ATE243186T1 - Verbindungen , die auf anorganische ionen- rezeptoren wirken - Google Patents
Verbindungen , die auf anorganische ionen- rezeptoren wirkenInfo
- Publication number
- ATE243186T1 ATE243186T1 AT97922601T AT97922601T ATE243186T1 AT E243186 T1 ATE243186 T1 AT E243186T1 AT 97922601 T AT97922601 T AT 97922601T AT 97922601 T AT97922601 T AT 97922601T AT E243186 T1 ATE243186 T1 AT E243186T1
- Authority
- AT
- Austria
- Prior art keywords
- inorganic ion
- compounds acting
- compounds
- ion receptors
- receptor
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/49—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C255/58—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the carbon skeleton
-
- 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
- A61K31/13—Amines
- A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
- A61K31/137—Arylalkylamines, e.g. amphetamine, epinephrine, salbutamol, ephedrine or methadone
-
- 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
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/357—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having two or more oxygen atoms in the same ring, e.g. crown ethers, guanadrel
- A61K31/36—Compounds containing methylenedioxyphenyl groups, e.g. sesamin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- 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
-
- 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
- A61P3/12—Drugs for disorders of the metabolism for electrolyte homeostasis
- A61P3/14—Drugs for disorders of the metabolism for electrolyte homeostasis for calcium homeostasis
-
- 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
-
- 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
- A61P5/14—Drugs for disorders of the endocrine system of the thyroid hormones, e.g. T3, T4
- A61P5/16—Drugs for disorders of the endocrine system of the thyroid hormones, e.g. T3, T4 for decreasing, blocking or antagonising the activity of the thyroid hormones
-
- 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
- A61P5/18—Drugs for disorders of the endocrine system of the parathyroid hormones
- A61P5/20—Drugs for disorders of the endocrine system of the parathyroid hormones for decreasing, blocking or antagonising the activity of PTH
-
- 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
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/01—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms
- C07C211/26—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing at least one six-membered aromatic ring
- C07C211/29—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by halogen atoms or by nitro or nitroso groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/01—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms
- C07C211/26—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing at least one six-membered aromatic ring
- C07C211/30—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing at least one six-membered aromatic ring the six-membered aromatic ring being part of a condensed ring system formed by two rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
- C07C217/54—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
- C07C217/56—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms
- C07C217/58—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms with amino groups and the six-membered aromatic ring, or the condensed ring system containing that ring, bound to the same carbon atom of the carbon chain
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
- C07C217/54—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
- C07C217/56—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms
