2008
DOI: 10.1016/j.jinorgbio.2008.01.022
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis and antioxidative activity of metalloporphyrins bearing 2,6-di-tert-butylphenol pendants

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
13
0
2

Year Published

2010
2010
2021
2021

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 38 publications
(15 citation statements)
references
References 39 publications
0
13
0
2
Order By: Relevance
“…CH 3 CN was purified and dried by a known procedure. [6] The concentration of the compounds was 1 mM. For the reaction of these porphyrins with DPPH the concentration ratio was 1:1 (C 0 = 0.1 mM) by measuring CVA curves in certain intervals of time (10 s, 30 s, 1, 3, 5 and 10 min) during 1 h. The compounds under investigation were obtained by procedures described in our previous work.…”
mentioning
confidence: 99%
“…CH 3 CN was purified and dried by a known procedure. [6] The concentration of the compounds was 1 mM. For the reaction of these porphyrins with DPPH the concentration ratio was 1:1 (C 0 = 0.1 mM) by measuring CVA curves in certain intervals of time (10 s, 30 s, 1, 3, 5 and 10 min) during 1 h. The compounds under investigation were obtained by procedures described in our previous work.…”
mentioning
confidence: 99%
“…The in vivo study has been performed for the most active compounds using fish (Asipenser gueldenstaedti B.) and Wistar rats [26][27][28][29][30][31][32][33][34][35][36][37][38][39][40][41][42].…”
Section: Metal Complexes Based On 26-di-tert-butylphenolsmentioning
confidence: 99%
“…In this respect the combination of alkyl phenol units with porphyrin macrocycle is rather promising. [1][2][3][4][5] Introduction of several sterically hindered phenol fragments to the periphery of the porphyrin macrocycle can lead to increased antioxidant activity, due to inhibition activity of phenolic moieties in respect to free radicals, and ability of the porphyrin itself to interact with free radicals and oxygen. [6][7] It is known that isobornylphenols possess membrane-protecting properties [8] and can be used as bio-and technical antioxidants.…”
Section: Introductionmentioning
confidence: 99%