WO1997001568A1 - New anticoagulants - Google Patents
New anticoagulants Download PDFInfo
- Publication number
- WO1997001568A1 WO1997001568A1 PCT/SE1996/000859 SE9600859W WO9701568A1 WO 1997001568 A1 WO1997001568 A1 WO 1997001568A1 SE 9600859 W SE9600859 W SE 9600859W WO 9701568 A1 WO9701568 A1 WO 9701568A1
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- WO
- WIPO (PCT)
- Prior art keywords
- unit
- trisaccharide
- acid
- idoa
- glca
- Prior art date
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H3/00—Compounds containing only hydrogen atoms and saccharide radicals having only carbon, hydrogen, and oxygen atoms
- C07H3/06—Oligosaccharides, i.e. having three to five saccharide radicals attached to each other by glycosidic linkages
Definitions
- the present invention relates to prevention and treatment of thromboembolic diseases by administration of a therapeutically effective dose of an active trisacc- haride comprising an iduronic acid, a glucopyranosyl or glucopyranosylamine unit and a hexuronic acid selected from iduronic acid and glucuronic acid.
- the specific trisaccharides of the present invention have potent activity towards thrombin and also potentiates the inhibition of FXa, even if the trisaccharides lack sulfate groups.
- safe and potent anticoagulants with a high oral absorption are potentially achievable, due to the much smaller mole ⁇ cular size and presence of very few, if any, sulfate groups compared to presently available anticoagulants.
- thromboembolic processes three groups of substances need to be considered: a) substances which prevent platelet aggregation (platelet antiaggregation agents), b) agents which inhibit the coagulation process (anticoagulants), and c) substances which eliminate fibrinogen from the circulation (defibrinogenating agents).
- anticoagulant and antithrombotic drugs are unfractionated (standard) heparin and the low molecular weight heparins (LMWHs), the latter compounds being introduced in clinical practice during the last decade.
- LMWHs low molecular weight heparins
- the major anticoagulant effect of standard as well as low molecular weight heparins, is through its interaction with AT III on coagulation enzymes particularly thrombin (factor II a) and factor Xa (FXa).
- Anticoagulant drugs that inhibit the synthesis of vitamin K - dependent coagula ⁇ tion factors, such as warfarin, are also well known.
- warfarin prophylaxes of venous thromboembolism is more complicated to use than fixed low-dose heparin therapy, warfarin is generally reserved for patients at very high risk (J. Hirsh, Oral anticoagulant Drugs, N. Engl. J. Med., 324 (1991) 1865-1875).
- LMWHs Today far more LMWHs than standard heparin are being used in clinical practice. This is because, the LMWHs cause less hemorrhage than standard heparin at doses producing an equivalent antithrombotic effect. Also, the LMWHs are effective and safe for the prevention of venous thromboembolism in surgical and medical patients who are at risk. Furthermore, for heparin numerous side-effects have been documented such as hemorrhage, thrombocytopenia with or without thrombosis, osteoporosis, skin necrosis, alopecia, hypersensitivity reaction and hypoaldosteronism. (J. Hirsh, Heparin, N. Engl. J. Med., 324 (1991) 1565-1574).
- the LMWHs are also more convenient to use than standard heparin. Generally, a once daily subcutaneous dose is sufficient for LMWH, whereas 2 to 3 daily doses are required for heparin. At present, however, no formulation is available for oral administration of heparin or LMWHs.
- a heparin-like anticoagulant of similar molecular weight (6 kDa) as the LMWHs is the heparinoid Danaparoid sodium (Orgaran ® , trademark of Akzo of the Nether ⁇ lands). It consists of a polydisperse mixture comprising sulfated glycosamino- glycans derived from animal mucosa, heparan sulfate (83 % w/w), of which some 4 to 5% has high affinity for antithrombin III (AT III), dermatan sulfate (12% w/w) and a minor amount of chondroitin sulfate (5% w/w).
