Nicotine Containing Dental Floss
Keep away cavities and cancer at the same time.
Make the Most of Our Site
See this month's Top Inventors and Most Cited Patents.
Stay on top of the latest innovations by subscribing to an RSS feed.
Registered users: Manage your profile.
| Number | Title | Issue Date |
| 8173843 | Amphiphilic derivatives of α-C-phenyl--butylnitrone Compounds derived from α-C-phenyl-N-tert-butylnitrone, a process for the preparation thereof and use thereof for the preparation of medicaments for use in preventing or treating oxidative stress-related diseases. ... | 05/08/2012 |
| 7696383 | N-oxides of venlafaxine and o-desmethylvenlafaxine as prodrugs Embodiments of the invention relate to a compound of formula (1), or a tautomer, stereoisomer, hydrate, or solvate thereof, wherein R1 is H or CH3. Other embodiments of the invention relate to a pharma... | 04/13/2010 |
| 7326730 | Aminoadamantane derivatives as therapeutic agents The present invention provides novel aminoadamantane derivatives, methods of making the derivatives, compositions including the novel aminoadamantane derivatives, and methods for the treatment and prevention of neurological diseases using the derivatives and composi... | 02/05/2008 |
| 6753429 | 1,4-disubstituted benzenes as insecticides Compounds of formula I: wherein A, B, D, and R are as defined herein and their agriculturally acceptable salts are disclosed as effective insecticides. In addition, compositions comprising an insecticidally effective amo... | 06/22/2004 |
| 6717012 | Antioxidant nitroxides and nitrones as therapeutic agents The invention provides novel adamantane compounds having one of the following formulas: wherein: R1 and R3 are H, OH, alkyl, cycloalkyl, amino or aryl, and can be the same or different; | 04/06/2004 |
| 6689911 | Process An integrated process for preparing -(2,4-disulfophenyl)-N-tert-butylnitrone and its salts is disclosed in which N-tert-butylhydroxylamine acid addition salt is incompletely neutralised so as to leave catalytic amounts of acid and the neutrali... | 02/10/2004 |
| 6512136 | Substituted 2-phenyl-1-(3,4-dihydroxy-5-nitrophenyl)-1-ethanones, their use in the treatment of some central and peripheral nervous system disorders and pharmaceutical compositions containing them New compounds of formula I are described ##STR1## The compounds have potentially valuable pharmaceutical properties in the treatment of some central and peripheral nervous system disorders, where a reduction in the O-methylation of catecholamines may be o... | 01/28/2003 |
| 6417401 | Ether diamines amine oxides The present invention is related to a series of derivatives of novel ether diamine compounds prepared by the cyanobutylation reaction of an alcohol having 3 to 22 carbon atoms with 2-pentenenitrile to form a branched alkyl ether nitrile. The etheraminonit... | 07/09/2002 |
| 6291702 | Azulenyl nitrone spin trapping agents, methods of making and using same The present invention relates to chromotropic nitrone spin trapping agents, methods of making these agents, compositions comprising same, and methods of their use. In particular, azulenyl nitrones of the present invention are effective agents for trapping... | 09/18/2001 |
| 6197825 | Azulenyl nitrone spin trapping agents, methods of making and using same The present invention relates to chromotropic nitrone spin trapping agents, methods of making these agents, compositions comprising same, and methods of their use. In particular, azulenyl nitrones of the present invention are effective agents for trapping... | 03/06/2001 |
| 6002002 | Anti-ischaemic hydroxylamine derivatives and pharmaceutical compositions The present invention provides novel hydroxylamine derivatives represented by the general formula: wherein: X is O, --NH, or a group of formula NR', wherein R and R' are independently selected from alkyl, cycloalkyl, phenylalkyl, phenyl optionally substit... | 12/14/1999 |
| 5892117 | Preparation and uses of N-methylnitrone Oxidation of secondary amines with hydrogen peroxide and sodium tungstate is reported to give good yields of nitrones. However, when using dimethylamine in this manner, a considerable amount of N,N-dimethylformamide was produced as a co-product. To more s... | 04/06/1999 |
