[go: up one dir, main page]

AR097279A1 - Derivados de benzimidazolil-metil urea como agonistas del receptor de alx - Google Patents

Derivados de benzimidazolil-metil urea como agonistas del receptor de alx

Info

Publication number
AR097279A1
AR097279A1 ARP140102978A ARP140102978A AR097279A1 AR 097279 A1 AR097279 A1 AR 097279A1 AR P140102978 A ARP140102978 A AR P140102978A AR P140102978 A ARP140102978 A AR P140102978A AR 097279 A1 AR097279 A1 AR 097279A1
Authority
AR
Argentina
Prior art keywords
group
alkyl
substituted once
unsubstituted
monocyclic
Prior art date
Application number
ARP140102978A
Other languages
English (en)
Original Assignee
Actelion Pharmaceuticals Ltd
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
Application filed by Actelion Pharmaceuticals Ltd filed Critical Actelion Pharmaceuticals Ltd
Publication of AR097279A1 publication Critical patent/AR097279A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D235/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/06Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
    • C07D235/14Radicals substituted by nitrogen atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/08Bronchodilators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D235/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/06Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
    • C07D235/16Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D453/00Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
    • C07D453/02Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pulmonology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Virology (AREA)
  • Biomedical Technology (AREA)
  • Immunology (AREA)
  • Oncology (AREA)
  • Pain & Pain Management (AREA)
  • Communicable Diseases (AREA)
  • Molecular Biology (AREA)
  • Hospice & Palliative Care (AREA)
  • Rheumatology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Cardiology (AREA)
  • AIDS & HIV (AREA)
  • Psychiatry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Epidemiology (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

