FR2214471A1 - Disteroidyl ethers - having improved and/or increased hormonal props - Google Patents
Disteroidyl ethers - having improved and/or increased hormonal propsInfo
- Publication number
- FR2214471A1 FR2214471A1 FR7321979A FR7321979A FR2214471A1 FR 2214471 A1 FR2214471 A1 FR 2214471A1 FR 7321979 A FR7321979 A FR 7321979A FR 7321979 A FR7321979 A FR 7321979A FR 2214471 A1 FR2214471 A1 FR 2214471A1
- Authority
- FR
- France
- Prior art keywords
- delta
- ethers
- contg
- pregnane
- androstane
- 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.)
- Granted
Links
- 150000002170 ethers Chemical class 0.000 title abstract 3
- 230000003054 hormonal effect Effects 0.000 title 1
- 150000003431 steroids Chemical class 0.000 abstract 3
- QZLYKIGBANMMBK-UGCZWRCOSA-N 5α-Androstane Chemical compound C([C@@H]1CC2)CCC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CCC[C@@]2(C)CC1 QZLYKIGBANMMBK-UGCZWRCOSA-N 0.000 abstract 2
- JWMFYGXQPXQEEM-NUNROCCHSA-N 5β-pregnane Chemical compound C([C@H]1CC2)CCC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H](CC)[C@@]2(C)CC1 JWMFYGXQPXQEEM-NUNROCCHSA-N 0.000 abstract 2
- XIIAYQZJNBULGD-UHFFFAOYSA-N (5alpha)-cholestane Natural products C1CC2CCCCC2(C)C2C1C1CCC(C(C)CCCC(C)C)C1(C)CC2 XIIAYQZJNBULGD-UHFFFAOYSA-N 0.000 abstract 1
- VMNRNUNYBVFVQI-QYXZOKGRSA-N (5s,8s,9s,10s,13s,14s)-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one Chemical compound C([C@@H]1CC2)C(=O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CCC[C@@]2(C)CC1 VMNRNUNYBVFVQI-QYXZOKGRSA-N 0.000 abstract 1
- QSHQKIURKJITMZ-OBUPQJQESA-N 5β-cholane Chemical compound C([C@H]1CC2)CCC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@H](C)CCC)[C@@]2(C)CC1 QSHQKIURKJITMZ-OBUPQJQESA-N 0.000 abstract 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 abstract 1
- 150000001241 acetals Chemical class 0.000 abstract 1
- 239000003377 acid catalyst Substances 0.000 abstract 1
- -1 anabolic Chemical class 0.000 abstract 1
- 230000001195 anabolic effect Effects 0.000 abstract 1
- 230000001548 androgenic effect Effects 0.000 abstract 1
- 230000003110 anti-inflammatory effect Effects 0.000 abstract 1
- 239000003874 central nervous system depressant Substances 0.000 abstract 1
- XIIAYQZJNBULGD-LDHZKLTISA-N cholestane Chemical compound C1CC2CCCC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 XIIAYQZJNBULGD-LDHZKLTISA-N 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 150000002084 enol ethers Chemical class 0.000 abstract 1
- GRXPVLPQNMUNNX-MHJRRCNVSA-N estrane Chemical compound C1CC2CCCC[C@@H]2[C@@H]2[C@@H]1[C@@H]1CCC[C@@]1(C)CC2 GRXPVLPQNMUNNX-MHJRRCNVSA-N 0.000 abstract 1
- 230000001114 myogenic effect Effects 0.000 abstract 1
- 230000001072 progestational effect Effects 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
Classifications
-
- 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
- C07J1/0051—Estrane derivatives
-
- 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
- C07J1/0003—Androstane derivatives
-
- 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
- C07J7/00—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Filling Or Emptying Of Bunkers, Hoppers, And Tanks (AREA)
- Steroid Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ES1972181237U ES181237Y (es) | 1972-06-07 | 1972-06-07 | Barredora mecanica para descarga de silos de gran diametro con cimentacion plana. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| FR2214471A1 true FR2214471A1 (en) | 1974-08-19 |
| FR2214471B1 FR2214471B1 (enExample) | 1976-12-31 |
Family
ID=8354227
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FR7321979A Granted FR2214471A1 (en) | 1972-06-07 | 1973-06-15 | Disteroidyl ethers - having improved and/or increased hormonal props |
Country Status (2)
| Country | Link |
|---|---|
| ES (1) | ES181237Y (enExample) |
| FR (1) | FR2214471A1 (enExample) |
-
1972
- 1972-06-07 ES ES1972181237U patent/ES181237Y/es not_active Expired
-
1973
- 1973-06-15 FR FR7321979A patent/FR2214471A1/fr active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| FR2214471B1 (enExample) | 1976-12-31 |
| ES181237Y (es) | 1974-02-16 |
| ES181237U (es) | 1973-03-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Djerassi et al. | Steroids. LIV. 1 Synthesis of 19-Nov-17α-ethynyltestosterone and 19-Nor-17α-methyltestosterone2 | |
| GB1494097A (en) | D-homo-20-keto-pregnanes | |
| GB1127746A (en) | Novel process for preparing unsaturated steroids | |
| FR2214471A1 (en) | Disteroidyl ethers - having improved and/or increased hormonal props | |
| NL7308395A (en) | Disteroidyl ethers - having improved and/or increased hormonal props | |
| GB1502326A (en) | 11-substituted steroids of the estrane series | |
| US3766223A (en) | Disteroidyl ethers | |
| US3793350A (en) | Process for preparing 17alpha,21-dihydroxy-20-keto-pregnanes,derivatives and intermediates thereof | |
| US3318923A (en) | Process for the preparation of delta1, 3, 5(10)-trienes and 3-keto-6-oxygenated-delta5(10)-dehydro intermediates therefor | |
| US3453295A (en) | Process for preparing 3-keto-19-nor-delta**4,9(10) steroids | |
| GB1228212A (enExample) | ||
| US3375167A (en) | 6-hydroxymethyl-3-oxo-4, 6-dienic steroids, acyl derivatives thereof, and process for preparing same | |
| US3717627A (en) | Process for the production of estrogenic steroids having a formyl group in the 1-or 4-position | |
| GB1097656A (en) | A process for the manufacture of steroids of the pregnane series | |
| GB1037891A (en) | Process for the manufacture of 19-nor-steroids | |
| GB1213118A (en) | PROCESS FOR PREPARING 9alpha-FLUORO-16-METHYLENE-PREDNISOLONE OR PREDNISONE, AND 21-ESTERS THEREOF | |
| GB1240698A (en) | Methylenation process and reagent | |
| US3445488A (en) | Novel 5beta,10alpha-steroids | |
| GB852847A (en) | Improvements in or relating to 6-methyl steroid compounds | |
| GB1128044A (en) | 13-(c) alkyl-11-oxygenated gonenes | |
| US3248405A (en) | Process for the preparation of 21-halo-19-nor-ethisterones and the 3-enol ethers thereof | |
| US3169135A (en) | 19-nor-delta1(10)-5alpha-pregnen-17alpha-ol-2, 20-dione and derivatives thereof | |
| Turner | Applications of high-potential quinones. Convenient syntheses of steroidal 1, 4, 6-trien-3-ones | |
| GB1237483A (en) | MICROBIAL REDUCTION OF Delta<5> STEROIDS | |
| Urushibara et al. | A New Synthesis of Progesterone |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| ST | Notification of lapse |