JP4845743B2 - サイクリン依存性キナーゼインヒビターとしてのピラゾロピリミジン誘導体 - Google Patents
サイクリン依存性キナーゼインヒビターとしてのピラゾロピリミジン誘導体 Download PDFInfo
- Publication number
- JP4845743B2 JP4845743B2 JP2006553181A JP2006553181A JP4845743B2 JP 4845743 B2 JP4845743 B2 JP 4845743B2 JP 2006553181 A JP2006553181 A JP 2006553181A JP 2006553181 A JP2006553181 A JP 2006553181A JP 4845743 B2 JP4845743 B2 JP 4845743B2
- Authority
- JP
- Japan
- Prior art keywords
- mmol
- prepared
- mixture
- added
- compound
- 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 - Lifetime
Links
- 0 Ic(cn[n]1c(*Cc2cnccc2)c2)c1nc2-c1ccccc1 Chemical compound Ic(cn[n]1c(*Cc2cnccc2)c2)c1nc2-c1ccccc1 0.000 description 9
- MZSREVLQRIKFFY-UHFFFAOYSA-N Clc(cccc1)c1-c(cc([n]1nc2)Cl)nc1c2Br Chemical compound Clc(cccc1)c1-c(cc([n]1nc2)Cl)nc1c2Br MZSREVLQRIKFFY-UHFFFAOYSA-N 0.000 description 3
- NDDIQYMTLDWZTO-UHFFFAOYSA-N Clc(cccc1)c1-c(cc(NCC1CNCCC1)[n]1nc2)nc1c2Br Chemical compound Clc(cccc1)c1-c(cc(NCC1CNCCC1)[n]1nc2)nc1c2Br NDDIQYMTLDWZTO-UHFFFAOYSA-N 0.000 description 2
- BPGWLQDYPPESDE-UHFFFAOYSA-N Brc(cn[n]1c(NCc2cnc(N3CCOCC3)nc2)c2)c1nc2-c1ccccc1 Chemical compound Brc(cn[n]1c(NCc2cnc(N3CCOCC3)nc2)c2)c1nc2-c1ccccc1 BPGWLQDYPPESDE-UHFFFAOYSA-N 0.000 description 1
- IRLUCSFLZGPVMM-UHFFFAOYSA-N Brc(cn[n]1c(NCc2cnccc2)c2)c1nc2NC1CCCC1 Chemical compound Brc(cn[n]1c(NCc2cnccc2)c2)c1nc2NC1CCCC1 IRLUCSFLZGPVMM-UHFFFAOYSA-N 0.000 description 1
- IUARYRNDPHIJMI-UHFFFAOYSA-N Brc1c2nc(C3CCNCC3)cc(NCc3cnccc3)[n]2nc1 Chemical compound Brc1c2nc(C3CCNCC3)cc(NCc3cnccc3)[n]2nc1 IUARYRNDPHIJMI-UHFFFAOYSA-N 0.000 description 1
- XETHRXRKOYUSND-UHFFFAOYSA-N Brc1c2nc(C3CNCCC3)cc(NCc3cnccc3)[n]2nc1 Chemical compound Brc1c2nc(C3CNCCC3)cc(NCc3cnccc3)[n]2nc1 XETHRXRKOYUSND-UHFFFAOYSA-N 0.000 description 1
- WBBAFJZODNMVGJ-UHFFFAOYSA-N C#Cc(cn[n]1c(NCc2cnccc2)c2)c1nc2-c(cccc1)c1F Chemical compound C#Cc(cn[n]1c(NCc2cnccc2)c2)c1nc2-c(cccc1)c1F WBBAFJZODNMVGJ-UHFFFAOYSA-N 0.000 description 1
- FHNZMVGLJCBDBB-FYJGNVAPSA-N C/N=C/c(cn[n]1c(NCc2cnccc2)c2)c1nc2-c1ccccc1 Chemical compound C/N=C/c(cn[n]1c(NCc2cnccc2)c2)c1nc2-c1ccccc1 FHNZMVGLJCBDBB-FYJGNVAPSA-N 0.000 description 1
- ILLIYQWQZAEKKT-UHFFFAOYSA-N CC(C)(C)OC(N(Cc1c[n+]([O-])ccc1)c([n]1nc2)cc(-c(cc3)ccc3F)nc1c2Br)=O Chemical compound CC(C)(C)OC(N(Cc1c[n+]([O-])ccc1)c([n]1nc2)cc(-c(cc3)ccc3F)nc1c2Br)=O ILLIYQWQZAEKKT-UHFFFAOYSA-N 0.000 description 1
- FMHZMTRZVKFANZ-UHFFFAOYSA-N CC(C)(C)OC(N(Cc1ccncc1)c1cc(-c(cccc2)c2F)nc2ccn[n]12)=O Chemical compound CC(C)(C)OC(N(Cc1ccncc1)c1cc(-c(cccc2)c2F)nc2ccn[n]12)=O FMHZMTRZVKFANZ-UHFFFAOYSA-N 0.000 description 1
- KLKBCNDBOVRQIJ-UHFFFAOYSA-N CC(C)(C)OC(N1CCC(CN)CC1)=O Chemical compound CC(C)(C)OC(N1CCC(CN)CC1)=O KLKBCNDBOVRQIJ-UHFFFAOYSA-N 0.000 description 1
- OTUYHXHSMKRCDK-UHFFFAOYSA-N CC(C)(C)OC(N1CCC(CNc([n]2nc3)cc(-c4ccccc4Cl)nc2c3Br)CC1)=O Chemical compound CC(C)(C)OC(N1CCC(CNc([n]2nc3)cc(-c4ccccc4Cl)nc2c3Br)CC1)=O OTUYHXHSMKRCDK-UHFFFAOYSA-N 0.000 description 1
- KLQQTJMQHIOKJL-UHFFFAOYSA-N CC(C)(C)OC(Nc1nccc(C=O)c1)=O Chemical compound CC(C)(C)OC(Nc1nccc(C=O)c1)=O KLQQTJMQHIOKJL-UHFFFAOYSA-N 0.000 description 1
- HMQFDFGFYVYALU-UHFFFAOYSA-N CC(C)(C)OC(Nc1nccc(CCl)c1)=O Chemical compound CC(C)(C)OC(Nc1nccc(CCl)c1)=O HMQFDFGFYVYALU-UHFFFAOYSA-N 0.000 description 1
- MTLPTFRZCYSDNT-UHFFFAOYSA-N CC(C)(C)OC(Nc1nccc(CN)c1)=O Chemical compound CC(C)(C)OC(Nc1nccc(CN)c1)=O MTLPTFRZCYSDNT-UHFFFAOYSA-N 0.000 description 1
- WWIMVFCGNYLUMJ-UHFFFAOYSA-N CC(C)(C)OC(Nc1nccc(CO)c1)=O Chemical compound CC(C)(C)OC(Nc1nccc(CO)c1)=O WWIMVFCGNYLUMJ-UHFFFAOYSA-N 0.000 description 1
- RDCODVKTTJWFAR-UHFFFAOYSA-N CCc1c[nH]nc1N Chemical compound CCc1c[nH]nc1N RDCODVKTTJWFAR-UHFFFAOYSA-N 0.000 description 1
