5-HT7激动剂1结构式
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常用名 | 5-HT7激动剂1 | 英文名 | 5-HT7 agonist 1 |
|---|---|---|---|---|
| CAS号 | 334974-31-1 | 分子量 | 325.83500 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C19H20ClN3 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
5-HT7激动剂1用途5-HT7 agonist 1 是一种选择性的 5-HT7 受体激动剂,IC50 值为 222.93 nM,可用于研究与 5-HT7 受体相关的疾病,例如中枢神经系统疾病。 |
| 中文名 | 5-HT7激动剂1 |
|---|---|
| 英文名 | [33] 4-(4-(2-chlorobenzyl)piperazin-1-yl)-1H-indole |
| 描述 | 5-HT7 agonist 1 是一种选择性的 5-HT7 受体激动剂,IC50 值为 222.93 nM,可用于研究与 5-HT7 受体相关的疾病,例如中枢神经系统疾病。 |
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| 相关类别 | |
| 靶点实验 |
IC50: 222.93 nM (5-HT7 receptor)[1] |
| 体外研究 | 5-HT7激动剂1(化合物33)是一种选择性5-HT7受体激动剂,IC50为222.93 nM,可用于5-HT7受体相关疾病,如CNS疾病[1]。 |
| 参考文献 |
[1]. Pascual-ramon, et al. 5HT7 RECEPTOR LIGANDS AND COMPOSITIONS COMPRISING THE SAME. 20110183991 A1. |
| 分子式 | C19H20ClN3 |
|---|---|
| 分子量 | 325.83500 |
| 精确质量 | 325.13500 |
| PSA | 22.27000 |
| LogP | 4.14640 |
| InChIKey | IKHUKLQDWXAECD-UHFFFAOYSA-N |
| SMILES | Clc1ccccc1CN1CCN(c2cccc3[nH]ccc23)CC1 |
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实验名称:Primary cell-based high-throughput screening assay for identification of compounds th...
来源:Johns Hopkins Ion Channel Center
靶标:regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id:JHICC_RGS_Act_HTS
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实验名称:qHTS Assay for Inhibitors of the Phosphatase Activity of Eya2
来源:NCGC
靶标:eyes absent homolog 2 isoform a [Homo sapiens]
External Id:EYA2477
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实验名称:Luminescence Cell-Free Homogeneous Counter Screen to Identify Inhibitors of ADP-glo R...
来源:Broad Institute
靶标:N/A
External Id:2046-03_INHIBITORS_DOSE-TITRATION_MLPCN-CHERRYPICK
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实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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实验名称:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
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实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1100
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实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1101
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实验名称:Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
来源:Broad Institute
靶标:N/A
External Id:2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
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实验名称:Primary cell-based high-throughput screening for identification of compounds that all...
来源:Johns Hopkins Ion Channel Center
靶标:MAS-related GPR member X1 [Homo sapiens]
External Id:JHICC_MrgX1_AlloAgonist_Primary
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实验名称:Primary cell-based high-throughput screening for identification of compounds that ant...
来源:Johns Hopkins Ion Channel Center
靶标:MAS-related GPR member X1 [Homo sapiens]
External Id:JHICC_MrgX1_Antagonist_Primary
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