FIELD: chemistry.
SUBSTANCE: invention relates to a novel 2-{4-[(E)-2-(4-ethoxyphenyl)vinyl]phenoxy}-N,N,N-trimethylethanamine bromide, having properties of a surface-active photosensitiser with a structure which enables to alter excitability of heart and neural tissue by blocking ion channels of cells. The compound facilitates selective irreversible blocking of ion channels of only those cells exposed to UV radiation in the presence of said compound. In particular, the compound can be used in pre-clinical studies of antiarrhythmic drugs when creating various novel model systems. The compound has the structural formula
EFFECT: compound has low toxicity.
5 dwg, 1 tbl, 1 ex
Title | Year | Author | Number |
---|---|---|---|
METHOD FOR SYNTHESIS OF 2-CARBOXY-N,N,N-TRIMETHYLETHANAMINIUM DERIVATIVE | 2021 |
|
RU2786884C2 |
METHOD OF PRODUCING DERIVATIVES OF PHENOXYBENZYL-2(4-ALKOXYPHENYL)-2-METHYLPROPYL ETHER | 0 |
|
SU1447275A3 |
HYDROCHLORIDE OF N-(2, 6-DIMETHYLPHENYL)AMIDE OF 2-(β-N,N-DIETHYLAMINE ETYLAMINO)-4-OXO-4-(4-ETHOXYPHENYL)-2-BUTENOIC ACID, HAVING LOCAL ANAESTHETIC ACTIVITY | 2009 |
|
RU2412159C2 |
METHOD OF THE N-ALKYL(PHENYL)-N,N-BIS[4-ALKOXY(PHENOXY-, BENZYLOXY-, PROP-2-YNYLOXY)-2-BUTYNYL]AMINES PREPARATION | 2016 |
|
RU2675505C2 |
METHOD OF PRODUCING 2-(4-HYDROXY-MORPHOLINYL)-2-CYCLOHEXENONE | 2007 |
|
RU2439066C2 |
USE OF N-(2-OXO-6-(3,4,5-TRIMETHOXYPHENYL)-2H-PYRAN-3-YL)BENZAMIDE AS AN ANTI-MICROBIAL AGENT | 2023 |
|
RU2809158C1 |
METHOD OF OBTAINING (±)-(12R*,13AR*,13BS*)-2,3,5,6,12,13,13A,13B- OCTAHYDRO-1H-INDOLO[3,2,1-DE]PYRIDO[3,2,1-IJ]NAPHTHYRIDINE-12-OL | 2023 |
|
RU2815974C1 |
CYCLOBUTYL (S)-2-[[[R)-2-(6-AMINOPURIN-9-YL)-1-METHYL-ETOXY]METHYL-PHENOXY-PHOSPHORYL]AMINO]-PROPANOATES, METHOD OF THEIR PRODUCTION AND APPLICATION | 2017 |
|
RU2647576C1 |
NEW DISPIRO-INDOLINONES, MDM2/p53 INTERACTION INHIBITORS, METHOD FOR PRODUCTION AND APPLICATION | 2015 |
|
RU2629750C2 |
NOVEL HYDROPHILIC DERIVATIVES OF 2-ARYL-4-QUINOLONES AS ANTICANCER AGENTS | 2007 |
|
RU2424245C2 |
Authors
Dates
2014-05-10—Published
2012-12-21—Filed