نتایج جستجو برای: hydroxamic acids alkyl substituents

تعداد نتایج: 283965  

2012
Nuha Z Abdelwahab Arthur T Crossman Lauren Sullivan Michael A J Ferguson Michael D Urbaniak

Disruption of glycosylphosphatidylinositol biosynthesis is genetically and chemically validated as a drug target against the protozoan parasite Trypanosoma brucei, the causative agent of African sleeping sickness. The N-acetylglucosamine-phosphatidylinositol de-N-acetylase (deNAc) is a zinc metalloenzyme responsible for the second step of glycosylphosphatidylinositol biosynthesis. We recently r...

Journal: :iranian journal of science and technology (sciences) 2005
y. k agrawal

calix(6)arene hydroxamic acids (iii) are synthesised for the first time by reactingcalix(6)arene acid chloride(ii) with substituted hydroxylamines at low temperature in the presence ofsodium bicarbonate. the p-carboxycalix(6)arene(i) is obtained by an acid catalysed condensationreaction of p-hydroxybenzoic acid and formaldehyde. these calixarenes are characterised by meltingpoint, uv, ir, 1h nm...

Journal: :Antimicrobial agents and chemotherapy 1977
C Y Wang L H Lee

Hydroxamic acids demonstrated mutagenic and antibacterial activities. These activities appear to be dependent on the hydroxamic acid function and are probably due to the interaction with deoxyribonucleic acid.

2017
Masakazu Morimoto Takaki Sumi Masahiro Irie

Photoswitching and fluorescent properties of sulfone derivatives of 1,2-bis(2-alkyl-4-methyl-5-phenyl-3-thienyl)perfluorocyclopentene, 1-5, having methyl, ethyl, n-propyl, i-propyl, and i-butyl substituents at the reactive carbons (2- and 2'-positions) of the thiophene 1,1-dioxide rings were studied. Diarylethenes 1-5 underwent isomerization reactions between open-ring and closed-ring forms upo...

2010
L. K. TIWARY

Hydroxamic acids serve as a monsulfhydril bisubstrate analog inhibition of fernesyl protein transferase (FPT), the enzyme catalysing fernesylation of p21ras. Tumor necrosis factor (TFN) is specifically prevented by synthetic hydroxamic acid-based metalloproteinase inhibitors. Suberoyanilide hydroxamic acid (SAHA) have been identified as histone deacetylase inhibitors based on their ability to i...

2017
Matthias Wünsch David Schröder Tanja Fröhr Lisa Teichmann Sebastian Hedwig Nils Janson Clara Belu Jasmin Simon Shari Heidemeyer Philipp Holtkamp Jens Rudlof Lennard Klemme Alessa Hinzmann Beate Neumann Hans-Georg Stammler Norbert Sewald

The amide moiety of peptides can be replaced for example by a triazole moiety, which is considered to be bioisosteric. Therefore, the carbonyl moiety of an amino acid has to be replaced by an alkyne in order to provide a precursor of such peptidomimetics. As most amino acids have a chiral center at Cα, such amide bond surrogates need a chiral moiety. Here the asymmetric synthesis of a set of 24...

Journal: :Journal of Japan Oil Chemists' Society 1988

2006
AHMED E. FAZARY MOHAMED M. KHALIL ALY FAHMY TANTAWY A. TANTAWY

Hydroxamic acids, a group of naturally occurring and synthetic weak organic acids of general formula RC(=O)N(R')OH, are widespread in the tissues of plants, in metabolites of bacteria and fungi, including complex compounds. Hydroxamic acids and their derivatives fulfill a variety of important roles in biology and medicine; here we provide a comprehensive brief review of the most basic medicinal...

Journal: :Acta Chemica Scandinavica 1957

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