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| Number | Title | Issue Date |
| 6225331 | Guanidinyl heterocycle compounds useful as alpha-2 adrenoceptor agonists This invention involves compounds having the following structure: ##STR1## as described in the claims; and enantiomers, optical isomers, stereoisomers, diastereomers, tautomers, addition salts, biohydrolyzable amides and esters thereof, as well as pharmac... | 05/01/2001 |
| 6224644 | Cyanine dyes and synthesis methods thereof A cyanine dye having the formula ##STR1## wherein R1 -R8 are each independently selected from a group consisting of hydrogen, C1 -C6 alkyl group, and C0 -C4 alkyl group having a hydrophilic... | 05/01/2001 |
| 6218359 | Screening method using the RZR receptor family The current invention concerns the use of a receptor from the RZR/ROR receptor family or of a functional fragment thereof in a test of a compound for anti-autoimmune, anti-arthritic, anti-tumor, melatonin-like and/or melatonin-antagonistic activity and th... | 04/17/2001 |
| 6204389 | Cyanine dyes and synthesis methods thereof A cyanine dye having the formula ##STR1## wherein R1 --R8 are each independently selected from a group consisting of hydrogen, C1 -C6 alkyl group, and C0 -C4 alkyl group having a hydrophili... | 03/20/2001 |
| 6197969 | Process for producing substituted alkylamines or salts thereof The present invention provides a process for producing a substituted alkylamine represented by formula (3): ##STR1## or a salt thereof, which process comprises reacting a 2-aminothiophenol derivative metal salt represented by formula (1): ##STR2## wi... | 03/06/2001 |
| 6197968 | Decolorizable dye Described is a decolorizable dye represented by the following formula (I): ##STR1## wherein R1 represents an alkyl, aryl or heterocyclic group; R2 and R3 independently each represents a hydrogen atom or has the same meanin... | 03/06/2001 |
| 6197956 | Cyanine dyes and synthesis methods thereof A cyanine dye having the formula ##STR1## wherein R1 -R8 are each independently selected from a group consisting of hydrogen, C1 -C6 alkyl group, and C0 -C4 alkyl group having a hydrophilic... | 03/06/2001 |
| 6177572 | Solid and liquid-phase synthesis of benzoxazoles and benzothiazoles and their use Methods for preparing benzoxazoles and benzothiazoles on solid supports. Substituted benzothiazoles and benzoxazoles, libraries of the compounds, and methods of using the compounds are also disclosed.... | 01/23/2001 |
| 6159983 | Method and composition for treatment of inflammatory bowel disease A composition in unit dosage form for the inhibition, prevention or treatment of inflammatory bowel disease comprising an effective amount of a compound having the formula: ##STR1## and a pharmaceutically acceptable carrier therefor. Also disclosed i... | 12/12/2000 |
| 6156772 | Antagonists of gonadotropin releasing hormone There are disclosed compounds of formula (I) ##STR1## and pharmaceutically acceptable salts thereof which are useful as antagonists of GnRH and as such may be useful for the treatment of a variety of sex-hormone related and other conditions in both m... | 12/05/2000 |
| 6136831 | Pyrazole derivatives and COX inhibitors containing them The purpose is to provide anti-inflammatory agents which have potent pharmacological actions and exert a selective inhibitory activity on COX-2, thereby being expected to reduce adverse effects such as disorders in gastric mucosa. The present invention en... | 10/24/2000 |
| 6124330 | N-[4-(Heteroarylmethyl)phenyl]-heteroarylamines The present invention is concerned with compounds of formula ##STR1## the N-oxides, the pharmaceutically acceptable addition salts and the stereochemically isomeric forms thereof, wherein R1 is hydrogen, hydroxy, C1-6 alkyl or a... | 09/26/2000 |
| 6114350 | Cyanine dyes and synthesis methods thereof A cyanine dye having the formula ##STR1## wherein R1 -R8 are each independently selected from a group consisting of hydrogen, C1 -C6 alkyl group, and C0 -C4 alkyl group having a hydrop... | 09/05/2000 |
