GLPBio

Formoterol

Catalog No.: GF11341Purity:>98.00%
Formoterol is a kind of long-acting β2-adrenergic receptor (β2AR) agonist.

製品は研究用途にのみ使用できます。人体には使用できません。患者への販売は行っておりません。


Formoterol
Cas No.: 73573-87-2
10mM (in 1mL DMSO)In Stock
$31.00
1
5mgIn Stock
$28.00
1
10mgIn Stock
$48.00
1
25mgIn Stock
$88.00
1
50mgIn Stock
$144.00
1
100mgIn Stock
$243.00
1
200mgIn Stock
$384.00
1

引用文献 (Citations)

1 publications本製品を使用した研究者による文献

製品説明 (Description)

Formoterol is a kind of long-acting β2-adrenergic receptor (β2AR) agonist [1]. Formoterol is widely used for symptomatic relief in asthma and control of chronic obstructive pulmonary disease (COPD) [2]. The therapeutic mechanism of Formoterol involves both bronchodilation through airway smooth muscle relaxation and anti-inflammatory activity [2].

Formoterol (0.1μM; 24h) inhibited secretion of TNFα in the bronchial epithelial (BE) cells infected with rhinovirus [3]. Formoterol (1μM; 24h) effectively reduced tert-butyl hydroperoxide-induced SH-SY5Y cell death [1]. Formoterol (0.1nM~1μM; 24h) inhibited the IgE-dependent release of histamine from human lung mast cells in a concentration-dependent manner [4].

Formoterol (1mg/kg; 4 weeks; s.c.) decreased the expression of Fbxo32 and Trim63 in muscle wasting Balb/c mice induced by doxorubicin hydrochloride [5]. Formoterol (1mg/kg; 2 weeks; i.p.) prevented abdominal aortic aneurysm formation in erythropoietin-induced ApoE−/− mice [2].

References:
[1] Chang J C, Chang H S, Chao Y C, et al. Formoterol acting via β2-adrenoreceptor restores mitochondrial dysfunction caused by parkinson's disease-related UQCRC1 mutation and improves mitochondrial homeostasis including dynamic and transport [J]. Biology, 2024, 13(4): 231.
[2] Zhang J, Cao Y, Ren R, et al. Medium-dose formoterol attenuated abdominal aortic aneurysm induced by EPO via β2AR/cAMP/SIRT1 pathway [J]. Advanced science, 2024, 11(15): e2306232.
[3] Bochkov Y A, Busse W W, Brockman-Schneider R A, et al. Budesonide and formoterol effects on rhinovirus replication and epithelial cell cytokine responses [J]. Respiratory research, 2013, 14(1): 98.
[4] Scola A M, Chong L K, Suvarna S K, et al. Desensitisation of mast cell beta2-adrenoceptor-mediated responses by salmeterol and formoterol [J]. British journal of pharmacology, 2004, 141(1): 163-171.
[5] De Lima Junior E A, Teixeira A A S, Silveira L S, et al. Formoterol reduces muscle wasting in mice undergoing doxorubicin chemotherapy [J]. Frontiers in oncology, 2023, 13: 1237709.

実験プロトコル (Protocol)

Cell experiment [1]:

Cell lines

Bronchial epithelial (BE) cells

Preparation Method

BE cells were obtained from airway brushings. Cells were incubated for 24h with Formoterol (0.01% DMSO drug vehicle), and then infected with 0.25 mL of rhinovirus-16 (5×106 plaque forming units [PFU]/mL). After 24h, cytokine secretion (TNFα) was analyzed.

Reaction Conditions

0.1μM; 24h

Applications

Formoterol inhibited secretion of TNFα in the cells.
Animal experiment [2]:

Animal models

Male Balb/c mice

Preparation Method

The mice received doxorubicin hydrochloride (DOX) to induce muscle wasting. One of the groups treated with Formoterol, and another not submitted to Formoterol treatment received saline solution (0.9%) by the corresponding route of administration. The mice were euthanized for sample collection after 4 weeks.

Dosage form

1mg/kg; 4 weeks; s.c.

Applications

Formoterol protected against DOX-induced increase in Fbxo32 and Trim63 gene expression.

References:
[1] Bochkov Y A, Busse W W, Brockman-Schneider R A, et al. Budesonide and formoterol effects on rhinovirus replication and epithelial cell cytokine responses [J]. Respiratory research, 2013, 14(1): 98.
[2] De Lima Junior E A, Teixeira A A S, Silveira L S, et al. Formoterol reduces muscle wasting in mice undergoing doxorubicin chemotherapy [J]. Frontiers in oncology, 2023, 13: 1237709.

製品資料 (Product Documents)

Purity:>98.00%Appearance:A solid

化学的性質 (Chemical Properties)

CAS番号
73573-87-2
分子式
C19H24N2O4
分子量
344.4
溶解性
DMSO : 250 mg/mL (725.90 mM; Need ultrasonic)
保存条件
-20°C
一般的な注意事項
製品の溶解性データに基づいて適切な溶媒を選択してください。調製後は、凍結融解の繰り返しを避けるため、ストック溶液を小分けしてください。
ストック溶液は、-80°Cで保存する場合は6か月以内、-20°Cで保存する場合は1か月以内に使用してください。
溶解性を高めるには、チューブを37°Cに温め、適切な時間超音波処理してください。
配送条件
評価用サンプルは保冷剤とともに発送します。その他の容量は室温で発送し、ご要望に応じて保冷剤を同梱します。

計算ツール (Calculators)モル濃度 / 希釈 / 分子量 / 単位変換 / in vivo製剤 / 溶解度

g/mol

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