cannabidiol dimethyl ether

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CAS:1242-67-7
Purity:98% Package:1G;10G;100G Remarks:Lipoxygenases (LOs) are non-heme iron-containing dioxygenases that catalyze the oxidation of polyunsaturated fatty acids to generate unsaturated fatty acid hydroperoxides. Cannabidiol dimethyl ether (
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CAS:1242-67-7
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Products Intro: Product Name:Cannabidiol Dimethyl Ether
CAS:1242-67-7
cannabidiol dimethyl ether Basic information
Product Name:cannabidiol dimethyl ether
Synonyms:cannabidiol dimethyl ether;(1R,6R)-1-(2,6-Dimethoxy-4-pentylphenyl)-3-methyl-6-isopropenyl-2-cyclohexene;(3R)-1-Methyl-3β-(2,6-dimethoxy-4-pentylphenyl)-4α-isopropenyl-1-cyclohexene;1-Methyl-3β-(2,6-dimethoxy-4-pentylphenyl)-4α-isopropenylcyclohexene;Benzene, 1,3-dimethoxy-2-[(1R,6R)-3-methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentyl-
CAS:1242-67-7
MF:C23H34O2
MW:342.51
EINECS:
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Mol File:1242-67-7.mol
cannabidiol dimethyl ether Structure
cannabidiol dimethyl ether Chemical Properties
Boiling point 438.4±45.0 °C(Predicted)
density 0.957±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility ≤14mg/ml in ethanol;1mg/ml in DMSO;2mg/ml in dimethyl formamide
form solution in acetate.
Safety Information
MSDS Information
cannabidiol dimethyl ether Usage And Synthesis
UsesLipoxygenases (LOs) are non-heme iron-containing dioxygenases that catalyze the oxidation of polyunsaturated fatty acids to generate unsaturated fatty acid hydroperoxides. The immediate products of 15-LO fatty acid oxidation act as mediators in inflammation, thrombosis, and cancer. CBDD is a cannabidiol derivative that potently and selectively inhibits 15-LO with an IC50 value of 0.28 μM. It does not inhibit 5-LO effectively (IC50 >200 μM).
Biological Activitycannabidiol dimethyl ether (cbdd) is a cannabidiol derivative that potently and selectively inhibits 15-lox with an ic50 value of 0.28 μm.15-lox can oxygenate cholesterol esters in the low-density lipoprotein (ldl) particle. thus, 15-lox has been involved in the development of atherosclerosis, and cbdd may be a useful prototype for producing medicines for atherosclerosis [1].cbdd showed a potent inhibitory effect on the catalytic activity of cytochrome p450 2c19 with an ic50 value of 14.8 μμ [2]. cbdd inhibited the cyp2b6 activity with the ic50values of 75.7 μm [3]. cytochrome p450 enzymes have been isolated from numerous mammalian tissues such as liver, kidney, lung, intestine, adrenal cortex. cytochrome p450 enzymes have also existed in insects, plants, yeasts, and bacteria. cytochrome p450 has been known to catalyze hydroxylations, epoxidations, n-, s-, and o-dealkylations, n-oxidations, sulfoxidations, dehalogenations, and other reactions [4].
references[1] takeda s, usami n, yamamoto i, et al. cannabidiol-2′, 6′-dimethyl ether, a cannabidiol derivative, is a highly potent and selective 15-lipoxygenase inhibitor[j]. drug metabolism and disposition, 2009, 37(8): 1733-1737.
[2] jiang r, yamaori s, okamoto y, et al. cannabidiol is a potent inhibitor of the catalytic activity of cytochrome p450 2c19[j]. drug metabolism and pharmacokinetics, 2013, 28(4): 332-338.
[3] yamaori s, maeda c, yamamoto i, et al. differential inhibition of human cytochrome p450 2a6 and 2b6 by major phytocannabinoids[j]. forensic toxicology, 2011, 29(2): 117-124.
[4] groves j t, han y z. models and mechanisms of cytochrome p450 action[m]//cytochrome p450. springer us, 1995: 3-48.
cannabidiol dimethyl ether Preparation Products And Raw materials
Tag:cannabidiol dimethyl ether(1242-67-7) Related Product Information
resorstatin CANNABIDIOL O-1918 cannabidiol dimethyl ether 1-Methyl-4-(3-methyl-3-butenyl)benzene 5-METHYL-2-[(1R,6R)-3-METHYL-6-(1-METHYLETHENYL)-2-CYCLOHEXEN-1-YL]-1,3-BENZENEDIOL 2,6-DIMETHOXY-P-XYLENE 4-(2-METHOXYPHENYL)-2-METHYL-1-BUTENE 3-(2,6-DIMETHOXYPHENYL)-1-PROPENE (+)-Dipentene