- C07C217/62—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms linked by carbon chains having at least three carbon atoms between the amino groups and the six-membered aromatic ring or the condensed ring system containing that ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/49—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C255/54—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and etherified hydroxy groups bound to the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/79—Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
- C07D307/81—Radicals substituted by nitrogen atoms not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
- C07D317/50—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to atoms of the carbocyclic ring
- C07D317/58—Radicals substituted by nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Physical Education & Sports Medicine (AREA)
- Diabetes (AREA)
- Endocrinology (AREA)
- Epidemiology (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Heart & Thoracic Surgery (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Emergency Medicine (AREA)
- Cardiology (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Furan Compounds (AREA)
- Eye Examination Apparatus (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Prostheses (AREA)
- Steroid Compounds (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US1667396P | 1996-05-01 | 1996-05-01 | |
PCT/US1997/007371 WO1997041090A1 (en) | 1996-05-01 | 1997-04-30 | Inorganic ion receptor-active compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
ATE243186T1 true ATE243186T1 (de) | 2003-07-15 |
Family
ID=21778338
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT02018228T ATE352537T1 (de) | 1996-05-01 | 1997-04-30 | Verbindungen, die auf anorganische ionen- rezeptoren wirken |
AT07000764T ATE430123T1 (de) | 1996-05-01 | 1997-04-30 | Inorganische am ionen-rezeptor aktive verbindungen |
AT97922601T ATE243186T1 (de) | 1996-05-01 | 1997-04-30 | Verbindungen , die auf anorganische ionen- rezeptoren wirken |
Family Applications Before (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT02018228T ATE352537T1 (de) | 1996-05-01 | 1997-04-30 | Verbindungen, die auf anorganische ionen- rezeptoren wirken |
AT07000764T ATE430123T1 (de) | 1996-05-01 | 1997-04-30 | Inorganische am ionen-rezeptor aktive verbindungen |
Country Status (12)
Country | Link |
---|---|
US (3) | US5981599A (de) |
EP (1) | EP0907631B1 (de) |
JP (2) | JP4117506B2 (de) |
AT (3) | ATE352537T1 (de) |
AU (1) | AU731146C (de) |
DE (3) | DE69737303T2 (de) |
DK (1) | DK0907631T3 (de) |
ES (3) | ES2201300T3 (de) |
HK (2) | HK1051995A1 (de) |
PT (1) | PT907631E (de) |
TW (1) | TW561150B (de) |
WO (1) | WO1997041090A1 (de) |
Families Citing this family (47)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4426245A1 (de) * | 1994-07-23 | 1996-02-22 | Gruenenthal Gmbh | 1-Phenyl-3-dimethylamino-propanverbindungen mit pharmakologischer Wirkung |
DK0907631T3 (da) * | 1996-05-01 | 2003-09-22 | Nps Pharma Inc | Uorganiske ionreceptoraktive forbindelser |
KR100860655B1 (ko) * | 1996-07-08 | 2008-09-26 | 기린 파마 가부시끼가이샤 | 칼슘 수용체 활성 화합물 |
IL133942A0 (en) * | 1997-07-09 | 2001-04-30 | Akzo Nobel Nv | Chelating agents and their manganic chelates |
AU1558899A (en) * | 1997-11-10 | 1999-05-31 | F. Hoffmann-La Roche Ag | Isoquinoline derivatives for use against cns disorders |
FR2800735B1 (fr) * | 1999-11-09 | 2002-02-01 | Centre Nat Rech Scient | Nouvelles aralkyle-1,2-diamines possedant une activite calcimimetique et leur mode de preparation |
US7176243B2 (en) | 2000-06-02 | 2007-02-13 | The General Hospital Corporation | CaR receptor as a mediator of migratory cell chemotaxis and/or chemokinesis |
FR2812875B1 (fr) * | 2000-08-08 | 2003-12-12 | Centre Nat Rech Scient | Nouvelles diamines possedant une activite modulatrice des casr et leur mode de preparation |