| 5837717 | Hydroxamic acid anesthetic compounds A compound of the following formula: ##STR1## and its pharmaceutically acceptable salt thereof, wherein R1 and R2 are independently hydrogen, C1-4 alkyl, C3-7 cycloalkyl, C2-4 alkenyl, C1-4 | 11/17/1998 |
| 5650425 | Permanently ionic derivatives of steroid hormones and their antagonists The present disclosure relates to compounds of the general formulae: ##STR1## wherein DRUG is a steroid agonist or antagonist, a mixed agonist-antagonist, or a partial agonist, and to the use of such compounds as anti-inflammatory and anti-tumor agen... | 07/22/1997 |
| 5639880 | Preparation of amine oxides A process for preparing amine oxides of the general formula I ##STR1## where R1, R2 and R3 are each C1 -C30 -alkyl, C3 -C12 -cycloalkyl, C1 -C30 -hydroxyalk... | 06/17/1997 |
| 5498791 | Nitrosamine and nitrite inhibition A synergistic mixture of a carbonate and/or bicarbonate with a phosphonate, especially an organoamino methylene phosphonate or an N-oxide thereof, inhibits or reduces nitrosamine contamination during preparation, storage and/or heating of products which a... | 03/12/1996 |
| 5461078 | Anti-cancer compounds Compounds of formula (I) ##STR1## in which R1 is CH.dbd.CHR, CH.dbd.NNHR, CH.dbd.N--A--N(O)R'R" or CH2 --NH--A--N(O)R'R" and R2 is separately selected from hydrogen, CH.dbd.CHR, CH.dbd.NNHR, CH.dbd.N--A--(O)R'R" and C... | 10/24/1995 |
| 5223541 | Tramadol N-oxide material, enantiomers and compositions thereof, and their use This invention relates to a tramadol N-oxide material, enantiomers and compositions thereof and their use. The tramadol N-oxide material and compositions thereof are pharmacologically useful in treating pain, diarrhea and tussive conditions. The tramadol ... | 06/29/1993 |
| 5164121 | Pourable composition containing an amine oxide -polyethylene glycol mixture A pourable amine oxide composition which is suitable for use in detergent compositions is obtained by reacting a tert-amine with aqueous hydrogen peroxide in a normally liquid polyethylene glycol as the sole organic solvent. When the composition has a low... | 11/17/1992 |
| 5162408 | N-alkenyl substituted amine-N-oxide stabilizers N-Alkenyl substituted hydroxylamines of formula I ##STR1## where R1 and R2 are independently hydrogen, alkyl, aryl or phenylalkyl, and R3 to R7 are independently hydrogen, alkyl or substituted alkyl are ver... | 11/10/1992 |
| 5087752 | Synthesis of nitroxides using dioxiranes The subject invention relates to a method of synthesizing nitroxides from secondary amines. This method uses a suitable dioxirane compound such as dimethyldioxirane (DMD), which is relatively stable and simple to synthesize, as the oxidizing agent. A quan... | 02/11/1992 |
| 5082938 | Organic materials containing poly(oxyalkylene) moieties having enhanced functionality and their preparation Enhanced branched chain hydroxyl compounds are provided of formula Y--(Z)1-6 wherein Y is the residue of a nucleophile devoid of conjugated divalent linking moieties, and each Z is a poly(oxyalkylene) moiety having a molecular weight of from about 2... | 01/21/1992 |
| 5082940 | Process for the production of oxides of aromatic tertiary amines Aromatic tertiary amines are oxidized by means of hydrogen peroxide in an inert solvent medium in the presence of a catalyst selected from metal selenium and compounds of selenium. The process is applied to the preparation of oxides of heterocyclic aromat... | 01/21/1992 |
| 5081300 | N-alkenyl substituted amine-N-oxide stabilizers N-substituted hydroxylamines of formula I ##STR1## where R1 and R2 are independently hydrogen, alkyl, alkenyl, aryl or phenylalkyl, and R3 to R7 are independently hydrogen, alkyl or substituted alkyl are ve... | 01/14/1992 |
| 5021429 | Pharmacologically active aminoalkylphenyl compounds and their use Compounds of the general formula: ##STR1## and physiologically acceptable salts, and hydrates, N-oxides and bioprecursors of such compounds and such salts in which R1 and R2, which may be the same or different, represent hydrogen ... | 06/04/1991 |
| 4992589 | Substituted phenyl hydroxyethyl sulfones, and process for their preparation Compounds of the formula (1) ##STR1## in which X denotes a sulfur atom or the group ##STR2## in which R denotes a hydrogen atom, an alkylene-C1 -C4 -alkoxy-C1 -C6 - or alkyl-C1 -C6 | 02/12/1991 |
