Clenbuterol
CAS No. 37148-27-9
Clenbuterol ( —— )
产品货号. M22407 CAS No. 37148-27-9
克仑特罗是一种取代的苯氨基乙醇,在非常低的剂量下具有β2肾上腺素样特性,并用作哮喘的支气管扩张剂。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥2623 | 有现货 |
|
| 10MG | ¥4380 | 有现货 |
|
| 25MG | ¥6476 | 有现货 |
|
| 50MG | ¥9916 | 有现货 |
|
| 100MG | 获取报价 | 有现货 |
|
| 200MG | 获取报价 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称Clenbuterol
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述克仑特罗是一种取代的苯氨基乙醇,在非常低的剂量下具有β2肾上腺素样特性,并用作哮喘的支气管扩张剂。
-
产品描述Clenbuterol is a substituted phenylaminoethanol that has β2 adrenomimetic properties at very low doses, and is used as a bronchodilator in asthma.
-
体外实验Clenbuterol (NAB-365) is a selective β2-adrenergic agonist (β2/β1 ratio = 4.0). Clenbuterol is a very potent inhibitor of the lipopolysaccharide (LPS)-induced release of TNF-α and IL-1β. Clenbuterol can inhibit the inflammatory process.Clenbuterol (10-200 μM; for 24 or 48 hours) decreases the viability of C2C12 myoblasts. Clenbuterol (100 μM) significantly decreases DNA synthesis. Clenbuterol (100 μM; for 12 h) increases the proportion of cells in G0/G1 phase. Clenbuterol treatment delays cell cycle progression. Clenbuterol (100 μM) induces cell cycle arrest, but not apoptosis, in C2C12 myoblasts. Cell Viability Assay Cell Line:C2C12 cells.Concentration:0, 10, 100, and 200 μM.Incubation Time:24 and 48 hours.Result:Treatment reduced viability of C2C12 cells for 24 and 48 h.
-
体内实验Treatment with Clenbuterol increases survival, rescues abnormalities in respiratory function and social recognition, and improves motor coordination in young male Mecp2-null (Mecp2?/y) mice. Clenbuterol is a bronchodilator. Clenbuterol (90 μg) is administered intratracheally to five horses. Peak serum concentrations of ~230 pg/mL are detected 10 min after administration, dropping to ~50 pg/mL within 30 min and declining much more slowly thereafter. Intratracheal administration of clenbuterol shortly before race time can be detected with this serum test. Animal Model:Male Mecp2?/y and female Mecp2?/+ mice Dosage:5 or 0.1 mg/kg.Administration:Injected i.p.; daily for 5 d, followed by a 2-d off period, repeated weekly Result:Significantly improved the phenotype during the second but not first day of testing, implying a modest effect on motor coordination in Mecp2-null mice.
-
同义词——
-
通路Angiogenesis
-
靶点Adrenergic Receptor
-
受体β2-adrenergic receptor
-
研究领域——
-
适应症——
化学信息
-
CAS Number37148-27-9
-
分子量277.19
-
分子式C12H18Cl2N2O
-
纯度>98% (HPLC)
-
溶解度——
-
SMILESCC(C)(C)NCC(O)c1cc(Cl)c(N)c(Cl)c1
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1. Nurul T , Faridah S , Yusran S . Development of Polyclonal Antibody against Clenbuterol for Immunoassay Application[J]. Molecules, 2018, 23(4):789.
产品手册
关联产品
-
Clonidine
可乐定是一种中枢活性α-肾上腺素能激动剂,主要用作抗高血压药,通常与其他药物联合使用。尽管可乐定已广泛使用多年,但尚未明确与血清转氨酶升高或临床上明显的肝损伤有关。
-
Dasotraline hydrochl...
Dasotraline Hydrochloride (SEP-225289 HydroHClide) 是一种三重再摄取抑制剂,可抑制多巴胺、去甲肾上腺素和血清素转运蛋白,IC50 值分别为 4、6 和 11 nM。
-
Bunazosin Hydrochlor...
Bunazosin Hydrochloride 是一种 α(1)-肾上腺素受体拮抗剂,用作全身抗高血压药和降眼压药。
021-51111890
购物车()
sales@molnova.cn

