WO2005047899A3 - Utilisation d'un recepteur de lipoxine, fprl1, en tant qu'outil d'identification de composes efficaces dans le traitement de douleurs et d'inflammations - Google Patents

Utilisation d'un recepteur de lipoxine, fprl1, en tant qu'outil d'identification de composes efficaces dans le traitement de douleurs et d'inflammations Download PDF

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Publication number
WO2005047899A3
WO2005047899A3 PCT/US2004/036952 US2004036952W WO2005047899A3 WO 2005047899 A3 WO2005047899 A3 WO 2005047899A3 US 2004036952 W US2004036952 W US 2004036952W WO 2005047899 A3 WO2005047899 A3 WO 2005047899A3
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Prior art keywords
fprl1
inflammation
pain
tool
treatment
Prior art date
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PCT/US2004/036952
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English (en)
Other versions
WO2005047899A2 (fr
Inventor
Norman Nash
Audra L Scully
Luis Gardell
Roger Olsson
Magnus Gustafsson
Original Assignee
Acadia Pharm Inc
Norman Nash
Audra L Scully
Luis Gardell
Roger Olsson
Magnus Gustafsson
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.)
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Application filed by Acadia Pharm Inc, Norman Nash, Audra L Scully, Luis Gardell, Roger Olsson, Magnus Gustafsson filed Critical Acadia Pharm Inc
Priority to AU2004290368A priority Critical patent/AU2004290368A1/en
Priority to CA002544983A priority patent/CA2544983A1/fr
Priority to EP04810415A priority patent/EP1692502A2/fr
Priority to JP2006539672A priority patent/JP2007516434A/ja
Priority to BRPI0416272-2A priority patent/BRPI0416272A/pt
Publication of WO2005047899A2 publication Critical patent/WO2005047899A2/fr
Publication of WO2005047899A3 publication Critical patent/WO2005047899A3/fr

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/16Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
    • C07D295/18Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
    • C07D295/182Radicals derived from carboxylic acids
    • C07D295/185Radicals derived from carboxylic acids from aliphatic carboxylic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41961,2,4-Triazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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Abstract

L'invention concerne des composés qui activent de manière sélective le récepteur FPRL1. L'invention concerne également des procédés destinés à soulager des réactions inflammatoires par régulation d'étapes clés dans le commerce illicite de leucocytes et dans la prévention de dommages tissulaires induits par des neutrophiles par administration à un sujet d'une quantité efficace sur le plan thérapeutique des composés de cette invention. En outre, cette invention concerne des procédés de modulation ou de production d'une action agoniste spécifique du récepteur FPRL1 par administration d'une quantité efficace des composés susmentionnés.
PCT/US2004/036952 2003-11-07 2004-11-04 Utilisation d'un recepteur de lipoxine, fprl1, en tant qu'outil d'identification de composes efficaces dans le traitement de douleurs et d'inflammations WO2005047899A2 (fr)

Priority Applications (5)

Application Number Priority Date Filing Date Title
AU2004290368A AU2004290368A1 (en) 2003-11-07 2004-11-04 Use of the lipoxin receptor, FPRL1, as a tool for identifying compounds effective in the treatment of pain and inflammation
CA002544983A CA2544983A1 (fr) 2003-11-07 2004-11-04 Utilisation d'un recepteur de lipoxine, fprl1, en tant qu'outil d'identification de composes efficaces dans le traitement de douleurs et d'inflammations
EP04810415A EP1692502A2 (fr) 2003-11-07 2004-11-04 Utilisation d'un recepteur de lipoxine, fprl1, en tant qu'outil d'identification de composes efficaces dans le traitement de douleurs et d'inflammations
JP2006539672A JP2007516434A (ja) 2003-11-07 2004-11-04 リポキシン受容体fprl1の、疼痛および炎症の治療に有効な化合物を識別する手段としての使用
BRPI0416272-2A BRPI0416272A (pt) 2003-11-07 2004-11-04 usos do receptor fprl1, e de compostos, uso profilático de compostos, métodos de triagem para um composto capaz de afetar uma ou mais atividades de um receptor fprl1, de tratamento ou prevenção de inflamação, de identificação de um composto de indução de vasodilatação, para antagonismo de uma resposta vasoconstrutiva a um sulfidopeptìdeo leucotrieno em um indivìduo, e para estimulação de proliferação celular em um indivìduo, e, composto

