JP2004532854A - 複素2環式fkbpリガンド - Google Patents
複素2環式fkbpリガンド Download PDFInfo
- Publication number
- JP2004532854A JP2004532854A JP2002586941A JP2002586941A JP2004532854A JP 2004532854 A JP2004532854 A JP 2004532854A JP 2002586941 A JP2002586941 A JP 2002586941A JP 2002586941 A JP2002586941 A JP 2002586941A JP 2004532854 A JP2004532854 A JP 2004532854A
- Authority
- JP
- Japan
- Prior art keywords
- compound
- mmol
- pharmaceutically acceptable
- found
- acceptable salt
- 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.)
- Abandoned
Links
- 0 C[C@@](Cc1c([C@@]2[C@@](C3)N4C3(*)CC[C@]43)cccc1)N2C3=O Chemical compound C[C@@](Cc1c([C@@]2[C@@](C3)N4C3(*)CC[C@]43)cccc1)N2C3=O 0.000 description 15
- HVRKZQJSFZCVOF-UHFFFAOYSA-N CC(C(CCCCC1)OCC23)=C(Cc4ccccn4)N2C1C(c1cccc(OC)c1CC1)N1C3=O Chemical compound CC(C(CCCCC1)OCC23)=C(Cc4ccccn4)N2C1C(c1cccc(OC)c1CC1)N1C3=O HVRKZQJSFZCVOF-UHFFFAOYSA-N 0.000 description 1
- OZCQFWUWBBZYAS-UHFFFAOYSA-N CC(C)(C)NC(N(C(CCC1)C2N3CCc4c2ccc(OC)c4)C1C3=O)=O Chemical compound CC(C)(C)NC(N(C(CCC1)C2N3CCc4c2ccc(OC)c4)C1C3=O)=O OZCQFWUWBBZYAS-UHFFFAOYSA-N 0.000 description 1
- JLPQUZSABGZAGB-UHFFFAOYSA-N CC(C)(C)c(cc1)ccc1S(N(C(CCC1)C2N3CCc4c2c(OC)cc(OC)c4)C1C3=O)(=O)=O Chemical compound CC(C)(C)c(cc1)ccc1S(N(C(CCC1)C2N3CCc4c2c(OC)cc(OC)c4)C1C3=O)(=O)=O JLPQUZSABGZAGB-UHFFFAOYSA-N 0.000 description 1
- GEFCMRYXLACVOF-UHFFFAOYSA-N CCNC(N(C(CCC1)C2N3CCc4c2cccc4OC)C1C3=O)=O Chemical compound CCNC(N(C(CCC1)C2N3CCc4c2cccc4OC)C1C3=O)=O GEFCMRYXLACVOF-UHFFFAOYSA-N 0.000 description 1
- HOVNKSUNKPSVPK-UHFFFAOYSA-N COc1cc(CCN(C2C(CCCC34)N3C(Cc(cc3Cl)ccc3Cl)=O)C4=O)c2c(OC)c1 Chemical compound COc1cc(CCN(C2C(CCCC34)N3C(Cc(cc3Cl)ccc3Cl)=O)C4=O)c2c(OC)c1 HOVNKSUNKPSVPK-UHFFFAOYSA-N 0.000 description 1
- GIXFPXROQMRZBA-UHFFFAOYSA-N COc1cc(CCN(C2C(CCCC34)N3C(c(ccc(Cl)c3)c3Cl)=O)C4=O)c2c(OC)c1 Chemical compound COc1cc(CCN(C2C(CCCC34)N3C(c(ccc(Cl)c3)c3Cl)=O)C4=O)c2c(OC)c1 GIXFPXROQMRZBA-UHFFFAOYSA-N 0.000 description 1
- DOJFLMJBDYXAJO-UHFFFAOYSA-N COc1cc(CCN(C2C(CCCC34)N3S(Cl)(=O)=O)C4=O)c2cc1 Chemical compound COc1cc(CCN(C2C(CCCC34)N3S(Cl)(=O)=O)C4=O)c2cc1 DOJFLMJBDYXAJO-UHFFFAOYSA-N 0.000 description 1
- RNRLITQZDJWKFW-UHFFFAOYSA-N COc1cc(CCN(C2C(CCCC34)N3SNc(cc3OC)cc(OC)c3OC)C4=O)c2cc1 Chemical compound COc1cc(CCN(C2C(CCCC34)N3SNc(cc3OC)cc(OC)c3OC)C4=O)c2cc1 RNRLITQZDJWKFW-UHFFFAOYSA-N 0.000 description 1
- NJCPLCNRNUTEHA-UHFFFAOYSA-N COc1cc(CON(C2C3NC4CCC3)C4=O)c2cc1 Chemical compound COc1cc(CON(C2C3NC4CCC3)C4=O)c2cc1 NJCPLCNRNUTEHA-UHFFFAOYSA-N 0.000 description 1
- VQSVNUICNDHWEW-UHFFFAOYSA-N COc1cc(N(CC2)CCN2C(C(N(CC2CC3)CC3(c(cc3)c(CC4)cc3OC)N4C2=O)=O)=O)ccc1 Chemical compound COc1cc(N(CC2)CCN2C(C(N(CC2CC3)CC3(c(cc3)c(CC4)cc3OC)N4C2=O)=O)=O)ccc1 VQSVNUICNDHWEW-UHFFFAOYSA-N 0.000 description 1
