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5-METHYL-2-[(1R,6R)-3-METHYL-6-(1-METHYLETHENYL)-2-CYCLOHEXEN-1-YL]-1,3-BENZENEDIOL

更新时间:2025-08-21 19:51:29

5-METHYL-2-[(1R,6R)-3-METHYL-6-(1-METHYLETHENYL)-2-CYCLOHEXEN-1-YL]-1,3-BENZENEDIOL结构式
5-METHYL-2-[(1R,6R)-3-METHYL-6-(1-METHYLETHENYL)-2-CYCLOHEXEN-1-YL]-1,3-BENZENEDIOL结构式
品牌特惠专场
常用名 5-METHYL-2-[(1R,6R)-3-METHYL-6-(1-METHYLETHENYL)-2-CYCLOHEXEN-1-YL]-1,3-BENZENEDIOL 英文名 5-METHYL-2-[(1R,6R)-3-METHYL-6-(1-METHYLETHENYL)-2-CYCLOHEXEN-1-YL]-1,3-BENZENEDIOL
CAS号 35482-50-9 分子量 258.355
密度 1.1±0.1 g/cm3 沸点 414.3±45.0 °C at 760 mmHg
分子式 C17H22O2 熔点 N/A
MSDS N/A 闪点 192.3±23.3 °C

 用途


Cannabidiorcol (CBDO、CBD-C1、O-1821) 与大麻二酚的衍生物,其戊基侧链缩短为甲基。 Cannabidiorcol 对大麻素受体 (CB) 的亲和力较低,是瞬时受体电位通道 (TRP channel) 的激动剂,通过该通道产生抗炎作用,但高浓度时还可促进肿瘤发生。

 名称

英文名 5-methyl-2-[(6R)-3-methyl-6-prop-1-en-2-ylcyclohex-2-en-1-yl]benzene-1,3-diol
英文别名 更多

 生物活性

描述 Cannabidiorcol (CBDO、CBD-C1、O-1821) 与大麻二酚的衍生物,其戊基侧链缩短为甲基。 Cannabidiorcol 对大麻素受体 (CB) 的亲和力较低,是瞬时受体电位通道 (TRP channel) 的激动剂,通过该通道产生抗炎作用,但高浓度时还可促进肿瘤发生。
相关类别
靶点实验

AChE:4.61 mM (Ki)

参考文献

[1]. Teresina Laragione, et al. Combination therapy of a TRPV2 agonist with a TNF inhibitor achieves sustained suppression of disease severity and reduced joint damage. Clin Exp Immunol. 2023 Mar; 211(3): 233–238.

[2]. Rongqi Huang, et al. Thermal stress involved in TRPV2 promotes tumorigenesis through the pathways of HSP70/27 and PI3K/Akt/mTOR in esophageal squamous cell carcinoma. Br J Cancer. 2022 Nov 1; 127(8): 1424–1439.

 物理化学性质

密度 1.1±0.1 g/cm3
沸点 414.3±45.0 °C at 760 mmHg
分子式 C17H22O2
分子量 258.355
闪点 192.3±23.3 °C
精确质量 258.161987
PSA 40.46000
LogP 4.91
InChIKey GKVOVXWEBSQJPA-UONOGXRCSA-N
SMILES C=C(C)C1CCC(C)=CC1c1c(O)cc(C)cc1O
蒸汽压 0.0±1.0 mmHg at 25°C
折射率 1.565
储存条件 -20°C,密闭,干燥

 靶点实验

查看更多实验

实验名称:Agonist activity at human CB2 receptor expressed in CHO cells assessed as forskolin-s...
来源:ChEMBL
靶标:Cannabinoid receptor 2
External Id:CHEMBL5529047
实验名称:Antagonist activity at human CB1 receptor expressed in CHO cells assessed as inhibiti...
来源:ChEMBL
靶标:Cannabinoid receptor 1
External Id:CHEMBL5529046
实验名称:Discovery of Small Molecules to Inhibit Human Cytomegalovirus Nuclear Egress
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:HCMV UL50
External Id:HMS1262
实验名称:Antagonist activity at human CB1 receptor expressed in CHO cells assessed as inhibiti...
来源:ChEMBL
靶标:Cannabinoid receptor 1
External Id:CHEMBL5529045
实验名称:A screen for small molecules that modulate mitochondrial supercomplex formation
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:N/A
External Id:HMS1482
实验名称:Cell-based high throughput primary assay to identify activators of GPR151
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL
External Id:GPR151_PHUNTER_AG_LUMI_1536_1X%ACT
实验名称:AlphaScreen-based biochemical high throughput primary assay to identify inhibitors of...
来源:The Scripps Research Institute Molecular Screening Center
External Id:MITF_INH_Alpha_1536_1X%INH PRUN
实验名称:Stabilization of p53 in human papillomavirus-positive cells
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:Cellular tumor antigen p53
External Id:HMS1485
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 英文别名

Cannabidiorcol
Cannabidiorocol
2-[(1R,6R)-6-Isopropenyl-3-methyl-2-cyclohexen-1-yl]-5-methyl-1,3-benzenediol
O 1821
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