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Identification and Characterization of Cannabichromene's Major Metabolite Following Incubation with Human Liver Microsomes
被引:0
|作者:
Ward, Alexandra M.
[1
]
Shokati, Touraj
[2
]
Klawitter, Jost
[2
]
Klawitter, Jelena
[2
]
Nguyen, Vu
[1
]
Kozell, Laura
[3
,4
,5
]
Abbas, Atheir I.
[3
,4
,5
]
Jones, David
[6
]
Christians, Uwe
[2
]
机构:
[1] Univ Colorado Anschutz Med Campus, Skaggs Sch Pharm & Pharmaceut Sci, Dept Pharmaceut Sci, Aurora, CO 80045 USA
[2] Univ Colorado Anschutz Med Campus, Sch Med, Dept Anesthesiol, iC42 Clin Res & Dev, iC42 Clin Res & Dev, Aurora, CO 80045 USA
[3] Oregon Hlth & Sci Univ, Dept Behav Neurosci, Portland, OR 97239 USA
[4] Oregon Hlth & Sci Univ, Dept Psychiat, Portland, OR 97239 USA
[5] Vet Affairs Portland Hlth Care Syst, Portland, OR 97239 USA
[6] Univ Colorado Anschutz Med Campus, Sch Med, Dept Pharmacol, Aurora, CO 80045 USA
来源:
关键词:
cannabichromene;
2 '-hydroxycannabicitran;
cannabicitran;
human drug metabolism;
phase I metabolism;
human liver microsomes;
gas chromatography-mass spectrometry;
nuclear magnetic resonance spectroscopy;
molecular docking;
CB1;
receptor;
CB2;
binding;
PLANT CANNABINOIDS;
ACCURATE DOCKING;
CANNABIDIOL;
POTENCY;
GLIDE;
DELTA(9)-TETRAHYDROCANNABINOL;
PHYTOCANNABINOIDS;
RECEPTORS;
SATIVA;
CB1;
D O I:
10.3390/metabo14060329
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Cannabichromene (CBC) is a minor cannabinoid within the array of over 120 cannabinoids identified in the Cannabis sativa plant. While CBC does not comprise a significant portion of whole plant material, it is available to the public in a purified and highly concentrated form. As minor cannabinoids become more popular due to their potential therapeutic properties, it becomes crucial to elucidate their metabolism in humans. Therefore, the goal of this was study to identify the major CBC phase I-oxidized metabolite generated in vitro following incubation with human liver microsomes. The novel metabolite structure was identified as 2 '-hydroxycannabicitran using gas chromatography-mass spectrometry and nuclear magnetic resonance spectroscopy. Following the identification, in silico molecular modeling experiments were conducted and predicted 2 '-hydroxycannabicitran to fit in the orthosteric site of both the CB1 and CB2 receptors. When tested in vitro utilizing a competitive binding assay, the metabolite did not show significant binding to either the CB(1 )or CB2 receptors. Further work necessitates the determination of potential activity of CBC and the here-identified phase I metabolite in other non-cannabinoid receptors.
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页数:21
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