MA29259B1 - 2-phénylindoles en tant qu'antagonistes du récepteur de la prostaglandine d2 - Google Patents

2-phénylindoles en tant qu'antagonistes du récepteur de la prostaglandine d2

Info

Publication number
MA29259B1
MA29259B1 MA30150A MA30150A MA29259B1 MA 29259 B1 MA29259 B1 MA 29259B1 MA 30150 A MA30150 A MA 30150A MA 30150 A MA30150 A MA 30150A MA 29259 B1 MA29259 B1 MA 29259B1
Authority
MA
Morocco
Prior art keywords
pharmaceutically acceptable
xvi
urticaria
solvate
inflammation
Prior art date
Application number
MA30150A
Other languages
English (en)
Inventor
Keith J Harris
Hans-Jochen Lang
Rose M Mathew
Stephen J Shimshock
Thaddeus R Nieduzak
Sharon Jackson
Zhaoxia Yang
Kenneth J Bordeau
Original Assignee
Aventis Pharma Inc
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 Aventis Pharma Inc filed Critical Aventis Pharma Inc
Publication of MA29259B1 publication Critical patent/MA29259B1/fr

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/12—Radicals substituted by oxygen atoms
    • 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
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404—Indoles, e.g. pindolol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/08—Bronchodilators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/04—Antipruritics
    • 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
    • A61P25/20—Hypnotics; Sedatives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • A61P27/12—Ophthalmic agents for cataracts
    • 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
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/08—Antiallergic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • 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
    • C07D209/22—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 with an aralkyl radical attached to the ring nitrogen atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • 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
    • C07D209/24—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 with an alkyl or cycloalkyl radical attached to the ring nitrogen atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—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
    • 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
    • C07D405/12—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 linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic 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
    • C07D413/06—Heterocyclic 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 carbon chain containing only aliphatic carbon atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pulmonology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Cardiology (AREA)
  • Dermatology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Immunology (AREA)
  • Anesthesiology (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Hospice & Palliative Care (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

LA PRÉSENTE INVENTION CONCERNE UN COMPOSÉ DE FORMULE (XVI) DANS LAQUELLE R, R2, R3, R4, R5, R6, R7 ET N SONT TELS QUE DÉFINIS ICI OU UN SEL, HYDRATE OU SOLVATE DE CELUI-CI ACCEPTABLES DU POINT DE VUE PHARMACEUTIQUE, UN PROMÉDICAMENT ACCEPTABLE DU POINT DE VUE PHARMACEUTIQUE DE CELUI-CI OU UN SEL, HYDRATE OU SOLVATE ACCEPTABLES DU POINT DE VUE PHARMACEUTIQUE DU PROMÉDICAMENT, UNE COMPOSITION PHARMACEUTIQUE COMPRENANT UNE QUANTITÉ EFFICACE DU POINT DE VUE PHARMACEUTIQUE D'UN OU PLUSIEURS COMPOSÉS SELON LA FORMULE (XVI) EN MÉLANGE AVEC UN VÉHICULE ACCEPTABLE DU POINT DE VUE PHARMACEUTIQUE, UN PROCÉDÉ CONSISTANT À TRAITER UN PATIENT SOUFFRANT D'UN TROUBLE MÉDIÉ PAR LA PGD2 DONT, MAIS IL N'EST PAS LIMITÉ À CEUX-CI, UNE MALADIE ALLERGIQUE (TELLE QUE LA RHINITE ALLERGIQUE, LA CONJONCTIVITE ALLERGIQUE, LA DERMATITE ATOPIQUE, L'ASTHME BRONCHIQUE ET UNE ALLERGIE ALIMENTAIRE), UNE MASTOCYTOSE SYSTÉMIQUE, DES TROUBLES S'ACCOMPAGNANT D'UNE ACTIVATION SYSTÉMIQUE DES MASTOCYTES, LE CHOC ANAPHYLACTIQUE, LA BRONCHOCONSTRICTION, LA BRONCHITE, L'URTICAIRE, L'ECZÉMA, DES MALADIES S'ACCOMPAGNANT DE DÉMANGEAISONS (TELLES QUE LA DERMATITE ATOPIQUE ET L'URTICAIRE), DES MALADIES (TELLES QUE LA CATARACTE, LE DÉCOLLEMENT DE LA RÉTINE, UNE INFLAMMATION, UNE INFECTION ET DES TROUBLES DU SOMMEIL) QUI SONT GÉNÉRÉES DE FAÇON SECONDAIRE EN CONSÉQUENCE D'UN COMPORTEMENT S'ACCOMPAGNANT DE DÉMANGEAISONS (TEL QU'UN GRATTEMENT ET UN BATTAGE), UNE INFLAMMATION, DES BRONCHO-PNEUMOPATHIES CHRONIQUES OBSTRUCTIVES, UNE PLAIE DE REPERFUSION ISCHÉMIQUE, UN ACCIDENT CÉRÉBROVASCULAIRE, LA POLYARTHRITE RHUMATOÏDE CHRONIQUE, LA PLEURÉSIE, LA RECTO-COLITE HÉMORRAGIQUE ET SIMILAIRES EN ADMINISTRANT AU DIT PATIENT UNE QUANTITÉ EFFICACE DU POINT DE VUE PHARMACEUTIQUE D'UN COMPOSÉ SELON LA FORMULE (XVI).
MA30150A 2005-01-26 2007-08-17 2-phénylindoles en tant qu'antagonistes du récepteur de la prostaglandine d2 MA29259B1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US64730705P 2005-01-26 2005-01-26