Reivindicación 1: Un compuesto de fórmula (1) donde n representa 0, 1, 2, 3, ó 4; D representa =N- o =C(R⁵)-; E representa =N- o =C(R⁴A)-; R⁹ representa alquilo C₁₋₄ o halógeno; R¹ representa alquilo C₁₋₄, alcoxi C₁₋₄, fluoroalquilo C₁₋₄, fluoroalcoxi C₁₋₄, ciano o halógeno; R² y R³ representan independientemente uno del otro hidrógeno o metilo; o R² y R³ forman, junto con el átomo de carbono al cual están unidos, un anillo cicloalquilo C₃₋₅ monocíclico; R⁴ y R⁴A representan independientemente uno del otro hidrógeno, alquilo C₁₋₄, alcoxi C₁₋₄, fluoroalquilo C₁₋₄, ciano, nitro o halógeno; R⁵ representa hidrógeno o halógeno; R⁶ representa hidrógeno o metilo; R⁷ representa hidrógeno, alquilo C₁₋₄ o hidroxi-alquilo C₁₋₄; R⁸ representa un grupo cicloalquilo C₃₋₈ mono- o bicíclico, dicho grupo está sin sustituir o está sustituido uno o dos veces, donde los sustituyentes son independientemente seleccionados del grupo que consiste en alquilo C₁₋₄, alcoxi C₁₋₄, hidroxi, hidroxi-alquilo C₁₋₄, halógeno, -COR¹⁰, y fenilo el cual está sin sustituir o está sustituido una o dos veces con alquilo C₁₋₄, fluoroalquilo C₁₋₄, halógeno, o -COOR¹¹; un grupo heterociclilo mono- o bicíclico, dicho grupo está sin sustituir; sustituido una vez en un átomo de nitrógeno con alquilo C₁₋₄, fluoroalquilo C₁₋₄, alquil C₁₋₄-carbonilo, alquil C₁₋₄-sulfonilo, fenil-alquilo C₁₋₄, cicloalquilo C₃₋₆ monocíclico o -COOR¹¹; sustituido una o dos veces en un átomo de carbono con flúor o oxo; o sustituido una, dos, tres, cuatro o cinco veces con metilo; un grupo cicloalquenilo C₅₋₆ monocíclico; un grupo arilo bicíclico parcialmente saturado o un grupo heteroarilo bicíclico parcialmente saturado, dichos grupos están independientemente sin sustituir o sustituidos una o dos veces, donde los sustituyentes son independientemente seleccionados del grupo que consiste en alcoxi C₁₋₄ y hidroxi; un grupo fenilo donde dicho grupo está sin sustituir o sustituido una vez con alcoxi C₁₋₄; un grupo heteroarilo monocíclico donde dicho grupo está sin sustituir o sustituido una o dos veces, donde los sustituyentes son independientemente seleccionados del grupo que consiste en alquilo C₁₋₄, cicloalquilo C₃₋₆ monocíclico, heteroarilo, bencilo y fenilo monocíclicos sin sustituir, donde el fenilo está sin sustituir o sustituido una o dos veces, donde los sustituyentes son independientemente seleccionados del grupo que consiste en alquilo C₁₋₄, alcoxi C₁₋₄, fluoroalcoxi C₁₋₄ y halógeno; un grupo alquilo C₄₋₆; o un grupo alquilo C₁₋₄ el cual está sustituido una vez con un sustituyente seleccionado del grupo X; sustituido una vez con un sustituyente seleccionado del grupo Y; sustituido dos veces con un sustituyente seleccionado del grupo X y un sustituyente seleccionado del grupo Y; o sustituido dos veces con un grupo heterociclilo monocíclico y un sustituyente seleccionado del grupo Y; donde X representa alcoxi C₁₋₄, fluoroalquilo C₁₋₄, ciano, hidroxi, dimetilamino, -COOR¹¹ o -CONH₂; Y representa un grupo cicloalquilo C₃₋₆ monocíclico, dicho grupo está sin sustituir o sustituido una vez con hidroxi o fenilo; un grupo heterociclilo monocíclico, dicho grupo está sin sustituir o está sustituido una vez en un átomo de nitrógeno con alquilo C₁₋₄, alquil C₁₋₄-carbonilo o -COOR¹¹; un grupo arilo bicíclico parcialmente saturado o un grupo heteroarilo bicíclico parcialmente saturado; un grupo arilo donde dicho grupo está sin sustituir o sustituido una, dos o tres veces, donde los sustituyentes son independientemente seleccionados del grupo que consiste en alquilo C₁₋₄, alcoxi C₁₋₄, alcoxi C₁₋₃-alquilo C₁₋₂, heterociclilo monocíclico-alquilo C₁₋₂, heteroarilo monocíclico -alquilo C₁₋₂, fluoroalquilo C₁₋₄, fluoroalcoxi C₁₋₄, ciano, halógeno, -COOR¹¹ y bis-(alquil C₁₋₂)-amino-alquilo C₁₋₂; o un grupo benzo[d][1,3]dioxolilo; o un grupo heteroarilo donde dicho grupo está sin sustituir o sustituido una o dos veces, donde los sustituyentes son independientemente seleccionados del grupo que consiste en alquilo C₁₋₄, cicloalquilo C₃₋₆ monocíclico, alcoxi C₁₋₄, fluoroalquilo C₁₋₄, fluoroalcoxi C₁₋₄, fluoroalcoxi C₁₋₄-alquilo C₁₋₂, halógeno, heterociclilo monocíclico y fenilo el cual está sin sustituir o sustituido una vez con alcoxi C₁₋₄; o R⁷ y R⁸ forman, junto con el átomo de nitrógeno al cual están unidos, un grupo heterociclilo mono- o bicíclico, dicho grupo está sin sustituir; o sustituido una vez en un átomo de nitrógeno con alquilo C₁₋₄, alquil C₁₋₄-carbonilo o -COOR¹¹; R¹⁰ representa hidroxi, alcoxi C₁₋₄ o amino; y R¹¹ representa alquilo C₁₋₄; o una sal de dicho compuesto.
ARP140102978A 2013-08-09 2014-08-07 Derivados de benzimidazolil-metil urea como agonistas del receptor de alx AR097279A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IB2013056530 2013-08-09

