| 常用名 | 1-[(5-氯-1H-吲哚-2-基)羰基]-4-甲基哌嗪 | CAS号 | 459168-41-3 |
|---|---|---|---|
| 价格 | ¥需询单/1kg ¥需询单/1g ¥需询单/1mg | 纯度 | 98.0% |
| 备货期 | 需询单 | 库存 | 询单 |
| 产品详情(用途,包装等)
用途: JNJ-7777120 is a selective H4R antagonist with Ki of 4 ±1 nM, exhibits >1000-fold selectivity over the other histamin receptors.IC50 value: 4 ±1 nM (Ki) [1] Target: histamine H4 receptorin vitro: JNJ-7777120 prevents fibronectin-induced lung fibroblast migration, thus suggesting that H4R could represent an attractive target for the development of new drugs for lung fibrosis treatment .[2]in vivo: JNJ 7777120 blocks histamine-induced chemotaxis and calcium influx in mouse bone marrow-derived mast cells. In addition, it can block the histamine-induced migration of tracheal mast cells from the connective tissue toward the epithelium in mice. JNJ 7777120 significantly blocks neutrophil infiltration in a mouse zymosan-induced peritonitis model. [3] 物理化学性质: CAS号:459168-41-3 常用中文名:1-[(5-氯-1H-吲哚-2-基)羰基]-4-甲基哌嗪 常用英文名:JNJ-7777120 分子式:C14H16ClN3O 分子量:277.749 密度:1.3±0.1 g/cm3 沸点:477.0±45.0 °C at 760 mmHg 熔点:N/A 闪点:242.3±28.7 °C 储存条件:Store at +4°C |