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7585872 |
Guanidinyl-substituted hydroxy-6-phenylphenanthridines as effective phosphodiesterase (PDE) 4 inhibitors
The compounds of a certain formula (1),
in which R1, R2, R3, R31, R4, R5, R6 and R7 have the meanings as given in the description, are novel effective PDE4 inhibitors.
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7378427 |
Processes for preparing 6-alkyl-5-arylsulfonyl-dihydrophenanthridines
Synthetic methods are provided for production of compounds of the formula:
where R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 12 , R 13 and R 14 are as defined in the...
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7358245 |
Treatment of gastroesophageal reflux disease
The administration of cannabinoid receptor agonists for inhibition of transient lower esophageal sphincter relaxations, gastroesophageal reflux disease and regurgitation is disclosed.
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7329676 |
2-hydroxy-6-phenylphenanthridines as PDE-4 inhibitors
The compounds of formula I
in which R1, R2, R3, R31, R4, R5, R6 and R7 have the meanings as indicated in the description, are novel effective PDE4 inhibitors.
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7304073 |
Method of treating myocardial ischemia-reperfusion injury using NF-kB inhibitors
The present invention concerns a method of treatment or prevention of myocardial ischemia-reperfusion injury by diagnosing that a person is in need of treatment or prevention of myocardial...
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7291596 |
Pharmaceutical composition for thrombin peptide derivatives
Disclosed are pharmaceutical compositions comprising a thrombin peptide derivatives and a chelating agent and/or a pharmaceutically acceptable thiol-containing compound. The pharmaceutical...
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7214685 |
Prodrugs for a selective cancer therapy
The chemotherapy of malignant tumours is greatly restricted by the generally slight differentiation of the available cytostatic agents between normal and malignant tissue. In order to achieve an...
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7087106 |
Materials and methods for inhibiting fouling of surfaces exposed to aquatic environments
The subject invention provides materials and methods for inhibiting the biofouling of surfaces exposed to aquatic environments. In one embodiment, the subject invention provides additives for...
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7074782 |
Carbamate caspase inhibitors and uses thereof
This invention provides caspase inhibitors of formula I:
wherein Z is oxygen or sulfur; R 1 is hydrogen, —CHN 2 , R, CH 2 OR, CH 2 SR, or —CH 2 Y; Y is an electronegative leaving group; R 2...
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7060729 |
Composition and method for treating skin
The present invention relates to a composition and method for treating individuals afflicted with rosacea by combining a dicarboxylic acid, at least an antimicrobial agent, and a pharmaceutically...
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7037919 |
Tetrahydroquinoline derivatives
Tetrahydroquinoline derivatives of general formula (I) or salts thereof, having a specific and strong binding affinity for AR and exhibiting AR agonism or antagonism; and pharmaceutical...
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6958347 |
Aminophenanthridinone and aminophenanthridine as NPY-5 antagonists
The present invention provides NPY-5 receptor antagonists having a Formula (I)
Methods and pharmaceutical compositions useful for treating diseases, conditions and/or disorders modulated by...
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6894061 |
Substituted dihydrophenanthridinesulfonamides
This invention provides a compound of formulae (I) or (II) having the structure
or a pharmaceutically acceptable salt thereof which are useful for the treatment of the inflammatory component...
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6884802 |
6-heteroarylphenanthridines
Compounds of formula 1, in which Het is an unsubstituted or R6- and/or R7-substituted pyrrolyl, furanyl, thiophenyl, pyrazolyl, imidazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl,...
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6770668 |
Pharmaceutically active compounds and methods of use
The present invention relates to pharmaceutically acceptable compounds, including certain substituted indolinyl and derivatives thereof, 1,2,3,4-tetrahydroquinolinyl and derivatives thereof,...
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6743817 |
Substituted fused pyrroleimines and pyrazoleimines
Disclosed are compounds of the formula and the pharmaceutically acceptable salts thereof wherein R, Ar, A, n, R 1 and R 2 are defined herein. These compounds are highly selective agonists,...
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6723733 |
Sulfonamide and carbamide derivatives of 6(5H)phenanthridinones and their uses
This invention relates to compounds, pharmaceutical compositions, and methods of using the disclosed compounds for inhibiting PARP.
