6-phenyl-2-sulfanylidene-1,3-diazinan-4-one
Modify Date: 2026-07-14 23:45:57
6-phenyl-2-sulfanylidene-1,3-diazinan-4-one structure
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Common Name | 6-phenyl-2-sulfanylidene-1,3-diazinan-4-one | ||
|---|---|---|---|---|
| CAS Number | 6300-96-5 | Molecular Weight | 206.26400 | |
| Density | 1.32g/cm3 | Boiling Point | N/A | |
| Molecular Formula | C10H10N2OS | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
| Name | 6-phenyl-2-sulfanylidene-1,3-diazinan-4-one |
|---|---|
| Synonym | More Synonyms |
| Density | 1.32g/cm3 |
|---|---|
| Molecular Formula | C10H10N2OS |
| Molecular Weight | 206.26400 |
| Exact Mass | 206.05100 |
| PSA | 73.22000 |
| LogP | 1.77970 |
| Index of Refraction | 1.664 |
| InChIKey | JIBRFUJNQRGYJA-UHFFFAOYSA-N |
| SMILES | O=C1CC(c2ccccc2)NC(=S)N1 |
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~33%
6-phenyl-2-sulf... CAS#:6300-96-5 |
| Literature: Svetlik, Jan; Veizerova, Lucia Helvetica Chimica Acta, 2011 , vol. 94, # 2 p. 199 - 205 |
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~%
6-phenyl-2-sulf... CAS#:6300-96-5 |
| Literature: Erlenmeyer; Heitz Helvetica Chimica Acta, 1942 , vol. 25, p. 832,834 |
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~%
6-phenyl-2-sulf... CAS#:6300-96-5 |
| Literature: Posner Chemische Berichte, 1905 , vol. 38, p. 2324,2719 |
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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: A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id: HMS979
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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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