返回ChemicalBook首页>CAS数据库列表>41570-61-0

41570-61-0

中文名称 妥布特罗
英文名称 Tulobuterol
CAS 41570-61-0
分子式 C12H18ClNO
MDL 编号 MFCD00867022
分子量 227.73
MOL 文件 41570-61-0.mol
更新日期 2024/04/18 11:50:10
41570-61-0 结构式 41570-61-0 结构式

基本信息

中文别名
alpha-[(叔丁基氨基)甲基]-邻氯苯甲醇
妥布特罗
妥洛特罗
英文别名
alpha-[(tert-butylamino)methyl]-o-chlorobenzyl alcohol
TULOBUTEROL
TULOBUTEROL BASE
TulobuterolHcl56776-01-3/Base
Tulobuterol(baseandorunspecifiedsalt)
2-Chloro-a-[[(1,1-dimethylethyl)amino]methyl]benzenemethano
Benzenemethanol, 2-chloro-a-[[(1,1-dimethylethyl)amino]methyl]- (9CI)
HN 078
o-Chloro-a-[(tert-butylamino)methyl]benzyl alcohol
Tulobuterol Bane
Tulobuterol (base and/or unspecified salts)
2-Chloro-a-[[(1,1-dimethylethyl)amino]methyl]benzenemethanol
2-(tert-Butylamino)-1-(o-chlorophenyl)ethanol
Sekinarin
Tulobunist
Tulobuten
α-[(tert-Butylamino)methyl]-2-chlorobenzenemethanol
所属类别
原料药:平喘药

物理化学性质

熔点89-91°C
沸点338.2±27.0 °C(Predicted)
密度1.098±0.06 g/cm3(Predicted)
RTECS号DA4734170
储存条件-20°C冷冻
溶解度可溶于DMSO(少许)、甲醇(少许)
酸度系数(pKa)13.62±0.20(Predicted)
形态固体
颜色白色至灰白色

安全数据

危险性符号(GHS)
GHS07
警示词警告
危险性描述H302
安全说明24/25
海关编码29214990
毒性LD50 in male mice, rats, rabbits (mg/kg): 305, 850, 563 orally; 170, 417, 164 s.c. (Kubo, 1975)
妥布特罗价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2024/01/25HY-B1810妥布特罗
Tulobuterol
41570-61-050mg700元
2024/01/25HY-B1810妥布特罗
Tulobuterol
41570-61-0100mg1200元
2024/01/16XW024157061004妥布特罗41570-61-025G5919元

常见问题列表

生物活性
Tulobuterol (C-78 free base) 是一种长效的 β2 肾上腺素受体 (β2-adrenoceptor) 激动剂,可减少慢性阻塞性肺疾病和支气管哮喘的发作频率。Tulobuterol 也是一种拟交感神经药,用作透皮贴剂,可增加正常的横膈膜肌肉力量。
靶点

β2-adrenoceptor

体外研究

Tulobuterol (0.1 μM; 24 hours or 72 hours; human tracheal epithelial cells) treatment decreases the RV14 RNA levels at 1 day and at 3 days after infection. The concentrations of sICAM-1 in the supernatants of the cells treated with tulobutero are significantly lower than those in the cells treated with vehicle before RV14 infection. Treatment with Tulobuterol reduces the number of acidic endosomes with green fluorescence in the cells and the fluorescence intensity of acidic endosomes in the cells. Also reduces the RV14 infection-induced secretion of IL-1β, IL-6, and IL-8. Tulobuterol treatment produces a small but significant reduction in the amount of p50, p65, and c-Rel of NF-κB induced by RV14 infection.

RT-PCR

Cell Line: Human tracheal epithelial cells infected with RV14
Concentration: 0.1 μM
Incubation Time: 24 hours or 72 hours
Result: Decreased the RV14 RNA levels at 1 day and at 3 days after infection. The concentrations of sICAM-1 in the supernatants of the cells were significantly lower. Reduced the number of acidic endosomes with green fluorescence in the cells and the fluorescence intensity of acidic endosomes in the cells. Also reduced the RV14 infection-induced secretion of IL-1β, IL-6, and IL-8. And produced a small but significant reduction in the amount of p50, p65, and c-Rel of NF-κB induced by RV14 infection.
体内研究

In vivo effect of Tulobuterol is examined the on the contractility of diaphragm muscles prepared from mice (BALBs/c mice; 21.7 ± 0.2 g) treated with Endotoxin. Contractile parameters of force-frequency curves and twitch kinetics using untreated or treated diaphragm muscles at 0 (E0) and 4 (E4) hours after E. coli endotoxin (20 mg/kg) administration are measured. E0 and E4 diaphragm muscles are analyzed at 0, 12, and 24 h after transdermal Tulobuterol treatment. The force-frequency curves of E0 and E4 diaphragm muscles at three time points are not significantly changed each other, indicating that Tulobuterol patch restores the muscle contractility. Thus, diaphragm muscle contractility is maintained during 4 h of endotoxin administration with Tulobuterol patch for over 24 h.

"41570-61-0" 相关产品信息
118-91-2 22483-09-6 95-57-8 2444-36-2 96-33-3 79-20-9 89-98-5 143390-89-0 67-56-1 99-76-3 623-04-1 6740-85-8 74-83-9 298-00-0 56776-01-3 41570-61-0