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6706729 |
Thiolesters and uses thereof
This invention pertains to the discovery of a novel family of thiolesters and uses thereof. Also provided for are viricidal compounds and pharmaceutical formulations comprising these novel...
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6696407 |
Huntington's disease treatment comprising administering aldose reductase inhibitors to increase striatal CNTF
The present invention provides methods of modulating neurotrophic factor-associated activity, especially CNTF-associated levels and activity, using aldose reductase inhibitors. These methods are...
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6677350 |
Beta-fluoroethyl thiourea compounds and use
The present invention relates to compounds, compositions and methods for the prevention or treatment of mycobacterium infections. The compounds are naturally occurring and synthetic biflavonoids,...
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6670369 |
Use of phanquinone for the treatment of alzheimer's disease
The use of phanquinone for the manufacture of a pharmaceutical composition for the prevention or the treatment of Alzheimer's disease is disclosed. Also methods of treatment or prevention of...
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6630483 |
Phenanthridine-N-oxides
N-oxides of the compounds of formula (I) in which R1 is hydroxyl, 1-4C-alkoxy, 3-7C-cycloalkoxy, 3-7C-cycloalkylmethoxy or completely or predominantly fluorine-substituted 1-4C-alkoxy, R2 is...
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6538005 |
Phenanthridine-N-oxides with PDE-IV inhibiting activity
The N-oxides of the compounds of formula (I), in which R1, R2, R3, R31, R4, R5, R51 and R6 have the meanings indicated in the description, arm novel active bronchial therapeutics.
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6534518 |
Polysubstituted 6-phenylphenanthridines with PDE-IV inhibiting activity
Compounds of formula (I), in which R1, R2, R3, R31, R4, R5, R51 and R6 have the meanings indicated in the description, are novel active bronchial therapeutics.
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6514988 |
Condensed-ring thiophene derivatives, their production and use
A gonadotropin-releasing hormone antagonistic composition, which comprises an optionally substituted condensed-bicyclic compound consisting of a homo or hetero 5 to 7 membered ring and a homo or...
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6479505 |
6-arylphenanthridines with PDE-IV inhibiting activity
Compounds of formula (I), in which R1, R2, R3, R31, R4, R5, R51 and Ar have the meanings indicated in the description, are novel active bronchial therapeutics.
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6476048 |
Substituted phenanthridinones and methods of use thereof
This invention provides a novel class of substituted 6(5H)phenanthridinone compounds. Pharmaceutical compositions, and methods of making and using the compounds, or a pharmaceutically acceptable...
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6476025 |
Phenylphennanthridines with PDE-IV inhibiting activity
Compounds of formula (I), in which R1, R2, R3, R31, R4, R5, R51, R6, R13 and R20 have the meaning indicated in the description, are novel active bronchial therapeutics
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6469047 |
Tyrosine derivatives
The compounds of the invention are inhibitors of alpha4 containing integrin-mediated binding to ligands such as VCAM-1 and MAdCAM.
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6391887 |
3,4-Dihydroquinoline derivatives as nitrogen monoxide synthase (NOS) inhibitors
The invention relates to compounds of formula (I), as defined herein. The invention also relates to the use of the inventive compounds for treatment of a disease caused by the effects of nitrogen...
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6268377 |
Method for treating androgen-related conditions
The present invention provides for the combined use of 5α-reductase inhibitors together with calcium channel blockers for the treatment of benign prostatic hyperplasia (BPH), prostate cancer,...
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6242432 |
Antithrombotic organic nitrates
Compounds or compositions containing compounds of the formula A-(X 1 --NO 2 ) to or salts thereof, for the preparation of antithrombotic medications wherein "to" is the integer 1 or 2X 1 is an...
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6214839 |
Substituted 6-alkylphenanthridines
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6177441 |
Treating red blood cell solutions with anti-viral agents
Methods and compositions for treating pathogens in material are described, including methods of decontaminating human fluids prior to processing in the clinical laboratory and methods for...
