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JP2024515215A |
Formula (I) useful as antineoplastic and antibacterial agents: [Formula 1] and compositions and methods of using the antineoplastic and antimicrobial compounds.
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JP2024514316A |
Enantiopure (S)-methadone, (R)-methadone, (R,S) with preservation of stereochemical configuration starting from optically active or racemic N-substituted cyclic sulfamidates or N-substituted aziridines -Methods for the synthesis of metha...
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JP7449913B2 |
Oxathiazin-like compounds, processes for making new oxathiazin-like compounds, compounds useful for making oxathiazin-like compounds, and their uses are disclosed. Processes of treating patients suffering from cancers, bacterial infectio...
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JP7339677B2 |
Disclosed in the present invention were a fluorosulfonyl-containing compound, an intermediate thereof, a preparation method therefor and use thereof. The fluorosulfonyl-containing compound disclosed in the present invention comprises a c...
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JP2023093679A |
To provide a composition and a method for producing high-purity acesulfame potassium.A method for producing high-purity acesulfame potassium comprising: forming a cyclic sulfur trioxide adduct; hydrolyzing the cyclic sulfur trioxide addu...
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JP2023093678A |
To provide a composition and a method for producing high-purity acesulfame potassium.A manufacturing method of an acesulfame potassium composition comprises: preparing a crude acesulfame potassium composition comprising acesulfame potass...
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JP7270670B2 |
Compositions and processes for producing high purity acesulfame potassium are described. One process comprises the steps of providing a crude acesulfame potassium composition comprising acesulfame potassium and acetoacetamide, concentrat...
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JP7270671B2 |
Compositions and processes for producing high purity acesulfame potassium are described. One process comprises the steps of forming a cyclic sulfur trioxide adduct; hydrolyzing the cyclic sulfur trioxide adduct to form an acesulfame-H co...
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JP2023052166A |
To provide a method of treating diseases.The present disclosure relates generally to eukaryotic initiation factor 2B modulators, or pharmaceutically acceptable salts thereof, stereoisomers, mixtures of stereoisomers, or prodrugs thereof,...
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JP2023502791A |
The present disclosure provides compounds of formula (I) or (II): [Chemical 1] and pharmaceutically acceptable salts or solvates thereof. The disclosure also relates to pharmaceutical compositions comprising said compounds, and therapeut...
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JP7169977B2 |
Compositions and processes for producing high purity acesulfame potassium are described. One process comprises the steps of forming a cyclic sulfur trioxide adduct; hydrolyzing the cyclic sulfur trioxide adduct to form an acesulfame-H co...
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JP7111796B2 |
Improved processes for producing high purity acesulfame potassium. In one embodiment, the process comprises the steps of contacting a solvent, e.g., dichloromethane, and a cyclizing agent, e.g., sulfur trioxide, to form a cyclizing agent...
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JP7108741B2 |
A process for producing acesulfame potassium, the process comprising the steps of providing a cyclizing agent composition comprising a cyclizing agent and a solvent and having an initial temperature, cooling the cyclizing agent compositi...
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JP7043096B2 |
This invention provides preparations, compositions, products, and applications of photo-crosslinked hydrogels. Component A - a photosensitive polymer derivative, component B - the photoinitiator, and auxiliary component C - other biocomp...
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JP2022517466A |
The present invention provides novel compounds and compositions thereof that release carbon monoxide for the treatment of carbon monoxide-reactive medical disorders, such as inflammation, pain, and dermatological disorders. [Selection di...
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JP7030093B2 |
Oxathiazin-like compounds, processes for making new oxathiazin-like compounds, compounds useful for making oxathiazin-like compounds, and their uses are disclosed. Processes of treating patients suffering from cancers, bacterial infectio...
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JP2022501411A |
The present invention provides a method for preparing a compound of formula C, formula D, or formula F.
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JP2021531303A |
The present invention relates to a composition of sodium ellagolix, as well as a method for preparing the composition and an intermediate for the preparation thereof.
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JP6914201B2 |
Inhibitors of HBV replication of Formula (I-A)including stereochemically isomeric forms, and salts, hydrates, solvates thereof, wherein Rato Rd, and R1to R8have the meaning as defined herein.The present invention also relates to processe...
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JP6913692B2 |
Oxathiazin-like compounds, processes for making new oxathiazin-like compounds, compounds useful for making oxathiazin-like compounds, and their uses are disclosed. Processes for efficient and safe manufacture of compounds useful for maki...
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JP6912582B2 |
A process for producing acesulfame potassium, the process comprising the steps of providing a cyclizing agent composition comprising a cyclizing agent and a solvent and having an initial temperature, cooling the cyclizing agent compositi...
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JP6912581B2 |
Compositions and processes for producing high purity acesulfame potassium are described. One process comprises the steps of providing a crude acesulfame potassium composition comprising acesulfame potassium and acetoacetamide, concentrat...
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JP6818896B2 |
Improved processes for producing high purity acesulfame potassium. In one embodiment, the process comprises the steps of contacting a solvent, e.g., dichloromethane, and a cyclizing agent, e.g., sulfur trioxide, to form a cyclizing agent...
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JP2020530446A |
The present disclosure generally describes eukaryotic initiation factor 2B modulators, or pharmaceutically acceptable salts thereof, stereoisomers, mixtures of stereoisomers, or prodrugs, and their manufacture and use. Regarding the meth...
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JP6746605B2 |
Oxathiazin-like compounds, processes for making new oxathiazin-like compounds, compounds useful for making oxathiazin-like compounds, and their uses are disclosed. Processes of treating patients suffering from cancers, bacterial infectio...
