AR057188A1 - 3-amino-2-arilpropil azaindoles y usos de los mismos - Google Patents
3-amino-2-arilpropil azaindoles y usos de los mismosInfo
- Publication number
- AR057188A1 AR057188A1 ARP060105231A ARP060105231A AR057188A1 AR 057188 A1 AR057188 A1 AR 057188A1 AR P060105231 A ARP060105231 A AR P060105231A AR P060105231 A ARP060105231 A AR P060105231A AR 057188 A1 AR057188 A1 AR 057188A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- optionally substituted
- pyrrolopyridin
- pyrrolopyrimidin
- oxide
- 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
- A61K31/435—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
- A61K31/437—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 nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
-
- 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
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- 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
- A61P13/10—Drugs for disorders of the urinary system of the bladder
-
- 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- 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
- A61P25/08—Antiepileptics; Anticonvulsants
-
- 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
-
- 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
- A61P25/22—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
- 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
- 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
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- 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
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- 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
-
- 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
-
- 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
- C07D487/12—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 three hetero rings
- C07D487/14—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (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)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Diabetes (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Urology & Nephrology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Psychology (AREA)
- Child & Adolescent Psychology (AREA)
- Hospice & Palliative Care (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Steroid Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
También se aportan composiciones farmacéuticas, métodos de utilizacion y métodos de preparacion de los compuestos. Reivindicacion 1: Un compuesto de formula (1) o una sal farmacéuticamente aceptable de los mismos, en la que p es 1 o 2; Ar es: pirrolopiridinilo seleccionado del grupo formado por pirrolopiridin-1-ilo, pirrolopiridin-2-ilo y pirrolopiridin-3-ilo, cada uno de los cuales puede ser opcionalmente sustituido; N-oxido de pirrolopiridinilo seleccionado del grupo formado por N- oxido de pirrolopiridin-1-ilo, N-oxido de pirrolopiridin-12ilo y N-oxido de pirrolopiridin-3-ilo, cada uno de los cuales puede ser opcionalmente sustituido; o pirrolopirimidinilo seleccionado del grupo formado por: pirrolopirimidin-5-ilo, pirrolopirimidin-6-ilo y pirrolopirimidin-7-ilo, cada uno de los cuales puede ser opcionalmente sustituido; R1 es: (a) arilo seleccionado de entre fenilo y naftilo, cada uno opcionalmente sustituido; o (b) heteroarilo seleccionado de entre