NO20050668L - 7,8,9,10-tetrahydro-6H-azepino6,7,8,9-tetrahydro-pyrido og 2,3-dihydro-2H-pyrrolo [2,1-B]-kinazolinon-derivater - Google Patents
7,8,9,10-tetrahydro-6H-azepino6,7,8,9-tetrahydro-pyrido og 2,3-dihydro-2H-pyrrolo [2,1-B]-kinazolinon-derivaterInfo
- Publication number
- NO20050668L NO20050668L NO20050668A NO20050668A NO20050668L NO 20050668 L NO20050668 L NO 20050668L NO 20050668 A NO20050668 A NO 20050668A NO 20050668 A NO20050668 A NO 20050668A NO 20050668 L NO20050668 L NO 20050668L
- Authority
- NO
- Norway
- Prior art keywords
- tetrahydro
- pyrido
- pyrrolo
- dihydro
- azepino6
- Prior art date
Links
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
- C07D471/04—Ortho-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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- 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
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- 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
- A61P25/20—Hypnotics; Sedatives
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Psychiatry (AREA)
- Epidemiology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Diabetes (AREA)
- Child & Adolescent Psychology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Anesthesiology (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP0207608 | 2002-07-09 | ||
PCT/EP2003/007297 WO2004004733A1 (fr) | 2002-07-09 | 2003-07-08 | Derives de 7,8,9,10-tetrahydro-6h-azepino, 6,7,8,9-tetrahydro-pyrido et 2,3-dihydro-2h-pyrrolo[2,1-b]-quinazolinone |
Publications (1)
Publication Number | Publication Date |
---|---|
NO20050668L true NO20050668L (no) | 2005-04-05 |
Family
ID=30011039
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO20050668A NO20050668L (no) | 2002-07-09 | 2005-02-08 | 7,8,9,10-tetrahydro-6H-azepino6,7,8,9-tetrahydro-pyrido og 2,3-dihydro-2H-pyrrolo [2,1-B]-kinazolinon-derivater |
Country Status (16)
Country | Link |
---|---|
US (1) | US7067519B2 (fr) |
EP (1) | EP1521583B1 (fr) |
JP (1) | JP4498922B2 (fr) |
CN (1) | CN1556705B (fr) |
AU (1) | AU2003246657A1 (fr) |
CA (1) | CA2460051A1 (fr) |
DE (1) | DE60311101T2 (fr) |
ES (1) | ES2278197T3 (fr) |
IL (1) | IL166100A0 (fr) |
MX (1) | MXPA04002269A (fr) |
NO (1) | NO20050668L (fr) |
NZ (1) | NZ538029A (fr) |
PL (1) | PL373223A1 (fr) |
RU (1) | RU2005103398A (fr) |
WO (1) | WO2004004733A1 (fr) |
ZA (1) | ZA200500026B (fr) |
Families Citing this family (36)
Publication number | Priority date | Publication date | Assignee | Title |
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CA2520839A1 (fr) * | 2003-04-28 | 2004-11-11 | Actelion Pharmaceuticals Ltd | Derives de quinoxalinone-3- one utilises comme antagonistes du recepteur d'orexine |
EP1607069B1 (fr) * | 2004-06-15 | 2009-12-23 | Tornier | Prothese totale d'epaule de type inverse |
AU2007272854B2 (en) | 2006-07-14 | 2013-08-01 | Merck Sharp & Dohme Corp. | Bridged diazepan orexin receptor antagonists |
WO2008026149A1 (fr) * | 2006-08-28 | 2008-03-06 | Actelion Pharmaceuticals Ltd | Dérivés de 1,4,5,6,7,8-hexahydro-1,2,5-triaza-azulène en tant qu'antagonistes de récepteur d'orexine |