US6979559B2 (en) * | 2000-10-12 | 2005-12-27 | Marical, Inc. | Polyvalent cation-sensing receptor in atlantic salmon |
US6463883B1 (en) | 2000-10-12 | 2002-10-15 | Marical, Llc | Methods for raising pre-adult anadromous fish |
US6475792B1 (en) | 2000-10-12 | 2002-11-05 | Marical, Llc | Methods for raising pre-adult anadromous fish |
US6979558B2 (en) * | 2000-10-12 | 2005-12-27 | Marical, Inc. | Polyvalent cation-sensing receptor in Atlantic salmon |
US6951739B2 (en) * | 2000-10-12 | 2005-10-04 | Marical, Inc. | Polyvalent cation-sensing receptor in atlantic salmon |
EP1324651B1 (de) * | 2000-10-12 | 2008-02-13 | Marical, Inc. | Verfahren zur züchtung von nichterwachsenen anadromen fischen |
US6481379B1 (en) * | 2000-10-12 | 2002-11-19 | Marical, Llc | Methods for raising pre-adult anadromous fish |
US6463882B1 (en) * | 2000-10-12 | 2002-10-15 | Marical, Llc | Growing marine fish in freshwater |
US7101988B2 (en) * | 2000-10-12 | 2006-09-05 | Marical, Inc. | Polyvalent cation-sensing receptor in Atlantic salmon |
EP1434482B9 (de) * | 2001-10-11 | 2007-11-28 | Marical, Inc. | Verfahren zum züchten und imprimieren von fischen mittels eines geruchstoffes |
US6908935B2 (en) * | 2002-05-23 | 2005-06-21 | Amgen Inc. | Calcium receptor modulating agents |
US7176322B2 (en) | 2002-05-23 | 2007-02-13 | Amgen Inc. | Calcium receptor modulating agents |
TR201910177T4 (tr) | 2003-09-12 | 2019-08-21 | Amgen Inc | Bir sinakalset HCl içeren hızlı çözünme formülasyonu. |
EG23529A (en) * | 2003-11-05 | 2006-04-11 | Amri Moosa E Al | System and method to broadcast the video or tv anddisplaying on pc tv by choosing the required prog ram from the internet |
WO2005065050A2 (ja) | 2003-12-25 | 2005-07-21 | Asahi Kasei Pharma Corporation | 2環化合物 |
WO2005115975A1 (ja) | 2004-05-28 | 2005-12-08 | Tanabe Seiyaku Co., Ltd. | アリールアルキルアミン化合物及びその製法 |
US7361789B1 (en) | 2004-07-28 | 2008-04-22 | Amgen Inc. | Dihydronaphthalene compounds, compositions, uses thereof, and methods for synthesis |
CN101184508A (zh) * | 2005-03-17 | 2008-05-21 | 安姆根有限公司 | 减少钙化的方法 |
DK1882684T3 (en) * | 2005-05-19 | 2015-01-05 | Astellas Pharma Inc | PYRROLIDE INGREDIENTS OR SALTS THEREOF |
CN101180261A (zh) * | 2005-05-23 | 2008-05-14 | 特瓦制药工业有限公司 | 用于制备盐酸西那卡塞晶型ⅰ的方法 |
JP5309014B2 (ja) | 2006-03-23 | 2013-10-09 | アムジエン・インコーポレーテツド | シナカルセットの多形体の製造および使用のための方法および組成物 |
CN101437490A (zh) | 2006-04-20 | 2009-05-20 | 安美基公司 | 稳定乳液配方 |
ES2449340T3 (es) | 2007-03-30 | 2014-03-19 | Amgen Inc. | Compuestos calcimiméticos para su uso en el tratamiento de trastornos intestinales |
ES2499015T3 (es) * | 2007-05-08 | 2014-09-26 | Ajinomoto Co., Inc. | Agente profiláctico o terapéutico para la diarrea |
CA2701792A1 (en) * | 2007-10-15 | 2009-04-23 | Amgen Inc. | Calcium receptor modulating agents |
WO2010010359A2 (en) * | 2008-07-24 | 2010-01-28 | Cilpa Limited | A process for the preparation of cinacalcet and its salts |
WO2010042642A1 (en) * | 2008-10-08 | 2010-04-15 | Amgen Inc. | Calcium receptor modulating agents |
WO2010104882A1 (en) | 2009-03-10 | 2010-09-16 | Amgen Inc. | Methods of modulating sperm motility |
US8785494B2 (en) | 2009-05-27 | 2014-07-22 | Leo-Pharma A/S | Calcium sensing receptor modulating compounds and pharmaceutical use thereof |
CA2762137A1 (en) | 2009-05-27 | 2010-12-02 | Leo Pharma A/S | Novel calcium sensing receptor modulating compounds and pharmaceutical use thereof |
WO2010136036A2 (en) * | 2009-05-27 | 2010-12-02 | Leo Pharma A/S | Calcium-sensing receptor-active compounds |
RU2599788C2 (ru) | 2010-06-30 | 2016-10-20 | Лео Фарма А/С | Новая полиморфная форма кальцимиметического соединения |
JP5968880B2 (ja) | 2010-06-30 | 2016-08-10 | レオ ファーマ アクティーゼルスカブ | カルシウム模倣化合物の新規多形 |
