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Furneaux

David Michael Furneaux, Berkshire GB

Patent application numberDescriptionPublished
20100234985BATCH RE-LOAD OF COIN RECYCLER - Replenishing coins in a coin store associated with a coin handling device includes feeding a batch of coins from a bulk coin store to a receptacle near the coin handling device, delivering coins from the receptacle to the coin handling device and routing at least some of those coins from the coin handling device to the coin store associated with the coin handling device.09-16-2010

David Michael Furneaux, Reading GB

Patent application numberDescriptionPublished
20090101469COIN SENSOR - A coin sensor performs time-domain eddy-current testing using an inductance in one arm of a Maxwell bridge which is driven by a bipolar square wave having randomly-selected intervals between transitions, the output of the bridge being sampled at a high frequency. A processor stores a model which receives the drive signal and adjusts coefficients of the model so that the output matches the sampled measurements. Acceptance criteria are applied to the adjusted coefficients for coin classification purposes.04-23-2009

Richard Hubert Furneaux, Wellington NZ

Patent application numberDescriptionPublished
20090233948Inhibitors of nucleoside phosphorylases and nucleosidases - The present invention relates to compounds of the general formula (I) which are inhibitors of purine nucleoside phosphorylases (PNP), purine phosphoribosyltransferases (PPRT), 5′-methylthioadenosine phosphorylases (MTAP), 5′-methylthioadenosine nucleosidases (MTAN) and/or nucleoside hydrolases (NH). The invention also relates to the use of these compounds in the treatment of diseases and infections including cancer, bacterial infections, protozoal infections, and T-cell mediated disease and to pharmaceutical compositions containing the compounds.09-17-2009
20090325986Deazapurine Analogs of 1'-Aza-L-Nucleosides - The invention relates to compounds of the formula (I), which are L-enantiomeric forms of nucleoside analogues, and to pharmaceutical compositions containing the compounds, methods of treating certain diseases, including cancer, bacterial infection, parasitic infection, and T-cell mediated diseases, using the compounds, processes for preparing the compounds, and intermediates useful in the preparation of the compounds.12-31-2009
20100168141AZETIDINE ANALOGUES NUCLEOSIDASE AND PHOSPHORYLASE INHIBITORS - Azetidine analogues of nucleosidase and nucleoside phosphorylase inhibitors having the general formula (I), the use of these compounds as pharmaceuticals, pharmaceutical compositions containing the compounds, methods of treating certain diseases using the compounds, processes for preparing the compounds, and intermediates useful in the preparation of the compounds wherein W and X are each independently selected from hydrogen, CH07-01-2010
20110046167ACYCLIC AMINE INHIBITORS OF 5-METHYTIOADENOSINE PHOSPHORYLASE AND NUCLEOSIDASE - The present invention relates to compounds of the general formula (I) which are inhibitors of 5′-methylthioadenosine phosphorylase or 5′-methylthioadenosine nucleosidase. The invention also relates to the use of these compounds in the treatment of diseases or conditions in which it is desirable to inhibit 5′-methylthioadenosine phosphorylase or 5′-methylthioadenosine nucleosidase including cancer, and to pharmaceutical compositions containing the compounds.02-24-2011
20110092521Methods of Treating Diseases Using Inhibitors of Nucleoside Phosphorylases and Nucleosidases - The invention relates to treating a disease or condition in which it is desirable to inhibit 5′-methylthioadenosine phosphorylase (MTAP) and/or 5′-methylthioadenosine nucleosidase (MTAN). The invention particularly relates to the co-administration of 5′-methylthioadenosine (MTA), or a prodrug of MTA, with one or more MTAP/MTAN inhibitors. Included among the diseases treatable are prostate cancer and head and neck cancer.04-21-2011
20110130412Acyclic amine inhibitors of nucleoside phosphorylases and hydrolases - The invention relates to compounds of the general formula (I) which are inhibitors of purine nucleoside phosphorylases (PNPs) and/or nucleoside hydrolases (NHs). The invention also relates to the use of these compounds in the treatment of diseases and infections including cancer, bacterial infections, protozoal infections, and T-cell mediated disease and to pharmaceutical compositions containing the compounds.06-02-2011

Patent applications by Richard Hubert Furneaux, Wellington NZ