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(-)-Cannabidiol, Natural cannabinoid (ab120448)

Price and availability

335 040 ₸

Availability

Order now and get it on Friday March 05, 2021

(-)-Cannabidiol, Natural cannabinoid (ab120448)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)

Key features and details

  • Common constituent of Cannabis
  • CAS Number: 13956-29-1
  • Purity: > 98%
  • Soluble in DMSO to 100 mM and in ethanol to 100 mM
  • Form / State: Solid
  • Source: Synthetic

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Overview

  • Product name

    (-)-Cannabidiol, Natural cannabinoid
  • Description

    Common constituent of Cannabis
  • Alternative names

    • CBD
  • Biological description

    Common constituent of Cannabis with much lower affinity at CB1 and CB2 receptors (Ki values are 4350 and 2860 nM, respectively) than Delta-9 THC. Elicits anticonvulsant, anticancer, anti-inflammatory and neuroprotective effects. Protects retinal neurons in diabetic models.

  • Purity

    > 98%
  • CAS Number

    13956-29-1
  • Chemical structure

    Chemical Structure

Properties

  • Chemical name

    2-[(1R,6R)-3-Methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentyl-1,3-benzenediol
  • Molecular weight

    314.47
  • Molecular formula

    C21H30O2
  • PubChem identifier

    644019
  • Storage instructions

    Store at -20°C. Store under desiccating conditions. The product can be stored for up to 12 months.
  • Solubility overview

    Soluble in DMSO to 100 mM and in ethanol to 100 mM
  • Handling

    Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

    Toxic, refer to SDS for further information

    Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

  • SMILES

    CC(=C)[C@@H]2CCC(C)=C[C@H]2c1c(O)cc(CCCCC)cc1O
  • Source

    Synthetic

  • Research areas

    • Neuroscience
    • Neurotransmission
    • Receptors / Channels
    • GPCR
    • Cannabinoid Receptor
    • Cardiovascular
    • Lipids / Lipoproteins
    • Lipid Metabolism
    • Cholesterol Metabolism
    • Cardiovascular
    • Atherosclerosis
    • Lipoprotein metabolism
    • Biochemicals
    • Chemical Type
    • Biochemicals
    • Biochemicals
    • Pharmacology
    • Receptors & Transporters
    • Cannabinoid
    • Non-selective
    • Biochemicals
    • Pharmacology
    • Receptors & Transporters
    • Cannabinoid
    • Non-selective
    • Agonists
    • Metabolism
    • Pathways and Processes
    • Metabolic signaling pathways
    • Lipid and lipoprotein metabolism
    • Cholesterol Metabolism
    • Metabolism
    • Pathways and Processes
    • Metabolic signaling pathways
    • Lipid and lipoprotein metabolism
    • Lipoprotein metabolism
    • Metabolism
    • Types of disease
    • Heart disease
    • Biochemicals
    • Research Area
    • Addiction
    • Cannabinoid
    • Non-selective
    • Biochemicals
    • Research Area
    • Addiction
    • Cannabinoid
    • Non-selective
    • Agonists
    • Biochemicals
    • Research Area
    • Obesity
    • Cannabinoid
    • Non-selective
    • Biochemicals
    • Research Area
    • Obesity
    • Cannabinoid
    • Non-selective
    • Agonists
    • Biochemicals
    • Research Area
    • Pain & inflammation
    • Cannabinoid
    • Non-selective
    • Biochemicals
    • Research Area
    • Pain & inflammation
    • Cannabinoid
    • Non-selective
    • Agonists
    • Biochemicals
    • Pharmacology
    • Signaling
    • Immunomodulators
    • Immunomodulators & Immunosuppressants
    • Biochemicals
    • Chemical Type
    • Controlled substances

Images

  • Functional Studies - (-)-Cannabidiol, Natural cannabinoid (ab120448)
    Functional Studies - (-)-Cannabidiol, Natural cannabinoid (ab120448)
    ab109225 staining Nox4 in HeLa cells treated with (-)-cannabidiol (ab120448), by ICC/IF. Increase in Nox4 expression correlates with increased concentration of (-)-cannabidiol, as described in literature.
    The cells were incubated at 37°C for 6h in media containing different concentrations of ab120847 ((-)-cannabidiol) in DMSO, fixed with 4% formaldehyde for 10 minutes at room temperature and blocked with PBS containing 10% goat serum, 0.3 M glycine, 1% BSA and 0.1% tween for 2h at room temperature. Staining of the treated cells with ab109225 (5 µg/ml) was performed overnight at 4°C in PBS containing 1% BSA and 0.1% tween. A DyLight 488 goat anti-rabbit polyclonal antibody (ab96899) at 1/250 dilution was used as the secondary antibody.

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