- GKWYRUSORJLJGT-UHFFFAOYSA-N CCc1c[nH]nc1NC(CC(OC)=O)=O Chemical compound CCc1c[nH]nc1NC(CC(OC)=O)=O GKWYRUSORJLJGT-UHFFFAOYSA-N 0.000 description 1
- YCHYGGNTIXJETG-UHFFFAOYSA-N CCc1cnc(N)nc1 Chemical compound CCc1cnc(N)nc1 YCHYGGNTIXJETG-UHFFFAOYSA-N 0.000 description 1
- BTVJTKWOCSGJDQ-UHFFFAOYSA-N CN(CC1)CCC1C(N)=O Chemical compound CN(CC1)CCC1C(N)=O BTVJTKWOCSGJDQ-UHFFFAOYSA-N 0.000 description 1
- DDUIMHOBPZTPQC-UHFFFAOYSA-N CSc1ncc(CNc([n]2nc3)cc(-c4ccccc4)nc2c3Br)cn1 Chemical compound CSc1ncc(CNc([n]2nc3)cc(-c4ccccc4)nc2c3Br)cn1 DDUIMHOBPZTPQC-UHFFFAOYSA-N 0.000 description 1
- KNTIGQDGKVIOEY-UHFFFAOYSA-N Fc(cccc1)c1-c1nc2c(C=C(Br)Br)cn[n]2c(NCc2cnccc2)c1 Chemical compound Fc(cccc1)c1-c1nc2c(C=C(Br)Br)cn[n]2c(NCc2cnccc2)c1 KNTIGQDGKVIOEY-UHFFFAOYSA-N 0.000 description 1
- ZAIYYXVHGBMLEC-UHFFFAOYSA-N Fc(cccc1)c1-c1nc2ccn[n]2c(NCc2ccncc2)c1 Chemical compound Fc(cccc1)c1-c1nc2ccn[n]2c(NCc2ccncc2)c1 ZAIYYXVHGBMLEC-UHFFFAOYSA-N 0.000 description 1
- CEMVEGUWOCCVMF-UHFFFAOYSA-N Ic(cn[n]1c(NCc2cccnc2)c2)c1nc2-c1ccccc1 Chemical compound Ic(cn[n]1c(NCc2cccnc2)c2)c1nc2-c1ccccc1 CEMVEGUWOCCVMF-UHFFFAOYSA-N 0.000 description 1
- DPBWFNDFMCCGGJ-UHFFFAOYSA-N NC(C1CCNCC1)=O Chemical compound NC(C1CCNCC1)=O DPBWFNDFMCCGGJ-UHFFFAOYSA-N 0.000 description 1
- XFKPORAVEUOIRF-UHFFFAOYSA-N NCc1cc(C#N)ccc1 Chemical compound NCc1cc(C#N)ccc1 XFKPORAVEUOIRF-UHFFFAOYSA-N 0.000 description 1
- CWFNBZZUAUSUII-UHFFFAOYSA-N NCc1cccc(CNc([n]2nc3)cc(-c(cccc4)c4Cl)nc2c3Br)c1 Chemical compound NCc1cccc(CNc([n]2nc3)cc(-c(cccc4)c4Cl)nc2c3Br)c1 CWFNBZZUAUSUII-UHFFFAOYSA-N 0.000 description 1
- HMWDLVRYRPUQOL-UHFFFAOYSA-N NCc1cnc(N)nc1 Chemical compound NCc1cnc(N)nc1 HMWDLVRYRPUQOL-UHFFFAOYSA-N 0.000 description 1
- GCWPGEWXYDEQAY-BQBZGAKWSA-N N[C@@H]1[C@H](CO)CCCC1 Chemical compound N[C@@H]1[C@H](CO)CCCC1 GCWPGEWXYDEQAY-BQBZGAKWSA-N 0.000 description 1
- KZBYHVHAUOAPIJ-UHFFFAOYSA-N Nc([n]1nc2)cc(-c3ccccc3)nc1c2Br Chemical compound Nc([n]1nc2)cc(-c3ccccc3)nc1c2Br KZBYHVHAUOAPIJ-UHFFFAOYSA-N 0.000 description 1
- DPOYRRAYGKTRAU-UHFFFAOYSA-N Nc1ncc(C=O)cn1 Chemical compound Nc1ncc(C=O)cn1 DPOYRRAYGKTRAU-UHFFFAOYSA-N 0.000 description 1
- NUGGQZDIPXLGQW-UHFFFAOYSA-N Nc1ncc(CO)cn1 Chemical compound Nc1ncc(CO)cn1 NUGGQZDIPXLGQW-UHFFFAOYSA-N 0.000 description 1
- OHYVNOXBJLONTP-UHFFFAOYSA-N O=Cc(cn[n]1c(NCc2cnccc2)c2)c1nc2-c1ccccc1 Chemical compound O=Cc(cn[n]1c(NCc2cnccc2)c2)c1nc2-c1ccccc1 OHYVNOXBJLONTP-UHFFFAOYSA-N 0.000 description 1
- ROYUZJRILJDVGJ-UHFFFAOYSA-N O=S(c1ccc(CNc([n]2nc3)cc(-c4ccccc4F)nc2c3Br)cc1)(Cl)=O Chemical compound O=S(c1ccc(CNc([n]2nc3)cc(-c4ccccc4F)nc2c3Br)cc1)(Cl)=O ROYUZJRILJDVGJ-UHFFFAOYSA-N 0.000 description 1
- BRQFIORUNWWNBM-KBPBESRZSA-N OC[C@H](CCCC1)[C@H]1NCc1ccccc1 Chemical compound OC[C@H](CCCC1)[C@H]1NCc1ccccc1 BRQFIORUNWWNBM-KBPBESRZSA-N 0.000 description 1
- CFSCYYOACNGJHX-UHFFFAOYSA-N OS(c1ccc(CNc([n]2nc3)cc(-c4ccccc4F)nc2c3Br)cc1)(=O)=O Chemical compound OS(c1ccc(CNc([n]2nc3)cc(-c4ccccc4F)nc2c3Br)cc1)(=O)=O CFSCYYOACNGJHX-UHFFFAOYSA-N 0.000 description 1
- OBPZGAMADBUOKY-UHFFFAOYSA-N [O-][n+]1cc(CNc([n]2nc3)cc(-c(cc4)ccc4F)nc2c3Br)ccc1 Chemical compound [O-][n+]1cc(CNc([n]2nc3)cc(-c(cc4)ccc4F)nc2c3Br)ccc1 OBPZGAMADBUOKY-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—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
- A61K31/495—Heterocyclic 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
-
- 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
- A61K31/495—Heterocyclic 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- 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
- 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
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurology (AREA)
- Oncology (AREA)
