7,14-Diazadispiro[5.1.5.2]pentadecane-15-thione结构式
|
常用名 | 7,14-Diazadispiro[5.1.5.2]pentadecane-15-thione | 英文名 | 7,14-Diazadispiro[5.1.5.2]pentadecane-15-thione |
|---|---|---|---|---|
| CAS号 | 4833-50-5 | 分子量 | 238.39200 | |
| 密度 | 1.14g/cm3 | 沸点 | 374.8ºC at 760 mmHg | |
| 分子式 | C13H22N2S | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 180.5ºC |
| 英文名 | 7,14-diazadispiro[5.1.58.26]pentadecane-15-thione |
|---|---|
| 英文别名 | 更多 |
| 密度 | 1.14g/cm3 |
|---|---|
| 沸点 | 374.8ºC at 760 mmHg |
| 分子式 | C13H22N2S |
| 分子量 | 238.39200 |
| 闪点 | 180.5ºC |
| 精确质量 | 238.15000 |
| PSA | 56.15000 |
| LogP | 3.52750 |
| InChIKey | URGJOYDECMYFMJ-UHFFFAOYSA-N |
| SMILES | S=C1NC2(CCCCC2)NC12CCCCC2 |
| 折射率 | 1.592 |
|
~91%
7,14-Diazadispi... 4833-50-5 |
| 文献:Paventi, Martino; Edward, John T. Canadian Journal of Chemistry, 1987 , vol. 65, p. 282 - 289 |
|
~98%
7,14-Diazadispi... 4833-50-5 |
| 文献:ROHM AND HAAS COMPANY Patent: EP1229023 A1, 2002 ; Location in patent: Example DDPT ; |
|
~%
7,14-Diazadispi... 4833-50-5 |
| 文献:Paventi, Martino; Edward, John T. Canadian Journal of Chemistry, 1987 , vol. 65, p. 282 - 289 |
|
~%
7,14-Diazadispi... 4833-50-5 |
| 文献:Christian Journal of Organic Chemistry, 1957 , vol. 22, p. 396 |
|
~%
7,14-Diazadispi... 4833-50-5 |
| 文献:Paventi, Martino; Chubb, Francis L.; Edward, John T. Canadian Journal of Chemistry, 1987 , vol. 65, p. 2114 - 2117 |
|
~%
7,14-Diazadispi... 4833-50-5
详细
|
| 文献:Paventi, Martino; Chubb, Francis L.; Edward, John T. Canadian Journal of Chemistry, 1987 , vol. 65, p. 2114 - 2117 |
|
~%
7,14-Diazadispi... 4833-50-5 |
| 文献:Christian Journal of Organic Chemistry, 1957 , vol. 22, p. 396 Full Text View citing articles Show Details Bucherer; Brandt Journal fuer Praktische Chemie (Leipzig), 1934 , vol. <2> 140, p. 129,135, 150 |
|
~5%
详细
|
| 文献:Paventi, Martino; Edward, John T. Canadian Journal of Chemistry, 1987 , vol. 65, p. 282 - 289 |
|
实验名称:Primary cell-based high-throughput screening assay for identification of compounds th...
来源:Johns Hopkins Ion Channel Center
靶标:regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id:JHICC_RGS_Act_HTS
|
|
实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
|
|
实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
|
|
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
|
|
实验名称:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
|
|
实验名称:Antibacterial activity against Klebsiella pneumoniae MDR ATCC 70063 (CO-ADD:GN_003); ...
来源:ChEMBL
靶标:Klebsiella pneumoniae
External Id:CHEMBL4296186
|
|
实验名称:High throughput fluorescence intensity-based biochemical assay to screen for small mo...
来源:University of Pittsburgh Molecular Library Screening Center
靶标:furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id:MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
|
|
实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
|
|
实验名称:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
来源:Broad Institute
靶标: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
|
|
实验名称:Identifying Sarm1 TIR NADase inhibitors through high throughput HPLC assay
来源:24386
靶标:N/A
External Id:Sarm1 TIR NADase inhibitors
|
| 15-Thioxo-7,14-diaza-dispiro<5.1.5.2>pentadecan |
| HMS2886A11 |