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| Number | Title | Issue Date |
| 7994340 | Azolylmethyloxiranes, their use for controlling phytopathogenic fungi, and compositions comprising them The present invention relates to azolylmethyloxiranes of the general formula (I) in which A stands for phenyl which is optionally substituted by one to three of the following substituents: halogen, NO2, amino, C1-C4-alkyl, C1 | 08/09/2011 |
| 7361673 | Agents for controlling plant pests The present invention relates to compositions for controlling plant pests containing the compound of the formula (I) in a mixture with specified fungicidally active compounds. ... | 04/22/2008 |
| 7307172 | 7-amino triazolopyrimidines for controlling harmful fungi The invention relates to 7-amino triazolopyrimidines of formula (I), in which the substituents have the following meanings: R1, R2 represent hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, phenyl, naphthyl; or 5-membered or 6-membered heterocycl... | 12/11/2007 |
| 7179814 | Agents for controlling plant pests The present invention relates to compositions for controlling plant pests containing the compound of the formula (I) in a mixture with specified fungicidally active compounds. ... | 02/20/2007 |
| RE39263 | Substituted aromatic thiocarboxylic acid amides and their use as herbicides There is disclosed substituted thiocarboxamides of the general formula (I) useful as herbicides. ... | 09/05/2006 |
| 7056932 | Heterocyclyl substituted 1-alkoxy acetic acid amides The invention is concerned with novel heterocyclyl substituted 1-alkoxy acetic acid derivatives of formula (I) wherein R1 to R6 and A are as defined in the description and in the claims, as ... | 06/06/2006 |
| 6933390 | Process for the arylation of aza-heterocycles with activated aromatics in presence of caesium carbonate The invention concerns a process for the preparation of N-aryl-aza-heterocycles of the general formula I by reaction of aza-heterocycles with activated aryl halides with use of caesium carbonate without addition of fur... | 08/23/2005 |
| 6916813 | (1-phenyl-2-heteoaryl)ethyl-guanidine compounds as inhibitors of mitochondrial F1F0 ATP hydrolase Compounds having the formula (I), and pharmaceutically acceptable salts thereof, are useful for modulating mitochondrial F1F0 ATPase activity and treating ischemic conditions including myocardial ... | 07/12/2005 |
| 6916924 | Process for synthesis of heteroaryl-substituted urea compounds useful as antiinflammatory agents This invention relates to novel processes for preparing heteroaryl-substituted urea compounds of formula (I): which are useful for treating diseases and pathological conditions involving inflammation such as chronic in... | 07/12/2005 |
| 6903092 | Naphthamide neurokinin antagonists for use as medicaments Compounds having the general formula wherein R1, R2, R3, R4, R5, X1 and X2 are as defined in the specification, methods of using such compoun... | 06/07/2005 |
| 6809098 | Compounds The present invention relates to compounds of formula I which are antagonists of gonadotropin releasing hormone (GnRH) activity. The invention also relates to pharmaceutical formulations, the use of a compound of the present invention in the manufacture of a medicam... | 10/26/2004 |
| 6541499 | Antithrombotic agents The invention relates to novel compounds of formula (I), and their pharmaceutically acceptable salts, as defined herein, processes and intermediates for their preparation, pharmaceutical formulations comprising the novel compounds of formula (I), and the ... | 04/01/2003 |
| 6410542 | Aminotetrazole derivatives useful as nitric oxide synthase inhibitors The current invention discloses aminotetrazole derivatives useful as nitric oxide synthase inhibitors.... | 06/25/2002 |