- heparin molecules with fewer than 18 saccharides are unable to bind thrombin and AT III simultaneously. Therefore, with less than 18 saccharides heparin molecules are unable to accelerate the inactivation of thrombin by AT III but retain their ability to catalyze the inhibition of FXa by AT III (J. Hirsh and M. N. Levine, Low Molecular Weight Heparin, Blood, 79 (1992) 1-17).
- LMWHs and Danaparoid sodium In order for heparin, LMWHs and Danaparoid sodium to bind to AT III and thereby express their anticoagulant effect they must contain a highly sulfated pentasaccharide sequence found in heparin, LMWHs and some heparan sulfates. Synthetic, highly sulfated pentasaccarides which bind to AT III and inhibit FXa and thus exhibit anticoagulant activity have been described. These highly sulfated pentasaccharides correspond to the natural hepta and octasulfated pentasaccha- rides as well as some additional non-natural octasulfated and nonasulfated penta ⁇ saccharides.
- Efficient and well-controlled anticoagulants of the prior art derived from heparin or heparan sulfate are highly sulfated and exhibit a molecular weight and size, making them unsuitable for oral administration.
- Tri-3 One of the trisaccharides presently claimed for treatment of thromboembolic diseases is known per se.
- the structure and synthesis of the claimed trisacc- haride designated in this specification as Tri-3 has been disclosed in M. Nilsson et al, Carbohydrate Res., 246 (1993) 161-172 and J. Westman et al, J. Carbohydrate Chem., 14(1) (1995) 95-113.
- These references do not disclose any infor ⁇ mation in general and much less any experimental support showing anticoagulant activity or potential administration by the oral route of the presently claimed trisaccharides.
- oligosaccharides with few saccharide units and containing idopyranosyl- uronic and /or glucopyranosyluronic acids are known from the prior art.
- carbohydrate derivatives comprising a trisaccharide unit are described. All of the trisaccharides are highly sulfated and have an ⁇ -D-glucopyranosyluronic acid at their non-reducing end. Furthermore, no anticoagulant nor antithrombotic activity have been shown.
- EP-A-0084999 (assigned to Choay), discloses production of mucopolysaccharide products having 2-12 saccharide units for use as antithrombotic agents. There are, however, up till now no disclosures connected to such oligosaccharides showing anticoagulant activity of such importance that administration of an anticoagulant e.g. by the oral route can be envisaged.
- Heparin and LMWHs are heterogeneous mixtures of polysaccharide fragments with multiple sites of pharmacological action, which cannot be used successfully by oral administration. Even the above mentioned synthetic pentasaccharides, although being more defined than heparin and LMWHs, are still being too large molecules and much to sulfated for oral administration.
- One object of the present invention is efficient inhibition of thrombin without the adverse side-effects encountered with standard heparin.
- Another object of the present invention is efficient inhibition of thrombin by AT III in the presence of compounds with a molecular weight and size which are sub ⁇ stantially smaller, more defined and less sulfated than conventional LMWHs.
- a further object of the present invention is efficient inhibition of FXa by AT III in the presence of compounds with a molecular weight and size which are substan ⁇ tially smaller, more defined and less sulfated than conventional LMWHs.
- Yet another object of the present invention is to provide potent inhibitors of thrombin and FXa having properties suitable for oral administration to the patients.
- IdoA idopyranosyluronic acid (at the non-reducing end)
- iduronic acid or IdoA are used as abbreviations for idopyranosyl ⁇ uronic acid, idopyranosyluronate or esters of any of these.
- glucuronic acid or GlcA are used as abbreviations for glucopyranosyluronic acid, glucopyranosyluronate or esters of any of these.
- a pharmaceutically acceptable salt is suitable, e.g. hydrogen chloride.
