A-933548结构式
|
常用名 | A-933548 | 英文名 | A-933548 |
|---|---|---|---|---|
| CAS号 | 1037826-43-9 | 分子量 | 439.47 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C25H21N5O3 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
A-933548用途A-933548是一种强效钙蛋白酶抑制剂。A-933548与相关半胱氨酸蛋白酶组织蛋白酶相比具有增强的选择性、良好的微粒体稳定性和在细胞测定中的功效。 |
| 英文名 | A-933548 |
|---|
| 描述 | A-933548是一种强效钙蛋白酶抑制剂。A-933548与相关半胱氨酸蛋白酶组织蛋白酶相比具有增强的选择性、良好的微粒体稳定性和在细胞测定中的功效。 |
|---|---|
| 参考文献 | 1. Kling A, Jantos K, Mack H, Hornberger W, Drescher K, Nimmrich V, Relo A, Wicke K, Hutchins CW, Lao Y, Marsh K, Moeller A. Discovery of Novel and Highly Selective Inhibitors of Calpain for the Treatment of Alzheimer's Disease: 2-(3-Phenyl-1H-pyrazol-1-yl)-nicotinamides. J Med Chem. 2017 Aug 24;60(16):7123-7138. doi: 10.1021/acs.jmedchem.7b00731. Epub 2017 Aug 15. PubMed PMID: 28759231. |
| 分子式 | C25H21N5O3 |
|---|---|
| 分子量 | 439.47 |
| InChIKey | YAJUREDVHDQEOI-UHFFFAOYSA-N |
| SMILES | NC(=O)C(=O)C(Cc1ccccc1)NC(=O)c1cccnc1-n1ccc(-c2ccccc2)n1 |
|
实验名称:Inhibition of human erythrocytes calpain-1 using Suc-Leu-Tyr-AMC as substrate by kine...
来源:ChEMBL
靶标:Calpain-1 catalytic subunit
External Id:CHEMBL4041003
|
|
实验名称:AUC (0 to infinity) in cynomolgus monkey at 1 mg/kg, po administered via gastric intu...
来源:ChEMBL
靶标:Macaca fascicularis
External Id:CHEMBL4255785
|
|
实验名称:Efflux ratio of apparent permeability in human Caco2 cells
来源:ChEMBL
靶标:N/A
External Id:CHEMBL4040998
|
|
实验名称:Thiol reactivity using recombinant human full length 13C-labeled La antigen (100 to 3...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL4041074
|
|
实验名称:Inhibition of calpain-1 in rat hippocampal slices assessed as prevention of NMDA-indu...
来源:ChEMBL
靶标:Calpain-1 catalytic subunit
External Id:CHEMBL4041008
|
|
实验名称:Reversible inhibition of human calpain 1 assessed as dissociation half life using Suc...
来源:ChEMBL
靶标:Calpain-1 catalytic subunit
External Id:CHEMBL4041072
|