KR101700229B1 - 화합물들 - Google Patents
화합물들 Download PDFInfo
- Publication number
- KR101700229B1 KR101700229B1 KR1020117024068A KR20117024068A KR101700229B1 KR 101700229 B1 KR101700229 B1 KR 101700229B1 KR 1020117024068 A KR1020117024068 A KR 1020117024068A KR 20117024068 A KR20117024068 A KR 20117024068A KR 101700229 B1 KR101700229 B1 KR 101700229B1
- Authority
- KR
- South Korea
- Prior art keywords
- alkyl
- optionally substituted
- aryl
- heterocycloalkyl
- group
- 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.)
- Expired - Fee Related
Links
- 0 *c1n[n]c2ccnc(*)c12 Chemical compound *c1n[n]c2ccnc(*)c12 0.000 description 6
- MUXCGFHODRXFPZ-UHFFFAOYSA-N C(CC1)CCC1Nc1c2c(-c3cccc(-[n]4nccc4)c3)n[nH]c2ccn1 Chemical compound C(CC1)CCC1Nc1c2c(-c3cccc(-[n]4nccc4)c3)n[nH]c2ccn1 MUXCGFHODRXFPZ-UHFFFAOYSA-N 0.000 description 1
- BPNYWJJIFGVHCG-UHFFFAOYSA-N C(CC1)CCC1Oc1c2c(-c3c[o]cc3)n[nH]c2ccn1 Chemical compound C(CC1)CCC1Oc1c2c(-c3c[o]cc3)n[nH]c2ccn1 BPNYWJJIFGVHCG-UHFFFAOYSA-N 0.000 description 1
- ZAJDWGYNMXZROW-UHFFFAOYSA-N C(CC1)CCC1Oc1c2c(-c3c[o]cc3)n[n](C(c3ccccc3)(c3ccccc3)c3ccccc3)c2ccn1 Chemical compound C(CC1)CCC1Oc1c2c(-c3c[o]cc3)n[n](C(c3ccccc3)(c3ccccc3)c3ccccc3)c2ccn1 ZAJDWGYNMXZROW-UHFFFAOYSA-N 0.000 description 1
- SAVORVAQVQNIKX-UHFFFAOYSA-N C(CC1)CN1c1n[n](C(c2ccccc2)(c2ccccc2)c2ccccc2)c2ccnc(OC3CCCCC3)c12 Chemical compound C(CC1)CN1c1n[n](C(c2ccccc2)(c2ccccc2)c2ccccc2)c2ccnc(OC3CCCCC3)c12 SAVORVAQVQNIKX-UHFFFAOYSA-N 0.000 description 1
- IQXQQNKHAXREMZ-UHFFFAOYSA-N C(CN1CCOCC1)[n]1ncc(-c2n[nH]c3ccnc(NC4CCCCC4)c23)c1 Chemical compound C(CN1CCOCC1)[n]1ncc(-c2n[nH]c3ccnc(NC4CCCCC4)c23)c1 IQXQQNKHAXREMZ-UHFFFAOYSA-N 0.000 description 1
- SLHXAMODMOMLFE-OAQYLSRUSA-N C(Cc1n[nH]c2ccnc(NC3CCCCC3)c12)CN(CCC1)C[C@@H]1c1ccccc1 Chemical compound C(Cc1n[nH]c2ccnc(NC3CCCCC3)c12)CN(CCC1)C[C@@H]1c1ccccc1 SLHXAMODMOMLFE-OAQYLSRUSA-N 0.000 description 1
- NLKKXPRHZNYOEC-UHFFFAOYSA-N COc1ccc(C[n](c2ccnc(OC3CCCCC3)c22)nc2I)cc1 Chemical compound COc1ccc(C[n](c2ccnc(OC3CCCCC3)c22)nc2I)cc1 NLKKXPRHZNYOEC-UHFFFAOYSA-N 0.000 description 1
- MRNQFRADJPXGJY-UHFFFAOYSA-N Cc1n[nH]c2ccnc(-c3ncc[o]3)c12 Chemical compound Cc1n[nH]c2ccnc(-c3ncc[o]3)c12 MRNQFRADJPXGJY-UHFFFAOYSA-N 0.000 description 1
- BEFKCSGSEJIZRG-UHFFFAOYSA-N Cc1n[nH]c2ccnc(Cc3ccccc3)c12 Chemical compound Cc1n[nH]c2ccnc(Cc3ccccc3)c12 BEFKCSGSEJIZRG-UHFFFAOYSA-N 0.000 description 1
- MQQIWQIHDIGEOF-UHFFFAOYSA-N Cc1n[nH]c2ccnc(Nc(cc3)ccc3C(NC3CCCC3)=O)c12 Chemical compound Cc1n[nH]c2ccnc(Nc(cc3)ccc3C(NC3CCCC3)=O)c12 MQQIWQIHDIGEOF-UHFFFAOYSA-N 0.000 description 1
- ZYHZNQNCDMBUMQ-UHFFFAOYSA-N Cc1n[n](Cc(cc2)ccc2OC)c2ccnc(C#N)c12 Chemical compound Cc1n[n](Cc(cc2)ccc2OC)c2ccnc(C#N)c12 ZYHZNQNCDMBUMQ-UHFFFAOYSA-N 0.000 description 1