- the charged groups are compensated by pharmaceutically acceptable counter ⁇ ions, such as hydrogen, alkali or alkaline-earth metal ions, such as sodium and calcium, respectively, or ammonium ions, which optionally may be substituted. It is also conceivable to use metal ions, primarily copper or zinc ions, as counter ⁇ ions.
- pharmaceutically acceptable counter ⁇ ions such as hydrogen, alkali or alkaline-earth metal ions, such as sodium and calcium, respectively, or ammonium ions, which optionally may be substituted. It is also conceivable to use metal ions, primarily copper or zinc ions, as counter ⁇ ions.
- Easily hydrolyzable ester groups can be substituted for one or more of the hydroxyl groups of the trisaccharides according to formula I. This is applicable to all three saccharide units of the trisaccharides.
- the introduction of easily hydrolyz ⁇ able ester groups, can also be made in one or both of the carboxylic groups of the uronic acids.
- the inventors of the present invention have found that certain trisaccharides potentiate the anticoagulant activity of AT III.
- the trisaccharides according to formula I have potent activity towards thrombin and also potentiates the inhibition of FXa. This is very surprising, since previously it has been believed that at least 18 saccharide units were necessary for binding thrombin and AT III simul ⁇ taneously. Even more surprisingly is the high activity exhibited by these trisaccha- rides, although they lacked sulfate groups.
- A an iduronic acid (IdoA) linked 1-4 to
- R H, alkyl or aryl
- the IdoA unit A, the glucopyranosyl or glucopyranosylamine unit B, as well as the uronic acid unit C can be either in their D or L forms.
- the IdoA unit A is in its L form
- the glucopyranosyl or glucopyranosylamine unit B is in its D form.
- the uronic acid unit C is in its D form when the uronic acid is a GlcA unit and in its L form when the uronic acid is a IdoA unit.
- L-IdoA (A), D-glucopyranosylamine unit (B) and D-GlcA (C) is a preferred embodiment.
- the IdoA unit A, the glucopyranosyl or glucopyranosylamine unit B, as well as the uronic acid unit C can be either in their ⁇ or ⁇ forms.
- the IdoA unit A is in its ⁇ form
- the glucopyranosyl or glucopyranosylamine unit B is in its ⁇ form.
- the uronic acid unit C is in its ⁇ form when the uronic acid is a GlcA unit and in its ⁇ form when the uronic acid is a IdoA unit.
- the combination of ⁇ -IdoA (A), ⁇ -glucopyranosylamine unit (B) and ⁇ -GlcA (C) is a preferred embodiment.
- Y can be an acetyl, propionyl or butyryl group, the two latter of which can be straight or branched.
- Y is an acetyl group and the glucopyranosylamine unit then is a 2- acetamido-2-deoxy-glucopyranosyl unit (GlcNAc).
- LMWHs and some heparan sulfates In order for heparin, LMWHs and some heparan sulfates to bind to AT III and thereby express their anticoagulant effect they must contain a highly sulfated pentasaccharide sequence, as already mentioned above. It is thus a prerequisite of these anticoagulants to contain at least four sulfate groups, and preferably seven or eight groups.
- one or two OH groups of the trisaccha ⁇ rides may be sulfated.
- a suitable position is the 6-position of the glucopyranosyl or glucopyranosylamine unit (B) (see formula II). This is, however, less preferred embodiments, since the presence of sulfate groups decreases the oral absorption.
- the low sulfate content facilitates administration of an inventive preparation con ⁇ taining the trisaccharides according to formula I, aimed for prevention and treat ⁇ ment of thrombosis and treatment of arteriosclerosis or use for manufacture of a medicament for prevention and treatment of thrombosis and treatment of arterio ⁇ sclerosis.
- This is further emphasized by the fact that a potentiation of AT III- mediated inhibition of FXa was observed for a trisaccharide according to formula I lacking sulfate groups.
- the inventive pharmaceutical compositions containing the trisaccharides according to formula I are suitable for parenteral administration, optionally with one or more pharmaceutically acceptable additives.
