JP2002544137A5 - - Google Patents
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- Publication number
- JP2002544137A5 JP2002544137A5 JP2000616220A JP2000616220A JP2002544137A5 JP 2002544137 A5 JP2002544137 A5 JP 2002544137A5 JP 2000616220 A JP2000616220 A JP 2000616220A JP 2000616220 A JP2000616220 A JP 2000616220A JP 2002544137 A5 JP2002544137 A5 JP 2002544137A5
- Authority
- JP
- Japan
- Prior art keywords
- cholesta
- group
- hydroxy
- tetraene
- homo
- 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.)
- Pending
Links
- 150000001875 compounds Chemical class 0.000 description 18
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 8
- 125000000217 alkyl group Chemical group 0.000 description 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 4
- 125000002252 acyl group Chemical group 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- -1 amino, nitro, carbamoyl Chemical group 0.000 description 4
- 125000000962 organic group Chemical group 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 3
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 125000000304 alkynyl group Chemical group 0.000 description 2
- 125000003435 aroyl group Chemical group 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 125000002861 (C1-C4) alkanoyl group Chemical group 0.000 description 1
- LSBDFXRDZJMBSC-UHFFFAOYSA-N 2-phenylacetamide Chemical group NC(=O)CC1=CC=CC=C1 LSBDFXRDZJMBSC-UHFFFAOYSA-N 0.000 description 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
- 208000023275 Autoimmune disease Diseases 0.000 description 1
- 208000020084 Bone disease Diseases 0.000 description 1
- KCDROUKZZKVJRE-UHFFFAOYSA-N CCNC1=C(C(=CC(=C1NC)N)C(=O)N(CC)NC)NC(=O)C Chemical group CCNC1=C(C(=CC(=C1NC)N)C(=O)N(CC)NC)NC(=O)C KCDROUKZZKVJRE-UHFFFAOYSA-N 0.000 description 1
- 208000028698 Cognitive impairment Diseases 0.000 description 1
- 206010012289 Dementia Diseases 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 206010020772 Hypertension Diseases 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 208000021642 Muscular disease Diseases 0.000 description 1
- 201000009623 Myopathy Diseases 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 102000003982 Parathyroid hormone Human genes 0.000 description 1
- 108090000445 Parathyroid hormone Proteins 0.000 description 1
- 201000001263 Psoriatic Arthritis Diseases 0.000 description 1
- 208000036824 Psoriatic arthropathy Diseases 0.000 description 1
- 208000005770 Secondary Hyperparathyroidism Diseases 0.000 description 1
- 201000002661 Spondylitis Diseases 0.000 description 1
- 206010052779 Transplant rejections Diseases 0.000 description 1
- 125000004450 alkenylene group Chemical group 0.000 description 1
- 125000003282 alkyl amino group Chemical group 0.000 description 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 125000004419 alkynylene group Chemical group 0.000 description 1
- 208000006673 asthma Diseases 0.000 description 1
- 230000023555 blood coagulation Effects 0.000 description 1
- 125000002837 carbocyclic group Chemical group 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 208000010877 cognitive disease Diseases 0.000 description 1
- 150000004292 cyclic ethers Chemical group 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 208000037902 enteropathy Diseases 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000004720 fertilization Effects 0.000 description 1
- 208000019622 heart disease Diseases 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 206010020718 hyperplasia Diseases 0.000 description 1
- 208000027866 inflammatory disease Diseases 0.000 description 1
- 208000028774 intestinal disease Diseases 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000009826 neoplastic cell growth Effects 0.000 description 1
- 230000001613 neoplastic effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 239000000199 parathyroid hormone Substances 0.000 description 1
