N?-Acyl derivatives of arginine, bearing the di(2-chloroethyl)-amino group

1964 ◽  
Vol 13 (10) ◽  
pp. 1805-1807
Author(s):  
S. �. Zurabyan ◽  
L. P. Rasteikene ◽  
O. V. Kil'disheva ◽  
I. L. Knunyants
Keyword(s):  
Amino Group ◽  
Derivatives Of ◽  
Acyl Derivatives

N?-acyl derivatives of histidine with the di-(2-chloroethyl)amino group

1965 ◽  
Vol 14 (5) ◽  
pp. 888-890
Author(s):  
M. I. Dagene ◽  
L. P. Rasteikene ◽  
O. V. Kil'disheva ◽  
I. L. Knunyants
Keyword(s):  
Amino Group ◽  
Derivatives Of ◽  
Acyl Derivatives

scholarly journals Synthesis of acyl derivatives of thiazolo[5.4-b]indole

2019 ◽  
Vol 55 (4) ◽  
pp. 436-441
Author(s):  
D. V. Lopatik ◽  
Z. I. Kuvaeva ◽  
O. M. Bondareva ◽  
V. E. Naidenov ◽  
L. Yu. Tychinskaya
Keyword(s):  
Chemical Modification ◽  
Free Amino ◽  
Amino Group ◽  
Therapeutic Activity ◽  
Functional Derivatives ◽  
Derivatives Of ◽  
Acyl Derivatives

2-Amino-4-acetylthiazolo[5,4-b]indole and its bromosubstituted analogue contain a free amino group and are initial compounds for chemical modification in order to obtain on their basis functional derivatives having high therapeutic activity. By the interaction of these 2-aminо-4-acetylthiazolo[5,4-b]indoles with succinic and maleic anhydrides, the corresponding imides and amides were obtained, which are of interest for use in order to create on their basis antihypoxic and actoprotective agents.

scholarly journals SYNTHESIS AND PROPERTIES OF NEW N-ACYL DERIVATIVES OF ANTHRANILIC ACID

2019 ◽  
Vol 85 (4) ◽  
pp. 59-70
Author(s):  
Oksana Slobodianiuk ◽  
Oleksandra Berezhnytska ◽  
Tetyana Kamens'ka ◽  
Мария Русакова
Keyword(s):  
Candida Albicans ◽  
Benzoic Acid ◽  
Anthranilic Acid ◽  
Yeast Cells ◽  
Ir Absorption ◽  
Amino Group ◽  
Synthetic Derivatives ◽  
Hydrolysis Of ◽  
Derivatives Of ◽  
Acyl Derivatives

A series of N-acyl derivatives of anthranil (or o -aminobenzoic acid) was first synthesized, namely 2-(4-octylbenzamido)benzoic acid, 2-(4-(heptyloxy)- benzamido)benzoic acid, 2-(4-(heptylsulfanyl)benz-amido)benzoic acid. 2-(4-octylbenzamido)benzoic acid was synthesized in five stages of octylbenzene, by acylating chloride acid using a Friedie-Crafts reaction. 2-(4-(heptyloxy)benzamido)benzoic acid was prepared from the methyl ester of p-hydroxybenzoic acid which, at the first stage, was activated with 1-bromoheptane in acetonitrile with potassium carbonate and catalytic amount of sodium iodide at heating. After that, hydrolysis of the ester group by hydroxide in the methanol–water system was performed. Synthesis of 2-(4-(heptylsulfanyl)benzamido)benzoic acid was carried out from p-sulfanylbenzoic acid, which was activated with 1-bromoheptane, in a system of ethanol–water with sodium hydroxide. Chlorinated hydrides of acids were obtained by reaction of acids with chlorinated thionyl in benzene. Acylation of the tret-butyl ester of anthranilic acid with formed chlorohydrides was carried out in pyridine upon heating and in dichloromethane with triethylamine (as the base), and dimethylaminopyridine (catalyst).At the last stage of the synthesis of all derivatives, the hydrolysis of tret-butyl esters with trifluoroacetic acid in dichloromethane to the formation of terminal compounds took place.The composition and structure of the synthesized compounds were determined using NMR 1H, infrared spectroscopy. The shape and position of the bands in the IR absorption spectra of the synthesized anthranilic acid derivatives are shifted and splited in comparison with the parent acid due to the presence of a secondary amino group, an additional aromatic moiety, and a different nature of the substitutes in the para-position to the amino group. For all synthesized derivatives, the sensitivity of various morphological forms Candida albicans was determined. The influence of the test substances on the cells of the yeast fungus was determined for 24–48 hours using Saburo and Spider nutrient media with the  addition of mannitol. Compared with the already known influence of anthranilic acid on Candida albicans cells grown in Saburo nutrient medium for 24 hours, the compounds studied were more effective at all stages of cultivation. It has been shown that the synthetic derivatives studied are more active with respect to the cells in the biofilm composition, which consists of the yeast-like form of Candida albicans, than those cells that form a hyphal type biofilm. The yeast-like form of the Candida albicans cell is susceptible to synthetic derivatives. It is shown that the level of sensitivity of compounds 1-3 is higher in 4-6 times compared with anthranilic acid. Glyphs have been found to be more susceptible to the effects of the compounds studied than Е yeast cells of Candida albicans

