|
Match
|
Document |
Document Title |
|
|
8071807 |
Antagonists of prostaglandin D2 receptors
Described herein are compounds that are antagonists of PGD2 receptors. Also described are pharmaceutical compositions that include the compounds described herein, and methods of using such...
|
|
|
7767714 |
Method of preventing infectious diseases
Effective preventive method for infectious diseases, an enhancing method of an infectious disease-preventive action of cystine and composition, food and feed effective for infectious diseases are...
|
|
|
7598232 |
Amino-substituted (E)-2,6-dialkoxystyryl 4-substituted-benzylsulfones for treating proliferative disorders
Compounds useful as antiproliferative agents, including, for example, anticancer agents, are provided according to formula (I); wherein: X, X1, X2, Ra, R1, R2,R3, R4, R5, R6, R7, g, M, y, a, b, d,...
|
|
|
7566738 |
Acyloxyalkyl carbamate prodrugs of sulfinic acids, methods of synthesis, and use
Acyloxyalkyl carbamate prodrugs of 3-aminopropylsulfinic acid and analogs thereof, pharmaceutical compositions of 3-aminopropylsulfinic acid and analogs thereof, methods of making prodrugs of...
|
|
|
7476754 |
Biphenyl derived thiamides as calpain inhibitors
The present invention relates to compounds derived from biphenyl with activity as calpain inhibitors. One compound of the present invention is a 2,2′-disubstituted biphenyl, where the s...
|
|
|
7217831 |
Insecticide and method of controlling insects
An insecticide of formula 1 and the agriculturally acceptable salts thereof, wherein: R1 is selected from the group consisting of:the group OR5 wherein R5 is selected from the group consisting of...
|
|
|
7173059 |
Intermediates useful in the synthesis of HIV-protease inhibitors and methods for preparing the same
Optically active 3-amino-butene and 1,2-dihydroxy-3-amino-butane intermediate compounds, useful in the synthesis of HIV-protease inhibitors and methods of preparing these intermediate compounds are...
|
|
|
7105545 |
N-p-propargyloxyphenethyl-thioacetic acid amides
The invention relates to N-propargyloxy-phenethyl thioacetic acid amide derivatives of the general formula (I) including the optical isomers thereof and mixtures of such isomers, wherein R1 is...
|
|
|
7034015 |
Aminobenzoephenones
The invention relates to a novel class of aminobenzophenones derivatives, to pharmaceutical preparations comprising said compounds, to dosage units of such preparations, to methods of treating...
|
|
|
6946474 |
Nitrogen-containing compounds and their use as glycine transport inhibitors
The present invention provides trichloroethyl-sulfonylurea-containing compounds that inhibit glycing transporters, pharmaceutical compositions comprising such compounds, methods for using such...
|
|
|
6878845 |
Oligomers from multifunctional acrylates
Oligomers from multifunctional acrylates and organonitro compounds are provided. Films obtained from crosslinked oligomers of the present invention are useful as protective or decorative coatings...
|
|
|
6838472 |
Substituted urea retinoid agonists
The current invention provide novel compounds, methods of treating or preventing emphysema, cancer and dermatological disorders, pharmaceutical compositions suitable for the treatment or prevention...
|
|
|
6803480 |
Diphenylmethane derivatives
The invention relates to novel diphenylmethane derivatives, processes for their preparation and their use in medicaments, in particular for the indications of arteriosclerosis and...
|
|
|
6683200 |
N-substituted-N′-substituted urea derivatives and pharmaceutical compositions containing the derivatives
N-Substituted-N′-substituted urea derivatives represented by the following formula, analogs thereof or pharmaceutically acceptable salts thereof are herein provided. These compounds show a TNF-α pr...
|
|
|
6559334 |
Polymers chromatographic separation of enantiomers
The invention relates to novel optically active polymerizable dipeptides, to the process for the preparation thereof, to the polymerization thereof and to the use of the polymers as adsorbents for...
|
|
|
6534546 |
Aniline derivatives possessing an inhibitory effect of nitric oxide synthase
Compounds represented by the general formula (1): (where R1 is SR6 or NR7R8, where R6 is typically an alkyl group having 1-6 carbon atoms, R7 is a hydrogen atom, an alkyl group having 1-6 carbon a...
|
|
|
6472430 |
Amino thioxomethyl amino oxyacetic acid derivatives
Antiatherosclerotic compounds are provided which have the following structure: whereinR is lower alkyl;R1 is hydroxy, amino, or lower alkoxy,R2 and R3 are each independently hydrogen, alkyl or...
