The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. 39711-79-0, Name is N-Ethyl-2-isopropyl-5-methylcyclohexanecarboxamide, SMILES is CC(C1)CCC(C(C)C)C1C(NCC)=O, in an article , author is Silva, Daniel G., once mentioned of 39711-79-0, HPLC of Formula: https://www.ambeed.com/products/39711-79-0.html.
We recently reported a series of naphthofuranic compounds as constrained agomelatine analogues. Herein, in order to explore alternative ethyl amide side chain rigidification, naphthocyclopentane and quinolinocyclopentane derivatives with various acetamide modulations were synthesized and evaluated at both melatonin (MT1, MT2) and serotonin (5-HT2c) receptors. These modifications has led to compounds with promising dual affinity and high MTs receptors agonist activity. Enantiomeric separation was then performed on selected compounds allowing us to identify levogyre enantiomers (-)-17g and (-)-17k as the highest (MT1 MT2)/5-HT2c dual ligands described nowadays. (C) 2017 Elsevier Masson SAS. All rights reserved.
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Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics