Results 91 to 100 of about 2,622 (202)

Development of a precolumn derivatization method for the determination of free amines in wastewater by high-performance liquid chromatography via fluorescent detection with 9-(2-hydroxyethyl)acridone

open access: yes, 2002
A simple, sensitive, and mild method for the determination of amino compounds based on a condensation reaction with fluorescence detection has been developed.
Zhang, WB   +5 more
core   +1 more source

Evaluation of Alkaloids Isolated from Ruta graveolens as Photosynthesis Inhibitors

open access: yesMolecules, 2018
Eight alkaloids (1–8) were isolated from Ruta graveolens, and their herbicide activities were evaluated through in vitro, semivivo, and in vivo assays.
Olívia Moreira Sampaio   +6 more
doaj   +1 more source

Inhibition of Subgenomic Hepatitis C Virus RNA Replication by Acridone Derivatives: Identification of an NS3 Helicase Inhibitor

open access: yes, 2016
We report the synthesis and structure−activity relationship (SAR) of a large series of acridones and acridone-fragment derivatives designed on the basis of the selective antihepatitis C virus (HCV) activity shown by acridone 2, previously studied as a ...
Giovanni Maga (10904)   +9 more
core   +1 more source

Long wavelength sensitizers for europium(III) luminescence based on acridone derivatives

open access: yes, 2002
The preparation of several acridone derivatives which have been shown to act as sensitizers for europium(III) luminescence at wavelengths longer than 400 nm is described.
Faulkner, Stephen   +5 more
core   +1 more source

Synthesis of New Acridone Derivatives, Inhibitors of NS3 Helicase, Which Efficiently and Specifically Inhibit Subgenomic HCV Replication

open access: yes, 2016
A new goup of acridone derivatives, obtained by reaction of acridone-4-carboxylic acid derivatives with aromatic amines, was tested to determine the inhibitory properties toward the NS3 helicase of hepatitis C virus (HCV). Six compounds inhibited the NS3
Anna Stankiewicz-Drogoń (2304214)   +3 more
core   +1 more source

Studies using radioisotopes. III. The biosynthesis of acridone alkaloids

open access: yes, 1969
The biosynthesis of acridone alkaloids has been investigated in Acronychia baueri and Evodia xanthoxyloides. Anthranilic acid, N- methylanthranilic acid (XI), acetate, and 4-hydroxy-N-methylquinol-2- one (X) are incorporated, and tryptophan appears not ...
RH Prager, HM Thredgold
core   +1 more source

Spectrophotometric Enzyme Assays for High-Throughput Screening

open access: yesFood Technology and Biotechnology, 2004
This paper reviews high-throughput screening enzyme assays developed in our laboratory over the last ten years. These enzyme assays were initially developed for the purpose of discovering catalytic antibodies by screening cell culture supernatants, but ...
Jean-Louis Reymond
doaj  

Acridones as promising drug candidates against Oropouche virus

open access: yesCurrent Research in Microbial Sciences
Oropouche virus (OROV) is an emerging vector-borne arbovirus found in South America that causes Oropouche fever, a febrile infection similar to dengue fever.
Marielena Vogel Saivish   +16 more
doaj   +1 more source

Lewis Acid Promoted Hetero [2 + 2] Cycloaddition Reactions of Aldehydes with 10-Propynyl-9(10H)-acridone. A Highly Stereoselective Synthesis of Acrylic Acid Derivatives and 1,3-Dienes Using an Electron Deficient Variant of Ynamine

open access: yes, 2016
Reactivities of 10-propynyl-9(10H)-acridone toward various aldehydes in BF3·Et2O-promoted hetero [2 + 2] cycloaddition reactions are described here. This electron deficient variant of ynamine is more stable and easier to handle than most ynamines but ...
Craig A. Zificsak (2471440)   +5 more
core   +1 more source

Synthesis of novel xanthone and acridone carboxamides with potent antiproliferative activities

open access: yes, 2020
Several new amino-substituted acridone and xanthone derivatives have been designed and synthesized, using an efficient methodology from suitable acridone- or xanthone-carboxylic acid intermediates.
Gioti, K.   +10 more
core   +1 more source

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