ZT-1A
| 中文名称 | ZT-1A |
|---|---|
| 中文同义词 | 化合物ZT-1A;化合物ZT-1A,10 MM DMSO 溶液 |
| 英文名称 | Benzamide, 5-chloro-N-[5-chloro-4-[(4-chlorophenyl)cyanomethyl]-2-methylphenyl]-2-hydroxy- |
| 英文同义词 | Benzamide, 5-chloro-N-[5-chloro-4-[(4-chlorophenyl)cyanomethyl]-2-methylphenyl]-2-hydroxy-;ZT-1a, 10 mM in DMSO;ZT-1a |
| CAS号 | 212135-62-1 |
| 分子式 | C22H15Cl3N2O2 |
| 分子量 | 445.73 |
| EINECS号 | |
| 相关类别 | |
| Mol文件 | 212135-62-1.mol |
| 结构式 | ![]() |
ZT-1A 性质
| 沸点 | 538.7±50.0 °C(Predicted) |
|---|---|
| 密度 | 1.442±0.06 g/cm3(Predicted) |
| 储存条件 | Store at -20°C |
| 溶解度 | 二甲基亚砜:125 mg/mL(280.44 mM) |
| 形态 | 固体 |
| 酸度系数(pKa) | 7+-.0.43(Predicted) |
| 颜色 | 白色至米白色 |
SPAK
ZT-1a inhibits Na-K-2Cl cotransporter (NKCC1) and stimulates K-Cl cotransporters (KCCs) by decreasing their SPS1-related proline/alanine-rich kinase (SPAK)-dependent phosphorylation.
ZT-1a inhibits phosphorylation of NKCC1 p-Thr203/207/212 by 72±5.2% at 1 µM ZT-1a and phosphorylation of KCC sites 1/2 by 65-77% at 3 µM in HEK-293 cells.
SPAK phosphorylation at Ser373 is inhibited by 70±3.8% inhibition at 3-10 µM ZT-1a.
ZT-1a (10 µM) inhibits NKCC1 but stimulates KCC3 activity.
ZT-1a (10-100 mg/kg) inhibits SPAK-dependent cation-Cl− cotransporters (CCC) phosphorylation in vivo.
| Animal Model: | Naive mice |
| Dosage: | 10, 30, 50, and 100 mg/kg |
| Administration: | Intraperitoneal (i.p.) administration |
| Result: | Inhibited SPAK-dependent cation-Cl - cotransporters (CCC) phosphorylation in vivo. |
安全信息
| 更新日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
|---|---|---|---|---|---|
| 2026/06/05 | HY-136532 | ZT-1a | 212135-62-1 | 5mg | 997元 |
| 2026/06/05 | HY-136532 | ZT-1a | 212135-62-1 | 10mM * 1mLin DMSO | 1096元 |
