SE328871B - - Google Patents
Info
- Publication number
- SE328871B SE328871B SE13050/67A SE1305067A SE328871B SE 328871 B SE328871 B SE 328871B SE 13050/67 A SE13050/67 A SE 13050/67A SE 1305067 A SE1305067 A SE 1305067A SE 328871 B SE328871 B SE 328871B
- Authority
- SE
- Sweden
- Prior art keywords
- alpha
- cyanoethynyl
- prepared
- diol
- free
- Prior art date
Links
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 8
- 125000000468 ketone group Chemical group 0.000 abstract 4
- 150000003431 steroids Chemical class 0.000 abstract 4
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 abstract 3
- 229960005309 estradiol Drugs 0.000 abstract 3
- 238000000034 method Methods 0.000 abstract 3
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 abstract 2
- MUMGGOZAMZWBJJ-DYKIIFRCSA-N Testostosterone Chemical compound O=C1CC[C@]2(C)[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 MUMGGOZAMZWBJJ-DYKIIFRCSA-N 0.000 abstract 2
- 150000001242 acetic acid derivatives Chemical class 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 150000002009 diols Chemical class 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- -1 propiolic acid nitrile Chemical class 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- DNXHEGUUPJUMQT-UHFFFAOYSA-N (+)-estrone Natural products OC1=CC=C2C3CCC(C)(C(CC4)=O)C4C3CCC2=C1 DNXHEGUUPJUMQT-UHFFFAOYSA-N 0.000 abstract 1
- IATKKATWPOVYCC-VMXHOPILSA-N (8s,9s,10r,13s,14s)-10,13-dimethyl-2,3,6,7,8,9,11,12,14,15,16,17-dodecahydro-1h-cyclopenta[a]phenanthrene Chemical class C1CC2=CCCC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CCC[C@@]1(C)CC2 IATKKATWPOVYCC-VMXHOPILSA-N 0.000 abstract 1
- HUHXLHLWASNVDB-UHFFFAOYSA-N 2-(oxan-2-yloxy)oxane Chemical compound O1CCCCC1OC1OCCCC1 HUHXLHLWASNVDB-UHFFFAOYSA-N 0.000 abstract 1
- KBXXJWDSHUJCMA-UHFFFAOYSA-N 3-(oxan-3-yloxy)oxane Chemical compound C1CCOCC1OC1COCCC1 KBXXJWDSHUJCMA-UHFFFAOYSA-N 0.000 abstract 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 1
- DNXHEGUUPJUMQT-CBZIJGRNSA-N Estrone Chemical compound OC1=CC=C2[C@H]3CC[C@](C)(C(CC4)=O)[C@@H]4[C@@H]3CCC2=C1 DNXHEGUUPJUMQT-CBZIJGRNSA-N 0.000 abstract 1
- CYSAMXITKBXZOP-UHFFFAOYSA-N [(2,2,2-trifluoroacetyl)amino] 2,2,2-trifluoroacetate Chemical compound FC(F)(F)C(=O)NOC(=O)C(F)(F)F CYSAMXITKBXZOP-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 abstract 1
- 150000001450 anions Chemical class 0.000 abstract 1
- 230000001833 anti-estrogenic effect Effects 0.000 abstract 1
- 230000003509 anti-fertility effect Effects 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- 239000000969 carrier Substances 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- QPJDMGCKMHUXFD-UHFFFAOYSA-N cyanogen chloride Chemical compound ClC#N QPJDMGCKMHUXFD-UHFFFAOYSA-N 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 150000002081 enamines Chemical class 0.000 abstract 1
- 239000000328 estrogen antagonist Substances 0.000 abstract 1
- 230000001076 estrogenic effect Effects 0.000 abstract 1
- 229960003399 estrone Drugs 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 229960004719 nandrolone Drugs 0.000 abstract 1
- 230000016087 ovulation Effects 0.000 abstract 1
- 150000002923 oximes Chemical class 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 229960003604 testosterone Drugs 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J41/00—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring
- C07J41/0033—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005
- C07J41/0094—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005 containing nitrile radicals, including thiocyanide radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J41/00—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring
- C07J41/0033—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005
- C07J41/0072—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005 the A ring of the steroid being aromatic
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Steroid Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEM0071056 | 1966-09-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SE328871B true SE328871B (cg-RX-API-DMAC10.html) | 1970-09-28 |
Family
ID=7313769
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE13050/67A SE328871B (cg-RX-API-DMAC10.html) | 1966-09-26 | 1967-11-22 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US3505364A (cg-RX-API-DMAC10.html) |
| BE (1) | BE704204A (cg-RX-API-DMAC10.html) |
| CH (1) | CH514560A (cg-RX-API-DMAC10.html) |
| DE (1) | DE1593090A1 (cg-RX-API-DMAC10.html) |
| ES (1) | ES345449A1 (cg-RX-API-DMAC10.html) |
| FR (1) | FR7564M (cg-RX-API-DMAC10.html) |
| GB (1) | GB1140642A (cg-RX-API-DMAC10.html) |
| NL (1) | NL6712574A (cg-RX-API-DMAC10.html) |
| SE (1) | SE328871B (cg-RX-API-DMAC10.html) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4898694A (en) * | 1987-11-25 | 1990-02-06 | Schwartz Arthur G | 17-Hydroxy-steroids |
| US20070129282A1 (en) * | 1998-11-24 | 2007-06-07 | Ahlem Clarence N | Pharmaceutical treatments and compositions |
| AU7736300A (en) * | 1999-09-30 | 2001-04-30 | Hollis-Eden Pharmaceuticals, Inc. | Therapeutic treatment of androgen receptor driven conditions |
| AU2005330504B2 (en) * | 2004-09-29 | 2010-10-28 | Harbor Biosciences, Inc. | Steroid analogs and characterization and treatment methods |
-
1966
- 1966-09-26 DE DE19661593090 patent/DE1593090A1/de active Pending
-
1967
- 1967-09-06 CH CH1247867A patent/CH514560A/de not_active IP Right Cessation
- 1967-09-07 GB GB40879/67A patent/GB1140642A/en not_active Expired
- 1967-09-14 NL NL6712574A patent/NL6712574A/xx unknown
- 1967-09-22 BE BE704204D patent/BE704204A/xx unknown
- 1967-09-25 ES ES345449A patent/ES345449A1/es not_active Expired
- 1967-09-25 US US670410A patent/US3505364A/en not_active Expired - Lifetime
- 1967-09-26 FR FR122295A patent/FR7564M/fr not_active Expired
- 1967-11-22 SE SE13050/67A patent/SE328871B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| FR7564M (cg-RX-API-DMAC10.html) | 1970-01-05 |
| ES345449A1 (es) | 1968-11-01 |
| CH514560A (de) | 1971-10-31 |
| GB1140642A (en) | 1969-01-22 |
| US3505364A (en) | 1970-04-07 |
| NL6712574A (cg-RX-API-DMAC10.html) | 1968-03-27 |
| BE704204A (cg-RX-API-DMAC10.html) | 1968-03-22 |
| DE1593090A1 (de) | 1970-06-04 |
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