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JP7158096B2 |
Described herein are methods for the production of oligosaccharides, including functionalized oligosaccharides, from one or more sugars, such as one or more monosaccharides, using polymeric and solid-supported catalysts containing acidic...
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JP7077165B2 |
To provide a method for producing a sulfate of a hydroxy compound capable of easily producing a sulfate without using special reagents, equipment or reaction conditions and suppressing the decomposition of the hydroxy compound compared w...
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JP2021530479A |
The present invention eliminates the use of protective groups on intermediates, improves stereoselectivity of glycosylation and reduces the number of process steps required to produce the compound, 4'-ethynyl 2'-deoxy. With respect to th...
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JP2021508732A |
Provided are compounds of formula (A) used in the prevention or treatment of joint and bone disorders in mammals, such as arthritis and osteoporosis, as well as pharmaceutically acceptable salts and esters thereof, and pharmaceutical com...
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JP2020534361A |
The compounds of formula (I) and pharmaceutically acceptable salts thereof are disclosed herein. [Chemical 1] The variables in formula (I) are described herein. Methods for synthesizing such compounds, as well as for treating diseases an...
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JP6765371B2 |
The present invention relates to a family of carbohydrate monosulphate fatty acid esters, which contain less than 10 mole % of carbohydrate polysulphate fatty acid esters, and to a method of preparation thereof. The monosulphate carbohyd...
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JP6662503B2 |
The present invention provides a pentosan polysulfate having a uronic acid content of 7.0 mass% to 15.0 mass% and an acetyl group content of 0 mass% to 2.0 mass%; a pharmaceutically acceptable salt thereof; or a pharmaceutically acceptab...
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JP6595460B2 |
A molecule responding to formula (I) of the glycocluster type with galactose residues at their extremities. Simple and efficient methods for the preparation of these compounds. Medical use of compounds (I) as inhibitors of infections by ...
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JP6526692B2 |
The present invention relates to synthesis of novel higher oligomers and process of preparing the same. In particular the present invention relates to the chemical synthesis of oligomers of Neisseria meningitidis serogroup X (‘hereinaf...
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JPWO2018043667A1 |
According to the present invention, as a production method in which the cost of acidic xylooligosaccharide is reduced, a step of depolymerizing a plant-derived raw material and a deacetylation step of adjusting the solution of the produc...
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JP6339673B2 |
The present invention provides novel processes for the preparation of Fondaparinux sodium by using the compound of formula ABC5. In some embodiments, the intermediates for the synthesis of Fondaparinux sodium, are also provided.
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JP6004586B2 |
The present invention relates to trisaccharide derivates comprising a substituted trisaccharide core, which trisaccharide core is fully substituted with fatty acid ester groups, and optionally one or more anionic groups, to a method for ...
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JP5998211B2 |
The invention relates to a sucrose octasulfate of magnesium, having general formula I, the preparation method thereof and the use of same in the pharmaceutical and/or cosmetic field, wherein 0≦n≦4, n is an integer and Y represents OH...
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JP5647899B2 |
The current invention provides polypeptides and polypeptide conjugates that include an exogenous N-linked glycosylation sequence. The N-linked glycosylation sequence is preferably a substrate for an oligosaccharyltransferase (e.g., bacte...
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JP5643844B2 |
A process for the preparation of topiramate in an one pot reaction comprises the following steps: A) reacting 2,3:4,5-bis-O-{1-methylethylidene)-β-D-fructopyranose with sulfurylchloride in xylene in the presence of an organic or inorgan...
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JP5535202B2 |
The present invention relates to novel synthetic analogs of phosphatidyl-myo-inositol mannosides (hereinafter referred to as PIMs) of general formula (I): or a pharmaceutically acceptable salt thereof, to the method for preparing same an...
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JP5484668B2 |
The present invention provides a process for synthesizing a compound having the structure: ides useful as a vaccine for inducing antibodies to human breast cancer cells in an adjuvant therapy therefor.
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JP2014040471A |
To provide compounds having activity against infectious Flaviviridae viruses and inhibiting viral RNA-dependent RNA polymerase to have antiviral activity.Provided are substituted carba-nucleoside analogs typically represented by the spec...
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JP5425187B2 |
Provided are pyrrolo[1,2-f][1,2,4]triazinyl, imidazo[1,5-f][1,2,4]triazinyl, imidazo[1,2-f][1,2,4]triazinyl, and [1,2,4]triazolo[4,3-f][1,2,4]triazinyl nucleosides, nucleoside phosphates and prodrugs thereof, wherein the 1' position of t...
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JP2014501730A |
The invention relates to a method of inhibiting the cytotoxic activity of extracellular histones in a subject, comprising administering an effective amount of a polyanion to the subject. In particular the invention relates to a method fo...
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JP5389140B2 |
New mixtures (A) of heparin-derived sulfated polysaccharides have average molecular weight 1500-3000, anti-Xa activity 120-200 IU/mg, anti-IIa activity 0-10 IU/mg and ratio of anti-Xa to anti-IIa activity more than 30; comprise 2-26 sacc...
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JP5371167B2 |
Partially desulfated glycosaminoglycan derivatives are described, particularly heparin, and more particularly formula (I) compounds where the U, R and R1 groups have the meanings indicated in the description. These glycosaminoglycan deri...
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JP5314745B2 |
Saccharide-protein conjugates having a new type of linker are described. The conjugates comprising the new linker are prepared from modified saccharides comprising a moiety of the formula (I): -A-N(R1)-L-M wherein: A is a bond, —C(O)â€...
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JP5268222B2 |
Saccharide-protein conjugates having a new type of linker are described. The conjugates comprising the new linker are prepared from modified saccharides comprising a moiety of the formula (I): -A-N(R1)-L-M wherein: A is a bond, —C(O)â€...