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
US51847603P 2003-11-07 2003-11-07
US60/518,476 2003-11-07
US51908503P 2003-11-10 2003-11-10
US60/519,085 2003-11-10
US59292604P 2004-07-30 2004-07-30
US60/592,926 2004-07-30

Publications (2)

Publication Number Publication Date
WO2005047899A2 WO2005047899A2 (fr) 2005-05-26
WO2005047899A3 true WO2005047899A3 (fr) 2006-03-30

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PCT/US2004/036952 WO2005047899A2 (fr) 2003-11-07 2004-11-04 Utilisation d'un recepteur de lipoxine, fprl1, en tant qu'outil d'identification de composes efficaces dans le traitement de douleurs et d'inflammations

Country Status (7)

Country Link
EP (1) EP1692502A2 (fr)
JP (1) JP2007516434A (fr)
KR (1) KR20060130064A (fr)
AU (1) AU2004290368A1 (fr)
BR (1) BRPI0416272A (fr)
CA (1) CA2544983A1 (fr)
WO (1) WO2005047899A2 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101724765B1 (ko) 2009-05-18 2017-04-07 액테리온 파마슈티칼 리미티드 Alx 수용체 및/또는 fprl2 아고니스트로서의 브릿지 스피로[2.4]헵탄 유도체

