1H-Imidazole-5-sulfonamide,4-nitro
Modify Date: 2025-08-25 18:49:48
1H-Imidazole-5-sulfonamide,4-nitro structure
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Common Name | 1H-Imidazole-5-sulfonamide,4-nitro | ||
|---|---|---|---|---|
| CAS Number | 6963-63-9 | Molecular Weight | 192.15300 | |
| Density | 1.888g/cm3 | Boiling Point | 652.4ºC at 760mmHg | |
| Molecular Formula | C3H4N4O4S | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 348.3ºC | |
| Name | 4-nitro-1H-imidazole-5-sulfonamide |
|---|---|
| Synonym | More Synonyms |
| Density | 1.888g/cm3 |
|---|---|
| Boiling Point | 652.4ºC at 760mmHg |
| Molecular Formula | C3H4N4O4S |
| Molecular Weight | 192.15300 |
| Flash Point | 348.3ºC |
| Exact Mass | 191.99500 |
| PSA | 143.04000 |
| LogP | 1.26960 |
| Index of Refraction | 1.646 |
| InChIKey | XARPOFSVXQKPFU-UHFFFAOYSA-N |
| SMILES | NS(=O)(=O)c1nc[nH]c1[N+](=O)[O-] |
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Name: Luminescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id: OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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Name: QFRET-based biochemical primary high throughput screening assay to identify exosite i...
Source: The Scripps Research Institute Molecular Screening Center
Target: disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id: ADAM17_INH_QFRET_1536_1X%INH PRUN
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Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1100
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Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1101
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Name: Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
Source: Broad Institute
Target: N/A
External Id: 2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
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Name: Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
Source: Broad Institute
Target: FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id: 2147-01_Inhibitor_SinglePoint_HTS_Activity
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Name: High throughput screen for small molecule inhibitors of a hypoxia-regulated fluoresce...
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
Target: N/A
External Id: HMS1149-MLP
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Name: qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
Source: NCGC
Target: apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id: AMA1100
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Name: Fluorescence polarization-based biochemical high throughput primary assay to identify...
Source: The Scripps Research Institute Molecular Screening Center
Target: abhydrolase domain-containing protein 4 isoform 1 [Mus musculus]
External Id: ABHD4_INH_FP_1536_1X%INH PRUN
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| 4-Nitro-5-sulfamoyl-imidazol |
| HMS3088C13 |
| 5-nitro-1(3)H-imidazole-4-sulfonic acid amide |
| 4(5)-Nitroimidazol-5(4)-sulfonamid |
| 4(5)-nitro-5(4)-sulphonamidoimidazole |