scholarly journals Prodrugs of Cephalosporin RWJ-333441 (MC-04,546) with Improved Aqueous Solubility

2003 ◽  
Vol 47 (6) ◽  
pp. 2043-2046 ◽  
Author(s):  
Scott J. Hecker ◽  
Trevor Calkins ◽  
Mary E. Price ◽  
Keith Huie ◽  
Sharon Chen ◽  
...  
Keyword(s):  
Staphylococcus Aureus ◽  
Aqueous Solubility ◽  
Amino Group ◽  
Methicillin Resistant ◽  
Ph Values ◽  
Primary Amino ◽  
Derivatives Of ◽  
Acyl Derivatives

ABSTRACT To improve the aqueous solubility of anti-methicillin-resistant Staphylococcus aureus cephalosporin RWJ-333441 for parenteral administration, acyl derivatives of the C-3 primary amino group were prepared and evaluated for solubility, cleavage in serum in vitro, and conversion to RWJ-333441 in vivo. Improved solubility at physiologic pH values and release of RWJ-333441 in vitro and in vivo were observed for several prodrugs, including the aspartate derivative RWJ-333442.

Oxime derivatives. IV. Attempted syntheses of N-acyl derivatives of oximes

1956 ◽  
Vol 21 (6) ◽  
pp. 1500-1512 ◽  
Author(s):  
O. Exner
Keyword(s):  
Oxime Derivatives ◽  
Derivatives Of ◽  
Acyl Derivatives

scholarly journals Synthesis, Antiproliferative Activity and Radical Scavenging Ability of 5-O-Acyl Derivatives of Quercetin

Molecules ◽  
2021 ◽  
Vol 26 (6) ◽  
pp. 1608
Author(s):  
Stephen Lo ◽  
Euphemia Leung ◽  
Bruno Fedrizzi ◽  
David Barker
Keyword(s):  
Antiproliferative Activity ◽  
Biological Activities ◽  
Radical Scavenging Activity ◽  
Radical Scavenging ◽  
Breast Cancer Cell Lines ◽  
Scavenging Activity ◽  
Plant Materials ◽  
Wide Range ◽  
Derivatives Of ◽  
Acyl Derivatives

Quercetin is a flavonoid that is found in many plant materials, including commonly eaten fruits and vegetables. The compound is well known for its wide range of biological activities. In this study, 5-O-acyl derivatives of quercetin were synthesised and assessed for their antiproliferative activity against the HCT116 colon cancer and MDA-MB-231 breast cancer cell lines; and their radical scavenging activity against the 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) radical cation and 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical species. Four derivatives were found to have improved the antiproliferative activity compared to quercetin whilst retaining radical scavenging activity.

Synthesis of Lactams and Other Nitrogen Heterocycles by Intramolecular Cyclizations of Carbamates and Acyl Derivatives of Aminosulfones.

ChemInform ◽  
2003 ◽  
Vol 34 (34) ◽  
Author(s):  
Nora M. Hernandez ◽  
Melina J. Sedano ◽  
Hollie K. Jacobs ◽  
Aravamudan S. Gopalan
Keyword(s):  
Nitrogen Heterocycles ◽  
Intramolecular Cyclizations ◽  
Derivatives Of ◽  
Acyl Derivatives
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