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Axt

Alexandra Axt, Rossdorf DE

Patent application numberDescriptionPublished
20080319015Insect Repellent Mixture - The present invention relates to the use of an insect repellent, preferably selected from the group 2-(2-hydroxyethyl)-1-methylpropyl 1-piperidinecarboxylate, N,N-diethyl-3-methylbenzamide, dimethyl phthalate, butopyronoxyl, 2,3,4,5-bis(2-butylene)-tetrahydro-2-furaldehyde, N,N-diethylcaprylamide, N,N-diethylbenzamide, o-chloro-N,N-diethylbenzamide, dimethyl carbate, di-n-propyl isocinchomeronate, 2-ethylhexane-1,3-diol, N-octylbicycloheptenedicarboximide or piperonyl butoxide, particularly preferably 2-(2-hydroxyethyl)-1-methylpropyl 1-piperidinecarboxylate, as action enhancer for a second insect repellent, to corresponding compositions, and to the preparation thereof.12-25-2008

Jakob Axt, Saulheim DE

Patent application numberDescriptionPublished
20100070890Method for Providing a Manufacturing Execution System (MES) Service to Third Parties - A computer-implemented method for providing on-demand manufacturing execution systems for clients in which a response to a questionnaire from a client with information relative to identification of a business and production process, a determination of process steps, and an identification of process step requirements is evaluated by the service provider according to GUI requirements for each one of a number of individual process steps. Based on the evaluation, a GUI is defined for each of the individual process steps by the service provider and provided to the client for installation on client computing devices in a manufacturing line of the client. Data is collected for each of the individual process steps via each GUI and sent to the service provider for storage and evaluation.03-18-2010

Sabine Axt, Sunnyvale, CA US

Patent application numberDescriptionPublished
20090149465AMINOTETRALIN COMPOUNDS AS MU OPIOID RECEPTOR ANTAGONISTS - The invention provides aminotetralin compounds of formula (I):06-11-2009
20090247627AMINO- AND AMIDO-AMINOTETRALIN DERIVATIVES AND RELATED COMPOUNDS AS MU OPIOID RECEPTOR ANTAGONISTS - The invention provides amino- and amido-aminotetralin compounds of formula (I):10-01-2009
20090253787SHORT-ACTING SEDATIVE HYPNOTIC AGENTS FOR ANESTHESIA AND SEDATION - The invention provides compounds compositions and methods useful for inducing or maintaining general anesthesia or sedation in mammals.10-08-2009
20100021395CRYSTALLINE FORMS OF A BIPHENYL COMPOUND - The invention provides crystalline forms of biphenyl-2-ylcarbamic acid 1-(2-{[4-(4-carbamoylpiperidin-1-ylmethyl)benzoyl]methylamino}ethyl)piperidin-4-yl ester, and pharmaceutically acceptable solvates thereof. The crystalline form can be a freebase, or a salt such as a diphosphate, monosulfate or dioxalate salt. The invention also provides pharmaceutical compositions comprising these crystalline compounds or prepared using these compounds; processes and intermediates for preparing the crystalline compounds; and methods of using these compounds to treat a pulmonary disorder.01-28-2010
20100048622CRYSTALLINE FORMS OF A BIPHENYL COMPOUND - The invention provides crystalline forms of biphenyl-2-ylcarbamic acid 1-(2-{[4-(4-carbamoylpiperidin-1-ylmethyl)benzoyl]methylamino}ethyl)piperidin-4-yl ester, and pharmaceutically acceptable solvates thereof. The crystalline form can be a freebase, or a salt such as a diphosphate, monosulfate or dioxalate salt. The invention also provides pharmaceutical compositions comprising these crystalline compounds or prepared using these compounds; processes and intermediates for preparing the crystalline compounds; and methods of using these compounds to treat a pulmonary disorder.02-25-2010

Patent applications by Sabine Axt, Sunnyvale, CA US

Steven D. Axt, Menlo Park, CA US

Patent application numberDescriptionPublished
20100056770PREPARATION OF NUCLEOSIDES RIBOFURANOSYL PYRIMIDINES - The present process provides an improved method for the preparation of 4-amino-1-((2R,3R,4R,5R)-3-fluoro-4-hydroxy-5-hydrox-ymethyl-3-methyl-tetrahydro-furan-2-yl)-1H-pyrimidin-2-one of the formula (IV) which is a potent inhibitor of Hepatitis C Virus (HCV) NS5B polymerase.03-04-2010