JP5205276B2 - 酵素阻害剤 - Google Patents
酵素阻害剤 Download PDFInfo
- Publication number
- JP5205276B2 JP5205276B2 JP2008546614A JP2008546614A JP5205276B2 JP 5205276 B2 JP5205276 B2 JP 5205276B2 JP 2008546614 A JP2008546614 A JP 2008546614A JP 2008546614 A JP2008546614 A JP 2008546614A JP 5205276 B2 JP5205276 B2 JP 5205276B2
- Authority
- JP
- Japan
- Prior art keywords
- mmol
- pyridine
- piperazine
- imidazo
- pyridin
- Prior art date
- Legal status (The legal status 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 status listed.)
- Active
Links
- 0 CN1CC*(*)CC1 Chemical compound CN1CC*(*)CC1 0.000 description 4
- XGTJAALWHZACGE-UHFFFAOYSA-N Bc1cnc2[nH]c(-c(cc3)ccc3N(C)C)nc2c1N(CC1)CCN1C=C Chemical compound Bc1cnc2[nH]c(-c(cc3)ccc3N(C)C)nc2c1N(CC1)CCN1C=C XGTJAALWHZACGE-UHFFFAOYSA-N 0.000 description 1
- XTWIBTGKSHFGFX-UHFFFAOYSA-N Bc1cnc2[nH]c(C3=CCC(CN4CCOCC4)C=C3)nc2c1N1CCN(Cc2c[s]c(C)n2)CC1 Chemical compound Bc1cnc2[nH]c(C3=CCC(CN4CCOCC4)C=C3)nc2c1N1CCN(Cc2c[s]c(C)n2)CC1 XTWIBTGKSHFGFX-UHFFFAOYSA-N 0.000 description 1
- DMJJAOQGCLCTHC-DDYQODIZSA-N CC(/C(/C=C\N=C)=C/C)N(CC1)CCN1c(c(nc(-c(cc1)ccc1OC)[nH]1)c1nc1)c1Br Chemical compound CC(/C(/C=C\N=C)=C/C)N(CC1)CCN1c(c(nc(-c(cc1)ccc1OC)[nH]1)c1nc1)c1Br DMJJAOQGCLCTHC-DDYQODIZSA-N 0.000 description 1
- PMOUTRVUUVWDQR-UHFFFAOYSA-N CC(C)(C)OC(N1CCN(Cc2n[o]c(C)c2)CC1)=O Chemical compound CC(C)(C)OC(N1CCN(Cc2n[o]c(C)c2)CC1)=O PMOUTRVUUVWDQR-UHFFFAOYSA-N 0.000 description 1
- BMJCQIUKICOIHH-UHFFFAOYSA-N CC(c1ccccc1)N(CC1)CCN1c(c(nc(-c(cc1)ccc1N(C)C)[nH]1)c1nc1)c1Cl Chemical compound CC(c1ccccc1)N(CC1)CCN1c(c(nc(-c(cc1)ccc1N(C)C)[nH]1)c1nc1)c1Cl BMJCQIUKICOIHH-UHFFFAOYSA-N 0.000 description 1
- AWOUTRVTXAOOOH-UHFFFAOYSA-N CC(c1ccccc1)N(CC1)CCN1c(c(nc(-c(cc1)ccc1N1CCN(C)CC1)[nH]1)c1nc1)c1Br Chemical compound CC(c1ccccc1)N(CC1)CCN1c(c(nc(-c(cc1)ccc1N1CCN(C)CC1)[nH]1)c1nc1)c1Br AWOUTRVTXAOOOH-UHFFFAOYSA-N 0.000 description 1
- CPHQNNZDTOMGME-UHFFFAOYSA-N CC(c1ccccc1)N(CC1)CCN1c(c(nc(-c1ccc(CN2CCOCC2)cc1)[nH]1)c1nc1)c1[Br]=C Chemical compound CC(c1ccccc1)N(CC1)CCN1c(c(nc(-c1ccc(CN2CCOCC2)cc1)[nH]1)c1nc1)c1[Br]=C CPHQNNZDTOMGME-UHFFFAOYSA-N 0.000 description 1
- VLYSXKFFDDERAO-UHFFFAOYSA-N CC(c1ccccn1)N(CC1)CCN1c(c([N+]([O-])=O)c(N)nc1)c1Br Chemical compound CC(c1ccccn1)N(CC1)CCN1c(c([N+]([O-])=O)c(N)nc1)c1Br VLYSXKFFDDERAO-UHFFFAOYSA-N 0.000 description 1
- CWSGKEIBGQREHF-UHFFFAOYSA-N CN(C(c(cc1)ccc1OC)N1)c2c1ncc(C=[BrH])c2N1CCN(Cc2c[s]cn2)CC1 Chemical compound CN(C(c(cc1)ccc1OC)N1)c2c1ncc(C=[BrH])c2N1CCN(Cc2c[s]cn2)CC1 CWSGKEIBGQREHF-UHFFFAOYSA-N 0.000 description 1