Publications (1)

Publication Number Publication Date
AR097279A1 true AR097279A1 (es) 2016-03-02

Family

ID=51688366

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP140102978A AR097279A1 (es) 2013-08-09 2014-08-07 Derivados de benzimidazolil-metil urea como agonistas del receptor de alx

Country Status (14)

Country Link
US (1) US9663473B2 (es)
EP (1) EP3030560B1 (es)
JP (1) JP6387411B2 (es)
KR (1) KR20160042019A (es)
CN (1) CN105473575B (es)
AR (1) AR097279A1 (es)
AU (1) AU2014304046B2 (es)
BR (1) BR112016002459A8 (es)
CA (1) CA2917954A1 (es)
ES (1) ES2641172T3 (es)
MX (1) MX2016001788A (es)
RU (1) RU2016107974A (es)
TW (1) TW201536756A (es)
WO (1) WO2015019325A1 (es)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR096686A1 (es) 2013-06-25 2016-01-27 Actelion Pharmaceuticals Ltd Derivados de espiro[2.4]heptano puenteados sustituidos con difluoroetil-oxazol como agonistas del receptor de alx
ES2639798T3 (es) 2013-07-18 2017-10-30 Idorsia Pharmaceuticals Ltd Derivados de espiro[2.4]heptano con puente sustituidos con piperazina como agonistas del receptor ALX
ES2752733T3 (es) 2013-11-28 2020-04-06 Kyorin Seiyaku Kk Derivados de urea deuterados o marcados isotópicamente o sales farmacológicamente aceptables de los mismos útiles como agonistas de FPRL-1
WO2016189877A1 (en) 2015-05-27 2016-12-01 Kyorin Pharmaceutical Co., Ltd. Urea derivative or pharmacologically acceptable salt thereof
JP6746613B2 (ja) 2015-05-27 2020-08-26 杏林製薬株式会社 ウレア誘導体、またはその薬理学的に許容される塩
ES3039644T3 (en) * 2015-10-23 2025-10-23 Vifor Int Ag Novel ferroportin inhibitors
WO2017087318A1 (en) * 2015-11-20 2017-05-26 Mingsight Pharmaceuticals, Inc. Treatment of autoimmune disease
KR20190068537A (ko) 2016-09-18 2019-06-18 에이치 리 모피트 캔서 센터 앤드 리서어치 인스티튜트 아이엔씨 Yap1과 oct4의 상호작용을 표적으로 하는 yap1 저해제
JOP20180036A1 (ar) 2017-04-18 2019-01-30 Vifor Int Ag أملاح لمثبطات فروبورتين جديدة
US20210147405A1 (en) * 2017-06-14 2021-05-20 European Molecular Biology Laboratory Bicyclic heteroaromatic urea or carbamate compounds for use in therapy
CN108003048A (zh) * 2017-12-07 2018-05-08 滨海吉尔多肽有限公司 一种o-甲基-苏/酪氨酸的制备方法
CN111868052B (zh) 2018-03-05 2024-03-08 百时美施贵宝公司 苯基吡咯烷酮甲酰肽2受体激动剂
PE20211450A1 (es) 2018-03-14 2021-08-05 H Lee Moffitt Cancer Ct & Res Inhibidores de yap1 que dirigen la interaccion de yap1 con oct4
EP3870169A4 (en) * 2018-10-23 2022-06-29 The Brigham and Women's Hospital, Inc. Lipoxin a4 analogs and uses thereof
CN112341451B (zh) * 2019-08-09 2022-06-17 成都先导药物开发股份有限公司 一种免疫调节剂
CN112341450B (zh) * 2019-08-09 2022-05-17 成都先导药物开发股份有限公司 一种免疫调节剂
CN114644577B (zh) * 2020-12-18 2023-06-27 新发药业有限公司 一种取代异腈化合物的环保制备方法
WO2024121709A1 (en) 2022-12-09 2024-06-13 Pfizer Inc. Papain-like protease (plpro) inhibitors