|
|
|
6444850 |
Fungicidial compounds having a fluorovinyloxphyenyl moiety and process for the preparation thereof
A fungicidal compound of formula (I) having a fluorovinyloxyphenyl moiety and stereoisomers thereof are useful for protecting crops from fungal diseases: wherein:X is CH or N;Y is O or S;Z is O or...
|
|
|
6420603 |
Process for the preparation of n,n'-bis&lsqb 2,3-dihydroxypropyl&rsqb -5-&lsqb (hydroxyacetyl) methylamino&rsqb -2, 4,6-triiodo-1, 3-benzenedi carboxamide
A novel process for the preparation of N,N′-bis[2,3-dihydroxypropyl]-5-[(hydroxyacetyl) methylamino]-2,4,6-triiodo-1, 3-benzenedi carboxamide of formula (I), commonly known as lomeprol, a novel n...
|
|
|
6407100 |
Fungicidal aromatic oximes
The invention relates to novel compounds of the formula in which R1 is C1-4alkyl and (Y—X) is CH2, C1-2alkylthio-CH═ or C1-2alkyl-ON═ and Z is an aldimino or ketimino group, and to their prepa...
|
|
|
6388122 |
Tryptase inhibitor and novel guanidino derivatives
A tryptase inhibitor comprising as an active ingredient at least one member selected from among guanidinoaliphatic acid derivatives of the formula (I), guanidinobenzoic acid derivatives of the...
|
|
|
6331627 |
Intermediates of benzoxazinone derivatives and preparation thereof
The present invention relates to novel antiobesity and hypocholesterolemic compounds, their derivatives, their analogs, their tautomeric forms, their stereoisomers, their polymorphs, their...
|
|
|
6284914 |
Highly water-soluble metalloproteinase inhibitors
New compounds of general formulae (III), (IV) and (V). ##STR1##
|
|
|
6265590 |
Nα-2-(4-nitrophenylsulfonyl)ethoxycarbonyl-amino acids
Protected amino acid derivatives of general formula (I) ##STR1##and methods for the prepatation of the derivatives are provided.
|
|
|
6265603 |
Inhibitors of isoprenyl transferase
Peptidomimetic isoprenyl transferase inhibitors R6SCHR1'CHR1WCHR2YC(:X)NR3CHR5COR4 wherein R1=OH, H, alkyl, amino group or R1 and R6 together form a heterocyclic ring; R1'=H, alkyl, aryl; R2=H,...
|
|
|
6239308 |
Method for producing α-hydroxy-β-aminocarboxylic acids
The present invention provides a simple and inexpensive method for producing α-hydroxy-β-aminocarboxylic acids and their esters.An ester of an N-protected α-amino acid ester is converted into a β-...
|
|
|
6235922 |
Processes and intermediates for preparing benzo-fused azepinone and piperidinone compounds useful in the inhibition of ACE and NEP
Compounds having the following formula I, and pharmaceutically acceptable salts thereof, including dual inhibitors of ACE and NEP and selective ACE inhibitors: ##STR1##wherein: Y1 and Y2 are each...
|
|
|
H001950 |
Processes for preparing indeno[1,2-E][1,3,4]oxadiazine-dicarboxylates
Oxadiazines of formula I, wherein R1 is F, Cl or fluoroalkoxy and R2 is alkyl, are prepared by reacting hydrazine derivatives of formula II with a dialkoxymethane in the presence of a protic acid...
|
|
|
6166072 |
Amino acid derivatives
Described herein are compounds having the general formula: ##STR1## wherein: Ar1 and Ar2 are independently selected aryl groups, optionally substituted with substituents selected from the group...
|
|
|
6153650 |
Substituted gamma aminobutyric acids as pharmaceutical agents
|
|
|
6066754 |
Process for manufacturing N-alkoxy(or aryloxy)carbonyl isothiocyanate derivatives using N,N-dialkylarylamine as catalyst
The present invention provides a process for making N-alkoxy(or aryloxy)carbonyl isothiocyanate derivatives by reacting a chloroformate with a thiocyanate, in the presence of an organic solvent and...
|
|
|
6030803 |
Dibenzodihydropyridinecarboxylic esters and their use in chemiluminescent assay methods
|
|
|
6028131 |
Antioxidants containing phenol groups and aromatic amine groups
The invention relates to compounds of the formula I ##STR1## in which R is C1 -C18 alkyl, C5 -C8 cycloalkyl, C7 -C9 phenylalkyl, --CH2 --A--R2 or a group of the formula II, ##STR2## R1 is C1 -C18...
|
|
|
6013829 |
Process for the asymmetric synthesis of S-acyl derivatives of 2-mercaptomethyl -3- phenyl propanoic acid, application to the synthesis of N-(mercaptoacyl) amino acid derivatives
Process for the asymmetric synthesis of S-acyl derivatives of 2-mercaptomethyl-3-phenylpropanoic acid of formula (I): characterized in that it comprises the steps consisting in: a) preparing the...