- NUJNIVFRVOPULY-UHFFFAOYSA-N CN(C)CCOc(cc1)ccc1-c([nH]1)nc2c1ncc(Br)c2N1CCN(Cc2cnccc2)CC1 Chemical compound CN(C)CCOc(cc1)ccc1-c([nH]1)nc2c1ncc(Br)c2N1CCN(Cc2cnccc2)CC1 NUJNIVFRVOPULY-UHFFFAOYSA-N 0.000 description 1
- ZZGCDTUWDYCDMK-UHFFFAOYSA-N CN(C)Cc(cc1)ccc1-c([nH]c1ncc2Br)nc1c2N1CCN(Cc2cccnc2)CC1 Chemical compound CN(C)Cc(cc1)ccc1-c([nH]c1ncc2Br)nc1c2N1CCN(Cc2cccnc2)CC1 ZZGCDTUWDYCDMK-UHFFFAOYSA-N 0.000 description 1
- XYGOLWNJJOEHQQ-UHFFFAOYSA-N CN(C)c(cc1)ccc1-c([nH]1)nc2c1ncc(Cl)c2N1CCN(CCOc2ccccc2)CC1 Chemical compound CN(C)c(cc1)ccc1-c([nH]1)nc2c1ncc(Cl)c2N1CCN(CCOc2ccccc2)CC1 XYGOLWNJJOEHQQ-UHFFFAOYSA-N 0.000 description 1
- VUSIBCSDUOMGIP-UHFFFAOYSA-N CN(C)c(cc1)ccc1-c([nH]1)nc2c1ncc(S)c2N(CC1)CCN1C(Nc1ccccc1)=O Chemical compound CN(C)c(cc1)ccc1-c([nH]1)nc2c1ncc(S)c2N(CC1)CCN1C(Nc1ccccc1)=O VUSIBCSDUOMGIP-UHFFFAOYSA-N 0.000 description 1
- PZPZWQJLZXJMOZ-UHFFFAOYSA-N COc(cc1)ccc1-c([nH]1)nc2c1ncc(Br)c2N1CCN(Cc2cnc(C(F)(F)F)cc2)CC1 Chemical compound COc(cc1)ccc1-c([nH]1)nc2c1ncc(Br)c2N1CCN(Cc2cnc(C(F)(F)F)cc2)CC1 PZPZWQJLZXJMOZ-UHFFFAOYSA-N 0.000 description 1
- SBFRYLGLYVWCPP-UHFFFAOYSA-N Cc(c(N1CCN(CC(Nc2ncc[s]2)=O)CC1)c1[N+]([O-])=O)cnc1N Chemical compound Cc(c(N1CCN(CC(Nc2ncc[s]2)=O)CC1)c1[N+]([O-])=O)cnc1N SBFRYLGLYVWCPP-UHFFFAOYSA-N 0.000 description 1
- UUZCMALYIRLDMB-UHFFFAOYSA-N Cc(cnc1c2nc(-c(cc3)ccc3N3CCOCC3)[nH]1)c2N1CCN(Cc2cccnc2)CC1 Chemical compound Cc(cnc1c2nc(-c(cc3)ccc3N3CCOCC3)[nH]1)c2N1CCN(Cc2cccnc2)CC1 UUZCMALYIRLDMB-UHFFFAOYSA-N 0.000 description 1
- UCMBJCSZCYRYBL-UHFFFAOYSA-N Cc(cnc1c2nc(-c3ccc(CN4CCNCC4)cc3)[nH]1)c2N1CCN(Cc2cncnc2)CC1 Chemical compound Cc(cnc1c2nc(-c3ccc(CN4CCNCC4)cc3)[nH]1)c2N1CCN(Cc2cncnc2)CC1 UCMBJCSZCYRYBL-UHFFFAOYSA-N 0.000 description 1
- FJRUVPMBOVLASK-UHFFFAOYSA-N Cc1cc(CN(CC2)CCN2c(c([N+]([O-])=O)c(N)nc2)c2Cl)n[o]1 Chemical compound Cc1cc(CN(CC2)CCN2c(c([N+]([O-])=O)c(N)nc2)c2Cl)n[o]1 FJRUVPMBOVLASK-UHFFFAOYSA-N 0.000 description 1
- ZDHLKZRRPUHBPW-UHFFFAOYSA-N Cc1nc(CN(CC2)CCN2c(c([N+]([O-])=O)c(N)nc2)c2Cl)c[s]1 Chemical compound Cc1nc(CN(CC2)CCN2c(c([N+]([O-])=O)c(N)nc2)c2Cl)c[s]1 ZDHLKZRRPUHBPW-UHFFFAOYSA-N 0.000 description 1
- WKGJPDSBQCJEBD-UHFFFAOYSA-N Cc1nc(CN(CC2)CCN2c(c(nc(-c(cc2)ccc2-[n]2nccc2)[nH]2)c2nc2)c2Br)c[s]1 Chemical compound Cc1nc(CN(CC2)CCN2c(c(nc(-c(cc2)ccc2-[n]2nccc2)[nH]2)c2nc2)c2Br)c[s]1 WKGJPDSBQCJEBD-UHFFFAOYSA-N 0.000 description 1
- SEBZZEUNOZDMLV-UHFFFAOYSA-N Cc1nc(CN(CC2)CCN2c(c(nc(-c(cc2)ccc2OC)[nH]2)c2nc2)c2Br)c[s]1 Chemical compound Cc1nc(CN(CC2)CCN2c(c(nc(-c(cc2)ccc2OC)[nH]2)c2nc2)c2Br)c[s]1 SEBZZEUNOZDMLV-UHFFFAOYSA-N 0.000 description 1
- RDOHVRMBAPAICL-UHFFFAOYSA-N Cc1nc(CN(CC2)CCN2c(c(nc(-c2ccc(CN3CCNCC3)cc2)[nH]2)c2nc2)c2Br)c[s]1 Chemical compound Cc1nc(CN(CC2)CCN2c(c(nc(-c2ccc(CN3CCNCC3)cc2)[nH]2)c2nc2)c2Br)c[s]1 RDOHVRMBAPAICL-UHFFFAOYSA-N 0.000 description 1