WO2012069402A1 (en) | 2010-11-26 | 2012-05-31 | Leo Pharma A/S | Substituted cyclopentyl - azines as casr- active compounds |
RU2013128973A (ru) | 2010-11-26 | 2015-01-10 | Лео Фарма А/С | Соединения, активные в отношении кальций-чувствительных рецепторов |
EP2643291A2 (de) | 2010-11-26 | 2013-10-02 | Leo Pharma A/S | Casr-aktive verbindungen |
RU2013128968A (ru) | 2010-11-26 | 2015-01-10 | Лео Фарма А/С | Соединения, активные в отношении кальций-чувствительного рецептора |
US9382216B2 (en) | 2011-03-10 | 2016-07-05 | Lupin Limited | Substituted morpholines as modulators for the calcium sensing receptor |
WO2013136288A1 (en) * | 2012-03-16 | 2013-09-19 | Lupin Limited | Substituted 3,4-dihydro-2h-benzo[b] [1,4]oxazine compounds as calcium sensing receptor modulators |
Family Cites Families (96)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2276618A (en) * | 1942-03-17 | N-phenylaliphatic bihxdroxithenyl- | ||
CH217009A (fr) * | 1940-10-25 | 1941-09-30 | Anonyme Taubert Freres Societe | Boîte de montre. |
US2930731A (en) * | 1952-04-08 | 1960-03-29 | Upjohn Co | Bis[beta-(ortho-hydrocarbonoxyphenyl)iso-propyl]amines |
BE570596A (de) * | 1957-08-26 | |||
NL281782A (de) * | 1961-08-14 | |||
US3262977A (en) * | 1962-03-10 | 1966-07-26 | Chinoin Gyogyszer Es Vegyeszet | N-aralkyl-1, 1-diphenyl-propylamine derivatives |
NL293886A (de) * | 1962-06-19 | 1965-04-12 | Merck Ag E | |
US3318952A (en) * | 1964-01-22 | 1967-05-09 | Sandoz Ag | Dibenzylsulfamides |
US3459767A (en) * | 1965-08-10 | 1969-08-05 | Pfizer & Co C | Aminomethylindoles |
GB1109924A (en) * | 1965-11-29 | 1968-04-18 | Roche Products Ltd | Novel substituted diphenylalkyl amines and a process for the manufacture thereof |
DE1618005A1 (de) * | 1966-09-22 | 1971-09-09 | Thomae Gmbh Dr K | Verfahren zur Herstellung von neuen Amino-dihalogen-phenyl-aethylaminen |
CH480791A (de) * | 1967-01-17 | 1969-11-15 | Ciba Geigy | Schädlingsbekämpfungsmittel |
GB1263987A (en) * | 1969-05-30 | 1972-02-16 | Allen & Hanburys Ltd | Phenethylamine derivatives |
GB1448437A (en) * | 1973-02-24 | 1976-09-08 | Beecham Group Ltd | Diphenylpropylamines |
US3862925A (en) * | 1973-07-05 | 1975-01-28 | American Home Prod | Preparation of somatotropin release inhibiting factor and intermediates therefor |
US4000197A (en) * | 1973-07-23 | 1976-12-28 | The University Of Iowa Research Foundation | Asymmetric synthesis of phenylisopropylamines |
US3842067A (en) * | 1973-07-27 | 1974-10-15 | American Home Prod | Synthesis of(des-asn5)-srif and intermediates |
JPS5726506B2 (de) * | 1974-03-08 | 1982-06-04 | ||
US4014937A (en) * | 1974-08-26 | 1977-03-29 | Pfizer Inc. | 3,4-And 3,5-dialkoxyphenethylamines |
HU169507B (de) * | 1974-09-25 | 1976-12-28 | ||
US3987201A (en) * | 1974-12-24 | 1976-10-19 | Eli Lilly And Company | Method for treating arrhythmia |
US4105602A (en) * | 1975-02-10 | 1978-08-08 | Armour Pharmaceutical Company | Synthesis of peptides with parathyroid hormone activity |
JPS5390272A (en) * | 1977-01-13 | 1978-08-08 | Sendai Fukusokan Kagaku Kenkiy | Method of producing optically active salsolizine |
US4608391A (en) * | 1977-07-05 | 1986-08-26 | Cornell Research Foundation Inc. | Catecholamine derivatives, a process for their preparation and pharmaceutical compositions thereof |
US4289787A (en) * | 1977-12-19 | 1981-09-15 | Eli Lilly And Company | Quaternary ammonium antiarrhythmic drugs |
DD144050A5 (de) * | 1978-06-05 | 1980-09-24 | Ciba Geigy Ag | Verfahren zur herstellung von n-alkylierten aminoalkoholen |
DE2825961A1 (de) * | 1978-06-14 | 1980-01-03 | Basf Ag | Fungizide amine |
IL57672A (en) * | 1978-07-03 | 1983-03-31 | Lilly Co Eli | Phenethanolamines,their preparation and pharmaceutical compositions containing the same |