PE20081229A1 (es) | 2006-12-01 | 2008-08-28 | Merck & Co Inc | Antagonistas de receptor de orexina de diazepam sustituido |
CA2669561A1 (fr) | 2006-12-22 | 2008-07-03 | Actelion Pharmaceuticals Ltd | Derives de 5,6,7,8-tetrahydro-imidazo[1,5-a]pyrazine |
US8263586B2 (en) | 2007-05-18 | 2012-09-11 | Merck Sharp & Dohme Corp. | OXO bridged diazepan orexin receptor antagonists |
WO2008150364A1 (fr) | 2007-05-23 | 2008-12-11 | Merck & Co., Inc. | Antagonistes du récepteur de la cyclopropylpyrrolidine orexine |
RS52200B (en) | 2007-05-23 | 2012-10-31 | Merck Sharp & Dohme Corp. | PIRIDIL PIPERIDIN ORREXIN ANTAGONIST RECEPTORA |
EP2161266A1 (fr) | 2008-08-22 | 2010-03-10 | EVOTEC Neurosciences GmbH | Dérivés de benzofurane en tant qu'antagonistes du récepteur de l'orexine |
CA2741125A1 (fr) | 2008-10-22 | 2010-04-29 | Merck Sharp & Dohme Corp. | Nouveaux derives de benzimidazole cycliques utiles comme agents anti-diabetiques |
WO2010051206A1 (fr) | 2008-10-31 | 2010-05-06 | Merck Sharp & Dohme Corp. | Nouveaux agents antidiabétiques utiles avec des dérivés de benzimidazole cycliques |
JP5847087B2 (ja) | 2009-10-23 | 2016-01-20 | ヤンセン ファーマシューティカ エヌ.ベー. | オレキシン受容体調節因子としての縮合複素環式化合物 |
US9062044B2 (en) | 2009-10-23 | 2015-06-23 | Janssen Pharmaceutica Nv | Disubstituted octahydropyrrolo[3,4-c]pyrroles as orexin receptor modulators |
MX2012004753A (es) | 2009-10-23 | 2012-09-07 | Janssen Pharmaceutica Nv | Octahidropirrolo[3,4-c]pirrolos disustituidos como moduladores del receptor de orexina. |
JP2013520502A (ja) | 2010-02-25 | 2013-06-06 | メルク・シャープ・エンド・ドーム・コーポレイション | 有用な抗糖尿病薬である新規な環状ベンズイミダゾール誘導体 |
WO2011138266A1 (fr) | 2010-05-03 | 2011-11-10 | Evotec Ag | Dérivés d'indolizine et d'imidazopyridine comme antagonistes de récepteurs d'orexine |
WO2011138265A2 (fr) | 2010-05-03 | 2011-11-10 | Evotec Ag | Dérivés d'indole et d'indazole utilisés comme antagonistes du récepteur de l'orexine |
JP5728099B2 (ja) | 2011-02-25 | 2015-06-03 | メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. | 抗糖尿病剤として有用な新規環状アザベンゾイミダゾール誘導体 |
US9586962B2 (en) | 2011-04-20 | 2017-03-07 | Janssen Pharmaceutica Nv | Disubstituted octahydropyrrolo [3,4-C] pyrroles as orexin receptor modulators |
ES2562903T3 (es) * | 2011-07-13 | 2016-03-09 | Santen Pharmaceutical Co., Ltd | Nuevo compuesto que tiene actividad inhibidora de PARP |
AR088352A1 (es) | 2011-10-19 | 2014-05-28 | Merck Sharp & Dohme | Antagonistas del receptor de 2-piridiloxi-4-nitrilo orexina |
US9440982B2 (en) | 2012-02-07 | 2016-09-13 | Eolas Therapeutics, Inc. | Substituted prolines/piperidines as orexin receptor antagonists |
CA2863413A1 (fr) | 2012-02-07 | 2013-08-15 | Eolas Therapeutics, Inc. | Piperidines/prolines substituees en tant qu'antagonistes du recepteur de l'orexine |
CA2880901A1 (fr) | 2012-08-02 | 2014-02-06 | Merck Sharp & Dohme Corp. | Composes tricycliques antidiabetiques |
RU2015140066A (ru) | 2013-02-22 | 2017-03-30 | Мерк Шарп И Доум Корп. | Противодиабетические бициклические соединения |