indolilo, piridinilo, tienilo, furanilo, pirimidinilo, piridazinilo, pirazinilo, oxazolilo, tiazolilo, isoxazolilo, isotiazolilo, imidazolilo, pirazolilo, quinolinilo e isoquinolinilo, cada uno opcionalmente sustituido; (c) arilalquilo opcionalmente sustituido; (d) heteroarilalquilo opcionalmente sustituido; (e) cicloalquilo; (f) cicloalquilmetilo; o (g) alquilo ramificado; R2 es: (a) H; (b) alquilo; (c) hidroxialquilo; (d) alcoxialquilo; fluoro; o alquilo; Rb es H, alquilo, hidroxi, alcoxi, fluoro, o hidroxialquilo; o uno de R2 y R3 junto con uno de Ra y Rb y los átomos a los que están unidos pueden constituir un anillo de 5 o 6 miembros que opcionalmente incluye un heteroátomo adicional seleccionado de entre O, N y S; Rc y Rd son cada uno de forma independiente: H o alquilo; o Rc y Rd juntos forman =O, =S, o =NRf, en el que Rf es H, alquilo, o -ORg, en el que Rg es H o alquilo; o uno de R2 y R3 junto con uno de Rc y Rd junto con los átomos a los que están unidos pueden constituir un anillo de 4 a 6 miembros que de forma opcional incluye un heteroátomo adicional seleccionado de entre O, N y s; y Re es H o alquilo.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US74127205P | 2005-11-30 | 2005-11-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR057188A1 true AR057188A1 (es) | 2007-11-21 |
Family
ID=37667384
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP060105231A AR057188A1 (es) | 2005-11-30 | 2006-11-28 | 3-amino-2-arilpropil azaindoles y usos de los mismos |
Country Status (17)
Country | Link |
---|---|
US (2) | US7638517B2 (es) |
EP (1) | EP1957488B1 (es) |
JP (1) | JP2009517432A (es) |
KR (1) | KR101026570B1 (es) |
CN (1) | CN101321752A (es) |
AR (1) | AR057188A1 (es) |
AT (1) | ATE442368T1 (es) |
AU (1) | AU2006319233B9 (es) |
BR (1) | BRPI0619184A2 (es) |
CA (1) | CA2632284A1 (es) |
DE (1) | DE602006009138D1 (es) |
ES (1) | ES2329413T3 (es) |
NO (1) | NO20082112L (es) |
RU (1) | RU2008120141A (es) |
TW (1) | TW200804376A (es) |
WO (1) | WO2007062998A1 (es) |
ZA (1) | ZA200804299B (es) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2912744B1 (fr) * | 2007-02-16 | 2012-09-07 | Centre Nat Rech Scient | Composes pyrrolo°2,3-b!pyridine,composes azaindoles utiles dans la synthese de ces composes pyrrolo°2,3-b!pyridine, leurs procedes de fabrication et leurs utilisations. |
US7871802B2 (en) * | 2007-10-31 | 2011-01-18 | E.I. Du Pont De Nemours And Company | Process for enzymatically converting glycolonitrile to glycolic acid |
CN102026988B (zh) * | 2008-06-05 | 2013-07-03 | 爱思开生物制药株式会社 | 3-取代的丙胺化合物 |
US8101642B2 (en) * | 2008-06-05 | 2012-01-24 | Sk Biopharmaceuticals Co., Ltd. | 3-substituted propanamine compounds |
WO2010059771A1 (en) | 2008-11-20 | 2010-05-27 | Osi Pharmaceuticals, Inc. | Substituted pyrrolo[2,3-b]-pyridines and-pyrazines |
US8222416B2 (en) * | 2009-12-14 | 2012-07-17 | Hoffmann-La Roche Inc. | Azaindole glucokinase activators |
WO2011143646A1 (en) * | 2010-05-14 | 2011-11-17 | OSI Pharmaceuticals, LLC | Fused bicyclic kinase inhibitors |
AR081039A1 (es) | 2010-05-14 | 2012-05-30 | Osi Pharmaceuticals Llc | Inhibidores biciclicos fusionados de quinasa |
US20140088114A1 (en) | 2011-05-16 | 2014-03-27 | OSI Pharmaceuticals ,LLC | Fused bicyclic kinase inhibitors |
AR098436A1 (es) * | 2013-11-19 | 2016-05-26 | Actelion Pharmaceuticals Ltd | Compuestos tricíclicos de piperidina |
CN108034283B (zh) * | 2017-12-15 | 2020-10-13 | 淮海工学院 | 一种聚乙二醇化苯并吲哚七甲川菁染料及其制备方法和应用 |
