Login| Sign Up| Help| Contact|

Patent Searching and Data


Matches 551 - 600 out of 3,606

Document Document Title
WO/2004/018414A2
The present invention relates to compounds of formula I or a pharmaceutically acceptable salt thereof, wherein X=NH Y=CO, CS, -C(=N-CN) or X and Y together form an alkene, or C3-C5 cycloalkyl; R1 is -COOH; R2 is an electron withdrawing g...  
WO/2004/018446A1
A process for producing high-purity &gammad -keto acetals in high yield by a simple and easy means, as represented by the following scheme: (I) wherein Ar is aryl; X is halogeno; Ra and Rb are each alkyl or the like; and W is alkylene.  
WO/2004/016213A2
The present invention relates to solid phase or solution phase combinatorial libraries of autoinducer analogs. The present invention also relates to autoinducer agonists and antagonists. In addition, the present invention relates to meth...  
WO/2004/014966A1
The invention relates to a method for producing optionally coupled, non-blocked polymers based on conjugated dienes or optionally coupled, non-blocked copolymers based on conjugated dienes and vinyl aromatic compounds by anionic polymeri...  
WO/2004/014871A1
Compounds having the general structure and compositions containing them, for the treatment of acute, inflammatory and neuropathic pain, dental pain, general headache, migraine, cluster headache, mixed-vascular and non-vascular syndromes,...  
WO/2004/014899A1
The present invention provides compounds of formula (I): (I) pharmaceutical compositions containing the same, processes for preparing the same and their use as pharmaceutical agents.  
WO/2004/014890A1
It is intended to provide a method of purifying lactide whereby crude lactide can be purified while consuming less energy and causing no heat denaturation to thereby give D- or L-lactide having a high optical purity. In a method of purif...  
WO/2004/013121A2
The present invention relates to preparing lactic acid derivatives that are useful as odorants and monomers for polymer synthesis.  
WO/2004/011418A1
Disclosed are novel compounds of the formula (I)or a pharmaceutically acceptable salt or solvate thereof. Also disclosed is the treatment of chemokine-mediated diseases using compounds of the formula (II)  
WO/2004/011420A1
A process by which an optically active 6-sulfonyloxymethyl-1,3-dioxan-4-ylacetic acid derivative useful as an intermediate for medicines can be easily produced through short steps from an inexpensive, easily available material. The proce...  
WO/2004/011451A1
A process for easily and safely producing from inexpensive materials an optically active 1,4-benzodioxane derivative useful as an intermediate for medicines, etc. The process comprises sulfonylating an optically active triol compound (5)...  
WO/2004/006878A1
The use is described of merocyanine derivatives of formula (1), wherein R1 and R2 are each independently of the other hydrogen; C1-C22alkyl; cyclo-C3C8alkyl; or unsubstituted or C1-C5alkyl- or C1-C5alkoxy-substituted C6-C20aryl; orl; or ...  
WO/2004/005478A2
This invention relates to a method to modulate exogenous gene expression in which an ecdysone receptor complex comprising: a DNA binding domain; a ligand binding domain; a transactivation domain; and a ligand is contacted with a DNA cons...  
WO/2004/005278A1
The present invention relates to the use of bisarylsulfonamide compounds of formula (I) wherein W is a CI-5 branched or unbranched alkyl group or a C2-5 alkenyl group; nis0or1; R1 is H, a C, 1-8 branched or unbranched alkyl group, a C2-8...  
WO/2004/000771A1
The invention relates to 3,3,4,4-tetrafluorocyclopentane compounds of formula (I), in which R1, A1, A2, Z1, Z2 and m are defined as cited in claim 1. Said compounds are suitable for use as components of liquid crystal media.  
WO/2004/000783A1
The present invention relates to Mannich base antimalarial aminoalkylphenol compounds and their use against protozoa of the genus Plasmodium, particularly emerging strains of drug-resistant Plasmodia. This invention further relates to co...  
