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Matches 551 - 600 out of 1,055

Document Document Title
JP4035852B2
An industrially excellent alternative process for producing cyclodepsipeptide derivatives, as represented in formula (1), having an excellent vermicidal activity as an animal and human anthelmintic, wherein R1 represents hydrogen or a hy...  
JP4033920B2
Endoparasitic activity of cyclic depsipeptides (I) comprising amino acid and hydroxycarboxylic acid units and having 6-30 ring atoms is increased by praziquantel (II) and epsiprantel (III). An endoparasitic agent contg. (I) together with...  
JP4029047B2
Production of polyisocyanates by catalytic conversion of aliphatic diisocyanates comprises using a catalyst consisting of a salt in which the anion comprises 5-97.1 wt.% of 1,2,3- and/or 1,2,4-triazolate structures.  
JP2007538106A
The invention provides N-cyclic sulfonamido compounds for use in treating or preventing cognitive disorders, such as Alzheimer's Disease. Compounds of particular interest are defined by Formula I, wherein R4, R5, R6, R7, and R8, are as d...  
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...  
JP4016097B2  
JP2007534696A
The invention is directed to compositions and methods useful for treating Central Nervous System (CNS) disorders. Furthermore, the invention provides compositions and methods of treating sleep disorders. More specifically, the invention ...  
JP4015192B2
Disclosed are "acid-amide" calixarenes of formula (I) wherein: L is [-CH2-] or [-O-CH2-O-] and may be the same or different between each aryl group; R5 is H, halogen, or C1-C10 aliphatic hydrocarbyl group, C6-C20 aryl group, C6-C20 hydro...  
JP2007533718A
Compounds having therapeutic utility are of general formula (1) wherein R, is H, C 1-C6 alkyl optionally substituted with F or C3-C6 cycloalkyl or C2-C4 alkenyl; A is O, CH2 or S(O)n where n is 0-2; one of W, X, Y and Z is N, CH or CR3 a...  
JP2007297303A
To provide an organic luminous element prevented from the depletion of luminous intensity. An organic luminous compound is provided, which has a specific structure having a site with the function of a dopant and the function of a host in...  
JP4001381B1
Novel derivatives of PF1022 substance, which are cyclodepsipeptides represented by the general formula (I) shown below or their salts are useful as anthelmintic agent for prevention or treatment of parasitic infections.  
JP3995300B2
Isocyanate trimers (or mixtures) (I) based on aliphatic,cycloaliphatic, aromatic or araliphatic mono- or poly-isocyanates (II) with a NCO content of less than 70%, optionally with other substituents in the organic groups, such as carbony...  
JP2007528420A
Muscarinic Acetylcholine receptor antagonists and methods of using them are provided.  
JP3985050B2
A novel industrial process for producing an anthelmintic depsipeptide derivative represented by structural formula (I), which is excellent in the yield etc.  
JP2007238510A
To provide an optically active compound highly sensitive and responsible in high speed. The optically active compound is expressed by general formula (I), wherein X1, X2, X3and X4express each independently -NH2, -N(CH3)2, -H, -CpF2p+1, -...  
JP3968933B2
To provide high luminance and shelf life electroluminescent element and highly luminescent color filter based on that electroluminescent element by using inorganic and/or rare-earth complex based phosphor. An electroluminescent element c...  
JP3954127B2
PURPOSE: To obtain a new cyclic amide derivative exhibiting excellent weeding activity to injurious weed generating in paddy field or upland field in soil treatment or stem and leaf-treatment and exhibiting high safety to crop and useful...  
JP2007519639A
The invention relates to compounds of formula wherein Het, A1, A2, A3, A4, D, W, T, Q, Y, X1, X2, R1, R2, R3, R4, k and m are as defined hereinabove, and, where applicable, to possible E/Z isomers, mixtures of E/Z isomers and/or tautomer...  
JP2007182456A
To provide a herbicide having a selective action for killing only weeds without damaging crops, even when simultaneously applied to both the crops and the weeds.A cyclic amide derivative represented by the general formula [I] [-A-B- is -...  
JP3932559B2
The invention refers to a pharmaceutical composition suitable for the protection of the mitochondrial genom and/or mitochondrium from damages or for the treatment of diseases connected with such damages, said composition comprising 0.1 t...  
JP3926662B2
To provide a new polymer responding to the chirality of a wide range of optically active substances in improved sensitivity and provide a monomer for the polymer. The invention relates to a polyaryl acetylene derivative and its monomer h...  
JP2007513166A
Certain noel N-(heteroarylalkyl)alkanediamine derivatives have provided unexpected insecticidal and acaricidal activity. These compounds are represented by formula I: wherein Ar, a, r, R, Ra, Rb, Rc, Rd, b, c, Re, Rf, Rg, Rh, R5, d, e, U...  
JP3909870B2
PURPOSE: To provide the novel compounds useful as immunosuppressants, anti- inflammatory agents, antifungal agents, antiproliferative agents and antitumor agents. CONSTITUTION: By protecting an alcoholic site of paramycin with a protecti...  
JP3907207B2
Provided is a compound of the formula: I This compound is an intermediate to and is used for preparing the arthropodicidal oxidiazine Compound II described in the specification.  
JP3887769B2
This invention relates to the use of a group of aryl ureas in treating cytokine mediated diseases and proteolytic enzyme mediated diseases, and pharmaceutical compositions for use in such therapy.  
JP3887784B2
PCT No. PCT/EP94/02533 Sec. 371 Date Feb. 5, 1996 Sec. 102(e) Date Feb. 5, 1996 PCT Filed Jul. 29, 1994 PCT Pub. No. WO95/04728 PCT Pub. Date Feb. 16, 1995The application relates to new azadioxacycloalkenes of the formula (I) (I) in whic...  