- Rheumatology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Hematology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Communicable Diseases (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Virology (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 (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/776,988 US7119200B2 (en) | 2002-09-04 | 2004-02-11 | Pyrazolopyrimidines as cyclin dependent kinase inhibitors |
| US10/776,988 | 2004-02-11 | ||
| PCT/US2005/003859 WO2005077954A2 (en) | 2004-02-11 | 2005-02-08 | Pyrazolopyrimidine-derivatives as cyclin dependent kinase inhibitors |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010157338A Division JP2010215675A (ja) | 2004-02-11 | 2010-07-09 | サイクリン依存性キナーゼインヒビターとしてのピラゾロピリミジン誘導体 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2007522220A JP2007522220A (ja) | 2007-08-09 |
| JP2007522220A5 JP2007522220A5 (https=) | 2010-08-26 |
| JP4845743B2 true JP4845743B2 (ja) | 2011-12-28 |
Family
ID=34860861
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006553181A Expired - Lifetime JP4845743B2 (ja) | 2004-02-11 | 2005-02-08 | サイクリン依存性キナーゼインヒビターとしてのピラゾロピリミジン誘導体 |
| JP2010157338A Withdrawn JP2010215675A (ja) | 2004-02-11 | 2010-07-09 | サイクリン依存性キナーゼインヒビターとしてのピラゾロピリミジン誘導体 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010157338A Withdrawn JP2010215675A (ja) | 2004-02-11 | 2010-07-09 | サイクリン依存性キナーゼインヒビターとしてのピラゾロピリミジン誘導体 |
Country Status (26)
| Country | Link |
|---|---|
| US (2) | US7119200B2 (https=) |
| EP (1) | EP1720882B1 (https=) |
| JP (2) | JP4845743B2 (https=) |
| KR (1) | KR101196498B1 (https=) |
| CN (1) | CN1946725B (https=) |
| AR (1) | AR047543A1 (https=) |
| AT (1) | ATE494287T1 (https=) |
| AU (1) | AU2005212409C1 (https=) |
| BR (1) | BRPI0507644B8 (https=) |
| CA (1) | CA2555345C (https=) |
| CY (1) | CY1112400T1 (https=) |
| DE (1) | DE602005025733D1 (https=) |
| DK (1) | DK1720882T3 (https=) |
| ES (1) | ES2359410T3 (https=) |
| HR (1) | HRP20110245T1 (https=) |
| IL (1) | IL177283A (https=) |
| MY (1) | MY149044A (https=) |
| NO (1) | NO337520B1 (https=) |
| NZ (1) | NZ590480A (https=) |
| PE (1) | PE20050774A1 (https=) |
| PL (1) | PL1720882T3 (https=) |
| RU (1) | RU2414472C9 (https=) |
| SI (1) | SI1720882T1 (https=) |
| TW (1) | TWI393566B (https=) |
| WO (1) | WO2005077954A2 (https=) |
| ZA (1) | ZA200606573B (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010215675A (ja) * | 2004-02-11 | 2010-09-30 | Schering Corp | サイクリン依存性キナーゼインヒビターとしてのピラゾロピリミジン誘導体 |
Families Citing this family (116)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7196092B2 (en) * | 2002-09-04 | 2007-03-27 | Schering Corporation | N-heteroaryl pyrazolopyrimidines as cyclin dependent kinase inhibitors |
| US7196078B2 (en) * | 2002-09-04 | 2007-03-27 | Schering Corpoartion | Trisubstituted and tetrasubstituted pyrazolopyrimidines as cyclin dependent kinase inhibitors |
| US7557110B2 (en) | 2003-02-28 | 2009-07-07 | Teijin Pharma Limited | Pyrazolo[1,5-A] pyrimidine derivatives |
| US20070179161A1 (en) * | 2003-03-31 | 2007-08-02 | Vernalis (Cambridge) Limited. | Pyrazolopyrimidine compounds and their use in medicine |
| GB0321475D0 (en) * | 2003-09-12 | 2003-10-15 | Glaxo Group Ltd | Novel compounds |
| US20070060595A1 (en) * | 2003-10-10 | 2007-03-15 | Toshio Yoshizawa | Novel fused heterocyclic compound and use thereof |
| JP2007536369A (ja) * | 2004-05-06 | 2007-12-13 | ファイザー・インク | プロリン及びモルホリン誘導体の新規化合物 |
| US20080287405A1 (en) * | 2004-05-14 | 2008-11-20 | Thannickal Victor J | Compositions and Methods Relating to Protein Kinase Inhibitors |
| KR20070034524A (ko) * | 2004-05-28 | 2007-03-28 | 버텍스 파마슈티칼스 인코포레이티드 | 무스카린 수용체 조정자 |
