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Matches 601 - 650 out of 1,401

Document Document Title
JP4032663B2  
JP2008500337A
Formula I [化 1] The medicine composite containing the salt which can be permitted on the compound of (the inside of a formula, R, R, R, R, m, and n are as defining in a specification like salt) or its medicine, and its compound is manu...  
JP4029454B2  
JP2007330268A
To provide a flavor or taste modifier and a flavor or taste enhancer for foods, drinks and other victuals, or orally administrable medicines and compositions. The method for controlling tastes of victuals or medicines comprises following...  
JP2007537215A
5H and (9H) -6 and 8-ジオキサベンゾ cyclohepten of the present invention is new -- it is related with the use as intermediate field in composition of 7 and 7 -2 substituted derivative, its manufacture method, and the nonsteroidal ...  
JP2007512283A5  
JP2007534827A
An acetal system composite useful as 造核剤, a gelling agent, a thickening agent, or a clarifying agent is indicated. This composite may be compounded or offered with the form from which many containing two or more carbon ジアセ ta...  
JP4015192B2  
JP2007528400A
The present invention relates to the method of dealing with amyloidosis-related at least one state, an obstacle, or a disease using new molecular entities and those compounds. A calmly related group in which A-beta protein of amyloidosis...  
JP2007528420A
Muscarinic acetylcholine receptor antagonists and those directions for use are offered.  
JP3989554B2  
JP2007527408A
ホスホイノシチド dependence kinase *1 (PDK*1) inhibitor of a new class of formula (I) ; here, X is chosen from the group which consists of アルキル and halo アルキル, and; Ar is a アリール radical chosen from phenyl, ...  
JP2007231005A
To provide a new collagen production inhibitor remarkably excellent in an effect for inhibiting the production of collagen. This collagen production inhibitor contains a compound of the general formula (1) or its salt as an active ingred...  
JP2007231020A
To provide a new compound which improves the lipid barrier penetrability of a biologically active substance comprising a fatty acid such as lipoic acid and simultaneously makes a biologically active substance comprising a different fatty...  
JP2007525406A
R is H or C1*C6 アルキル, and; R the present invention H, C1*C6 アルキル, (CH) Are R, phenyl, or Ben Jill, ; n is 0 to 6, ; R is アリール, a ヘテロア reel, cycloalkyl, or hetero cycloalkyl, and; R becomes independent abou...  
JP2003521479A5  
JP2007204481A
To provide a new derivative of 3,3-diphenylpropylamines, to provide a method for producing the same, to provide a pharmaceutical composition comprising the new compound and to provide uses of the compound for preparing drugs. The derivat...  
JP3960481B2  
JP2007518849A
The present invention relates to the compound of a new class useful as chiral dopant. This compound can be obtained with the form of two mirror image isomers. Such a combination thing is useful for a display or other various products.  
JP2007518763A
How to use alpha* amino amide derivative specific in order to deal with a lower urinary tract obstacle. Without being substantially accompanied by side effects, a lower urinary tract obstacle is reduced or the medical treatment agent of ...  
JP2007517493A
The invention relates to compounds that specifically bind a T1R1/T1R3 or T1R2/T1R3 receptor or fragments or sub-units thereof. The present invention also relates to the use of hetero-oligomeric and chimeric taste receptors comprising T1R...  
JP2007516245A
The present invention is a method for dealing with the disease, especially bone arthritis of ADAMTS*5 relation, and relates to a method including prescribing for the patient a medicine with the capability to adjust ADAMTS*5 activity to t...  
JP3929702B2  
JPWO2007063925A
Provide medical treatment or a preventive medicine based on capsaicin receptor VR1 activation depressant action which was new and excellent in a nociceptive pain, a neuropathic pain, cancerous sharp pain, headache, bladder dysfunction, e...  
JP2007084552A5  
JP2007512283A
The delta* amino *gamma* ヒドロキシ *omega* アリール * alkane acid amide compound of formula (I) [化 1] which has the renin prevention characteristic, and its salt are indicated. Moreover, the medicine composite in which being ...  
JP2007509997A
The present invention relates to the compound shown by formula (I) (as B, X, Y, Z, R, and R were defined during the statement), and its salt which may be permitted pharmacologically. The present invention relates also to the use for the ...  
JP3904491B2
To provide a method for producing a compound useful as an HIV protease inhibitor in high efficiency and provide a method for producing an intermediate compound. The amide derivative expressed by formula 3 (R5, R7 and R8 are each H, an al...  