| 6169089 | Aminotetrazole derivatives useful as nitric oxide synthase inhibitors The current invention discloses aminotetrazole derivatives useful as nitric oxide synthase inhibitors.... | 01/02/2001 |
| 6066662 | Hydroxylamine derivatives and their use as metalloproteinase inhibiting agents The invention provides hydroxylamine derivatives of formula (I) wherein A, R1, R2 and R3 have the significance given in the description, which are matrix metalloproteinase inhibitors and which also prevent TNF release. The... | 05/23/2000 |
| 5919787 | Aminotetrazole derivatives useful as nitric oxide synthase inhibitors The current invention discloses aminotetrazole derivatives useful as nitric oxide synthase inhibitors.... | 07/06/1999 |
| 5854268 | Azetidine, pyrrolidine and piperidine derivatives A class of substituted azetidine, pyrrolidine and piperidine derivatives are selective agonists of 5-HT1 -like receptors, being potent agonists of the human 5-HT1D receptor subtype whilst possessing at least a 10-fold selecti... | 12/29/1998 |
| 5854251 | Aminotetrazole derivatives useful as nitric oxide synthase inhibitors Aminotetrazole derivatives of the formula (I) wherein the variables are as defined in the disclosure are useful as nitric oxide synthase inhibitors. ##STR1##... | 12/29/1998 |
| 5795905 | CRF receptor antagonists and methods relating thereto CRF receptor antagonists are disclosed. Such receptor antagonists are thiadiazole-, pyrimidine-, triazine-, and triazole-containing compounds substituted with both a C3-C14 monocyclic or fused, homoaryl or heteroaryl group and a substituted amine group. T... | 08/18/1998 |
| 5684008 | Aminotetrazole derivatives useful as nitric oxide synthase inhibitors The current invention discloses aminotetrazole derivatives useful as nitric oxide synthase inhibitors.... | 11/04/1997 |
| 5621010 | Urea derivatives and their use as ACAT inhibitors Urea derivatives of formula (I) ##STR1## wherein the valuable groups are as defined in the specification, which possess both an ACAT inhibitory activity and an antioxidative activity. Those derivatives are useful in the prophylaxis and treatment of ... | 04/15/1997 |
| 5436259 | Substituted 1,2,4-triazolin-3-one compounds bearing acidic functional groups as balanced angiotensin II antagonists Novel substituted 1,2,4-triazolin-3-ones of the formula (I) are useful as angiotensin II antagonists. ##STR1##... | 07/25/1995 |
| 5359078 | Signal transduction inhibitor compounds A compound having the formula: Y--(CH2)p --Ar11 --X--Ar12 wherein: p is an integer of from 0 to 4; Ar11 and Ar12 are each aromatic moieties independently selected from the group consisting of phenyl,... | 10/25/1994 |
| 5336778 | Substituted triazoles as angiotensin II antagonists Novel substituted triazoles of the formula (I), which are useful as angiotensin II antagonists, are disclosed. ##STR1##... | 08/09/1994 |
| 5245040 | Process for the preparation of nitroguanidine derivatives A process for the preparation of 1,3-disubstituted 2-nitroguanidines of the formula I ##STR1## in which R1 is hydrogen or C1 -C4 alkyl, R2 is hydrogen, C1 -C6 alkyl, C3 -C | 09/14/1993 |
| 5214206 | Aminosulfonyl urea ACAT inhibitors The present invention provides pharmaceutically useful compounds which are aminosulfonyl urea compounds which are ACAT inhibitors rendering them useful in controlling blood cholesterol levels, pharmaceutical compositions and methods of using the ACAT inhi... | 05/25/1993 |
| 5177214 | Aminal and isocyanate intermediates for fundicidal N,N'-diacylaminals Aminal and isocyanate intermediates of the formulas ##STR1## for fungicidal N,N'-diacylaminals of the formula ##STR2## in which R1 is optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl or cycloalkenyl, R2 and R... | 01/05/1993 |
| 5110986 | Synthesis of N-t-alkyl-1,2-diacylhydrazines This application relates to a process for preparing a N-t-alkyl-1,2-diacylhydrazine by reacting a 1,3,4-oxadiazole with a tertiary alkyl cation precursor in the presence of a strong acid catalyst. Preferably, the 1,3,4-oxadiazole is a 2,5-disubstituted-1,... | 05/05/1992 |