| UY29223A1 (es) * | 2004-11-23 | 2006-06-30 | Astrazeneca Ab | Ácidos fenoxiacéticos sustituidos, composiciones farmacéuticas que los contienen y procesos para su preparación |
| US7850960B2 (en) * | 2004-12-30 | 2010-12-14 | University Of Washington | Methods for regulation of stem cells |
| WO2006133322A2 (en) | 2005-06-09 | 2006-12-14 | Schering Corporation | Synthesis of 3-amino-4-substituted pyrazole derivatives |
| US7932257B2 (en) * | 2005-07-22 | 2011-04-26 | Sunesis Pharmaceuticals, Inc. | Substituted pyrazolo[4,3-d]pyrimidines as aurora kinase inhibitors |
| WO2007017678A1 (en) * | 2005-08-09 | 2007-02-15 | Eirx Therapeutics Limited | Pyrazolo[1,5-a] pyrimidine compounds and pharmaceutical compositions containing them |
| BRPI0616985B1 (pt) * | 2005-10-06 | 2021-10-26 | Merck Sharp & Dohme Corp. | Composto de pirazolo[1,5-a]pirimidina, e, uso de um composto |
| AU2006336504C9 (en) * | 2005-12-28 | 2015-05-14 | Vertex Pharmaceuticals Incorporated | 1-(benzo [D] [1,3] dioxol-5-yl) -N- (phenyl) cyclopropane- carboxamide derivatives and related compounds as modulators of ATP-Binding Cassette transporters for the treatment of Cystic Fibrosis |
| US7671221B2 (en) * | 2005-12-28 | 2010-03-02 | Vertex Pharmaceuticals Incorporated | Modulators of ATP-Binding Cassette transporters |
| US20090069315A1 (en) * | 2006-03-08 | 2009-03-12 | Rajeev Sivasankaran | Use of Pyrazolo(1,5A)Pyrimidin-7-YL Amine Derivatives in the Treatment of Neurological Disorders |
| WO2007139732A1 (en) * | 2006-05-22 | 2007-12-06 | Schering Corporation | Pyrazolo [1, 5-a] pyrimidines as cdk inhibitors |
| WO2008005469A2 (en) | 2006-06-30 | 2008-01-10 | Schering Corporation | Igfbp2 biomarker |
| CA2660953A1 (en) * | 2006-08-18 | 2008-02-21 | Schering Corporation | Process for resolving chiral piperidine alcohol and process for synthesis of pyrazolo [1,5-a] pyrimidine derivatives using same |
| US7786306B2 (en) * | 2006-08-18 | 2010-08-31 | Schering Corporation | Process for resolving chiral piperidine alcohol and process for synthesis of pyrazolo[1,5-a] pyrimidine derivatives using same |
| CN101627041A (zh) * | 2006-08-28 | 2010-01-13 | 先灵公司 | 合成(3-烷基-5-哌啶-1-基-3,3a-二氢-吡唑并[1,5-a]嘧啶-7-基)-氨基衍生物和中间体的方法和中间体 |
| WO2008027220A2 (en) * | 2006-08-28 | 2008-03-06 | Schering Corporation | Process and intermediates for the synthesis of (3-alkyl-5-piperidin-1-yl-3, 3a-dihydropyrazol0 [1, 5-a] pyrimidin-7-yl) -amino derivatives |
| CA2686848A1 (en) | 2007-05-08 | 2008-11-20 | Schering Corporation | Methods of treatment using intravenous formulations comprising temozolomide |
| AU2008261027A1 (en) * | 2007-06-05 | 2008-12-11 | Emory University | Selective inhibitors for cyclin-dependent kinases |
| WO2009020140A1 (ja) * | 2007-08-06 | 2009-02-12 | Dainippon Sumitomo Pharma Co., Ltd. | アダマンチルウレア誘導体 |
| WO2009023160A2 (en) * | 2007-08-11 | 2009-02-19 | The Uab Research Foundation | Novel inhibitors of bacterial sortase enzymes and methods of using the same |
| ES2799897T3 (es) | 2007-08-31 | 2020-12-22 | Whitehead Inst Biomedical Res | Estimulación de la vía wnt en la reprogramación de células somáticas |
| EP2200584A2 (en) * | 2007-09-17 | 2010-06-30 | Schering Corporation | Formulation containing cyclin-dependent kinase inhibiting compound and method of treating tumors using the same |
| US20100286038A1 (en) * | 2007-09-21 | 2010-11-11 | Valentyn Antochshuk | Formulation containing cyclin-dependent kinase inhibiting compound and method of treating tumors using the same |
| JP2011500086A (ja) * | 2007-10-22 | 2011-01-06 | シェーリング コーポレイション | 完全ヒト抗vegf抗体および使用方法 |
| US20110039857A1 (en) * | 2008-04-30 | 2011-02-17 | Hamed Aissaoui | Piperidine and pyroolidine compounds |
| CN102131389A (zh) * | 2008-06-20 | 2011-07-20 | 健泰科生物技术公司 | 三唑并吡啶jak抑制剂化合物和方法 |
