CAS: 1076198-80-5; 4-(2-Aminoethoxy)-3-Methoxyphenol

相似化合物

87780-27-6 1836-62-0 64464-07-9

上下游产品

4-(2-Bromoethoxy)-3-Methoxyphenol 1262778-69-7
Formic Acid 4-(2-Bromoethoxy)-3-Methoxyphenyl Ester 1262778-68-6

📜4-(2-Bromoethoxy)-3-Methoxyphenol置于ammonium Hydroxide体系中,用 水 用作溶剂,化学反应 4.0H,反应生成4-(2-氨基乙氧基)-3-甲氧基苯酚
参考文献:Suppression Of Store Overload-Induced Calcium Release By Hydroxylated Metabolites Of Carvedilol
标题:Suppression Of Store Overload-Induced Calcium Release By Hydroxylated Metabolites Of Carvedilol
摘要:Carvedilol Is A Drug Widely Used In The Treatment Of Heart Failure And Associated Cardiac Arrhythmias. A Unique Action Of Carvedilol Is Its Suppression Of Store Overload-Induced Calcium Release (Soicr) Through The Cardiac Ryanodine Receptor (Ryr2),Which Can Trigger Ventricular Arrhythmias. Since The Effects Of Carvedilol Metabolites On Soicr Have Not Yet Been Investigated,Three Carvedilol Metabolites Hydroxylated At The 3-,4' And 5'-Positions Were Synthesized And Assayed For Soicr Inhibition In Mutant Hek 293 Cells Expressing The Ryr2 Mutant R4496C. This Cell Line Is Especially Prone To Soicr And Calcium Release Through The Defective Ryr2 Channel Was Measured With A Calcium-Sensitive Fluorescent Dye. These Results Revealed That The 3-And 4'-Hydroxy Derivatives Are Slightly More Effective Than Carvedilol In Suppressing Soicr,While The 5'-Analog Proved Slightly Less Active. Metabolic Deactivation Of Carvedilol Via These Hydroxylation Pathways Is Therefore Insignificant. (C) 2015 Elsevier Ltd. All Rights Reserved.
Doi:10.1016/j.Bmcl.2015.11.008