WO2020160174A1 (en) * | 2019-01-29 | 2020-08-06 | Universita Degli Studi Di Padova | Uses of compounds having anti-hsv-1 activity |
Family Cites Families (47)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE849108C (de) | 1948-10-01 | 1952-09-11 | Hoechst Ag | Verfahren zur Herstellung von 1-disubstituierten 3-Aminopropanen |
GB705652A (en) | 1948-10-01 | 1954-03-17 | Farbewerke Hoechst Ag | Manufacture of 3-aminopropane compounds |
NL82464C (es) | 1952-01-05 | |||
US2708197A (en) | 1952-05-24 | 1955-05-10 | Upjohn Co | Preparation of (hydroxy-3-indole)-alkylamines |
US2984670A (en) | 1959-05-22 | 1961-05-16 | Upjohn Co | Novel 3-(1-hydroxy-1-phenyl-3-aminopropyl) indoles |
GB992731A (en) | 1962-09-28 | 1965-05-19 | Koninklijke Pharma Fab Nv | Aminoalkyl-indolyl-benzyl alcohols |
US4616080A (en) | 1984-07-02 | 1986-10-07 | Eli Lilly And Company | Simplified process of forming crystalline ceftazidime pentahydrate |
US4956388A (en) * | 1986-12-22 | 1990-09-11 | Eli Lilly And Company | 3-aryloxy-3-substituted propanamines |
KR880007433A (ko) * | 1986-12-22 | 1988-08-27 | 메리 앤 터커 | 3-아릴옥시-3-치환된 프로판아민 |
JP2779240B2 (ja) * | 1987-12-11 | 1998-07-23 | 三井化学株式会社 | 新規アミン類およびその用途 |
JPH0314562A (ja) | 1988-04-11 | 1991-01-23 | Nippon Chemiphar Co Ltd | 新規なアルキレンジアミン誘導体およびグルタミン酸遮断剤 |
US4902710A (en) * | 1988-12-14 | 1990-02-20 | Eli Lilly And Company | Serotonin and norepinephrine uptake inhibitors |
FR2674522B1 (fr) | 1991-03-26 | 1993-07-16 | Lipha | Nouveaux derives de l'indole, procedes de preparation et medicaments les contenant. |
US5177088A (en) | 1991-04-17 | 1993-01-05 | Hoechst-Roussel Pharmaceuticals Incorporated | Substituted 3-(pyridinylamino)-indoles |
US5185350A (en) | 1991-09-23 | 1993-02-09 | Hoechst-Roussel Pharmaceuticals Incorporated | Substituted pyridinylamino-1h-indoles,1h-indazoles,2h-indazoles, benzo (b)thiophenes and 1,2-benzisothiazoles |
EP0600830A1 (de) | 1992-11-27 | 1994-06-08 | Ciba-Geigy Ag | Substituierte Derivate von Diaminophthalimid als Protein-Tyrosin-Kinase-Hemmer |
GB9225141D0 (en) | 1992-12-01 | 1993-01-20 | Smithkline Beecham Corp | Chemical compounds |
GB9518552D0 (en) | 1995-09-11 | 1995-11-08 | Fujisawa Pharmaceutical Co | New heterocyclic compounds |
GB9523948D0 (en) | 1995-11-23 | 1996-01-24 | Univ East Anglia | Process for preparing n-benzyl indoles |
JPH09176162A (ja) | 1995-12-22 | 1997-07-08 | Toubishi Yakuhin Kogyo Kk | チアゾリジンジオン誘導体及びその製造法並びにそれを含む医薬組成物 |
CA2256492C (en) | 1996-05-20 | 2006-04-04 | Teijin Limited | Diarylalkyl cyclic diamine derivatives as chemokine receptor antagonists |
EP0912494A1 (en) | 1996-06-07 | 1999-05-06 | Nps Pharmaceuticals, Inc. | Coumpounds active at a novel site on receptor-operated calcium channels useful for treatment of neurological disorders and diseases |
SE9701144D0 (sv) | 1997-03-27 | 1997-03-27 | Pharmacia & Upjohn Ab | Novel compounds, their use and preparation |
EP0887348A1 (en) | 1997-06-25 | 1998-12-30 | Boehringer Mannheim Italia S.p.A. | Bis-Indole derivatives having antimetastatic activity, a process for their preparation and pharmaceutical compositions containing them |
AU744939B2 (en) | 1997-09-26 | 2002-03-07 | Merck & Co., Inc. | Novel angiogenesis inhibitors |
EP1027046A4 (en) | 1997-10-28 | 2002-04-03 | Merck & Co Inc | GONADOTROPIN RELEASING HORMON ANTAGONISTS |
JP2001520997A (ja) | 1997-10-28 | 2001-11-06 | メルク エンド カムパニー インコーポレーテッド | 性腺刺激ホルモン放出ホルモン拮抗薬 |