| WO2009155565A1 (en) * | 2008-06-20 | 2009-12-23 | Genentech, Inc. | Triazolopyridine jak inhibitor compounds and methods |
| MY169791A (en) | 2008-10-22 | 2019-05-15 | Array Biopharma Inc | Substituted pyrazolo [1,5-a] pyrimidine compounds as trk kinase inhibitors |
| US8507673B2 (en) * | 2008-12-11 | 2013-08-13 | Emory University | Process for preparing 5,7 diaminopyrazolo [1,5-A] pyrimidine compounds |
| WO2010068838A2 (en) * | 2008-12-11 | 2010-06-17 | Emory University | PROCESSES FOR PREPARING 5,7 DIAMINOPYRAZOLO[1,5-α] PYRIMIDINE COMPOUNDS |
| US8591943B2 (en) | 2009-04-09 | 2013-11-26 | Merck Sharp & Dohme Corp. | Pyrazolo[1,5-a]pyrimidine derivatives as mTOR inhibitors |
| WO2010124290A2 (en) * | 2009-04-24 | 2010-10-28 | Whitehead Institute For Biomedical Research | Compositions and methods for deriving or culturing pluripotent cells |
| AR077468A1 (es) | 2009-07-09 | 2011-08-31 | Array Biopharma Inc | Compuestos de pirazolo (1,5 -a) pirimidina sustituidos como inhibidores de trk- quinasa |
| EP2473041B1 (en) | 2009-09-04 | 2018-03-07 | Merck Sharp & Dohme Corp. | Modulators of cell cycle checkpoints and their use in combination with checkpoint kinase inhibitors |
| WO2011090738A2 (en) | 2009-12-29 | 2011-07-28 | Dana-Farber Cancer Institute, Inc. | Type ii raf kinase inhibitors |
| EP2552917B1 (en) * | 2010-03-26 | 2014-11-05 | Merck Sharp & Dohme Corp. | Process for synthesizing 6-bromo-3-(1-methyl-1h-pyrazol-4-yl)-5-(3(r)-piperidinyl)pyrazolo[1,5-a]pyrimidin-7-amine |
| ME03376B (me) | 2010-05-20 | 2020-01-20 | Array Biopharma Inc | Makrociklička jedinjenja kао inhibiтori trk kinaze |
| WO2012044562A2 (en) * | 2010-09-30 | 2012-04-05 | Merck Sharp & Dohme Corp. | Pyrazolopyrimidine pde10 inhibitors |
| US9309250B2 (en) | 2011-06-22 | 2016-04-12 | Vertex Pharmaceuticals Incorporated | Substituted pyrrolo[2,3-b]pyrazines as ATR kinase inhibitors |
| ES2769270T3 (es) | 2011-09-30 | 2020-06-25 | Bluebird Bio Inc | Compuestos para transducción viral mejorada |
| US9382239B2 (en) | 2011-11-17 | 2016-07-05 | Dana-Farber Cancer Institute, Inc. | Inhibitors of c-Jun-N-terminal kinase (JNK) |
| EP2634189A1 (en) * | 2012-03-01 | 2013-09-04 | Lead Discovery Center GmbH | Pyrazolo-triazine derivatives as selective cyclin-dependent kinase inhibitors |
| EP2634190A1 (en) * | 2012-03-01 | 2013-09-04 | Lead Discovery Center GmbH | Pyrazolo-triazine derivatives as selective cyclin-dependent kinase inhinitors |
| ES2685709T3 (es) | 2012-03-30 | 2018-10-10 | Merck Sharp & Dohme Corp. | Biomarcador predictivo mediado por un inhibidor de CDK útil para la terapia contra el cáncer |
| EP2909194A1 (en) | 2012-10-18 | 2015-08-26 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinase 7 (cdk7) |
| USRE48175E1 (en) | 2012-10-19 | 2020-08-25 | Dana-Farber Cancer Institute, Inc. | Hydrophobically tagged small molecules as inducers of protein degradation |
| CA2889919C (en) | 2012-11-16 | 2021-08-17 | University Health Network | Pyrazolopyrimidine compounds |
| LT2925757T (lt) | 2012-11-19 | 2017-12-27 | Novartis Ag | Junginiai ir kompozicijos, skirti parazitinių ligų gydymui |
| US8871754B2 (en) | 2012-11-19 | 2014-10-28 | Irm Llc | Compounds and compositions for the treatment of parasitic diseases |
| SI2941432T1 (en) | 2012-12-07 | 2018-07-31 | Vertex Pharmaceuticals Incorporated | 2-AMINO-6-FLUORO-N- (5-FLUORO-4- (4- (4- (OXETHAN-3-YL) PIPERAZIN-1-CARBONYL) PIPERIDIN-1-YLIPRIDIN-3-YL) 1,5 ALFA) PYRIMIDINE-3-CARBOXAMIDE AS ATR KINAZE INHIBITOR |
| WO2014143240A1 (en) | 2013-03-15 | 2014-09-18 | Vertex Pharmaceuticals Incorporated | Fused pyrazolopyrimidine derivatives useful as inhibitors of atr kinase |
