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7348335 |
Compositions useful as inhibitors of JAK and other protein kinases
The present invention provides a compound of formula I:
or a pharmaceutically acceptable salt thereof. The invention also provides pharmaceutically acceptable compositions comprising the...
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7348333 |
Cycloalkyl derivatives as inhibitors of bone resorption and vitronectin receptor antagonists
There are described cycloalkyl derivatives of the formula (I)
R 1 —Y-A-B-D-E-F-G (I)
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7338959 |
Diamino-pyrimidines and their use as angiogenesis inhibitors
Benzimidazole derivatives, which are useful as TIE-2 and/or VEGFR-2 inhibitors are described herein. The described invention also includes methods of making such benzimidazole derivatives as well...
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7335672 |
Vanilloid receptor ligands and their use in treatments
Substituted pyridines and pyrimidines and compositions containing them, for the treatment of acute, inflammatory and neuropathic pain, dental pain, general headache, migraine, cluster headache,...
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7335663 |
Heteroaryl compounds which inhibit leukocyte adhesion mediated by α4 integrins
Disclosed are compounds which bind α 4 integrins, where the α 4 integrin is preferably VLA-4. Certain of these compounds also inhibit leukocyte adhesion and, in particular, leukocyte adhesion...
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7329670 |
Inhibition of RAF kinase using aryl and heteroaryl substituted heterocyclic ureas
The compounds are aryl and heteroaryl substituted heterocyclic ureas of the formula A—NH—C(O)—NH—B where A is the aryl or hetaryl substituted heterocyclic group and B is an aryl or...
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7329661 |
N-phenyl-3-pyrimidine-amine derivatives
The invention relates to N-phenyl-2-pyrimidine-amine derivatives of formula I
wherein the substituents are defined as indicated in the description, to processes for the preparation thereof, to...
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7326717 |
Pyrimidine n-oxide compounds for stimulating the growth of keratin fibers and/or reducing loss thereof
Novel pyrimidine N-oxide compounds and salts thereof, well suited for stimulating the growth of keratin fibers (e.g., the hair or the eyelashes) and/or limiting the loss thereof and/or increasing...
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7326705 |
Heterocyclic sodium/proton exchange inhibitors and method
Heterocyclic are provided which are sodium/proton exchange (NHE) inhibitors which have the structure
wherein n is 1 to 5; X is N or C—R 5 wherein R 5 is H, halo, alkenyl, alkynyl, alkoxy,...
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7323464 |
Pyridine and pyrimidine derivatives
Compounds of formula (1) are described in which R a and R b is each independently a hydrogen atom or a group R c , or R a and R b together form an oxo (═O) or thio (═S) group; X is a N atom...
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7319104 |
hPPARs activators
Compounds of formula (1) or a pharmaceutically acceptable salt, solvate, acid isostere, or hydrolyzable ester thereof, are disclosed. Methods of making and using the compounds are also disclosed....
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7312216 |
N-phenyl-2-pyrimidine-amine derivatives
The invention relates to N-phenyl-2-pyrimidine-amine derivatives of formula I
wherein the substituents are defined as indicated in the description, to processes for the preparation thereof, to...
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7312227 |
Compositions useful as inhibitors of JAK and other protein kinases
The present invention provides a compound of formula I:
or a pharmaceutically acceptable salt thereof. The invention also provides pharmaceutically acceptable compositions comprising the...
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7309704 |
Heteroaryl urea neuropeptide Y Y5 receptor antagonists
The present invention relates to compounds represented by the structural Formula I:
or a pharmaceutically acceptable salt thereof, which are useful for the treatment of metabolic and eating...
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7304071 |
Protein kinase inhibitors and uses thereof
Described herein are compounds that are useful as protein kinase inhibitors having the formulae I and V:
or a pharmaceutically acceptable salt thereof, wherein Ring B, Z 1 , Z 2 , U, T, m, n,...
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7304072 |
Spiro compounds
Compounds represented by the general formula (I)
wherein Ar 1 represents an aryl or heteroaryl which may be substituted; n represents 0 or 1; T, U, V and W each independently represent a...