Publications (1)

Publication Number Publication Date
MA29259B1 true MA29259B1 (fr) 2008-02-01

Family

ID=36282872

Family Applications (1)

Application Number Title Priority Date Filing Date
MA30150A MA29259B1 (fr) 2005-01-26 2007-08-17 2-phénylindoles en tant qu'antagonistes du récepteur de la prostaglandine d2

Country Status (25)

Country Link
US (1) US20070265278A1 (fr)
EP (1) EP1844011A1 (fr)
JP (1) JP2008528606A (fr)
KR (1) KR20070110277A (fr)
CN (1) CN101146770A (fr)
AR (1) AR054726A1 (fr)
AU (1) AU2006209213A1 (fr)
BR (1) BRPI0607079A2 (fr)
CA (1) CA2595728A1 (fr)
CR (1) CR9214A (fr)
DO (1) DOP2006000016A (fr)
GT (1) GT200600030A (fr)
IL (1) IL184816A0 (fr)
MA (1) MA29259B1 (fr)
MX (1) MX2007008277A (fr)
NO (1) NO20074336L (fr)
PA (1) PA8661201A1 (fr)
PE (1) PE20060878A1 (fr)
RU (1) RU2007132166A (fr)
SG (1) SG158918A1 (fr)
TN (1) TNSN07251A1 (fr)
TW (1) TW200639151A (fr)
UY (1) UY29346A1 (fr)
WO (1) WO2006081343A1 (fr)
ZA (1) ZA200705449B (fr)