| EP2970288A1 (en) | 2013-03-15 | 2016-01-20 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of atr kinase |
| US8957078B2 (en) | 2013-03-15 | 2015-02-17 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of ATR kinase |
| AU2014309199B2 (en) | 2013-08-20 | 2018-04-19 | Merck Sharp & Dohme Llc | Treating cancer with a combination of a PD-1 antagonist and dinaciclib |
| WO2015058126A1 (en) | 2013-10-18 | 2015-04-23 | Syros Pharmaceuticals, Inc. | Heteroaromatic compounds useful for the treatment of prolferative diseases |
| EP3057956B1 (en) | 2013-10-18 | 2021-05-05 | Dana-Farber Cancer Institute, Inc. | Polycyclic inhibitors of cyclin-dependent kinase 7 (cdk7) |
| PT3077397T (pt) | 2013-12-06 | 2020-01-22 | Vertex Pharma | Composto de 2-amino-6-fluoro-n-[5-fluoro-piridin-3-il]pirazolo[1,5-a]pirimidin-3-carboxamida útil como inibidor da atr quinase, a sua preparação, diferentes formas sólidas e derivados radiomarcados do mesmo |
| WO2015095840A1 (en) * | 2013-12-20 | 2015-06-25 | Biomed Valley Discoveries, Inc. | Cancer treatments using combinations of cdk and erk inhibitors |
| ES2728932T3 (es) | 2014-01-09 | 2019-10-29 | Intra Cellular Therapies Inc | Compuestos orgánicos |
| EP3476392A1 (en) | 2014-02-28 | 2019-05-01 | Merck Sharp & Dohme Corp. | Method for treating cancer |
| US9388239B2 (en) | 2014-05-01 | 2016-07-12 | Consejo Nacional De Investigation Cientifica | Anti-human VEGF antibodies with unusually strong binding affinity to human VEGF-A and cross reactivity to human VEGF-B |
| US10555931B2 (en) | 2014-05-28 | 2020-02-11 | Piramal Enterprises Limited | Pharmaceutical combination for the treatment of cancer |
| MX373102B (es) | 2014-06-05 | 2020-04-17 | Vertex Pharma | Derivados radiomarcados de un compuesto de 2-amino-6-fluoro-n-[5-fluoro-piridin-3-il]-pirazolo[1,5-a]pirimidin-3-carboxamida útil como inhibidor de ataxia telangiectasia mutada y rad3 relacionado (atr) cinasa, preparación de tal compuesto y diferentes formas sólidas del mismo. |
| SG11201610500WA (en) | 2014-06-17 | 2017-01-27 | Vertex Pharma | Method for treating cancer using a combination of chk1 and atr inhibitors |
| US20170114323A1 (en) | 2014-06-19 | 2017-04-27 | Whitehead Institute For Biomedical Research | Uses of kinase inhibitors for inducing and maintaining pluripotency |
| FI3218005T3 (fi) | 2014-11-12 | 2023-03-31 | Seagen Inc | Glykaanin kanssa vuorovaikutteisia yhdisteitä ja käyttömenetelmiä |
| CN113354649B (zh) | 2014-11-16 | 2024-12-10 | 阵列生物制药公司 | 一种新的晶型 |
| JP6854762B2 (ja) | 2014-12-23 | 2021-04-07 | ダナ−ファーバー キャンサー インスティテュート, インコーポレイテッド | サイクリン依存性キナーゼ7(cdk7)の阻害剤 |
| USRE50776E1 (en) | 2015-03-27 | 2026-02-03 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinases |
| CN106146515B (zh) * | 2015-04-17 | 2020-09-04 | 常州隆赛医药科技有限公司 | 新型激酶抑制剂的制备及应用 |
| WO2016201370A1 (en) | 2015-06-12 | 2016-12-15 | Dana-Farber Cancer Institute, Inc. | Combination therapy of transcription inhibitors and kinase inhibitors |
| AU2016319125B2 (en) | 2015-09-09 | 2021-04-08 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinases |
| AU2016331955B2 (en) | 2015-09-30 | 2022-07-21 | Vertex Pharmaceuticals Incorporated | Method for treating cancer using a combination of DNA damaging agents and ATR inhibitors |
| EP3368039A1 (en) | 2015-10-26 | 2018-09-05 | The Regents of The University of Colorado, A Body Corporate | Point mutations in trk inhibitor-resistant cancer and methods relating to the same |
| JP6692423B2 (ja) * | 2015-11-01 | 2020-05-13 | ザ リージェンツ オブ ザ ユニヴァーシティ オブ コロラド,ア ボディ コーポレイト | Wee1キナーゼ阻害剤、並びにそれを作製及び使用する方法 |
| CA3002097A1 (en) | 2015-11-12 | 2017-05-18 | Siamab Therapeutics, Inc. | Glycan-interacting compounds and methods of use |
