PDM 2结构式
|
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。 |
| 中文名 | PDM 2 |
|---|---|
| 英文名 | 1,3-dichloro-5-[2-(4-chlorophenyl)ethenyl]benzene |
| 英文别名 | 更多 |
| 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 |
| 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℃ |
|
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
|
| 1,3-Dichloro-5-[(E)-2-(4-chlorophenyl)vinyl]benzene |
| 1,3-dichloro-5-[(E)-2-(4-chlorophenyl)ethenyl]benzene |
| PDM 2 |