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KR20090039735A (ko) * 2006-07-25 2009-04-22 사노피-아벤티스 프로스타글란딘 d2 수용체 길항제로서의 2-페닐-인돌
EP2316824A1 (fr) 2006-08-07 2011-05-04 Actelion Pharmaceuticals Ltd. Derivees du (3-amino-1,2,3,4-tetrahydro-9H-carbazol-9-yl)-acide acetique
WO2008061006A1 (fr) * 2006-11-10 2008-05-22 Wyeth Indan-2-yl arylsulfonamides substitués et leurs procédés d'utilisation
US8362056B2 (en) * 2007-11-05 2013-01-29 Array Biopharma Inc. 4-heteroaryl-substituted phenoxyphenylacetic acid derivatives
MX2012010820A (es) 2010-03-22 2012-10-10 Actelion Pharmaceuticals Ltd Derivados de 3-(heteroaril-amino)-1, 2, 3, 4-tetrahidro-9h-carbazo l y sus uso como moduladores del receptor de prostaglandina d2.
EP2626349A4 (fr) * 2010-10-06 2014-03-12 Kureha Corp Composé amine et son utilisation
WO2012140612A1 (fr) 2011-04-14 2012-10-18 Actelion Pharmaceuticals Ltd Dérivés d'acide 7-(hétéroaryl-amino)-6,7,8,9-tétrahydropyrido[1,2-a]indolacétique et leur utilisation en tant que modulateurs du récepteur aux prostaglandines d2
EP2548863A1 (fr) * 2011-07-18 2013-01-23 Almirall, S.A. Nouveaux antagonistes de CRTH2
EP2762141A4 (fr) * 2011-09-29 2015-03-25 Shionogi & Co Produit pharmaceutique thérapeutique contre la rhinite allergique comportant un antagoniste de pgd2 et un antagoniste d'histamine
TW201331179A (zh) 2011-12-21 2013-08-01 Actelion Pharmaceuticals Ltd 雜環衍生物及其作為前列腺素d2受體調節劑之用途
EP2885307A1 (fr) 2012-07-05 2015-06-24 Actelion Pharmaceuticals Ltd. Dérivés hétérocyclylés 1-phényl-substitués et leur utilisation en tant que modulateurs du récepteur de la prostaglandine d2
EP2912458B1 (fr) 2012-10-24 2018-07-18 NYU Winthrop Hospital Biomarqueurs non-invasifs pour identifier les sujets à risque d'accouchement prématuré
JP6168520B2 (ja) * 2013-09-17 2017-07-26 国立大学法人 千葉大学 インドール化合物、dpプロスタノイド受容体アンタゴニスト、それを用いた薬剤、及びdpプロスタノイド受容体アンタゴニストの使用。
JP2015089886A (ja) * 2013-11-06 2015-05-11 国立大学法人名古屋大学 嵩高い置換基を有する化合物を用いた植物成長調整剤
PH12016501764B1 (en) 2014-03-17 2024-05-17 Idorsia Pharmaceuticals Ltd Azaindole acetic acid derivatives and their use as prostaglandin d2 receptor modulators
WO2015140701A1 (fr) 2014-03-18 2015-09-24 Actelion Pharmaceuticals Ltd Dérivés d'acide aza-indol-acétique et leur utilisation comme modulateurs des récepteurs de la prostaglandine d2
WO2017046125A1 (fr) 2015-09-15 2017-03-23 Actelion Pharmaceuticals Ltd Formes cristallines
KR20200109293A (ko) 2017-09-13 2020-09-22 프로제너티, 인크. 자간전증 바이오마커 및 관련된 시스템 및 방법
EP3759090A1 (fr) 2018-03-02 2021-01-06 Inflazome Limited Nouveaux composés
WO2021113710A1 (fr) 2019-12-04 2021-06-10 Progenity, Inc. Évaluation de la prééclampsie à l'aide de dosages du facteur de croissance placentaire libre et dissocié
CN113173877B (zh) * 2020-10-30 2023-10-27 江西师范大学 吲哚乙酰基亚氨基砜系列化合物及其制备方法
CN115925606B (zh) * 2023-01-05 2023-10-13 宁夏医科大学 一种5-(3-(磺酰胺基)苯基)-1h-吡咯-2-羧酸衍生物及其制备方法和应用
US12220411B1 (en) 2023-07-25 2025-02-11 The Eye Hospital Of Wenzhou Medical University Application of PTGDS inhibitor in preparation of drug for treating cataracts
CN117599052B (zh) * 2023-07-25 2026-07-24 温州医科大学附属眼视光医院 Ptgds的抑制剂在制备治疗白内障药物上的应用

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US7868037B2 (en) * 2004-07-14 2011-01-11 Ptc Therapeutics, Inc. Methods for treating hepatitis C

Also Published As

Publication number Publication date
CN101146770A (zh) 2008-03-19
TW200639151A (en) 2006-11-16
CR9214A (es) 2007-11-23
IL184816A0 (en) 2007-12-03
EP1844011A1 (fr) 2007-10-17
JP2008528606A (ja) 2008-07-31
KR20070110277A (ko) 2007-11-16
UY29346A1 (es) 2006-08-31
TNSN07251A1 (en) 2008-12-31
PE20060878A1 (es) 2006-10-18
NO20074336L (no) 2007-10-23
MX2007008277A (es) 2007-09-07
PA8661201A1 (es) 2006-09-08
SG158918A1 (en) 2010-02-26
AR054726A1 (es) 2007-07-11
CA2595728A1 (fr) 2006-08-03
GT200600030A (es) 2006-09-27
US20070265278A1 (en) 2007-11-15
BRPI0607079A2 (pt) 2009-08-04
WO2006081343A1 (fr) 2006-08-03
ZA200705449B (en) 2009-01-28
DOP2006000016A (es) 2006-07-31
AU2006209213A1 (en) 2006-08-03
RU2007132166A (ru) 2009-03-10

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