| MX2018006250A (es) | 2015-11-18 | 2018-09-05 | Genzyme Corp | Biomarcador de enfermedad poliquistica renal y usos del mismo. |
| WO2017139561A1 (en) | 2016-02-12 | 2017-08-17 | Bluebird Bio, Inc. | Vcn enhancer compositions and methods of using the same |
| IL261002B2 (en) | 2016-02-12 | 2024-07-01 | Bluebird Bio Inc | Vcn enhancer compositions and methods of using the same |
| FI3439662T3 (fi) | 2016-04-04 | 2024-09-04 | Loxo Oncology Inc | (s)-n-(5-((r)-2-(2,5-difluorifenyyli)pyrrolidin-1-yyli)pyratsolo[1,5-a]pyrimidin-3-yyli)-3-hydroksipyrrolidiini-1-karboksamidin nesteformulaatioita |
| US10045991B2 (en) | 2016-04-04 | 2018-08-14 | Loxo Oncology, Inc. | Methods of treating pediatric cancers |
| WO2017178844A1 (en) * | 2016-04-15 | 2017-10-19 | Cancer Research Technology Limited | Heterocyclic compounds as ret kinase inhibitors |
| SI3442535T1 (sl) | 2016-04-15 | 2023-01-31 | Cancer Research Technology Limited | Heterociklične spojine kot zaviralci RET-kinaze |
| EP3458456B1 (en) | 2016-05-18 | 2020-11-25 | Loxo Oncology Inc. | Preparation of (s)-n-(5-((r)-2-(2,5-difluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide |
| JOP20190092A1 (ar) | 2016-10-26 | 2019-04-25 | Array Biopharma Inc | عملية لتحضير مركبات بيرازولو[1، 5-a]بيريميدين وأملاح منها |
| CN108017641B (zh) * | 2016-11-02 | 2021-01-05 | 深圳铂立健医药有限公司 | 吡唑并嘧啶化合物作为pi3k抑制剂及其应用 |
| WO2018094143A1 (en) | 2016-11-17 | 2018-05-24 | Siamab Therapeutics, Inc. | Glycan-interacting compounds and methods of use |
| HUE057337T2 (hu) * | 2017-02-10 | 2022-05-28 | Novartis Ag | 1-(4-amino-5-bróm-6-(1H-pirazol-1-il)pirimidin-2-il)-1H-pirazol-4-ol és alkalmazása rák kezelésében |
| WO2018160909A1 (en) | 2017-03-03 | 2018-09-07 | Siamab Therapeutics, Inc. | Glycan-interacting compounds and methods of use |
| JOP20190213A1 (ar) | 2017-03-16 | 2019-09-16 | Array Biopharma Inc | مركبات حلقية ضخمة كمثبطات لكيناز ros1 |
| GB201705971D0 (en) | 2017-04-13 | 2017-05-31 | Cancer Res Tech Ltd | Inhibitor compounds |
| SI3658557T1 (sl) | 2017-07-28 | 2024-10-30 | Takeda Pharmaceutical Company Limited | Zaviralci TYK2 in njihova uporaba |
| KR20200141487A (ko) | 2018-04-11 | 2020-12-18 | 주식회사 큐리언트 | 사이클린 의존성 키나아제의 선택적 억제제로서의 피라졸로-트리아진 및/또는 피라졸로피리미딘 유도체 |
| EP3810132A4 (en) | 2018-06-25 | 2022-06-22 | Dana-Farber Cancer Institute, Inc. | TAIRE FAMILY KINASE INHIBITORS AND RELATED USES |
| JP7179161B2 (ja) | 2018-09-10 | 2022-11-28 | イーライ リリー アンド カンパニー | 乾癬および全身性エリテマトーデスの処置に有用なピラゾロ[1,5-a]ピリミジン-3-カルボキサミド誘導体 |
| CN113271940A (zh) | 2018-10-15 | 2021-08-17 | 林伯士拉克许米公司 | Tyk2抑制剂和其用途 |
| US11155560B2 (en) | 2018-10-30 | 2021-10-26 | Kronos Bio, Inc. | Substituted pyrazolo[1,5-a]pyrimidines for modulating CDK9 activity |
| AR117177A1 (es) | 2018-12-10 | 2021-07-14 | Lilly Co Eli | DERIVADOS DE 7-(METILAMINO)PIRAZOLO[1,5-A]PIRIMIDIN-3-CARBOXAMIDA COMO INHIBIDORES DE IL-23 E INFa |
| US20220040324A1 (en) | 2018-12-21 | 2022-02-10 | Daiichi Sankyo Company, Limited | Combination of antibody-drug conjugate and kinase inhibitor |
| US12281126B2 (en) | 2018-12-28 | 2025-04-22 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinase 7 and uses thereof |
| CA3134814A1 (en) | 2019-03-26 | 2020-10-01 | Ventyx Biosciences, Inc. | Tyk2 pseudokinase ligands |
| JP7635228B2 (ja) | 2019-11-08 | 2025-02-25 | ベンティックス バイオサイエンシーズ,インク. | Tyk2偽キナーゼリガンド |
| TWI810520B (zh) | 2020-02-12 | 2023-08-01 | 美商美國禮來大藥廠 | 7-(甲基胺基)吡唑并[1,5-a]嘧啶-3-甲醯胺化合物 |
| CN115052660B (zh) | 2020-02-12 | 2024-01-09 | 伊莱利利公司 | 取代的7-(甲氨基)吡唑并[1,5-a]嘧啶-3-甲酰胺衍生物 |
| EP4146797A1 (en) | 2020-05-06 | 2023-03-15 | Orchard Therapeutics (Europe) Limited | Treatment for neurodegenerative diseases |
