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Matches 701 - 750 out of 1,375

Document Document Title
JP3842132B2
N-(4-carbamimidoyl-phenyl)-glycine derivatives have the formula:wherein X and R1 to R5 are as defined herein, and includes hydrates or solvates and/or physiologically acceptable salts thereof and/or physiologically acceptable esters ther...  
JP3836425B2
A synthesis method which comprises reacting NH group-containing compounds with thiocyanates, cyanamides, nitriles or esters in the presence of a silylating agent to synthesize the corresponding nitrogen-containing addition or substitutio...  
JP3838657B2
PCT No. PCT/DE94/00756 Sec. 371 Date Feb. 6, 1996 Sec. 102(e) Date Feb. 6, 1996 PCT Filed Jun. 28, 1994 PCT Pub. No. WO95/01168 PCT Pub. Date Jan. 12, 1995The invention relates to a novel pharmaceutical preparation, containing an active ...  
JP3836892B2
PURPOSE: To obtain a new substituted cyclic amine compound having a strong and selective serotonin 2 receptor antagonistic effect and useful for prevention and therapy of hypertension, ischemic heart diseases, cerebrovascular diseases, e...  
JP2006523223A
The present invention relates to compounds of Formula (I): which are agonists of the M-1 muscarinic receptor  
JP3827530B2
Compounds that prolong thrombin time. Exemplary are:(a) rac-4-{3-[5-ethoxycarbonylmethyl-2-methyl-4-(2-methyl-pyrrol idinocarbonyl)-phenyl]-propargylamino}benzamidine,(b) rac-4-{3-[2,5-dimethyl-4-(2-methyl-pyrrolidinocarbonyl)-phen yl]-p...  
JP3821544B2
To obtain a formamidine compound being normally liquid and lowly viscous and having good compatibility with synthetic polymers. There is provided a formamidine compound represented by formula I, being normally liquid and lowly viscous an...  
JP3817263B2
The present invention provide novel substituted amidinonaphthyl ester compounds effective for treatment of thrombosis. The present invention relates to compounds represented by the following formula (I) and pharmaceutically acceptable ac...  
JP2006519832A
Methods of selectively removing counterions from compounds are disclosed. Compounds derived from the methods, such as the compound S-[2-[(1-Iminoethyl)amino]ethyl]-2-methyl-L-cysteine zwitterion with between zero and up to 2 molar equiva...  
JP3816543B2
PURPOSE: To obtain an N-arylhydrazine deriv. controlling insects and mite as harmful organisms and effective in protection from damage and loss caused by the harmful organisms. CONSTITUTION: A compd. represented by formula I {A is CR4 or...  
JP3814683B2
To prepare an amino acid composition having effects for supplementing the decrease of amino acids in blood due to strong physical exercises, reducing the changes in the concentrations of the amino acids in the blood, improving motor func...  
JP2006516671A
Novel monoamidine, monoamidoxime and bisamidine curatives, co-curatives and cure accelerators are provided for use with perfluoroelastomeric compositions as well as novel synthesis methods for making monoamidine- and monoamidoxime-based ...  
JP2006514824A
The present invention provides compositions and methods for assessing profiles of catalytically active enzymes in compositions containing a plurality of proteins. In preferred embodiments, the enzyme is a hydrolase, most preferably a cys...  
JP3770706B2
To obtain a new compound useful as a constituting component of a medicine carrier capable of efficiently and safely carrying out transfection of a nucleic acid, a polynucleotide, etc., to a cell and delivery of a medicine, a peptide, etc...  
JP3763828B2
To provide a method for producing a compound useful as an intermediate for synthesizing a precursor of a substituted benzopyran compound so as to synthesize the substituted benzopyran compound with a few steps. The method for producing a...  
JP3762790B2
This invention is directed to benzamidine derivatives substituted by amino acid and hydroxy acid derivatives which are useful as anti-coagulants. This invention is also directed to pharmaceutical compositions containing the compounds of ...  
