|
Match
|
Document |
Document Title |
|
|
7365069 |
Pyrimidone derivatives
The present invention relates to novel pyrimidones of the general formula (I), their derivatives, their analogs, their tautomeric forms, their stereoisomers, their polymorphs, their hydrates, their...
|
|
|
7361691 |
Method of treating cancers using β-lapachone or analogs or derivatives thereof
Cancers and/or malignancies can be treated by administration of a cell cycle checkpoint activator, which is preferably β-lapachone, or a derivative or analog thereof, combined with an oncogenic...
|
|
|
7354924 |
Composition and antiviral activity of substituted azaindoleoxoacetic piperazine derivatives
This invention provides Compounds I having drug and bio-affecting properties, their pharmaceutical compositions and method of use. In particular, the invention is concerned with azaindoleoxoacetyl...
|
|
|
7345046 |
Heteroaryl-fused pyrimidinyl compounds as anticancer agents
Heteroaryl-fused pyrimidinyl compounds, pharmaceutically acceptable salts, and prodrugs thereof; compositions that include a pharmaceutically acceptable carrier and one or more of the...
|
|
|
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...
|
|
|
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...
|
|
|
7307081 |
Piperidine derivatives useful as CCR5 antagonists
The present invention provides a compound of the formula
or a pharmaceutically acceptable salt or solvate thereof, wherein the various moieties are as defined in the specification. The present...
|
|
|
7300938 |
Polymorphs of imatinib mesylate
The present invention relates to novel polymorphs of imatinib mesylate, to processes for their preparation and to pharmaceutical compositions containing them.
|
|
|
7300937 |
Derivatives of cyano-aryl (or cyanoheteroaryl)-carbonyl-piperazinyl-pyrimidines, their preparation and application as medication
New derivatives of cyanoaryl (or cyanoheteroaryl)-carbonyl-piperazinyl-pyrimidines (I), where R 1 represents an OR 3 radical, where R 3 represents a radical derived from a saturated hydrocarbon,...
|
|
|
7238525 |
Strategy for leukemia therapy
The chimeric Bcr-Abl oncoprotein is the molecular hallmark of chronic myelogenous leukemia (CML). In the cytoplasm, the protein transduces a growth signal that is responsible for overexpansion of...
|
|
|
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...
|
|
|
7196080 |
Phenylpyridinecarbonylpiperazinederivative
The present invention relates to a compound which is represented by the following general formula and has type 4 phosphodiesterase inhibitory action, and uses and an intermediate compound thereof. ...
|
|
|
7186723 |
Tyrosine kinase inhibitors
The present invention relates to compounds which inhibit, regulate and/or modulate tyrosine kinase signal transduction, compositions which contain these compounds, and methods of using them to...
|
|
|
7173025 |
Aminoheterocyclic derivatives as antithrombotic or anticoagulant agents
Compounds of formula (I), wherein G 1 is CH or N; G 2 is CH or N; R 1 is a variety of optional substituents; L 1 is (1-4C)alkylene; T 1 is CH or N; R 2 and R 3 are independently hydrogen or...
|
|
|
7166597 |
Fused pyrazole derivatives being protein kinase inhibitors
Compounds of Formula (I): salts or solvates or physiologically functional derivatives thereof, wherein Z is CH or N, and R 1 , R 2 , and R 4 are various substituent groups, are protein kinase...
|
|
|
7163940 |
Pyrazolopyridinyl pyrimidine therapeutic compounds
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...
|
|
|
7157455 |
4-Aminopyrimidine-5-one derivatives
Novel 4-aminopyrimidine-5-one derivatives are disclosed. These compounds inhibit cyclin-dependent kinases, in particular cyclin-dependent kinase 4 (Cdk4). These compounds and their pharmaceutically...
|
|
|
7141569 |
Antiviral pyrazolopyridine compounds
The present invention provides compounds of formula (I):
pharmaceutical compositions containing the same, processes for preparing the same and their use as pharmaceutical agents.
|
|
|
7109197 |
N-phenyl-4-(4-pyridyl)-2-pyrimidineamine derivatives
The present invention relates to a method of protecting plants against attack or infestation by phytopathogenic organisms, such as nematodes or especially microorganisms, preferably fungi, bacteria...
