HK1148016A1 - - Google Patents
Info
- Publication number
- HK1148016A1 HK1148016A1 HK11102219.8A HK11102219A HK1148016A1 HK 1148016 A1 HK1148016 A1 HK 1148016A1 HK 11102219 A HK11102219 A HK 11102219A HK 1148016 A1 HK1148016 A1 HK 1148016A1
- Authority
- HK
- Hong Kong
- Prior art keywords
- pyridine
- imidazo
- carboxamide
- alkyl
- alkoxy
- Prior art date
Links
- 125000000217 alkyl group Chemical group 0.000 abstract 11
- 125000003545 alkoxy group Chemical group 0.000 abstract 7
- 125000005843 halogen group Chemical group 0.000 abstract 6
- 102100022676 Nuclear receptor subfamily 4 group A member 2 Human genes 0.000 abstract 4
- 101001109698 Homo sapiens Nuclear receptor subfamily 4 group A member 2 Proteins 0.000 abstract 3
- 108020005497 Nuclear hormone receptor Proteins 0.000 abstract 3
- 102000006255 nuclear receptors Human genes 0.000 abstract 3
- 108020004017 nuclear receptors Proteins 0.000 abstract 3
- 101001109694 Rattus norvegicus Nuclear receptor subfamily 4 group A member 2 Proteins 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical compound OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 102000004169 proteins and genes Human genes 0.000 abstract 2
- 108090000623 proteins and genes Proteins 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- -1 1,1-dimethylethoxy Chemical group 0.000 abstract 1
- UPSCSXUIMGDVSR-UHFFFAOYSA-N 6-(2-bromoacetyl)-n-phenylimidazo[1,2-a]pyridine-2-carboxamide Chemical compound C=1N2C=C(C(=O)CBr)C=CC2=NC=1C(=O)NC1=CC=CC=C1 UPSCSXUIMGDVSR-UHFFFAOYSA-N 0.000 abstract 1
- ICPHWBWBUHXEJO-UHFFFAOYSA-N 6-[6-[(2-methylpropan-2-yl)oxycarbonylamino]pyridin-2-yl]imidazo[1,2-a]pyridine-2-carboxylic acid Chemical compound CC(C)(C)OC(=O)NC1=CC=CC(C2=CN3C=C(N=C3C=C2)C(O)=O)=N1 ICPHWBWBUHXEJO-UHFFFAOYSA-N 0.000 abstract 1
- TVNRQGCHTDNMMK-UHFFFAOYSA-N 6-bromo-n-phenylimidazo[1,2-a]pyridine-2-carboxamide Chemical compound C=1N2C=C(Br)C=CC2=NC=1C(=O)NC1=CC=CC=C1 TVNRQGCHTDNMMK-UHFFFAOYSA-N 0.000 abstract 1
- QGYSDCUABQPBLN-UHFFFAOYSA-N 6-cyano-n-phenylimidazo[1,2-a]pyridine-2-carboxamide Chemical compound C=1N2C=C(C#N)C=CC2=NC=1C(=O)NC1=CC=CC=C1 QGYSDCUABQPBLN-UHFFFAOYSA-N 0.000 abstract 1
- ZPNPNJFWUJEMHV-UHFFFAOYSA-N 6-ethenyl-n-phenylimidazo[1,2-a]pyridine-2-carboxamide Chemical compound C=1N2C=C(C=C)C=CC2=NC=1C(=O)NC1=CC=CC=C1 ZPNPNJFWUJEMHV-UHFFFAOYSA-N 0.000 abstract 1
- WUFMZQMQOKCTCU-UHFFFAOYSA-N 6-formyl-n-phenylimidazo[1,2-a]pyridine-2-carboxamide Chemical compound C=1N2C=C(C=O)C=CC2=NC=1C(=O)NC1=CC=CC=C1 WUFMZQMQOKCTCU-UHFFFAOYSA-N 0.000 abstract 1
- ZFHZWMMMOXCBEI-UHFFFAOYSA-N 6-imidazo[1,2-a]pyridin-6-ylpyridin-2-amine propanoic acid Chemical compound CCC(=O)O.NC1=CC=CC(=N1)C=1C=CC=2N(C1)C=CN2 ZFHZWMMMOXCBEI-UHFFFAOYSA-N 0.000 abstract 1
- AVXDQXWDDPHUAG-UHFFFAOYSA-N 6-iodo-n-phenylimidazo[1,2-a]pyridine-2-carboxamide Chemical compound C=1N2C=C(I)C=CC2=NC=1C(=O)NC1=CC=CC=C1 AVXDQXWDDPHUAG-UHFFFAOYSA-N 0.000 abstract 1
- UTRHHBXFIAIQFN-UHFFFAOYSA-N 6-pyridin-2-ylimidazo[1,2-a]pyridine-2-carboxylic acid Chemical compound C1=CC2=NC(C(=O)O)=CN2C=C1C1=CC=CC=N1 UTRHHBXFIAIQFN-UHFFFAOYSA-N 0.000 abstract 1
- NUJLYEFXZKOOQP-UHFFFAOYSA-N CCC(=O)O.C1(=CC=CC=C1)C(N1C=NC(=C1)C=1C=CC=2N(C1)C=CN2)(C2=CC=CC=C2)C2=CC=CC=C2 Chemical compound CCC(=O)O.C1(=CC=CC=C1)C(N1C=NC(=C1)C=1C=CC=2N(C1)C=CN2)(C2=CC=CC=C2)C2=CC=CC=C2 NUJLYEFXZKOOQP-UHFFFAOYSA-N 0.000 abstract 1