|
|
|
5994539 |
Mercapto acyl aminoacid derivatives endowed with dual ACE-NEP inhibitory activity, useful in the treatment of cardiovascular diseases
Compounds of formula ##STR1## wherein R, R1, R2, R3, R4, m and n have the meanings reported in the description, processes for their preparation and pharmaceutical compositions which contain them as...
|
|
|
5959120 |
Acetate ester compounds
The present invention provides an acetate ester compound of formula (III), ##STR1## a process for synthesizing compound (III), and a process for using that compound to prepare a pyrazolone...
|
|
|
5945548 |
Process for the synthesis of α-substituted acrylic acids and their application
Process for the synthesis of α-substituted acrylic acids of general formula (I) and their application to the synthesis of N-(mercaptoacyl)aminoacid derivatives of formula (II). ##STR1##
|
|
|
5888972 |
Peptide compounds, their preparation and uses
A compound of the formula: ##STR1## in which R4 is acyl, R5 is lower alkyl, R6 is optionally substituted ar(lower)alkyl or optionally substituted heterocyclic-(lower)alkyl, R7 is lower alkyl or...
|
|
|
5866604 |
Thiol derivatives with metallopeptidase inhibitory activity
Compounds of formula (I) wherein R, R1, R2, R3, R4, m and n have the meanings reported in the description, processes for their preparation and pharmaceutical compositions which contain them as...
|
|
|
5847125 |
Amino acid derivatives with anticholecystokinin activity
Compounds of formula (II) wherein Ar is naphthyl, naphthylmethyl, 1,2,3,4-tetrahydronaphthyl, phenethyl, styryl, indanyl or a substituted derivative of any of the foregoing, or 3,4-dichlorophenyl,...
|
|
|
5783735 |
Process for preparing polymeric amides useful as additives in fuels and lubricating oils
A process for preparing polymeric amides is disclosed. The process comprises sequentially reacting a hydrocarbon polymer functionalized (e.g., via the Koch reaction) to contain acid, ester,...
|
|
|
5739163 |
Aromatic compounds containing basic and acidic termini useful as fibrinogen receptor antagonists
This invention relates to novel compounds containing basic and acidic termini, pharmaceutical compositions containing such compounds, processes for preparing such compounds, and to methods of using...
|
|
|
5693847 |
Heteroatom functionalized α-methyl ketones
The present invention relates to functionalized ketones and novel processes for synthesizing those ketones. The processes of this invention are especially well suited for synthesizing α-methyl ...
|
|
|
5686633 |
Inks, particularly for ink jet printing
Inks, particularly inks for ink jet printing, contain at least one compound of the formula I ##STR1## as a stabilizer. The symbols R1, R2, R3, R4, R3 ' and R4 ' are as defined in claim 1. The...
|
|
|
5650428 |
Arylsulfonamide derivative and pharmaceutical compositions and use thereof
An arylsulfonamide derivative of the formula (I): ##STR1## wherein R1 is unsubstituted phenyl or naphthyl, or phenyl substituted by 1 to 3 same or different substituents selected from the group...
|
|
|
5637616 |
Method for treating diseases mediated by proteases
A method for the topical or systemic treatment of disorders mediated by proteases which result in skin or mucosal lesions, and in particular, pemphigus, cicatricial pemphigoid, bullous pemphigoid,...
|
|
|
5635608 |
α-carboxy caged compounds
The invention relates to caged compounds for the study of biological processes, where the caged compound has a photoremoveable α-carboxy-substituted o-nitrobenzyl group. Covalent attachment of the ...
|
|
|
5631405 |
Method of forming amino acid-derived diaminopropanols useful as chemical intermediates for protease-inhibitors
The present invention relates to a method of forming a 1,3-diamino-3-substituted-2-propanol chemical intermediate from which various chemicals, such as selected protease-inhibitors and other drugs,...
|
|
|
5618966 |
Method forming protease inhibitor synthetic intermediates
The present invention relates to a method of forming a 1,3-diamino-3-substituted-2-propanol chemical intermediate from which various chemicals, such as selected protease-inhibitors and other drugs,...
|
|
|
5618775 |
Mixtures of optically active cyclohexenone oxime ethers, their preparation, intermediates for this purpose and their use as herbicides
Mixtures of optically active cyclohexenone oxime ethers having R- and S-configuration in the oxime ether moiety of the formula I ##STR1## (R1 =C1 -C6 -alkyl; ##STR2## X=C1-C4 -alkyl, C1 -C4...
|