- Parenteral administration here refers to intravenous, subcutaneous or intradermal administration.
- trisaccharides in general exhibit a much smaller molecular size and weight than conventionally used heparin-derived anticoagulants. This implies a higher proba ⁇ bility of good oral absorption.
- the inventive pharmaceutical compositions con ⁇ taining the trisaccharides according to formula I, optionally with one or more pharmaceutically acceptable additives are particularly suitable for oral, buccal, sublingual or rectal administration. This is because the present trisaccharides are less sulfated than hitherto known oligosaccharides.
- a particularly preferred embodiment of the inventive pharmaceutical compositions are those trisaccha ⁇ rides where sulfate ⁇ roups are completely lacking, since this means a particularly low molecular weignt and size and good oral, buccal or sublingual absorption
- Tri-3 and other trisaccharides as well as certain di, tri and tetrasaccharides has been disclosed in M. Nilsson et al, Carbohydrate Res., 246 (1993) 161-172 and J. Westman et al, J. Carbohydrate Chem., 14(1) (1995) 95- 113.
- the trisaccharides may also be prepared by chemical and or enzymatic treat ⁇ ment of heparin followed by fractionation and purification.
- the trisaccharides of formula I are covalently attached to a soluble or insoluble support.
- the trisaccharide is attached at its non-reducing end, optionally by a spacer between the trisaccharide and the support.
- Tri-3 is a tri ⁇ saccharide used to illustrate the present invention.
- Tri-1 and Tri-2 two trisaccharides (Tri-1 and Tri-2), five disaccharides and two tetrasaccharides were also tested.
- the reaction mixture contained 150 nM of antithrombin (AT III) and 66 ⁇ M of one oligosaccharide in each experiment.
- the reaction was initiated bv the addition of 2-3 nM of thrombin.
- the reaction buffer contained 0.15 M of NaCl, 20 mM of Tris- HCl with pH 7.4, and 0.1% of PEG 8000. 50 ⁇ l samples were then taken out every 15 seconds for quantification of the residual thrombin activity.
- Residual thrombin activity was measured by adding the 50 ⁇ l aliquots to 250 ⁇ l of 300 ⁇ M of the chro ⁇ mogenic substrate S-2238 (obtained from Chromogenix of M ⁇ lndal, Sweden), 5.4 ⁇ g/ml polybrene, and 0J2 klU/ml aprotinin. The residual thrombin activity was determined by calculating the rate of hydrolysis of S-2238 over 2 min.
- the residual thrombin activity versus the time at which the residual thrombin activity was determined was plotted.
- the curve obtained was fitted to a single exponential to give a pseudo 1st order rate constant.
- the pseudo 1st order rate constant was divided by the inhibitor (AT III) concentration to give the 2nd order rate constant.
- Assays were performed at room temperature with reaction mixtures containing 150 nM of AT III and increasing amounts of Tri-3 in a buffer similar to that described in Example 1. The reaction was initiated by the addition of 2-3 nM of thrombin. Samples of 50 ⁇ l were removed every 15 seconds for quantification of the residual thrombin activity by determining the rate of hydrolysis of S-2238 as described in Example 1. Residual thrombin activity versus time was plotted and values for the first order rate constant (k') were determined by fitting data by non ⁇ linear least-squares regression to equation 1:
- k' pseudo-first-order rate constant
- the correlation coefficient (R) of the fit was greater than 0.96 in all cases.
- the second-order rate constant of inhibition, k 2 was then obtained by dividing the pseudo-first-order rate constant by the inhibitor concentration (I).
- thrombins with k, ⁇ 1 x IO 7 were assayed as above.
- Thrombins with , >1 x 10 7 were assayed by monitoring the progress curves in the presence of 75-150 ⁇ M S- 2238, 150 nM antithrombin and 0.5-3 nM thrombin.
