The purpose of this work is the synthesis new isonicotinic acid hydrazones, study their structure, reactivity and biological screening some synthesized compounds. reactions leading to N-arylidene(alkylidene) hydrazones via condensation hydrazide with various derivatives aromatic aldehydes were studied. structure functionally substituted was established by FTIR, 1H 13C NMR, two-dimensional COSY ...

The anthranilic scaffold plays an important role as a pharmacophore and toxophore in medicinal and agricultural chemistry and contributes to a variety of biological activities [1 – 9]. Although ring-closure reactions of N-unsubstituted anthranilic acid derivates have been extensively elaborated, investigations towards the corresponding chemistry of N-alkyl(aryl)-anthranilic acids remained fragm...

A series of novel 4-amino-5-mercapto-3-[(3-aralkyl amido/imidoalkyl) phenyl]-1,2,4-triazoles (5a-d) were obtained by treating m-(aralkyl amido/imidoalkyl) benzoic acid hydrazides (3a-d) with carbon disulphide in alcoholic KOH and hydrazine hydrate, respectively. These triazole derivatives were employed in the synthesis of 5-[(3'-aralkyl amido/imidoalkyl) phenyl]-1,2,4-triazolo[3,4-b]-1,3,4-thia...

One of the rising demands in the field of protein chemical synthesis is the development of facile strategies that yield the protein in workable quantities and homogeneity, with fewer handling steps. Although the native chemical ligation of peptide hydrazides has recently been shown to be useful for the chemical synthesis of proteins carrying acid-sensitive modification groups, previous hydrazid...

A series of 2,6-disubstituted pyridine derivatives were prepared from 2,6-diacetylpyridine or 2,6dicarbonyl pyridine dichloride as starting materials. Reaction of 2,6-diacetylpyridine 1 with hydroxylamine hydrochloride or different aromatic aldehydes afforded the corresponding 2,6-diacetylpyridine dioxime and 2,6-bis-[β -(2-thienyl)acryloyl]pyridine derivatives 2 and 3, respectively. Additional...

We present a streamlined approach to sidechain acyl hydrazides of aspartic and glutamic acids – user friendly precursors peptide macrocycles glycopeptide analogues.

A simple method to label oligosaccharides with a multifunctional fluorescent group was developed. Oligosaccharides were quantitatively labeled at their reducing termini with pyrene butanoic acid hydrazide. The pyrene-labeled oligosaccharides were successfully applied to fluorescence polarization measurements and ELISA at picomole quantity, which was not previously reached by other procedures. T...