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332108-65-3

中文名称 N-(5-bromo-2-methoxybenzyl)tricyclo[3.3.1.1~3,7~]decan-1-amine
英文名称 N-(5-bromo-2-methoxybenzyl)tricyclo[3.3.1.1~3,7~]decan-1-amine
CAS 332108-65-3
分子式 C18H24BrNO
分子量 350.29
MOL 文件 332108-65-3.mol
更新日期 2025/06/25 16:26:32
332108-65-3 结构式 332108-65-3 结构式

基本信息

中文别名
化合物ABMA
化合物 T10222
英文别名
ABMA
N-(5-bromo-2-methoxybenzyl)tricyclo[3.3.1.1~3,7~]decan-1-amine

物理化学性质

沸点428.2±30.0 °C(Predicted)
密度1.35±0.1 g/cm3(Predicted)
储存条件-20°C储存
溶解度DMSO: 125 mg/mL (356.85 mM)
酸度系数(pKa)9.86±0.20(Predicted)
形态Solid
颜色White to off-white
N-(5-bromo-2-methoxybenzyl)tricyclo[3.3.1.1~3,7~]decan-1-amine价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2025/05/22HY-124801ABMA332108-65-35 mg937元
2025/05/22HY-124801N-(5-bromo-2-methoxybenzyl)tricyclo[3.3.1.1~3,7~]decan-1-amine
ABMA
332108-65-310mg1500元
2025/05/22HY-124801N-(5-bromo-2-methoxybenzyl)tricyclo[3.3.1.1~3,7~]decan-1-amine
ABMA
332108-65-310mM * 1mLin DMSO1650元

常见问题列表

生物活性
ABMA 是一种细胞内毒素和病原体的广谱抑制剂。ABMA 有效地保护细胞免受各种毒素和病原体的侵害,包括病毒,细胞内细菌和寄生虫。ABMA 选择性作用于宿主细胞晚期内体,而不是针对毒素或病原体本身,具有广谱抗感染活性。
靶点

Intracellular bacteria
Viruses
Parasite

体外研究

ABMA protects cells against four bacterial toxins ( Corynebacterium diphtheriae (DT; EC 50 of 62.9 μM), Bacillus anthracis (LT), Clostridium difficile toxin B (TcdB; EC 50 of 73.3 µM), Clostridium sordellii lethal toxin (TcsL; EC 50 of 86.7 μM)), three viruses (Ebola (EC 50 of 3.3 µM), rabies (EC 50 of 19.4 µM), dengue-4 virus ( EC 50 of 8.2 µM)), two species of Chlamydiales intracellular bacteria ( Simkania negevensis and Chlamydia trachomatis ), and the parasite Leishmania infantum (EC 50 of 7.1 µM) at micromolar level.
In A549 cells, ABMA treatment induces a decrease in ricin cytotoxicity with an EC 50 of 3.8 µM, and a protection factor (R) at 30 µM ranging from 5 to 10. ABMA retained almost 100% of its biological activity against ricin-induced cytotoxicity up to six days.

体内研究

ABMA (2-200 mg/kg; intraperitoneal injection; female BALB/c mice) treatment protects mice from nasal instillation of an LD 90 of ricin.

Animal Model: Pathogen-free female BALB/c mice (6 week-old) with ricin
Dosage: 2 mg/kg, 20 mg/kg, 200 mg/kg
Administration: Intraperitoneal injection
Result: A statistically significant protection according to survival curves was observed with a single ip dose of 2 mg/kg. The 20 mg/kg dose fully protected animals through to day 21. The 200 mg/kg dose resulted in 80% of protection of mice against ricin challenge with a single animal succumbing on day 15.
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