EP2970119B1 (fr) | 2013-03-14 | 2021-11-03 | Merck Sharp & Dohme Corp. | Nouveaux dérivés d'indole utiles en tant qu'agents antidiabétiques |
WO2015051496A1 (fr) | 2013-10-08 | 2015-04-16 | Merck Sharp & Dohme Corp. | Composés tricycliques antidiabétiques |
JP6663909B2 (ja) | 2014-08-13 | 2020-03-13 | エオラス セラピューティクス, インコーポレイテッド | オレキシンレセプターモジュレーターとしてのジフルオロピロリジン |
HRP20220906T1 (hr) | 2016-02-12 | 2022-10-14 | Astrazeneca Ab | Halo-supstituirani piperidini kao modulatori receptora oreksina |
PL3426251T3 (pl) | 2016-03-10 | 2022-07-18 | Janssen Pharmaceutica Nv | Sposoby leczenia depresji za pomocą antagonistów receptora typu 2 oreksyny |
EP3454857A1 (fr) | 2016-05-10 | 2019-03-20 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Méthodes et compositions pharmaceutiques pour le traitement de maladies inflammatoires auto-immunes |
US11072602B2 (en) | 2016-12-06 | 2021-07-27 | Merck Sharp & Dohme Corp. | Antidiabetic heterocyclic compounds |
WO2018118670A1 (fr) | 2016-12-20 | 2018-06-28 | Merck Sharp & Dohme Corp. | Composés de spirochromane antidiabétiques |
BR112020001698A2 (pt) | 2017-08-03 | 2020-07-21 | Galectin Sciences, Llc | compostos para prevenção e tratamento de distúrbios médicos e usos dos mesmos |
US12071434B2 (en) | 2018-12-12 | 2024-08-27 | Takeda Pharmaceutical Company Limited | Heterocyclic compound |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
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HU173438B (hu) * | 1975-11-27 | 1979-05-28 | Chinoin Gyogyszer Es Vegyeszet | Sposob poluchenija novykh proizvodnykh 4-okso-1,6,7,8-/tetragidro-4h-pirido/1,2/pirimidina s zaderzhivajuhhejj vozgoranie aktivnot'ju i protivosvertivajuhhem effektom |
HU191192B (en) * | 1982-11-16 | 1987-01-28 | Chinoin Gyogyszer Es Vegyeszeti Termekek Gyara Rt,Hu | Process for producing new azepino /1,2-a/ pyrimidine derivatives of bronchodilating activity and acid additional salts thereof and pharmaceiutical compositions containing them |
US4678499A (en) * | 1985-03-11 | 1987-07-07 | E. I. Du Pont De Nemours And Company | Herbicidal sulfonamides |
US5753664A (en) * | 1995-03-16 | 1998-05-19 | Takeda Chemical Industries, Ltd. | Heterocyclic compounds, their production and use |
US6057315A (en) * | 1996-12-09 | 2000-05-02 | Warner-Lambertt Company | Antibacterial agents |
AR016817A1 (es) | 1997-08-14 | 2001-08-01 | Smithkline Beecham Plc | Derivados de fenilurea o feniltiourea, procedimiento para su preparacion, coleccion de compuestos, compuestos intermediarios, composicion farmaceutica,metodo de tratamiento y uso de dichos compuestos para la manufactura de un medicamento |
CA2331735A1 (fr) | 1998-05-08 | 1999-11-18 | Smithkline Beecham P.L.C. | Derives de phenyluree et de (phenylthio)uree |
ATE282614T1 (de) | 1999-02-12 | 2004-12-15 | Smithkline Beecham Plc | Phenylharnstoff und phenylthioharnstoffderivate |
WO2000047576A1 (fr) | 1999-02-12 | 2000-08-17 | Smithkline Beecham Plc | Derives de cinnamide utilises en tant qu'antagonistes des recepteurs de l'orexine-1 |
