GB788855A - Improvements in or relating to mandelo-nitrile-glucuronosides and method of making the same - Google Patents

Improvements in or relating to mandelo-nitrile-glucuronosides and method of making the same

Info

Publication number
GB788855A
GB788855A GB18671/54A GB1867154A GB788855A GB 788855 A GB788855 A GB 788855A GB 18671/54 A GB18671/54 A GB 18671/54A GB 1867154 A GB1867154 A GB 1867154A GB 788855 A GB788855 A GB 788855A
Authority
GB
United Kingdom
Prior art keywords
mandelo
nitrile
beta
glucoside
acid
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
GB18671/54A
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.)
ERNST THEODORE KREBS
ERNST THEODORE KREBS JR
Original Assignee
ERNST THEODORE KREBS
ERNST THEODORE KREBS JR
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 ERNST THEODORE KREBS, ERNST THEODORE KREBS JR filed Critical ERNST THEODORE KREBS
Publication of GB788855A publication Critical patent/GB788855A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H15/00Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
    • C07H15/20Carbocyclic rings
    • C07H15/203Monocyclic carbocyclic rings other than cyclohexane rings; Bicyclic carbocyclic ring systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • Biotechnology (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Saccharide Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

The invention comprises l-mandelo-nitrile-beta-glucuronoside acid and derivatives thereof of the general formula: <FORM:0788855/IV (b)/1> wherein R1 represents hydrogen, a metal or hydrocarbon radical, and wherein the benzene ring may be substituted by a hydroxyl, methyl or nitro radical, preferablyin the para-position, and the preparation of the above compounds where R1 represents hydrogen by oxidizing an aqueous solution of an l-mandelo-nitrile-glucoside of the general formula: <FORM:0788855/IV (b)/2> in which the benzene ring may be substituted by a hydroxyl, methyl or nitro group, with molecular oxygen in the presence of platinum black, by condensing the required l-mandelo-nitrile with beta-glucuronic acid, or by hydrolysing a compound of the formula: <FORM:0788855/IV (b)/3> in which the benzene ring may be substituted by a hydroxyl, methyl or nitro group, by treatment with brewer's yeast, and oxidizing the resulting l-mandelo-nitrile-beta-glucoside with molecular oxygen in the presence of palladium black. The esters and metal salts are formed by usual methods, suitable esters being the ethyl, n- and iso-propyl and various butyl esters, and suitable salts being the sodium and potassium salts. The above processes using the l-mandelo-nitrile-beta-glucoside may be modified in that the l-mandelo-nitrile-beta-glucoside is prepared by condensing the required l-mandelo-nitrile with beta-glucose. The racemic form of mandelo-nitrile may be used in place of l-mandelo-nitrile in processes referred to above, and d-mandelo-nitrile-beta-glucoside or the d-mandelo-nitrile-beta-glucuronoside acid may then be selectively destroyed in or removed from the resulting mixture of d- and l-mandelo-nitrile-beta-glucuside or d- and l-mandelo-nitrile-beta-glucuronoside acid respectively, e.g. by the use of a specific enzyme. In the example, l-mandelo-nitrile-beta-glucuronoside acid and the sodium salt thereof are prepared from l-mandelo-nitrile-beta-glucoside which is obtained by the hydrolysis of amygdalin with yeast.ALSO:A therapeutic composition having bactericidal activity contains as the active ingredient l - mandelo - nitrile - beta - glucuronoside acid or a derivative thereof represented by the general formula <FORM:0788855/VI/1> wherein R1 represents hydrogen, a hydrocarbon radical or a metal such as sodium or potassium, and wherein the benzene ring may be substituted by a hydroxyl, methyl or nitro radical. The diluent may be a solid extender suitable for oral administration, or may be an isotonic solution suitable for parenteral administration. The active ingredient may be present in an amount from about 1/4 to 2 per cent by weight of the composition. The solid extender is preferably an alkaline extender, e.g. magnesium carbonate, magnesium oxide, brewer's yeast or rice bran. Suitable isotonic solutions are Ringer's isotonic solution, Ringer-Tyrode's solution, and sodium chloride solutions. A suitable compoition is 100 mgs. of active ingredient, e.g. sodium l-mandelonitrile-betaglucuronate, in about 3 to 5 c.c. of isotonic solution.
GB18671/54A 1953-06-30 1954-06-25 Improvements in or relating to mandelo-nitrile-glucuronosides and method of making the same Expired GB788855A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US788855XA 1953-06-30 1953-06-30

Publications (1)

Publication Number Publication Date
GB788855A true GB788855A (en) 1958-01-08

Family

ID=22146796

Family Applications (1)

Application Number Title Priority Date Filing Date
GB18671/54A Expired GB788855A (en) 1953-06-30 1954-06-25 Improvements in or relating to mandelo-nitrile-glucuronosides and method of making the same

Country Status (1)

Country Link
GB (1) GB788855A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2440374A1 (en) * 1978-10-13 1980-05-30 Schwimmer Adolf NOVEL GLUCURONIDES, PROCESSES FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS HAVING B-GLUCURONIDASE ACTIVITY AND / OR PH-DEPENDENT ACTIVITY, CONTAINING SAID GLUCORONIDES
US4481195A (en) * 1978-10-13 1984-11-06 Adolf Schwimmer Method for the treatment of tumors with β-glucuronidase activity dependent pharmaceuticals
US4490523A (en) * 1981-11-10 1984-12-25 Ely J. Rubin Mandelonitrile triacetyl glucuronate and process for preparing same
CN103214529A (en) * 2013-05-10 2013-07-24 浙江省农业科学院 Method for extracting amygdalin from kernel of red bayberry fruit
US20160002277A1 (en) * 2013-03-12 2016-01-07 Laszlo Sichtnik Compositions and methods for treating infectious disease

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2440374A1 (en) * 1978-10-13 1980-05-30 Schwimmer Adolf NOVEL GLUCURONIDES, PROCESSES FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS HAVING B-GLUCURONIDASE ACTIVITY AND / OR PH-DEPENDENT ACTIVITY, CONTAINING SAID GLUCORONIDES
US4481195A (en) * 1978-10-13 1984-11-06 Adolf Schwimmer Method for the treatment of tumors with β-glucuronidase activity dependent pharmaceuticals
US4490523A (en) * 1981-11-10 1984-12-25 Ely J. Rubin Mandelonitrile triacetyl glucuronate and process for preparing same
US20160002277A1 (en) * 2013-03-12 2016-01-07 Laszlo Sichtnik Compositions and methods for treating infectious disease
US10183964B2 (en) * 2013-03-12 2019-01-22 Laszlo Sichtnik Compositions and methods for treating infectious disease
US10723751B2 (en) * 2013-03-12 2020-07-28 Laszlo Sichtnik Compositions and methods for treating infectious disease
CN103214529A (en) * 2013-05-10 2013-07-24 浙江省农业科学院 Method for extracting amygdalin from kernel of red bayberry fruit

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