FR2780890B3 (fr) | 1998-07-10 | 2000-09-01 | Sanofi Sa | Utilisation d'une composition pharmaceutique contenant, en association, un antagoniste des recepteurs at1 de l'angiotensine ii et l'indomethacine pour le traitement des glomerulonephrites chroniques |
DE69935331T2 (de) | 1998-07-13 | 2007-10-31 | NPS Pharmaceuticals, Inc., Salt Lake City | Verfahren und verbindungen zur behandlung der depression |
SE9903998D0 (sv) | 1999-11-03 | 1999-11-03 | Astra Ab | New compounds |
FR2814073B1 (fr) | 2000-09-21 | 2005-06-24 | Yang Ji Chemical Company Ltd | Composition pharmaceutique antifongique et/ou antiparasitaire et nouveaux derives de l'indole a titre de principes actifs d'une telle composition |
CN1235583C (zh) | 2001-03-05 | 2006-01-11 | 特兰斯泰克制药公司 | 用作治疗剂的苯并咪唑衍生物 |
GB0112122D0 (en) * | 2001-05-18 | 2001-07-11 | Lilly Co Eli | Heteroaryloxy 3-substituted propanamines |
EP1448557A4 (en) | 2001-10-26 | 2005-02-02 | Univ Connecticut | HETEROINDANE: A NEW CLASS OF HIGH-ACTIVITY CANNABIMIMETIC LIGANDS |
AU2002347022A1 (en) | 2001-12-20 | 2003-07-09 | Novo Nordisk A/S | Benzimidazols and indols as glucagon receptor antagonists/inverse agonisten |
AU2002360819A1 (en) | 2001-12-28 | 2003-07-24 | Bayer Corporation | Cyclohexano- and cycloheptapyrazole derivative compounds, for use in diseases associated with the 5-ht2c receptor |
US7244847B2 (en) | 2002-02-06 | 2007-07-17 | Isis Pharmaceuticals, Inc. | Benzimidazole compounds |
EP1496838B1 (en) * | 2002-03-12 | 2010-11-03 | Merck Sharp & Dohme Corp. | Substituted amides |
EP1494997A4 (en) * | 2002-04-05 | 2007-04-11 | Merck & Co Inc | SUBSTITUTED ARYLAMID |
US7667053B2 (en) * | 2002-04-12 | 2010-02-23 | Merck & Co., Inc. | Bicyclic amides |
MXPA05011841A (es) * | 2003-05-09 | 2006-01-26 | Hoffmann La Roche | Metil-indoles y metil-pirrolopiridinas como agonistas adrenergicos de alfa-1. |
WO2005005439A1 (en) | 2003-07-09 | 2005-01-20 | Suven Life Sciences Limited | Benzothiazino indoles |
EP1663113A4 (en) * | 2003-09-18 | 2007-06-13 | Merck & Co Inc | SUBSTITUTED SULFONAMIDES |
CN1871208A (zh) * | 2003-10-30 | 2006-11-29 | 默克公司 | 作为大麻素受体调节剂的芳烷基胺 |
US7517899B2 (en) * | 2004-03-30 | 2009-04-14 | Wyeth | Phenylaminopropanol derivatives and methods of their use |
NZ551292A (en) * | 2004-06-01 | 2009-11-27 | Hoffmann La Roche | 3-Amino-1-arylpropyl indoles as monoamine reuptake inhibitor |
JP2009510066A (ja) * | 2005-09-29 | 2009-03-12 | ワイス | 血管運動症状(vms)の治療のためのモノアミン再取り込みのモジュレータである1−(1h−インドール−1−イル)−3−(メチルアミノ)−1−フェニルプロパン−2−オール誘導体および関連の化合物 |
-
2006
- 2006-11-20 CN CNA2006800451404A patent/CN101321752A/zh active Pending
- 2006-11-20 KR KR1020087012919A patent/KR101026570B1/ko not_active IP Right Cessation
- 2006-11-20 ES ES06819602T patent/ES2329413T3/es active Active
- 2006-11-20 CA CA002632284A patent/CA2632284A1/en not_active Abandoned
- 2006-11-20 WO PCT/EP2006/068650 patent/WO2007062998A1/en active Application Filing
- 2006-11-20 AT AT06819602T patent/ATE442368T1/de active
- 2006-11-20 DE DE602006009138T patent/DE602006009138D1/de active Active
- 2006-11-20 AU AU2006319233A patent/AU2006319233B9/en not_active Ceased
- 2006-11-20 JP JP2008542715A patent/JP2009517432A/ja active Pending
- 2006-11-20 EP EP06819602A patent/EP1957488B1/en not_active Not-in-force
- 2006-11-20 BR BRPI0619184-3A patent/BRPI0619184A2/pt not_active IP Right Cessation
- 2006-11-20 RU RU2008120141/04A patent/RU2008120141A/ru not_active Application Discontinuation
