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| Number | Title | Issue Date |
| 7081436 | Paste formulation for seed treatment of plants Disclosed herein is a composition comprising a seed treatment formulation and an organosilicone additive of the formula: wherein: X is a number from 0 to 30; Y ... | 07/25/2006 |
| 6916347 | Primary intermediates for oxidative coloration of hair Primary intermediates for hair coloring compositions for oxidative dyeing of hair are compounds of the formula (1): where R1 and R2 are each individually selected from a hydrogen atom, a C1 | 07/12/2005 |
| 6849733 | Neuropeptide-Y ligands There are disclosed novel neuropeptide Y ligands having the general formula I Wherein the symbols W, A, D, R1, R2, R3, R4 are further defined in the description. Compounds of... | 02/01/2005 |
| 6750355 | Primary intermediates for oxidative coloration of hair Primary intermediates for hair coloring compositions for oxidative dyeing of hair are compounds of the formula (1): where R1 and R2 are each individually selected from a hydrogen atom, a C1 | 06/15/2004 |
| 6673932 | Primary intermediates for oxidative coloration of hair Primary intermediates for hair coloring compositions for oxidative dyeing of hair are compounds of the formula (1): ##STR1## wherein R is hydrogen, hydroxy, nitro, amino, halogen, C1 to C5 alkyl or haloalkyl, C1 to C5... | 01/06/2004 |
| 6635650 | Substituted dimeric compounds The invention relates to compounds of formula (I): wherein: A represents NR1 C(Q)R2, C(Q)NR2 R3 or NR1 C(Q)NR2 R3, B represents NR1 C(Q)R2, C(Q)NR2... | 10/21/2003 |
| 6593479 | Coating composition comprising a bicyclo- or spiro-orthoester functional compound The invention pertains to a coating composition comprising a first compound comprising at least one bicyclo- or spiro-orthoester group and a second compound comprising at least two hydroxyl-reactive groups. The invention also comprises a process for curin... | 07/15/2003 |
| 6376468 | Protein:prenyl transferase inhibitors The invention pertains to novel peptide analogs suitable for inhibiting protein:prenyl transferases. As such they are therapeutically useful in e.g. inhibiting oncogenesis and other unwanted cell proliferation, and in supressing aberrant high signal trans... | 04/23/2002 |
| 6310245 | 3-aminocarbonyl/3-aminothiocarbonyl-substituted 2-benzoyl-cyclohexan-1,3-diones with herbicidal effect The invention relates to 2-benzoylcyclohexane-1,3-diones of the formula I ##STR1## where R1, R2 are hydrogen, nitro, halogen, cyano, thiocyanato, alkyl, haloalkyl, alkoxyalkyl, alkenyl, alkynyl, --OR5, --OCOR6, ... | 10/30/2001 |
| 6307067 | Palladium and boron co-catalyzed addition of oxygen nucleophiles to vinyl epoxides Nucleophilic oxygen species, such as primary alcohols, carboxylates, and water, are added to vinyl epoxides in a highly regioselective and enantioselective manner, providing a convenient route to enantiomerically enriched 1,2-diols and oxygen-containing h... | 10/23/2001 |
| 6040339 | Urea derivatives having ACAT inhibitory activity, their preparation and their therapeutic and prophylactic use Compounds of formula (I): ##STR1## wherein: R1 is alkyl; R2a, R2b, R2c and R2d are the same or different and each is hydrogen, optionally substituted alkyl or various other organic groups; R... | 03/21/2000 |
| 6034087 | Nucleoside derivatives and process for preparing thereof Nucleoside derivatives represented by formula (I); ##STR1## wherein, R1 represents hydrogen, phosphate or phosphonate group, R2 represents substituted or unsubstituted pyrimidine or purine base, and Z represents S, SO, SO2 | 03/07/2000 |
| 5916914 | Compounds and method of treating psychosis and schizophrenia This invention relates to compounds that are antagonists of dopamine D4 receptors, and to methods of treating psychosis and schizophrenia using a compound that is an antagonist of dopamine D4 receptors.... | 06/29/1999 |
| 5914351 | Anti-viral aromatic hydrazones Compounds of the formula ##STR1## wherein Q is a hydrazone derivative; R1 is hydrogen, halogen, alkyl or alkoxy; R2 is hydrogen, halogen, alkyl, alkoxy, alkenoxy, alkynyloxy, halomethyl, trifluoromethoxy, alkylthio, nitro or cyano; a... | 06/22/1999 |