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6127378 |
Phenanthridines substituted in the 6 position
Compounds of the formula I in which R1, R2, R3, R31, R4, R5, R51 and R6 have the meanings indicated in the description, are novel efficacious bronchial therapeutics.
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6121279 |
Substituted 6-phenylphenanthridines
The invention relates to compounds of formula (I): wherein R1, R2, R3, R31, R4, R5, R51 and R6 are as defined in the specification. The compounds are phosphodiesterase inhibitors. Also disclosed...
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6071929 |
Octahydro phenanthridine derivatives useful as NMDA-R receptor subtype blockers
The present invention relates to the use of tetrahydroisoquinoline derivatives of the general formula: ##STR1## wherein: A is aryl R 1 is hydrogen, hydroxy, lower alkyl, lower alkoxy, R--CO--...
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6054448 |
2-amino-2-(3-substituted cyclobutyl) acetic acid derivatives
Compounds of the formula ##STR1## in which R 1 is Y or Y--C 1 -6 alkyl, where Y is carboxy, tetrazolyl, --SO 2 H, --SO 3 H, --OSO 3 H, --CONHOH, or --P(OH)OR', --PO(OH)OR', --OP(OH)OR' or...
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6025365 |
Chelerythrine and radiation combined tumor therapy
Combination of low doses of irradiation and chelerythrine results in increased apoptosis in tumor cells. The doses of either irradiation or chelerythrine alone are such that increased apoptosis or...
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5939429 |
Cardiovascular uses of cannabinoid compounds
Hemorrhagic shock and in other conditions associated with excessive vasoconstriction, such as hypertension, peripheral vascular disease, cirrhosis of the liver, or certain forms of angina pectoris...
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5827856 |
Method of treating insulin resistance
The present invention provides a novel method for the clinical treatment of painful, hyperalgesic and/or inflammatory conditions in which C-fibers play a pathophysiological role by eliciting...
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5728719 |
Systemic control of parasites
The present invention is a method for controlling ectoparasites. More particularly, the invention relates to a method of treatment in which the warm blooded animal is dosed with an ovicidally...
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5670514 |
Compositions for inhibiting bone loss
The present invention provides methods of inhibiting bone loss in mammals via the administration to a mammal in need of such treatment an effective amount of a compound from a series of...
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5654298 |
Amine derivatives
This invention concerns novel aminopyridinium compounds of the formula I wherein R 1 , R 2 , R 3 , R 5 and R 6 are selected from the following combinations: ##STR1## (a) one of R 2 and R 6 is a...
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5631279 |
Perhydroisoindole derivatives, preparation thereof and pharmaceutical compositions containing same
This invention relates to perhydroisoindole derivatives of 08/448,402 formula (I), wherein radicals R are phenyl radicals optionally 2-or 3-substituted by a halogen atom or a methyl radical; R 1 ...
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5605906 |
Cannabinoid receptor agonists
Disclosed are novel cannabinoid (CB2) receptor agonists, their compositions, and the methods of their preparation. The compounds are useful for lowering ocular intra ocular pressure, treating...
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5580888 |
Styryl derivatives as anti-inflammatory agents
Compounds of general formula (1) ##STR1## are described wherein Y is a halogen atom or a group --OR 1 , wherein R 1 is an optionally substituted alkyl group; X is --O--, --S-- or --N(R 6 )--,...
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5550134 |
Methods for inhibiting bone loss
The present invention provides methods of inhibiting bone loss in mammals via the administration to a mammal in need of such treatment an effective amount of a compound from a series of...
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5543433 |
Azine-substituted phenylacetic acid derivatives and fungicides containing these
Compounds of the formula I ##STR1## where X is hydrogen, halogen, alkyl, alkoxy, trifluoromethyl, cyano or nitro, Y is an amino, methylamino or dimethylamino group, Z is a group CHCH 3 ,...
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5215986 |
5-hydroxy-2-pyrimidinylmethylene oxaza heterocycles
Novel 5, 6, or 7 membered oxaza heterocycles substituted at the 4-carbon by a 5-hydroxypyrimidinylmethylene group inhibitors of 5-lipoxygenase and/or cyclooxygenase and are thus useful in treating...
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