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7300933 |
Diazabicyclic biaryl derivatives
This invention relates to novel diazabicyclic biaryl derivatives, which are found to be cholinergic ligands at the nicotinic acetylcholine receptors and modulators of the monoamine receptors and...
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7300940 |
Integrin α-v β-3 antagonists for use in imaging and therapy
Integrin receptor antagonists whose molecular structure includes a tetrahydropyridimidinylaminoethyloxybenzoyl group on a sulfonylamino-β-alanine nucleus exhibit increased binding affinity for the...
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7300941 |
Non-imidazole compounds
Disclosed are novel compounds of the formula
Also disclosed are pharmaceutical compositions comprising the compounds of Formula I. Also disclosed are methods of treating various diseases or...
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7294635 |
Substituted isoquinolinones
Isoquinolinone compounds are provided that are useful for the inhibition of ADP-platelet aggregation, particularly in the treatment of thrombosis and thrombosis related conditions or disorders.
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7291624 |
CDK-inhibitory pyrimidines, their production and use as pharmaceutical agents
This invention relates to pyrimidine derivatives of general formula I
in which R 1 , R 2 , X, A and B have the meanings that are contained in the description, as inhibitors of the...
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7288547 |
CDK-inhibitory 2-heteroaryl-pyrimidines, their production and use as pharmaceutical agents
This invention relates to 2-heteroaryl-pyrimidine derivatives of general formula I or I f as inhibitors of the cyclin-dependent kinases, their production as well as their use as medications for...
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7288544 |
Pyrimidine compounds useful as N-type calcium channel antagonists
Achiral pyrimidine derivatives and pyridine derivatives of the following formulae or analogs thereof have selective N-type calcium channel antagonistic activity and showed analgesic action when...
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7285560 |
Indole derivatives or benzimidazole derivatives for modulating IκB kinase
The present invention relates to indole derivatives or benzimidazole derivatives, to processes for preparing such compounds, to pharmaceutical compositions comprising such compounds, and methods...
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7285551 |
Fused-ring compounds and use thereof as drugs
The present invention provides a fused ring compound of the following formula [I]
wherein each symbol is as defined in the specification, a pharmaceutically acceptable salt thereof, and a...
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7282504 |
Kinase inhibitors
The invention relates to inhibitors of kinases, compositions comprising the inhibitors, and methods of using the inhibitors and inhibitor compositions. The inhibitors and compositions comprising...
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7276510 |
HIV replication inhibitors
This invention concerns HIV replication inhibitors of formula
the N-oxides, the pharmaceutically acceptable addition salts, the quaternary amines and the stereochemically isomeric forms...
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7276502 |
Thiazoles useful as inhibitors of protein kinases
The present invention relates to compounds useful of inhibitors of protein kinases. The invention also provides pharmaceutically acceptable compositions comprising said compounds and methods of...
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7273862 |
Aminoalkyl substituted (benzodioxan, benzofuran or benzopyran) derivatives
The present invention concerns compounds of formula (I)
a stereochemically isomeric form thereof, an N-oxide form thereof or a pharmaceutically acceptable acid addition salt thereof, wherein -Z...
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7265115 |
Diazabicyclic CNS active agents
Compounds of formula I:
or pharmaceutically acceptable salts thereof, are useful for controlling synaptic transmission in mammals.
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7262203 |
Pyrimidineamines as angiogenesis modulators
Pyrimidine derivatives, which are useful as VEGFR2 inhibitors are described herein. The described invention also includes methods of making such pyrimidine derivatives as well as methods of using...
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7262202 |
Inhibitors of cyclin dependent kinases as anti-cancer agent
The present invention relates to 2-substituted 4-heteroaryl-pyrimidines, their preparation, pharmaceutical compositions containing them and their use as inhibitors of cyclin-dependent kinases...
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7256192 |
Aromatic diamide derivatives, chemicals for agricultural or horticultural use and usage thereof
The present invention relates to an aromatic diamide derivative represented by the general formula (I):
[A 1 is optionally substituted (C 1 -C 8 )alkylene group, (C 3 -C 8 )alkenylene...
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7253174 |
N-heterocyclic inhibitors of TNF-α expression
N-heterocyclic compounds that block cytokine production via inhibition of p38 kinase are disclosed. In one embodiment, compounds of the present invention are represented by Formula (I):
Methods...