- IZRXRZKKTJHSGV-UHFFFAOYSA-N Clc1ccc(CN(CC2)CCN2c(c(nc(-c2ccc(CN3CCOCC3)cc2)[nH]2)c2nc2)c2Br)cc1 Chemical compound Clc1ccc(CN(CC2)CCN2c(c(nc(-c2ccc(CN3CCOCC3)cc2)[nH]2)c2nc2)c2Br)cc1 IZRXRZKKTJHSGV-UHFFFAOYSA-N 0.000 description 1
- RWVPUUWFAXNOJL-UHFFFAOYSA-N Nc(c([N+]([O-])=O)c1N2CCN(CC(Nc3ccccc3)=O)CC2)ncc1Br Chemical compound Nc(c([N+]([O-])=O)c1N2CCN(CC(Nc3ccccc3)=O)CC2)ncc1Br RWVPUUWFAXNOJL-UHFFFAOYSA-N 0.000 description 1
- PUFSTYPSVFGZJM-UHFFFAOYSA-N O=C(CN(CC1)CCN1c(c(nc(-c(cc1)ccc1N(CC1)CCS1(=O)=O)[nH]1)c1nc1)c1Cl)Nc1ncc[s]1 Chemical compound O=C(CN(CC1)CCN1c(c(nc(-c(cc1)ccc1N(CC1)CCS1(=O)=O)[nH]1)c1nc1)c1Cl)Nc1ncc[s]1 PUFSTYPSVFGZJM-UHFFFAOYSA-N 0.000 description 1
- XZJMUBUWAJLUOS-UHFFFAOYSA-N O=C(CN(CC1)CCN1c(c(nc(-c1ccc2OCCOc2c1)[nH]1)c1nc1)c1Cl)Nc1ncc[s]1 Chemical compound O=C(CN(CC1)CCN1c(c(nc(-c1ccc2OCCOc2c1)[nH]1)c1nc1)c1Cl)Nc1ncc[s]1 XZJMUBUWAJLUOS-UHFFFAOYSA-N 0.000 description 1
- QGUCXPYHWHDNGM-UHFFFAOYSA-N OCCOc(cc1)ccc1-c([nH]1)nc2c1ncc(Cl)c2N1CCN(CC(Nc2ncc[s]2)=O)CC1 Chemical compound OCCOc(cc1)ccc1-c([nH]1)nc2c1ncc(Cl)c2N1CCN(CC(Nc2ncc[s]2)=O)CC1 QGUCXPYHWHDNGM-UHFFFAOYSA-N 0.000 description 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
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- 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
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Immunology (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Rheumatology (AREA)
- Pulmonology (AREA)
- Transplantation (AREA)
- Pain & Pain Management (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0526169.8 | 2005-12-22 | ||
| GB0526169A GB0526169D0 (en) | 2005-12-22 | 2005-12-22 | Enzyme inhibitors |
| GB0620884A GB0620884D0 (en) | 2006-10-20 | 2006-10-20 | Enzyme inhibitors |
| GB0620884.7 | 2006-10-20 | ||
| PCT/GB2006/004854 WO2007072017A2 (en) | 2005-12-22 | 2006-12-21 | Enzyme inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2009520791A JP2009520791A (ja) | 2009-05-28 |
| JP2009520791A5 JP2009520791A5 (enExample) | 2010-02-12 |
| JP5205276B2 true JP5205276B2 (ja) | 2013-06-05 |
Family
ID=38091678
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008546614A Active JP5205276B2 (ja) | 2005-12-22 | 2006-12-21 | 酵素阻害剤 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US8088761B2 (enExample) |
| EP (1) | EP1963315B1 (enExample) |
| JP (1) | JP5205276B2 (enExample) |
| ES (1) | ES2526813T3 (enExample) |
| WO (1) | WO2007072017A2 (enExample) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008121064A1 (en) * | 2007-03-30 | 2008-10-09 | Astrazeneca Ab | New imidazo[4,5-b]pyridine-6-halo-7-aryl/heteroaryl compounds 705 |
