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PDM 2

更新时间:2025-08-25 10:27:53

PDM 2结构式
PDM 2结构式
品牌特惠专场
常用名 PDM 2 英文名 PDM 2
CAS号 688348-25-6 分子量 283.580
密度 1.4±0.1 g/cm3 沸点 394.2±42.0 °C at 760 mmHg
分子式 C14H9Cl3 熔点 N/A
MSDS N/A 闪点 276.5±23.5 °C

 PDM 2用途


PDM2 是一种选择性的高亲和力芳烃受体 (AhR) 拮抗剂,Ki 为 1.2±0.4 nM。

 PDM 2名称

中文名 PDM 2
英文名 1,3-dichloro-5-[2-(4-chlorophenyl)ethenyl]benzene
英文别名 更多

 PDM 2生物活性

描述 PDM2 是一种选择性的高亲和力芳烃受体 (AhR) 拮抗剂,Ki 为 1.2±0.4 nM。
相关类别
靶点实验

Ki: 1.2±0.4 nM(AhR)[1]

体外研究 PDM2(化合物4b)对于AhR表现出1.2±0.4nM的Ki并且对雌激素受体(ER)没有亲和力,证实用氯取代羟基消除了对ER的结合并且显着增加了对AhR的亲和力[1]。
参考文献

[1]. de Medina P, et al. Synthesis and biological properties of new stilbene derivatives of resveratrol as new selective aryl hydrocarbon modulators. J Med Chem. 2005 Jan 13;48(1):287-91.

 PDM 2物理化学性质

密度 1.4±0.1 g/cm3
沸点 394.2±42.0 °C at 760 mmHg
分子式 C14H9Cl3
分子量 283.580
闪点 276.5±23.5 °C
精确质量 281.976990
LogP 6.58
InChIKey JMYNPQVCVQVODQ-OWOJBTEDSA-N
SMILES Clc1ccc(C=Cc2cc(Cl)cc(Cl)c2)cc1
蒸汽压 0.0±0.9 mmHg at 25°C
折射率 1.675
储存条件 2-8℃

 PDM 2靶点实验

查看更多实验

实验名称:Tested for cytotoxicity towards A549 cell line (human lung carcinoma); Not active
来源:ChEMBL
靶标:A549
External Id:CHEMBL825830
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:Tested for cytotoxicity towards T47D cell line (human breast cancer); Not active
来源:ChEMBL
靶标:T47D
External Id:CHEMBL826646
实验名称:Binding affinity to aryl hydrocarbon receptor (unknown origin)
来源:ChEMBL
靶标:Aryl hydrocarbon receptor
External Id:CHEMBL3055293
实验名称:Tested for cytotoxicity towards MCF-7 cell line (human breast cancer); Not active
来源:ChEMBL
靶标:MCF7
External Id:CHEMBL825831
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: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
实验名称:Discovering small molecule activators of G protein-gated inwardly-rectifying potassiu...
来源:15621
靶标:G protein-activated inward rectifier potassium channel 2
External Id:VANDERBILT_HTS_GIRK2_MPD
实验名称:Inhibition of human TRPA1 expressed in HEK293 cells assessed as decrease in AITC-indu...
来源:ChEMBL
靶标:Transient receptor potential cation channel subfamily A member 1
External Id:CHEMBL4022612
实验名称:In Vitro Binding Assay from Article 10.1021/jm0498194: "Synthesis and biological prop...
来源:BindingDB
靶标:N/A
External Id:BindingDB_2736_1
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 PDM 2英文别名

1,3-Dichloro-5-[(E)-2-(4-chlorophenyl)vinyl]benzene
1,3-dichloro-5-[(E)-2-(4-chlorophenyl)ethenyl]benzene
PDM 2
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