- SVCIAQKWMPVRGD-UHFFFAOYSA-N CCC(=O)O.CC(C)(OC(=O)NC=1SC=C(N1)C=1C=CC=2N(C1)C=CN2)C Chemical compound CCC(=O)O.CC(C)(OC(=O)NC=1SC=C(N1)C=1C=CC=2N(C1)C=CN2)C SVCIAQKWMPVRGD-UHFFFAOYSA-N 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 abstract 1
- 108010093175 Member 2 Group A Nuclear Receptor Subfamily 4 Proteins 0.000 abstract 1
- ZUBQCVLPVVRZLM-UHFFFAOYSA-N N-(3-fluorophenyl)-7-(1H-1,2,4-triazol-5-yl)imidazo[1,2-a]pyridine-2-carboxamide Chemical compound FC=1C=C(C=CC1)NC(=O)C=1N=C2N(C=CC(=C2)C2=NNC=N2)C1 ZUBQCVLPVVRZLM-UHFFFAOYSA-N 0.000 abstract 1
- 210000001744 T-lymphocyte Anatomy 0.000 abstract 1
- 102100024671 Zinc finger protein 3 Human genes 0.000 abstract 1
- 101710180928 Zinc finger protein 3 Proteins 0.000 abstract 1
- XQZLRSPDYDSZDK-UHFFFAOYSA-N [2-(phenylcarbamoyl)imidazo[1,2-a]pyridin-6-yl]boronic acid Chemical compound C=1N2C=C(B(O)O)C=CC2=NC=1C(=O)NC1=CC=CC=C1 XQZLRSPDYDSZDK-UHFFFAOYSA-N 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 230000003266 anti-allergic effect Effects 0.000 abstract 1
- 230000002456 anti-arthritic effect Effects 0.000 abstract 1
- 230000001088 anti-asthma Effects 0.000 abstract 1
- 230000001773 anti-convulsant effect Effects 0.000 abstract 1
- 230000001430 anti-depressive effect Effects 0.000 abstract 1
- 230000003178 anti-diabetic effect Effects 0.000 abstract 1
- 230000003110 anti-inflammatory effect Effects 0.000 abstract 1
- 230000000648 anti-parkinson Effects 0.000 abstract 1
- 230000003356 anti-rheumatic effect Effects 0.000 abstract 1
- 230000000767 anti-ulcer Effects 0.000 abstract 1
- 239000000924 antiasthmatic agent Substances 0.000 abstract 1
- 239000001961 anticonvulsive agent Substances 0.000 abstract 1
- 239000000935 antidepressant agent Substances 0.000 abstract 1
- 229940005513 antidepressants Drugs 0.000 abstract 1
- 239000003472 antidiabetic agent Substances 0.000 abstract 1
- 229960003965 antiepileptics Drugs 0.000 abstract 1
- 239000000939 antiparkinson agent Substances 0.000 abstract 1
- 239000003435 antirheumatic agent Substances 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 210000004027 cell Anatomy 0.000 abstract 1
- 230000001966 cerebroprotective effect Effects 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000000824 cytostatic agent Substances 0.000 abstract 1
- 230000001085 cytostatic effect Effects 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 210000001320 hippocampus Anatomy 0.000 abstract 1
- 239000002955 immunomodulating agent Substances 0.000 abstract 1
- 230000002584 immunomodulator Effects 0.000 abstract 1
- 229940121354 immunomodulator Drugs 0.000 abstract 1
- 230000001506 immunosuppresive effect Effects 0.000 abstract 1
- 230000010534 mechanism of action Effects 0.000 abstract 1
- OXJHFELWRIRKLL-UHFFFAOYSA-N n-(3,5-difluorophenyl)-6-iodoimidazo[1,2-a]pyridine-2-carboxamide Chemical compound FC1=CC(F)=CC(NC(=O)C=2N=C3C=CC(I)=CN3C=2)=C1 OXJHFELWRIRKLL-UHFFFAOYSA-N 0.000 abstract 1
- LLLARNVVXAQHTI-UHFFFAOYSA-N n-(4-bromophenyl)-6-(1-methylpiperidin-2-yl)imidazo[1,2-a]pyridine-2-carboxamide Chemical compound CN1CCCCC1C1=CN2C=C(C(=O)NC=3C=CC(Br)=CC=3)N=C2C=C1 LLLARNVVXAQHTI-UHFFFAOYSA-N 0.000 abstract 1
- XRWSMMDFINJOOL-UHFFFAOYSA-N n-phenyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)imidazo[1,2-a]pyridine-2-carboxamide Chemical compound O1C(C)(C)C(C)(C)OB1C1=CN2C=C(C(=O)NC=3C=CC=CC=3)N=C2C=C1 XRWSMMDFINJOOL-UHFFFAOYSA-N 0.000 abstract 1
