posted on 2013-07-08, 00:00authored bySvetlana Botov, Eleni Stamellou, Steffen Romanski, Miguel Guttentag, Roger Alberto, Jörg-Martin Neudörfl, Benito Yard, Hans-Günther Schmalz
Novel
η4-acyloxy-cyclohexadiene-Fe(CO)3 complexes
(with variable length of the acyloxy chain) were synthesized as potential
enzyme-triggered carbon monoxide (CO)-releasing molecules (ET-CORMs).
The molecular structure of two complexes was additionally confirmed
by X-ray crystallography. The enzyme-triggered CO-releasing activity
of the compounds was assessed under physiological conditions (37 °C,
0.1 M phosphate buffer, pH = 7.4) by headspace gas chromatography
(GC) and additionally by means of a myoglobin assay (UV). The relative
rate of CO release and the amount of liberated CO were found to depend
on the length of the acyloxy chain and its position at the diene unit
(outer or inner position). Some of the new ET-CORMs exhibited very
good biological activity as assessed in different cellular assays
(cytotoxicity, protective effect against hypothermia-associated cell
damage, and inhibition of TNF-α-mediated VCAM-1 expression).