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THE IN VITRO ANTIOXIDANT PROPERTIES OF 2-ALKOXYPHENYLCARBAMIC ACID DERIVATIVES CONTAINING A 4 '-(SUBSTITUTED PHENYL) PIPERAZIN- 1 '- YL MOIETY DETERMINED BY THE 2,2 '- AZINOBIS(3-ETHYLBENZOTHIAZOLINE-6-SULFONIC ACID) DERIVED RADICAL CATION (ABTS(center dot+)) AND FERRIC REDUCING ANTIOXIDANT POWER (FRAP) ASSAYS

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F62157124%3A16370%2F17%3A43876152" target="_blank" >RIV/62157124:16370/17:43876152 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.14499/indonesianjpharm28iss1pp1" target="_blank" >http://dx.doi.org/10.14499/indonesianjpharm28iss1pp1</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.14499/indonesianjpharm28iss1pp1" target="_blank" >10.14499/indonesianjpharm28iss1pp1</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    THE IN VITRO ANTIOXIDANT PROPERTIES OF 2-ALKOXYPHENYLCARBAMIC ACID DERIVATIVES CONTAINING A 4 '-(SUBSTITUTED PHENYL) PIPERAZIN- 1 '- YL MOIETY DETERMINED BY THE 2,2 '- AZINOBIS(3-ETHYLBENZOTHIAZOLINE-6-SULFONIC ACID) DERIVED RADICAL CATION (ABTS(center dot+)) AND FERRIC REDUCING ANTIOXIDANT POWER (FRAP) ASSAYS

  • Original language description

    In an effort to comprehensively characterize an antioxidant profile of 2-alkoxyphenylcarbamic acid-based compounds containing a 4 &apos;-(substituted phenyl) piperazin-1 &apos;- yl fragment, they were in vitro screened in the 2,2 &apos; -azino-bis(3-ethylbenzothiazoline-6- sulfonic acid) derived radical cation (ABTS(center dot+)) and ferric reducing antioxidant power (FRAP) assay using the UV/VIS spectrophotometry. The ABTS(center dot+) scavenging (reducing) potential of 1-[3-(2-methoxyphenylcarbamoyl) oxy-2- hydroxypropyl]-4-(4-fluorophenyl) piperazin-1-ium chloride was found to be the most promising and it was comparable to the efficiency of the carvedilol reference drug. Moreover, that 4 &apos; - fluoro group-containing compound was regarded as more active than the atenolol standard. When testing the molecules &apos; power to reduce the ferric 2,4,6-tris (2-pyridyl)-s-triazine complex [Fe(III)(TPTZ) 2] (3+), the most prospective was 1-[3-(2-ethoxyphenylcarbamoyl) oxy-2- hydroxypropyl]- 4-( 4-fluorophenyl) piperazin-1-ium chloride. On the other hand, its Fe3+ reducing power was lower compared to both standards carvedilol and atenolol. The study discussed structure-antioxidant properties relationships considering electronic, steric and lipophilic features.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>ost</sub> - Miscellaneous article in a specialist periodical

  • CEP classification

  • OECD FORD branch

    30104 - Pharmacology and pharmacy

Result continuities

  • Project

  • Continuities

    V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Others

  • Publication year

    2017

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Indonesian journal of pharmacy

  • ISSN

    2338-9427

  • e-ISSN

  • Volume of the periodical

    28

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    ID - INDONESIA

  • Number of pages

    9

  • Pages from-to

    1-9

  • UT code for WoS article

    000411629700001

  • EID of the result in the Scopus database