JP3882411B2
To provide a method for readily and environmentally-friendly producing 3,3-alkyleneoxaziridine in high yield. A cycloalkanone is reacted with ammonia and hydrogen peroxide, and the product is reacted with a carboxylic acid and/or a carbo...  
JP3882195B2
A method for making a compound of Formula I which is racemic or enantiomerically enriched at chiral center* comprising hydrogenating a compound of Formula V in the presence of a compound of Formula VII wherein: R 1 is F, Cl, or C 1 -C 3 ...  
JP2007501769A
The present invention relates to the use of sulphonamide salts as catalysts for oligomerizing isocyanates and also to a process for NCO oligomerization using the catalysts of the invention.  
JP3855538B2
To provide a processing solution for a silver halide photographic sensitive material having rapid desilvering performance, not causing the stain of an edge part and excellent in liquid preservation stability and environmental suitability...  
JP2006527763A
The present invention concerns the use of a sphingoid-polyalkylamine conjugate as a capturing agent of biologically active molecules, such as antigens. In a particular embodiment, the spinogid-polyalkylamines are used for the preparation...  
JP2006308474A
To provide a means which simply and highly sensitively measures heavy metal ions including trivalent heavy metal ions, without using any flame.A mass analyzing reagent for measuring the heavy metal ions is provided, which is composed of ...  
JPWO2005023788A1
Microbes belonging to Beauveria sp. And capable of producing FKI-1366 substance A and / or FKI-1366 substance B and / or FKI-1366 substance C (Beauveria sp. FKI-1366, FERM BP- 08459) was cultured in a medium, FKI-1366 substance A and / o...  
JP3837461B2
To obtain the subject new compound having crown ether structure, high in ion transfer ability, capable of solid phase polymerization, and useful as a raw material for functional materials such as electroconductive materials, electrode ma...  
JP2006523691A
Disclosed herein is an antioxidant that is an alkylated iminodibenzyl of the general formula: wherein: R1, R2, R3, and R4 are independently selected from the group consisting of hydrogen, alkyl moieties, and alkenyl moieties; and R5, R6,...  
JP2006523232A
Compounds useful for treating cellular proliferative diseases and disorders by inhibiting the activity of KSP are disclosed.  
JP2006232691A
To provide a method for synthesizing the oligomer by using a lactic acid modified with amino acid (for example, glycyl-lactic acid or the like).The oligodepside compound is a compound represented by any of formula (1), formula (2) and fo...  
JP3790424B2
A compound having formula (I) or a pharmaceutically acceptable salt or prodrug thereof, is an immunomodulatory agent and is useful in the treatment of restenosis and immune and autoimmune diseases. Also disclosed are cancer-, fungal grow...  
JP2006514939A
Methods of making substituted phenylalkynes of formula (I).  
JP3749253B2
PCT No. PCT/GB95/00019 Sec. 371 Date Jun. 20, 1996 Sec. 102(e) Date Jun. 20, 1996 PCT Filed Jan. 6, 1995 PCT Pub. No. WO95/18808 PCT Pub. Date Jul. 13, 1995Linked polyamine cyclic compounds of general formula V-R-A-R'-W where V and W are...  
JP2006501291A
Serratamolide, also named cycloÄ(3R)-3-hydroxydecanoyl-L-seryl-(3R)-3-hydroxydecanoyl -L-serylÜ, is a cyclic depsipeptide isolated from cultures of bacteria of the species Serratia marcescens. Serratamolide decreases the viability of, ...  
JP2005538926A
An ammonium selective ionophore for use in ion selective electrodes.  
JP2005533030A
The invention provides a method for preventing or reducing the effects of oxidative stress on a substrate. The method includes the step of treating the substrate with a compound of formula (I), or a pharmaceutically acceptable salt there...  
JP2005272452A
To provide a new agricultural chemical, particularly an insecticide or acaricide.This invention relates to a substituted benzanilide compound represented by general formula (1) [wherein G is a ring such as G-7, G-13, G-71 or the like; W1...  
JP2005247716A
To provide an ABC(ATP-binding cassette) transporter inhibitor overcoming the multidrug resistance(MDR) to anticancer drugs due to the amplification and expression of MDR1 gene as the most important problem in cancer chemotherapy or the d...  
JP3693366B2
PURPOSE: To provide a new compound useful as a endoparasiticide for human beings and animals, etc. CONSTITUTION: A compound of the formula I [R1, R2, R11 and R12 are each 1-8C alkyl, 1-8C halogenoalkyl, 3-6C cycloalkyl, aralkyl or aryl; ...  
JP2005523925A
It has now been found that certain novel heterocyclic derivitives have provided unexpected insecticidal activity. These compounds are represented by formula (I): R Preferred are those compounds of formula (I) where R2 and R3 taken togeth...  
JP2005162760A
To provide a fungicide for protecting plants.The new azadioxacycloalkene is represented by formula (I) (wherein A is an alkanediyl; Ar is an arylene or the like; E is 1-alkene-1 or the like having a R1 group; R1 is hydrogen, a halogen or...  
JP2005132727A
To provide a new dioxazine derivative useful as an insecticidal and acaricidal active ingredient.The dioxazine derivative is represented by general formula (1) [wherein, R1 denotes a hydrogen atom, an alkyl group or an alkoxyalkyl group;...  
JP3652986B2
The present invention relates to novel herbicidally active 3-hydroxy-4-aryl-5-oxopyrazoline derivatives, to processes for their preparation, to compositions which comprise these compounds and may additionally comprise safeners, and to th...  

Matches 551 - 600 out of 1,055