Benzenesulfonic acid,3,4-dimethoxy-, 2-[(1-oxido-2-pyridinyl)methylene]hydrazide结构式
|
常用名 | Benzenesulfonic acid,3,4-dimethoxy-, 2-[(1-oxido-2-pyridinyl)methylene]hydrazide | 英文名 | Benzenesulfonic acid,3,4-dimethoxy-, 2-[(1-oxido-2-pyridinyl)methylene]hydrazide |
|---|---|---|---|---|
| CAS号 | 73736-93-3 | 分子量 | 337.35100 | |
| 密度 | 1.34g/cm3 | 沸点 | 497.1ºC at 760 mmHg | |
| 分子式 | C14H15N3O5S | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 英文名 | Benzenesulfonic acid, 3,4-dimethoxy-, (2-pyridinylmethylene)hydrazide, N-oxide |
|---|---|
| 英文别名 | 更多 |
| 密度 | 1.34g/cm3 |
|---|---|
| 沸点 | 497.1ºC at 760 mmHg |
| 分子式 | C14H15N3O5S |
| 分子量 | 337.35100 |
| 精确质量 | 337.07300 |
| PSA | 110.83000 |
| LogP | 2.91640 |
| InChIKey | KSEMBTCMTKECGJ-MJOFCVHYSA-N |
| SMILES | COc1ccc(S(=O)(=O)N=NC=C2C=CC=CN2O)cc1OC |
| 折射率 | 1.595 |
|
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:Inhibition of ribonuclease H activity of HIV1 reverse transcriptase using as poly(dC)...
来源:ChEMBL
靶标:Reverse transcriptase/RNaseH
External Id:CHEMBL1959154
|
|
实验名称:Inhibition of RNA-dependent DNA polymerase activity of Human immunodeficiency virus 1...
来源:ChEMBL
靶标:Reverse transcriptase/RNaseH
External Id:CHEMBL1959233
|
|
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: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
|
| 2-pyridinecarboxaldehyde-1-oxide-3,4-dimethoxybenzene sulfonylhydrazone |