- NSHZAVKHMIWWFO-UHFFFAOYSA-O COc1cccc(C2C(CCCC34)N3C(Nc(cc3)ccc3[N+](O)=O)=O)c1CCN2C4=O Chemical compound COc1cccc(C2C(CCCC34)N3C(Nc(cc3)ccc3[N+](O)=O)=O)c1CCN2C4=O NSHZAVKHMIWWFO-UHFFFAOYSA-O 0.000 description 1
- QDVRPEUQLXECOX-QQMFLWPESA-N C[C@@H](Cc1c([C@@H]2[C@@H](C3)N([C@H]4CC5)C35S(c(cc3)ccc3Oc3ccncc3)(=O)=O)cccc1)N2C4=O Chemical compound C[C@@H](Cc1c([C@@H]2[C@@H](C3)N([C@H]4CC5)C35S(c(cc3)ccc3Oc3ccncc3)(=O)=O)cccc1)N2C4=O QDVRPEUQLXECOX-QQMFLWPESA-N 0.000 description 1
- SIHLLLMQPYFXJF-OADPDTJPSA-N C[C@@H](Cc1c([C@@H]2[C@@H]3N[C@H]4CCC3)cccc1)N2C4=O Chemical compound C[C@@H](Cc1c([C@@H]2[C@@H]3N[C@H]4CCC3)cccc1)N2C4=O SIHLLLMQPYFXJF-OADPDTJPSA-N 0.000 description 1
- VBEWDGCWKFTBLH-UHFFFAOYSA-N C[NH+]([NH+]([O-])OC)[O-] Chemical compound C[NH+]([NH+]([O-])OC)[O-] VBEWDGCWKFTBLH-UHFFFAOYSA-N 0.000 description 1
- MWOXUWAIZBDNFI-UHFFFAOYSA-N Cc(cc1)ccc1NC(N(CC1(CCC2)N3CCc4c1ccc(OC)c4)C2C3=O)=O Chemical compound Cc(cc1)ccc1NC(N(CC1(CCC2)N3CCc4c1ccc(OC)c4)C2C3=O)=O MWOXUWAIZBDNFI-UHFFFAOYSA-N 0.000 description 1
- AQHBHTILUWPTBG-UHFFFAOYSA-N Cc1cc(C(C2NCC3CC2)N(CC2)C3=O)c2cc1 Chemical compound Cc1cc(C(C2NCC3CC2)N(CC2)C3=O)c2cc1 AQHBHTILUWPTBG-UHFFFAOYSA-N 0.000 description 1
- QUAKRCBKUVIWEZ-UHFFFAOYSA-N Cc1cc(S(N(C(CCC2)C3N4CCc5c3cc(C)cc5)C2C4=O)(=O)=O)ccc1 Chemical compound Cc1cc(S(N(C(CCC2)C3N4CCc5c3cc(C)cc5)C2C4=O)(=O)=O)ccc1 QUAKRCBKUVIWEZ-UHFFFAOYSA-N 0.000 description 1
- PJUBIPBBMMPWRN-UHFFFAOYSA-N O=C(C1NC2CCC1)N(CC1)C2c2c1ccc(F)c2 Chemical compound O=C(C1NC2CCC1)N(CC1)C2c2c1ccc(F)c2 PJUBIPBBMMPWRN-UHFFFAOYSA-N 0.000 description 1
- HMHWQHGKOIYUMI-UQOMOVTASA-N O=C([C@H]1NC2CCC1)N([C@H](C1)[U])[C@@H]2c2c1cccc2 Chemical compound O=C([C@H]1NC2CCC1)N([C@H](C1)[U])[C@@H]2c2c1cccc2 HMHWQHGKOIYUMI-UQOMOVTASA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/08—Bridged systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/14—Drugs for dermatological disorders for baldness or alopecia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
- A61P21/02—Muscle relaxants, e.g. for tetanus or cramps
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/16—Otologicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/52—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing halogen
- C07C57/58—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing halogen containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/40—Unsaturated compounds
- C07C59/58—Unsaturated compounds containing ether groups, groups, groups, or groups
- C07C59/64—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Vascular Medicine (AREA)
- Psychology (AREA)
- Urology & Nephrology (AREA)
- Hospice & Palliative Care (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Psychiatry (AREA)
- Ophthalmology & Optometry (AREA)
