GB916778A - Oral compositions containing 3-substituted 17-ª--methyl testosterones - Google Patents
Oral compositions containing 3-substituted 17-ª--methyl testosteronesInfo
- Publication number
- GB916778A GB916778A GB34990/59A GB3499059A GB916778A GB 916778 A GB916778 A GB 916778A GB 34990/59 A GB34990/59 A GB 34990/59A GB 3499059 A GB3499059 A GB 3499059A GB 916778 A GB916778 A GB 916778A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methyl
- tertosterone
- enol
- ethyl
- alkyl
- 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
- C07J7/00—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J1/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
-
- 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)
- Medicinal Preparation (AREA)
Abstract
The invention comprises inter alia the 3-enol alkyl or cycloalkyl ethers of free or acylated 17a -methyl testosterone having from 4-8 carbon atoms in the alkyl or cycloalkyl group. The compounds are prepared by (a) reacting methyl magnesium bromide with the corresponding enol ether of androstene-3,17-dione or (b) reacting the appropriate alcohol with the 3-enol ethyl ether of 17a -methyl testerone free or acylated in the presence of an acid catalyst, e.g. p-toluene sulphonic acid. The above process (b) may be used to prepare other 3-enol alkyl and benzyl ethers of 17a -methyltestosterone especially those substituted with functional substituents such as nitro and halo substituents. 3-Alkylene ketals of 17a -methyltestosterone are prepared by reacting 3-alkylene ketals of D 4-androstene-3,17-dione with methyl magnesium halide.ALSO:An oral composition having a high androgenic and anobolic activity comprises a 3-enol ether or a 3-glycol ketal of 17a methyl tertosterone or a 17b ester thereof, mixed with an orally ingestible pharmaceutical carrier. The 3-enol ether of tertosterone has at the 3 position a residue of an aliphatic, alicyclic arylaliphatic, aromatic or heterocyclic alcohol. The residue may contain a straight or branch chain alkyl group, which may be substituted e.g. by halogen; an alkylene group e.g. ethylene, a tetrahydropyraryl group or maybe a sugar residue such as that of glucose, galactose or maltose. Preferred ethers have a straight alkyl chain of 4 to 8 carbon atoms with or without methyl or ethyl substituents, at the 3 position. Preferred glycol ketals are alkylene glycol ketals having 2 to 4 carbon atoms in the glycol group. The compositions may be in the form of coated or uncoated tablets, powders, syrups and capsules e.g. keratin or gelatin capsules and are stabilised by adding an alkaline oxide e.g. MgO or an alkaline carbonate. The preferred carrier is a lipid from animal or vegetable sources, specified lipid carriers are (a) oils e.g. coconut, corn, cottonseed, lard, linseed, olive, sunflower seed, palm, peanut, sesame, soya bean, wheat germ and egg yolk oil. (b) Fats e.g. butter fat, lard, cocoa butter or margarine fat; (c) esters of glycerol with high molecular weight long chain fatty acids of 10-22 C atoms; (d) the free fatty acids contained in fats or oils having 10 to 22 carbon atoms e.g. decenoic, decosanoic lauric, palmitic, stearic, archidic, oleic, linoleic and linolenic acids. Other adjuvants specified are magnesium stearate, talc, lactose, rice starch. The compositions may also contain androgenic and/or anabolic steroid hormones, antiseptics, antioxidants e.g. propyl gallate and/or preservatives. The active ingredient is present in an amount ranging from 0.1 to 7% by weight of the final composition. Specified active ingredients are the 3-sec.-butyl, 3-n-amyl -, 3 isoamyl -, 3 hexyl -, 3 - (2 - methyl) pentyl -, 3 - n - heptyl -, 3 cyclohexyl -, 3 benzyl -, 3 - isobutyl -, 3 - sec - (3,3 - dimethyl)-butyl -, 3 - (2 - ethyl) - butyl, 3 - octyl, 3-chloroethyl, 3 - n - butyl and 3 ethyl enol ether of 17a methyl tertosterone, the 3-ethyl-enol ether of 17a methyl tertosterone acetate and the 3 glycol ketal of 17a methyl tertosterone.