- WADDCOJZSBKBFM-UHFFFAOYSA-N Cc1n[n](Cc(cc2)ccc2OC)c2ccnc(Nc(cc3)ccc3C(O)=O)c12 Chemical compound Cc1n[n](Cc(cc2)ccc2OC)c2ccnc(Nc(cc3)ccc3C(O)=O)c12 WADDCOJZSBKBFM-UHFFFAOYSA-N 0.000 description 1
- GWSJLYHWTLYEKJ-UHFFFAOYSA-N OC(c1ccc(CCc2n[nH]c3ccnc(NC4CCCCC4)c23)cc1)=O Chemical compound OC(c1ccc(CCc2n[nH]c3ccnc(NC4CCCCC4)c23)cc1)=O GWSJLYHWTLYEKJ-UHFFFAOYSA-N 0.000 description 1
- FPEKOKIMAJMGBM-UHFFFAOYSA-N OCCCc1n[nH]c2ccnc(NC3CCCCC3)c12 Chemical compound OCCCc1n[nH]c2ccnc(NC3CCCCC3)c12 FPEKOKIMAJMGBM-UHFFFAOYSA-N 0.000 description 1
Images
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
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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
- A61P25/28—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
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D471/12—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 three hetero rings
- C07D471/14—Ortho-condensed systems
-
- 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
- C07F9/65611—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings containing the ring system (X = CH2, O, S, NH) optionally with an additional double bond and/or substituents, e.g. penicillins and analogs
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Neurosurgery (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Psychology (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0904746.5 | 2009-03-19 | ||
| GB0904746A GB0904746D0 (en) | 2009-03-19 | 2009-03-19 | Compounds |
| US16202409P | 2009-03-20 | 2009-03-20 | |
| US61/162,024 | 2009-03-20 | ||
| GB0912238A GB0912238D0 (en) | 2009-07-14 | 2009-07-14 | Compounds |
| GB0912238.3 | 2009-07-14 | ||
| GB1001418.1 | 2010-01-28 | ||
| GBGB1001418.1A GB201001418D0 (en) | 2010-01-28 | 2010-01-28 | Compounds |
| PCT/GB2010/000498 WO2010106333A1 (en) | 2009-03-19 | 2010-03-19 | Compounds |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20110128925A KR20110128925A (ko) | 2011-11-30 |
| KR101700229B1 true KR101700229B1 (ko) | 2017-01-26 |
Family
ID=42226628
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020117024068A Expired - Fee Related KR101700229B1 (ko) | 2009-03-19 | 2010-03-19 | 화합물들 |
Country Status (13)
| Country | Link |
|---|---|
| US (2) | US20100317646A1 (https=) |
| EP (1) | EP2408772B1 (https=) |
| JP (1) | JP5732036B2 (https=) |
| KR (1) | KR101700229B1 (https=) |
| CN (1) | CN102428084B (https=) |
| AU (1) | AU2010224693B2 (https=) |
| CA (1) | CA2754605C (https=) |
| CL (1) | CL2011002267A1 (https=) |
| IL (1) | IL215147A0 (https=) |
| MX (1) | MX2011009807A (https=) |
| PE (1) | PE20120506A1 (https=) |
| RU (1) | RU2011142182A (https=) |
| WO (1) | WO2010106333A1 (https=) |
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2658984C (en) * | 2006-08-16 | 2014-12-02 | Joshua Kennedy-Smith | Non-nucleoside reverse transcriptase inhibitors |