| WO2009001021A1 (en) * | 2007-06-26 | 2008-12-31 | Chroma Therapeutics Ltd. | Imidazopyridine derivatives useful as enzyme inhibitors for the treatment of cell proliferative and autoimmune diseases |
| US8987307B2 (en) | 2011-03-03 | 2015-03-24 | Hoffmann-La Roche Inc. | 3-amino-pyridines as GPBAR1 agonists |
| WO2013116291A1 (en) * | 2012-01-30 | 2013-08-08 | Cephalon, Inc. | Imidazo [4, 5 - b] pyridine derivatives as alk and jak modulators for the treatment of proliferative disorders |
| SG11201406818VA (en) | 2012-04-23 | 2014-11-27 | Genentech Inc | Intermediates and processes for preparing compounds |
| GB201211021D0 (en) * | 2012-06-21 | 2012-08-01 | Cancer Rec Tech Ltd | Pharmaceutically active compounds |
| GB201211019D0 (en) * | 2012-06-21 | 2012-08-01 | Cancer Rec Tech Ltd | Inhibitor compounds |
| ES2620119T3 (es) | 2012-11-16 | 2017-06-27 | Merck Patent Gmbh | Derivados heterocíclicos novedosos como moduladores de la actividad de quinasa |
| UY36390A (es) * | 2014-11-05 | 2016-06-01 | Flexus Biosciences Inc | Compuestos moduladores de la enzima indolamina 2,3-dioxigenasa (ido), sus métodos de síntesis y composiciones farmacéuticas que los contienen |
| WO2016073738A2 (en) | 2014-11-05 | 2016-05-12 | Flexus Biosciences, Inc. | Immunoregulatory agents |
| EP3253754B1 (en) | 2015-02-02 | 2021-03-31 | Kancera AB | 2-phenyl-3h-imidazo[4,5-b]pyridine derivates useful as inhibitors of mammalian tyrosine kinase ror1 activity |
| US11660303B2 (en) | 2016-07-11 | 2023-05-30 | Kancera Ab | 2-phenylimidazo[4,5-b]pyridin-7-amine derivates useful as inhibitors of mammalian tyrosine kinase ROR1 activity |
| ES2899113T3 (es) | 2016-07-11 | 2022-03-10 | Kancera Ab | Derivados de 2-fenilimidazo[4,5-b]piridin-7-amina útiles como inhibidores de la actividad tirosina quinasa ROR1 de mamíferos |
| CN112239465A (zh) | 2019-07-16 | 2021-01-19 | 微境生物医药科技(上海)有限公司 | 极光激酶抑制剂及其用途 |
| WO2024017977A1 (en) * | 2022-07-20 | 2024-01-25 | Sanofi | Imidazopyridine compounds, preparation thereof and therapeutic uses thereof |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ID24300A (id) * | 1997-08-05 | 2000-07-13 | Pfizer Prod Inc | 4-AMINOPIROL(3,2-d)PIRIMIDIN SEBAGAI ANTAGONIS-ANTAGONIS RESEPTOR NEUROPEPTIDA Y |
| US6943174B2 (en) | 2000-06-14 | 2005-09-13 | Warner-Lambert Company | 6,5-Fused bicyclic heterocycles |
| SE0202462D0 (sv) | 2002-08-14 | 2002-08-14 | Astrazeneca Ab | Novel use |
| US7534796B2 (en) | 2005-02-18 | 2009-05-19 | Wyeth | Imidazo[4,5-b]pyridine antagonists of gonadotropin releasing hormone receptor |
-
2006
- 2006-12-21 US US12/158,339 patent/US8088761B2/en active Active
