RU2000119753A - SYNTHETIC POLYSACCHARIDES, METHOD FOR PRODUCING THERE AND THEIR PHARMACEUTICAL COMPOSITIONS - Google Patents

SYNTHETIC POLYSACCHARIDES, METHOD FOR PRODUCING THERE AND THEIR PHARMACEUTICAL COMPOSITIONS

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Publication number
RU2000119753A
RU2000119753A RU2000119753/04A RU2000119753A RU2000119753A RU 2000119753 A RU2000119753 A RU 2000119753A RU 2000119753/04 A RU2000119753/04 A RU 2000119753/04A RU 2000119753 A RU2000119753 A RU 2000119753A RU 2000119753 A RU2000119753 A RU 2000119753A
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RU
Russia
Prior art keywords
glucopyranosyl
methyl
sulfo
tri
polysaccharide
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Application number
RU2000119753/04A
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Russian (ru)
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RU2211224C2 (en
Inventor
Йоханнес БАСТЕН
Корнелия ДРЕФ-ТРОМП
Пьер-Александр ДРИГЭЗ
Филипп Дюшоссуа
Жан-Марк Эрбер
Морис ПТИТУ
БУККЕЛ Констант ВАН
Original Assignee
Санофи-Синтелябо
Акзо Нобел Н.В.
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Priority claimed from FR9800515A external-priority patent/FR2773804B1/en
Application filed by Санофи-Синтелябо, Акзо Нобел Н.В. filed Critical Санофи-Синтелябо
Publication of RU2000119753A publication Critical patent/RU2000119753A/en
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Publication of RU2211224C2 publication Critical patent/RU2211224C2/en

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Claims (11)