WO/2003/106443A1
Compounds of formula (I) (R and R1 are a wide range of substituents, Q is CO, CHOH or CHOR2, R2 is alkyl, alkenyl, alkynyl or cycloalkyl group, each of which is optionally substituted, or is alkanoyl, alkanoyoxy, aminocarbonyl, alkylamin...  
WO/2003/106447A1
Process for the preparation of an ester of formula (1), wherein R1represents a leaving group, CN, OH or a COOR5 group, R3 and R4each independently represent a 1-3 C alkyl group, and R2 and R5 each independently represent an ester residue...  
WO/2003/103660A1
Compounds of Formula I, wherein R1-R8 are defined herein are provided, together with pharmaceutically acceptable salts, hydrates, metabolites, and/or prodrugs thereof. Uses of these compounds for inhibiting beta amyloid production and fo...  
WO/2003/104203A1
Methods of inhibiting the cytokine or biological activity of Macrophage Migration Inhibitory Factor (MIF) comprising contacting MIF with a compound of formula (I) as defined herein, is provided. The invention also relates to methods of t...  
WO/2003/104178A1
Where Y, R¿1?-R¿8? and R¿101?-R¿108? are as defined in the specification. Compounds of formula (II) and methods of inhibiting the cytokine or biological activity of Macrophage Migrating Inhibitory Factor (MIF) comprising contacting M...  
WO/2003/102536A2
Destructible surfactants and methods of using same are provided. The invention includes anionic surfactants having a dioxolane or dioxane functional group that enable degradation of the surfactant under acidic conditions. The invention a...  
WO/2003/099284A1
Compounds having the general structure and compositions containing them, for the treatment of acute, inflammatory and neuropathic pain, dental pain, general headache, migraine, cluster headache, mixed-vascular and non-vascular syndromes,...  
WO/2003/099776A1
The compounds of the invention are represented by the following general structure (I) or a pharmaceutically acceptable salt thereof, and compositions containing them, wherein the variables are defined herein, and their use to reduce or i...  
WO/2003/097619A1
A novel class of compounds of the general formula (I), which act to antagonize the action of the glucagon hormone on the glucagon receptor. Owing to their antagonizing effect of the glucagon receptor the compounds may be suitable for the...  
WO/2003/095439A1
This invention relates to dihydro-furan-2-one derivatives, their intermediates and methods of manufacture. As such, the present invention includes methods of making a compound of the formula (V-1), wherein R2 and p are herein defined. Th...  
WO/2003/093223A1
Disclosed are novel biphenyl carboxamides of formula (I), in which R1, R2, m, n, R3, Y, and A have the meanings indicated in the description, several methods for producing said substances, the use thereof for controlling undesired microo...  
WO/2003/091238A1
A catalyst and depolymerization conditions for efficiently converting a lactic acid polymer into a lactide having a high optical purity. These are used for the purpose of, e.g., subjecting a waste high-molecular lactic acid polymer to ch...  
WO/2003/089424A1
Methods for preparation of cyclic alkylene carbonates which include a six-membered ring as part of their chemical structure are disclosed. According to the present invention, an oxide, alkoxide, or carboxylate salt of a metal selected fr...  
WO/2003/087034A1
The invention relates to 3-aminophenol derivatives of formula (I) or to their physiologically compatible, water-soluble salts, wherein R1 is identical to a radical of formula (II) or to a radical of formula (III), and to dyes that contai...  
WO/2003/086288A2
Novel compounds of the structural formula (I) are antagonists and/or inverse agonists of the Cannabinoid-1 (CB1) receptor and are useful in the treatment, prevention and suppression of diseases mediated by the CB1 receptor. The compounds...  
WO/2003/086673A1
A method and a device for removing harmful substances capable of safely processing the harmful substances and improving a processing efficiency, the device comprising a harmful substance separating and extracting device (10) for storing ...  
WO/2003/085002A1
Cyclodextrins cross-linked by reaction with organic carbonates and the use thereof as agents capable or removing pollutants from fluids of various origin, in particular from contaminated waters.  