| 5880147 | Amide derivatives having ACAT inhibitory activity, their preparation and their therapeutic and prohylactic use Compounds of formula (I): ##STR1## wherein: R1 is alkyl; R2a, R2b, R2c and R2d are the same or different and each is hydrogen, optionally substituted alkyl, --(C.dbd.O)--B1 (wherein B | 03/09/1999 |
| 5856529 | Benzofuran and dihydrobenzofuran melatonergic agents Novel derivatives of benzofuran and dihydrobenzofuran are provided which are useful as melatonergic agents.... | 01/05/1999 |
| 5756772 | Reducing polyethercyclicpolyol metal adhesion Reduction of the adhesion of polyethercyclicpolyol (PECP) to metals by preparing the PECP by condensing polyol molecules by reactive distillation and replacing part of the polyol with an alcohol of lower hydroxyl content than the polyol.... | 05/26/1998 |
| 5756639 | Copolymerization of polyetherpolyols with epoxy resins A method for producing an epoxy polyetherpolyol having 15 to 75 wt. % epoxy comprising heating a polyol and catalyst to initiate condensation, removing water, introducing sufficient epoxy into the reaction mixture to give 15 to 75 wt. % epoxy in the produ... | 05/26/1998 |
| 5718845 | Tricyanovinyl substitution process for NLO polymers Nonlinear optical compounds which contain a heteroaromatic ring and may further comprise a tricyanovinyl group attached to the heteroaromatic ring.... | 02/17/1998 |
| 5693827 | Treatment of HIV infections and compounds useful therein A method of inhibiting the growth or replication of viruses of the HIV group is disclosed. Also disclosed are compounds useful in the method and pharmaceutical formulations incorporating such compounds. The method involves the use of compounds having the ... | 12/02/1997 |
| 5674894 | Amidine derivatives useful as platelet aggregation inhibitors and vasodilators The current invention discloses novel amidine derivatives with nitric oxide donating property that can inhibit platelet aggregation and promote vasodilation in a single compound.... | 10/07/1997 |
| 5675022 | Recovery of dioxanone by melt crystallization Processes are disclosed for the recovery of 1,4-dioxanone by melt crystallization from a feed containing impurities capable of initiating the polymerization of 1,4-dioxanone, e.g., diethylene glycol. The processes of the present invention utilize melt cry... | 10/07/1997 |
| 5656656 | Tartronic acids, their acetalic ethers and O-esters Tartronic acid acetalic ethers and esters of the general formula: ##STR1## are provided and are useful in treatment of bone dysmetabolism. As examples, Ra and Rb may be hydrogen, B is a C2 -C12 acyl group, R is phenyl and n is 0... | 08/12/1997 |
| 5604256 | Octahydronaphthalene oxime derivatives for cholesterol biosynthesis inhibition Compounds of formula (I): ##STR1## (in which: R is hydrogen, methyl or hydroxy; X is alkyl, alkenyl, cycloalkyl, aryl, aralkyl, or a heterocyclic group; A is a single bond, or an alkylene, alkenylene, alkynylene or alkadienylene group; Y is hydrogen,... | 02/18/1997 |
| 5550280 | Hindered aromatic ester compounds useful as anti-viral agents Compounds of the formula ##STR1## wherein X is O or S; Y is O or S; R1 is hydrogen, halogen, C1 -C4 alkyl or C1 -C4 alkoxy; R2 is hydrogen, halogen, C1 -C4 alkyl, C | 08/27/1996 |
| 5514642 | Cyclohexenone oxime ethers, their preparation and their use Cyclohexenone oxime ethers of the formula I ##STR1##... | 05/07/1996 |
| 5502219 | Low calorie substitute for an edible oil A polyglycerol composition of the formula ##STR1## wherein R may be ##STR2## C comprises up to about 3 percent of all N+M units, and N+M is a number from about 3 to about 15, and wherein the polyglycerol is essentially free of low molecular... | 03/26/1996 |
| 5428178 | Polyethercyclipolyols from epihalohydrins, polyhydric alcohols, and metal hydroxides or epoxy alcohols and optionally polyhydric alcohols with thermal condensation Method for preparing polyethercyclicpolyol by heating alkali and/or alkaline earth hydroxide optionally with polyol, its precursors or derivatives, admixing epoxy alcohol or epihalohydrin therewith to initiate an addition reaction, and thermally condensin... | 06/27/1995 |