JP3904490B2
To provide a method with which a compound useful as an HIV protease inhibitor can be manufactured stereoselectively in an extremely efficient manner. A compound of formula 3 having HIV protease inhibitor activity can be obtained as follo...  
JP2007084552A
To provide novel 3,3-diphenylpropylamine derivatives, their production, pharmaceutical compositions containing the novel compound and the use of these compounds to prepare drugs.The novel 3,3-diphenylpropylamine derivatives are exemplifi...  
JPWO2007032362A
And it has the operation which controls cell responses, such as intracellular signaling or cell activation caused with toxin, and superfluous production of an inflammatory mediator resulting from them, A substitution cycloalkene derivati...  
JP2007506751A
A new calcium rivalry compound and its directions for use are offered.  
JP3895795B2
To provide a method for the control of phytopathogenic bacteria, fungi and diseases caused thereby by using a benzophenone compound having a specific structure, capable of selectively controlling the phytopathogenic bacteria, fungi and d...  
JP2002538109A5  
JP3887428B2
PURPOSE: To obtain a new compound excellent in oxidation stability, having fragrant characteristics advantageous from the viewpoint of fragrance tenacity and useful as a perfume. CONSTITUTION: A compound of formula I [X is CHO, a group o...  
JP3886196B2
To obtain a new phorbol ester derivative that has excellent inhibitory action on production of tumor necrosis factor (hereinafter abbreviated as TNF), anti-inflammatory action, anti-HIV action, etc., and is able to provide excellent phar...  
JP2007039414A
To provide an optically anisotropic compound having polymerizability, polymerization rate of a polymer, polymerization degree, transparency of the polymer, mechanical strength, applicability, solubility, crystallinity, shrinking degree, ...  
JP3867433B2
To provide a method for optically resolving the subject compound useful as an intermediate for synthesizing a chiral ketone compound, by allowing a specified chiral compound to act on a specified racemic compound and then separating and ...  
JP2006527715A
[化 1] The present invention relates to the compound of new formula (I) which has 5HT* rivalry nature. The production method of still such [the present invention] a new compound -- this -- it is related with the use as a medicine of the...  
JPWO2006129736A
The subject of the present invention provides an advantageous manufacturing method industrially [cyclic ester], It is providing an advantageous manufacturing method industrially [the annular オキシ ester which is poly (hydroxy alkylox...  
JP3852140B2
To provide the subject compound which is useful in immunoassay as a chemiluminescent substrate. This compound is represented by formula I (R1 is H, methyl, phenyl), typically (3,3-(bicyclo[3.3.l]nonane-(3,7-diyl)-4-(4-formyl-3-hydroxy- ...  
JP2006525372A
: which the present invention provides with the new beta adrenaline action nature receptor agonist compound of formula (I) -- here, R*R and w have either of the values described by this detailed letter. The medicine manufacture composite...  
JP2006290879A
To provide an external preparation for skin comprising a new ingredient having excellent bleaching effects.The external preparation for skin comprises a compound represented by general formula (1) [wherein, A represents a -(CR2R3)n- {whe...  
JP2006523196A
The present invention relates to a new molecular entity useful as a modulator of a KCNQ channel, the pharmacological preparation thing containing this compound, and the medical treatment method using this.  
JP3828161B2
PURPOSE: To provide a hydroformylation method capable of being performed under relatively mild operation conditions and enabling to achieve a high reaction rate and a high selectivity to the produced aldehyde, even when the reaction is p...  
JP2006520465A
the present invention is characterized by making following type (I) and the signaling compound come out of and expressed react to a peroxide about the method and compound which are useful for detection of the source of hydrogen peroxide....  
JPWO2005007151A1
Following general formula (I) : (the number of atoms of a main chain expresses the connection machine (the connection machine may have a substitution machine) which are 2 thru/or 5, and the inside of a formula and X are A) E expresses th...  
JP2002520385A5  
JP3809215B2
To provide a method for economically and efficiently producing a cyclic ester from an oligomer of an alkylene oxalate. This method for producing an oxalic acid alkylene cyclic ester by depolymerizing an oligomer of an alkylene oxalate co...  
JP2006206548A
To provide a new method for producing a nitrile compound on the basis of the addition reaction of R-CN to a carbon-carbon multiple bond.This method for producing the nitrile compound is characterized by using a nickel catalyst. Concrete ...  

Matches 601 - 650 out of 1,401