Pyridine,4,4'-(1,2,4-thiadiazole-3,5-diyl)bis- (9CI)结构式
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常用名 | Pyridine,4,4'-(1,2,4-thiadiazole-3,5-diyl)bis- (9CI) | 英文名 | Pyridine,4,4'-(1,2,4-thiadiazole-3,5-diyl)bis- (9CI) |
|---|---|---|---|---|
| CAS号 | 16225-38-0 | 分子量 | 240.28400 | |
| 密度 | 1.317g/cm3 | 沸点 | 475.9ºC at 760mmHg | |
| 分子式 | C12H8N4S | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 238.6ºC |
| 英文名 | 3,5-dipyridin-4-yl-1,2,4-thiadiazole |
|---|---|
| 英文别名 | 更多 |
| 密度 | 1.317g/cm3 |
|---|---|
| 沸点 | 475.9ºC at 760mmHg |
| 分子式 | C12H8N4S |
| 分子量 | 240.28400 |
| 闪点 | 238.6ºC |
| 精确质量 | 240.04700 |
| PSA | 79.80000 |
| LogP | 2.66210 |
| InChIKey | RJDDHKWIIGWQNR-UHFFFAOYSA-N |
| SMILES | c1cc(-c2nsc(-c3ccncc3)n2)ccn1 |
| 蒸汽压 | 9.14E-09mmHg at 25°C |
| 折射率 | 1.645 |
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~96%
Pyridine,4,4'-(... 16225-38-0 |
| 文献:Forlani, Luciano; Lugli, Andrea; Boga, Carla; Corradi, Anna Bonamartini; Sgarabotto, Paolo Journal of Heterocyclic Chemistry, 2000 , vol. 37, # 1 p. 63 - 69 |
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~%
Pyridine,4,4'-(... 16225-38-0 |
| 文献:Mayhoub, Abdelrahman S.; Kiselev, Evgeny; Cushman, Mark Tetrahedron Letters, 2011 , vol. 52, # 38 p. 4941 - 4943 |
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~%
Pyridine,4,4'-(... 16225-38-0 |
| 文献:Mayhoub, Abdelrahman S.; Marler, Laura; Kondratyuk, Tamara P.; Park, Eun-Jung; Pezzuto, John M.; Cushman, Mark Bioorganic and Medicinal Chemistry, 2012 , vol. 20, # 1 p. 510 - 520 |
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~%
Pyridine,4,4'-(... 16225-38-0 |
| 文献:Oda, Kazuaki; Machida, Minoru; Kanaoka, Yuichi Heterocycles, 1984 , vol. 21, # 2 p. 622 |
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~%
Pyridine,4,4'-(... 16225-38-0
详细
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| 文献:Oda, Kazuaki; Machida, Minoru; Kanaoka, Yuichi Heterocycles, 1984 , vol. 21, # 2 p. 622 |
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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
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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
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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
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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
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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
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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.
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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
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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
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实验名称:Induction of QR1 activity in mouse Hepa-1c1c7 cells using MTT as substrate by spectro...
来源:ChEMBL
靶标:NAD(P)H dehydrogenase [quinone] 1
External Id:CHEMBL1941483
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实验名称:Induction of QR1 activity in mouse Hepa-1c1c7 cells using MTT as substrate assessed a...
来源:ChEMBL
靶标:NAD(P)H dehydrogenase [quinone] 1
External Id:CHEMBL1941482
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| hms2780n13 |