- YJWNPRCOKOKATB-UHFFFAOYSA-N n-phenyl-6-trimethylstannylimidazo[1,2-a]pyridine-2-carboxamide Chemical compound C=1N2C=C([Sn](C)(C)C)C=CC2=NC=1C(=O)NC1=CC=CC=C1 YJWNPRCOKOKATB-UHFFFAOYSA-N 0.000 abstract 1
- 239000003176 neuroleptic agent Substances 0.000 abstract 1
- 230000000701 neuroleptic effect Effects 0.000 abstract 1
- 230000000324 neuroprotective effect Effects 0.000 abstract 1
- 230000001777 nootropic effect Effects 0.000 abstract 1
- 125000000369 oxido group Chemical group [*]=O 0.000 abstract 1
- IBBMAWULFFBRKK-UHFFFAOYSA-N picolinamide Chemical compound NC(=O)C1=CC=CC=N1 IBBMAWULFFBRKK-UHFFFAOYSA-N 0.000 abstract 1
- UXRUJTKYYCGQBB-UHFFFAOYSA-N propanoic acid 6-pyridin-2-ylimidazo[1,2-a]pyridine Chemical compound CCC(=O)O.N1=C(C=CC=C1)C=1C=CC=2N(C1)C=CN2 UXRUJTKYYCGQBB-UHFFFAOYSA-N 0.000 abstract 1
- LAAQFBNTFJQJKJ-UHFFFAOYSA-N tert-butyl N-(6-imidazo[1,2-a]pyridin-6-ylpyridin-2-yl)-N-[(2-methylpropan-2-yl)oxycarbonyl]carbamate propanoic acid Chemical compound CCC(=O)O.CC(C)(OC(=O)N(C1=CC=CC(=N1)C=1C=CC=2N(C1)C=CN2)C(=O)OC(C)(C)C)C LAAQFBNTFJQJKJ-UHFFFAOYSA-N 0.000 abstract 1
- 229940125725 tranquilizer Drugs 0.000 abstract 1
- 239000003204 tranquilizing agent Substances 0.000 abstract 1
- 230000002936 tranquilizing effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- 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
-
- 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
- A61P25/08—Antiepileptics; Anticonvulsants
-
- 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
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- 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
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- 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
- A61P25/24—Antidepressants
-
- 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
- A61P25/26—Psychostimulants, e.g. nicotine, cocaine
-
- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- 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
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
- C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
- C07F7/0814—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring said ring is substituted at a C ring atom by Si
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin compounds
- C07F7/2208—Compounds having tin linked only to carbon, hydrogen and/or halogen
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Addiction (AREA)
- Heart & Thoracic Surgery (AREA)
- Hospice & Palliative Care (AREA)
- Psychology (AREA)
- Cardiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0800005A FR2925903B1 (fr) | 2008-01-02 | 2008-01-02 | DERIVES 6-HETEROCYCLIQUE-IMIDAZO°1,2-a!PYRIDINE-2- CARBOXAMIDES, LEUR PREPARATION ET LEUR APPLICATION EN THERAPEUTIQUE |
| PCT/FR2008/001836 WO2009106750A2 (fr) | 2008-01-02 | 2008-12-31 | Dérivés 6-heterocyclique-imidazo[1,2-a]pyrroine-2-carboxamides, leur préparation et leur application en thérapeutique |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HK1148016A1 true HK1148016A1 (es) | 2011-08-26 |
Family
ID=39745373
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HK11102219.8A HK1148016A1 (es) | 2008-01-02 | 2011-03-07 |
Country Status (25)
| Country | Link |
|---|---|
| US (2) | US8314109B2 (es) |
| EP (1) | EP2225240B1 (es) |