- the hydrolysis of S-2238 to yield p-nitroaniline product (P) was determined continuously at an optical density of 405 nm (OD 405 ) over time (t).
- the data were fitted by non-linear regression (Marquardt algorithm) to equation 2, to obtain estimates of initial velocity (v 0 ), steady state velocity (v s ), and the apparent first-order rate constant (k'):
- Fig. 1 is a dose-response curve for Tri-3.
- Fig. 1 is a dose-response curve for Tri-3.
- k the second- order rate constant of inhibition
- the assay was carried out in a 0.05 M Tris-HCl buffer with pH 7.5, the buffer containing 0.15 M NaCl, 0.01 M CaCl. and 0.01% Tween 80. The same buffer was used for dilution of the human proteins employed, whereas saccharides were diluted in water.
- Human FXa was obtained from Enzyme Research Laboratories of South Bend, IL, USA and human antithrombin (AT III) from Chromogenix of M ⁇ lndal, Sweden. FXa was active site titrated with NPBG using the method of Chase and Shaw (Methods in Enzymology, 1970).
- Tri-3 gives a significant decrease in FXa activity whereas the other synthetic oligosaccharides show only minor or insignificant effects.
Abstract
Description
Claims
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP96922351A EP0837868A1 (en) | 1995-06-29 | 1996-06-28 | New anticoagulants |
AU63249/96A AU706002B2 (en) | 1995-06-29 | 1996-06-28 | New anticoagulants |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US104095P | 1995-06-29 | 1995-06-29 | |
US60/001,040 | 1995-06-29 | ||
SE9502656A SE9502656D0 (en) | 1995-07-19 | 1995-07-19 | New anticoagulants |
SE9502656-3 | 1995-07-19 |
Publications (1)
Publication Number | Publication Date |
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WO1997001568A1 true WO1997001568A1 (en) | 1997-01-16 |
Family
ID=26662353
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/SE1996/000859 WO1997001568A1 (en) | 1995-06-29 | 1996-06-28 | New anticoagulants |
Country Status (3)
Country | Link |
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EP (1) | EP0837868A1 (en) |
AU (1) | AU706002B2 (en) |
WO (1) | WO1997001568A1 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0871761A1 (en) | 1995-08-21 | 1998-10-21 | The Procter & Gamble Company | Solvent extraction of polyhydroxy-alkanoates from biomass |
WO2007138263A1 (en) * | 2006-05-25 | 2007-12-06 | Ulive Enterprises Limited | Prevention and/or treatment of neurodegenerative disorders |
CN102898487A (en) * | 2012-11-13 | 2013-01-30 | 麦科罗夫(南通)生物制药有限公司 | Fondaparinux sodium disaccharide intermediate fragment BA and synthetic method thereof |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0004823A2 (en) * | 1978-04-10 | 1979-10-17 | ANVAR Agence Nationale de Valorisation de la Recherche | Process for the preparation of oside derivatives, derivatives so obtained and their biological applications |
EP0113599A1 (en) * | 1982-10-27 | 1984-07-18 | Choay S.A. | Process for the organic synthesis of oligonucleotides containing galactosamin-uron-acid motives, oligosaccharides obtained and their biological applications |
EP0347964A1 (en) * | 1988-06-21 | 1989-12-27 | Akzo N.V. | New oligosaccharides with internal spacer |
WO1990006755A1 (en) * | 1988-12-15 | 1990-06-28 | Glycomed Incorporated | Heparin fragments as inhibitors of smooth muscle cell profileration |
-
1996
- 1996-06-28 EP EP96922351A patent/EP0837868A1/en not_active Withdrawn
