نتایج جستجو برای: hexahydroquinoline 3 carboxamide

تعداد نتایج: 1812884  

Journal: :Acta Crystallographica Section E Structure Reports Online 2009

Journal: :Bioorganic & medicinal chemistry 2013
Tomas Gonec Jiri Kos Iveta Zadrazilova Matus Pesko Stanislava Keltosova Jan Tengler Pavel Bobal Peter Kollar Alois Cizek Katarina Kralova Josef Jampilek

In this study, a series of 22 ring-substituted 1-hydroxynaphthalene-2-carboxanilides were prepared and characterized. Primary in vitro screening of the synthesized compounds was performed against Mycobacterium marinum, Mycobacterium kansasii and Mycobacterium smegmatis. The compounds were also tested for their activity related to inhibition of photosynthetic electron transport (PET) in spinach ...

Journal: :Acta Crystallographica Section E Structure Reports Online 2010

2012
Gabriele Murineddu Battistina Asproni Stefania Ruiu Francesco Deligia Matteo Falzoi Amedeo Pau Brian F Thomas Yanan Zhang Gérard A Pinna Luca Pani Paolo Lazzari

In search of new selective CB2 ligands, the synthesis and preliminary biological evaluation of novel 1,4-dihydroindeno[1,2-c]pyrazole hybrids of the highly potent prototypicals 5-(4-chloro-3-methylphenyl)-1-(4-methylbenzyl)-N-fenchyl-1H-pyrazole-3-carboxamide 1 and 1-(2,4-dichlorophenyl)-6-methyl-N-(piperidin-1-yl)-1,4-dihydroindeno[1,2-c]pyrazole-3-carboxamide 2 are detailed.We postulated that...

Journal: :Organic & biomolecular chemistry 2015
Yanhua He Lingling Yan Wenwen Zang Weiping Zheng

Built upon the catalytic mechanism-based pan-SIRT1/2/3 inhibitory warhead L-2-amino-7-carboxamidoheptanoic acid (L-ACAH, a close structural analog of N(ε)-acetyl-lysine) that our laboratory discovered recently, in the current study, its carboxamide NH2-ethylated analog was found to be a ∼2.4-6.6-fold stronger SIRT1/2/3 inhibitory warhead than L-ACAH. Carboxamide NH2-dodecylated and carboxymethy...

Journal: :Russian Journal of General Chemistry 2021

The reaction of cyanothioacetamide with aromatic aldehydes and 1,3-dicarbonyl compounds followed by aminomethylation or S-alkylation gave a series heterocyclic derivatives 1,2,3,4-tetrahydropyridine 1,4,5,6,7,8-hexahydroquinoline fragment. resulting were tested for analgesic activity in vivo. Some the prepared showed an antinociceptive effect superior to that ketorolac dynamics.

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