2006
DOI: 10.1016/j.bmc.2006.05.042
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Synthesis, pulse radiolysis, and in vitro radioprotection studies of melatoninolipoamide, a novel conjugate of melatonin and α-lipoic acid

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Cited by 33 publications
(13 citation statements)
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“…This compound named melatoninolipoamide was used to carry out pulse radiolysis study. The results indicate that melatonin moiety of the conjugate reacts preferably with oxidizing radicals, and the lipoic acid moiety exhibits preferential reaction with reducing radicals [71]. Thus, our rationale behind the choice of melatonin and ALA was essentially to quench all forms of free radicals leading to overall protection of myocardium.…”
Section: Resultsmentioning
confidence: 96%
“…This compound named melatoninolipoamide was used to carry out pulse radiolysis study. The results indicate that melatonin moiety of the conjugate reacts preferably with oxidizing radicals, and the lipoic acid moiety exhibits preferential reaction with reducing radicals [71]. Thus, our rationale behind the choice of melatonin and ALA was essentially to quench all forms of free radicals leading to overall protection of myocardium.…”
Section: Resultsmentioning
confidence: 96%
“…It was found that the melatonin moiety of the conjugate reacts preferably with oxidizing radicals and the LA moiety exhibits preferential reaction with reducing radical. Using c-radiation induced lipid peroxidation in liposomes and hemolysis of erythrocytes as a model, the radioprotection ability was compared with those of melatonin and LA and the results suggest that the conjugate can be explored as a probable radioprotector [97].…”
Section: Antioxidant Defensementioning
confidence: 99%
“…The conjugate was named melatoninolipoamide [97]. It was found that the melatonin moiety of the conjugate reacts preferably with oxidizing radicals and the LA moiety exhibits preferential reaction with reducing radical.…”
Section: Antioxidant Defensementioning
confidence: 99%
“…3 Using this approach, several research groups have recently designed and synthesized hybrid molecules by coupling LA with other bioactive molecules. These efforts resulted in new molecules with antioxidant activity hyphenated with a wide variety of other activities such as: protection against reperfusion arrhythmias, 4,5 nitric oxide synthase inhibition, 6 erythrocyte protection from hemolysis, 7 antiproliferative activity, 8,9 acetylcholinesterase inhibition, 10 butyrylcholinesterase inhibition, 11 as well as radioprotective, 12 and anti-inflammatory activity. 13,14 Moreover, combination of 1,2-dithiolane-3-alkyl group with the catechol moiety through five-membered heterocyclic rings, as bioisosters, 15 of the amide bond led to compounds which exhibited strong neuroprotective activity.…”
Section: Introductionmentioning
confidence: 99%