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JP2013116856A |
To provide an amyloid β-binding material that excellently binds to an amyloid β, and to provide a sensor device using the same.The present invention relates to an amyloid β-binding material which contains sugar, or a sugar residue der...
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JP2013519706A |
The present invention relates to the use of a specific family of glycerolipid compounds of formula (I) described in the detailed description or the manufacture of a medicament for the prevention or for the treatment of cancer metastasis.
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JP5198538B2 |
It is intended to provide: an analytical method whereby the structure of a sulfated polysaccharide or a sulfated oligosaccharide can be highly sensitively analyzed; a pharmaceutical composition and a drug containing a sulfated polysaccha...
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JP5137403B2 |
The present invention provides a phosphoramidate compound having the structure (I) wherein X comprises a monosaccharide group comprising the structure (II) or (III) or a pharmaceutically acceptable salt, ester or salt of such ester. The ...
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JP5139797B2 |
The invention relates to compounds which are polysulfated oligosaccharide derivatives having activity as inhibitors of heparan sulfate-binding proteins and inhibitors of the enzyme heparanase; methods for the preparation of the compounds...
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JP5047807B2 |
The present invention relates to a method for improving stability of non fluoridated sugar derivatives, and in particular glucose derivatives such as 1,3,4,6-tetra-O-acetyl-2-O-trifluoromethanesulfonyl-ß-D-man
nopyranose which are used ...
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JP2012188373A |
To provide a means to stereoselectively produce a compound which is composed of a sugar 1-phosphate compound with phosphoric acid bonded to an anomer position (C1 position) thereof (a sugar 1-phosphate compound).A sugar 1-oxazaphospholid...
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JP5035940B2 |
The present invention provides phosphotetrahydropyran compounds and the use thereof in treating diseases or conditions that are dependent on T-lymphocyte migration, as well as compositions containing said compounds.
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JP5021898B2 |
New mixtures (A) of heparin-derived sulfated polysaccharides have average molecular weight 1500-3000, anti-Xa activity 120-200 IU/mg, anti-IIa activity 0-10 IU/mg and ratio of anti-Xa to anti-IIa activity more than 30; comprise 2-26 sacc...
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JP5004261B2 |
Methods for treating infections or autoimmune disease or an allergic condition using monophosphonyl lipid 4 or a mimetic thereof (an aminoalkyl glucosaminide phosphate).
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JP5001989B2 |
A keratan sulfate oligosaccharide which comprises from two to five sugar units and has sulfated N-acetylglucosamine at the reducing end and in a molecule of which at least two hydroxyl groups are sulfated, preferably, which contains at l...
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JP4939934B2 |
A method for synthesizing Salacinol, its stereoisomers, and analogues, homologues and other derivatives thereof potentially useful as glycolsidase inhibitors. The compounds of the invention may have the general formula (I) or (II): The s...
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JP2012092109A |
To provide new strategies and protocols for oligosaccharide synthesis.There are provided a method for synthesizing a compound having the structure (I) (wherein R is H) and related oligosaccharides useful as a vaccine for inducing antibod...
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JP2012509305A |
The Invention relates to the methyl pentasaccharide O-2,3,4-tri-O-methyl-α-D-glucopyranosyl-(1→4)-O-2,3-di-O-
methyl-β-D-glucopyranosyluronic acid-(1→4)-O-α-D-glucopyranosyl-(1→4)-O-2,3-di-O-méthy
l-α-L-idopyranosyluronic acid...
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JP4913272B2 |
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JP2012046511A |
To provide a polysulfated hyaluronic acid derivative useful for preventing and/or treating allergic diseases.A low molecular weight polysulfated hyaluronic acid derivative expressed by general formula (IA) or (IB) or a pharmaceutically a...
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JP4892191B2 |
The present invention is directed to a continuous process for the preparation of fructopyranose sulfamate derivatives of the general formula (I)
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JP4838706B2 |
Compounds that are adjuvants and immunoeffectors are described and claimed. The compounds augment antibody production in immunized animals as well as stimulate cytokine production and activate macrophages. Compositions and methods for us...
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JP2011246481A |
To provide compositions used as adjuvants and immunoeffectors.There are provided certain aminoalkyl glucosaminide phosphate compounds (AGP) represented by formula (I), or pharmaceutically acceptable salts thereof.
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JP4810558B2 |
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JP4806394B2 |
The invention provides methods for analyzing heparins, low-molecular-weight heparins, ultralow-molecular-weight heparins, and oligosaccharides by high performance liquid chromatography a stationary phase dynamically coated with a quatern...
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JP4755333B2 |
To provide a method for producing a water-soluble composition of bivalent metal salts such as Ca salts of a phosphorylated oligosaccharide (POS) and/or a phosphorylated dextrin (PDN) having excellent filterability without forming precipi...
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JP4733329B2 |
The invention concerns oligosaccharides of formula (I), their mixtures, their diastereomers, methods for preparing them and pharmaceutical compositions containing them.
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JP4731477B2 |
The invention relates to a compound of formula (I): wherein P1, P2, P3, and P4 are each independently hydrogen or a protecting group; and n is an integer of from 2 to 20 and to the use of such compounds for the synthesis of 18F-FDG.
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JP4725976B2 |
The present invention is directed to a one-step process for the preparation of fructopyranose sulfamate derivatives of the general formula (I) wherein X, R1, R3, R4, R5 and R6 are as described in the specification.
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JP4712001B2 |
Novel substituted liposaccharides useful as in the prophylactic and affirmative treatment of endotoxemia including sepsis, septicemia and various forms of septic shock and methods of using these agents are provided. Also provided are met...
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