| GB201008134D0 (en) * | 2010-05-14 | 2010-06-30 | Medical Res Council Technology | Compounds |
| GB201015949D0 (en) * | 2010-09-22 | 2010-11-03 | Medical Res Council Technology | Compounds |
| US9233977B2 (en) * | 2010-10-29 | 2016-01-12 | Merck Sharp & Dohme Corp. | Leucine-rich repeat kinase enzyme activity |
| WO2012118679A1 (en) | 2011-02-28 | 2012-09-07 | Merck Sharp & Dohme Corp. | Compounds inhibiting leucine-rich repeat kinase enzyme activity |
| WO2012135631A1 (en) | 2011-03-30 | 2012-10-04 | Arrien Pharmaeuticals Llc | Substituted 5-(pyrazin-2-yl)-1h-pyrazolo [3, 4-b] pyridine and pyrazolo [3, 4-b] pyridine derivatives as protein kinase inhibitors |
| EP2699572B1 (en) * | 2011-04-21 | 2016-08-10 | Origenis GmbH | Heterocyclic compounds as kinase inhibitors |
| AU2012258977A1 (en) | 2011-05-23 | 2014-01-16 | Imago Pharmaceuticals, Inc. | Inhibitors of LRRK2 kinase activity |
| CN102558174B (zh) * | 2011-08-23 | 2014-03-19 | 天津市斯芬克司药物研发有限公司 | 一种全新吡唑并[4,3-c]吡啶化合物的发明及其合成方法 |
| BR112014007654A8 (pt) * | 2011-09-30 | 2018-06-12 | Ipsen Pharma | Inibidores de lrrk2 quinase macrocíclicos. |
| GB201204985D0 (en) | 2012-03-21 | 2012-05-02 | Genentech Inc | Compounds |
| WO2013182612A1 (en) | 2012-06-07 | 2013-12-12 | Bayer Pharma Aktiengesellschaft | Glucose transport inhibitors |
| WO2014001973A1 (en) * | 2012-06-29 | 2014-01-03 | Pfizer Inc. | NOVEL 4-(SUBSTITUTED-AMINO)-7H-PYRROLO[2,3-d]PYRIMIDINES AS LRRK2 INHIBITORS |
| WO2014026330A1 (en) * | 2012-08-15 | 2014-02-20 | Merck Sharp & Dohme Corp. | 3-AMINOCYCLOALKYL COMPOUNDS AS RORgammaT INHIBITORS AND USES THEREOF |
| US10000482B2 (en) | 2012-10-19 | 2018-06-19 | Origenis Gmbh | Kinase inhibitors |
| EP2914597B1 (en) * | 2012-10-31 | 2017-12-06 | RaQualia Pharma Inc | Pyrazolopyridine derivatives as ttx-s blockers |
| MD20150037A2 (ro) * | 2012-11-08 | 2015-11-30 | Pfizer Inc. | Compuşi heteroaromatici şi utilizarea lor ca liganzi de dopamină D1 |
| EP2968995B1 (en) * | 2013-03-15 | 2018-05-09 | Elan Pharmaceuticals LLC | Inhibitors of lrrk2 kinase activity |
| US9045477B2 (en) * | 2013-03-15 | 2015-06-02 | Epizyme, Inc. | Substituted 6,5-fused bicyclic heteroaryl compounds |
| TW201533043A (zh) * | 2013-04-18 | 2015-09-01 | Lundbeck & Co As H | 作爲lrrk2抑制劑的芳基吡咯并吡啶衍生化合物 |
| TW201534597A (zh) | 2013-06-20 | 2015-09-16 | Ab Science | 作為選擇性蛋白質激酶抑制劑之苯并咪唑衍生物 |
| WO2015026683A1 (en) * | 2013-08-22 | 2015-02-26 | Merck Sharp & Dohme Corp. | Compounds inhibiting leucine-rich repeat kinase enzyme activity |
| JP6487921B2 (ja) | 2013-12-17 | 2019-03-20 | ファイザー・インク | LRRK2阻害薬としての新規の3,4−二置換−1H−ピロロ[2,3−b]ピリジンおよび4,5−二置換−7H−ピロロ[2,3−c]ピリダジン |
| EP3134405B1 (en) | 2014-04-25 | 2019-08-28 | Pfizer Inc | Heteroaromatic compounds and their use as dopamine d1 ligands |
| CR20160525A (es) * | 2014-05-14 | 2016-12-20 | Pfizer | Pirazolopiridinas y pirazolopirimidinas |
