59-42-7
59-42-7 结构式
基本信息
去氧肾上腺素碱
去羟肾上腺素
去氧肾上腺
新交感酚
新辛内井林
L-PHENYLEPHRINE
(-)-PHENYLEPHRINE
PHENYLEPHRINE BASE
(-)-m-Hydroxy-alpha-(methylaminomethyl)benzyl alcohol
(-)-m-hydroxy-alpha-(methylaminomethyl)benzylalcohol
(-)-m-oxedrine
(R)-3-Hydroxy-alpha-[(methylamino)methyl]benzenemethanol hydrochloride
(r)-benzenemethano
(r)-phenylephrine
Adrianol
Ak-dilate
Ak-nefrin
Alcon efrin
Benzyl alcohol, m-hydroxy-alpha-((methylamino)methyl)-, (-)-
Biomydrin
component of Cerose dm
component of Comhist
component of Cyclomydril
component of Decongestant
物理化学性质
安全数据
| 报价日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
| 2025/02/08 | HY-B0769 | 去氧肾上腺素碱 Phenylephrine | 59-42-7 | 500mg | 500元 |
| 2025/02/08 | HY-B0769 | 去氧肾上腺素碱 Phenylephrine | 59-42-7 | 10mM * 1mLin DMSO | 550元 |
| 2025/02/05 | P0395 | L-苯肾上腺素 L-Phenylephrine | 59-42-7 | 5G | 720元 |
常见问题列表
(R)-(-)-Phenylephrine is a selective α 1 -adrenoceptor agonist with pK i values of 5.86, 4.87 and 4.70 for α 1D , α 1B and α 1A receptors respectively. Phenylephrine promotes cardiac fibroblast proliferation. Phenylephrine activates CaN and evokes NFAT3 nuclear translocation. It suggests that the Ca( 2+ )/CaN/NFAT pathway mediates phenylephrine -induced cardiac fibroblast proliferation, and this pathway might be a possible therapeutic target in cardiac fibrosis.
Perfusion of hearts with 100 μM phenylephrine causes a rapid (maximal at 10 min) 12-fold activation of two p38-MAPK isoforms. α 1 -adrenoceptor agonists such as phenylephrine increase the contractility of the heart. Phenylephrine also activates SAPKs/JNKs in neonatal ventricular myocytes. Phenylephrine could increase the alveolar fluid clearance in high tidal volume-ventilated rats and accelerate the absorption of pulmonary edema.