JP2014526469A5 - - Google Patents
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- JP2014526469A5 JP2014526469A5 JP2014529913A JP2014529913A JP2014526469A5 JP 2014526469 A5 JP2014526469 A5 JP 2014526469A5 JP 2014529913 A JP2014529913 A JP 2014529913A JP 2014529913 A JP2014529913 A JP 2014529913A JP 2014526469 A5 JP2014526469 A5 JP 2014526469A5
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- 150000001875 compounds Chemical class 0.000 claims description 86
- 229910052739 hydrogen Inorganic materials 0.000 claims description 38
- 239000001257 hydrogen Substances 0.000 claims description 38
- 125000000217 alkyl group Chemical group 0.000 claims description 26
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 25
- 150000003839 salts Chemical class 0.000 claims description 18
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 16
- 201000010099 disease Diseases 0.000 claims description 10
- 125000005843 halogen group Chemical group 0.000 claims description 10
- 150000002431 hydrogen Chemical class 0.000 claims description 10
- 239000008194 pharmaceutical composition Substances 0.000 claims description 10
- 125000005842 heteroatom Chemical group 0.000 claims description 9
- 208000030886 Traumatic Brain injury Diseases 0.000 claims description 8
- 230000009529 traumatic brain injury Effects 0.000 claims description 8
- 208000035475 disorder Diseases 0.000 claims description 6
- 125000002947 alkylene group Chemical group 0.000 claims description 5
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims description 4
- 208000021384 Obsessive-Compulsive disease Diseases 0.000 claims description 4
- 125000003342 alkenyl group Chemical group 0.000 claims description 4
- 125000000304 alkynyl group Chemical group 0.000 claims description 4
- 208000029560 autism spectrum disease Diseases 0.000 claims description 4
- ZPUCINDJVBIVPJ-LJISPDSOSA-N cocaine Chemical compound O([C@H]1C[C@@H]2CC[C@@H](N2C)[C@H]1C(=O)OC)C(=O)C1=CC=CC=C1 ZPUCINDJVBIVPJ-LJISPDSOSA-N 0.000 claims description 4
- 206010015037 epilepsy Diseases 0.000 claims description 4
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- 125000001072 heteroaryl group Chemical group 0.000 claims description 3
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- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 2
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- 206010012289 Dementia Diseases 0.000 claims description 2
- 208000027534 Emotional disease Diseases 0.000 claims description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 2
- 208000023105 Huntington disease Diseases 0.000 claims description 2
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- 206010041250 Social phobia Diseases 0.000 claims description 2
- 208000007271 Substance Withdrawal Syndrome Diseases 0.000 claims description 2
- 208000009205 Tinnitus Diseases 0.000 claims description 2
- 206010048010 Withdrawal syndrome Diseases 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000002837 carbocyclic group Chemical group 0.000 claims description 2
- 125000004452 carbocyclyl group Chemical group 0.000 claims description 2
- 229960003920 cocaine Drugs 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims description 2
- 208000024732 dysthymic disease Diseases 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical group 0.000 claims description 2
- 125000000623 heterocyclic group Chemical group 0.000 claims description 2
