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PE20081375A1 - Derivados octahidro-pirrolo[3,4-c]pirrol como antagonistas del receptor ccr5 - Google Patents

Derivados octahidro-pirrolo[3,4-c]pirrol como antagonistas del receptor ccr5

Info

Publication number
PE20081375A1
PE20081375A1 PE2007001255A PE2007001255A PE20081375A1 PE 20081375 A1 PE20081375 A1 PE 20081375A1 PE 2007001255 A PE2007001255 A PE 2007001255A PE 2007001255 A PE2007001255 A PE 2007001255A PE 20081375 A1 PE20081375 A1 PE 20081375A1
Authority
PE
Peru
Prior art keywords
alkyl
phenyl
pirrolo
octahydro
antagonists
Prior art date
Application number
PE2007001255A
Other languages
English (en)
Inventor
Remy Lemoine
Chris Richard Melville
David Mark Rotstein
Jutta Wanner
Original Assignee
Hoffmann La Roche
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=38787632&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20081375(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of PE20081375A1 publication Critical patent/PE20081375A1/es

Links

Classifications

    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A61P31/18—Antivirals for RNA viruses for HIV
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Communicable Diseases (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Oncology (AREA)
  • Virology (AREA)
  • Molecular Biology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • AIDS & HIV (AREA)
  • Immunology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

SE REFIERE A COMPUESTOS OCTAHIDRO-PIRROLO[3,4-c]PIRROL DE FORMULA (I), EN DONDE R1 ES FENILO, PIRIDINILO, PIRIMIDILO, OPCIONALMENTE SUSTITUIDOS CON ALQUILO(C1-C6), HALOALQUILO(C1-C6), ENTRE OTROS; UNO DE R2 Y R3 ES H. Y EL OTRO ES A1, A2 O A3; O BIEN JUNTOS CON (CH2)mNR4(CH2)n; DONDE m Y n SON 1 0 2; R4 ES ALQUILO(C1-C6), HALOALQUILO(C1-C6), CH2C=N, -C(=O)R5 O -SO2R5; Ar ES FENILO OPCIONALMENTE SUSTITUIDO CON HALO, ALQUILO(C1-C6), ENTRE OTROS; R7 ES H O ALQUILO (C1-C3). SON SELECCIONADOS: 4-{2-[5-(4,6-DIMETIL-PIRIMIDINA-5-CARBONIL)-HEXAHIDRO-PIRROLO[3,4-c]PIRROL-2-IL]-ETIL}-4-FENIL-PIPERIDINA-1-CARBOXILATO DE TERT-BUTILO, (5-{2-[1-BENZOIL-4-(3-FLUOR-FENIL)-PIPERIDIN-4-IL]-ETIL}-HEXAHIDRO-PIRROLO[3,4-c]PIRROL-2-IL)-(4,6-DIMETIL-PIRIMIDIN-5-IL)-METANONA, ENTRE OTROS. TAMBIEN SE REFIERE A UNA COMPOSICION FARMACEUTICA. ESTOS COMPUESTOS SON ANTAGONISTAS DE LOS RECEPTORES CCR5 DE QUIMIOQUINA, SIENDO UTILES EN EL TRATAMIENTO Y PREVENCION DE LA INFECCION DEL VIRUS DE INMUNODEFICIENCIA (VIH)
PE2007001255A 2006-09-18 2007-09-17 Derivados octahidro-pirrolo[3,4-c]pirrol como antagonistas del receptor ccr5 PE20081375A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US84533406P 2006-09-18 2006-09-18

Publications (1)

Publication Number Publication Date
PE20081375A1 true PE20081375A1 (es) 2008-10-17

Family

ID=38787632

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2007001255A PE20081375A1 (es) 2006-09-18 2007-09-17 Derivados octahidro-pirrolo[3,4-c]pirrol como antagonistas del receptor ccr5

Country Status (13)