JP2006045245A
To provide a new phenylcyclohexan-1-ylcarboxylic acid, a pharmaceutical composition containing the compound, the use of the compound in treating allergic and inflammatory diseases and the use of the compound to inhibit the production of ...  
JP2006036770A
To selectively inhibit virus (particularly influenza virus), especially glycolytic enzymes like neuraminidase, above all, viral or bacterial neuraminidase.Novel compounds of Formula (III) or Formula (IV) are described. The compounds gene...  
JP2006028021A
To produce a new organic molecule catalyst which is used for realizing an industrially useful asymmetric reaction and does not contain an organic metal.The new organic molecule catalyst is represented by formula (1) or (2). In addition, ...  
JP2006502134A
The present invention relates to new compounds of formula I, wherein P, Q, X1, X2, X3, X4, X5, R, R1, R2, R3, R4, R5, G, M1, M2, M3, m and n, are defined as in formula I, a process for their preparation and new intermediates prepared the...  
JP2006501160A
The present invention relates to the use of amidine compounds in the treatment of amyloid related diseases. In particular, the invention relates to a method of treating or preventing an amyloid-related disease in a subject comprising adm...  
JP2005538950A
Non-natural amino acids such as 2-alkylated amino acids allow for the synthesis of a wider variety of peptidal and non-peptidal pharmaceutically active agents. A method of preparing a 2-alkyl amino acid involves a Michael-type addition o...  
JP3727334B2
Compounds, compositions, and method for modulating processes mediated by Retinoid X Receptors using retinoid-like compounds which have activity selective for members of the subclass of Retinoid X Receptors (RXRs), in preference to member...  
JP2005535710A
This invention provides certain compounds, methods of their preparation, pharmaceutical compositions comprising the compounds, and their use in treating human or animal disorders. The compounds of the invention are useful as antagonists,...  
JP2005535570A
The present invention relates to novel amino substituted pyrimidinone derivatives of the general formula (I), their derivatives, their analogs, their tautomeric forms, their stereoisomers, their polymorphs, their hydrates, their solvates...  
JP3712208B2
The present invention is related to novel intermediates and processes which are useful in the preparation of certain antihistaminic piperidine derivatives of formula (I) wherein W represents -C(=O)- or -CH(OH)-; R 1 represents hydrogen o...  
JP3704649B2
Compounds of the formula Iin whichY is hydrogen, C1-C4alkyl, C1-C4alkoxy, OH, CN, NO2, Si(CH3)3, CF3 or halogen,Z is a group a)R1 is hydrogen, C1-C4alkyl, C2-C4alkenyl, C2-C4alkynyl, C3-C6cycloalkyl, phenyl which is unsubstituted or at m...  
JP2005529934A
A process for preparing xanthine phosphodiesterase V inhibitors, and compounds utilized in said process. The process includes a five-step methodology for efficient synthesis of Compound 5 without intermediate purifications or separations...  
JP2005263809A
To provide a method for protecting important agronomic crops from harmful and damaging action caused by noxious organisms of insects and ticks.The N-aryl hydrazine derivative is represented by formula I [for example, 2,2-dimethyl propion...  
JP2005525413A
The present invention relates to compounds, and prodrugs thereof, compositions and methods useful for preventing and treating thrombotic conditions in mammals. The compounds of the present invention, and prodrugs thereof, selectively inh...  
JP2005524706A
Compounds of the formula (R5)m-(R6A)-2-(R4)-1-[N-C(R1)N(R2)(R3)]benzene and their agriculturally suitable salts, are disclosed which are useful as fungicides, wherein R1 is H, OH, SH, SO3H, CN, -OR7 or -SR7; C1-C10 alkyl, C2-C10 alkenyl,...  
JP3676236B2
The invention is concerned with novel N-(4-carbamimidoyl-phenyl)-glycine derivatives of the formula: wherein R1, E, X1 to X4 and G1 and G2 are as defined in the description and the claims, as well as hydrates or solvates and physiologica...  
