5-Thiazolecarboxamide,4-amino-2-(methylthio)-N,N-diphenyl结构式
|
常用名 | 5-Thiazolecarboxamide,4-amino-2-(methylthio)-N,N-diphenyl | 英文名 | 5-Thiazolecarboxamide,4-amino-2-(methylthio)-N,N-diphenyl |
|---|---|---|---|---|
| CAS号 | 63238-15-3 | 分子量 | 341.45100 | |
| 密度 | 1.38g/cm3 | 沸点 | 560.5ºC at 760mmHg | |
| 分子式 | C17H15N3OS2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 292.8ºC |
| 英文名 | 4-amino-2-methylsulfanyl-N,N-diphenyl-1,3-thiazole-5-carboxamide |
|---|---|
| 英文别名 | 更多 |
| 密度 | 1.38g/cm3 |
|---|---|
| 沸点 | 560.5ºC at 760mmHg |
| 分子式 | C17H15N3OS2 |
| 分子量 | 341.45100 |
| 闪点 | 292.8ºC |
| 精确质量 | 341.06600 |
| PSA | 112.76000 |
| LogP | 5.00690 |
| InChIKey | ZHZGJKSCJQMOGC-UHFFFAOYSA-N |
| SMILES | CSc1nc(N)c(C(=O)N(c2ccccc2)c2ccccc2)s1 |
| 折射率 | 1.718 |
|
~%
5-Thiazolecarbo... 63238-15-3 |
| 文献:Wobig,D. Justus Liebigs Annalen der Chemie, 1977 , p. 400 - 406 |
|
~%
5-Thiazolecarbo... 63238-15-3 |
| 文献:Wobig,D. Justus Liebigs Annalen der Chemie, 1977 , p. 400 - 406 |
|
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:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1100
|
|
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1101
|
|
实验名称:Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
来源:Broad Institute
靶标:N/A
External Id:2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
|
|
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:qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
来源:NCGC
靶标:apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id:AMA1100
|
|
实验名称:Fluorescence polarization-based biochemical high throughput primary assay to identify...
来源:The Scripps Research Institute Molecular Screening Center
靶标:abhydrolase domain-containing protein 4 isoform 1 [Mus musculus]
External Id:ABHD4_INH_FP_1536_1X%INH PRUN
|
|
实验名称:High Throughput Screen to Identify Inhibitors Targeting HIV-1 Vif-dependent Degradati...
来源:Southern Research Institute
靶标:HIV-1 Vif
External Id:HIV1-VIF_MS
|
| 4-Amino-N-phenyl-2-methylthio-5-thiazolcarboxanilid |
| 4-amino-2-methylsulfanyl-thiazole-5-carboxylic acid diphenylamide |