Family Cites Families (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4407746A (en) 1981-12-14 1983-10-04 G. D. Searle & Co. Cyclohexyl and phenyl substituted enkephalins
RU2106592C1 (ru) 1996-07-12 1998-03-10 Слипченко Николай Николаевич Подводный спортивный пистолет
WO1998027108A2 (en) * 1996-12-16 1998-06-25 Fujisawa Pharmaceutical Co., Ltd. New amide compounds and their use as nitric oxide synthase inhibitors
WO1999038867A1 (en) 1998-01-29 1999-08-05 Suntory Limited 1-cycloalkyl-1,8-naphthyridin-4-one derivatives with phosphodiesterase iv inhibitory activity
US7087632B2 (en) 2001-03-05 2006-08-08 Transtech Pharma, Inc. Benzimidazole derivatives as therapeutic agents
FR2822827B1 (fr) 2001-03-28 2003-05-16 Sanofi Synthelabo Nouveaux derives de n-(arylsulfonyl) beta-aminoacides comportant un groupe aminomethyle substitue, leur procede de preparation et les compositions pharmaceutiques en contenant
DE10211770A1 (de) 2002-03-14 2003-10-02 Boehringer Ingelheim Pharma Neue substituierte Piperidine, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung
US20050164305A1 (en) 2002-04-03 2005-07-28 Bayer Healthcare Ag Diagnostics and therapeutics for diseases associated with n-formyl peptide receptor like 1 (fprl1)
WO2004007459A2 (en) 2002-07-12 2004-01-22 Janssen Pharmaceutica N.V. Naphthol, quinoline and isoquinoline-derivatives as modulators of vanilloid vr1 receptor
PE20040804A1 (es) 2002-12-19 2004-12-31 Boehringer Ingelheim Pharma DERIVADOS DE CARBOXAMIDAS COMO INHIBIDORES DEL FACTOR Xa
US7615568B2 (en) 2003-05-30 2009-11-10 Eli Lilly And Company Antithrombotic ethers
US7141596B2 (en) 2003-10-08 2006-11-28 Incyte Corporation Inhibitors of proteins that bind phosphorylated molecules
CN1894580A (zh) * 2003-11-07 2007-01-10 阿卡蒂亚药品公司 脂氧素受体fprl1作为一种用于鉴定能有效治疗疼痛和炎症化合物的工具
WO2005047899A2 (en) 2003-11-07 2005-05-26 Acadia Pharmaceuticals Inc. Use of the lipoxin receptor, fprl1, as a tool for identifying compounds effective in the treatment of pain and inflammation
US7371743B2 (en) 2004-02-28 2008-05-13 Boehringer Ingelheim International Gmbh Carboxylic acid amides, the preparation thereof and their use as medicaments
TW200538098A (en) 2004-03-22 2005-12-01 Astrazeneca Ab Therapeutic agents
US7453002B2 (en) 2004-06-15 2008-11-18 Bristol-Myers Squibb Company Five-membered heterocycles useful as serine protease inhibitors
ATE546430T1 (de) 2004-06-29 2012-03-15 Aventis Pharma Inc Fkbp bindende zusammensetzung und deren pharmazeutische verwendung
JP4885958B2 (ja) 2005-08-12 2012-02-29 エフ.ホフマン−ラ ロシュ アーゲー フルオロ置換2−オキソアゼパン誘導体
TW200902533A (en) 2007-05-02 2009-01-16 Boehringer Ingelheim Int Carboxylic acid amides, manufacturing and use thereof as medicaments
JP2010536723A (ja) 2007-08-16 2010-12-02 エフ.ホフマン−ラ ロシュ アーゲー 置換ヒダントイン
AR069650A1 (es) 2007-12-14 2010-02-10 Actelion Pharmaceuticals Ltd Derivados de aminopirazol como agonistas no peptidicos del receptor alx humano