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003023007A2 (fr) 2001-09-07 2003-03-20 Bristol-Myers Squibb Company Polynucleotide codant pour un recepteur lie a une nouvelle proteine g humaine, hgprmby39
US20100291089A1 (en) * 2005-07-07 2010-11-18 Postech Academy-Industry Foundation Ligand of regulating immune response, and use thereof in treating an immune response-related disease
AR069650A1 (es) * 2007-12-14 2010-02-10 Actelion Pharmaceuticals Ltd Derivados de aminopirazol como agonistas no peptidicos del receptor alx humano
TWI434685B (zh) * 2007-12-18 2014-04-21 Actelion Pharmaceuticals Ltd 胺基三唑衍生物
EP2440555B1 (fr) 2009-06-09 2016-05-18 Actelion Pharmaceuticals Ltd Dérivés fluorés de l'aminotriazole
KR20120046159A (ko) 2009-06-12 2012-05-09 액테리온 파마슈티칼 리미티드 Alx 수용체 아고니스트로서의 옥사졸 및 티아졸 유도체
ES2553635T3 (es) 2010-11-17 2015-12-10 Actelion Pharmaceuticals Ltd. Derivados de éster spiro[2.4]heptano puenteados
AU2011336973A1 (en) * 2010-12-03 2013-07-11 Allergan, Inc. Pharmaceutical compositions comprising 3,4- dihydroisoquinolin-2(1 H)-yl-3-phenylurea derivatives having formyl peptide receptor like-1 (FPRL-1) agonist or antagonist activity
US9346793B2 (en) 2010-12-07 2016-05-24 Actelion Pharmaceuticals, Ltd. Hydroxylated aminotriazole derivatives as ALX receptor agonists
WO2012077049A1 (fr) 2010-12-07 2012-06-14 Actelion Pharmaceuticals Ltd Dérivés d'oxazolyl-méthyléther convenant comme agonistes du récepteur alx
AU2012214265A1 (en) * 2011-02-11 2013-09-05 Allergan, Inc. Novel 1-(1-oxo-1,2,3,4-tetrahydroisoquinolin-7-yl)urea derivatives as N-formyl peptide receptor like-1 (FPRL-1) receptor modulators
EP2770989B1 (fr) * 2011-10-26 2018-09-05 Allergan, Inc. Dérivés amides d'acides aminés substitués par une n-urée à titre de modulateurs des récepteurs de type 1 du peptide formyle (fprl-1)
EP2597160B1 (fr) 2011-11-23 2015-09-23 Universita' Degli Studi "G. d'Annunzio" Chieti-Pescara Outil de criblage pour la découverte de médicament anti-inflammatoire comportant le promoteur de gène FPR2/ALX
US9284288B2 (en) 2012-05-16 2016-03-15 Actelion Pharmaceuticals Ltd. 1-(p-tolyl) cyclopropyl substituted bridged spiro[2.4]heptane derivatives as ALX receptor agonists
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
BR122017004254B1 (pt) 2013-03-06 2021-04-13 Allergan, Inc. Uso de agonistas de receptor de formil peptídeo 2 para tratar doenças inflamatórias oculares
WO2014204229A2 (fr) * 2013-06-21 2014-12-24 성균관대학교산학협력단 Composition pharmaceutique pour la prévention ou le traitement de l'arthrite rhumatoïde, comprenant un peptide en tant que principe actif
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
EP3022174B1 (fr) * 2013-07-16 2018-09-05 Allergan, Inc. Dérivés d'acides aminés substitués par une n-urée utilisés comme modulateurs des récepteurs des peptides formylés
KR20160033747A (ko) 2013-07-18 2016-03-28 액테리온 파마슈티칼 리미티드 Alx 수용체 아고니스트로서의 피페라진 치환된 브릿지연결 스피로[2.4]헵탄 유도체
AR097279A1 (es) 2013-08-09 2016-03-02 Actelion Pharmaceuticals Ltd Derivados de benzimidazolil-metil urea como agonistas del receptor de alx
NZ720508A (en) 2013-11-28 2019-03-29 Kyorin Seiyaku Kk Urea derivative or pharmacologically acceptable salt thereof
CA2948876A1 (fr) 2014-05-21 2015-11-26 Allergan, Inc. Derives d'imidazole en tant que modulateurs des recepteurs de peptide formyle
CN107849049B (zh) 2015-05-27 2021-03-16 杏林制药株式会社 脲衍生物或其药用盐
US10858314B2 (en) 2015-05-27 2020-12-08 Kyorin Pharmaceutical Co., Ltd. Urea derivative or pharmacologically acceptable salt thereof
KR101731303B1 (ko) 2015-06-11 2017-05-02 가톨릭대학교 산학협력단 인터루킨―1베타 억제제의 스크리닝 방법
EA202092094A1 (ru) 2018-03-05 2020-12-10 Бристол-Маерс Сквибб Компани Фенилпирролидиноновые агонисты формилпептидного рецептора 2
IT202100004964A1 (it) * 2021-03-03 2022-09-03 Univ Degli Studi Di Bari Aldo Moro Agonisti del recettore fpr2 (formyl peptide receptor 2) e loro uso nel trattamento del disturbo dello spettro autistico.

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000031261A2 (fr) * 1998-11-25 2000-06-02 Cadus Pharmaceutical Corporation Methodes et compositions d'identification d'effecteurs de recepteurs
WO2001057074A1 (fr) * 2000-02-04 2001-08-09 The Government Of The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Ligands des recepteurs de la classe fpr qui induisent une reponse immunitaire de l'hote a un agent pathogene ou inhibent l'infection par le vih
WO2003074069A2 (fr) * 2002-03-07 2003-09-12 Bayer Healthcare Ag Diagnostic et therapeutique destines a des maladies associees au recepteur peptidique n-formyl 1 (fpr1)
WO2003106683A1 (fr) * 2002-06-14 2003-12-24 武田薬品工業株式会社 Procede de criblage
WO2004027427A1 (fr) * 2002-09-19 2004-04-01 Astrazeneca Ab Analyse de ligands fprl-1
WO2005024057A1 (fr) * 2003-09-10 2005-03-17 Galapagos Genomics N.V. Procede pour identifier un compose qui modifie le traitement d'une proteine precurseur de la beta-amyloide dans une cellule

