A new application about 2-Methylthiazole-4-carboxylic acid

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Safety of 2-Methylthiazole-4-carboxylic acid, you can also check out more blogs about35272-15-2

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.35272-15-2, Name is 2-Methylthiazole-4-carboxylic acid, molecular formula is C5H5NO2S. In a Article,once mentioned of 35272-15-2, Safety of 2-Methylthiazole-4-carboxylic acid

In this study, we reported the synthesis and biological characterization of a novel series of furan-carboxamide derivatives that were potent inhibitors of the influenza A H5N1 virus. The systematic structure-activity relationship (SAR) studies demonstrated that the 2,5-dimethyl-substituted heterocyclic moiety (furan or thiophene) had significant influence on the anti-influenza activity. In particular, 2,5-dimethyl-N-(2-((4-nitrobenzyl)thio)ethyl)-furan-3-carboxamide 1a showed the best activity against the H5N1 virus with an EC50 value of 1.25 muM. For the first time, the simple scaffold furan-carboxamide derivatives were identified as novel inhibitors of lethal H5N1 influenza A virus.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Safety of 2-Methylthiazole-4-carboxylic acid, you can also check out more blogs about35272-15-2

Reference:
Thiazole | C3H3848NS – PubChem,
Thiazole | chemical compound | Britannica