Country Link
US (1) US7625905B2 (es)
EP (1) EP2066674B1 (es)
JP (1) JP2010503714A (es)
CN (1) CN101516884A (es)
AR (1) AR062798A1 (es)
AT (1) ATE472549T1 (es)
CA (1) CA2662835A1 (es)
CL (1) CL2007002671A1 (es)
DE (1) DE602007007497D1 (es)
ES (1) ES2345130T3 (es)
PE (1) PE20081375A1 (es)
TW (1) TW200821311A (es)
WO (1) WO2008034731A1 (es)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2491031B1 (en) 2009-10-23 2013-08-07 Janssen Pharmaceutica N.V. Fused heterocyclic compounds as orexin receptor modulators
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
PH12012500796A1 (en) 2009-10-23 2012-11-26 Janssen Pharmaceutica Nv Disubstituted octahydropyrrolo [3,4-c] pyrroles as orexin receptor modulators
WO2012145581A1 (en) 2011-04-20 2012-10-26 Janssen Pharmaceutica Nv Disubstituted octahy-dropyrrolo [3,4-c] pyrroles as orexin receptor modulators
MY165115A (en) 2011-06-19 2018-02-28 Univ New York Leukotoxin e/d as a new anti-inflammatory agent and microbicide
SG11201607839UA (en) 2014-03-26 2016-10-28 Hoffmann La Roche Bicyclic compounds as autotaxin (atx) and lysophosphatidic acid (lpa) production inhibitors
US10214520B2 (en) 2014-07-15 2019-02-26 Gruenenthal Gmbh Substituted azaspiro(4.5)decane derivatives
TW201607923A (zh) 2014-07-15 2016-03-01 歌林達有限公司 被取代之氮螺環（４．５）癸烷衍生物
KR20180043837A (ko) 2015-09-04 2018-04-30 에프. 호프만-라 로슈 아게 페녹시메틸 유도체
KR102448342B1 (ko) 2016-03-10 2022-09-27 얀센 파마슈티카 엔.브이. 오렉신-2 수용체 길항제를 사용한 우울증의 치료 방법
JP7090099B2 (ja) 2017-03-16 2022-06-23 エフ．ホフマン－ラ ロシュ アーゲー Ａｔｘインヒビターとしての新規二環式化合物
US11629196B2 (en) 2020-04-27 2023-04-18 Incelldx, Inc. Method of treating SARS-CoV-2-associated hypercytokinemia by administering a human monoclonal antibody (PRO-140) that inhibits CCR5/CCL5 binding interactions

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002070523A1 (en) * 2001-03-07 2002-09-12 Pfizer Products Inc. Modulators of chemokine receptor activity
AU2003296992A1 (en) * 2002-12-13 2004-07-09 Smithkline Beecham Corporation Pyrrolidine and azetidine compounds as ccr5 antagonists
JP2006511554A (ja) * 2002-12-13 2006-04-06 スミスクライン ビーチャム コーポレーション Ｃｃｒ５アンタゴニストとしてのピペリジン誘導体
EP1776362A1 (en) * 2003-07-18 2007-04-25 Virochem Pharma Inc. Spiro compounds and methods for the modulation of chemokine receptor activity
JP2007500694A (ja) 2003-07-31 2007-01-18 アストラゼネカ・アクチエボラーグ Ｃｃｒ５受容体モジュレーターとしてのピペリジン誘導体
TW200610761A (en) * 2004-04-23 2006-04-01 Astrazeneca Ab Chemical compounds
RU2006146608A (ru) * 2004-06-09 2008-07-20 Ф.Хоффманн-Ля Рош Аг (Ch) ОКТАГИДРОПИРРОЛО[3,4-с]-ПРОИЗВОДНЫЕ И ИХ ПРИМЕНЕНИЕ В КАЧЕСТВЕ ПРОТИВОВИРУСНЫХ АГЕНТОВ
SE0401657D0 (sv) 2004-06-24 2004-06-24 Astrazeneca Ab Chemical compounds
SE0403106D0 (sv) 2004-12-20 2004-12-20 Astrazeneca Ab Chemical compounds
JP2009526803A (ja) 2006-02-15 2009-07-23 エフ．ホフマン−ラ ロシュ アーゲー ヘテロ二環式抗ウイルス化合物
AU2007214602A1 (en) 2006-02-15 2007-08-23 F. Hoffmann-La Roche Ag Heterocyclic antiviral compounds

Also Published As

Publication number Publication date
US20080103125A1 (en) 2008-05-01
CA2662835A1 (en) 2008-03-27
JP2010503714A (ja) 2010-02-04
EP2066674B1 (en) 2010-06-30
DE602007007497D1 (de) 2010-08-12
CL2007002671A1 (es) 2008-04-18
ES2345130T3 (es) 2010-09-15
ATE472549T1 (de) 2010-07-15
TW200821311A (en) 2008-05-16
CN101516884A (zh) 2009-08-26
WO2008034731A1 (en) 2008-03-27
US7625905B2 (en) 2009-12-01
AR062798A1 (es) 2008-12-03
EP2066674A1 (en) 2009-06-10

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