|
|
|
7098213 |
CCR5 antagonists useful for treating AIDS
Compounds of the formula
or a pharmaceutically acceptable salt or isomer thereof, wherein:
Q, X and Z are CH or N; R, R 4 –R 7 and R 13 are H or alkyl; R 1 is H, alkyl, fluoroalkyl,...
|
|
|
7094785 |
Method of treating polycythemia vera
The invention is directed to the use of imatinib mesylate for treating polycythemia vera. Imatinib mesylate is surprisingly effective at controlling the symptoms of polycythemia vera and reducing...
|
|
|
7087608 |
Use of PDGF receptor tyrosine kinase inhibitors for the treatment of diabetic nephropathy
The present invention relates to the use of PDGF receptor tyrosine kinase inhibitors, especially of N-phenyl-2-pyrim-idine-amine derivatives of formula (I), in which the symbols and substituents...
|
|
|
7064127 |
Treatment of hepatic fibrosis with imatinib mesylate
Disclosed herein is a method for treating hepatic fibrosis comprising administering to a patient in need of such treatment an amount effective to treat hepatic fibrosis of imatinib mesylate. This...
|
|
|
7060701 |
CCR5 antagonists useful for treating AIDS
Compounds of the formula
or a pharmaceutically acceptable salt or isomer thereof, wherein:
Q, X and Z are CH or N; R, R 4 –R 7 and R 13 are H or alkyl; R 1 is H, alkyl, fluoroalkyl,...
|
|
|
7045523 |
Combination comprising N-{5-[4-(4-methyl-piperazino-methyl)-benzoylamido]-2-methylphenyl}-4-(3-pyridyl)-2-pyrimidine-amine and telomerase inhibitor
A method of treating BCR-ABL positive leukemia in a warm-blooded animal comprising administering the combination of...
|
|
|
7045519 |
Inhibitors of glycogen synthase kinase 3
New pyrimidine or pyridine based compounds, compositions and methods of inhibiting the activity of glycogen synthase kinase (GSK3) in vitro and of treatment of GSK3 mediated disorders in vivo are...
|
|
|
7022695 |
Thioether-substituted benzamides as inhibitors of Factor Xa
Thioether-substituted benzamide compounds having the formula:
are provided that exhibit exceptionally strong inhibition of Factor Xa in combination with weak hERG binding.
|
|
|
7008946 |
CCR5 antagonists useful for treating AIDS
Compounds of the formula
or a pharmaceutically acceptable salt or isomer thereof, wherein:
Q, X and Z are CH or N; R, R 4 –R 7 and R 13 are H or alkyl; R 1 is H, alkyl, fluoroalkyl,...
|
|
|
6995159 |
5-HT receptor ligands and uses thereof
Compounds of Formula (IC) that act as 5-HT receptor ligands and their uses in the treatment of diseases linked to the activation of 5-HT 2 receptors in animals are described herein
.
|
|
|
6974816 |
Combination for the treatment of endothelial damage
The invention relates to a combination of (a) an inhibitor of platelet-derived growth factor (PDGF) activity and (b) a vector for vascular endothelial growth factor (VEGF-, especially VEGF-C) gene...
|
|
|
6958335 |
Treatment of gastrointestinal stromal tumors
4-(4-methylpiperazin-1-ylmethyl)-N-[4-methyl-3-(4-pyridin-3-
yl)pyrimidin-2-ylamino)phenyl]-benzamide of the formula I
or a pharmaceutically acceptable salt thereof can be used in the...
|
|
|
6953803 |
Pyrimidine compounds
Pyrmidinone compounds of formula (I)
are inhibitors of the enzyme Lp-PLA 2 and of use in therapy, in particular for treating atherosclerosis.
|
|
|
6949552 |
Remedial agent for anxiety neurosis or depression and piperazine derivative
There are provided a therapeutic preparation for anxiety neurosis or depression which comprises a MC 4 receptor antagonist as an effective ingredient; and a piperazine derivative represented by...
|
|
|
6916804 |
Pyrimidine A2b selective antagonist compounds, their synthesis and use
The subject invention provides compounds having the structure:
wherein R 1 is substituted or unsubstituted phenyl or a 5-6 membered heterocyclic or heteroaromatic ring containing from 1 to 5...