1. Синтетический полисахарид в кислотной форме и его фармацевтически приемлемые соли. анионная форма которого соответствует одной из формул (I)-(V), приведенных ниже (см. графическую часть).1. Synthetic polysaccharide in acid form and its pharmaceutically acceptable salts. the anionic form of which corresponds to one of the formulas (I) - (V) below (see graphic part). 2. Полисахарид по п. 1 в форме натриевой или калиевой соли. 2. The polysaccharide according to claim 1 in the form of sodium or potassium salt. 3. Полисахарид по любому из пп. 1 и 2 формулы: метил-O-(2,3,4,6-тетра-O-сульфо-α-D-глюкопиранозил)-(1-->4)-O-(2,3,6-три-O-сульфо-α-D-глюкопиранозил)-(1-->4)-O-(2,3,6-три-O-сульфо-β-D-глюкопиранозил)-(1-->4)-O-(2,3-ди-O-метил-6-O-сульфо-α-D-глюкопиранозил)-(1-->4)-O-(2,3,6-три-O-метилβ-D-глюкопиранозил)-(1-->4)-[O-(2,3,6-три-O-метил-α-D-глюкопиранозил)-(1-->4)-O-(2,3,6-три-O-метил-β-D-глюкопиранозил)-(1-->4)] 3-O-(2,3-ди-O-метил-6-O-сульфо-α-D-глюкопиранозил)-(1-->4)-O-(2,3-ди-O-метил-β-D-глюкопиранозилуроновая кислота)-(1-->4)-O-(2,3,6-три-O-сульфо-α-D-глюкопиранозил)-(1-->4)-O-(2,3-ди-O-метил-α-L-идопиранозилуроновая кислота)-(1-->4)-3-O-метил-2,6-ди-O-сульфо-α-D-глюкопиранозида натриевая соль.3. The polysaccharide according to any one of paragraphs. 1 and 2 of the formula: methyl-O- (2,3,4,6-tetra-O-sulfo-α-D-glucopyranosyl) - (1 -> 4) -O- (2,3,6-tri- O-sulfo-α-D-glucopyranosyl) - (1 -> 4) -O- (2,3,6-tri-O-sulfo-β-D-glucopyranosyl) - (1 -> 4) -O - (2,3-di-O-methyl-6-O-sulfo-α-D-glucopyranosyl) - (1 -> 4) -O- (2,3,6-tri-O-methylβ-D- glucopyranosyl) - (1 -> 4) - [O- (2,3,6-tri-O-methyl-α-D-glucopyranosyl) - (1 -> 4) -O- (2,3,6 -tri-O-methyl-β-D-glucopyranosyl) - (1 -> 4)] 3 -O- (2,3-di-O-methyl-6-O-sulfo-α-D-glucopyranosyl) - (1 -> 4) -O- (2,3-di-O-methyl-β-D-glucopyranosyluronic acid) - (1 -> 4) -O- (2,3,6-tri-O- sulfo-α-D-glucopyranosyl) - (1 -> 4) -O- (2,3-di-O-methyl-α-L-idopyranosyluronic acid) - (1 -> 4) -3-O- methyl 2,6-di-O-sulfo-α-D-glucopyranoside on rievaya salt. 4. Фармацевтические композиции, содержащие в качестве активного начала полисахарид по любому из пп. 1-3 в форме соли с фармацевтически приемлемым основанием или в кислотной форме, в сочетании или в виде смеси с инертным, нетоксичным, фармацевтически приемлемым эксципиентом. 4. Pharmaceutical compositions containing, as an active principle, the polysaccharide according to any one of claims. 1-3 in the form of a salt with a pharmaceutically acceptable base or in acid form, in combination or as a mixture with an inert, non-toxic, pharmaceutically acceptable excipient. 5. Фармацевтическая композиция по п. 4 в форме единиц дозирования. в которых активное начало смешано с по меньшей мере одним фармацевтическим эксципиентом. 5. The pharmaceutical composition according to claim 4 in the form of dosage units. in which the active principle is mixed with at least one pharmaceutical excipient. 6. Композиция по п. 5, где каждая единица дозирования содержит 0,1 - 100 мг активного начала. 6. The composition according to p. 5, where each dosage unit contains 0.1 to 100 mg of active principle. 7. Композиция по п. 6, где каждая единица дозирования содержит 0,5 - 50 мг активного начала. 7. The composition according to p. 6, where each dosage unit contains 0.5 to 50 mg of active principle. 8. Применение полисахарида по пп. 1-3, для приготовления лекарства, которое полезно при патологиях, связанных с дисфункцией коагуляции. 8. The use of the polysaccharide in paragraphs. 1-3, for the preparation of a medicine that is useful in pathologies associated with coagulation dysfunction. 9. Применение полисахарида по пп. 1-3 для приготовления лекарства, которое полезно при лечении и предупреждении расстройств сердечно-сосудистой и цереброваскулярной систем, тромбоэмболических расстройств, связанных с артериосклерозом и с диабетами, или тромбоэмболических расстройств, связанных с ретромбозом после тромболиза, с инфарктом, с деменцией ишемического происхождения, с периферическими артериальными заболеваниями, с гемодиализом или с аурикулярными фибрилляциями, или, альтернативно, при использовании сосудистых протезов аортокоронарного шунтирования. 9. The use of the polysaccharide in paragraphs. 1-3 for the preparation of a medicine that is useful in the treatment and prevention of disorders of the cardiovascular and cerebrovascular systems, thromboembolic disorders associated with arteriosclerosis and diabetes, or thromboembolic disorders associated with retrombosis after thrombolysis, heart attack, dementia of ischemic origin, with peripheral arterial diseases, with hemodialysis or with auricular fibrillation, or, alternatively, when using vascular prostheses of coronary artery bypass grafting. 10. Применение по п. 9, отличающееся тем, что приготовленные лекарства используют при предупреждении или лечении тромбоэмболических заболеваний. 10. The use according to claim 9, characterized in that the prepared drugs are used in the prevention or treatment of thromboembolic diseases. 11. Применение по п. 10, отличающееся тем. что приготовленные лекарства используют при предупреждении или лечении нестабильной стенокардии, ударов, рестеноза после ангиопластики, эндартерэктомии или инсталляции эндоваскулярных протезов. 11. The use of claim 10, wherein that the prepared drugs are used in the prevention or treatment of unstable angina, strokes, restenosis after angioplasty, endarterectomy or the installation of endovascular prostheses.
RU2000119753/04A 1998-01-19 1999-01-13 Synthetic polysaccharides, method of preparation thereof, and pharmaceutical compositions containing thereof RU2211224C2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR9800515A FR2773804B1 (en) 1998-01-19 1998-01-19 SYNTHESIS POLYSACCHARIDES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME
FR98/00515 1998-01-19