US4391826A (en) * | 1978-07-03 | 1983-07-05 | Eli Lilly And Company | Phenethanolamines, compositions containing the same, and method for effecting weight control |
ZA794872B (en) * | 1978-09-20 | 1980-11-26 | Schering Corp | A phenylalkylaminoethylsalicylamide,its preparation and pharmaceutical compositions containing it |
FR2436773A1 (fr) * | 1978-09-22 | 1980-04-18 | Roussel Uclaf | Nouveaux derives du 3-(aminoethyl) phenol et leurs sels, procede de preparation et application a titre de medicaments |
US4360511A (en) * | 1978-11-29 | 1982-11-23 | Medi-Physics, Inc. | Amines useful as brain imaging agents |
DD150456A5 (de) * | 1979-03-01 | 1981-09-02 | Ciba Geigy Ag | Verfahren zur herstellung von derivaten des 3-amino-1,2-propandiols |
US4338333A (en) * | 1979-06-16 | 1982-07-06 | Beecham Group Limited | Ethanamine derivatives their preparation and use in pharmaceutical compositions |
JPS603387B2 (ja) * | 1980-07-10 | 1985-01-28 | 住友化学工業株式会社 | 新規光学活性イミダゾリジン−2−オン誘導体およびその製法 |
HU183430B (en) * | 1981-05-12 | 1984-05-28 | Chinoin Gyogyszer Es Vegyeszet | Process for producing cyclodextrine inclusion complexes of n-bracket-1-phenylethyl-bracket closed-3,3-diphenylpropylamine or n-bracket-1-phenylethyl-bracket closed-3,3-diphenylpropylamine-hydrochloride |
US4591605A (en) * | 1981-11-10 | 1986-05-27 | Research Foundation Of State University Of New York | Method and ingestible formulation for inhibiting the secretion of stomach acid |
US4658060A (en) * | 1982-04-26 | 1987-04-14 | Schering Corporation | Preparation of (-)-5-(beta)-1-hydroxy-2-((beta)-1-methyl-3-phenylpropyl)aminoethyl) salicylamide |
DE3225879A1 (de) * | 1982-07-10 | 1984-01-12 | Basf Ag, 6700 Ludwigshafen | Trans-3-(4'-tert.-butylcyclohexyl-1')-2-methyl-1-dialkyl-aminopropane, ihre herstellung und verwendung als arzneimittel |
CA1258454A (en) * | 1982-08-10 | 1989-08-15 | Leo Alig | Phenethanolamines |
US4647446A (en) * | 1982-08-18 | 1987-03-03 | The Regents Of The University Of California | Rapid brain scanning radiopharmaceutical |
JPS5950358A (ja) * | 1982-09-14 | 1984-03-23 | Sumitomo Chem Co Ltd | 光学活性なカルボン酸をグラフトしたクロマトグラフ充填剤およびそれを用いる鏡像体混合物の分離法 |
US4677101A (en) * | 1983-09-26 | 1987-06-30 | Merck & Co., Inc. | Substituted dihydroazepines useful as calcium channel blockers |
US4661635A (en) * | 1983-11-21 | 1987-04-28 | Mcneilab, Inc. | Aralykyl (arylethynyl)aralkyl amines and their use as vasodilators and antihypertensives |
US5334628A (en) * | 1984-06-09 | 1994-08-02 | Kaken Pharmaceutical Co., Ltd. | Amine derivatives, processes for preparing the same and fungicides containing the same |
US4587253A (en) * | 1984-07-30 | 1986-05-06 | Merck & Co., Inc. | Bridged pyridine compounds useful as calcium channel blockers and analgesics |
US4609494A (en) * | 1985-02-21 | 1986-09-02 | Merck & Co., Inc. | 5-acetyl-3,4,5,6-tetrahydro-4-oxo-2,6-methano-2H-1,3,5-benzothiazocine(benzodiazocine)-11-carboxylates useful as calcium channel blockers |
US4839369A (en) * | 1985-04-16 | 1989-06-13 | Rorer Pharmaceutical Corporation | Aryl and heteroaryl ethers as agents for the treatment of hypersensitive ailments |
GB8522186D0 (en) * | 1985-09-06 | 1985-10-09 | Erba Farmitalia | Cycloalkyl-substituted 4-aminophenyl derivatives |
DE3541181A1 (de) * | 1985-11-21 | 1987-05-27 | Basf Ag | Propylamine, verfahren zu ihrer herstellung und ihre verwendung als fungizide |
US4675321A (en) * | 1986-02-07 | 1987-06-23 | Merck & Co., Inc. | Substituted pyrimidines useful as calcium channel blockers |
US5034514A (en) * | 1986-03-17 | 1991-07-23 | Cetus Corporation | Novel cross-linking agents |
US5030576A (en) * | 1986-04-30 | 1991-07-09 | Genentech, Inc. | Receptors for efficient determination of ligands and their antagonists or agonists |