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000031261A2 (fr) * 1998-11-25 2000-06-02 Cadus Pharmaceutical Corporation Methodes et compositions d'identification d'effecteurs de recepteurs
WO2001057074A1 (fr) * 2000-02-04 2001-08-09 The Government Of The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Ligands des recepteurs de la classe fpr qui induisent une reponse immunitaire de l'hote a un agent pathogene ou inhibent l'infection par le vih
WO2003074069A2 (fr) * 2002-03-07 2003-09-12 Bayer Healthcare Ag Diagnostic et therapeutique destines a des maladies associees au recepteur peptidique n-formyl 1 (fpr1)
WO2003106683A1 (fr) * 2002-06-14 2003-12-24 武田薬品工業株式会社 Procede de criblage
EP1514930A1 (fr) * 2002-06-14 2005-03-16 Takeda Pharmaceutical Company Limited Procede de criblage
WO2004027427A1 (fr) * 2002-09-19 2004-04-01 Astrazeneca Ab Analyse de ligands fprl-1
WO2005024057A1 (fr) * 2003-09-10 2005-03-17 Galapagos Genomics N.V. Procede pour identifier un compose qui modifie le traitement d'une proteine precurseur de la beta-amyloide dans une cellule

Non-Patent Citations (14)

* Cited by examiner, † Cited by third party
Title
CUI Y ET AL: "Potential role of the formyl peptide receptor-like 1 (FPRL1) in inflammatory aspects of Alzheimer's disease", JOURNAL OF LEUKOCYTE BIOLOGY 01 OCT 2002 UNITED STATES, vol. 72, no. 4, 1 October 2002 (2002-10-01), pages 628 - 635, XP009047055, ISSN: 0741-5400 *
DENG X ET AL: "A synthetic peptide derived from human immunodeficiency virus type 1 gp120 downregulates the expression and function of chemokine receptors CCR5 and CXCR4 in monocytes by activating the 7-transmembrane G-protein-coupled receptor FPRL1/LXA4R", BLOOD, W.B.SAUNDERS COMPANY, ORLANDO, FL, US, vol. 94, no. 4, 15 August 1999 (1999-08-15), pages 1165 - 1173, XP002154093, ISSN: 0006-4971 *
GEWIRTZ ANDREW T ET AL: "Mechanisms of active intestinal inflammation and potential down-regulation via lipoxins.", ADVANCES IN EXPERIMENTAL MEDICINE AND BIOLOGY. 2002, vol. 507, 2002, pages 229 - 236, XP009047056, ISSN: 0065-2598 *
GRONERT K ET AL: "Identification of a human enterocyte lipoxin A4 receptor that is regulated by interleukin (IL)-13 and interferon gamma and inhibits tumor necrosis factor alpha-induced IL-8 release", JOURNAL OF EXPERIMENTAL MEDICINE, TOKYO, JP, vol. 187, no. 8, 20 April 1998 (1998-04-20), pages 1285 - 1294, XP002226394, ISSN: 0022-1007 *
KLEIN C ET AL: "Identification of surrogate agonists for the human FPRL-1 receptor by autocrine selection in yeast", NATURE BIOTECHNOLOGY, NATURE PUBLISHING, US, vol. 16, no. 13, December 1998 (1998-12-01), pages 1334 - 1337, XP002137534, ISSN: 1087-0156 *