JP2005519994A
The invention relates to novel substituted aryl and heteroaryl derivatives of general formula (I), in which A, Ar, n, X, Y1, Y2, Y3, Y4, R1, and R5 are defined as per claim 1, to their prodrugs, tautomers, stereoisomers, mixtures and sal...  
JP2005519866A
The present invention relates to compounds, and prodrugs thereof, compositions and methods useful for preventing and treating thrombotic conditions in mammals. The compounds of the present invention, and prodrugs thereof, selectively inh...  
JP2005516062A
The present invention relates to compounds of formula (I):  
JP2005126332A
To provide a means for producing high-purity formamidine acetate in high yield by an economical and simple method.A method for production is carried out as follows. A reaction is made to proceed under refluxing conditions when the formam...  
JP2005514332A
The present invention relates to compounds, and prodrugs thereof, composition and methods useful for preventing and treating thrombotic conditions in mammals. The compounds of the present invention, and prodrugs thereof, selectively inhi...  
JPWO2003027060A1
Provided are a compound represented by the following general formula (1), which has a higher selectivity for a smooth muscle muscarinic receptor than a cardiac muscarinic receptor and has a strong antagonistic effect, and a salt and hydr...  
JP2005509606A
The present invention relates to prodrug compounds, comprising a 5- or 6- membered heterocyclic or aromatic ring substituted with a derivatized amidine, as well as compositions and methods useful for preventing and treating thrombotic co...  
JP2005508874A
Substituted N-acylaniline derivatives of general formula wherein R<1 >to R<5>, A, X, Y, and Z are as defined herein, and the tautomers, prodrugs, and derivatives thereof which contain, instead of a carboxy group, a group which is negativ...  
JP2005508307A
There are provided novel compounds of formula (I), wherein R1, R2, R3, T, U, X, Y, V and W are as defined in the specification, and pharmaceutically acceptable salts thereof, and enantiomers and racemates thereof; together with processes...  
JP2005507380A
This invention concerns HIV replication inhibitors of formulathe N-oxides, the pharmaceutically acceptable addition salts, the quaternary amines and the stereochemically isomeric forms thereof, wherein the ring containing -a1=a2-a3=a4- a...  
JP2005504827A
Disclosed are novel cathepsin S, K, F, L and B reversible inhibitory compounds of the formulas (Ia) and (Ib) where R1, R2, R3, R4, R5, R6, R8, R9 and X are defined herein. The compounds are useful for treating autoimmune and other diseas...  
JP2005504053A
The present invention relates to the use of amidine compounds in the treatment of amyloid-related diseases. In particular, the invention relates to a method of treating or preventing an amyloid-related disease in a subject comprising adm...  
JP3614711B2
To obtain a new compound useful for a production intermediate compound of a selective inhibitor for an inducible nitric-oxide synthase. This compound is expressed by formula I (Q is H or a carboxy protecting group; Q' is a protecting gro...  
JP3611517B2
A new family of aminoamidine derivatives is claimed, which are oil soluble and have good filtering properties for UV-A and UV-B radiation and thus protection from solar irradiation. Cosmetic compositions for external use, particularly fo...  
JP2005500259A
Agents and methods for chemoprevention and treatment of neoplasia are described, the agents including a selective inhibitor of inducible nitric oxide synthase and a combination of a selective inhibitor of inducible nitric oxide synthase ...  
JP2004359609A
To provide a method by which cyclopropylcarbamidine hydrochloride can economically and industrially advantageously be produced in a favorable yield.The production method for cyclopropylcarbamidine hydrochloride represented by formula (II...  
JP2004535379A
Energy-reversible acyl conjugates, intermediates, and related compositions are disclosed. In preferred aspects, examples of such compositions include:  
JP2004535362A5  

Matches 701 - 750 out of 1,375