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GB834913A - Steroids and biologically active preparations containing steroids - Google Patents

Steroids and biologically active preparations containing steroids

Info

Publication number
GB834913A
GB834913A GB36527/56A GB3652756A GB834913A GB 834913 A GB834913 A GB 834913A GB 36527/56 A GB36527/56 A GB 36527/56A GB 3652756 A GB3652756 A GB 3652756A GB 834913 A GB834913 A GB 834913A
Authority
GB
United Kingdom
Prior art keywords
acid
allopregnane
esters
salts
derived
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
GB36527/56A
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.)
Organon Laboratories Ltd
Original Assignee
Organon Laboratories Ltd
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 Organon Laboratories Ltd filed Critical Organon Laboratories Ltd
Publication of GB834913A publication Critical patent/GB834913A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J5/00Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J75/00Processes for the preparation of steroids in general

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Steroid Compounds (AREA)

Abstract

The invention comprises 3-acid polycarboxylic esters of pregnanes and allopregnanes of the general formula <FORM:0834913/IV (b)/1> wherein Y represents an oxo or 11b -hydroxy group and the polycarboxylic acids contain 2 to 8 carbon atoms and the preparation of the salts by reacting free 3-hydroxy-substituted pregnanes or allopregnanes with the polycarboxylic acids or anhydrides thereof and converting the resulting acid esters into alkali metal, ammonium or substituted ammonium salts. The esters may be derived from malonic, adipic, succinic, glutaric, pimelic, fumaric, maleic, malic, tartaric, citric, aconitic, tricarballylic, aspartic, suberic, glutamic or phthalic acid. A preferred acid is an aliphatic dicarboxylic acid having from 2 to 8 carbon atoms. The esters may be prepared by reacting an excess of the required acid anhydride with the pregnane or allopregnane preferably in the presence of pyridine. The salts may be prepared by reacting the 3-acid polycarboxylic ester with the required base such as sodium bicarbonate or sodium hydroxide, in aqueous solution. Suitable salts mentioned are the ammonium, potassium and sodium salts and salts derived from dimethylamine, trimethylamine, diethylamine, triethylamine, diethanolamine, dimethylethanolamine, dimethylbenzylamine, N : N1-tetramethyl - hexamethylene - diamine, procaine and "Xylocaine" (Registered Trade Mark) and other amines containing alkyl, aryl and/or aralkyl groups. A number of detailed examples are given in which the steroid reactants are 3a (and 3b -dihydroxy-20-oxo-pregnane, 3a - hydroxy - 11,20 - dioxo - pregnane and allopregnane, and 3b - hydroxy - 11,20-dioxo-allopregnane. The Specification also refers to 3-esters of compounds of the above general formula derived from monocarboxylic acids containing from 1 to 10 carbon atoms, e.g. derived from aliphatic, aromatic and araliphatic carboxylic acids, a large number of which are detailed.ALSO:A therapeutic preparation suitable for oral or parenteral administration contains as the active ingredient a pregnane or allopregnane of the general formula <FORM:0834913/VI/1> wherein X represents an oxo or an a - or b -hydroxy group, or an a - or b -acyloxy group derived from a monocarboxylic acid containing from 1 to 10 carbon atoms or a 3-acid ester thereof derived from a polycarboxylic acid containing from 2 to 8 carbon atoms or an alkali metal, ammonium or substituted ammonium salt of said polycarboxylic ester and Y represents an oxo or b -hydroxy group. Thus any of the following steroid compounds may be incorporated in the composition: 3,11,20-trioxopregnane and allopregnane, 3a -hydroxy-11,20-dioxo - pregnane and allopregnane, 3b - hydroxy - 11,20 - dioxo - allopregnane, and 3a (and 3b ), 11b -dihydroxy-20-oxo-pregnane, and the 3-esters thereof-particularly those derived from formic, acetic, propionic, butyric, valeric, capronic, venanthic, caprylic, crotonic, b -cyclopentylpropionic, g - cyclohexylbutyric, chloracetic, trifluoro - acetic, trimethyl - acetic, diethyl - acetic, carbamic, glycine, alanine, serine, leucine, benzoic, phenyl-acetic, b -phenylpropionic, furane-2-carboxylic acid and isonicotinic acid; and the dicarboxylic acids such as malonic, succinic, glutaric, pimelic, fumaric, maleic, malic, tartaric, citric, aconitic, tricarballylic, aspartic, glutamic and phthalic acids. The salts of the 3-acid esters may be a sodium, potassium, dimethylamine, trimethylamine, diethylamine, triethylamine, diethanolamine, dimethylethanolamine, dimethylbenzylamine, N,N1 - tetramethyl - hexamethylene-diamine, procaine or "Xylocaine" (Registered Trade Mark). Suitable diluents are water, sodium chloride, glucose, lactose, starch, talc, magnesium stearate, benzyl alcohol, arachis oil, polyoxyethylene - sorbitan - monolaurate, carboxymethylcellulose, and sodium phosphates.
GB36527/56A 1955-12-23 1956-11-29 Steroids and biologically active preparations containing steroids Expired GB834913A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
NL834913X 1955-12-23

Publications (1)

Publication Number Publication Date
GB834913A true GB834913A (en) 1960-05-11

Family

ID=19843105

Family Applications (1)

Application Number Title Priority Date Filing Date
GB36527/56A Expired GB834913A (en) 1955-12-23 1956-11-29 Steroids and biologically active preparations containing steroids

Country Status (1)

Country Link
GB (1) GB834913A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7674783B2 (en) 2002-11-22 2010-03-09 Dimera Inc. Estrogen beta receptor agonists to prevent or reduce the severity of cardiovascular disease

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7674783B2 (en) 2002-11-22 2010-03-09 Dimera Inc. Estrogen beta receptor agonists to prevent or reduce the severity of cardiovascular disease

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