Publications (2)

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RU2000119753A true RU2000119753A (en) 2002-09-10
RU2211224C2 RU2211224C2 (en) 2003-08-27

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JP (1) JP4402835B2 (en)
KR (1) KR100513196B1 (en)
CN (1) CN1165550C (en)
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WO (1) WO1999036443A1 (en)
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FR2814463B1 (en) * 2000-09-22 2002-11-15 Sanofi Synthelabo NOVEL POLYSACCHARIDES WITH ANTITHROMBOTIC ACTIVITY COMPRISING AT LEAST ONE COVALENT BINDING WITH BIOTIN OR A BIOTINE DERIVATIVE
FR2874924B1 (en) * 2004-09-09 2006-12-01 Sanofi Aventis Sa BIOTINYLATED HEXADECASACCHARIDES, THEIR PREPARATION AND THEIR THERAPEUTIC USE
TWI403334B (en) * 2004-12-23 2013-08-01 Merck Sharp & Dohme Antithrombotic dual inhibitors comprising a biotin residue
GB0507577D0 (en) 2005-04-14 2005-05-18 Novartis Ag Organic compounds
IL188647A0 (en) 2008-01-08 2008-11-03 Orina Gribova Adaptable structured drug and supplements administration system (for oral and/or transdermal applications)
US8791064B2 (en) * 2008-04-24 2014-07-29 Technion Research And Development Foundation Ltd. Beta-lactoglobulin-polysaccharide nanoparticles for hydrophobic bioactive compounds
EP2279249A4 (en) 2008-05-30 2014-03-05 Momenta Pharmaceuticals Inc Saccharide structures and methods of making and using such structures
FR2935386B1 (en) * 2008-08-26 2010-09-10 Sanofi Aventis NOVEL POLYSACCHARIDES WITH ANTITHROMBOTIC ACTIVITY COMPRISING A COVALENT LIAISON WITH AN AMINO CHAIN
AU2010234779A1 (en) * 2009-03-30 2011-10-20 University Of Georgia Research Foundation, Inc. Heparan sulfate synthesis
MX340134B (en) 2009-07-09 2016-06-28 Oshadi Drug Administration Ltd Matrix carrier compositions, methods and uses.
EP3666786A1 (en) * 2009-07-31 2020-06-17 Reliable Biopharmaceutical Corporation Process for preparing fondaparinux sodium and intermediates useful in the synthesis thereof
FR2949115B1 (en) 2009-08-14 2012-11-02 Sanofi Aventis FGF RECEPTOR ACTIVATOR N-SULFATE OLIGOSACCHARIDES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION
FR2949114B1 (en) 2009-08-14 2011-08-26 Sanofi Aventis FGF RECEPTOR ACTIVATORY N-ACYLATED OCTASACCHARIDES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION
US8420790B2 (en) 2009-10-30 2013-04-16 Reliable Biopharmaceutical Corporation Efficient and scalable process for the manufacture of Fondaparinux sodium
EP2614089A1 (en) 2010-09-10 2013-07-17 Sanofi-Aventis Biotinylated polysaccharides having an antithrombotic activity and improved metabolic stability
US9005664B2 (en) 2010-10-17 2015-04-14 Technion Research And Development Foundation Ltd. Denatured lactoglobulin and polyphenol coassemblies
FR2970969B1 (en) 2011-01-27 2013-10-18 Sanofi Aventis OLIGOSACCHARIDES 3-O-ALKYL ACTIVATORS OF FGFS RECEPTORS, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION

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NZ260933A (en) * 1993-07-16 1996-07-26 Hercules Inc Cation-complexed polysaccharides; use in foods and pharmaceuticals
FR2749849B1 (en) * 1996-06-14 1998-09-04 Sanofi Sa SYNTHETIC POLYSACCHARIDES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
CZ427499A3 (en) * 1998-05-29 2000-05-17 The Procter & Gamble Company Fine topic antimicrobial preparations

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