4-Thiazolidinone,5-[(2-bromophenyl)methylene]-2-thioxo
Modify Date: 2025-09-18 20:12:29
![4-Thiazolidinone,5-[(2-bromophenyl)methylene]-2-thioxo Structure](https://image.chemsrc.com/caspic/270/5503-75-3.png)
4-Thiazolidinone,5-[(2-bromophenyl)methylene]-2-thioxo structure
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Common Name | 4-Thiazolidinone,5-[(2-bromophenyl)methylene]-2-thioxo | ||
|---|---|---|---|---|
| CAS Number | 5503-75-3 | Molecular Weight | 300.19500 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C10H6BrNOS2 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
| Name | 5-[(2-bromophenyl)methylidene]-2-sulfanylidene-1,3-thiazolidin-4-one |
|---|---|
| Synonym | More Synonyms |
| Molecular Formula | C10H6BrNOS2 |
|---|---|
| Molecular Weight | 300.19500 |
| Exact Mass | 298.90700 |
| PSA | 86.49000 |
| LogP | 3.26670 |
| InChIKey | HCQIPSCNDYWABJ-UHFFFAOYSA-N |
| SMILES | O=C1NC(=S)SC1=Cc1ccccc1Br |
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~60%
4-Thiazolidinon... CAS#:5503-75-3 |
| Literature: Opletalova, Veronika; Dolezel, Jan; Kralova, Katarina; Pesko, Matus; Kunes, Jiri; Jampilek, Josef Molecules, 2011 , vol. 16, # 6 p. 5207 - 5227 |
| Precursor 2 | |
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| DownStream 0 | |
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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
|
|
Name: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
Source: Broad Institute
Target: 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
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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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