Novel hybrid inhibitors of the phage T7 RNA polymerase : synthesis, docking and screening in vitro

A number of new hybrid heteroaromatic compounds, consisting of tricyclic fragments (acridone, thioxanthone and phenazine) and bicyclic fragments (benzimidazole, benzothiazole and benzoxazole) were synthesized using the method, developed by the authors. As a result of screening against the transcription model system of the phage T7 DNA-dependent RNA polymerase three effective inhibitors of the RNA syntheses with the IC50 value of 8.9, 5.7 and 19.8 microM were detected. To cast light on the mode of interaction between the synthesized compounds and the target, the molecular docking was applied to the model pocket of the phage T7 RNA polymerase transcription complex. It was established that these ligands form networks of H-bonds with residues of the pocket conservative amino acids and pi-interaction with the Mg2+ ion. A planar geometry of the hybrid molecules, realized due to the intramolecular H-bonds, proved to be an important structural feature, which correlates with an efficacious inhibitory activity.

Medienart:

Artikel

Erscheinungsjahr:

2012

Erschienen:

2012

Enthalten in:

Zur Gesamtaufnahme - volume:84

Enthalten in:

Ukrains'kyi biokhimichnyi zhurnal (1999 ) - 84(2012), 5 vom: 10. Sept., Seite 38-47

Sprache:

Ukrainisch

Beteiligte Personen:

Kostina, V H [VerfasserIn]
Pal'chykovs'ka, L H [VerfasserIn]
Platonov, M O [VerfasserIn]
Vasyl'chenko, O V [VerfasserIn]
Lysenko, N A [VerfasserIn]
Alekseeva, I V [VerfasserIn]

Themen:

Acridones
Bacteriophage T7 RNA polymerase
Benzimidazoles
Benzothiazoles
Benzoxazoles
DNA-Directed RNA Polymerases
EC 2.7.7.-
EC 2.7.7.6
English Abstract
Enzyme Inhibitors
I38ZP9992A
Journal Article
Magnesium
Phenazines
RNA, Viral
Solutions
Viral Proteins

Anmerkungen:

Date Completed 05.02.2013

Date Revised 03.08.2015

published: Print

Citation Status MEDLINE

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM224392298