Final Thoughts on Chemistry for 4-(tert-Butoxycarbonyl)thiomorpholine-3-carboxylic acid

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. 128453-98-5, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 128453-98-5, in my other articles.

128453-98-5, One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, such as the rate of change in the concentration of reactants or products with time.In a article, authors is Mattmann, Margrith E., mentioned the application of 128453-98-5, Name is 4-(tert-Butoxycarbonyl)thiomorpholine-3-carboxylic acid, molecular formula is C10H17NO4S

Identification of (R)-N-(4-(4-methoxyphenyl)thiazol-2-yl)-1- tosylpiperidine-2-carboxamide, ML277, as a novel, potent and selective K v7.1 (KCNQ1) potassium channel activator

A high-throughput screen utilizing a depolarization-triggered thallium influx through KCNQ1 channels was developed and used to screen the MLSMR collection of over 300,000 compounds. An iterative medicinal chemistry approach was initiated and from this effort, ML277 was identified as a potent activator of KCNQ1 channels (EC50 = 260 nM). ML277 was shown to be highly selective against other KCNQ channels (>100-fold selectivity versus KCNQ2 and KCNQ4) as well as against the distantly related hERG potassium channel.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. 128453-98-5, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 128453-98-5, in my other articles.

Reference£º
Thiomorpholine – Wikipedia,
Thiomorpholine | C4H9NS – PubChem