DZ3513A1 - Derives d'imidazole a noyau aryle ou heteroaryle condense, utiles comme agents anti-inflammatoires analgesiques - Google Patents
Derives d'imidazole a noyau aryle ou heteroaryle condense, utiles comme agents anti-inflammatoires analgesiquesInfo
- Publication number
- DZ3513A1 DZ3513A1 DZ013513A DZ013513A DZ3513A1 DZ 3513 A1 DZ3513 A1 DZ 3513A1 DZ 013513 A DZ013513 A DZ 013513A DZ 013513 A DZ013513 A DZ 013513A DZ 3513 A1 DZ3513 A1 DZ 3513A1
- Authority
- DZ
- Algeria
- Prior art keywords
- arylated
- condensed
- useful
- inflammatory agents
- imidazole derivatives
- Prior art date
Links
Classifications
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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
- A61K31/4164—1,3-Diazoles
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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US24182500P | 2000-10-19 | 2000-10-19 | |
PCT/IB2001/001940 WO2002032900A2 (fr) | 2000-10-19 | 2001-10-15 | Composes imidazoles condenses avec aryle ou heteroaryle, utiles en tant qu'agents analgesiques anti-inflammatoires |
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DZ3513A1 true DZ3513A1 (fr) | 2002-04-25 |
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DZ013513A DZ3513A1 (fr) | 2000-10-19 | 2001-10-15 | Derives d'imidazole a noyau aryle ou heteroaryle condense, utiles comme agents anti-inflammatoires analgesiques |
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IL94805A (en) * | 1989-06-28 | 1994-04-12 | Ciba Geigy Ag | Certain translocated carboxylic acids (a) Arylsulfonamide - and pyridyl - or imidazolil (), process for their preparation and pharmaceutical preparations containing them |
GB9009469D0 (en) * | 1990-04-27 | 1990-06-20 | British Bio Technology | Compounds |
GB9010404D0 (en) * | 1990-05-09 | 1990-06-27 | Pfizer Ltd | Therapeutic agents |
GB2330307A (en) * | 1998-02-07 | 1999-04-21 | Glaxo Group Ltd | EP4 Receptor antagonists as bone resorption inhibitors |
EP1071648A2 (fr) * | 1998-03-13 | 2001-01-31 | Merck Frosst Canada & Co. | Acides carboxyliques et acylsulfonamides, compositions contenant ces composes et methodes de traitement |
EP1148877A4 (fr) | 1998-10-15 | 2003-01-22 | Merck & Co Inc | Inhibition de la resorption osseuse |
EP1121133A1 (fr) * | 1998-10-15 | 2001-08-08 | Merck & Co., Inc. | Methodes de stimulation de la formation osseuse |
JP2000191615A (ja) * | 1998-10-20 | 2000-07-11 | Takeda Chem Ind Ltd | 芳香族アミン誘導体、その製造法および剤 |
DK1183245T3 (da) | 1999-04-22 | 2007-09-24 | Lundbeck & Co As H | Selektive NPY(Y5)-antagonister |
HUP0201291A3 (en) | 1999-04-28 | 2002-11-28 | Sanofi Aventis Deutschland | Di-aryl acid derivatives as ppar receptor ligands and pharmaceutical compositions containing them |
GB0031302D0 (en) | 2000-12-21 | 2001-01-31 | Glaxo Group Ltd | Napthalene derivatives |
GB0031315D0 (en) | 2000-12-21 | 2001-02-07 | Glaxo Group Ltd | Indole derivatives |
GB0031295D0 (en) | 2000-12-21 | 2001-01-31 | Glaxo Group Ltd | Naphthalene derivatives |
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2001
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- 2001-10-15 KR KR1020037005443A patent/KR100582319B1/ko active IP Right Grant
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2003
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2004
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2006
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2007
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