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Matches 601 - 650 out of 1,363

Document Document Title
JP2009521505A
The present invention is formula (I) generally:The inside of [type, variable portion A, B, and L, M, W, Z, R1R2R3R4R5R6R7R8R9And R10It is related with a new macrocyclic molecule or its stereoisomeric form, a tautomerism object, salt perm...  
JP2009107953A
To provide a new agricultural/horticultural bactericide and to provide a production method of a new compound as an effective ingredient thereof.The agricultural/horticultural bactericide comprises as an effective ingredient at least one ...  
JP2009108054A
To provide a new compound useful for treating infection with vancomycin-resistant bacteria.The new peptoid compound is useful especially against infection with gram-positive bacteria including the vancomycin-resistant and methicillin-res...  
JP2009519252A
The present invention relates to the new macrolide compound of general formula I which has antibacterial activity and antitumor activity useful as at least 1 side of the medicine and agricultural chemicals which are used for the medical ...  
JP2009102437A
To provide the intermediate compounds useful for production of 3-(1-hydroxyphenyl-1-alkoximinomethyl)-dioxazines which are known as intermediates for preparing compounds having fungicidal properties.There are provided the compounds of -n...  
JP4263200B2  
JP4259620B2  
JP2009513510A
The present invention is formula I. [Formula 1][Inside of a formula, R1は (C)1*8アルキル (C),1*4Alkoxy (C)1*4アルキル, hydroxy (C)1*6アルキル (C),1*4アルキルチオ (C)1*4アルキル (C),1*6アルケニル (C),3*7Cycloal...  
JP2009062355A
To provide a new nitrogen-containing heterocyclic compound or its salt, and to provide a pest control agent containing the compound as an active ingredient.Provided are a nitrogen-containing heterocyclic compound represented by formula (...  
JP2009511430A
Amide is formed by making amine containing the nitrogen which carried out the covalent bond, or its salt react to the atom chosen from alpha* keto acid or its salt, oxygen and nitrogen, and sulfur by a 脱 carboxyl condensation reaction....  
JP2009510013A
The compound of formula (I) with the present invention useful for the medical treatment of the medical treatment of human immunodeficiency virus (HIV) infection, prevention, AIDS (AIDS), or ARC (inside of a formula, R)1*R4It provides as ...  
JP2008526912A5  
JP2008546815A
The present invention indicates the substitution p* truffe ルオロ methylphenyl ether shown by formula (I), its manufacture, and use [here, each substituent is as a definition during detailed explanation]. This invention compound has e...  
JP4202898B2  
JP4181632B2  
JP4176077B2  
JP4172895B2  
JP2008247806A
To efficiently synthesize cyclic octadepsipeptide PF1022.The PF1022 represented by the general formula (II) (wherein, R1, R2, R3 and R4 represent each a hydrocarbon group which may have the same or different substituent) are efficiently ...  
JP4160115B2  
JP2008222568A
To provide an oligomer-type chiral salen compound, and to provide a method for producing the chiral compound from a racemic epoxide.The oligomer-type chiral salen compound is represented by formula (1). The method for producing the chira...  
JP4149532B2
Arylalkyldiazinone derivs. of formula (I) and their salts are new: B = aromatic heterocycle with 1-4H, O and/or S atoms bonded to N or C (opt. mono-, di- or tri-substd. by Hal, A and/or OA and opt. condensed with a benzene or pyridyl rin...  
JP2008528507A
The present invention explains arbitrarily at least one cardiovascular compound containing at least one heterocyclic nitric oxide donor machine, the composite containing at least one nitric oxide reinforcement compound and/or at least on...  
JP4126121B2  
JP2008526912A
R, R, V, V, X, X, Y, Z, Ar, AA, and n of the present invention are as the definition with a specification among the formula [化 1] [type of separated type or acid addition salt type, and the number of the ring atoms contained in this si...  
JP2008162953A
To provide a new cyclic ether amide lipid constructing molecular aggregates by self-organization, and a lipid membrane forming a moderate intramolecular hydrogen bond.This new cyclic ether amide lipid of 2 glycerol derivatives and 2 long...  
JP2008523059A
The compound of formula (I) or a stereoisomeric form, a tautomer, or its pharmacological composite that contains pharmacologically the salt which can be received or a solvation thing, and the compound of formula (I) is indicated. Moreove...  
JP4105805B2  
JP4106134B2  
JP2008520670A
The present invention is inhibitor of beta* secretase enzyme, and relates to the large annular tertiary-amine compound expressed to the medical treatment of the illness in which beta* secretase enzyme participates, for example, Alzheimer...  
JPWO2006080323A1
骨粗鬆症や骨折などの骨疾患、さらには緑内 障又は潰瘍性大腸炎の予防及び/又は治療に 有効な医薬の有効成分として利用可能な一般 式(I):[化1][Tは酸素原子等を示...  
JP2008520598A
The present invention relates to use of the 殺内部 verminousness デプシ peptide for manufacture of the medicine for prevention of perpendicular internal parasitism insect infection.  
JP4104653B2  
JP2008517965A
The manufacture method of [1, 4, 5] -オキシジアゼピン derivative by making 4 and 5-Zia シル- [1, 4, 5] -オキシジアゼピン react to a base.  
JP4090514B2
The present invention relates to compounds of the formula Q is selected from the group consisting of G is selected from the group consisting of alkyl, substituted alkyl, substituted or unsubstituted aryl, heterocyclo, W is O or NR15; X i...  
JP4090070B2  
JP2008515827A
general formula (I) of the present invention is new -- 1, 3, and a 4* オキサジ azine *5* ON derivative --those use for manufacturing the medicine used for those use for the disposal of those production methods and a disease, and/or p...  
JPWO2006011466A1
The compound concerning the present invention and its salt which can be permitted in medicine are denoted by the following general formula (1). [R1, R2, R3, R4, and X show R1, R2, R3, R4, and X and the meaning in a specification among a ...  
JP2008092952A
To provide an effective method for preparation of substituted aryl lactic acid containing cyclodepsipeptides.The invention relates to the new method for the preparation of substituted aryl lactic acid containing cyclodepsipeptides with 2...  
JP4070270B2  
JP4065053B2  
JP4054063B2  
JP2008503458A
The present invention offers the macrocyclic compound in which a new high order structure where it was proved that it is an alternative modulator (a growth hormone secretion promotion medicine receptor (GHS*R 1a) and its subtype, an iso ...  
JP4035852B2  
JP4033920B2  
JP4029047B2  
JP2007538106A
The present invention offers N* ring type sulfonamide compound for using it in the medical treatment or prevention of Alzheimer's disease etc. Of consciousness disorder. Especially an important compound is defined by formula (I) and R, R...  
JP2007314580A
To enhance the endoparasiticidal activity of cyclic depsipeptides. The present invention relates to the use of praziquantel and epsiprantel for enhancing the endoparasiticidal activity of cyclic depsipeptides in endoparasiticidal composi...  
JP2007535568A
The present invention offers the directions of the compound for dealing with or preventing the disease or obstacle relevant to activity of a compound, the medicine composite containing this compound, and the cathepsin S to apply.  
JP4016097B2  
JP2007534696A
The present invention relates to a composite and a method useful although it deals with a central nervous system (CNS) obstacle. Furthermore, the present invention offers the composite and method of dealing with sleep disorder. Furthermo...  

Matches 601 - 650 out of 1,363