| JP (1) | JP5258899B2 (es) |
| KR (1) | KR101600635B1 (es) |
| CN (1) | CN101959884B (es) |
| AR (1) | AR070074A1 (es) |
| AU (1) | AU2008351928B2 (es) |
| BR (1) | BRPI0821458A2 (es) |
| CA (1) | CA2710947C (es) |
| CL (1) | CL2008003928A1 (es) |
| CO (1) | CO6331309A2 (es) |
| EA (1) | EA019122B1 (es) |
| FR (1) | FR2925903B1 (es) |
| HK (1) | HK1148016A1 (es) |
| IL (1) | IL206669A (es) |
| MA (1) | MA32527B1 (es) |
| ME (1) | ME01157B (es) |
| MX (1) | MX2010007353A (es) |
| MY (1) | MY155468A (es) |
| NZ (1) | NZ586474A (es) |
| SG (1) | SG187408A1 (es) |
| TW (1) | TWI432432B (es) |
| UY (1) | UY31589A1 (es) |
| WO (1) | WO2009106750A2 (es) |
| ZA (1) | ZA201004644B (es) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2925907B1 (fr) * | 2008-01-02 | 2010-10-15 | Sanofi Aventis | DERIVES DE 2-HETEROAROYL-IMIDAZO°1,2-a!PYRIDINE, LEUR PREPARATION ET LEUR APPLICATION EN THERAPEUTIQUE |
| CA2852615A1 (en) * | 2011-10-21 | 2013-04-25 | Torrent Pharmaceuticals Limited | Novel substituted imidazopyrimidines as gpbar1 receptor modulators |
| KR101716993B1 (ko) | 2012-12-25 | 2017-03-15 | 닛뽕소다 가부시키가이샤 | 할로겐화 아닐린 및 그 제조 방법 |
| CN108295074B (zh) * | 2018-02-01 | 2020-08-28 | 华中农业大学 | 一种噻二唑并三嗪类化合物在制备单胺氧化酶抑制剂中的用途 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2638161B1 (fr) * | 1988-10-24 | 1991-01-11 | Centre Nat Rech Scient | Nouvelles benzoyl-2 imidazo (1,2-a) pyridines et leurs sels, leur procede de preparation, leur application a titre de medicaments et les compositions pharmaceutiques les renfermant |
| IE904346A1 (en) * | 1989-12-04 | 1991-06-05 | Searle & Co | IMIDAZO[1,2-a]PYRIDINYLALKYL COMPOUNDS FOR TREATMENT OF¹NEUROTOXIC INJURY |
| AU2003269354B2 (en) * | 2002-09-24 | 2008-03-06 | Neuro Therapeutics Ab | Methods for promoting dopaminergic neuronal development by using NG4A-subfamily and Wnt-ligands |
| EP1567527A1 (en) * | 2002-11-27 | 2005-08-31 | Eli Lilly And Company | Condensed pyrazolo derivatives |
| WO2004103991A1 (fr) * | 2003-05-20 | 2004-12-02 | 'chemical Diversity Research Institute', Ltd. | Piperidines 2-substituees, bibliotheque focalisee et composition pharmaceutique |
| DE102005019181A1 (de) * | 2005-04-25 | 2006-10-26 | Novartis Ag | Peptid-Deformylase (PDF) Inhibitoren 1 |
| FR2903108B1 (fr) * | 2006-07-03 | 2008-08-29 | Sanofi Aventis Sa | Utilisation de derives d'imidazo[1,2-a] pyridine-2-carboxamides en therapeutique. |
| FR2903107B1 (fr) * | 2006-07-03 | 2008-08-22 | Sanofi Aventis Sa | Derives d'imidazopyridine-2-carboxamides, leur preparation et leur application en therapeutique |
| FR2903106B1 (fr) * | 2006-07-03 | 2010-07-30 | Sanofi Aventis | Utilisations de 2-benzoyl-imidazopyridines en therapeutique |
-
2008
- 2008-01-02 FR FR0800005A patent/FR2925903B1/fr not_active Expired - Fee Related
- 2008-12-30 UY UY31589A patent/UY31589A1/es not_active Application Discontinuation
- 2008-12-30 AR ARP080105779A patent/AR070074A1/es unknown
- 2008-12-30 CL CL2008003928A patent/CL2008003928A1/es unknown
- 2008-12-31 WO PCT/FR2008/001836 patent/WO2009106750A2/fr active Application Filing
- 2008-12-31 ME MEP-2010-103A patent/ME01157B/me unknown
- 2008-12-31 EP EP08872775.5A patent/EP2225240B1/fr active Active
- 2008-12-31 CN CN2008801277669A patent/CN101959884B/zh not_active Expired - Fee Related
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