- 229960001319 parathyroid hormone Drugs 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 206010039073 rheumatoid arthritis Diseases 0.000 description 1
- 230000001568 sexual effect Effects 0.000 description 1
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 1
- 208000017520 skin disease Diseases 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 230000029663 wound healing Effects 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB9910934.0A GB9910934D0 (en) | 1999-05-11 | 1999-05-11 | Chemical compounds |
| GB9910934.0 | 1999-05-11 | ||
| PCT/GB2000/001813 WO2000068246A1 (en) | 1999-05-11 | 2000-05-11 | Steroid compounds with a c17-alkyl side chain and an aromatic a-ring for use in therapy |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2002544137A JP2002544137A (ja) | 2002-12-24 |
| JP2002544137A5 true JP2002544137A5 (enExample) | 2007-06-21 |
Family
ID=10853250
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000616220A Pending JP2002544137A (ja) | 1999-05-11 | 2000-05-11 | Ｃ１７アルキル側鎖および芳香族ａ環をもつ治療に使用するステロイド化合物 |
Country Status (21)
| Country | Link |
|---|---|
| US (2) | US6881730B1 (enExample) |
| EP (1) | EP1179005B1 (enExample) |
| JP (1) | JP2002544137A (enExample) |
| KR (1) | KR100690040B1 (enExample) |
| CN (1) | CN1158297C (enExample) |
| AT (1) | ATE254629T1 (enExample) |
| AU (1) | AU779743B2 (enExample) |
| CA (1) | CA2373443A1 (enExample) |
| CZ (1) | CZ297316B6 (enExample) |
| DE (1) | DE60006665T2 (enExample) |
| DK (1) | DK1179005T3 (enExample) |
| ES (1) | ES2207509T3 (enExample) |
| GB (1) | GB9910934D0 (enExample) |
| HK (1) | HK1046001B (enExample) |
| HU (1) | HUP0201047A3 (enExample) |
| IL (2) | IL146442A0 (enExample) |
| NO (1) | NO319949B1 (enExample) |
| NZ (1) | NZ515482A (enExample) |
| PT (1) | PT1179005E (enExample) |
| WO (1) | WO2000068246A1 (enExample) |
| ZA (1) | ZA200109272B (enExample) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6908910B2 (en) | 1993-08-06 | 2005-06-21 | The Children's Medical Center Corporation | Estrogenic compounds as anti-mitotic agents |
| GB9910934D0 (en) * | 1999-05-11 | 1999-07-14 | Res Inst Medicine Chem | Chemical compounds |
| US7087592B1 (en) | 1999-08-23 | 2006-08-08 | Entre Med, Inc. | Compositions comprising purified 2-methoxyestradiol and methods of producing same |
| NZ523042A (en) * | 2000-05-11 | 2004-05-28 | Res Inst Medicine Chem | 2-substituted pregna-1, 3, 5 (10) -triene and chola-1, 3, 5 (10)-triene derivatives and their biological activity |
| US6995278B2 (en) | 2000-08-18 | 2006-02-07 | Entre Med, Inc. | Antiangiogenic agents |
| US7135581B2 (en) | 2000-08-18 | 2006-11-14 | Entremed, Inc. | Antiangiogenic agents |
| JP2004537499A (ja) * | 2000-11-27 | 2004-12-16 | エントレメッド インコーポレイテッド | 抗血管新生薬 |
| WO2002092100A1 (en) * | 2001-05-11 | 2002-11-21 | Marsden, John, Christopher | 17-(c(ch3) (ch2) o-3c (r4, r5) n (r6, r7))-substituted 19-nor-pregna-1, 3, 5(10)-triene derivatives and their medical use |
| AU2004275693A1 (en) | 2003-05-28 | 2005-04-07 | Entremed, Inc. | Antiangiogenic agents |
| JP2007529426A (ja) | 2004-03-12 | 2007-10-25 | エントレメッド インコーポレイテッド | 抗血管新生薬 |
| CA2646065C (en) | 2006-03-20 | 2014-01-14 | Entremed, Inc. | Disease modifying anti-arthritic activity of 2-methoxyestradiol |
| NZ581081A (en) * | 2007-06-19 | 2012-12-21 | Kythera Biopharmaceuticals Inc | Synthetic deoxycholic acid (dca) or an ester, hydroxamale, or hydroxyamide thereof |
| US8242294B2 (en) | 2007-06-19 | 2012-08-14 | Kythera Biopharmaceuticals, Inc. | Synthetic bile acid compositions and methods |
| JOP20180077A1 (ar) | 2007-06-19 | 2019-01-30 | Kythera Biopharmaceuticals Inc | تركيبات وطرق لحمض صفراوي تخليقي |
| US20080318870A1 (en) | 2007-06-19 | 2008-12-25 | Kythera Biopharmaceuticals, Inc. | Synthetic bile acid compositions and methods |
| WO2013036835A1 (en) * | 2011-09-08 | 2013-03-14 | Sage Therapeutics, Inc. | Neuroactive steroids, compositions, and uses thereof |
| RS67266B1 (sr) | 2013-03-13 | 2025-10-31 | Sage Therapeutics Inc | Neuroaktivni steroidi i postupci za njihovu upotrebu |
