VU0134992结构式
|
常用名 | VU0134992 | 英文名 | VU 0134992 |
|---|---|---|---|---|
| CAS号 | 755002-90-5 | 分子量 | 411.38 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C20H31BrN2O2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
VU0134992用途VU0134992 是一种选择性的内向整流钾通道 Kir4.1 阻滞剂,IC50 值为 0.97 μM。 |
| 中文名 | VU0134992 |
|---|---|
| 英文名 | VU0134992 |
| 描述 | VU0134992 是一种选择性的内向整流钾通道 Kir4.1 阻滞剂,IC50 值为 0.97 μM。 |
|---|---|
| 相关类别 | |
| 靶点实验 |
IC50: 0.97 µM (Kir4.1)[1] |
| 体外研究 | 对Kir4.1而言,VU0134992对Kir4.1的选择性大于30倍,Kir2.1和Kir2.2对Kir2.3,Kir6.2/SUR1和Kir7.1具有弱活性,并且同样对Kir3.1/3.2,Kir3.1/3.4和Kir4.2 [1]。 |
| 参考文献 |
| 分子式 | C20H31BrN2O2 |
|---|---|
| 分子量 | 411.38 |
| InChIKey | OTTDLWFVHQYRDA-UHFFFAOYSA-N |
| SMILES | CC(C)c1ccc(OCC(=O)NC2CC(C)(C)NC(C)(C)C2)c(Br)c1 |
| 储存条件 | -20°C,密封,干燥 |
|
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
|
|
实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
|
|
实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
|
|
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
|
|
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
|
|
实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
|
|
实验名称:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
来源:Broad Institute
靶标:N/A
External Id:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
|
|
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
|
|
实验名称:Fluorescence polarization-based biochemical high throughput primary assay to identify...
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=Sialate O-acetylesterase; AltName: Full=H-Lse; AltName: Full=Sialic acid-specific 9-O-acetylesterase; Flags: Precursor [Homo sapiens]
External Id:SIAE_INH_FP_1536_1X%INH PRUN
|
|
实验名称:Absorbance-based primary biochemical high throughput screening assay to identify acti...
来源:The Scripps Research Institute Molecular Screening Center
靶标:caspase-3 preproprotein [Homo sapiens]
External Id:PROCASPASE3_ACT_EPIABS_1536_1X%ACT PRUN
|