2010
DOI: 10.1016/j.jtemb.2009.09.002
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Superoxidedismutase-mimetic copper(II) complexes containing saccharinate and 4-aminopyridine/4-cyanopyridine

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Cited by 5 publications
(2 citation statements)
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“…13, it can be seen that the poor antioxidant capacities of the sartans were improved by complexation (IC 50 [1] =6.8×10 −6 M and IC 50 [2] = 3.7× 10 −6 M). The prepared mimetic complexes were not as effective as the enzyme (bovine erythrocyte SOD, IC 50 = 2.1× 10 −7 M) [41] but it has been previously determined that when the experimental IC 50 values occurred below 20 ×10 −6 M the compounds are considered to act as strong SOD mimics [42].…”
Section: Antioxidant Activitiesmentioning
confidence: 94%
“…13, it can be seen that the poor antioxidant capacities of the sartans were improved by complexation (IC 50 [1] =6.8×10 −6 M and IC 50 [2] = 3.7× 10 −6 M). The prepared mimetic complexes were not as effective as the enzyme (bovine erythrocyte SOD, IC 50 = 2.1× 10 −7 M) [41] but it has been previously determined that when the experimental IC 50 values occurred below 20 ×10 −6 M the compounds are considered to act as strong SOD mimics [42].…”
Section: Antioxidant Activitiesmentioning
confidence: 94%
“…Many complexes of copper(II) have similar to SOD ability to neutralize superoxides ( 14 – 27 ). These SOD-mimicking complexes of copper were proposed as non-analgesic anti-inflammatory drugs by various authors: Cu complexes of aromatic acids ( 14 – 16 ) (Suksrichavalit et al 2008), saccharinate and pyridine derivates ( 17 – 18 ) (Ferrer et al 2010), tolfenamic acid ( 19 ) (Kovala-Demertzi et al 2004), 2-amino-2-thiazoline and polyamines ( 20 – 25 ) (Pontiki et al 2006), o-vanillin ( 26 ) (González-Baró et al 2010), oxaprozinate ( 27 ) (Dutta et al 2004). …”
Section: Biological Activity Of Complexes Of Stable Copper Isotopesmentioning
confidence: 99%