CAS 41570-61-0|Tulobuterol

Introduction:Basic information about CAS 41570-61-0|Tulobuterol, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameTulobuterol
CAS Number41570-61-0Molecular Weight227.73000
Density1.098 g/cm3Boiling Point338.2ºC at 760 mmHg
Molecular FormulaC12H18ClNOMelting Point89-91ºC
MSDS/Flash Point158.3ºC

Names

NameTulobuterol
SynonymMore Synonyms

Tulobuterol BiologicalActivity

DescriptionTulobuterol (C-78 free base) is a long-acting β2-adrenoceptor agonist, which reduces the frequency of exacerbations of chronic obstructive pulmonary disease and bronchial asthma. Tulobuterol is also a sympathomimetic agent used as a transdermal patch, and increases normal diaphragm muscle strength[1].
Related CatalogResearch Areas >>Endocrinology
Target

β2-adrenoceptor[1]

In VitroTulobuterol (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[1]. RT-PCR[1] 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.
In VivoIn 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[2].
References

[1]. Yamaya M, et al. Tulobuterol inhibits rhinovirus infection in primary cultures of human tracheal epithelial cells. Physiol Rep. 2013 Aug;1(3):e00041.

[2]. Shindoh C, et al. Tulobuterol patch maintains diaphragm muscle contractility for over twenty-four hours in a mouse model of sepsis. Tohoku J Exp Med. 2009 Aug;218(4):271-8.

Chemical & Physical Properties

Density1.098 g/cm3
Boiling Point338.2ºC at 760 mmHg
Melting Point89-91ºC
Molecular FormulaC12H18ClNO
Molecular Weight227.73000
Flash Point158.3ºC
Exact Mass227.10800
PSA32.26000
LogP3.15240
InChIKeyYREYLAVBNPACJM-UHFFFAOYSA-N
SMILESCC(C)(C)NCC(O)c1ccccc1Cl
Storage condition-20°C Freezer

Safety Information

HS Code2922199090

Customs

HS Code2922199090
Summary2922199090. other amino-alcohols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Synonyms

MFCD00867022
2-(tert-butylamino)-1-(2-chlorophenyl)ethanol
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