Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C21H30O2 |
| Molecular Weight | 314.4617 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCC1=CC(O)=C2C=CC(C)(CCC=C(C)C)OC2=C1
InChI
InChIKey=UVOLYTDXHDXWJU-UHFFFAOYSA-N
InChI=1S/C21H30O2/c1-5-6-7-10-17-14-19(22)18-11-13-21(4,23-20(18)15-17)12-8-9-16(2)3/h9,11,13-15,22H,5-8,10,12H2,1-4H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Flavonoid glycosides and cannabinoids from the pollen of Cannabis sativa L. | 2005 Jan-Feb |
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| Neurophysiological and subjective profile of marijuana with varying concentrations of cannabinoids. | 2005 Sep |
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| Antitumor activity of plant cannabinoids with emphasis on the effect of cannabidiol on human breast carcinoma. | 2006 Sep |
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| Cannabinoids in health and disease. | 2007 |
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| Recent advances in Cannabis sativa research: biosynthetic studies and its potential in biotechnology. | 2007 Aug |
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| Phytochemical and genetic analyses of ancient cannabis from Central Asia. | 2008 |
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| Antibacterial cannabinoids from Cannabis sativa: a structure-activity study. | 2008 Aug |
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| Cannabinoids in the management of difficult to treat pain. | 2008 Feb |
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| Plant-derived cannabinoids modulate the activity of transient receptor potential channels of ankyrin type-1 and melastatin type-8. | 2008 Jun |
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| Evaluation of prevalent phytocannabinoids in the acetic acid model of visceral nociception. | 2009 Nov 1 |
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| Thermal isomerization of cannabinoid analogues. | 2009 Nov 25 |
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| Cannabinoid receptor 1 binding activity and quantitative analysis of Cannabis sativa L. smoke and vapor. | 2010 Feb |
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| Antidepressant-like effect of delta9-tetrahydrocannabinol and other cannabinoids isolated from Cannabis sativa L. | 2010 Jun |
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| Pharmacological evaluation of the natural constituent of Cannabis sativa, cannabichromene and its modulation by Δ(9)-tetrahydrocannabinol. | 2010 Nov 1 |
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| Disposition of cannabichromene, cannabidiol, and Δ⁹-tetrahydrocannabinol and its metabolites in mouse brain following marijuana inhalation determined by high-performance liquid chromatography-tandem mass spectrometry. | 2010 Oct |
Patents
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Code | English |
| Code System | Code | Type | Description | ||
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CANNABICHROMENE
Created by
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2585216
Created by
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291831
Created by
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C010695
Created by
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DTXSID80942873
Created by
admin on Fri Dec 15 15:04:43 GMT 2023 , Edited by admin on Fri Dec 15 15:04:43 GMT 2023
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DB14735
Created by
admin on Fri Dec 15 15:04:43 GMT 2023 , Edited by admin on Fri Dec 15 15:04:43 GMT 2023
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K4497H250W
Created by
admin on Fri Dec 15 15:04:43 GMT 2023 , Edited by admin on Fri Dec 15 15:04:43 GMT 2023
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30219
Created by
admin on Fri Dec 15 15:04:43 GMT 2023 , Edited by admin on Fri Dec 15 15:04:43 GMT 2023
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20675-51-8
Created by
admin on Fri Dec 15 15:04:43 GMT 2023 , Edited by admin on Fri Dec 15 15:04:43 GMT 2023
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K4497H250W
Created by
admin on Fri Dec 15 15:04:43 GMT 2023 , Edited by admin on Fri Dec 15 15:04:43 GMT 2023
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PRIMARY |
ACTIVE MOIETY
