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 PDFInfo
- 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
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- fprl1
- inflammation
- pain
- tool
- treatment
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 206010061218 Inflammation Diseases 0.000 title 1
- 102100021126 N-formyl peptide receptor 2 Human genes 0.000 title 1
- 101710091942 N-formyl peptide receptor 2 Proteins 0.000 title 1
- 230000004054 inflammatory process Effects 0.000 title 1
- 101000818546 Homo sapiens N-formyl peptide receptor 2 Proteins 0.000 abstract 2
- 102000057492 human FPR2 Human genes 0.000 abstract 2
- 230000028709 inflammatory response Effects 0.000 abstract 1
- 210000000265 leukocyte Anatomy 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 210000000440 neutrophil Anatomy 0.000 abstract 1
- 230000001105 regulatory effect Effects 0.000 abstract 1
- 230000000451 tissue damage Effects 0.000 abstract 1
- 231100000827 tissue damage Toxicity 0.000 abstract 1
- 230000032258 transport Effects 0.000 abstract 1
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- C07D295/00—Heterocyclic 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
- C07D295/16—Heterocyclic 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
- C07D295/18—Heterocyclic 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
- C07D295/182—Radicals derived from carboxylic acids
- C07D295/185—Radicals derived from carboxylic acids from aliphatic carboxylic acids
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic 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
- A61K31/4196—1,2,4-Triazoles
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- A61K31/495—Heterocyclic 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
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- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/18—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/88—Nitrogen atoms, e.g. allantoin
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- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D401/00—Heterocyclic 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
- C07D401/02—Heterocyclic 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
- C07D401/12—Heterocyclic 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
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- C07D405/02—Heterocyclic 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
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- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/435—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans
- G01N2333/705—Assays involving receptors, cell surface antigens or cell surface determinants
- G01N2333/72—Assays involving receptors, cell surface antigens or cell surface determinants for hormones
- G01N2333/726—G protein coupled receptor, e.g. TSHR-thyrotropin-receptor, LH/hCG receptor, FSH
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Pulmonology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Hematology (AREA)
- Manufacturing & Machinery (AREA)
- Dermatology (AREA)
- Immunology (AREA)
- Physical Education & Sports Medicine (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Ceramic Engineering (AREA)
- Epidemiology (AREA)
- Endocrinology (AREA)
- Materials Engineering (AREA)
- Psychiatry (AREA)
- Orthopedic Medicine & Surgery (AREA)
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Abstract
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 |
Family
ID=34595924
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
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)
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)
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 |
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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)
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 |
-
2004
- 2004-11-04 KR KR1020067011178A patent/KR20060130064A/ko not_active Application Discontinuation
- 2004-11-04 EP EP04810415A patent/EP1692502A2/fr not_active Withdrawn
- 2004-11-04 WO PCT/US2004/036952 patent/WO2005047899A2/fr active Application Filing
- 2004-11-04 BR BRPI0416272-2A patent/BRPI0416272A/pt not_active Application Discontinuation
- 2004-11-04 CA CA002544983A patent/CA2544983A1/fr not_active Abandoned
- 2004-11-04 JP JP2006539672A patent/JP2007516434A/ja active Pending
- 2004-11-04 AU AU2004290368A patent/AU2004290368A1/en not_active Abandoned
Patent Citations (7)
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)
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)
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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CA2544983A1 (fr) | 2005-05-26 |
EP1692502A2 (fr) | 2006-08-23 |
AU2004290368A1 (en) | 2005-05-26 |
JP2007516434A (ja) | 2007-06-21 |
KR20060130064A (ko) | 2006-12-18 |
WO2005047899A2 (fr) | 2005-05-26 |
BRPI0416272A (pt) | 2007-01-09 |
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