5-hydroxy-3-methyl-5-(1,2,3,4-tetrahydroxybutyl)thiazolidine-2-thione structure
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Common Name | 5-hydroxy-3-methyl-5-(1,2,3,4-tetrahydroxybutyl)thiazolidine-2-thione | ||
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| CAS Number | 10225-81-7 | Molecular Weight | 269.33800 | |
| Density | 1.7g/cm3 | Boiling Point | 574ºC at 760mmHg | |
| Molecular Formula | C8H15NO5S2 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 300.9ºC | |
| Name | 5-hydroxy-3-methyl-5-(1,2,3,4-tetrahydroxybutyl)-1,3-thiazolidine-2-thione |
|---|---|
| Synonym | More Synonyms |
| Density | 1.7g/cm3 |
|---|---|
| Boiling Point | 574ºC at 760mmHg |
| Molecular Formula | C8H15NO5S2 |
| Molecular Weight | 269.33800 |
| Flash Point | 300.9ºC |
| Exact Mass | 269.03900 |
| PSA | 161.78000 |
| Vapour Pressure | 1.45E-15mmHg at 25°C |
| Index of Refraction | 1.737 |
| InChIKey | PJYWOSZGVKJXLI-UHFFFAOYSA-N |
| SMILES | CN1CC(O)(C(O)C(O)C(O)CO)SC1=S |
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5-hydroxy-3-met... CAS#:10225-81-7 |
| Literature: Dalton,L.K. Australian Journal of Chemistry, 1966 , vol. 19, p. 445 - 450 |
| Precursor 2 | |
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| DownStream 0 | |
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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: 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: 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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Name: High Throughput Screen to Identify Inhibitors Targeting HIV-1 Vif-dependent Degradati...
Source: Southern Research Institute
Target: HIV-1 Vif
External Id: HIV1-VIF_MS
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| 2-Thiazolidinethione,5-hydroxy-3-methyl-5-(1,2,3,4-tetrahydroxybutyl) |
| 3-Methyl-5-hydroxy-5-<D-arabino-tetrahydroxy-butyl>-thiazolidin-2-thion |
| 5-hydroxy-3-methyl-5-(1,2,3,4-tetrahydroxybutyl)thiazolidine-2-thione |
| EINECS 233-542-3 |
| methyl-D-fructos-1-yl-dithiocarbamic acid |