6-hydroxy-5-nitroso-naphthalene-2-sulfonic acid结构式
|
常用名 | 6-hydroxy-5-nitroso-naphthalene-2-sulfonic acid | 英文名 | 6-hydroxy-5-nitroso-naphthalene-2-sulfonic acid |
|---|---|---|---|---|
| CAS号 | 6345-59-1 | 分子量 | 253.23100 | |
| 密度 | 1.65g/cm3 | 沸点 | N/A | |
| 分子式 | C10H7NO5S | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 英文名 | 6-hydroxy-5-nitrosonaphthalene-2-sulfonic acid |
|---|---|
| 英文别名 | 更多 |
| 密度 | 1.65g/cm3 |
|---|---|
| 分子式 | C10H7NO5S |
| 分子量 | 253.23100 |
| 精确质量 | 253.00400 |
| PSA | 112.41000 |
| LogP | 1.78830 |
| InChIKey | ZDPZWHLPCUZHPA-UHFFFAOYSA-N |
| SMILES | O=Nc1c(O)ccc2cc(S(=O)(=O)O)ccc12 |
| 折射率 | 1.693 |
|
~%
6-hydroxy-5-nit... 6345-59-1 |
| 文献:Feldmann Giorn.Chim.ind.appl., vol. 7, p. 406 Chem. Zentralbl., 1926 , vol. 97, # I p. 84 |
|
~%
6-hydroxy-5-nit... 6345-59-1 |
| 文献:Meldola Journal of the Chemical Society, 1881 , vol. 39, p. 47 Chemische Berichte, 1881 , vol. 14, p. 532 |
| 上游产品 2 | |
|---|---|
| 下游产品 1 | |
|
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: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:High throughput screen for small molecule inhibitors of a hypoxia-regulated fluoresce...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:N/A
External Id:HMS1149-MLP
|
|
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:High Throughput Screen to Identify Inhibitors Targeting HIV-1 Vif-dependent Degradati...
来源:Southern Research Institute
靶标:HIV-1 Vif
External Id:HIV1-VIF_MS
|
| 5-Hydroxyimino-6-oxo-5,6-dihydro-naphthalin-2-sulfonsaeure |
| 5-hydroxyimino-6-oxo-5,6-dihydro-naphthalene-2-sulfonic acid |
| HMS3091G18 |