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Phenol group in pyridoxamine acts as a stabilizing element for its carbinolamines and Schiff bases.
Chem Biodivers. 2011 Jul;8(7):1318-32. doi: 10.1002/cbdv.201000296.
Chem Biodivers. 2011.
PMID: 21766453
Understanding non-enzymatic aminophospholipid glycation and its inhibition. Polar head features affect the kinetics of Schiff base formation.
Caldés C, Vilanova B, Adrover M, Muñoz F, Donoso J.
Caldés C, et al.
Bioorg Med Chem. 2011 Aug 1;19(15):4536-43. doi: 10.1016/j.bmc.2011.06.018. Epub 2011 Jun 16.
Bioorg Med Chem. 2011.
PMID: 21719301
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Formation of Schiff bases of O-phosphorylethanolamine and O-phospho-D,L-serine with pyridoxal 5'-phosphate. experimental and theoretical studies.
Vilanova B, Gallardo JM, Caldés C, Adrover M, Ortega-Castro J, Muñoz F, Donoso J.
Vilanova B, et al. Among authors: caldes c.
J Phys Chem A. 2012 Mar 1;116(8):1897-905. doi: 10.1021/jp2116033. Epub 2012 Feb 14.
J Phys Chem A. 2012.
PMID: 22280506
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The hydrophobic substituent in aminophospholipids affects the formation kinetics of their Schiff bases.
Caldés C, Vilanova B, Adrover M, Donoso J, Muñoz F.
Caldés C, et al.
Bioorg Med Chem Lett. 2013 Apr 1;23(7):2202-6. doi: 10.1016/j.bmcl.2013.01.100. Epub 2013 Feb 4.
Bioorg Med Chem Lett. 2013.
PMID: 23462644
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Basic cancer research: why it is essential for the future of cancer therapy.
Yarden Y, Caldes C.
Yarden Y, et al. Among authors: caldes c.
Bull Cancer. 2014 Sep;101(9):E25-6. doi: 10.1684/bdc.2014.2024.
Bull Cancer. 2014.
PMID: 25295602
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