- 1996-06-28 WO PCT/SE1996/000859 patent/WO1997001568A1/en not_active Application Discontinuation
- 1996-06-28 AU AU63249/96A patent/AU706002B2/en not_active Ceased
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0004823A2 (en) * | 1978-04-10 | 1979-10-17 | ANVAR Agence Nationale de Valorisation de la Recherche | Process for the preparation of oside derivatives, derivatives so obtained and their biological applications |
EP0113599A1 (en) * | 1982-10-27 | 1984-07-18 | Choay S.A. | Process for the organic synthesis of oligonucleotides containing galactosamin-uron-acid motives, oligosaccharides obtained and their biological applications |
EP0347964A1 (en) * | 1988-06-21 | 1989-12-27 | Akzo N.V. | New oligosaccharides with internal spacer |
WO1990006755A1 (en) * | 1988-12-15 | 1990-06-28 | Glycomed Incorporated | Heparin fragments as inhibitors of smooth muscle cell profileration |
Non-Patent Citations (5)
Title |
---|
PATENT ABSTRACTS OF JAPAN, Vol. 9, No. 237, C-305; & JP,A,60 094 989 (RIKAGAKU KENKYUSHO), 28 May 1985. * |
PATENT ABSTRACTS OF JAPAN, Vol. 9, No. 96, C-278; & JP,A,59 227 896 (RIKAGAKU KENKYUSHO), 21 December 1984. * |
SNT INTERNATIONAL, FILE CA, CHEMICAL ABSTRACTS, Volume 122, No. 21, 22 May 1995 (Columbus, Ohio, US), WESTMAN, JACOB et al., "Synthesis and Fibroblast Growth Factor Binding of Oligosaccharides Related to Heparin and Heparin Sulfate", Abstract No. 265852; & J. CARBOHYDR. CHEM. (1995), 14(1), 95-113. * |
STN INTERNATIONAL, FILE CA, CHEMICAL ABSTRACTS, Volume 107, No. 19, 9 November 1987 (Columbus, Ohio, US), VAN BOECKEL, C.A.A. et al: "Conformational Analysis of Synthetic Heparin-Like Oligosaccharides Containing .alpha.-L-Idopyranosyluronic Acid", Abstract No. 176382; & RECL. TRAV. CHIM. PAYS-BAS (1987), 106(1), 19-29. * |
STN INTERNATIONAL, FILE CA, CHEMICAL ABSTRACTS, Volume 120, No. 5, 31 January 1994 (Columbus, Ohio, US), NILSSON, MARIANNE et al: "Synthesis of the Methyl Glycosides of a Tri- and a Tetra-Saccharide Related to Heparin and Heparan Sulfate", Abstract No. 54861; & CARBOHYDR. RES. (1993), 246, 161-72. * |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0871761A1 (en) | 1995-08-21 | 1998-10-21 | The Procter & Gamble Company | Solvent extraction of polyhydroxy-alkanoates from biomass |
WO2007138263A1 (en) * | 2006-05-25 | 2007-12-06 | Ulive Enterprises Limited | Prevention and/or treatment of neurodegenerative disorders |
JP2009537622A (en) * | 2006-05-25 | 2009-10-29 | ザ ユニバーシティ オブ リバプール | Prevention and / or treatment of neurodegenerative diseases |
EP2384757A1 (en) * | 2006-05-25 | 2011-11-09 | The University of Liverpool | Prevention and/ortreatment of neurodegenerative disorders |
AU2007266849B2 (en) * | 2006-05-25 | 2012-05-24 | The University Of Liverpool | Prevention and/or treatment of neurodegenerative disorders |
US8673880B2 (en) | 2006-05-25 | 2014-03-18 | The University Of Liverpool | Prevention and/or treatment of neurodegenerative disorders |
CN102898487A (en) * | 2012-11-13 | 2013-01-30 | 麦科罗夫(南通)生物制药有限公司 | Fondaparinux sodium disaccharide intermediate fragment BA and synthetic method thereof |
Also Published As
Publication number | Publication date |
---|---|
AU706002B2 (en) | 1999-06-03 |
AU6324996A (en) | 1997-01-30 |
EP0837868A1 (en) | 1998-04-29 |
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