- Pain & Pain Management (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US28982801P | 2001-05-10 | 2001-05-10 | |
| PCT/US2002/014966 WO2002089806A1 (en) | 2001-05-10 | 2002-05-10 | Heterobicycles fkbp-ligands |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2004532854A true JP2004532854A (ja) | 2004-10-28 |
| JP2004532854A5 JP2004532854A5 (https=) | 2005-12-22 |
Family
ID=23113278
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002586941A Abandoned JP2004532854A (ja) | 2001-05-10 | 2002-05-10 | 複素2環式fkbpリガンド |
Country Status (6)
| Country | Link |
|---|---|
| EP (1) | EP1423119A4 (https=) |
| JP (1) | JP2004532854A (https=) |
| BR (1) | BR0210060A (https=) |
| CA (1) | CA2446795A1 (https=) |
| MX (1) | MXPA03010255A (https=) |
| WO (1) | WO2002089806A1 (https=) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009506988A (ja) * | 2005-08-19 | 2009-02-19 | エラン ファーマシューティカルズ,インコーポレイテッド | ガンマセクレターゼの架橋n−環状スルホンアミド阻害剤 |
| JP2017523990A (ja) * | 2014-08-27 | 2017-08-24 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | Cns障害を処置するための置換ピラジノ[2,1−a]イソキノリン誘導体 |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2690102A1 (en) | 2012-07-24 | 2014-01-29 | Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. | Bicyclic aza-amides for treatment of psychiatric disorders |
| EP2899192A1 (en) * | 2014-01-24 | 2015-07-29 | Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. | Diazabicyclo[4.3.1]decane derivatives for treatment of psychiatric disorders |
| WO2015110271A1 (en) * | 2014-01-24 | 2015-07-30 | MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. | Diazabicyclo[4.3.1]decane derivatives for treatment of psychiatric disorders |
| US10597378B2 (en) | 2017-09-08 | 2020-03-24 | National Health Research Institutes | Tetrahydroisoquinolines for use as MOR/NOP dual agonists |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3880927A (en) * | 1972-06-19 | 1975-04-29 | Lilly Co Eli | {62 -Phenyl-{62 ,{62 -difluoroethylamines |
| PT1098897E (pt) * | 1998-07-17 | 2004-10-29 | Agouron Pharma | Compostos composicoes e metodos para estimular o crescimento e a elongacao neuronal |
| US6818643B1 (en) * | 1999-12-08 | 2004-11-16 | Bristol-Myers Squibb Company | Neurotrophic bicyclic diamides |
| AU2001292160A1 (en) * | 2000-10-19 | 2002-04-29 | Pfizer Products Inc. | Bridged piperazine derivatives |
| HUP0304058A2 (hu) * | 2001-01-30 | 2004-04-28 | Bristol-Myers Squibb Company | Xa faktor szulfonamid-laktám inhibitorok és alkalmazásuk és ezeket tartalmazó gyógyszerkészítmények |
-
2002
- 2002-05-10 BR BR0210060-6A patent/BR0210060A/pt not_active IP Right Cessation
- 2002-05-10 JP JP2002586941A patent/JP2004532854A/ja not_active Abandoned
- 2002-05-10 WO PCT/US2002/014966 patent/WO2002089806A1/en not_active Ceased
