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(±)-Cannabichromene
🥰Excellent
Catalog No. TN3575Cas No. 20675-51-8
Alias Cannabichromene
(±)-Cannabichromene is a major non-psychotropic phytocannabinoid that inhibits endocannabinoid inactivation and activates the transient receptor potential ankyrin-1 (TRPA1), it selectively reduces inflammation-induced hypermotility in vivo in a manner that is not dependent on cannabinoid receptors or TRPA1.
(±)-Cannabichromene
🥰Excellent
Purity: 99.1%
Catalog No. TN3575Alias CannabichromeneCas No. 20675-51-8
(±)-Cannabichromene is a major non-psychotropic phytocannabinoid that inhibits endocannabinoid inactivation and activates the transient receptor potential ankyrin-1 (TRPA1), it selectively reduces inflammation-induced hypermotility in vivo in a manner that is not dependent on cannabinoid receptors or TRPA1.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | $173 | In Stock | |
| 5 mg | $432 | In Stock | |
| 10 mg | $628 | In Stock | |
| 25 mg | $986 | In Stock | |
| 50 mg | $1,320 | In Stock | |
| 100 mg | $1,790 | In Stock | |
| 500 mg | $3,590 | In Stock | |
| 1 mL x 10 mM (in DMSO) | $550 | In Stock |
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Purity:99.1%
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All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.Product Introduction
Bioactivity
Chemical Properties
| Description | (±)-Cannabichromene is a major non-psychotropic phytocannabinoid that inhibits endocannabinoid inactivation and activates the transient receptor potential ankyrin-1 (TRPA1), it selectively reduces inflammation-induced hypermotility in vivo in a manner that is not dependent on cannabinoid receptors or TRPA1. |
| In vitro | Cannabichromene (CBC)? activated CB2 but not CB1 receptors to produce hyperpolarization of AtT20 cells.?This activation was inhibited by a CB2 receptor antagonist AM630, and sensitive to Pertussis toxin.?Application of CBC reduced activation of CB2 , but not CB1 , receptors by subsequent co-application of CP55,940, an efficacious CB1 and CB2 receptor agonist.?Continuous CBC application induced loss of cell surface CB2 receptors and desensitization of the CB2 receptor-induced hyperpolarization[2]. |
| Alias | Cannabichromene |
| Molecular Weight | 314.46 |
| Formula | C21H30O2 |
| Cas No. | 20675-51-8 |
| Smiles | OC1=C2C(OC(CCC=C(C)C)(C)C=C2)=CC(CCCCC)=C1 |
| Relative Density. | 1.0536 g/cm3 (Estimated) |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 55 mg/ml (174.88 mM)  | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
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(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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