Blunder_2011_Bioorg.Med.Chem.Lett_21_363

Reference

Title : Silanetriols as in vitro inhibitors for AChE - Blunder_2011_Bioorg.Med.Chem.Lett_21_363
Author(s) : Blunder M , Hurkes N , Spirk S , List M , Pietschnig R
Ref : Bioorganic & Medicinal Chemistry Lett , 21 :363 , 2011
Abstract : Three stable silanetriols with increasing steric protection of the silicon atom have been tested for inhibition of acetylcholinesterase (AChE). For all tested silanetriols we found reversible inhibition of the AChE activity at a 100 muM concentration. The highest inhibition rate was found for the sterically least hindered cyclohexylsilanetriol with 45% inhibition relative to galanthamine hydrobromide for which an IC(50) value of 121 +/- 3 muM was determined as well. The cytotoxicity of the silanetriols used was found to be negligible at concentrations relevant for inhibition.
ESTHER : Blunder_2011_Bioorg.Med.Chem.Lett_21_363
PubMedSearch : Blunder_2011_Bioorg.Med.Chem.Lett_21_363
PubMedID: 21111617

Related information

Citations formats

Blunder M, Hurkes N, Spirk S, List M, Pietschnig R (2011)
Silanetriols as in vitro inhibitors for AChE
Bioorganic & Medicinal Chemistry Lett 21 :363

Blunder M, Hurkes N, Spirk S, List M, Pietschnig R (2011)
Bioorganic & Medicinal Chemistry Lett 21 :363