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Dining Table Having Integral Dishwasher
A space-saving dishwasher, which may be installed within a counter top or table, having a dish-carrying rack that is vertically shiftable through the open top of the dishwasher for facilitating loading and unloading of the dishes.
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| Number | Title | Issue Date |
| 8026374 | Process for preparing (meth)acrylic esters of N-hydroxyalkylated imidazoles A process for preparing (meth)acrylic esters (F) of N-hydroxyalkylated imidazoles, wherein N-hydroxyalkylated imidazoles (I), in which R1 and R2 may each independently be hydrogen or C | 09/27/2011 |
| 7312350 | Process for preparing arylalkynes The invention relates to a process for preparing arylvinyl halides and sulphonates and arylalkynes by reacting haloaromatics or aryl sulphonates with vinyl halides or sulphonates in the presence of a palladium catalyst and a base and, if appropriate, subsequent elim... | 12/25/2007 |
| 7250434 | CCK-1 receptor modulators Certain imidazole compounds are CCK1 modulators useful in the treatment of CCK1 mediated diseases. ... | 07/31/2007 |
| 7247732 | Method for producing optically active compound The present invention provides a method for producing an optically active β-hydroxy ester compound represented by the general formula: wherein R1 represents an optionally substituted hydrocarb... | 07/24/2007 |
| 7223871 | Process for preparing substituted imidazole derivatives and intermediates used in the process The invention relates to a process for preparing substituted imidazole derivatives of formula (I) and acid addition salts thereof in which formula Y is —CH2— or —CO—, R1 is H, halo o... | 05/29/2007 |
| RE39634 | Bisarylimidazoly fatty acid amide hydrolase inhibitors The present invention relates to bisarylimidazolyl derivatives and pharmaceutical compositions comprising said compounds inhibiting fatty acid amide hydrolase and useful for the treatment of pain, particularly neuropathic pain, psychomotor disorder, hypertension, ca... | 05/15/2007 |
| 7183370 | Phosphonic-acid grafted hybrid inorganic-organic proton electrolyte membranes (PEMs) A proton conducting polymer is formed by the copolymerization of a plurality of compounds, including a silicon compound comprising an organic chain, and a compound including at least one acid group. The polymer comprises a hybrid organic-inorganic matrix having acid... | 02/27/2007 |
| 7125725 | Biaryl-type compounds, CD color fixing agent and method for determination of absolute configuration A novel achiral biaryl-type compound and a circular dichroism(CD) color fixing agent are provided. Furthermore, a method for determining an absolute configuration of a chiral compound is carried out by introducing the above achiral biaryl-type compound into the chir... | 10/24/2006 |
| 7102012 | Process for preparing N,N'-carbonyldiazoles A process is provided for preparing N,N′-carbonyldiazoles by reacting azoles with phosgene in halogenated aliphatic hydrocarbon solvents, the entirety of the azole for reaction being introduced in the solvent, followed by the addition of phosgene. ... | 09/05/2006 |
| 7084278 | Process for production of optically active compounds The present invention provides a method for producing an optically active β-hydroxy ester compound represented by the general formula: wherein R1 represents an optio... | 08/01/2006 |
| 7026357 | Diphenylurea compounds Compound of formula (I): and medicinal products containing the same are useful as dual α2/5-HT2c antagonist receptors. ... | 04/11/2006 |
| 6984645 | Dual inhibitors of adipocyte fatty acid binding protein and keratinocyte fatty acid binding protein Compounds that are dual aP2/k-FABP inhibitors are provided having the formula wherein A, B, X, Y, R1, R2 and R3 are as described herein. A method is also provided for treating diabetes ... | 01/10/2006 |
| 6979696 | Method for detecting a gram-negative bacterial autoinducer molecule This invention relates to compounds which are alpha-1 receptor agonists, preferably alpha-1A/L receptor agonists, and which are represented by Formula I: wherein m, A, X, Y, R1, R2, R3,... | 12/27/2005 |
