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34391-04-3

中文名称 左旋沙丁胺醇
英文名称 Salbutamol
CAS 34391-04-3
分子式 C13H21NO3
MDL 编号 MFCD00869868
分子量 239.31
MOL 文件 34391-04-3.mol
更新日期 2023/02/10 16:49:10
34391-04-3 结构式 34391-04-3 结构式

基本信息

中文别名
左旋沙丁胺醇
左旋沙丁胺醇盐酸盐
4-[2-(叔丁氨基)-1-羟乙基]-2-(羟甲基)苯酚
英文别名
(L)-ALBUTEROL
LEVALBUTEROL
LEVALBUTEROL HCL
R-SALBUTAMOL HCL
(-)-alpha(sup1)-(((1,1-dimethylethyl)amino)methyl)-4-hydroxy-1,3-benzenedime
1,3-benzenedimethanol,alpha(sup1)-(((1,1-dimethylethyl)amino)methyl)-4-hydrox
alpha’-diol,alpha(sup1)-((tert-butylamino)methyl)-4-hydroxy-m-xylene-alph
r-albuterol
Levalbutreol
2-(hydroxymethyl)-4-[1-hydroxy-2-(tert-butylamino)ethyl]phenol
LEVOSALBUTEROLHCL
1,3-Benzenedimethanol, a1-[[(1,1-dimethylethyl)amino]methyl]-4-hydroxy-, (a1R)- (9CI)
1,3-Benzenedimethanol, a1-[[(1,1-dimethylethyl)amino]methyl]-4-hydroxy-, (R)-
Levosalbutamol
m-Xylene-a,a'-diol, a1-[(tert-butylamino)methyl]-4-hydroxy-, (R)-(-)- (8CI)
2-(hydroxymethyl)-4-[(1R)-1-hydroxy-2-(tert-butylamino)ethyl]phenol
4-[2-(tert-Butylamino)-1-hydroxyethyl]-2-(hydroxymethyl)phenol
Salbutamol
(R)-1-(4-Hydroxy-3-hydroxymethylphenyl)-2-(1,1-dimethylethylamino)ethanol
(R)-1-(4-Hydroxy-3-hydroxymethylphenyl)-2-tert-butylaminoethanol
所属类别
有机原料:氨基化合物

物理化学性质

沸点433.5±40.0 °C(Predicted)
密度1.152±0.06 g/cm3(Predicted)
酸度系数(pKa)9.99±0.31(Predicted)

安全数据

危险品标志Xn
危险类别码R22
安全说明S36

常见问题列表

生物活性
Levalbuterol ((R)-Albuterol; (R)-Salbutamol) 是短效 β2-肾上腺素受体 (β2-adrenergic receptor) 激动剂和 Salbutamol 的活性 R 型对映异构体。Levalbuterol 是一种比 Salbutamol 更有效的支气管扩张试剂,可用于哮喘和慢性阻塞性肺疾病 (COPD) 的研究。
体外研究

Levalbuterol (10 μM; 24 hours) induces 11β-HSD1 mRNA expression, however, it does not influence 11β-HSD2 expression in airway epithelial cells.Levalbuterol (10 μM; 24 hours) significantly reduces both LPS- and TNF-α-induced NF-κB activity while increasing GRE activation in an 11β-HSD1 dependent manner in a transformed mouse airway epithelial cell line.

RT-PCR

Cell Line: Murine Club (MTCC) cells
Concentration: 10 μM
Incubation Time: 24 hours
Result: Increased 11β-HSD1 mRNA expression selectively.
体内研究

Levalbuterol (subcutaneous injection; 1 mg/kg; 14 days) significantly decreases pulmonary inflammation in OVA mice, demonstrated a decrease in eosinophilia and IgE.

Animal Model: C57BL/6 female mice with a pulmonary allergic model
Dosage: 1 mg/kg
Administration: Subcutaneous injection; 1 mg/kg; 14 days
Result: Decreased pulmonary inflammation after OVA sensitization.
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