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB34990/59A GB916778A (en) | 1959-10-15 | 1959-10-15 | Oral compositions containing 3-substituted 17-ª--methyl testosterones |
AT334760A AT243446B (en) | 1959-05-04 | 1960-05-03 | Process for the preparation of enol ethers of Δ <4> -3-keto steroids |
CH504460A CH389595A (en) | 1959-05-04 | 1960-05-03 | Process for the preparation of enol ethers of 4-3-keto steroids |
BE590424A BE590424A (en) | 1959-05-04 | 1960-05-03 | Hormonal compositions. |
FR837301A FR568M (en) | 1959-05-04 | 1960-08-31 | |
OA51016A OA00921A (en) | 1959-10-15 | 1964-12-24 | A process for the preparation of 2-enole ethers of 17α-methyl testosterone. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB34990/59A GB916778A (en) | 1959-10-15 | 1959-10-15 | Oral compositions containing 3-substituted 17-ª--methyl testosterones |
Publications (1)
Publication Number | Publication Date |
---|---|
GB916778A true GB916778A (en) | 1963-01-30 |
Family
ID=10372503
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB34990/59A Expired GB916778A (en) | 1959-05-04 | 1959-10-15 | Oral compositions containing 3-substituted 17-ª--methyl testosterones |
Country Status (2)
Country | Link |
---|---|
GB (1) | GB916778A (en) |
OA (1) | OA00921A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996037201A2 (en) * | 1995-05-16 | 1996-11-28 | Arch Development Corporation | METHODS AND COMPOSITIONS FOR INHIBITING 5α-REDUCTASE ACTIVITY |
WO2000066612A1 (en) * | 1999-05-04 | 2000-11-09 | Strakan Limited | Androgen glycosides and androgenic activity thereof |
US8466137B2 (en) | 2005-10-12 | 2013-06-18 | Unimed Pharmaceuticals, Llc | Testosterone gel and method of use |
US9125816B2 (en) | 2000-08-30 | 2015-09-08 | Besins Healthcare Inc. | Pharmaceutical composition and method for treating hypogonadism |
-
1959
- 1959-10-15 GB GB34990/59A patent/GB916778A/en not_active Expired
-
1964
- 1964-12-24 OA OA51016A patent/OA00921A/en unknown
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996037201A2 (en) * | 1995-05-16 | 1996-11-28 | Arch Development Corporation | METHODS AND COMPOSITIONS FOR INHIBITING 5α-REDUCTASE ACTIVITY |
WO1996037201A3 (en) * | 1995-05-16 | 1997-01-03 | Arch Dev Corp | METHODS AND COMPOSITIONS FOR INHIBITING 5α-REDUCTASE ACTIVITY |
WO2000066612A1 (en) * | 1999-05-04 | 2000-11-09 | Strakan Limited | Androgen glycosides and androgenic activity thereof |
US6630453B1 (en) | 1999-05-04 | 2003-10-07 | Strakan Limited | Androgen derivatives and uses thereof |
US9132089B2 (en) | 2000-08-30 | 2015-09-15 | Besins Healthcare Inc. | Pharmaceutical composition and method for treating hypogonadism |
US9125816B2 (en) | 2000-08-30 | 2015-09-08 | Besins Healthcare Inc. | Pharmaceutical composition and method for treating hypogonadism |
US8466136B2 (en) | 2005-10-12 | 2013-06-18 | Unimed Pharmaceuticals, Llc | Testosterone gel and method of use |
US8486925B2 (en) | 2005-10-12 | 2013-07-16 | Unimed Pharmaceuticals, Llc | Testosterone gel and method of use |
US8729057B2 (en) | 2005-10-12 | 2014-05-20 | Unimed Pharmaeuticals, LLC | Testosterone gel and method of use |
US8741881B2 (en) | 2005-10-12 | 2014-06-03 | Unimed Pharmaceuticals, Llc | Testosterone gel and method of use |
US8754070B2 (en) | 2005-10-12 | 2014-06-17 | Unimed Pharmaceuticals, Llc | Testosterone gel and method of use |
US8759329B2 (en) | 2005-10-12 | 2014-06-24 | Unimed Pharmaceuticals, Llc | Testosterone gel and method of use |
US8466138B2 (en) | 2005-10-12 | 2013-06-18 | Unimed Pharmaceuticals, Llc | Testosterone gel and method of use |
US8466137B2 (en) | 2005-10-12 | 2013-06-18 | Unimed Pharmaceuticals, Llc | Testosterone gel and method of use |
Also Published As
Publication number | Publication date |
---|---|
OA00921A (en) | 1968-03-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4147783A (en) | Oral pharmaceutical preparation | |
EP0159739B1 (en) | Steroids for use as immunomodulators | |
US4071623A (en) | Pharmaceutical preparation adapted for oral administration | |
US4098802A (en) | Oral pharmaceutical preparation having androgenic activity | |
KR100666016B1 (en) | Formulation comprising testosteron undecanoate and castor oil | |
CA1038760A (en) | Oral pharmaceutical preparation | |
CN101100480A (en) | New etonogestrel esters | |
CN101217963A (en) | Pharmaceutical delivery systems for hydrophobic drugs and compositions comprising same | |
GB916778A (en) | Oral compositions containing 3-substituted 17-ª--methyl testosterones | |
EP0808845B1 (en) | New 1- or 6-hydroxylated steroids, a process for their production, their use as medicaments and pharmaceutical compositions containing them | |
SU1277943A1 (en) | Zootechnical composition | |
EP0001851B1 (en) | Highly concentrated pharmaceutical formulations of steroids and processes for their preparation | |
HU179069B (en) | Process for preparing 1,3/diesters with benzoic acid of 17alpha-ethynyl-7alpha-methyl-1,3,5/10/-estratriene-1,3,17beta-triol | |
US4076811A (en) | Novel agents and methods for treatment of climacteric disturbances | |
US5102912A (en) | Hydroxyoctadecadienic acid for the treatment of estrogen-dependent disease | |
US20180333423A1 (en) | Methods of treating testosterone deficiency | |
GB1339142A (en) | Process for producing emulsified fats | |
US3939265A (en) | Novel zootechnical compositions | |
Barnes et al. | Effects of the Prevention of Coprophagy in the Rat: V. Essential Fatty Acid Deficiency | |
JP2001064169A (en) | Pai-1 lowering agent | |
US3342682A (en) | Oral compositions containing 3-enol ethers of progesterone or 6-methyl derivatives thereof and method of using the same | |
GB931115A (en) | Pharmaceutical preparations containing sitosterols | |
JP6945874B2 (en) | Pharmaceutical composition for oral administration | |
GB1132518A (en) | Medicinal composition | |
GB893315A (en) | Steroid compounds and therapeutic compositions containing steroid compounds |