- 206010022437 insomnia Diseases 0.000 claims description 2
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- 125000000547 substituted alkyl group Chemical group 0.000 claims description 2
- 208000011580 syndromic disease Diseases 0.000 claims description 2
- 231100000886 tinnitus Toxicity 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 3
- 238000000034 method Methods 0.000 description 5
- 125000004450 alkenylene group Chemical group 0.000 description 4
- 125000004419 alkynylene group Chemical group 0.000 description 4
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- HBKQWULJDAALRY-NLIMMPQESA-N CC([C@@H](CC1)C(C)(CC2)C1C1C2[C@@H](CC[C@@H](C2)O)C2=CC1)C(CO)(F)F Chemical compound CC([C@@H](CC1)C(C)(CC2)C1C1C2[C@@H](CC[C@@H](C2)O)C2=CC1)C(CO)(F)F HBKQWULJDAALRY-NLIMMPQESA-N 0.000 description 1
- RVXHMRSBDNBDEY-UHFFFAOYSA-N CCOC(C(C)C)(F)F Chemical compound CCOC(C(C)C)(F)F RVXHMRSBDNBDEY-UHFFFAOYSA-N 0.000 description 1
- VOXRDLZRMKBAFE-UHFFFAOYSA-N CCO[IH][IH]CC(C)OCC(C)(F)F Chemical compound CCO[IH][IH]CC(C)OCC(C)(F)F VOXRDLZRMKBAFE-UHFFFAOYSA-N 0.000 description 1
- UIIQWGBQZPMASR-UHFFFAOYSA-N COCC(F)(F)I Chemical compound COCC(F)(F)I UIIQWGBQZPMASR-UHFFFAOYSA-N 0.000 description 1
- ZOOUPKHXFIPMMF-DYNRJKDWSA-N C[C@@H]([C@@H](CC1)[C@@](C)(CC2)C1C1C2[C@@](C)(CC[C@@](C)(C2)O)C2=CC1)OC(c1ccccc1)=O Chemical compound C[C@@H]([C@@H](CC1)[C@@](C)(CC2)C1C1C2[C@@](C)(CC[C@@](C)(C2)O)C2=CC1)OC(c1ccccc1)=O ZOOUPKHXFIPMMF-DYNRJKDWSA-N 0.000 description 1
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- BJHUPERNCXCFTH-JFBOSTTDSA-N C[C@H](CCC(C)(C)O)[C@@H](CC1)[C@@](C)(CC2)C1C1C2[C@@H](CCC(C2)=O)C2=CC1 Chemical compound C[C@H](CCC(C)(C)O)[C@@H](CC1)[C@@](C)(CC2)C1C1C2[C@@H](CCC(C2)=O)C2=CC1 BJHUPERNCXCFTH-JFBOSTTDSA-N 0.000 description 1
- LLAUXVXYDZUXBL-VKHMYHEASA-N C[C@H](OC(C)(F)F)I Chemical compound C[C@H](OC(C)(F)F)I LLAUXVXYDZUXBL-VKHMYHEASA-N 0.000 description 1
- ZOOUPKHXFIPMMF-HZKWPTRHSA-N C[C@H]([C@@H](CC1)[C@@](C)(CC2)C1C1C2[C@@](C)(CC[C@@](C)(C2)O)C2=CC1)OC(c1ccccc1)=O Chemical compound C[C@H]([C@@H](CC1)[C@@](C)(CC2)C1C1C2[C@@](C)(CC[C@@](C)(C2)O)C2=CC1)OC(c1ccccc1)=O ZOOUPKHXFIPMMF-HZKWPTRHSA-N 0.000 description 1
- ZZLABZROPODDLV-DNCNGORPSA-N C[C@](CC1)(C(CC2)C3C1[C@@](C)(CC[C@@](C)(C1)O)C1=CC3)[C@H]2OCC(C(F)(F)F)=O Chemical compound C[C@](CC1)(C(CC2)C3C1[C@@](C)(CC[C@@](C)(C1)O)C1=CC3)[C@H]2OCC(C(F)(F)F)=O ZZLABZROPODDLV-DNCNGORPSA-N 0.000 description 1
- JLWWULDDVJQPID-HHZWQIATSA-N C[C@](CC1)(C(CC2)C3C1[C@@](C)(CC[C@@](C)(C1)O)C1=CC3)[C@H]2OCCC(C(F)(F)F)=O Chemical compound C[C@](CC1)(C(CC2)C3C1[C@@](C)(CC[C@@](C)(C1)O)C1=CC3)[C@H]2OCCC(C(F)(F)F)=O JLWWULDDVJQPID-HHZWQIATSA-N 0.000 description 1
- 206010012335 Dependence Diseases 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161532427P | 2011-09-08 | 2011-09-08 | |
| US61/532,427 | 2011-09-08 | ||
| PCT/US2012/054261 WO2013036835A1 (en) | 2011-09-08 | 2012-09-07 | Neuroactive steroids, compositions, and uses thereof |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017169737A Division JP2018021059A (ja) | 2011-09-08 | 2017-09-04 | 神経刺激性のステロイド、組成物、およびそれらの使用 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2014526469A JP2014526469A (ja) | 2014-10-06 |
| JP2014526469A5 true JP2014526469A5 (enExample) | 2015-10-29 |
| JP6205362B2 JP6205362B2 (ja) | 2017-09-27 |
Family
ID=46964032