- 2006-12-21 JP JP2008546614A patent/JP5205276B2/ja active Active
- 2006-12-21 WO PCT/GB2006/004854 patent/WO2007072017A2/en not_active Ceased
- 2006-12-21 EP EP06820620.0A patent/EP1963315B1/en active Active
- 2006-12-21 ES ES06820620.0T patent/ES2526813T3/es active Active
Also Published As
| Publication number | Publication date |
|---|---|
| WO2007072017A2 (en) | 2007-06-28 |
| ES2526813T3 (es) | 2015-01-15 |
| WO2007072017A3 (en) | 2007-08-16 |
| EP1963315B1 (en) | 2014-10-08 |
| EP1963315A2 (en) | 2008-09-03 |
| US8088761B2 (en) | 2012-01-03 |
| US20090247507A1 (en) | 2009-10-01 |
| JP2009520791A (ja) | 2009-05-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US11773110B2 (en) | Heterocycle amines and uses thereof | |
| JP4471665B2 (ja) | ヒストンデアセチラーゼ阻害剤として有用なベンズアミド誘導体 | |
| US20040106574A1 (en) | 2-Arylamino-pyrimidines for the treatment of gsk3-related disorders | |
| US7547779B2 (en) | Preparation of 1,6-disubstituted azabenzimidazoles as kinase inhibitors | |
| JP5205276B2 (ja) | 酵素阻害剤 | |
| JP2014510154A (ja) | 神経変性疾患の治療方法及び治療用組成物 | |
| JP2019519534A (ja) | 五員複素環[3,4−d]ピリダジノン系化合物、その製造方法、医薬組成物及び応用 | |
| JP2025522274A (ja) | Pargの阻害剤 | |
| AU2012233246A1 (en) | Novel furanone derivative | |
| JP7763538B2 (ja) | Parp7阻害剤及びその使用 | |
| US20080255106A1 (en) | Novel 2-Phenyl-Imidazo[4,5-B]Pyridine Derivatives as Inhibitors of Glycogen Synthase Kinase for the Treatment of Dementia and Neurodegenerative Disorders | |
| CA3181351A1 (en) | Nampt modulators | |
| HK40083035B (zh) | Parp7抑制剂及其用途 | |
| WO2022028556A1 (zh) | Cdk9抑制剂及其用途 | |
| HK1197677B (en) | Heterocycle amines and uses thereof | |
| AU2002232346A1 (en) | 2-arylamino-pyrimidines for the treatment of GSK3-related disorders | |
| HK1197677A (en) | Heterocycle amines and uses thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20091217 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20091217 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20120724 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20120724 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20121016 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20121023 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20121221 |
|
| TRDD | Decision of grant or rejection written | ||
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20130129 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20130218 |
|
| R150 | Certificate of patent or registration of utility model |
Ref document number: 5205276 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20160222 Year of fee payment: 3 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |