IGS-1.76结构式
|
常用名 | IGS-1.76 | 英文名 | IGS-1.76 |
|---|---|---|---|---|
| CAS号 | 313480-47-6 | 分子量 | 358.456 | |
| 密度 | 1.3±0.1 g/cm3 | 沸点 | N/A | |
| 分子式 | C22H18N2OS | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
IGS-1.76用途IGS-1.76是人NCS-1/Ric8a相互作用的小分子抑制剂,亲和力为1.25 uM(hNCS-1);表现出比吩噻嗪FD44更高的结合效力,降低异常高的突触数并增强FXS中的联想学习。动物模型。 |
| 英文名 | N-(1,3-Benzothiazol-2-yl)-3,3-diphenylpropanamide |
|---|---|
| 英文别名 | 更多 |
| 描述 | IGS-1.76是人NCS-1/Ric8a相互作用的小分子抑制剂,亲和力为1.25 uM(hNCS-1);表现出比吩噻嗪FD44更高的结合效力,降低异常高的突触数并增强FXS中的联想学习。动物模型。 |
|---|---|
| 参考文献 | References 1. Roca C, et al. J Med Chem. 2018 Jul 17. doi: 10.1021/acs.jmedchem.8b00088. View Related Products by Target Other Targets |
| 密度 | 1.3±0.1 g/cm3 |
|---|---|
| 分子式 | C22H18N2OS |
| 分子量 | 358.456 |
| 精确质量 | 358.113983 |
| LogP | 5.65 |
| InChIKey | GYQWKTIZRYVFEM-UHFFFAOYSA-N |
| SMILES | O=C(CC(c1ccccc1)c1ccccc1)Nc1nc2ccccc2s1 |
| 折射率 | 1.700 |
| 储存条件 | -20°C |
|
实验名称:Inhibition of human recombinant CK-1delta using casein as substrate at 10 uM after 60...
来源:ChEMBL
靶标:Casein kinase I isoform delta
External Id:CHEMBL3239315
|
|
实验名称:Inhibition of human recombinant CK-1delta using casein as substrate after 60 mins by ...
来源:ChEMBL
靶标:Casein kinase I isoform delta
External Id:CHEMBL3239314
|
|
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:AlphaScreen-based biochemical high throughput primary assay to identify activators of...
来源:The Scripps Research Institute Molecular Screening Center
靶标:N/A
External Id:FBW7_ACT_ALPHA_1536_1X%ACT PRUN
|
|
实验名称:AlphaScreen-based biochemical high throughput primary assay to identify inhibitors of...
来源:The Scripps Research Institute Molecular Screening Center
External Id:MITF_INH_Alpha_1536_1X%INH PRUN
|
|
实验名称:Inhibition of human NCS1 and V5-tagged Ric8a interaction expressed in HEK293 cells at...
来源:ChEMBL
靶标:Synembryn-A
External Id:CHEMBL4145364
|
| N-(1,3-Benzothiazol-2-yl)-3,3-diphenylpropanamide |