| WO2015195967A1 (en) | 2014-06-18 | 2015-12-23 | Sage Therapeutics, Inc. | Oxysterols and methods of use thereof |
| BR112018000129B1 (pt) | 2015-07-06 | 2024-01-09 | Sage Therapeutics, Inc | Compostos oxiesteróis, seus usos e composição farmacêutica |
| SMT202100476T1 (it) | 2015-07-06 | 2021-09-14 | Sage Therapeutics Inc | Ossisteroli e metodi di uso degli stessi |
| JP6882996B2 (ja) | 2015-07-06 | 2021-06-02 | セージ セラピューティクス， インコーポレイテッド | オキシステロールおよびそれらの使用の方法 |
| SI3436022T1 (sl) | 2016-04-01 | 2022-08-31 | Sage Therapeutics, Inc. | Oksisteroli in postopki za uporabo le-teh |
| WO2017193046A1 (en) | 2016-05-06 | 2017-11-09 | Sage Therapeutics, Inc. | Oxysterols and methods of use thereof |
| ES2884071T3 (es) | 2016-07-07 | 2021-12-10 | Sage Therapeutics Inc | 24-hidroxiesteroles sustituidos en 11 para el tratamiento de afecciones relacionadas con NMDA |
| MX392270B (es) | 2016-09-30 | 2025-03-24 | Sage Therapeutics Inc | Oxisteroles sustituidos en c7 y metodos de uso de los mismos. |
| EP4105223B1 (en) | 2016-10-18 | 2025-04-30 | Sage Therapeutics, Inc. | Oxysterols and methods of use thereof |
| CN110267966B (zh) | 2016-10-18 | 2022-07-08 | 萨奇治疗股份有限公司 | 氧甾醇及其使用方法 |
| CN115040524A (zh) * | 2022-07-27 | 2022-09-13 | 深圳市中西医结合医院 | 4-胆甾烯-3-酮用于治疗多发性骨髓瘤骨病的应用 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3562260A (en) * | 1965-08-23 | 1971-02-09 | Ormonoterapia Richter Spa | 2-carbonyl-estratrienes and method of their preparation |
| GB1267915A (en) * | 1968-05-24 | 1972-03-22 | Glaxo Lab Ltd | Ring a-substituted ring a-aromatic steroids |
| FR2528434B1 (fr) * | 1982-06-11 | 1985-07-19 | Roussel Uclaf | Nouveaux 19-nor steroides substitues en 11b et eventuellement en 2, leur procede de preparation et leur application comme medicament |
| JP2623285B2 (ja) * | 1988-03-09 | 1997-06-25 | 雪印乳業株式会社 | ２（３―ハイドロキシ―１，３，５（１０）―エストリエン―１７―イル）プロピオン酸の製造法 |
| GB9910934D0 (en) * | 1999-05-11 | 1999-07-14 | Res Inst Medicine Chem | Chemical compounds |
| US6967195B2 (en) * | 2000-05-11 | 2005-11-22 | Research Institute For Medicine And Chemistry, Inc. | 2-substituted pregna-1-3,5(10) triene and chola-1,3,5(10) triene derivatives and their biological activity |
-
1999
- 1999-05-11 GB GBGB9910934.0A patent/GB9910934D0/en not_active Ceased
-
2000
- 2000-05-11 CN CNB008095175A patent/CN1158297C/zh not_active Expired - Fee Related
- 2000-05-11 HU HU0201047A patent/HUP0201047A3/hu unknown
- 2000-05-11 DE DE60006665T patent/DE60006665T2/de not_active Expired - Fee Related
- 2000-05-11 NZ NZ515482A patent/NZ515482A/en unknown
- 2000-05-11 ES ES00927569T patent/ES2207509T3/es not_active Expired - Lifetime
- 2000-05-11 CA CA002373443A patent/CA2373443A1/en not_active Abandoned
- 2000-05-11 AU AU45960/00A patent/AU779743B2/en not_active Ceased
- 2000-05-11 EP EP00927569A patent/EP1179005B1/en not_active Expired - Lifetime
- 2000-05-11 CZ CZ20014049A patent/CZ297316B6/cs not_active IP Right Cessation
- 2000-05-11 WO PCT/GB2000/001813 patent/WO2000068246A1/en not_active Ceased
- 2000-05-11 AT AT00927569T patent/ATE254629T1/de not_active IP Right Cessation
- 2000-05-11 KR KR1020017014382A patent/KR100690040B1/ko not_active Expired - Fee Related
- 2000-05-11 PT PT00927569T patent/PT1179005E/pt unknown
- 2000-05-11 JP JP2000616220A patent/JP2002544137A/ja active Pending
- 2000-05-11 IL IL14644200A patent/IL146442A0/xx active IP Right Grant
- 2000-05-11 HK HK02105910.4A patent/HK1046001B/en not_active IP Right Cessation
- 2000-05-11 DK DK00927569T patent/DK1179005T3/da active
-
2001
- 2001-11-09 ZA ZA200109272A patent/ZA200109272B/xx unknown
- 2001-11-11 IL IL146442A patent/IL146442A/en not_active IP Right Cessation
- 2001-11-12 NO NO20015520A patent/NO319949B1/no not_active IP Right Cessation
-
2003
- 2003-05-11 US US09/926,491 patent/US6881730B1/en not_active Expired - Fee Related
-
2005
- 2005-02-11 US US11/055,620 patent/US20050171075A1/en not_active Abandoned
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