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JP6630671B2 |
The present invention relates to bis aryl analogs, pharmaceutical compositions containing them and their use as Nrf2 regulators.
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JP6577951B2 |
The present invention relates to compounds according to general formula (I) which are analogues of epoxymetabolites produced by cytochrome P450 (CYP) enzymes from omega-3 (n-3) polyunsaturated fatty acids (PUFAs). The present invention f...
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JP6281952B2 |
The present invention provides a novel compound having an antiviral activity, in particular, an HIV replication inhibiting activity, as well as a pharmaceutical composition, in particular, an anti-HIV agent. wherein ring A is substituted...
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JP6262228B2 |
Compounds of the formula I: or pharmaceutically acceptable salts thereof, wherein m, n, p, q, r, A, W, X1, X2, X3, X4, Y, Z, R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R11, and R12 are as defined herein. Also disclosed are methods of makin...
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JP6111276B2 |
The conformationally restricted, spatially defined macrocyclic ring system of formula (I) is constituted by three distinct molecular parts: Template A, conformation Modulator B and Bridge C. Macrocycles described by this ring system I ar...
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JP6013403B2 |
The invention relates to methods, compounds, compositions and vehicles for delivering 3-amino-1 -propanesulfonic acid (3APS) in a subject, preferably a human subject. The invention encompasses compounds that will yield or generate 3APS, ...
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JP5991766B2 |
Compounds and compositions comprising epoxyeicosatrienoic acid (EET) analogs that act as EET agonists and are useful as medications in the treatment of drug-induced nephrotoxicity, hypertension and other related conditions. Methods of ma...
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JP5892612B2 |
The invention pertains to compound of Formula (I) wherein X, Y, Z, R1, R2, R3, R4, A and A′ are as described hereinabove. Formula (I) and (II) compounds can be used in pharmaceutical compositions, useful for the treatment of diseases.
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JP2015145401A |
To provide compounds for medicament to inhibit histone deacetylase.This invention provides a compound such as phenyl hydroxamic acid substituted with a group comprising, for example, oxazepine, diazepine, thiazepine skeletons, pyrimidine...
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JP5638250B2 |
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JP2014521592A |
To provide pesticidal allylAryl heterocycle derivatives that are useful as a pesticidal compound. Pesticidal allylAryl heterocycle derivatives that are expressed by the Formula (I), and pesticides and an agent for controlling animal para...
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JP2014516343A |
This invention relates to novel compounds suitable for labelling by 18F and the corresponding 18F labelled compounds themselves, 19F-fluorinated analogues thereof and their use as reference standards, methods of preparing such compounds,...
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JP5519862B2 |
The object of the present invention is to provide an ionic liquid having a chiral center in the structure of a cation contained therein, a lithium secondary battery electrolyte includes the ionic liquid, and a lithium secondary battery i...
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JP5410677B2 |
There are provided a process for preparing an optically active aminopentane derivative that is promising as a psychotropic agent, an antidepressant agent, an antiparkinsonian agent, an anti-Alzheimer's agent, an apoptosis inhibitor, or t...
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JP2013537216A |
Phenoxy-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine-dioxide compounds (I) and their enantiomers and diastereoisomers, and addition salts with an acid or a base, are new. Phenoxy-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine-dioxide compoun...
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JP5219323B2 |
This invention relates to compounds of the formula: ##STR00001## wherein: the substituent groups defined by R.sub.1, R.sub.2 are each independently selected of H, C(.dbd.O)R', C.sub.1 C.sub.18 alkyl, C.sub.2 C.sub.18 alkenyl, C.sub.2 C.s...
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JP2013104031A |
To provide an electrically conductive composition which becomes a film having excellent electrical conductivity and contains an electrically conductive polymer having excellent thermal stability, and to further provide an electrically co...
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JP2013512893A |
The present invention relates to processes for the preparation of deferasirox, an oral iron chelator developed to treat iron overload due to e.g. multiple blood transfusions. The present invention further provides novel deferasirox pseud...
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JP2012232910A |
To provide pesticidal allyl heterocycle derivatives that are useful as a pesticidal compound.This invention relates to: the pesticidal allyl heterocycle derivatives are expressed by the Formula (I); and pesticides and an agent for contro...
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JP5063860B2 |
Diamidine derivatives of formula (I) and their salts are new. Amidine derivatives of formula (I) and their salts are new. [Image] X : a group of formula (ii) or R 4; Z : -(CH 2) m-; m : 8 - 21; n : 0 or 1; Y : R 3 or a group of formula (...
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JP5008812B2 |
Antitumor compounds have the five membered fused ring ecteinascidin structure of the formula (XIV). The present compounds lack a 1,4-bridging group as found in the ecteinascidins. They have at the C-1 position a substituent selected from...
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JP2012512141A |
4-Amino-1,2,3-benzoxathiazine compounds (I) and their salts, are new. 4-Amino-1,2,3-benzoxathiazine compounds of formula (I) and their salts are new. R1-R4 : H, halo, carbamoyl, thiocarbamoyl, nitro, cyano, hydroxy, SF 5 , 1-6C-alkyl, 2-...
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JPWO2010044371A1 |
Sweet receptor agonists such as Acesulfarm K, sucralose, saccharin or glycyrrhizin are used as active ingredients of insulin secretagogues. In addition, a test compound is added to cells expressing a sweet taste receptor, the sweet taste...
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JP4854853B2 |
Disclosed are compounds capable of facilitating transport of biologically active agents or substances into cells having general structure (A):
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JP4818114B2 |
Compounds of formula I: inhibit gamma-secretase and hence find use in treatment or prevention of Alzheimer's disease.
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