Effect of 8-methoxypsoralen and 4,5'-dimethylangelicin on ribonucleic acid synthesis in vitro

Photobinding of 8-methoxypsoralen (8-MOP) to DNA leads to mono- and diadduct formation while 4,5'-dimethylangelicin (4,5'-DMA) binds monofunctionally. The effect of the irreversible binding of furocoumarins to DNA on different steps of RNA synthesis has been assayed in this study.

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Veröffentlicht in:Biochemical pharmacology 1988-05, Vol.37 (9), p.1827-1828
Hauptverfasser: Czyz, M, Piestrzeniewicz, K, Wilmańska, D, Studzian, K, Szmigiero, L, Gniazdowski, M
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container_end_page 1828
container_issue 9
container_start_page 1827
container_title Biochemical pharmacology
container_volume 37
creator Czyz, M
Piestrzeniewicz, K
Wilmańska, D
Studzian, K
Szmigiero, L
Gniazdowski, M
description Photobinding of 8-methoxypsoralen (8-MOP) to DNA leads to mono- and diadduct formation while 4,5'-dimethylangelicin (4,5'-DMA) binds monofunctionally. The effect of the irreversible binding of furocoumarins to DNA on different steps of RNA synthesis has been assayed in this study.
doi_str_mv 10.1016/0006-2952(88)90466-2
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source MEDLINE; Elsevier ScienceDirect Journals Complete
subjects DNA-Directed RNA Polymerases - antagonists & inhibitors
Escherichia coli
Furocoumarins - pharmacology
In Vitro Techniques
Methoxsalen - pharmacology
RNA - biosynthesis
Templates, Genetic
title Effect of 8-methoxypsoralen and 4,5'-dimethylangelicin on ribonucleic acid synthesis in vitro
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