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Submit ReviewCimaterol
Discontinued Product
0435 has been discontinued.
View all Non-selective Adrenergic β Receptors products.
说明： β agonist
化学名： 2-Amino-5-[1-hydroxy-2-[(1-methylethyl)amino]ethyl]benzonitrile
纯度： ≥99% (HPLC)
生物活性 for Cimaterol
Cimaterol is a β-Adrenergic agonist.
技术数据 for Cimaterol
| 分子量 | 219.29 |
| 公式 | C12H17N3O |
| 储存 | Store at RT |
| 纯度 | ≥99% (HPLC) |
| CAS Number | 54239-37-1 |
| PubChem ID | 2755 |
| InChI Key | BUXRLJCGHZZYNE-UHFFFAOYSA-N |
| Smiles | CC(C)NCC(O)C1=CC=C(N)C(=C1)C#N |
上方提供的技术数据仅供参考。批次相关数据请参见分析证书。
Tocris products are intended for laboratory research use only, unless stated otherwise.
产品说明书 for Cimaterol
参考文献 for Cimaterol
参考文献是支持产品生物活性的出版物。
Engelhardt (1984) Structure activity relationships in further series of amino-halogen substituted phenyl-aminoethanols. Arzneimittelforschung 11A 1625 PMID: 6152155
Strosberg and Pietri-Rouxel (1996) Function and regulation of the β3-adrenoceptor. TiPS 17 373 PMID: 8979772
Lafontan et al (1988) Mechanisms of actions of β-adrenergic agonists - lipomobilization and anabolism. Reprod.Nutr.Develop. 28 61
Merck Index 12 2336
关键词: Cimaterol, Cimaterol supplier, β-adrenoceptor, beta-adrenoceptors, b-adrenoceptors, agonists, β-adrenergic, beta-adrenergic, b-adrenergic, Receptors, Non-Selective, Non-selective, Adrenergic, Beta, 0435, Tocris Bioscience
2 篇 Cimaterol 的引用文献
引用文献是使用了 Tocris 产品的出版物。 Cimaterol 的部分引用包括：
Mistry et al (2013) Synthesis and in vitro and in vivo characterization of highly β1-selective β-adrenoceptor partial agonists. J Med Chem 56 3852 PMID: 23614528
Kaya et al (2009) Coupling of β2-adrenoceptors to XLαs and Gαs: a new insight into ligand-induced G protein activation. J Pharmacol Exp Ther 329 350 PMID: 19144685
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该领域的文献
Tocris offers the following scientific literature in this area to showcase our products. We invite you to request* your copy today!
*请注意，Tocris 仅会向正规科研企业/机构地址发送文献。
Depression Poster
Major depressive disorder is characterized by depressed mood and a loss of interest and/or pleasure. Updated in 2015 this poster highlights presynaptic and postsynaptic targets for the potential treatment of major depressive disorder, as well as outlining the pharmacology of currently approved antidepressant drugs.