(-)-Cannabidiol

Pricing Availability   Qty
说明: Natural cannabinoid; GPR55 antagonist, weak CB1 antagonist, CB2 inverse agonist and AMT inhibitor
别名: CBD
化学名: 2-[(1R,6R)-3-Methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentyl-1,3-benzenediol
纯度: ≥99% (HPLC)
说明书
引用文献 (5)
评论
文献 (1)

生物活性 for (-)-Cannabidiol

(-)-Cannabidiol is a non-psychotropic constituent of cannabis that is anticonvulsive, antihyperalgesic and neuroprotective in vivo. GPR55 and weak CB1 antagonist (IC50 values are 0.445 and 3.35 μM), CB2 receptor inverse agonist and inhibitor of anandamide uptake (IC50 = 27.5 μM). Also inhibits FABPs and a weak agonist at TRP vanilloid receptors (EC50 = 3.5 μM).

技术数据 for (-)-Cannabidiol

分子量 314.47
公式 C21H30O2
储存 Store at -20°C
纯度 ≥99% (HPLC)
CAS Number 13956-29-1
PubChem ID 12302390
InChI Key QHMBSVQNZZTUGM-ROUUACIJSA-N
Smiles CCCCCC1=CC(O)=C([C@H]2C=C(C)CC[C@H]2C(C)=C)C(O)=C1

上方提供的技术数据仅供参考。批次相关数据请参见分析证书。

Tocris products are intended for laboratory research use only, unless stated otherwise.

溶解性数据 for (-)-Cannabidiol

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
ethanol 23.59 75
DMSO 23.59 75

制备储备液 for (-)-Cannabidiol

以下数据基于产品分子量 314.47。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

选择批次从而根据批次分子量重新计算:
浓度/溶剂体积/质量 1 mg 5 mg 10 mg
0.75 mM 4.24 mL 21.2 mL 42.4 mL
3.75 mM 0.85 mL 4.24 mL 8.48 mL
7.5 mM 0.42 mL 2.12 mL 4.24 mL
37.5 mM 0.08 mL 0.42 mL 0.85 mL

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产品说明书 for (-)-Cannabidiol

分析证书/产品说明书
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关键词: (-)-Cannabidiol, (-)-Cannabidiol supplier, Natural, cannabinoids, AMT, inhibitors, inhibits, GPR55, antagonists, weak, CB1, CB2, inverse, agonists, Anandamide, Transporters, Monoamine, Neurotransmitter, Non-Selective, Receptors, cb2r, cb1r, FABP, FABPs, fatty, acid, binding, proteins, CBD, Cannabinoid, Non-selective, Cannabinoids, Fatty, Acid, Binding, Proteins, 1570, Tocris Bioscience

5 篇 (-)-Cannabidiol 的引用文献

引用文献是使用了 Tocris 产品的出版物。 (-)-Cannabidiol 的部分引用包括:

Esposito et al (2011) Cannabidiol reduces Aβ-induced neuroinflammation and promotes hippocampal neurogenesis through PPARγ involvement. Proc Natl Acad Sci U S A 6 e28668 PMID: 22163051

Whyte et al (2009) The putative cannabinoid receptor GPR55 affects osteoclast function in vitro and bone mass in vivo. PLoS One 106 16511 PMID: 19805329

Rodríguez-Muñoz et al (2018) Cannabidiol enhances MOR antinociception, diminishes NMDA-mediated seizures and reduces stroke damage via the sigma 1 receptor. Mol Brain 11 51 PMID: 30223868

Hamtiaux et al (2011) Increasing antiproliferative properties of endocannabinoids in N1E-115 neuroblastoma cells through inhibition of their metabolism. PLoS One 6 e26823 PMID: 22046372

Panja et al (2019) Paraneoplastic cerebellar degeneration: Yo antibody alters mitochondrial calcium buffering capacity. Neuropathol Appl Neurobiol 45 141 PMID: 29679372


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该领域的文献

Tocris offers the following scientific literature in this area to showcase our products. We invite you to request* your copy today!

*请注意,Tocris 仅会向正规科研企业/机构地址发送文献。


Cannabinoid Receptor Ligands Scientific Review

Cannabinoid Receptor Ligands Scientific Review

Written by Roger Pertwee, this review discusses compounds which affect the activity of the endocannabinoid system, focusing particularly on ligands that are most widely used as experimental tools and denotes compounds available from Tocris.