| 6100405 | Benzothiazole-containing two-photon chromophores exhibiting strong frequency upconversion There are provided asymmetrical two-photon chromophores of the formula: D--Ar--A wherein Ar is selected from the group consisting of ##STR1## wherein Fl is a fluorene group of the formula: ##STR2## wherein R1 and R2 are alkyl gr... | 08/08/2000 |
| 6090834 | Substituted oxazoles for the treatment of inflammation A class of substituted oxazolyl compounds is described for use in treating inflammation and inflammation-related disorders. Compounds of particular interest are defined by Formula II ##STR1## wherein R is selected from halo, mercapto, hydroxyl, lower... | 07/18/2000 |
| 6045696 | Process for the purification of waste waters containing organic and inorganic sulphur compounds This invention relates to a process for the purification of waste waters containing organic and, should the situation arise, inorganic sulphur compounds, which waste waters contain a proportion of mercaptobenzothiazole and/or derivatives thereof and, shou... | 04/04/2000 |
| 6034246 | 2-arylbenzazole compounds There are disclosed herein 2-phenylbenzazole compounds having a 3'-substituent and a 4'-NR2 R6 substituent in the phenyl group where R5 and R6 are each hydrogen or alkyl, or where the $'-NR5 R6 | 03/07/2000 |
| 6011045 | Vitronectin receptor antagonists, their preparation and their use The present invention relates to compounds of the formula I A--B--D--E--F--G (I) in which A, B, D, E, F and G have the meanings given in the patent claims, to their preparation and to their use as medicaments. The compounds... | 01/04/2000 |
| 6007865 | Reversing the formation of advanced glycosylation endproducts The present invention relates to compositions and methods for inhibiting and reversing nonenzymatic cross-linking (protein aging). Accordingly, compositions are disclosed which comprise an agent capable of inhibiting the formation of advanced glycosylatio... | 12/28/1999 |
| 6004536 | Lipophilic cyanine dyes with enchanced aqueous solubilty The present invention relates to a family of cyanine dyes possessing lipophilic alkyl chains and either one or more reactive functional groups, bromo or chloro, or phenyl, sulfophenyl or polysulfophenyl substituents or combinations thereof. The dyes of th... | 12/21/1999 |
| 5990145 | Vitronectin receptor antagonists, their preparation and their use The present invention relates to compounds of the formula I, A--B--D--E--F--G (I) in which A, B, D, E, F and G have the meanings given in the patent claims, to their preparation and to their use as medicaments. The compound... | 11/23/1999 |
| 5980779 | Liquid crystalline compound and use thereof A process for producing a liquid crystalline compound represented by the following general formula (A): ##STR1##... | 11/09/1999 |
| 5981559 | Azole derivative with leukotriene (LTs) antagonizing activity and thromboxane (TX) A2 antagonizing activity An azole derivative represented by general formula (I) or a pharmaceutically acceptable salt thereof, having both of a leukotriene antagonistic effect and a thromboxane A2 antagonistic effect and being useful in preventing or treating allergic diseases, i... | 11/09/1999 |
| 5955458 | Penicillin glycolate New solvates of penicillin, in particular amoxycillin glycolate has been provided for together with a simple one-step process to prepare the same.... | 09/21/1999 |
| 5952354 | Tris carbamic acid esters: inhibitors of cholesterol absorption Inhibition of the enzymes cholesterol ester hydrolase (CEH) and/or acyl coenzyme A: cholesterol acyltransferase (ACAT) results in the inhibition of the esterification of cholesterol and are therefore implicated in the inhibition of absorption of cholester... | 09/14/1999 |
| 5942535 | a!-Annelated pyrrole derivatives and pharmaceutical use thereof The present invention relates to heterocyclic compounds of the formula ##STR1## in which R1 -R7, B, a and X have the meanings recited in the specification. These compounds are usable in the treatment of diseases of the rheumatoi... | 08/24/1999 |
| 5939415 | A!-annellated pyrrole derivatives and their use in pharmacology The present invention relates to heterocyclic compounds with the formula ##STR1## in which R1 to R7, B, a, and X have the meanings indicated in the specification. These compounds can be used for the treatment of diseases of the ... | 08/17/1999 |