DK2225231T3 (da) 2007-12-18 2011-10-17 Actelion Pharmaceuticals Ltd Aminotriazolderivater som alx-agonister
EP2300427A1 (en) * 2008-05-05 2011-03-30 Amgen Inc. Urea compounds as gamma secretase modulators
US8476470B2 (en) 2008-08-07 2013-07-02 Kyorin Pharmaceutical Co., Ltd. Process for production of bicyclo[2.2.2]octylamine derivative
WO2010083246A1 (en) 2009-01-15 2010-07-22 Amgen Inc. Fluoroisoquinoline substituted thiazole compounds and methods of use
JP5510945B2 (ja) 2009-05-18 2014-06-04 アクテリオン ファーマシューティカルズ リミテッド Alx受容体及び/又はfprl2アゴニストとしての架橋スピロ[2.4]ヘプタン誘導体
JP5095035B2 (ja) 2009-06-09 2012-12-12 アクテリオン ファーマシューティカルズ リミテッド フッ素化アミノトリアゾール誘導体
ES2440790T3 (es) 2009-06-12 2014-01-30 Actelion Pharmaceuticals Ltd. Derivados de oxazol y tiazol como agonistas del receptor del ALX
US9062076B2 (en) * 2009-10-22 2015-06-23 Fibrotech Therapeutics Pty Ltd Fused ring analogues of anti-fibrotic agents
GB201009731D0 (en) 2010-06-10 2010-07-21 Pulmagen Therapeutics Inflamma Kinase inhibitors
US9187435B2 (en) 2010-11-17 2015-11-17 Actelion Pharmaceuticals Ltd. Bridged Spiro[2.4]heptane ester derivatives
SI2649068T1 (sl) 2010-12-07 2015-01-30 Actelion Pharmaceuticals Ltd. Derivati oksazolil-metiletra kot agonisti alx-receptorja
AR084172A1 (es) 2010-12-07 2013-04-24 Actelion Pharmaceuticals Ltd Derivados aminotriazol hidroxilados como agonistas del receptor alx
BR112014002353B1 (pt) 2011-08-01 2022-09-27 Genentech, Inc Usos de antagonistas de ligação do eixo pd-1 e inibidores de mek, composições farmacêuticas, e kit
JP5982001B2 (ja) 2011-10-26 2016-08-31 アラーガン、インコーポレイテッドAllergan,Incorporated ホルミルペプチド受容体様1(fprl−1)受容体モジュレーターとしてのn−尿素置換アミノ酸のアミド誘導体
US8492556B2 (en) 2011-11-10 2013-07-23 Allergan, Inc. 2,5-Dioxoimidazolidin-1-yl-3-phenylurea derivatives as formyl peptide receptor like-1 (FPRL-1) receptor modulators
US8541577B2 (en) 2011-11-10 2013-09-24 Allergan, Inc. Aryl urea derivatives as N-formyl peptide receptors like-1 (FPRL-1) receptor modulators
MA37618B1 (fr) 2012-05-16 2017-08-31 Actelion Pharmaceuticals Ltd Dérivés pontés fluorés de spiro[2.4]heptane en tant qu'agonistes de récepteur alx
TW201348219A (zh) 2012-05-16 2013-12-01 Actelion Pharmaceuticals Ltd 作爲alx受體激動劑之經1-(對-甲苯基)環丙基取代橋聯螺[2.4]庚烷衍生物
RU2696487C2 (ru) 2013-03-06 2019-08-02 Аллерган, Инк. Применение агонистов формилпептидного рецептора 2 для лечения дерматологических заболеваний
CA2898301C (en) 2013-03-06 2021-11-16 Allergan, Inc. Use of agonists of formyl peptide receptor 2 for treating ocular inflammatory diseases
AR096686A1 (es) 2013-06-25 2016-01-27 Actelion Pharmaceuticals Ltd Derivados de espiro[2.4]heptano puenteados sustituidos con difluoroetil-oxazol como agonistas del receptor de alx
ES2639798T3 (es) 2013-07-18 2017-10-30 Idorsia Pharmaceuticals Ltd Derivados de espiro[2.4]heptano con puente sustituidos con piperazina como agonistas del receptor ALX
WO2015042071A1 (en) 2013-09-19 2015-03-26 Allergan, Inc. Diphenyl urea derivatives as formyl peptide receptor modulators