| 5412115 | Polycondensation of phenolic hydroxyl-containing compounds and polyhydric alcohols and thermal condensation to form polyethercyclicpolyols Polyethercyclicpolyols are prepared by thermally condensing a polyol having at least three hydroxyl groups of which at least two of the hydroxyl groups are vicinal, precursors of the polyol, cyclic derivatives of the polyol, or mixtures thereof, and contr... | 05/02/1995 |
| 5405968 | Polyketomethine dyes Methine dyes with a polyketo group I ##STR1## where A is ##STR2## R1 is a 5- or 6-membered cycloaliphatic radical which contains one or two hetero atoms from the group --NR4 --, --O-- and --S-- and which may be fused t... | 04/11/1995 |
| 5401860 | Copolymerization of polyethercyclicpolyols with epoxy resins Polyethercyclicpolyols are prepared by thermally condensing a polyol having at least three hydroxyl groups of which at least two of the hydroxyl groups are vicinal, precursors of the polyol, cyclic derivatives of the polyol, or mixtures thereof, and contr... | 03/28/1995 |
| 5399371 | Low calorie substitute for an edible oil A polyglycerol composition of the formula ##STR1## wherein R may be ##STR2## C comprises up to about 3 percent of all N+M units, and N+M is a number from about 3 to about 15, and wherein the polyglycerol is essentially free of low molecular... | 03/21/1995 |
| 5371243 | Polyethercyclicpolyols from epihalohydrins, polyhydric alcohols, and metal hydroxides Method for preparing polyethercyclicpolyol by heating a reaction mixture of an alkali or alkaline earth metal hydroxide with a polyol, adding epihalohydrin to initiate an addition reaction, and heating the mixture until the reaction is complete.... | 12/06/1994 |
| 5371244 | Polycondensation of dihydric alcohols and polyhydric alcohols and thermal condensation to form polyethercyclicpolyols Polyethercyclicpolyols are prepared by thermally condensing a polyol having at least three hydroxyl groups of which at least two of the hydroxyl groups are vicinal, precursors of the polyol, cyclic derivatives of the polyol, or mixtures thereof, and contr... | 12/06/1994 |
| 5367089 | Polyethercyclicpolyols from epihalohydrins, polyhydric alcohols and metal hydroxides or epoxy alcohol and optionally polyhydric alcohols with addition of epoxy resins Method for preparing polyethercyclicpolyol by heating an alkali or alkaline earth metal hydroxide with a polyol and epihalohydrin or epoxy alcohol to initiate an addition reaction, and adding epoxy resin to the addition reaction mixture prior to the addit... | 11/22/1994 |
| 5338870 | Thermal condensation of polyhydric alcohols to form polyethercyclicpolyols Polyethercyclicpolyols are prepared by thermally condensing a polyol having at least three hydroxyl groups of which at least two of the hydroxyl groups are vicinal, precursors of the polyol, cyclic derivatives of the polyol, or mixtures thereof, and contr... | 08/16/1994 |
| 5302728 | Polycondensation of phenolic hydroxyl-containing compounds and polyhydric alcohols and thermal condensation to form polyethercyclipolyols Polyethercyclicpolyols are prepared by thermally condensing a polyol having at least three hydroxyl groups of which at least two of the hydroxyl groups are vicinal, precursors of the polyol, cyclic derivatives of the polyol, or mixtures thereof, and contr... | 04/12/1994 |
| 5292961 | Process for the preparation of halogenated polyethers Process for the preparation of halogenated polyethers of the general formula: ##STR1## wherein X=Cl or F, RF and R'F either equal to or different from each other, are selected from fluorinated alkyl radicals with from 1 to 20 ... | 03/08/1994 |
| 5286882 | Polyethercyclicpolyols from epihalohydrins, polyhydric alcohols and metal hydroxides or epoxy alcohol and optionally polyhydric alcohols with addition of epoxy resins Method for preparing polyethercyclicpolyol by heating an alkali or alkaline earth metal hydroxide with a polyol and epihalohydrin or epoxy alcohol to initiate an addition reaction, and adding epoxy resin to the addition reaction mixture prior to the addit... | 02/15/1994 |
| 5266708 | New intermediates, process for their preparation, and their use for the synthesis of vitamins A and E New intermediates and processes for the preparation of vitamins A and E, which are the acetals of 5,6-dihalo-3-methyl-3-hydroxyhexanal or of 6-halo-3-hydroxy-3-methyl-5-hexenal or 3-methyl-3-hydroxy-5-hexenal, as well as processes for making the intermedi... | 11/30/1993 |
