A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
Stability of the Phosphotriester PDE6D Inhibitors
Tekijät: Rosenqvist Petja, Sabt Ahmed, Dyunyasheva Venera, Abankwa Daniel, Virta Pasi, Ora Mikko
Kustantaja: WILEY-V C H VERLAG GMBH
Julkaisuvuosi: 2021
Journal: ChemistrySelect
Tietokannassa oleva lehden nimi: CHEMISTRYSELECT
Lehden akronyymi: CHEMISTRYSELECT
Vuosikerta: 6
Numero: 3
Aloitussivu: 488
Lopetussivu: 493
Sivujen määrä: 6
ISSN: 2365-6549
eISSN: 2365-6549
DOI: https://doi.org/10.1002/slct.202004426
Tiivistelmä
The kinetics for the cleavage of the phosphotriester PDE6D inhibitors 1 (Deltaflexin-2) and 3 (Deltaflexin-1) and their derivatives 2, 4 and 5 is presented under various conditions in aqueous solutions. The conversion of the phosphotriesters (1-5) into the phosphodiesters 1**-5** was detected to take place as a major degradation process. In the absence of enzyme, the 4-acetylthio-2,2-dimethyl-3-oxobutyl protected compounds (1, 4 and 5) are one order of magnitude more stable than the 4-acetylthio-2-ethoxycarbonyl-3-oxo-2-methylbutyl protected ones (2 and 3). In cell culture (DMEM) containing fetal bovine serum and l-glutamine, an intermediary formation of S-S-dimer competed with the removal of the protecting group after deacetylation of the starting material. In addition, the susceptibility of the compounds to amine nucleophiles as well as their stability under acidic and basic condition were determined in non-aqueous solutions.
The kinetics for the cleavage of the phosphotriester PDE6D inhibitors 1 (Deltaflexin-2) and 3 (Deltaflexin-1) and their derivatives 2, 4 and 5 is presented under various conditions in aqueous solutions. The conversion of the phosphotriesters (1-5) into the phosphodiesters 1**-5** was detected to take place as a major degradation process. In the absence of enzyme, the 4-acetylthio-2,2-dimethyl-3-oxobutyl protected compounds (1, 4 and 5) are one order of magnitude more stable than the 4-acetylthio-2-ethoxycarbonyl-3-oxo-2-methylbutyl protected ones (2 and 3). In cell culture (DMEM) containing fetal bovine serum and l-glutamine, an intermediary formation of S-S-dimer competed with the removal of the protecting group after deacetylation of the starting material. In addition, the susceptibility of the compounds to amine nucleophiles as well as their stability under acidic and basic condition were determined in non-aqueous solutions.
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