返回ChemicalBook首页>CAS数据库列表>712313-35-4

712313-35-4

中文名称 HAMI3379
英文名称 HAMI3379
CAS 712313-35-4
分子式 C34H45NO8
分子量 595.72
MOL 文件 712313-35-4.mol
712313-35-4 结构式 712313-35-4 结构式

基本信息

中文别名
哈密3379
化合物 T15463
英文别名
HAMI3379
(Rac)-HAMI 3379
HRJWSEPIRZRGCL-UHFFFAOYSA-N

物理化学性质

储存条件-20°C储存
溶解度≤5mg/ml in ethanol;20mg/ml in DMSO;20mg/ml in dimethyl formamide
形态结晶固体

常见问题列表

生物活性
HAMI 3379 是一种有效的,选择性的半胱氨酸白三烯 (CysLT2) 受体拮抗剂。HAMI 3379 对急性和亚急性缺血性脑损伤具有保护作用,并减轻小胶质细胞相关的炎症。
靶点

CysLT 2

体外研究

In a CysLT 2 receptor reporter cell line, HAMI 3379 antagonizes leukotriene D 4 - (LTD 4 -) and leukotriene C 4 - (LTC 4 -) induced intracellular calcium mobilization with IC 50 values of 3.8 nM and 4.4 nM, respectively. In contrast, HAMI 3379 exhibits very low potency on a recombinant CysLT 1 receptor cell line (IC 50 >10000 nM).

体内研究

HAMI 3379 (ip; 0.025-0.4 mg/kg; 24 hours) attenuates the acute brain injury 24 hours after middle cerebral artery occlusion (MCAO) with effective doses of 0.1-0.4 mg/kg and a therapeutic window of ∼1 hour. It attenuates the neurological deficits, and reduces infarct volume, brain edema, and neuronal loss and degeneration 24 and 72 hours after MCAO.
HAMI 3379 (infused into the aortic cannula at a rate of 1% of the total flow rate; 0.01, 0.1, 1 μM; 20 min) concentration-dependently inhibits and reverses the LTC 4 -induced perfusion pressure increase and contractility decrease.

Animal Model: Male Sprague-Dawley rats (250-300 g) after MCAO
Dosage: 0.025, 0.05, 0.1, 0.2, 0.4 mg/kg
Administration: IP; 24 hours
Result: Attenuated the acute brain injury 24 hours after MCAO with effective doses of 0.1-0.4 mg/kg and a therapeutic window of ∼1 hour.
"712313-35-4" 相关产品信息