US4808718A (en) * | 1986-05-06 | 1989-02-28 | Merck & Co., Inc. | Fused polycyclic and bridged compounds useful as calcium channel blockers |
HU200591B (en) * | 1986-07-11 | 1990-07-28 | Chinoin Gyogyszer Es Vegyeszet | Process for producing new diphenyl propylamine derivatives and pharmaceutical compositions comprising such compounds |
US4797411A (en) * | 1986-07-18 | 1989-01-10 | Farmitalia Carlo Erba S.P.A. | Cycloalkyl-substituted 4-pyridyl derivatives and use as aromatase inhibitors |
HU207280B (en) * | 1986-09-25 | 1993-03-29 | Chinoin Gyogyszer Es Vegyeszet | Process for producing new phenyl-alkyl-amines and pharmaceutical compositions containing them |
US4925664A (en) * | 1986-10-20 | 1990-05-15 | University Of Utah | Spider toxins and methods for their use as blockers of calcium channels and amino acid receptor function |
US5064657A (en) * | 1986-10-20 | 1991-11-12 | University Of Utah | Spider toxins and methods for their use as blockers of amino acid receptor function |
EP0270376B1 (de) * | 1986-12-04 | 1992-09-30 | Asahi Kasei Kogyo Kabushiki Kaisha | Vom Calcitonin-Gen abgeleitete Peptidderivate |
GB8720115D0 (en) * | 1987-08-26 | 1987-09-30 | Cooper G J S | Treatment of diabetes mellitus |
GB8709871D0 (en) * | 1987-04-27 | 1987-06-03 | Turner R C | Peptides |
US4916145A (en) * | 1987-07-10 | 1990-04-10 | Hoffmann-La Roche Inc. | Substituted n-[(pyridyl)alkyl]aryl-carboxamide |
DE68924372T2 (de) * | 1988-01-11 | 1996-05-09 | Amylin Pharmaceuticals Inc | Behandlung von diabetes mellitus typ 2. |
US5001251A (en) * | 1988-01-15 | 1991-03-19 | E. R. Squibb & Sons, Inc. | Optical resolution of DL-3-acylthio-2-methylpropanoic acid |
WO1989009834A1 (en) * | 1988-04-04 | 1989-10-19 | The Salk Institute Biotechnology/Industrial Associ | Calcium channel compositions and methods |
US5082837A (en) * | 1988-06-28 | 1992-01-21 | Merrell Dow Pharmaceuticals | Lactamimides as calcium antagonists |
US4925873A (en) * | 1988-09-01 | 1990-05-15 | E. R. Squibb & Sons, Inc. | Method of treating skin injuries using thromboxane A2 receptor antagonists |
JPH02200658A (ja) * | 1989-01-28 | 1990-08-08 | Kumiai Chem Ind Co Ltd | N―(置換)ベンジルカルボン酸アミド誘導体及び除草剤 |
US5011834A (en) * | 1989-04-14 | 1991-04-30 | State Of Oregon, Acting By And Through The Oregon State Board Of Higher Education, Acting For And On Behalf Of The Oregon Health Sciences University And The University Of Oregon | PCP receptor ligands and the use thereof |
DD298412A5 (de) * | 1989-04-28 | 1992-02-20 | ������@���Kk�� | Verfahren zur herstellung von polypeptiden, die geeignet sind als antagonisten exzitatorischer aminosaeure-neurotransmitter und/oder blocker der calciumkanaele |
EP0597830A1 (de) * | 1989-07-03 | 1994-05-25 | New York University Nyu Medical Center | Verwendung von Polyaminen als die Ionenkanäle regulierenden Wirkstoffe |
GB8915712D0 (en) * | 1989-07-08 | 1989-08-31 | Macintyre Iain | Medical treatment |
US5021599A (en) * | 1989-08-31 | 1991-06-04 | Serpentix Conveyor Corporation | Redox-responsive anion receptors |
US5053337A (en) * | 1989-10-30 | 1991-10-01 | Neurogenetic Corporation | DNA encoding an α2B -adrenergic receptor |
EP0507863A4 (en) * | 1989-12-28 | 1993-07-07 | Virginia Commonwealth University | Sigma receptor ligands and the use thereof |
JP2818958B2 (ja) * | 1990-02-23 | 1998-10-30 | 塩野義製薬株式会社 | 4―(4―アルコキシフェニル)―2―ブチルアミン誘導体およびその製造法 |
US5096908A (en) * | 1990-05-04 | 1992-03-17 | Eli Lilly And Company | Method of inhibiting gastric acid secretion |
WO1992007829A1 (en) * | 1990-11-02 | 1992-05-14 | The Upjohn Company | Indole-3-methanamines useful as anti-diabetic, anti-obesity and anti-atherosclerotic agents |