| 5080815 | Method for preparing engine seal compatible dispersant for lubricating oils comprising reacting hydrocarbyl substituted discarboxylic compound with aminoguanirise or basic salt thereof A dispersant composition having improved compatibility with fluorohydrocarbon-containing elastomeric engine seals, said dispersant composition comprising the reaction product obtained by reacting a C30 -C250 hydrocarbyl-substituted s... | 01/14/1992 |
| 5077306 | Fungicidal N,N'-diacylaminals Fungicidal N,N'-diacylaminals of the formula ##STR1## in which R1 is optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl or cycloalkenyl, R2 and R3 are hydrogen or various organic radicals, and X is oxygen or sulphu... | 12/31/1991 |
| 5061311 | Substituted triazolinone herbicides and plant growth regulators Novel herbicides and plant growth regulants of the formula ##STR1## in which R1 represents hydrogen alkyl, alkenyl, alkinyl, halogenoalkyl, halogenoalkenyl, halogenoalkinyl, alkoxyalkyl, alkoxy, cycloalkylalkyl or cycloalkyl, or represents... | 10/29/1991 |
| 5055471 | Fungicides This invention relates to derivatives of propanoic acid of the formula ##STR1## Useful as fungicides, insecticides and miticides, to processes for preparing them, to compositions containing them, and to methods of using them to combat fungi, especial... | 10/08/1991 |
| 5041155 | Herbicidal aryl triazolinones Herbicidal compounds of the formula ##STR1## in which, for example, X is Br, Cl or F; Y is Cl or Br, R2 is CHF2, R3 is CH3, R is alkyl, dialkylamino, carboxymethyl, hydroxy, haloalkyl, or aryl, and R1 | 08/20/1991 |
| 5015644 | Antihyperlipidemic and antiatherosclerotic urea and carbamate compounds Certain substituted urea, thiourea, carbamate, and thiocarbamate compounds are potent inhibitors of the enzyme acyl-CoA: cholesterol acyltransferase and are thus useful agents for inhibiting the intestinal absorption of cholesterol, and for lowering blood... | 05/14/1991 |
| 4945111 | Fungicidal N,N'-diacylaminals Fungicidal N,N'-diacylaminals of the formula ##STR1## in which R1 is optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl or cycloalkenyl, R2 and R3 are hydrogen or various organic radicals, and X is oxygen or sulphu... | 07/31/1990 |
| 4795755 | Heterocyclic derivatives This invention relates to heterocyclic derivatives which are histamine H-2 antagonists and which inhibit gastric acid secretion. According to the invention there is provided a guanidine derivative of the formula I: ##STR1## in which R1 and... | 01/03/1989 |
| 4748165 | Amidine derivatives This invention relates to amidine derivatives which are histamine H-2 antagonists and which inhibit gastric acid secretion. According to the invention there is provided a guanidine derivative of the formula I: ##STR1## in which R1 is hydro... | 05/31/1988 |
| 4696933 | Guanidine compounds useful as histamine H2-antagonists The invention relates to amide derivatives which are histamine H-2 antagonists and which inhibit gastric acid secretion. According to the invention there is provided a guanidine derivative of the formula I: ##STR1## in which R1 is a hydrog... | 09/29/1987 |
| 4670448 | Triazole amine compounds, their pharmaceutical compositions and method of use The invention provides compounds of the general formula (I) ##STR1## and physiologically acceptable salts, hydrates and bioprecursors thereof, in which the substituents are defined in the detailed description. The compounds show pharmaceutical activity as... | 06/02/1987 |
| 4576957 | N-(Substituted phenyl)-N'-[(1H-imidazol-1-yl) and (1H-1,2,4-triazol-1-yl)alkyl]ureas N-(Substituted phenyl)-N'-[(1H-imidazol-1-yl) and (1H-1,2,4-triazol-1-yl)alkyl]ureas which are inhibitors of thromboxane synthetase enzyme.... | 03/18/1986 |