Family Applications (6)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014529913A Active JP6205362B2 (ja) | 2011-09-08 | 2012-09-07 | 神経刺激性のステロイド、組成物、およびそれらの使用 |
| JP2017169737A Withdrawn JP2018021059A (ja) | 2011-09-08 | 2017-09-04 | 神経刺激性のステロイド、組成物、およびそれらの使用 |
| JP2019011169A Active JP6777773B2 (ja) | 2011-09-08 | 2019-01-25 | 神経刺激性のステロイド、組成物、およびそれらの使用 |
| JP2020170611A Withdrawn JP2021008504A (ja) | 2011-09-08 | 2020-10-08 | 神経刺激性のステロイド、組成物、およびそれらの使用 |
| JP2023001738A Active JP7786665B2 (ja) | 2011-09-08 | 2023-01-10 | 神経刺激性のステロイド、組成物、およびそれらの使用 |
| JP2025064398A Pending JP2025108535A (ja) | 2011-09-08 | 2025-04-09 | 神経刺激性のステロイド、組成物、およびそれらの使用 |
Family Applications After (5)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017169737A Withdrawn JP2018021059A (ja) | 2011-09-08 | 2017-09-04 | 神経刺激性のステロイド、組成物、およびそれらの使用 |
| JP2019011169A Active JP6777773B2 (ja) | 2011-09-08 | 2019-01-25 | 神経刺激性のステロイド、組成物、およびそれらの使用 |
| JP2020170611A Withdrawn JP2021008504A (ja) | 2011-09-08 | 2020-10-08 | 神経刺激性のステロイド、組成物、およびそれらの使用 |
| JP2023001738A Active JP7786665B2 (ja) | 2011-09-08 | 2023-01-10 | 神経刺激性のステロイド、組成物、およびそれらの使用 |
| JP2025064398A Pending JP2025108535A (ja) | 2011-09-08 | 2025-04-09 | 神経刺激性のステロイド、組成物、およびそれらの使用 |
Country Status (20)
| Country | Link |
|---|---|
| US (5) | US20150158903A1 (enExample) |
| EP (2) | EP2753632B1 (enExample) |
| JP (6) | JP6205362B2 (enExample) |
| CN (4) | CN107936076B (enExample) |
| AU (6) | AU2012304412A1 (enExample) |
| BR (1) | BR112014005373B1 (enExample) |
| CA (1) | CA2848212C (enExample) |
| DK (1) | DK2753632T3 (enExample) |
| ES (1) | ES2951664T3 (enExample) |
| FI (1) | FI2753632T3 (enExample) |
| HR (1) | HRP20230747T1 (enExample) |
| HU (1) | HUE062616T2 (enExample) |
| LT (1) | LT2753632T (enExample) |
| PL (1) | PL2753632T3 (enExample) |
| PT (1) | PT2753632T (enExample) |
| RS (1) | RS64332B1 (enExample) |
| RU (1) | RU2665571C2 (enExample) |
| SI (1) | SI2753632T1 (enExample) |
| SM (1) | SMT202300232T1 (enExample) |
| WO (1) | WO2013036835A1 (enExample) |
Families Citing this family (80)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006047022A1 (en) | 2004-10-25 | 2006-05-04 | Virginia Commonwealth University | Nuclear sulfated oxysterol, potent regulator of cholesterol homeostasis, for therapy of hypercholesterolemia, hyperlipidemia, and atherosclerosis |
| KR20120107533A (ko) | 2005-11-28 | 2012-10-02 | 마리누스 파마슈티컬스 | ganaxolone 제형, 이의 제조방법 및 용도 |
| US9034859B2 (en) | 2011-04-06 | 2015-05-19 | Virginia Commonwealth University | Sulfated oxysterol and oxysterol sulfation by hydroxysterol sulfotransferase promote lipid homeostasis and liver proliferation |
| CN107936076B (zh) * | 2011-09-08 | 2021-10-15 | 萨奇治疗股份有限公司 | 神经活性类固醇、组合物、及其用途 |
| US10478505B2 (en) | 2011-09-23 | 2019-11-19 | The Regents Of The University Of California | Edible oils to enhance delivery of orally administered steroids |
| AU2012323888A1 (en) | 2011-10-14 | 2014-05-29 | Sage Therapeutics, Inc. | 3,3 disubstituted 19-nor pregnane compounds, compositions, and uses thereof |
| HRP20192348T1 (hr) | 2012-01-23 | 2020-03-20 | Sage Therapeutics, Inc. | Formulacije neuroaktivnog steroida koje uključuju kompleks alopregnanolona i sulfobutil eter beta-ciklodekstrina |
| WO2014028398A2 (en) | 2012-08-13 | 2014-02-20 | The Regents Of The University Of California | Mitigation of epileptic seizures by combination therapy using benzodiazepines and neurosteroids |
| KR102121633B1 (ko) | 2012-08-21 | 2020-06-10 | 세이지 테라퓨틱스, 인크. | 간질 또는 간질지속 상태를 치료하는 방법 |
