabielsoin I[1]
Identifiers
3D model (JSmol)
AbbreviationsCBE
ChemSpider
KEGG
UNII
  • InChI=1S/C21H30O3/c1-5-6-7-8-14-11-16(22)19-17(12-14)24-20-18(19)15(13(2)3)9-10-21(20,4)23/h11-12,15,18,20,22-23H,2,5-10H2,1,3-4H3/t15-,18+,20-,21-/m0/s1
    Key: RBEAVAMWZAJWOI-MTOHEIAKSA-N
  • CCCCCC1=CC(=C2[C@H]3[C@@H](CC[C@]([C@H]3OC2=C1)(C)O)C(=C)C)O
Properties
C21H30O3
Molar mass330.468 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Cannabielsoin (CBE) is a metabolite ofcannabidiol, one of the major chemical components ofcannabis.[2]

History

[edit]

Cannabielsoin in scientific journals was first cited in 1973. It was concluded that cannabielsoin was formed from cannabidiol as part of the metabolic process and is non-psychoactive.[3][unreliable source?]

See also

[edit]

References

[edit]
  1. ^"Cannabielsoin (CAS 52025-76-0)".www.caymanchem.com.
  2. ^Yamamoto I, Gohda H, Narimatsu S, Watanabe K, Yoshimura H (November 1991). "Cannabielsoin as a new metabolite of cannabidiol in mammals".Pharmacology, Biochemistry, and Behavior.40 (3):541–6.doi:10.1016/0091-3057(91)90360-e.PMID 1806944.S2CID 21038637.
  3. ^"Cannabielsoin (CBE) Cannabis".Marijuana Doctors.
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