ES2226785T3 (es) | 1999-02-12 | 2005-04-01 | Smithkline Beecham Plc | Derivados de fenilurea como antagonistas de los receptores de orexina. |
DE19906975B4 (de) * | 1999-02-19 | 2004-04-15 | Lts Lohmann Therapie-Systeme Ag | Arzneiform zur Behandlung von Alzheimer'scher Demenz |
WO2001066099A2 (fr) * | 2000-03-06 | 2001-09-13 | Astrazeneca Ab | Therapie |
WO2001085693A1 (fr) | 2000-05-11 | 2001-11-15 | Banyu Pharmaceutical Co., Ltd. | Dérivés n-acyltétrahydroisoquinoline |
JP4611608B2 (ja) | 2000-06-16 | 2011-01-12 | スミスクライン ビーチャム ピー エル シー | オレキシン受容体アンタゴニストとして使用するためのピペリジン |
ES2234929T3 (es) | 2000-11-28 | 2005-07-01 | Smithkline Beecham Plc | Derivados de morfolina como antagonistas de los receptores de orexina. |
GB0121214D0 (en) * | 2001-08-31 | 2001-10-24 | Btg Int Ltd | Synthetic method |
EP1438048A1 (fr) * | 2001-10-18 | 2004-07-21 | Boehringer Ingelheim Pharmaceuticals Inc. | Composes d'uree benzo fusionnes 1,4-disubstitues utilises comme inhibiteurs des cytokines |
US6676976B2 (en) * | 2002-03-21 | 2004-01-13 | Council Of Scientific And Industrial Research | Process for the production of vasicine |
-
2003
- 2003-07-08 PL PL03373223A patent/PL373223A1/xx not_active Application Discontinuation
- 2003-07-08 NZ NZ538029A patent/NZ538029A/en unknown
- 2003-07-08 WO PCT/EP2003/007297 patent/WO2004004733A1/fr active IP Right Grant
- 2003-07-08 AU AU2003246657A patent/AU2003246657A1/en not_active Abandoned
- 2003-07-08 JP JP2004518740A patent/JP4498922B2/ja not_active Expired - Fee Related
- 2003-07-08 EP EP03762653A patent/EP1521583B1/fr not_active Expired - Lifetime
- 2003-07-08 CA CA002460051A patent/CA2460051A1/fr not_active Abandoned
- 2003-07-08 MX MXPA04002269A patent/MXPA04002269A/es unknown
- 2003-07-08 CN CN038011042A patent/CN1556705B/zh not_active Expired - Fee Related
- 2003-07-08 US US10/489,350 patent/US7067519B2/en not_active Expired - Fee Related
- 2003-07-08 RU RU2005103398/04A patent/RU2005103398A/ru not_active Application Discontinuation
- 2003-07-08 ES ES03762653T patent/ES2278197T3/es not_active Expired - Lifetime
- 2003-07-08 DE DE60311101T patent/DE60311101T2/de not_active Expired - Lifetime
-
2005
- 2005-01-03 ZA ZA200500026A patent/ZA200500026B/en unknown
- 2005-01-03 IL IL16610005A patent/IL166100A0/xx unknown
- 2005-02-08 NO NO20050668A patent/NO20050668L/no unknown
Also Published As
Publication number | Publication date |
---|---|
EP1521583B1 (fr) | 2007-01-10 |
CN1556705A (zh) | 2004-12-22 |
NZ538029A (en) | 2006-08-31 |
IL166100A0 (en) | 2006-01-15 |
WO2004004733A1 (fr) | 2004-01-15 |
DE60311101D1 (de) | 2007-02-22 |
EP1521583A1 (fr) | 2005-04-13 |
CA2460051A1 (fr) | 2004-01-15 |
ES2278197T3 (es) | 2007-08-01 |
ZA200500026B (en) | 2005-10-20 |
PL373223A1 (en) | 2005-08-22 |
JP2005532381A (ja) | 2005-10-27 |
AU2003246657A1 (en) | 2004-01-23 |
US20050009852A1 (en) | 2005-01-13 |
CN1556705B (zh) | 2010-04-28 |
JP4498922B2 (ja) | 2010-07-07 |
US7067519B2 (en) | 2006-06-27 |
MXPA04002269A (es) | 2004-06-29 |
DE60311101T2 (de) | 2007-06-21 |
RU2005103398A (ru) | 2006-06-27 |
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