| 5932740 | Thioheterocyclic near-infrared dyes Disclosed is a novel near-infrared absorbing dye of formula: ##STR1## wherein X1, X2 independently represents --CR8 R9 --, --S--, --Se--, --NR10 --, --CH.dbd.CH-- or --O--; n is an integer of 2 or 3; ... | 08/03/1999 |
| 5889022 | Indole, indoline and quinoline derivatives with 5HT1D (anti-depressive) activity Novel indole, indoline and quinoline derivatives of formula (I) processes for their preparation, pharmaceutical compositions containing them, and their use in medicine is disclosed. A structurally distinct class of compounds have now been discovered and h... | 03/30/1999 |
| 5874431 | Benzazole compounds There are disclosed herein benzazole compounds, exemplified by 2-(4-aminophenyl)benzothiazole and analogues or salts thereof, which exhibit very significant selective cytotoxic activity in respect of tumor cells, especially breast cancer cells, and which ... | 02/23/1999 |
| 5853703 | Preventing and reversing the formation of advanced glycosylation endproducts The present invention relates to compositions and methods for inhibiting and reversing nonenzymatic cross-linking (protein aging). Accordingly, compositions are disclosed which comprise an agent capable of inhibiting the formation of advanced glycosylatio... | 12/29/1998 |
| 5843972 | Heterocyclic ଲ-adrenergic agonists The present invention relates to certain compounds of the formula (I) the racemic-enantiomeric mixtures and optical isomers of said compounds and the pharmaceutically acceptable salts or prodrugs thereof, depicted below, which are ଲ-adrenergic recep... | 12/01/1998 |
| 5840721 | Imidazole derivatives as MDR modulators The present invention relates to polysubsituted imidazole having formula 1 ##STR1## These compounds are useful for restoring the sensitivity of multidrug resistant cells to cancer chemotherapeutic agents.... | 11/24/1998 |
| 5821362 | Method of desilylating silylether compounds Method of desilylating a silylether compound by reacting a silylether compound of the general formula (I): ##STR1## or a salt thereof with an amine hydrogen fluoride salt or a pyridine hydrogen fluoride salt in an organic solvent to produce a compoun... | 10/13/1998 |
| 5801246 | Substituted heteroarylphenyloxazolidinones The present invention discloses novel substituted aryl- and heteroarylphenyloxazolidinones which are useful as anti-bacterial agents. More specifically, the substituted aryl- and heteroarylphenyloxazolidinones of the invention are characterized by ox... | 09/01/1998 |
| 5766510 | Liquid crystalline compound and use thereof A process for producing a liquid crystalline compound represented by the following general formula (A): ##STR1##... | 06/16/1998 |
| 5733648 | Organic compounds suitable as reactive diluents, and binder precursor compositions including same Organic compounds having at least one ethylenically-unsaturated group are described, the organic compounds being suitable for use in coatable compositions as reactive diluents; compounds of the invention preferably have a divalent organic linking moiety d... | 03/31/1998 |
| 5714479 | Endothelin antagonistic heteroaromatic ring-fused cyclopentene derivatives A heteroaromatic ring-fused cyclopentene derivative of the formula: ##STR1## wherein the variables are as defined in the specification; or a pharmaceutically acceptable salt thereof.... | 02/03/1998 |
| 5698574 | 5-membered heteroaryl-oxazolidinones The present invention relates to 5-membered heteroaryl-oxazolidinones, to processes for their preparation and to their use as medicaments, in particular as antibacterial medicaments.... | 12/16/1997 |
| 5684152 | Preparation of carboxyalkyl derivatives as inhibitors of matrix metalloproteinases Carboxy-peptidyl compounds of Formula I are found to be useful inhibitors of matrix metalloendoproteinase-mediated diseases including osteoarthritis, rheumatoid arthritis, septic arthritis, tumor invasion in certain cancers, periodontal disease, corneal u... | 11/04/1997 |