CA2099245A1 (en) * | 1991-02-08 | 1992-08-09 | Stanley M. Goldin | Substituted guanidines and derivatives thereof as modulators of neurotransmitter release and novel methodology for identifying neurotransmitter release blockers |
US5312928A (en) * | 1991-02-11 | 1994-05-17 | Cambridge Neuroscience | Calcium channel antagonists and methodology for their identification |
DE69206306T2 (de) * | 1991-04-08 | 1996-06-13 | Sumitomo Chemical Co | Optisch aktive Sekundär-Aminverbindung, Verfahren zur Herstellung einer optisch aktiven Sekundär-Aminverbindung und Verfahren zur Herstellung optisch aktiver Carbonsäure durch die Verwendung dieser Verbindung. |
CN1065857A (zh) * | 1991-04-16 | 1992-11-04 | 北京农业大学 | 光活性1,1′-联萘-2,2′-二酚的合成方法 |
US5763569A (en) * | 1991-08-23 | 1998-06-09 | The Brigham And Women's Hospital, Inc | Calcium receptor-active molecules |
US6001884A (en) * | 1991-08-23 | 1999-12-14 | Nps Pharmaceuticals, Inc. | Calcium receptor-active molecules |
JP4555401B2 (ja) * | 1991-08-23 | 2010-09-29 | エヌピーエス ファーマシューティカルズ インコーポレイテッド | カルシウム受容体に活性なアリールアルキルアミン |
DK1281702T3 (da) * | 1991-08-23 | 2006-04-18 | Nps Pharma Inc | Calciumreceptoraktive molekyler |
CA2123403C (en) * | 1991-11-12 | 2002-02-05 | Brian T. O'neill | Acyclic ethylenediamine derivatives as substance p receptor antagonists |
US5407961A (en) * | 1991-12-30 | 1995-04-18 | Janssen Pharmaceutica N.V. | α-substituted benzenemethanamine derivatives and pharmaceutical use |
AU3588693A (en) * | 1992-01-29 | 1993-09-01 | Smithkline Beecham Corporation | N-benzyloxamic acid, oxamate, and oxamide derivatives and their use as TNF and PDE IV inhibitors |
WO1994018959A1 (en) * | 1993-02-23 | 1994-09-01 | Brigham And Women's Hospital, Inc. | Calcium receptor-active molecules |
GB9326403D0 (en) * | 1993-12-24 | 1994-02-23 | Oxford Asymmetry Ltd | Improvements in or relating to chiral syntheses |
US5504253A (en) * | 1994-07-15 | 1996-04-02 | Nps Pharmaceuticals, Inc. | Amine preparation |
PT1203761E (pt) * | 1994-10-21 | 2005-04-29 | Nps Pharma Inc | Compostos activos do receptor de calcio |
US5648541A (en) * | 1995-09-28 | 1997-07-15 | Nps Pharmaceuticals, Inc. | Chiral reductions of imines leading to the syntheses of optically active amines |
DK0907631T3 (da) * | 1996-05-01 | 2003-09-22 | Nps Pharma Inc | Uorganiske ionreceptoraktive forbindelser |
-
1997
- 1997-04-30 DK DK97922601T patent/DK0907631T3/da active
- 1997-04-30 ES ES97922601T patent/ES2201300T3/es not_active Expired - Lifetime
- 1997-04-30 US US08/846,721 patent/US5981599A/en not_active Expired - Lifetime
- 1997-04-30 WO PCT/US1997/007371 patent/WO1997041090A1/en active IP Right Grant
- 1997-04-30 AT AT02018228T patent/ATE352537T1/de not_active IP Right Cessation
- 1997-04-30 ES ES07000764T patent/ES2326004T3/es not_active Expired - Lifetime
- 1997-04-30 DE DE69737303T patent/DE69737303T2/de not_active Expired - Lifetime
- 1997-04-30 DE DE69739388T patent/DE69739388D1/de not_active Expired - Lifetime
- 1997-04-30 DE DE69722934T patent/DE69722934T2/de not_active Expired - Lifetime
- 1997-04-30 PT PT97922601T patent/PT907631E/pt unknown
- 1997-04-30 JP JP53923197A patent/JP4117506B2/ja not_active Expired - Fee Related
- 1997-04-30 ES ES02018228T patent/ES2280460T3/es not_active Expired - Lifetime
- 1997-04-30 EP EP97922601A patent/EP0907631B1/de not_active Expired - Lifetime
- 1997-04-30 AT AT07000764T patent/ATE430123T1/de not_active IP Right Cessation
- 1997-04-30 AT AT97922601T patent/ATE243186T1/de active
- 1997-04-30 AU AU28229/97A patent/AU731146C/en not_active Ceased
- 1997-05-01 TW TW086105804A patent/TW561150B/zh not_active IP Right Cessation
-
1999
- 1999-10-06 US US09/415,179 patent/US6342532B1/en not_active Expired - Lifetime
-
2002
- 2002-01-29 US US10/060,959 patent/US6710088B2/en not_active Expired - Lifetime
