1-(噻吩-2-基磺酰基)哌啶结构式
|
常用名 | 1-(噻吩-2-基磺酰基)哌啶 | 英文名 | 1-thiophen-2-ylsulfonylpiperidine |
|---|---|---|---|---|
| CAS号 | 53442-04-9 | 分子量 | 231.33500 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C9H13NO2S2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 中文名 | 1-(噻吩-2-基磺酰基)哌啶 |
|---|---|
| 英文名 | 1-thiophen-2-ylsulfonylpiperidine |
| 英文别名 | 更多 |
| 分子式 | C9H13NO2S2 |
|---|---|
| 分子量 | 231.33500 |
| 精确质量 | 231.03900 |
| PSA | 74.00000 |
| LogP | 2.94140 |
| InChIKey | FUKURDMUOQFWNI-UHFFFAOYSA-N |
| SMILES | O=S(=O)(c1cccs1)N1CCCCC1 |
|
~83%
1-(噻吩-2-基磺酰基)哌啶 53442-04-9 |
| 文献:Katritzky, Alan R.; Rodriguez-Garcia, Valerie; Nair, Satheesh K. Journal of Organic Chemistry, 2004 , vol. 69, # 6 p. 1849 - 1852 |
|
~%
1-(噻吩-2-基磺酰基)哌啶 53442-04-9 |
| 文献:Lube, Andreas; Neumann, Wilhelm P.; Niestroj, Michael Chemische Berichte, 1995 , vol. 128, # 12 p. 1195 - 1198 |
| 1-(噻吩-2-基磺酰基)哌啶上游产品 3 | |
|---|---|
| 1-(噻吩-2-基磺酰基)哌啶下游产品 0 | |
|
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: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
|
|
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
|
|
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
|
|
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:Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
来源:Broad Institute
靶标:N/A
External Id:7124-01_Inhibitor_SinglePoint_HTS_Activity
|
|
实验名称:qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
来源:NCGC
靶标:apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id:AMA1100
|
|
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:abhydrolase domain-containing protein 4 isoform 1 [Mus musculus]
External Id:ABHD4_INH_FP_1536_1X%INH PRUN
|
| HMS1425N11 |
| 1-(thiophen-2-ylsulfonyl)piperidine |
| 1-(thiophene-2-sulfonyl)-piperidine |
| 1-(2-Thienylsulfonyl)piperidine |