- 2002-05-10 CA CA002446795A patent/CA2446795A1/en not_active Abandoned
- 2002-05-10 MX MXPA03010255A patent/MXPA03010255A/es unknown
- 2002-05-10 EP EP02731761A patent/EP1423119A4/en not_active Withdrawn
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009506988A (ja) * | 2005-08-19 | 2009-02-19 | エラン ファーマシューティカルズ,インコーポレイテッド | ガンマセクレターゼの架橋n−環状スルホンアミド阻害剤 |
| JP2017523990A (ja) * | 2014-08-27 | 2017-08-24 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | Cns障害を処置するための置換ピラジノ[2,1−a]イソキノリン誘導体 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1423119A1 (en) | 2004-06-02 |
| WO2002089806A1 (en) | 2002-11-14 |
| BR0210060A (pt) | 2004-08-17 |
| EP1423119A4 (en) | 2005-04-13 |
| CA2446795A1 (en) | 2002-11-14 |
| MXPA03010255A (es) | 2005-03-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR102449652B1 (ko) | Rock의 억제제로서의 스피로-융합 시클릭 우레아 | |
| US6544987B2 (en) | Compounds, compositions, and methods for stimulating neuronal growth and elongation | |
| JP2022503942A (ja) | イソインドリン化合物、その調製方法、医薬組成物および使用 | |
| JP5643818B2 (ja) | Katii阻害剤としての二環式および三環式化合物 | |
| WO2019014308A1 (en) | 5-CHAIN AND BICYCLIC HETEROCYCLIC AMIDES AS ROCK INHIBITORS | |
| CA2881566A1 (en) | 1-(cycloalkyl-carbonyl)proline derivative | |
| KR20190005838A (ko) | 이중 lsd1/hdac 억제제로서 사이클로프로필-아마이드 화합물 | |
| AU2004251830A1 (en) | Pyrido[2, 1-A]-isoquinoline derivatives as DPP-IV inhibitors | |
| EP3828174A1 (en) | Pyridazinone derivative | |
| JP5538421B2 (ja) | H3モジュレーターとして使用される置換されたピペリジンスピロピロリジノン及びピペリジノン | |
| KR102842676B1 (ko) | Khk 억제 효과를 갖는 화합물 | |
| AU2018326497A1 (en) | Spirocycle compounds and methods of making and using same | |
| EP2961746A1 (en) | Phenylpyrazole derivatives as potent rock1 and rock2 inhibitors | |
| JP5139307B2 (ja) | ナトリウムチャネルモジュレーターとしてのプロリンアミド誘導体 | |
| KR20180016485A (ko) | 무스카린성 m2 수용체의 양성 알로스테릭 조정제 | |
| KR101857931B1 (ko) | 아제티디닐옥시페닐피롤리딘 화합물 | |
| AU2008284746A1 (en) | Aminopyrazole amide derivative | |
| PT2178858E (pt) | Novos compostos heterocíclicos como antagonistas de mglu5 | |
| JP5139306B2 (ja) | 電位依存性ナトリウムチャネルの調節因子としての第四級α−アミノカルボキサミド誘導体 | |
| KR20230035437A (ko) | 7-치환된 1-아릴-나프티리딘-3-카르복실산 아미드 및 그의 용도 | |
| JP2004532854A (ja) | 複素2環式fkbpリガンド | |
| EA009059B1 (ru) | Замещенные производные азабициклогексана в качестве антагонистов мускаринового рецептора | |
| JP2022545314A (ja) | プログラニュリンモジュレーターおよびその使用方法 | |
| TW201639836A (zh) | 二氮雜-苯並熒蒽類化合物 | |
| FR2814167A1 (fr) | Preparation de la camptothecine et de ses derives |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20050509 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20050509 |
|
| A762 | Written abandonment of application |
Free format text: JAPANESE INTERMEDIATE CODE: A762 Effective date: 20071228 |