JP2002539135A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2002539135A5 JP2002539135A5 JP2000604054A JP2000604054A JP2002539135A5 JP 2002539135 A5 JP2002539135 A5 JP 2002539135A5 JP 2000604054 A JP2000604054 A JP 2000604054A JP 2000604054 A JP2000604054 A JP 2000604054A JP 2002539135 A5 JP2002539135 A5 JP 2002539135A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- halogen
- hydrogen
- cyano
- alkoxy
- 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
- 229910052739 hydrogen Inorganic materials 0.000 description 51
- 125000000217 alkyl group Chemical group 0.000 description 46
- 229910052736 halogen Inorganic materials 0.000 description 45
- 150000002367 halogens Chemical class 0.000 description 45
- 239000001257 hydrogen Substances 0.000 description 41
- 125000004093 cyano group Chemical group *C#N 0.000 description 39
- 125000003545 alkoxy group Chemical group 0.000 description 33
- 150000002431 hydrogen Chemical group 0.000 description 33
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 27
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 description 21
- 125000004043 oxo group Chemical group O=* 0.000 description 21
- 229910052799 carbon Inorganic materials 0.000 description 20
- 125000004432 carbon atom Chemical group C* 0.000 description 16
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 description 15
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 13
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 13
- 125000000304 alkynyl group Chemical group 0.000 description 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 8
- 125000002252 acyl group Chemical group 0.000 description 7
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 7
- 125000000392 cycloalkenyl group Chemical group 0.000 description 6
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 4
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 4
- 239000008194 pharmaceutical composition Substances 0.000 description 4
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 3
- 0 **[C@](C(*)C1O*)(C(*)(*)*)[C@@](*)(C(*)C2*)[C@@]1(*)C(C(*)C1*)C2[C@@](*)(CC2)C1C(*)[C@@]2(*)I Chemical compound **[C@](C(*)C1O*)(C(*)(*)*)[C@@](*)(C(*)C2*)[C@@]1(*)C(C(*)C1*)C2[C@@](*)(CC2)C1C(*)[C@@]2(*)I 0.000 description 3
- 125000003342 alkenyl group Chemical group 0.000 description 3
- 125000002070 alkenylidene group Chemical group 0.000 description 3
- 125000001118 alkylidene group Chemical group 0.000 description 3
- 150000001924 cycloalkanes Chemical class 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- -1 steroid compound Chemical class 0.000 description 3
- 239000002583 male contraceptive agent Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 150000003431 steroids Chemical group 0.000 description 2
- 206010002261 Androgen deficiency Diseases 0.000 description 1
- WAHQVRCNDCHDIB-QZYSPNBYSA-N [(3s,8r,9s,10r,13s,14s,17r)-17-acetyl-17-acetyloxy-6,10,13-trimethyl-1,2,3,8,9,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-3-yl] 3-cyclopentylpropanoate Chemical compound O([C@@H]1C=C2C(C)=C[C@H]3[C@@H]4CC[C@]([C@]4(CC[C@@H]3[C@@]2(C)CC1)C)(OC(=O)C)C(C)=O)C(=O)CCC1CCCC1 WAHQVRCNDCHDIB-QZYSPNBYSA-N 0.000 description 1
- 239000003098 androgen Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000003937 drug carrier Substances 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000583 progesterone congener Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP99200665.0 | 1999-03-08 | ||
| EP99200665 | 1999-03-08 | ||
| PCT/EP2000/001755 WO2000053619A1 (en) | 1999-03-08 | 2000-03-02 | 14.beta., 17-alpha-hydroxymethylandrostane derivatives as androgens |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2002539135A JP2002539135A (ja) | 2002-11-19 |
| JP2002539135A5 true JP2002539135A5 (enExample) | 2007-05-10 |
| JP4749550B2 JP4749550B2 (ja) | 2011-08-17 |
Family
ID=8239953
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000604054A Expired - Lifetime JP4749550B2 (ja) | 1999-03-08 | 2000-03-02 | アンドロゲンとしての14β,17α−ヒドロキシメチルアンドロスタン誘導体 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US6881728B1 (enExample) |