- 2006-11-28 TW TW095143987A patent/TW200804376A/zh unknown
- 2006-11-28 AR ARP060105231A patent/AR057188A1/es unknown
- 2006-11-29 US US11/605,729 patent/US7638517B2/en not_active Expired - Fee Related
-
2008
- 2008-05-06 NO NO20082112A patent/NO20082112L/no not_active Application Discontinuation
- 2008-05-19 ZA ZA200804299A patent/ZA200804299B/xx unknown
-
2009
- 2009-11-16 US US12/619,275 patent/US20100056499A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
DE602006009138D1 (de) | 2009-10-22 |
ATE442368T1 (de) | 2009-09-15 |
BRPI0619184A2 (pt) | 2011-09-13 |
KR101026570B1 (ko) | 2011-03-31 |
TW200804376A (en) | 2008-01-16 |
KR20080064192A (ko) | 2008-07-08 |
RU2008120141A (ru) | 2010-01-10 |
AU2006319233B2 (en) | 2011-06-02 |
US7638517B2 (en) | 2009-12-29 |
CN101321752A (zh) | 2008-12-10 |
CA2632284A1 (en) | 2007-06-07 |
ES2329413T3 (es) | 2009-11-25 |
ZA200804299B (en) | 2009-04-29 |
EP1957488B1 (en) | 2009-09-09 |
AU2006319233A1 (en) | 2007-06-07 |
WO2007062998A1 (en) | 2007-06-07 |
US20070123535A1 (en) | 2007-05-31 |
JP2009517432A (ja) | 2009-04-30 |
EP1957488A1 (en) | 2008-08-20 |
NO20082112L (no) | 2008-06-23 |
US20100056499A1 (en) | 2010-03-04 |
AU2006319233B9 (en) | 2011-09-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AR057188A1 (es) | 3-amino-2-arilpropil azaindoles y usos de los mismos | |
PE20220143A1 (es) | Agonistas de glp-1r y usos de los mismos | |
JP6073677B2 (ja) | 縮合複素環式化合物およびそれらの使用 | |
BR112019012957A2 (pt) | derivados de tetra-hidroimidazo[4,5-c]piridina como indutores de internalização de pd-l1 | |
AR080754A1 (es) | Derivados de imidazo (1,2-a) pirazina y su uso como inhibidores de pde10 | |
AR078841A1 (es) | Derivados de imidazo(1,2-b) piridazina y su uso como inhibidores de pde10 | |
ES2292130T3 (es) | Pirido(2,3-d)pirimidin-7-onas pirrolil-sustituidas y derivados de las mismas como agentes terapeuticos. | |
ES2320955B1 (es) | Nuevos derivados de 3-((1,2,4)triazolo(4,3-a)piridin-7-il)benzamida. | |
HRP20230595T1 (hr) | Inhibitori lizina specifične demetilaze-1 | |
HRP20201469T1 (hr) | Derivati tetrahidroizokinolina | |
HRP20190604T1 (hr) | Supstituirani spojevi dihidroizokinolinona | |
ES2661510T3 (es) | Uso de inhibidores de la actividad o función de PI3K | |
PE20190653A1 (es) | Nuevos derivados de pirrol, su procedimiento de preparacion y las composiciones farmaceuticas que los contienen | |
JP2010506850A5 (es) | ||
AR060537A1 (es) | 1,2,4-triazoles trisustituidos | |
AR044940A1 (es) | Compuestos heterociclicos y su uso como moduladores de gamma opioides | |
AR092684A1 (es) | Compuestos de sulfonamida sustituidos | |
JP2016512834A5 (es) | ||
HRP20212021T1 (hr) | 4-IMIDAZOPIRIDAZIN-1-iL-BENZAMIDI I 4-IMIDAZOTRIAZIN-1-IL-BENZAMIDI KAO INHIBITORI BTK | |
JP2008525498A5 (es) | ||
AR040047A1 (es) | 1-(aminoalquil)-3-sulfonilazaindoles como ligandos de la 5-hidroxitriptamina-6 | |
KR20130006664A (ko) | 인다졸 화합물 및 그의 용도 | |
AR119018A1 (es) | Inhibidores de proteína quinasas dependientes de adn | |
PE20171057A1 (es) | Derivados espirodiamina como inhibidores de la aldosterona sintasa | |
AR073687A1 (es) | Agonistas de receptores cb2, derivados de oxazoles y/o triazoles, composiciones farmaceuticas que los contienen y uso de los mismos en el tratamiento del dolor, enfermedades autoinmunes y alergicas, entre otras. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FB | Suspension of granting procedure |