| WO2016036586A1 (en) * | 2014-09-03 | 2016-03-10 | Merck Sharp & Dohme Corp. | Compounds inhibiting leucine-rich repeat kinase enzyme activity |
| KR102161364B1 (ko) | 2015-09-14 | 2020-09-29 | 화이자 인코포레이티드 | LRRK2 억제제로서 이미다조[4,5-c]퀴놀린 및 이미다조[4,5-c][1,5]나프티리딘 유도체 |
| WO2017215600A1 (en) | 2016-06-15 | 2017-12-21 | Suzhou Yabao Pharmaceutical R&D Co., Ltd. | Substituted tricyclic herteocyclic compounds and use thereof |
| KR101923852B1 (ko) | 2017-02-24 | 2018-11-29 | 재단법인 대구경북첨단의료산업진흥재단 | 혈액 뇌관문을 통과할 수 있는 화합물을 유효성분으로 함유하는 뇌암의 예방 또는 치료용 약학적 조성물 |
| WO2019134985A1 (en) | 2018-01-08 | 2019-07-11 | F. Hoffmann-La Roche Ag | Octahydropyrido[1,2-alpha]pyrazines as magl inhibitors |
| KR101990738B1 (ko) * | 2018-07-24 | 2019-06-19 | 재단법인 대구경북첨단의료산업진흥재단 | 혈액 뇌관문을 통과할 수 있는 화합물을 유효성분으로 함유하는 뇌암의 예방 또는 치료용 약학적 조성물 |
| AU2020395783A1 (en) * | 2019-12-04 | 2022-06-09 | Arcus Biosciences, Inc. | Inhibitors of HIF-2alpha |
| CR20220644A (es) | 2020-06-22 | 2023-02-17 | Hoffmann La Roche | Derivados de sulfona |
| MX2023002224A (es) * | 2020-09-03 | 2023-03-15 | Hoffmann La Roche | Compuestos heterociclicos. |
| AU2023225858B2 (en) * | 2022-02-25 | 2026-03-19 | Suzhou Yabao Pharmaceutical R & D Co., Ltd. | Substituted fused ring compound, pharmaceutical composition thereof, preparation method therefor and uses thereof |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1994017062A1 (en) | 1993-01-28 | 1994-08-04 | Zeneca Limited | Substituted fused pyrazolo compounds and their use as herbicides |
| WO2006077319A1 (fr) | 2005-01-19 | 2006-07-27 | Aventis Pharma S.A. | Pyrazolo pyridines substituees, compositions les contenant, procede de fabrication et utilisation |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3835144A (en) * | 1972-06-16 | 1974-09-10 | Squibb & Sons Inc | Amino derivatives of (4,3-c pyrazolopyridine cabroxylic acids and esters |
| NZ207394A (en) | 1983-03-08 | 1987-03-06 | Commw Serum Lab Commission | Detecting or determining sequence of amino acids |
| US5478830A (en) * | 1992-05-29 | 1995-12-26 | The Du Pont Merck Pharmaceutical Company | Fused-ring heterocycles for the treatment of atherosclerosis |
| CA2482838A1 (en) * | 2002-05-31 | 2003-12-11 | Eisai Co., Ltd. | Pyrazole compounds and pharmaceutical compositions containing the compound |
| EP1545515A1 (en) * | 2002-08-12 | 2005-06-29 | Sugen, Inc. | 3-pyrrolyl-pyridopyrazoles and 3-pyrrolyl-indazoles as novel kinase inhibitors |
| US7348338B2 (en) * | 2003-07-17 | 2008-03-25 | Plexxikon, Inc. | PPAR active compounds |
| EP1653946A4 (en) * | 2003-08-06 | 2007-04-04 | Sugen Inc | 3-CYCLOPENTYLIDENE-1,3-DIHYDROINDOL-2-ONES GEOMETRICALLY LIMITED AS POWERFUL INHIBITORS OF PROTEIN KINASES |
| WO2005121094A1 (en) * | 2004-06-09 | 2005-12-22 | Pfizer Limited | Piperazine and piperidine derivatives as anti-hiv-agents |
