9-butyl-1,3-dimethyl-8-sulfanylidene-7H-purine-2,6-dione
Modify Date: 2026-07-05 04:05:36
9-butyl-1,3-dimethyl-8-sulfanylidene-7H-purine-2,6-dione structure
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Common Name | 9-butyl-1,3-dimethyl-8-sulfanylidene-7H-purine-2,6-dione | ||
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| CAS Number | 7501-78-2 | Molecular Weight | 268.33500 | |
| Density | 1.39g/cm3 | Boiling Point | 346.3ºC at 760 mmHg | |
| Molecular Formula | C11H16N4O2S | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 163.2ºC | |
| Name | 9-butyl-1,3-dimethyl-8-sulfanylidene-7H-purine-2,6-dione |
|---|---|
| Synonym | More Synonyms |
| Density | 1.39g/cm3 |
|---|---|
| Boiling Point | 346.3ºC at 760 mmHg |
| Molecular Formula | C11H16N4O2S |
| Molecular Weight | 268.33500 |
| Flash Point | 163.2ºC |
| Exact Mass | 268.09900 |
| PSA | 96.81000 |
| LogP | 0.89640 |
| Index of Refraction | 1.658 |
| InChIKey | URMPBQMVAJIEQW-UHFFFAOYSA-N |
| SMILES | CCCCn1c(=S)[nH]c2c(=O)n(C)c(=O)n(C)c21 |
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~%
9-butyl-1,3-dim... CAS#:7501-78-2 |
| Literature: Blicke; Schaaf Journal of the American Chemical Society, 1956 , vol. 78, p. 5857,5860 |
| Precursor 2 | |
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| DownStream 0 | |
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Name: C. difficile toxins: Counterscreen in absence of substrate UDPG Measured in Biochemic...
Source: Broad Institute
Target: N/A
External Id: 7074-02_Inhibitor_Dose_CherryPick_Activity
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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
|
|
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
|
|
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
|
|
Name: C. difficile toxins: HTS for inhibitors of TcdB glycohydrolase activity Measured in B...
Source: Broad Institute
Target: Toxin B [Clostridium difficile 630]
External Id: 7074-01_Inhibitor_Dose_CherryPick_Activity
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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: 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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