Theoretical study of the scavenging mechanism to 1,4-dicarbonyls by pyridoxamine: The water-assisted reaction-Reference-Cited by-同舟云学术

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Theoretical study of the scavenging mechanism to 1,4-dicarbonyls by pyridoxamine: The water-assisted reaction

Published:2009-10 Issue:1-3 Volume:911 Page:70-74
ISSN:0166-1280
Container-title:Journal of Molecular Structure: THEOCHEM
language:en
Short-container-title:Journal of Molecular Structure: THEOCHEM

Author:

Chen Xin,Qiao Qing-An,Jin Yue-Qing,Jing Jie,Liu Quan-Wen,Sun Li-Xiang,Wang Mei-Shan,Yang Chuan-Lu

Publisher

Elsevier BV

Subject

Physical and Theoretical Chemistry,Condensed Matter Physics,Biochemistry

Reference30 articles.

1. Pyridoxamine: An Extremely Potent Scavenger of 1,4-Dicarbonyls

2. Intermediates in the Paal-Knorr Synthesis of Pyrroles. 4-Oxoaldehydes

3. A Post-Amadori Inhibitor Pyridoxamine Also Inhibits Chemical Modification of Proteins by Scavenging Carbonyl Intermediates of Carbohydrate and Lipid Degradation

4. Pyridoxamine Protects Proteins from Functional Damage by 3-Deoxyglucosone: Mechanism of Action of Pyridoxamine

5. Pyridoxamine Traps Intermediates in Lipid Peroxidation Reactions in Vivo

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