1289166-87-5Relevant academic research and scientific papers
Acyloxybutadiene iron tricarbonyl complexes as enzyme-triggered CO-releasing molecules (ET-CORMs)
Romanski, Steffen,Kraus, Birgit,Schatzschneider, Ulrich,Neud?rfl, J?rg-Martin,Amslinger, Sabine,Schmalz, Hans-Günther
, p. 2392 - 2396 (2011)
(Chemical Equation Presented) Molecular hazardous materials transport: Enzyme-triggered CO-releasing molecules (ET-CORMs) offer new options for the delivery of CO. The cleavage of dienylester iron tricarbonyl complexes by an esterase under mild oxidative
Acyloxybutadiene tricarbonyl iron complexes as enzyme-triggered CO-releasing molecules (ET-CORMs): A structure-activity relationship study
Romanski, Steffen,Kraus, Birgit,Guttentag, Miguel,Schlundt, Waldemar,Rücker, Hannelore,Adler, Andreas,Neud?rfl, J?rg-Martin,Alberto, Roger,Amslinger, Sabine,Schmalz, Hans-Günther
supporting information, p. 13862 - 13875 (2013/01/15)
A series of η4-acyloxycyclohexadiene-Fe(CO)3 complexes was prepared and fully characterized by spectroscopic methods including single crystal X-ray diffraction. For this purpose a new synthetic access to differently acylated 1,3- and 1,5-dienol-Fe(CO)3 complexes was developed. The enzymatically triggered CO release from these compounds was monitored (detection of CO through GC and/or by means of a myoglobin assay) and the anti-inflammatory effect of the compounds was assessed by a cellular assay based on the inhibition of NO-production by inducible NO synthase (iNOS). It was demonstrated that the properties (rate of esterase-triggered CO release, iNOS inhibition, cytotoxicity) of the complexes strongly depend on the substitution pattern of the π-ligand and the nature of the acyloxy substituent.