-
2003
- 2003-05-20 HK HK03103590A patent/HK1051995A1/xx not_active IP Right Cessation
-
2007
- 2007-10-04 HK HK07110801.1A patent/HK1102806A1/xx not_active IP Right Cessation
- 2007-12-04 JP JP2007313755A patent/JP4431609B2/ja not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
US6710088B2 (en) | 2004-03-23 |
ES2280460T3 (es) | 2007-09-16 |
DE69722934D1 (de) | 2003-07-24 |
EP0907631A1 (de) | 1999-04-14 |
TW561150B (en) | 2003-11-11 |
AU731146B2 (en) | 2001-03-22 |
US20030008876A1 (en) | 2003-01-09 |
ES2201300T3 (es) | 2004-03-16 |
ATE430123T1 (de) | 2009-05-15 |
EP0907631B1 (de) | 2003-06-18 |
JP2008115184A (ja) | 2008-05-22 |
DE69722934T2 (de) | 2004-05-27 |
DK0907631T3 (da) | 2003-09-22 |
JP2000509395A (ja) | 2000-07-25 |
JP4117506B2 (ja) | 2008-07-16 |
US6342532B1 (en) | 2002-01-29 |
DE69739388D1 (de) | 2009-06-10 |
JP4431609B2 (ja) | 2010-03-17 |
DE69737303T2 (de) | 2007-08-30 |
PT907631E (pt) | 2003-10-31 |
DE69737303D1 (de) | 2007-03-15 |
AU2822997A (en) | 1997-11-19 |
ATE352537T1 (de) | 2007-02-15 |
HK1102806A1 (en) | 2007-12-07 |
US5981599A (en) | 1999-11-09 |
AU731146C (en) | 2005-02-03 |
HK1051995A1 (en) | 2003-08-29 |
WO1997041090A1 (en) | 1997-11-06 |
ES2326004T3 (es) | 2009-09-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
ATE243186T1 (de) | Verbindungen , die auf anorganische ionen- rezeptoren wirken | |
WO1996012697A3 (en) | Calcium receptor-active compounds | |
HK1012620A1 (en) | Calcium receptor-active arylalkyl amines. | |
AU6602296A (en) | Chimeric receptors and methods for identifying compounds active at metabotropic glutamate receptors and the use of such compounds in the treatment of neurological disorders and diseases | |
DK0841928T3 (da) | Sustained release-formulering af d-threo-methylphenidat | |
YU59098A (sh) | Derivati spiro-piperidina, postupak njihovog dobijanja, njihova upotreba u proizvodnji leka korisnog za lečenje ili prevenciju bolova, upalnih procesa, migrene, povraćanja i postherpetične neuralgije i farmaceutski sastav koji ih sadrži | |
FR2773075B1 (fr) | Utilisation d'activateurs de ppar-gamma en dermatologie | |
NO944578L (no) | Eksitatoriske aminosyre reseptor antagonister | |
DK1482973T3 (da) | Fremgangsmåde til modulering af CD200-receptorer | |
WO2003014321A3 (en) | Compositions and methods for modulation of darpp-32 phosphorylation | |
DK0778890T3 (da) | DNA, som koder for en human calciumkanal-alpha-1E-underenhed | |
NO994850L (no) | Farmakologiske midler | |
YU41998A (sh) | Tetrahidrobetakarbolinska jedinjenja | |
DE59910781D1 (de) | Verteiles steuerungssystem mit lagebestimmung der komponenten | |
DE69524623D1 (de) | Verwendung von cck-b rezeptor antagonisten zur behandlung von schlafstörungen | |
PT628033E (pt) | Derivados de benzodiazepina uteis como antagonistas dos receptores-cck | |
DE60033576D1 (de) | Methoden zum screening knochenmorphogenetishemimetika | |
DK1506313T3 (da) | Fremgangsmåder til screening af modulatorer af den mitokondrielle NAD-afhængige deacetylase SIRT3 | |
EP1258471A3 (de) | Verbindungen, die auf anorganische Ionen-Rezeptoren wirken | |
CA2253407A1 (en) | Inorganic ion receptor-active compounds | |
AU2003221878A8 (en) | G-protein coupled receptor ligands and methods | |
DE69714247D1 (de) | Heterozyklische verbindungen | |
ATE342055T1 (de) | Verwendung von steroidalen estrogenrezeptorantagonisten zur männlichen fertilitätskontrolle | |
ES2169161T3 (es) | Metodologia de evaluacion de deposito de la delta-endotoxina del bacillus thuringiensis. | |
TR199900672T2 (xx) | Benzotiofenlerin sentezi i�in i�lem. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
UEP | Publication of translation of european patent specification |
Ref document number: 0907631 Country of ref document: EP |