N-(5-((2-((4-acetamidophenyl)amino)-2-oxoethyl)thio)-1,3,4-thiadiazol-2-yl)-2-fluorobenzamide结构式
|
常用名 | N-(5-((2-((4-acetamidophenyl)amino)-2-oxoethyl)thio)-1,3,4-thiadiazol-2-yl)-2-fluorobenzamide | 英文名 | N-(5-((2-((4-acetamidophenyl)amino)-2-oxoethyl)thio)-1,3,4-thiadiazol-2-yl)-2-fluorobenzamide |
|---|---|---|---|---|
| CAS号 | 893133-85-2 | 分子量 | 445.5 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C19H16FN5O3S2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
本表展示该化学物质的中文名称、英文系统名、各类中文与英文别名信息。
| 英文名 | N-(5-((2-((4-acetamidophenyl)amino)-2-oxoethyl)thio)-1,3,4-thiadiazol-2-yl)-2-fluorobenzamide |
|---|
本表包含该物质理化参数,如熔点、沸点、密度、溶解度、旋光性等理化指标,无数据项标记为N/A。
| 分子式 | C19H16FN5O3S2 |
|---|---|
| 分子量 | 445.5 |
| InChIKey | XOVPOACJCSMJQT-UHFFFAOYSA-N |
| SMILES | CC(=O)Nc1ccc(NC(=O)CSc2nnc(NC(=O)c3ccccc3F)s2)cc1 |
本表记录该化合物靶点、体外体内实验、生物测定实验相关实验数据。
|
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:Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
来源:Broad Institute
靶标:N/A
External Id:7124-01_Inhibitor_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
|
本部分为该化合物相关常见问答,包含基础参数、性状、储存条件等高频咨询问题与对应答案。
| Q: 893133-85-2的英文名称是什么? |
| A: 893133-85-2英文名称为N-(5-((2-((4-acetamidophenyl)amino)-2-oxoethyl)thio)-1,3,4-thiadiazol-2-yl)-2-fluorobenzamide。 |
| Q: 893133-85-2的InChIKey是什么? |
| A: 893133-85-2InChIKey为XOVPOACJCSMJQT-UHFFFAOYSA-N。 |
| Q: 893133-85-2的SMILES表达式是什么? |
| A: 893133-85-2SMILES表达式为CC(=O)Nc1ccc(NC(=O)CSc2nnc(NC(=O)c3ccccc3F)s2)cc1。 |
| Q: 893133-85-2的中文名称是什么? |
| A: 893133-85-2的中文名称为893133-85-2。 |
| Q: 893133-85-2的制备方法是什么? |
| A: 893133-85-2制备方法:CC(=O)Nc1ccc(NC(=O)CSc2nnc(NC(=O)c3ccccc3F)s2)cc1。 |
| Q: 893133-85-2的分子量是多少? |
| A: 893133-85-2分子量为445.5。 |
| Q: 893133-85-2的分子式是什么? |
| A: 893133-85-2分子式为C19H16FN5O3S2。 |
| Q: 893133-85-2的CAS号是多少? |
| A: 893133-85-2CAS号为893133-85-2。 |