| 4960934 | Amine oxide process The reaction of aqueous hydrogen peroxide with tert-amines to yield tert-amine oxides is catalyzed by the addition of a promoter amount of ammonium carbonate, ammonium bicarbonate or ammonium carbamate or mixtures thereof.... | 10/02/1990 |
| 4942260 | Amine oxide process with CO2 and aluminum Amine oxides which have low levels of nitrosamines or are substantially-free of nitrosamines are made by reacting tert-amines with hydrogen peroxide in the presence of carbon dioxide and aluminum metal.... | 07/17/1990 |
| 4696949 | Novel tri-phenyl alkane and alkene derivatives and their preparation and use The invention provides novel compounds of the formula: ##STR1## wherein n is 0 to 4, R1 and R2, which can be the same or different are H, OH, alkoxy of 1 to 4 carbon atoms, benzyloxy or methoxymethoxy; R3 is H, OH, ha... | 09/29/1987 |
| 4677049 | Spin castable photobleachable layer forming compositions Spin castable mixtures having aryl nitrones are provided which are useful in making photobleachable layers for use in contrast enhanced photolithography.... | 06/30/1987 |
| 4661433 | Storage stable aryl nitrone compositions Aryl nitrones, of the type used in contrast enhancement photolithography techniques, are stabilized by adding thereto a drying agent such as molecular sieve, silica gel or an alkylalkoxysilane. The resulting compositions are substantially storage stable.... | 04/28/1987 |
| 4399077 | Certain polyoxy perfluorinated surface active oligomers Perfluorinated surface-active block or random oligomers of the formula ##STR1## where R denotes a C2 -C18 -hydrocarbon or- hydrofluorocarbon radical, Y denotes a C6 -C13 -fluorocarbon or- hydrofluorocarbon radic... | 08/16/1983 |
| 4347381 | Method of treating long chain alkyl amines or products derived therefrom The pink color content often produced in products such as amine salts, amine oxides, betaines, quaternary ammonium compounds or other compounds derived from long chain alkyl amines is eliminated by treating the products with trace amounts of a bleaching a... | 08/31/1982 |
| 4275236 | Tertiary di-(ଲ-hydroxy organo) amine oxides and their preparation Disclosed are tertiary amine oxides which comprise an amine oxide nucleus substituted with an organic group and with two hydroxy groups which have carbon atoms in at least the , ଲ and γ positions, a hydroxyl group on the ଲ-carbon atom,... | 06/23/1981 |
| 4264776 | Production of secondary amines Tertiary amines such as alkyl or benzyl amines are catalytically oxidized by oxygen over an activated carbon catalyst to selectively produce secondary amines.... | 04/28/1981 |
| 4172093 | Pharmacodynamically active indan derivatives The present invention relates to new pharmacodynamically active compounds of the general structure ##STR1## as well as the corresponding amine oxides, quarternary ammonium compounds and salts with physiologically acceptable acids. In formula I R... | 10/23/1979 |
| 4169156 | N-(2-aminocycloheptyl)alkanoylanilides N-(2-aminocycloheptyl)N-alkanoylanilides and their 2-N-oxides of the formula ##STR1## e.g., trans-3,4-dichloro-N-[2-(allylamino)cycloheptyl]propionanilide, and their pharmacologically acceptable salts, have been found to possess potent Central N... | 09/25/1979 |
| 4153629 | 9,10-Dihydro-9,10-methanoanthracene N-oxide 9,10-Dihydro-9,10-methanoanthracene N-oxide derivatives represented by the formula: ##STR1## wherein A represents a straight or branched C1 -C6 alkylene; R1 and R2 each represents C1 -C4 | 05/08/1979 |
| 3957872 | Benzobicycloalkane amine N-oxides and the salts thereof Benzobicycloalkane amines, their pharmacologically acceptable addition salts, intermediates therefore the processes for their preparation and use. The compounds of the invention exert analgesic and antiinflammatory activity.... | 05/18/1976 |
| 3952017 | Tricyclic compounds 1-Methyl(or acetyl)-5H-dibenzo[a,d]cycloheptenes and 1-methyl(or acetyl)-10,11-dihydro-5H-dibenzo[a,d]cycloheptenes bearing a basic side chain at the 5-position, such as a 3-mono- or dimethylaminopropylidene, a 3-mono- or dimethylaminopropyl or a 3-dimeth... | 04/20/1976 |