LE Y ET AL: "Formyl-peptide receptors revisited", TRENDS IN IMMUNOLOGY, ELSEVIER, CAMBRIDGE, GB, vol. 23, no. 11, 1 November 2002 (2002-11-01), pages 541 - 548, XP004388300, ISSN: 1471-4906 *
LE Y ET AL: "PLEIOTROPIC ROLES OF FORMYL PEPTIDE RECEPTORS", CYTOKINE AND GROWTH FACTOR REVIEWS, OXFORD, GB, vol. 12, no. 1, March 2001 (2001-03-01), pages 91 - 105, XP001133719, ISSN: 1359-6101 *
LE Y ET AL: "Receptors for chemotactic formyl peptides as pharmacological targets", INTERNATIONAL IMMUNOPHARMACOLOGY, ELSEVIER, AMSTERDAM, NL, vol. 2, no. 1, January 2002 (2002-01-01), pages 1 - 13, XP002249587, ISSN: 1567-5769 *
LE Y ET AL: "The neurotoxic prion peptide fragment PrP(106-126) is a chemotactic agonist for the G protein-coupled receptor formyl peptide receptor-like 1", JOURNAL OF IMMUNOLOGY, THE WILLIAMS AND WILKINS CO. BALTIMORE, US, vol. 166, no. 3, 1 February 2001 (2001-02-01), pages 1448 - 1451, XP002973363, ISSN: 0022-1767 *
MADERNA P ET AL: "INFLUENCE OF LIPOXIN A4 AND OTHER LIPOXYGENASE-DERIVED EICOSANOIDS ON TISSUE FACTOR EXPRESSION", AMERICAN JOURNAL OF PHYSIOLOGY, AMERICAN PHYSIOLOGICAL SOCIETY, BETHESDA, MD, US, vol. 279, no. 4, PART 1, 2000, pages C945 - C953, XP008003788, ISSN: 0002-9513 *
MURPHY P M ET AL: "A STRUCTURAL HOMOLOGUE OF THE N FORMYL PEPTIDE RECEPTOR CHARACTERIZATION AND CHROMOSOME MAPPING OF A PEPTIDE CHEMOATTRACTANT RECEPTOR FAMILY", JOURNAL OF BIOLOGICAL CHEMISTRY, AMERICAN SOCIETY OF BIOLOGICAL CHEMISTS, BALTIMORE, MD, US, vol. 267, no. 11, 15 April 1992 (1992-04-15), pages 7637 - 7643, XP002137531, ISSN: 0021-9258 *
SERHAN C N: "Lipoxins and aspirin-triggered 15-epi-lipoxin biosynthesis: an update and role in anti-inflammation and pro-resolution", PROSTAGLANDINS, BUTTERWORTH, STONEHAM, MA, US, vol. 68-69, August 2002 (2002-08-01), pages 433 - 455, XP004380640, ISSN: 0090-6980 *
WANG J ET AL: "THE INVOLVEMENT OF THE G-PROTEIN COUPLED RECEPTOR FPRL1 IN PROINFLAMMATORY ASPECTS OF ALZHEIMER'S DISEASE", FASEB JOURNAL (FEDERATION OF AMERICAN SOCIETIES FOR EXPERIMENTAL BIOLOGY), BETHESDA, US, vol. 15, no. 4, 31 March 2001 (2001-03-31), pages A682, XP008027947, ISSN: 0892-6638 *
YAZAWA HIROSHI ET AL: "beta amyloid peptide (Abeta42) is internalized via the G-protein-coupled receptor FPRL1 and forms fibrillar aggregates in macrophages", FASEB JOURNAL (FEDERATION OF AMERICAN SOCIETIES FOR EXPERIMENTAL BIOLOGY), BETHESDA, US, vol. 15, no. 13, November 2001 (2001-11-01), pages 2454 - 2462, XP002280686, ISSN: 0892-6638 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101724765B1 (ko) 2009-05-18 2017-04-07 액테리온 파마슈티칼 리미티드 Alx 수용체 및/또는 fprl2 아고니스트로서의 브릿지 스피로[2.4]헵탄 유도체

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