MA29071B1 - Amino-pyridimidine 2, 6-substituee-4-monosubstituee en tant qu'antagonistes de recepteur de la prostaglandine d2 - Google Patents

Amino-pyridimidine 2, 6-substituee-4-monosubstituee en tant qu'antagonistes de recepteur de la prostaglandine d2

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Publication number
MA29071B1
MA29071B1 MA29872A MA29872A MA29071B1 MA 29071 B1 MA29071 B1 MA 29071B1 MA 29872 A MA29872 A MA 29872A MA 29872 A MA29872 A MA 29872A MA 29071 B1 MA29071 B1 MA 29071B1
Authority
MA
Morocco
Prior art keywords
pyridimidine
prostaglandin
substituted
receptor antagonists
monosubstituted amino
Prior art date
Application number
MA29872A
Other languages
English (en)
Inventor
Sungtaek Lim
Keith John Harris
David Stefany
Charles J Gardner
Bin Cao
Ray Boffey
Timothy A Gillespy
Joacy C Aguiar
Hazel J Hunt
Elsa A Dechaux
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 MA29071B1 publication Critical patent/MA29071B1/fr

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    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
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    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
    • C07D239/32One oxygen, sulfur or nitrogen atom
    • C07D239/42One nitrogen atom
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • 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
    • A61K31/50Pyridazines; Hydrogenated pyridazines
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    • 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Pulmonology (AREA)
  • Immunology (AREA)
  • Dermatology (AREA)
  • Epidemiology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Otolaryngology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
MA29872A 2004-10-15 2007-05-04 Amino-pyridimidine 2, 6-substituee-4-monosubstituee en tant qu'antagonistes de recepteur de la prostaglandine d2 MA29071B1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US61927204P 2004-10-15 2004-10-15

Publications (1)

Publication Number Publication Date
MA29071B1 true MA29071B1 (fr) 2007-12-03

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ID=36072155

Family Applications (1)

Application Number Title Priority Date Filing Date
MA29872A MA29071B1 (fr) 2004-10-15 2007-05-04 Amino-pyridimidine 2, 6-substituee-4-monosubstituee en tant qu'antagonistes de recepteur de la prostaglandine d2

Country Status (36)

Country Link
US (2) US8193183B2 (fr)
EP (1) EP1891019B1 (fr)
JP (1) JP4970274B2 (fr)
KR (1) KR101280268B1 (fr)
CN (1) CN101039920B (fr)
AR (1) AR053770A1 (fr)
AU (1) AU2005295502B2 (fr)
BR (1) BRPI0516482A (fr)
CA (1) CA2583742C (fr)
CR (1) CR9003A (fr)
DK (1) DK1891019T3 (fr)
EC (1) ECSP077398A (fr)
ES (1) ES2392091T3 (fr)
GT (1) GT200500284A (fr)
HK (1) HK1108429A1 (fr)
HN (1) HN2005000795A (fr)
IL (1) IL182090A (fr)
MA (1) MA29071B1 (fr)
MX (1) MX2007003155A (fr)
MY (2) MY142453A (fr)
NO (1) NO339772B1 (fr)
NZ (1) NZ553919A (fr)
PA (1) PA8649801A1 (fr)
PE (1) PE20060936A1 (fr)
PL (1) PL1891019T3 (fr)
PT (1) PT1891019E (fr)
RU (1) RU2417990C2 (fr)
SG (1) SG156653A1 (fr)
SI (1) SI1891019T1 (fr)
SV (1) SV2006002272A (fr)
TN (1) TNSN07098A1 (fr)
TW (1) TWI372751B (fr)
UA (1) UA88485C2 (fr)
UY (1) UY29167A1 (fr)
WO (1) WO2006044732A2 (fr)
ZA (1) ZA200702209B (fr)

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AR060403A1 (es) * 2006-04-12 2008-06-11 Sanofi Aventis Compuestos de amino- pirimidina 2,6- sustituidos -4- monosustituidos como antagonistas del receptor de prostaglandina d2
WO2008039882A1 (fr) * 2006-09-30 2008-04-03 Sanofi-Aventis U.S. Llc Combinaison de niacine et d'un antagoniste du récepteur de prostaglandine d2
AU2008232771B2 (en) * 2007-03-30 2012-12-20 Sanofi-Aventis Pyrimidine hydrazide compounds as PGDS inhibitors
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EP2014657A1 (fr) * 2007-06-21 2009-01-14 Bayer Schering Pharma Aktiengesellschaft Diaminopyrimidine en tant que modulateurs du récepteur EP2
JP2010532366A (ja) 2007-06-29 2010-10-07 サノフィ−アベンティス 2−(3−{6−[2−(2,4−ジクロロフェニル)−エチルアミノ]−2−メトキシピリミジン−4−イル}−フェニル)−2−メチルプロピオン酸を製造する新しい方法
AU2008282728B2 (en) * 2007-08-02 2012-04-19 Amgen Inc. Pl3 kinase modulators and methods of use
WO2009055730A1 (fr) * 2007-10-25 2009-04-30 Genentech, Inc. Procédé de préparation de composés de thiénopyrimidine
BRPI0817135A2 (pt) * 2007-11-06 2014-10-07 Du Pont Composto, método de controle de doenças de plantas e composições fungicidas
CA2710194C (fr) 2007-12-19 2014-04-22 Amgen Inc. Inhibiteurs de la p13 kinase
AU2008345573B2 (en) 2007-12-20 2013-12-19 Envivo Pharmaceuticals, Inc. Tetrasubstituted benzenes
CA2714743C (fr) 2008-02-19 2017-01-17 Janssen Pharmaceutica N.V. Aryl-hydroxyethylamino-pyrimidines et triazines en tant que modulateurs d'amide d'acide gras hydrolase
WO2009127949A1 (fr) * 2008-04-17 2009-10-22 Pfizer Inc. Composés aryl carboxamides de 4-[3-(aryloxy)benzylidène]-3-méthyl pipéridine utiles comme inhibiteurs de la faah
GB2463788B (en) * 2008-09-29 2010-12-15 Amira Pharmaceuticals Inc Heteroaryl antagonists of prostaglandin D2 receptors
UY32251A (es) * 2008-11-20 2010-05-31 Glaxosmithkline Llc Compuestos quimicos
AR074776A1 (es) * 2008-12-18 2011-02-09 Sanofi Aventis Metodo para tratar la degeneracion macular; modulando el sistema inmunitario del paciente
WO2011022348A1 (fr) 2009-08-18 2011-02-24 Janssen Pharmaceutica Nv Modulateurs d'éthylène diamine d'une amide hydrolase d'acide gras
CN103038228A (zh) * 2010-03-16 2013-04-10 安万特药物公司 作为前列腺素d2受体拮抗剂的取代的嘧啶类化合物
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