| 6951948 | Method for synthesis of substituted azole libraries The invention relates to methods of synthesizing libraries of diverse and complex 2-substituted azole compounds of the general formula (I) or (II) wherein X, R2 and the ring components ... | 10/04/2005 |
| 6911595 | Charge transfer material, and photoelectric conversion device and photoelectric cell using same, and pyridine compound A charge transfer material comprising a basic compound having negative charge and represented by the following general formula (I): (A1-L)n1-A2·M (I), wherein A1 represents a group having negativ... | 06/28/2005 |
| 6812349 | Process and intermediates for the preparation of imidazopyridines The invention relates to compounds of formula (2) in which R1, R2, R3 and R4 have the meanings indicated in the description, their preparation and their further reaction to give compounds of formula (1), in which A1, A2 and R4 have the meanings... | 11/02/2004 |
| 6787552 | PPAR delta activators Compounds of the general formula (I) or salts thereof and activators of PPARδ (peroxisome proliferator activated receptor δ) containing the compounds or the salts as the active ingredient: wherein R1 and R2 each are hydrogen, C1-8 ... | 09/07/2004 |
| 6750352 | Polymerizable molten salt monomer, electrolyte composition and electrochemical cell A polymerizable molten salt monomer represented by the following general formula (I): wherein Q represents a nitrogen-containing aromatic heterocyclic atomic group which can form a cation; Y1 represents a diva... | 06/15/2004 |
| 6737418 | Aryl substituted pyrazoles, imidazoles, oxazoles, thiazoles and pyrroles, and the use thereof This invention relates to compounds having the Formula I: or a pharmaceutically acceptable salt, prodrug or solvate thereof, wherein Het and R5-R13 are set in the specification. The invention also i... | 05/18/2004 |
| 6727098 | Biaryl-type compounds, CD color fixing agent and method for determination of absolute configuration A novel achiral biaryl-type compound and a circular dichroism (CD) color fixing agent are provided. Furthermore, a method for determining an absolute configuration of a chiral compound is carried out by introducing the above achiral biaryl-type compound into the chi... | 04/27/2004 |
| 6716990 | Process and intermediates for the preparation of imidazopyridines The invention relates to compounds of formula (2) in which R1, R2, R3 and R4 have the meanings indicated in the description, their preparation and their further reaction to give compounds of formula (1), in which A1, A2 and R4 have the meanings... | 04/06/2004 |
| 6713632 | Process for the preparation of imidazole derivatives A method for producing a compound of the formula: wherein R is an optionally substituted hydrocarbon group or an optionally substituted heterocyclic group and ring A is an imidazole ring which is optionally substituted f... | 03/30/2004 |
| 6649643 | Imidazol-4-ylmehanols and their use as inhibitors of steroid C17-20 lyase Imidazol-4-ylmethanols and their uses for preventing and treating primary tumors, metastasis and recurrence of tumors, various symptoms accompanying tumors, prostatic hypertrophy, virilism, hirsutism, male pattern alopecia, precocious puberty, endometrios... | 11/18/2003 |
| 6645991 | v댣 integrin inhibitors The invention describes novel compounds of the formula I which are biologically active as ligands of integrin vଲ.sub.3 in which X, Y, Z, R1, R2, R4 and R5 are as defined in claim 1, and their ... | 11/11/2003 |
| 6603019 | 1-imidazolyl substituted tetrahydronaphthalene derivatives as inhibitors of eytochrome P450RAI Compounds having Formula 4 wherein the symbols have the meaning defined in the specification are inhibitors of the cytochrome P450RAI (retinoic acid inducible) enzyme, and are used for treating diseases responsive to treatment by retinoids ##STR1##... | 08/05/2003 |
| 6573289 | Naphthalene derivatives, their production and use A composition containing a compound of the formula: ##STR1## wherein A is a nitrogen-containing heterocyclic group which may be substituted, R1 is a hydrogen atom, hydrocarbon group which may be substituted, or monocyclic aromatic heterocyclic ... | 06/03/2003 |
