PUMA
Istituto di Biofisica     
Macchia B., Gentili D., Macchia M., Mamone F., Martinelli A., Orlandini E., Rossello A., Cercignani G., Pierotti R., Allegretti M., Asti C., Caselli G. Synthesis, inhibitory activity towards human leukocyte elastase and molecular modelling studies of 1-carbamoyl-4-methyleneaminoxyazetidinones. In: European Journal of Medicinal Chemistry, vol. 35 (1) pp. 53 - 67. Elsevier, 2000.
 
 
Abstract
(English)
Some monocyclic β-lactam derivatives of type 3 (MAOAs) in which the leaving group (LG) on the C(4) is a methyleneaminoxy moiety, were synthesised and tested in vitro and in vivo for their inhibitory activity towards human leukocyte elastase (HLE). Some compounds showed an appreciable in vitro inhibitory activity against this enzyme. Effects on the anti-HLE activity due to the nature of the substituents R and R1 present on their LG were observed and rationalised by means of molecular modelling techniques. The results of in vivo pharmacological tests indicated that MAOAs, while showing an inhibitory activity on the haemorrhage induced by HLE, did not exhibit any effects due to the R and R1 substituents.
DOI: 10.1016/S0223-5234(00)00111-2
Subject Elastase inhibitor
β-lactam monocyclic inhibitor
1-carbamoyl-4-methyleneaminoxyazetidinone derivative
Oxime derivative


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