ZA200802339B - Indol-3-yl-carbonyl-azaspiro derivatives as vasopressin receptor antagonists - Google Patents
Indol-3-yl-carbonyl-azaspiro derivatives as vasopressin receptor antagonistsInfo
- Publication number
- ZA200802339B ZA200802339B ZA200802339A ZA200802339A ZA200802339B ZA 200802339 B ZA200802339 B ZA 200802339B ZA 200802339 A ZA200802339 A ZA 200802339A ZA 200802339 A ZA200802339 A ZA 200802339A ZA 200802339 B ZA200802339 B ZA 200802339B
- Authority
- ZA
- South Africa
- Prior art keywords
- indol
- carbonyl
- receptor antagonists
- vasopressin receptor
- azaspiro derivatives
- Prior art date
Links
- 239000002536 vasopressin receptor antagonist Substances 0.000 title 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
- C07D471/10—Spiro-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4355—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having oxygen as a ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/08—Drugs for genital or sexual disorders; Contraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
-
- 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
- A61P25/22—Anxiolytics
-
- 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
- A61P25/24—Antidepressants
-
- 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
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/02—Drugs for disorders of the endocrine system of the hypothalamic hormones, e.g. TRH, GnRH, CRH, GRH, somatostatin
-
- 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
-
- 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
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- 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
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Cardiology (AREA)
- Neurosurgery (AREA)
- Heart & Thoracic Surgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Reproductive Health (AREA)
- Endocrinology (AREA)
- Pain & Pain Management (AREA)
- Diabetes (AREA)
- Psychiatry (AREA)
- Gynecology & Obstetrics (AREA)
- Pregnancy & Childbirth (AREA)
- Hospice & Palliative Care (AREA)
- Gastroenterology & Hepatology (AREA)
- Urology & Nephrology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP05108966 | 2005-09-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200802339B true ZA200802339B (en) | 2009-10-28 |
Family
ID=37156049
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200802339A ZA200802339B (en) | 2005-09-28 | 2008-03-12 | Indol-3-yl-carbonyl-azaspiro derivatives as vasopressin receptor antagonists |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US7790752B2 (xx) |
| EP (1) | EP1931680B1 (xx) |
| JP (1) | JP4908513B2 (xx) |
| KR (1) | KR101018934B1 (xx) |
| CN (1) | CN101273046B (xx) |
| AR (1) | AR057136A1 (xx) |
| AT (1) | ATE488519T1 (xx) |
| AU (1) | AU2006298828B2 (xx) |
| BR (1) | BRPI0616618A2 (xx) |
| CA (1) | CA2623715A1 (xx) |
| DE (1) | DE602006018334D1 (xx) |
| ES (1) | ES2354909T3 (xx) |
| IL (1) | IL189981A (xx) |
| RU (1) | RU2418801C2 (xx) |
| TW (1) | TWI327571B (xx) |
| WO (1) | WO2007039438A1 (xx) |
| ZA (1) | ZA200802339B (xx) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20070072795A1 (en) * | 2005-09-28 | 2007-03-29 | Anton Haselbeck | Treatment of neurodegenerative disorders |
| DE602007007512D1 (de) * | 2006-12-08 | 2010-08-12 | Hoffmann La Roche | Als via-rezeptor-antagonisten verwendbare indole |
| CN101838269B (zh) * | 2009-03-18 | 2012-09-26 | 中国人民解放军军事医学科学院毒物药物研究所 | 1,3,8-三氮杂-螺[4.5]癸烷-4-酮类化合物及其医药用途 |
| JO3109B1 (ar) * | 2012-05-10 | 2017-09-20 | Ferring Bv | منبهات لمستقبلات v1a |
| WO2017005583A1 (en) * | 2015-07-03 | 2017-01-12 | F. Hoffmann-La Roche Ag | Triaza-spirodecanones as ddr1 inhibitors |
| EP3414247B1 (en) | 2016-02-08 | 2021-04-21 | F. Hoffmann-La Roche AG | Spiroindolinones as ddr1 inhibitors |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2769578B2 (ja) * | 1989-10-13 | 1998-06-25 | 大塚製薬株式会社 | バソプレシン拮抗剤 |
| JP2002515891A (ja) * | 1997-12-19 | 2002-05-28 | スミスクライン・ビーチャム・コーポレイション | 新規なピペリジン含有化合物 |
| HU225703B1 (en) * | 1999-07-15 | 2007-06-28 | Sanofi Aventis | Process for producing spiro[cis-4-(betha-hydroxy-ethyloxi)-cyclohexane-[3h]indole]-2'[1'h]-one derivatives |
| US6150365A (en) * | 1999-08-05 | 2000-11-21 | Bristol-Myers Squibb Company | Anxiety method |
| EA009369B1 (ru) * | 2002-09-09 | 2007-12-28 | Янссен Фармацевтика, Н.В. | Производные гидроксизамещенного 1,3,8-триазинспиро[4,5]декан-4-она, полезные для лечения расстройств, опосредованных orl-рецептором |
| US20080287478A1 (en) * | 2003-05-23 | 2008-11-20 | Lars Bo Laurenborg Hansen | Nociceptin Analogues and Uses Thereof |