| 6562846 | Bisarylimidazolyl fatty acid amide hydrolase inhibitors The present invention relates to bisarylimidazolyl derivatives and pharmaceutical compositions comprising said compounds inhibiting fatty acid amide hydrolase and useful for the treatment of pain, particularly neuropathic pain, psychomotor disorder, hyper... | 05/13/2003 |
| 6559100 | 2-benzoyl-cyclohexane-1,3-diones Substituted 2-benzoylcyclohexane-1,3-diones of the formula I ##STR1## where: R1 and R2 are each hydrogen, mercapto, nitro, halogen, cyano, thiocyanato, C1 -C6 -alkyl, C1 -C6 -haloalkyl, C1 | 05/06/2003 |
| 6545009 | Retinoid-related receptor function regulating agent 1,3-Azole derivatives, pharmaceutical compositions thereof and methods for regulating the function of retinoid-related receptors with 1,3-azole derivatives are disclosed. Such regulation may be useful for preventing or treating diabetes, preventing or tre... | 04/08/2003 |
| 6518257 | 1-substituted phenyl-1-(1h-imidazol-4-yl) alcohols, process for producing the same and use thereof To provide a composition having a steroid C17,20 -lyase inhibitory activity and useful as an agent for the prophylaxis or treatment of prostatism and tumors such as breast cancer. A compound represented by the formula: ##STR1## wherein R i... | 02/11/2003 |
| 6514966 | Compounds for the treatment of obesity NPY antagonists, methods of using such NPY antagonists and pharmaceutical compositions containing such NPY antagonists. The NPY antagonists are useful for the treatment of NPY mediated disease/conditions including obesity.... | 02/04/2003 |
| 6482859 | Microbicidal N-sulfonylglycin alkynyloxyphenethyl amide derivatives The invention relates to novel pesticidally active compounds of the general formula I ##STR1## as well as possible isomers and mixtures of isomers thereof, wherein n is a number zero or one; and R1 is C1 -C12 alkyl that is unsu... | 11/19/2002 |
| 6465647 | Oxygen, sulfur and nitrogen substituted cyclohexene and cyclohexane derivatives having retinoid-like biological activity Compounds of the Formula 1, Formula 2, Formula 3 and Formula 4 wherein the symbols have the meaning assigned to them in the disclosure have retinoid-like biological activity. ##STR1##... | 10/15/2002 |
| 6465646 | 1-alkoxy and 1-acyloxy substituted cyclohex-1-ene compounds and sulfur and 1-alkoxycarbonyl analogs having retinoid-like biological activity Compounds of Formula 1 and of Formula 2 ##STR1## where the symbols have the meaning defined in the specification, have retinoid, retinoid antagonist or retinoid negative hormone like biological activity.... | 10/15/2002 |
| 6459003 | Ether compounds The present invention relates to novel ether compounds, compositions comprising ether compounds, and methods useful for treating and preventing cardiovascular diseases, dyslipidemias, dysproteinemias, and glucose metabolism disorders comprising administer... | 10/01/2002 |
| 6407258 | Method for producing S-alkyl(aryl)-substituted imidazol derivatives The invention relates to a process for the preparation of compounds of the formula (I) ##STR1## in which R(2) and R(3) independently of one another are --SR(4) or --COOR(5) and R(1), R(4) and R(5) have the meaning indicated in the description, which ... | 06/18/2002 |
| 6380396 | Quaternary ammonium compounds The present invention provides intermediates for the preparation of compounds of the formula ##STR1## wherein R, R1, W, X, Y, Ar and ZA are defined herein.... | 04/30/2002 |
| 6372693 | Substituted 2-(3-alkenyl-benzoyl)-cyclohexane-1,3-diones The invention relates to 2-(3-alkenylbenzoyl)cyclohexane-1,3-diones of the formula I ##STR1## where the variables have the following meanings: R1, R2 are hydrogen, nitro, halogen, cyano, thiocyanato, alkyl, haloalkyl, alkoxyalkyl, al... | 04/16/2002 |
| 6313311 | Imidazole derivatives having affinity for alpha2 receptors Imidazole derivatives of formula (I) ##STR1## wherein n is 0 or 1, R1 is hydrogen or C1 -C4 -alkyl, R2 is hydrogen or R2 and R3 together form a double bond, R3 is hydrogen or C | 11/06/2001 |
| 6310067 | Urocanic acid derivatives Urocanic acid derivatives useful as antiallergic agents represented by the following formula (I) or a pharmacologically acceptable salt thereof: ##STR1## wherein R2 denotes hydrogen or lower alkyl, R3 denotes nitro, amino, cyano or C... | 10/30/2001 |
