A pulse radiolysis study of one-electron oxidation and .OH radical reaction of a new class of antioxidants: 2,5 dimethylpyrrole—amino acid N-conjugates
Author:
Publisher
Elsevier BV
Subject
Physiology (medical),Biochemistry
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1. A Highly Efficient Paal-Knorr Synthesis of Chiral Pyrrole Derivatives Catalyzed by MgI2;Chinese Journal of Organic Chemistry;2016
2. Evaluation of the anti-inflammatory and anti-nociceptive activities of novel synthesized melatonin analogues;European Journal of Medicinal Chemistry;2007-10
3. N-conjugates of 2,5-disubstituted pyrrole and glutathione evaluation of their potency as antioxidants against photosensitization of NCTC 2544 keratinocytes by excess endogenous protoporphyrin IX;Journal of Photochemistry and Photobiology B: Biology;1997-05
4. Amino acid-pyrrole N-conjugates; a new class of antioxidants II. Effectiveness of singlet oxygen quenching by luminescence measurements;Journal of Photochemistry and Photobiology B: Biology;1995-10
5. Glutathione Peroxidase and Glutathione Reductase Activities toward Glutathione-Derived Antioxidants;Biochemical and Biophysical Research Communications;1994-09
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