| DK2925327T3 (da) | 2012-11-30 | 2024-03-25 | Univ California | Allopregnanolon til behandling, reduktion eller lindring af symptomer på fødselsdepression |
| ES2699445T3 (es) | 2013-03-13 | 2019-02-11 | Sage Therapeutics Inc | Esteroides neuroactivos y métodos de utilización de los mismos |
| RU2015143463A (ru) * | 2013-03-13 | 2017-04-19 | Сейдж Терапьютикс, Инк. | Нейроактивные стероиды, композиции и их применение |
| US20160068563A1 (en) | 2013-04-17 | 2016-03-10 | Boyd L. Harrison | 19-nor neuroactive steroids and methods of use thereof |
| EP2986623B1 (en) * | 2013-04-17 | 2018-11-07 | Sage Therapeutics, Inc. | 19-nor c3,3-disubstituted c21-n-pyrazolyl steroids and methods of use thereof |
| HUE051403T2 (hu) | 2013-04-17 | 2021-03-01 | Sage Therapeutics Inc | Neuroaktív 19-nor-szteroidok kezelési eljárásokhoz |
| WO2014169831A1 (en) * | 2013-04-17 | 2014-10-23 | Sage Therapeutics, Inc. | 19-nor c3,3-disubstituted c21-c-bound heteroaryl steroids and methods of use thereof |
| CN103333216A (zh) * | 2013-06-04 | 2013-10-02 | 苏州大学 | 5α-6-酮-胆甾烷类似物及其应用 |
| LT3021852T (lt) | 2013-07-19 | 2021-04-12 | Sage Therapeutics, Inc. | Neuroaktyvūs steroidai, jų kompozicijos ir panaudojimas |
| EP3035940B1 (en) | 2013-08-23 | 2018-10-17 | Sage Therapeutics, Inc. | Neuroactive steroids, compositions, and uses thereof |
| ES2922501T3 (es) | 2013-12-24 | 2022-09-15 | Univ Virginia Commonwealth | Uso de sulfatos de colesterol oxigenados (OCS) para el tratamiento de disfunción renal |
| EP3157528B1 (en) * | 2014-06-18 | 2023-09-13 | Sage Therapeutics, Inc. | Oxysterols and methods of use thereof |
| US10246482B2 (en) | 2014-06-18 | 2019-04-02 | Sage Therapeutics, Inc. | Neuroactive steroids, compositions, and uses thereof |
| JOP20200195A1 (ar) | 2014-09-08 | 2017-06-16 | Sage Therapeutics Inc | سترويدات وتركيبات نشطة عصبياً، واستخداماتها |
| MY202135A (en) * | 2014-10-07 | 2024-04-05 | Sage Therapeutics Inc | Uses of neuroactive compounds |
| CN112961206A (zh) | 2014-10-16 | 2021-06-15 | 萨奇治疗股份有限公司 | 靶向cns障碍的组合物和方法 |
| EP3206493B1 (en) | 2014-10-16 | 2020-05-06 | Sage Therapeutics, Inc. | Compositions and methods for treating cns disorders |
| HUE049014T2 (hu) | 2014-11-27 | 2020-09-28 | Sage Therapeutics Inc | Készítmények és módszerek a központi idegrendszer rendellenességeinek kezelésére |
| ES2857082T3 (es) | 2015-01-26 | 2021-09-28 | Sage Therapeutics Inc | Composiciones y métodos para el tratamiento de trastornos del SNC |
| US10329320B2 (en) | 2015-02-20 | 2019-06-25 | Sage Therapeutics, Inc. | Neuroactive steroids, compositions, and uses thereof |
| HK1255500A1 (zh) | 2015-07-06 | 2019-08-16 | Sage Therapeutics, Inc. | 氧固醇及其使用方法 |
| KR20240137111A (ko) * | 2015-07-06 | 2024-09-19 | 세이지 테라퓨틱스, 인크. | 옥시스테롤 및 그의 사용 방법 |
| US11117924B2 (en) | 2015-07-06 | 2021-09-14 | Sage Therapeutics, Inc. | Oxysterols and methods of use thereof |
| BR112018001869A2 (pt) * | 2015-07-30 | 2018-09-18 | Intercept Pharmaceuticals Inc | método para preparação de ácidos biliares e derivados dos mesmos |
| AU2016324310B2 (en) | 2015-09-17 | 2021-04-08 | Modernatx, Inc. | Compounds and compositions for intracellular delivery of therapeutic agents |
| EP3362042A1 (en) | 2015-10-16 | 2018-08-22 | Marinus Pharmaceuticals, Inc. | Injectable neurosteroid formulations containing nanoparticles |
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