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7244740 |
Imidazo-pyridine derivatives for use in the treatment of herpes viral infection
The present invention provides compounds of formula (I):
wherein all variables are as defined herein, pharmaceutical compositions containing the same, processes for preparing the same and their...
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7244735 |
Heterocyclic protein kinase inhibitors and uses thereof
Described herein are compounds that are useful as protein kinase inhibitors of formula I:
or a pharmaceutically acceptable salt thereof, wherein Ring B, Z 1 , Z 2 , U, p, Q, R 1 , R 2 , R 3 ,...
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7241756 |
Combinations of dipeptidyl peptidase IV inhibitors and other antidiabetic agents for the treatment of diabetes mellitus
A method for the treatment of diabetes mellitus, especially Type 2 diabetes and conditions associated with diabetes mellitus in a mammal such as a human, which method comprises administering an...
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7241458 |
Antiviral compositions
The present invention is concerned with pharmaceutical compositions of antiviral compounds which can be administered to a mammal, in particular a human, suffering from a viral infection. These...
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7241769 |
Pyrimidines as PLK inhibitors
The present invention comprises compounds of general formula (1)
wherein
A, X, Y, Z, R a , R b , R c , R 1 , R 2 and R 3 are defined as in claim 1 , which are suitable for the treatment of...
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7238697 |
Pyridylpyrimidines for use as pesticides
The present invention relates to novel pyridylpyrimidines of the formula
in which R 1 , R 2 , X, n, Y, Z and R have the meanings given in the disclosure, to a plurality of processes for...
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7235561 |
Compound and a composition including such a compound
This invention relates to pyrimidine derivatives of general formula I
in which R 1 , R 2 , X, A and B have the meanings that are contained in the description, as inhibitors of the...
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7232825 |
Phenylaminopyrimidine derivatives and methods of use
The present invention relates to phenylaminopyrimidine derivatives, processes for their preparation, pharmaceutical compositions containing them as active ingredient, methods for the treatment of...
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7230002 |
Dipeptidyl peptidase IV inhibitors; processes for their preparation and compositions thereof
The present invention relates to novel dipeptidyl peptidase IV (DPP-IV) inhibitors their analogs, isomers, pharmaceutical compositions, therapeutic uses and methods of making the same.
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7226919 |
Compositions useful as inhibitors of protein kinases
The present invention provides a compound of formula (I):
or a pharmaceutically acceptable salt thereof. These compounds are inhibitors of protein kinases, particularly inhibitors of...
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7220736 |
Pyrimidine compounds
A cyclic compound of the formula (I) or a pharmacologically acceptable salt thereof,
wherein X is ═CH— or ═N—, Y is —NH—, —NR 4 —, —S—, —O—, —CH═N—,...
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7217716 |
N-substituted nonaryl-heterocyclic NMDA/NR2B antagonists
Compounds represented by Formula (I): (I) or pharmaceutically acceptable salts thereof, are effective as NMDA NR2B antagonists useful for relieving pain
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7208499 |
Pyrimidine derivatives for the treatment of abnormal cell growth
The present invention relates to a compound of the formula 1
wherein A and Ar are as defined herein. Such novel pyrimidine derivatives are useful in the treatment of abnormal cell growth, such...
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7205301 |
Microbiocidal N-phenyl-n-[4-(4-pyridyl)-2-pyrimidin-2-yl]-amine derivatives
Fungicidal compounds of Formula (I) wherein m is 0, 1, 2 or 3; n and p are independently of each other 0 or 1; R 1 is halogen, optionally substituted alkyl, optionally substituted alkoxy,...
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7205297 |
Substituted 5-alkynyl pyrimidines having neurotrophic activity
The present invention relates to a series of novel substituted 5-alkynyl pyrimidines, pharmaceutical compositions which contain them, methods for their preparation, and their use in therapy,...
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7205310 |
Pyrimidine hydantoin analogues which inhibit leukocyte adhesion mediated by VLA-4
Disclosed are compounds which bind VLA-4 and/or LPAM-1. Certain of these compounds also inhibit leukocyte adhesion and, in particular, leukocyte adhesion mediated by VLA-4 and/or LPAM-1. Such...
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