3-(2-苯并噻唑基)-7-羟基香豆素结构式
|
常用名 | 3-(2-苯并噻唑基)-7-羟基香豆素 | 英文名 | 3-(2-BENZOTHIAZOLYL)UMBELLIFERONE FOR |
|---|---|---|---|---|
| CAS号 | 58851-99-3 | 分子量 | 295.31300 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C16H9NO3S | 熔点 | 290-292ºC(lit.) | |
| MSDS | N/A | 闪点 | N/A |
| 中文名 | 3-(2-苯并噻唑基)-7-羟基香豆素 |
|---|---|
| 英文名 | (3E)-3-(3H-1,3-benzothiazol-2-ylidene)chromene-2,7-dione |
| 英文别名 | 更多 |
| 熔点 | 290-292ºC(lit.) |
|---|---|
| 分子式 | C16H9NO3S |
| 分子量 | 295.31300 |
| 精确质量 | 295.03000 |
| PSA | 91.57000 |
| LogP | 3.77530 |
| InChIKey | CYONGLVNBSZCQH-UHFFFAOYSA-N |
| SMILES | O=c1oc2cc(O)ccc2cc1-c1nc2ccccc2s1 |
| 安全声明 (欧洲) | 22-24/25 |
|---|---|
| WGK德国 | 3 |
| 3-(2-苯并噻唑基)-7-羟基香豆素上游产品 5 | |
|---|---|
| 3-(2-苯并噻唑基)-7-羟基香豆素下游产品 1 | |
|
实验名称:Discovery of Small Molecules to Inhibit Human Cytomegalovirus Nuclear Egress
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:HCMV UL50
External Id:HMS1262
|
|
实验名称:Small-molecule inhibitors of ST2 (IL1RL1)
来源:20881
靶标:interleukin-1 receptor-like 1 isoform [homo sapiens]
External Id:ST2_IL33_Inhibitors_Primary_Screening_77700
|
|
实验名称:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
|
|
实验名称:Cell-based high throughput primary assay to identify activators of GPR151
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL
External Id:GPR151_PHUNTER_AG_LUMI_1536_1X%ACT
|
|
实验名称:A screen for compounds that inhibit viral RNA polymerase binding and polymerization a...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:Chain A, Poliovirus Polymerase With Gtp
External Id:HMS750
|
|
实验名称:Inhibition of mouse recombinant PI3Kalpha expressed in baculovirus-infected Sf21 cell...
来源:ChEMBL
靶标:Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
External Id:CHEMBL1039894
|
|
实验名称:Inhibition of human recombinant PI3Kbeta expressed in baculovirus-infected Sf21 cells...
来源:ChEMBL
靶标:Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
External Id:CHEMBL1039895
|
|
实验名称:Inhibition of bovine recombinant PI3Kgamma expressed in baculovirus-infected Sf21 cel...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL1039892
|
|
实验名称:Inhibition of recombinant PI3Kdelta expressed in baculovirus-infected Sf21 cells at 1...
来源:ChEMBL
靶标:Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform
External Id:CHEMBL1039893
|
| 3-(benzothiazol-2yl)-7-hydroxycoumarin |
| 3-(2-benzothioazolyl)-7-hydroxycoumarin |
| 3-(benzo[d]thiazol-2-yl)-7-hydroxy-2H-chromen-2-one |
| 3-benzothiazol-2-yl-7-hydroxy-chromen-2-one |
| 3-(2-benzothiazolyl)-7-hydroxycoumarin |
| Coumarin 16 |
| 3-(1,3-benzothiazol-2-yl)-7-hydroxy-2H-chromen-2-one |