WO/2003/082205A3
Disclosed is a compound having the formula (I) pharmaceutically acceptable salts or solvates thereof and pharmaceutical compositions containing the same, wherein the structural variables are as defined herein. The compounds, salts and so...  
WO/2003/082850A1
The present invention relates to the field of perfumery. More particularly, it concerns an aldoxane derivative of Formula (I) capable of protecting an active aldehyde R¿1?CHO, for example a perfumery or flavor aldehyde, from a chemicall...  
WO/2003/082205A2
Disclosed is a compound having the formula (I) pharmaceutically acceptable salts or solvates thereof and pharmaceutical compositions containing the same, wherein the structural variables are as defined herein. The compounds, salts and so...  
WO/2003/083063A2
The present invention provides common ligand mimics that act as common ligands for a receptor family. The present invention also provides bi-ligands containing these common ligand mimics. Bi-ligands of the invention provide enhanced affi...  
WO/2003/080564A1
This invention is directed to menthol-substituted compounds and their pharmaceutically acceptable salts which are useful as antithrombotic agents by inhibiting plasminogen activator inhibitor-1 (PAI-1). In addition, the present invention...  
WO/2003/078417A1
A process for formation of N-aryl piperazines with chiral side-chains having the structure shown in formula below, and for making intermediate compounds therefor: (Formula I). In this process, chirality is introduced at the piperazine ri...  
WO/2003/078409A1
Carboxylic acid compounds represented by the following general formula (I) (wherein each symbol is as defined in the description) and drugs containing these compounds: (I) Because of binding to DP receptor and antagonizing the same, the ...  
WO/2003/078420A2
A process for a stereoselective preparation of novel chiral nitrogen mustard derivatives useful in synthesizing optically active 1,4-disubstituted piperazines of formula (I) wherein R, Ar, and Q are defined as set forth herein, and inter...  
WO/2003/076374A1
A process for producing a compound (I) which comprises the step of reacting a compound (II) with a base in an aprotic solvent as shown by the scheme: (II) (I) wherein R1 and R2 each independently represents lower alkyl.  
WO/2003/076405A1
The present invention relates to monocyclic aroylpyridinones, processes for their preparation, and their use in medicaments, especially for the treatment of COPD: (formula I).  
WO/2003/074467A2
The present invention provides HIV aspartyl protease inhibitors of the formula (I): and when the compound of formula I comprises an amino group, pharmaceutically acceptable ammonium salts thereof, wherein n is 3 or 4, Y is O, S, NH or N...  
WO/2003/072537A2
Compounds of formula (I), or therapeutically acceptable salts thereof, are selective protein tyrosine kinase-B (PTP1B) inhibitors. Preparation of the compounds, compositions containing the compounds, and treatment of disorders using the ...  
WO/2003/070713A1
The present invention relates to novel compounds possessing specific hot, pungent and spicy taste when subjected to direct pungency evaluation, which may be useful as food additives and anti-oxidants, however the said compounds do not ad...  
WO/2003/070676A1
A process for easily producing from an inexpensive material an optically active 3-halo-1,2-propanediol derivative useful as an intermediate for medicines. The process comprises reacting 2-chloroallyl alcohol, which is easily available at...  
WO/2003/070719A1
Biologically active compounds related to the bryostatin family of compounds, having simplified spacer domains and&sol or improved recognition domains are disclosed, including methods of preparing and utilizing the same.  
WO/2003/070714A1
The present invention relates to a method for the synthesis of highly fluorinated compounds and to novel highly fluorinated compounds. In particular, the present invention relates to the synthesis of highly fluorinated acetals and ketals...  
WO/2003/064408A1
The present invention relates to an improved process for the preparation of ethyl 2,3-dihydrobenzo[1,4]dioxin-2-carboxylate. More particularly the present invention provides a process for the preparation of ethyl 2,3-dihydrobenzo[1,4]dio...  

Matches 551 - 600 out of 3,606