| EP (1) | EP1163259B1 (enExample) |
| JP (1) | JP4749550B2 (enExample) |
| AR (1) | AR022852A1 (enExample) |
| AT (1) | ATE228143T1 (enExample) |
| AU (1) | AU3162200A (enExample) |
| CA (1) | CA2359218A1 (enExample) |
| CO (1) | CO5150195A1 (enExample) |
| DE (1) | DE60000826T2 (enExample) |
| PE (1) | PE20001489A1 (enExample) |
| WO (1) | WO2000053619A1 (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL202999B1 (pl) * | 1999-12-02 | 2009-08-31 | Organon Nv | Androgeny zawierające pierścień cyklopropanowy w pozycjach 14, 15 i zastosowanie takich androgenów |
| DE60134266D1 (de) | 2000-12-11 | 2008-07-10 | Organon Nv | Methylensteroide als neue androgene |
| DE10104327A1 (de) * | 2001-01-24 | 2002-07-25 | Schering Ag | 11beta-Halogensteroide, deren Herstellung und Verwendung zur Herstellung von Arzneimitteln sowie 11beta-Halogensteroide enthaltende pharmazeutische Präparate |
| TWI221154B (en) * | 2001-09-12 | 2004-09-21 | Akzo Nobel Nv | 17alpha-hydroxy-14beta-steroids with hormonal effect |
| PE20050677A1 (es) | 2003-12-22 | 2005-10-04 | Akzo Nobel Nv | Esteroides con perfil androgenico y progestagenico mixto |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4002746A (en) * | 1959-09-25 | 1977-01-11 | Herchel Smith | Synthesis of gon-4-enes |
| US3086027A (en) | 1960-01-22 | 1963-04-16 | Lilly Co Eli | 19-nor-4, 9(10)-steroids and process |
| IE60780B1 (en) * | 1987-01-23 | 1994-08-10 | Akzo Nv | New 11-aryl steroid derivatives |
| US5264427A (en) * | 1992-01-29 | 1993-11-23 | Research Corporation Technologies, Inc. | 20-substituted pregnene derivatives and their use as androgen synthesis inhibitors |
| US6180682B1 (en) * | 1999-01-26 | 2001-01-30 | Virgil A. Place | Buccal drug delivery system for use in male contraception |
-
2000
- 2000-03-02 WO PCT/EP2000/001755 patent/WO2000053619A1/en not_active Ceased
- 2000-03-02 DE DE60000826T patent/DE60000826T2/de not_active Expired - Lifetime
- 2000-03-02 JP JP2000604054A patent/JP4749550B2/ja not_active Expired - Lifetime
- 2000-03-02 AT AT00909281T patent/ATE228143T1/de not_active IP Right Cessation
- 2000-03-02 EP EP00909281A patent/EP1163259B1/en not_active Expired - Lifetime
- 2000-03-02 CA CA002359218A patent/CA2359218A1/en not_active Abandoned
- 2000-03-02 AU AU31622/00A patent/AU3162200A/en not_active Abandoned
- 2000-03-02 US US09/890,845 patent/US6881728B1/en not_active Expired - Lifetime
- 2000-03-07 AR ARP000101000A patent/AR022852A1/es unknown
- 2000-03-07 PE PE2000000200A patent/PE20001489A1/es not_active Application Discontinuation
- 2000-03-08 CO CO00016933A patent/CO5150195A1/es unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2003512474A5 (enExample) | ||
| RU96115774A (ru) | Производные 11-(замещенный фенил)-эстра-4,9-диена | |
| JP2005533807A5 (enExample) | ||
| JP4845320B2 (ja) | (7α,11β)−ジメチル−17β−ヒドロキシ−4−エストレン−3−オンの4−N−ブチルシクロヘキサン酸エステル及びウンデカン酸エステルの製造方法及びそれらの医学用途 | |
| KR970010784A (ko) | 11-(치환된 페닐)-에스트라-4,9-디엔 유도체 | |
| RU2009107537A (ru) | Новые стероидные соединения, обладающие повышенной растворимостью в воде и устойчивостью к метаболизму, и способы их приготовления | |
| JP2010510210A5 (enExample) | ||
| JP2003531119A5 (enExample) | ||
| RU2002103883A (ru) | Перорально активные андрогены | |
| JP2010507685A5 (enExample) | ||
| SE463074B (sv) | Anvaendning av aromatashaemmare och antiandrogener foer framstaellning av laekemedel foer profylax och terapi av benign prostatahyperplasi | |
| JP2008512426A5 (enExample) | ||
| EP0863760B1 (fr) | Utilisation des composes antimineralocorticoides contre le syndrome de sevrage des narcotiques | |
| JP2009512658A5 (enExample) | ||
| JP2003515543A5 (enExample) | ||
| JP2008540482A5 (enExample) | ||
| JP2002539135A5 (enExample) | ||
| RU2002117440A (ru) | Новые андрогены | |
| KR960014152A (ko) | 17-스피로메틸렌 락톤 또는 락톨 그룹을 갖는 스테로이드 | |
| RU95118123A (ru) | Стероиды с 17-спирометилен-лактоновой или -лактольной группой | |
| JP2001524525A5 (enExample) | ||
| JP2002541153A5 (enExample) | ||
| KR910005873A (ko) | 항프로게스테론양 화합물의 신규 용도 | |
| JP2005509610A5 (enExample) | ||
| JP2003522795A5 (enExample) |