| US7745630B2 (en) * | 2003-12-22 | 2010-06-29 | Justin Stephen Bryans | Triazolyl piperidine arginine vasopressin receptor modulators |
| PL1904477T3 (pl) * | 2005-07-14 | 2009-07-31 | Hoffmann La Roche | Pochodne indolo-3-karbonylo-spiro-piperydyny jako antagoniści receptora V1a |
| US7351706B2 (en) * | 2006-01-05 | 2008-04-01 | Hoffmann-La Roche Inc. | Indol-3-yl-carbonyl-spiro-piperidine derivatives |
| RU2009119393A (ru) * | 2006-12-07 | 2011-01-20 | Ф. Хоффманн-Ля Рош Аг (Ch) | Производные спиропиперидина |
-
2006
- 2006-09-18 KR KR1020087007377A patent/KR101018934B1/ko not_active Expired - Fee Related
- 2006-09-18 AU AU2006298828A patent/AU2006298828B2/en not_active Ceased
- 2006-09-18 WO PCT/EP2006/066441 patent/WO2007039438A1/en not_active Ceased
- 2006-09-18 CA CA002623715A patent/CA2623715A1/en not_active Abandoned
- 2006-09-18 CN CN2006800358570A patent/CN101273046B/zh not_active Expired - Fee Related
- 2006-09-18 BR BRPI0616618-0A patent/BRPI0616618A2/pt not_active IP Right Cessation
- 2006-09-18 JP JP2008532722A patent/JP4908513B2/ja not_active Expired - Fee Related
- 2006-09-18 ES ES06793584T patent/ES2354909T3/es active Active
- 2006-09-18 DE DE602006018334T patent/DE602006018334D1/de active Active
- 2006-09-18 EP EP06793584A patent/EP1931680B1/en not_active Not-in-force
- 2006-09-18 RU RU2008110409/04A patent/RU2418801C2/ru not_active IP Right Cessation
- 2006-09-18 AT AT06793584T patent/ATE488519T1/de active
- 2006-09-21 US US11/524,978 patent/US7790752B2/en not_active Expired - Fee Related
- 2006-09-25 TW TW095135364A patent/TWI327571B/zh not_active IP Right Cessation
- 2006-09-26 AR ARP060104192A patent/AR057136A1/es unknown
-
2008
- 2008-03-06 IL IL189981A patent/IL189981A/en not_active IP Right Cessation
- 2008-03-12 ZA ZA200802339A patent/ZA200802339B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ATE488519T1 (de) | 2010-12-15 |
| BRPI0616618A2 (pt) | 2011-06-28 |
| IL189981A (en) | 2012-09-24 |
| US20070072888A1 (en) | 2007-03-29 |
| TW200804392A (en) | 2008-01-16 |
| CN101273046A (zh) | 2008-09-24 |
| CN101273046B (zh) | 2011-05-25 |
| KR20080049780A (ko) | 2008-06-04 |
| EP1931680B1 (en) | 2010-11-17 |
| IL189981A0 (en) | 2008-08-07 |
| JP2009510010A (ja) | 2009-03-12 |
| DE602006018334D1 (de) | 2010-12-30 |
| EP1931680A1 (en) | 2008-06-18 |
| AU2006298828B2 (en) | 2011-12-01 |
| AR057136A1 (es) | 2007-11-21 |
| CA2623715A1 (en) | 2007-04-12 |
| ES2354909T3 (es) | 2011-03-21 |
| AU2006298828A1 (en) | 2007-04-12 |
| RU2008110409A (ru) | 2009-11-10 |
| JP4908513B2 (ja) | 2012-04-04 |
| RU2418801C2 (ru) | 2011-05-20 |
| WO2007039438A1 (en) | 2007-04-12 |
| KR101018934B1 (ko) | 2011-03-02 |
| US7790752B2 (en) | 2010-09-07 |
| TWI327571B (en) | 2010-07-21 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ZA200800320B (en) | Indol-3-carbonyl-spiro-piperidine derivatives as Via receptor antagonists | |
| TWI318206B (en) | Histamine-3 receptor antagonists | |
| ZA200803811B (en) | Neuropolin antagonists | |
| IL202561A0 (en) | Benzazepine derivatives useful as vasopressin antagonists | |
| IL187424A0 (en) | C5a RECEPTOR ANTAGONISTS | |
| IL184816A0 (en) | 2-phenyl-indoles as prostaglandin d2 receptor antagonists | |
| ZA200709147B (en) | Pyrimidindione derivatives as prokineticin 2 receptor antagonists | |
| ZA200801432B (en) | Carboxamide derivatives as muscarinic receptor antagonists | |
| IL184278A0 (en) | C5a RECEPTOR ANTAGONISTS | |
| ZA200806065B (en) | Oxazoloisoquinoline derivatives as thrombin receptor antagonists | |
| AP2007004047A0 (en) | Substituted triazole derivatives as oxtocin antagonists | |
| AP2008004441A0 (en) | Piperdin-4-ylpyrazin-2-ylamine derivatives as fastdissociating dopamine 2 receptor antagonists | |
| ZA200904479B (en) | Nitroderivatives as angiotensin II receptor antagonists | |
| EP1874302A4 (en) | ANTAGONISTS OF ANGIOTENSIN II RECEPTORS | |
| ZA200802339B (en) | Indol-3-yl-carbonyl-azaspiro derivatives as vasopressin receptor antagonists | |
| PL1912976T3 (pl) | Pochodne indol-3-ilokarbonylopiperydynobenzoimidazolu jako antagoniści receptora V1a | |
| IL185640A0 (en) | Use of 2-anilino-3 ,4-dihydro-quinazolines as 5ht5a receptor antagonists | |
| HU0501169D0 (en) | New phenantridine derivatives as selective bradykinin b1 receptor antagonists | |
| AP2008004537A0 (en) | Muscarinic receptor antagonists | |
| GB0525029D0 (en) | Receptor Antagonist | |
| ZA200806223B (en) | Muscarinic receptor antagonists | |
| ZA200800516B (en) | Indol-3-yl-carbonyl-piperidin-benzoimidazol derivatives as V1a receptor antagonists | |
| GB0516617D0 (en) | EP2 Receptor antagonists |