GB834913A - Steroids and biologically active preparations containing steroids - Google Patents
Steroids and biologically active preparations containing steroidsInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J5/00—Normal 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J75/00—Processes 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.
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)
| 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 |
-
1956
- 1956-11-29 GB GB36527/56A patent/GB834913A/en not_active Expired
Cited By (1)
| 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 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| GB834913A (en) | Steroids and biologically active preparations containing steroids | |
| US3089881A (en) | Sulfocarboxylic acid esters of hydroxylated steroids | |
| GB1380065A (en) | 5-amino-isophthalic acid derivatives | |
| GB704185A (en) | Improvement in electroplating of nickel | |
| GB862248A (en) | Di-isopropylammonium salts of chloroacetic and chloropropionic acids | |
| GB940701A (en) | Novel therapeutic salts of steroid compounds and processes for their manufacture | |
| US2241235A (en) | Sulphocarboxylic acid esters of cellulose | |
| US3276959A (en) | Stabilized steroid compositions | |
| GB868975A (en) | New steroid compounds and process for their manufacture | |
| GB1298005A (en) | ||
| GB499794A (en) | Manufacture of new esters of compounds of the oestrone series | |
| GB1475075A (en) | Derivatives of glycyrrhetinic and oleanolic acids | |
| GB940138A (en) | Improvements in or relating to phosphonic acid | |
| GB814000A (en) | Steroid compounds and the preparation thereof | |
| US3026335A (en) | 17-esters of 16alpha, 17alpha-dihydroxyprogesterone | |
| GB1107036A (en) | Esters of dibenzocycloheptenyl-carboxylic acids | |
| GB1115039A (en) | Process for the preparation of cycloalkene-dicarboxylic acids | |
| GB1387499A (en) | Derivatives of glycyrrhetinic acid | |
| US3012939A (en) | New dihalogenandrostenes and process for their manufacture | |
| GB815809A (en) | Esters of the pregnane and pregnene series and process of preparing these compounds | |
| GB1301778A (en) | ||
| US3291813A (en) | 3 mono and 3, 16-diesters of delta5-androstene-3beta, 16alpha-diol-17 one and process for the production thereof | |
| US3278564A (en) | 6, 16-substituted progesterones | |
| GB724146A (en) | Steroids | |
| DE3361150D1 (en) | Steroid esters of n-(2-halogen-ethyl)-n-nitroso-carbamoyl amino acids and their peptides, and process for their preparation |