pyridine; sulfosulfanylbenzene
Modify Date: 2026-08-16 16:30:40
pyridine; sulfosulfanylbenzene structure
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Common Name | pyridine; sulfosulfanylbenzene | ||
|---|---|---|---|---|
| CAS Number | 14265-87-3 | Molecular Weight | 269.34000 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C11H11NO3S2 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
| Name | pyridine,sulfosulfanylbenzene |
|---|---|
| Synonym | More Synonyms |
| Molecular Formula | C11H11NO3S2 |
|---|---|
| Molecular Weight | 269.34000 |
| Exact Mass | 269.01800 |
| PSA | 100.94000 |
| LogP | 3.74390 |
| InChIKey | IWCDXMBDDTUZMD-UHFFFAOYSA-N |
| SMILES | O=S(=O)(O)Sc1ccccc1.c1ccncc1 |
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~%
pyridine; sulfo... CAS#:14265-87-3 |
| Literature: Baumgarten Patent: DE530733 , 1930 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 18, p. 476 Full Text Show Details Baumgarten Chemische Berichte, 1930 , vol. 63, p. 1330,1332 |
| 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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| Thioschwefelsaeure-S-phenylester,Verbindung mit Pyridin |
| Pyridinium-S-phenylthiosulfat |
| Pyridin,S-Phenyl-thiosulfat |
| Pyridiniumsalz der Phenylthioschwefelsaeure |
| pyridinium phenyl thiosulfate |
| sulfosulfanylbenzene |
| thiosulfuric acid S-phenyl ester,compound with pyridine |