|
|
|
6908920 |
Pyrimidine derivatives
Compounds of formula (I), wherein R 1 , p, R 2 , q, R 3 and R 4 are defined within, and a pharmaceutically acceptable salts and in vivo hydrolysable esters are described. Also described are...
|
|
|
6818645 |
Benzocycloalkylenylamine derivatives as muscarinic receptor antagonists
This invention relates to compounds which are generally muscarinic M2/M3 receptor antagonists and which are represented by Formula I: wherein X, Y, and Z are O, S, or NR 4 , and the other...
|
|
|
6794386 |
β-amino acid compounds as integrin antagonists
The present invention relates to a compound of the general formula (I), wherein R 1 together with the C atom to which it is attached, and R 2 together with the N atom to which it is attached,...
|
|
|
6777415 |
Methods of inducing cancer cell death and tumor regression
Methods are provided for treating cancer, comprising administering (1) a farnesyl protein transferase inhibitor in conjunction with (2) an additional Ras signaling pathway inhibitor to induce...
|
|
|
6756380 |
5-phenyl-pyrimidine derivatives
Compounds of the general formula are described: wherein R 1 is hydrogen or halogen; R 2 is hydrogen, halogen, lower alkyl or lower alkoxy; R 3 is halogen, trifluoromethyl, lower alkoxy or...
|
|
|
6734183 |
Compounds
Compounds of the formula I useful as metalloproteinase inhibitors, especially as inhibitors of MMP 13.
|
|
|
6727254 |
Heteroaryl tropane derivatives as superior ligands for nociceptin receptor ORL-1
Novel compounds of the formula wherein R is optionally substituted heteroaryl or R 1 is H or C 1 -C 6 alkyl; and R 2 and R 3 are —CH 3 , —OCH 3 or halo; or a pharmaceutically...
|
|
|
6727249 |
Azabicyclic ether derivatives and their use as therapeutic agents
The present invention relates compounds of the formula (I): wherein X represents hydrogen, C 1-4 alkyl optionally substituted by a hydroxy, methoxy or benzyloxy group, or CO 2 (C 1-2 alkyl); Z...
|
|
|
6713474 |
Pyrrolopyrimidines as therapeutic agents
Chemical compounds having structural formula I and physiologically acceptable salts and metabolites thereof, are inhibitors of serine/threonine and tyrosine kinase activity. Several of the...
|
|
|
6696449 |
Sulfonyl aryl hydroxamates and their use as matrix metalloprotease inhibitors
This invention is directed to sulfonyl aromatic hydroxamic acid compounds and salts thereof that, inter alia, inhibit matrix metalloprotease (MMP) activity and/or aggrecanase activity. In some...
|
|
|
6696439 |
5-HT1F agonists
The present invention relates to substituted furo[3,2-b]pyridine compounds of formula I: or a pharmaceutical acid addition salt thereof; where; R is E—D is C═CH or CH—CH 2 ; R 1 is...
|
|
|
6689783 |
Aryl oxime-piperazines useful as CCR5 antagonists
In one embodiment, this invention provides a novel class of aryl oxime-piperazine compounds as antagonists of the CCR5 receptor, methods of preparing such compounds, pharmaceutical compositions...
|
|
|
6656957 |
Pyridine derivatives
A compound of formula I wherein X represents an optionally halo-substituted (C 2-4 )alkynylene group bonded via vicinal unsaturated carbon atoms.
|
|
|
6645972 |
Methods of treating leukemia
The present invention provides a novel method for treating leukemia in a host that has been previously treated with a Bcr-Abl tyrosine kinase inhibitor comprising administering to the host a...
|
|
|
6638935 |
Heteroary1 derivatives and their use as medicaments
The invention relates to novel pyridine derivatives of formula 1, to their preparation and to their use as medicaments, in particular for treating tumors
|
|
|
6593331 |
Method for treatment of pain
A method of treating pain with acetaminophen comprises the concurrent administration of a hydroxyazapirone selected from 6-hydroxybuspirone or 3-hydroxygepirone. This combination of agents results...
|