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GB603571A - Compounds having a retarding action on the coagulation of blood and processes of preparing the same - Google Patents

Compounds having a retarding action on the coagulation of blood and processes of preparing the same

Info

Publication number
GB603571A
GB603571A GB20952/44A GB2095244A GB603571A GB 603571 A GB603571 A GB 603571A GB 20952/44 A GB20952/44 A GB 20952/44A GB 2095244 A GB2095244 A GB 2095244A GB 603571 A GB603571 A GB 603571A
Authority
GB
United Kingdom
Prior art keywords
dextrane
ester
sulphuric acid
partially hydrolysed
alcohol
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB20952/44A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pfizer Health AB
Original Assignee
Pharmacia AB
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Pharmacia AB filed Critical Pharmacia AB
Publication of GB603571A publication Critical patent/GB603571A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B37/00Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
    • C08B37/0006Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
    • C08B37/0009Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid alpha-D-Glucans, e.g. polydextrose, alternan, glycogen; (alpha-1,4)(alpha-1,6)-D-Glucans; (alpha-1,3)(alpha-1,4)-D-Glucans, e.g. isolichenan or nigeran; (alpha-1,4)-D-Glucans; (alpha-1,3)-D-Glucans, e.g. pseudonigeran; Derivatives thereof
    • C08B37/0021Dextran, i.e. (alpha-1,4)-D-glucan; Derivatives thereof, e.g. Sephadex, i.e. crosslinked dextran

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Sulphuric acid esters of dextrane are prepared by subjecting dextrane, which may be partially hydrolysed, to the action of a sulphating agent, for example sulphur trioxide, concentrated sulphuric acid, oleum, sulphuryl chloride, N-pyridinium sulphonic or, preferably, chlorsulphonic acid. The esterification may vary from less than one esterified OH-group per glucose unit up to complete esterification. The acid esters may be partially or completely neutralized by means of a basic compound, preferably by alkali or alkaline earth bases. The salt or ester may be freed of sulphuric acid by dialysis, by precipitation of the salt or ester from aqueous solution with alcohol or by precipitating the sulphuric acid by means of Ca or Ba ions. The salts or esters may be used as anti-coagulating agents in the treatment of blood (see Group VI). In an example, a partially hydrolysed dextrane, prepared by boiling a 4 per cent aqueous dextrane solution with hydrochloric acid for 3 minutes followed by neutralization with caustic soda and precipitation as the sodium salt by addition of alcohol, was reacted with chlorsulphonic acid in anhydrous pyridine and the resulting sulphuric acid ester of dextrane precipitated by addition of alcohol. The ester was then dissolved in water, neutralized with caustic soda, the solution dialysed until free of sulphuric acid after which the sodium salt of the ester was precipitated by addition of alcohol. A suitable partially hydrolysed dextrane may also be of the kind disclosed in Specification 583,378.ALSO:In an example, a partially hydrolysed dextrane is prepared by boiling an aqueous solution of dextrane with concentrated hydrochloric acid for 3 minutes, the solution then being cooled and neutralised with caustic soda; the partially hydrolysed dextrane obtained is precipitated by addition of alcohol. Reference is made to the preparation of such dextrane disclosed in Specification 583,378, [Group IV].ALSO:Sulphuric acid esters of dextrane in the neutralised or unneutralised state (see Group IV) may be employed as agents for retarding the coagulation of blood. Preferably the esters are derived from partially hydrolysed dextrane of the kind disclosed in Specification 583,378 (as open to inspection under Sect. 91) [Group IV]. Salts of these esters, particularly of alkali or alkaline earth metals in water, saline solutions or other therapeutic fluids yield alone or in admixture with other physiologically suitable salts and therapeutic substances, solutions well adapted for intravenous injection. The degree of esterification of the dextrane may vary from a sulphur content below that of the mono-ester up to complete esterification while p the neutralisation may be partial or complete. An example describes the preparation of the sodium salt of the sulphur ester of a partially hydrolysed dextrane.
GB20952/44A 1943-11-13 1944-10-27 Compounds having a retarding action on the coagulation of blood and processes of preparing the same Expired GB603571A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SE603571X 1943-11-13

Publications (1)

Publication Number Publication Date
GB603571A true GB603571A (en) 1948-06-18

Family

ID=20312868

Family Applications (1)

Application Number Title Priority Date Filing Date
GB20952/44A Expired GB603571A (en) 1943-11-13 1944-10-27 Compounds having a retarding action on the coagulation of blood and processes of preparing the same

Country Status (1)

Country Link
GB (1) GB603571A (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2638469A (en) * 1950-05-19 1953-05-12 American Home Prod Process for alginic acid sulfate production
US2638470A (en) * 1950-05-19 1953-05-12 American Home Prod Process for the production of alginic acid sulfate
US2689848A (en) * 1951-02-06 1954-09-21 Wander Ag Dr A Salts of sulfuric acid esters of xylan
US2715091A (en) * 1949-11-28 1955-08-09 Nat Res Dev Dextran sulfate as anticoagulant, process of preparing same, and sterile solution thereof
US2729633A (en) * 1952-05-13 1956-01-03 American Home Prod Sulfated pectic acid blood anticoagulant
US2786833A (en) * 1953-11-24 1957-03-26 Nat Starch Products Inc Sulfation of amylaceous materials
US2897193A (en) * 1954-05-28 1959-07-28 Ohio Commw Eng Co Sulfuric acid esters of dextranic acid
US2914444A (en) * 1950-12-12 1959-11-24 David F Smith Cellulosic hemostatic composition
WO1988007060A1 (en) * 1987-03-19 1988-09-22 Arthropharm Pty. Limited Anti-inflammatory compounds and compositions
US5668116A (en) * 1987-03-19 1997-09-16 Anthropharm Pty. Limited Anti-inflammatory compounds and compositions

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2715091A (en) * 1949-11-28 1955-08-09 Nat Res Dev Dextran sulfate as anticoagulant, process of preparing same, and sterile solution thereof
US2638469A (en) * 1950-05-19 1953-05-12 American Home Prod Process for alginic acid sulfate production
US2638470A (en) * 1950-05-19 1953-05-12 American Home Prod Process for the production of alginic acid sulfate
US2914444A (en) * 1950-12-12 1959-11-24 David F Smith Cellulosic hemostatic composition
US2689848A (en) * 1951-02-06 1954-09-21 Wander Ag Dr A Salts of sulfuric acid esters of xylan
US2729633A (en) * 1952-05-13 1956-01-03 American Home Prod Sulfated pectic acid blood anticoagulant
US2786833A (en) * 1953-11-24 1957-03-26 Nat Starch Products Inc Sulfation of amylaceous materials
US2897193A (en) * 1954-05-28 1959-07-28 Ohio Commw Eng Co Sulfuric acid esters of dextranic acid
WO1988007060A1 (en) * 1987-03-19 1988-09-22 Arthropharm Pty. Limited Anti-inflammatory compounds and compositions
US5145841A (en) * 1987-03-19 1992-09-08 Arthropharm Pty. Limited Anti-inflammatory compounds and compositions
US5470840A (en) * 1987-03-19 1995-11-28 Arthropharm Pty Limited Anti-inflammatory compounds and compositions
US5668116A (en) * 1987-03-19 1997-09-16 Anthropharm Pty. Limited Anti-inflammatory compounds and compositions

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