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SML2913

Dehydroxylcannabidiol

≥98% (HPLC)

Synonym(s):

2-[(1R,6R)-3-Methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentylphenol, DH-CBD

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Pack SizeSKUAvailabilityPrice
5 mg
Please contact Customer Service for Availability
PLN 274.00
25 mg
Please contact Customer Service for Availability
PLN 1,390.00

About This Item

Empirical Formula (Hill Notation):
C21H30O
CAS Number:
Molecular Weight:
298.46
NACRES:
NA.77
UNSPSC Code:
12352200
Assay:
≥98% (HPLC)
Form:
oil
Quality level:

PLN 274.00


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Quality Level

assay

≥98% (HPLC)

form

oil

optical activity

[α]/D -135 to -120°, c = 0.5 in chloroform-d

color

colorless to light brown

storage temp.

2-8°C

Biochem/physiol Actions

Dehydroxylcannabidiol (DH-CBD) is a synthetic nonpsychoactive cannabinoid that alleviate acute pain and chronic inflammatory pain by targeting α3 GlyRs. Dehydroxylcannabidio restores the function of both hyperekplexic mutant GlyRα1 and GABAAR in the presence of GlyRα1R271Q. Apparently dehydroxylcannabidiol interrupts the protein interaction GlyRα1 and GABAAR.
Synthetic nonpsychoactive cannabinoid that alleviate acute pain and chronic inflammatory pain by targeting α3 GlyRs

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This Item
10891491089161SML3112
form

oil

form

-

form

-

form

powder

assay

≥98% (HPLC)

assay

-

assay

-

assay

≥98% (HPLC)

Quality Level

100

Quality Level

-

Quality Level

-

Quality Level

100

storage temp.

2-8°C

storage temp.

-

storage temp.

−20°C

storage temp.

2-8°C

color

colorless to light brown

color

-

color

-

color

white to beige

optical activity

[α]/D -135 to -120°, c = 0.5 in chloroform-d

optical activity

-

optical activity

-

optical activity

-


pictograms

Health hazardExclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Repr. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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Wei Xiong et al.
The Journal of experimental medicine, 209(6), 1121-1134 (2012-05-16)
Certain types of nonpsychoactive cannabinoids can potentiate glycine receptors (GlyRs), an important target for nociceptive regulation at the spinal level. However, little is known about the potential and mechanism of glycinergic cannabinoids for chronic pain treatment. We report that systemic
Jieping Lu et al.
Neuropharmacology, 133, 224-232 (2018-02-07)
Some cannabinoids have been shown to suppress chronic pain by targeting glycine receptors (GlyRs). Although cannabinoid potentiation of α3 GlyRs is thought to contribute to cannabinoid-induced analgesia, the role of cannabinoid potentiation of α1 GlyRs in cannabinoid suppression of chronic
Guichang Zou et al.
The Journal of biological chemistry, 295(1), 138-145 (2019-11-24)
The functions of the glycine receptor (GlyR) and GABAA receptor (GABAAR) are both impaired in hyperekplexia, a neurological disorder usually caused by GlyR mutations. Although emerging evidence indicates that cannabinoids can directly restore normal GlyR function, whether they affect GABAAR



Global Trade Item Number

SKUGTIN
SML2913-5MG04061841806622
SML2913-25MG04061841806615

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