| WO2006009245A1 (ja) * | 2004-07-23 | 2006-01-26 | Tanabe Seiyaku Co., Ltd. | 含窒素縮合二環式化合物 |
| US7553639B2 (en) * | 2006-01-31 | 2009-06-30 | Elan Pharma International Limited | Alpha-synuclein kinase |
| CA2647543A1 (en) * | 2006-03-29 | 2007-11-08 | Foldrx Pharmaceuticals, Inc. | Inhibition of alpha-synuclein toxicity |
| EP2346868B1 (en) * | 2008-09-26 | 2016-01-27 | Boehringer Ingelheim International Gmbh | Azaindazole compounds as ccr1 receptor antagonists |
| GB201015949D0 (en) * | 2010-09-22 | 2010-11-03 | Medical Res Council Technology | Compounds |
-
2010
- 2010-03-19 MX MX2011009807A patent/MX2011009807A/es not_active Application Discontinuation
- 2010-03-19 US US12/727,754 patent/US20100317646A1/en not_active Abandoned
- 2010-03-19 CN CN201080021866.0A patent/CN102428084B/zh active Active
- 2010-03-19 PE PE2011001662A patent/PE20120506A1/es not_active Application Discontinuation
- 2010-03-19 WO PCT/GB2010/000498 patent/WO2010106333A1/en not_active Ceased
- 2010-03-19 CA CA2754605A patent/CA2754605C/en not_active Expired - Fee Related
- 2010-03-19 EP EP10711443.1A patent/EP2408772B1/en not_active Not-in-force
- 2010-03-19 JP JP2012500308A patent/JP5732036B2/ja not_active Expired - Fee Related
- 2010-03-19 AU AU2010224693A patent/AU2010224693B2/en not_active Ceased
- 2010-03-19 RU RU2011142182/04A patent/RU2011142182A/ru unknown
- 2010-03-19 KR KR1020117024068A patent/KR101700229B1/ko not_active Expired - Fee Related
-
2011
- 2011-09-13 CL CL2011002267A patent/CL2011002267A1/es unknown
- 2011-09-14 IL IL215147A patent/IL215147A0/en unknown
-
2017
- 2017-04-03 US US15/478,141 patent/US20170320870A1/en not_active Abandoned
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1994017062A1 (en) | 1993-01-28 | 1994-08-04 | Zeneca Limited | Substituted fused pyrazolo compounds and their use as herbicides |
| WO2006077319A1 (fr) | 2005-01-19 | 2006-07-27 | Aventis Pharma S.A. | Pyrazolo pyridines substituees, compositions les contenant, procede de fabrication et utilisation |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2010106333A1 (en) | 2010-09-23 |
| PE20120506A1 (es) | 2012-05-14 |
| IL215147A0 (en) | 2011-12-29 |
| EP2408772B1 (en) | 2015-07-01 |
| CN102428084A (zh) | 2012-04-25 |
| CA2754605A1 (en) | 2010-09-23 |
| AU2010224693A1 (en) | 2011-09-15 |
| JP2012520861A (ja) | 2012-09-10 |
| JP5732036B2 (ja) | 2015-06-10 |
| RU2011142182A (ru) | 2013-04-27 |
| CA2754605C (en) | 2018-04-17 |
| CL2011002267A1 (es) | 2012-05-11 |
| EP2408772A1 (en) | 2012-01-25 |
| KR20110128925A (ko) | 2011-11-30 |
| AU2010224693B2 (en) | 2016-07-28 |
| US20170320870A1 (en) | 2017-11-09 |
| MX2011009807A (es) | 2011-09-29 |
| CN102428084B (zh) | 2016-05-18 |
| US20100317646A1 (en) | 2010-12-16 |
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