Also Published As

Publication number Publication date
RU2016107974A (ru) 2017-09-15
BR112016002459A2 (pt) 2017-08-22
TW201536756A (zh) 2015-10-01
US20160200686A1 (en) 2016-07-14
WO2015019325A1 (en) 2015-02-12
MX2016001788A (es) 2016-05-18
CN105473575B (zh) 2017-11-24
EP3030560B1 (en) 2017-06-21
KR20160042019A (ko) 2016-04-18
AU2014304046B2 (en) 2018-07-05
JP6387411B2 (ja) 2018-09-05
AU2014304046A1 (en) 2016-03-17
CA2917954A1 (en) 2015-02-12
EP3030560A1 (en) 2016-06-15
CN105473575A (zh) 2016-04-06
BR112016002459A8 (pt) 2017-12-26
US9663473B2 (en) 2017-05-30
JP2016529251A (ja) 2016-09-23
ES2641172T3 (es) 2017-11-08

Similar Documents

Publication Publication Date Title
AR097279A1 (es) Derivados de benzimidazolil-metil urea como agonistas del receptor de alx
AR095311A1 (es) 3-pirimidin-4-il-oxazolidin-2-onas como inhibidores de idh mutante
AR093921A1 (es) Derivados de indol carboxamida como antagonistas del receptor p2x7
AR108388A2 (es) Compuestos de oxazol sustituidos con indazol como inhibidores de pi3-quinasas
AR112348A1 (es) Compuestos bicíclicos de pirazolo y triazolo como inhibidores de quinasas jak
AR100033A1 (es) Compuestos y composiciones para inhibir la actividad de shp2
AR093580A1 (es) Inhibidores bmi-1 de pirimidina sustituidos
AR107061A1 (es) Heteroarilhidroxipirimidinonas como agonistas del receptor de apj
AR099789A1 (es) Derivados de 8-(piperazin-1-il)-1,2,3,4-tetrahidro-isoquinolina
AR091981A1 (es) Dihidropiridona p1 como inhibidores del factor xia
AR096788A1 (es) Compuestos tricíclicos de carboxamida como inhibidores potentes de rock
AR096450A1 (es) Compuestos para la modulación de quinasas, y sus indicaciones
AR100058A1 (es) DERIVADOS DE PIRIMIDIN-PIRAZINAS FUSIONADAS MODULADORES DE RORg
AR097936A1 (es) Compuestos herbicidas
AR098171A1 (es) Piridinilimidazolonas como herbicidas
AR095359A1 (es) Compuestos heteroaromáticos y su uso como ligandos d1 de dopamina
AR088630A1 (es) Inhibidores del virus de la hepatitis c
AR087274A1 (es) Derivados de amidas heterociclicas como antagonistas de receptores p2x7
AR110498A1 (es) DERIVADOS DE ISOXAZOLIL ÉTER COMO MODULADORES ALOSTÉRICOS POSITIVOS (PAM) DE RECEPTORES DE GABAA a5
AR106604A1 (es) Compuestos de criptoficina y productos conjugados, su preparación y su uso terapéutico
AR094053A1 (es) Derivados de indol carboxamida como antagonistas del receptor p2x₇
AR091185A1 (es) Derivados de 1,2,4-triazol
AR101561A1 (es) Nucleósidos de 2-cloro aminopirimidinona y pirimidina diona
AR102544A1 (es) Compuestos derivados de dihidrohidantoína como herbicidas
AR100776A1 (es) Compuestos herbicidas

Legal Events

Date Code Title Description
FB Suspension of granting procedure