| US12371667B2 (en) | 2021-05-13 | 2025-07-29 | Washington University | Enhanced methods for inducing and maintaining naive human pluripotent stem cells |
| CN116262752A (zh) * | 2021-12-15 | 2023-06-16 | 上海壹迪生物技术有限公司 | 吡唑并嘧啶类化合物及其用途 |
| CN119707984A (zh) * | 2023-09-28 | 2025-03-28 | 中国科学院上海药物研究所 | 吡唑并三嗪及吡唑并嘧啶衍生物、其制备方法、药物组合物及其用途 |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4864097A (https=) * | 1971-12-09 | 1973-09-05 | ||
| JPS6157587A (ja) * | 1984-08-29 | 1986-03-24 | Shionogi & Co Ltd | 縮合複素環誘導体および抗潰瘍剤 |
| US5602137A (en) * | 1993-06-10 | 1997-02-11 | Beiersdorf-Lilly Gmbh | Pyrimidine compounds and their use as pharmaceuticals |
| JP2006502163A (ja) * | 2002-09-04 | 2006-01-19 | シェーリング コーポレイション | サイクリン依存性キナーゼインヒビターとしてのピラゾロピリミジン |
| JP2006519226A (ja) * | 2003-02-28 | 2006-08-24 | 帝人ファーマ株式会社 | ピラゾロ[1,5−a]ピリミジン誘導体 |
Family Cites Families (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US619131A (en) * | 1899-02-07 | Chester l | ||
| GB9013750D0 (en) * | 1990-06-20 | 1990-08-08 | Pfizer Ltd | Therapeutic agents |
| AU651986B2 (en) | 1991-04-22 | 1994-08-11 | Otsuka Pharmaceutical Factory, Inc. | Pyrazolo{1,5-a}pyrimidine derivative and anti-inflammatory containing the same |
| CZ284157B6 (cs) * | 1992-12-17 | 1998-08-12 | Pfizer Inc. | Pyrazolové a pyrazolopyrimidinové sloučeniny jako takové a pro léčbu chorob a farmaceutické prostředky na jejich bázi |
| EP0628559B1 (en) | 1993-06-10 | 2002-04-03 | Beiersdorf-Lilly GmbH | Pyrimidine compounds and their use as pharmaceuticals |
| JP3710502B2 (ja) * | 1993-10-21 | 2005-10-26 | 塩野義製薬株式会社 | 三環性化合物 |
| WO1995035298A1 (en) | 1994-06-21 | 1995-12-28 | Otsuka Pharmaceutical Factory, Inc. | PYRAZOLO[1,5-a]PYRIMIDINE DERIVATIVE |
| US5919815A (en) | 1996-05-22 | 1999-07-06 | Neuromedica, Inc. | Taxane compounds and compositions |
| FR2750048B1 (fr) * | 1996-06-21 | 1998-08-14 | Oreal | Compositions de teinture des fibres keratiniques contenant des derives pyrazolo-(1, 5-a)-pyrimidine, procede de teinture, nouveaux derives pyrazolo-(1, 5-a)-pyrimidine et leur procede de preparation |
| US6191131B1 (en) | 1997-07-23 | 2001-02-20 | Dupont Pharmaceuticals Company | Azolo triazines and pyrimidines |
| JP3621706B2 (ja) * | 1996-08-28 | 2005-02-16 | ファイザー・インク | 置換された6,5―ヘテロ―二環式誘導体 |
| US6040321A (en) | 1997-11-12 | 2000-03-21 | Bristol-Myers Squibb Company | Aminothiazole inhibitors of cyclin dependent kinases |
| US6262096B1 (en) | 1997-11-12 | 2001-07-17 | Bristol-Myers Squibb Company | Aminothiazole inhibitors of cyclin dependent kinases |
| AU747705C (en) | 1997-12-13 | 2004-09-23 | Bristol-Myers Squibb Company | Use of pyrazolo (3,4-b) pyridine as cyclin dependent kinase inhibitors |
| US6413974B1 (en) | 1998-02-26 | 2002-07-02 | Aventis Pharmaceuticals Inc. | 6,9,-disubstituted 2-[trans-(4-aminocyclohexyl) amino] purines |
| FR2805160B1 (fr) * | 2000-02-23 | 2002-04-05 | Oreal | Compositions pour la teinture d'oxydation des fibres keratiniques comprenant un n(2-hydroxybenzene)-carbramate ou un n-(2-hydroxybenzene)-uree et une pyrazolopyrimidine, et procedes de teinture |
| EP1317453B1 (en) | 2000-09-15 | 2006-08-09 | Vertex Pharmaceuticals Incorporated | Isoxazoles and their use as inhibitors of erk |
| US7067520B2 (en) | 2000-11-17 | 2006-06-27 | Ishihara Sangyo Kaisha, Ltd. | Preventive or therapeutic medicines for diabetes containing fused-heterocyclic compounds or their salts |
| EP1345941A1 (fr) | 2000-12-20 | 2003-09-24 | Societe De Conseils De Recherches Et D'applications Scientifiques (S.C.R.A.S.) | Inhibiteurs de kinases dependantes des cylines (cdk) et de la glycogene synthase kinase-3 (gsk-3) |
| US7662826B2 (en) | 2002-04-23 | 2010-02-16 | Shionogi & Co., Ltd. | Pyrazolo [1,5-a] pyrimidine derivative and nad (p) h oxidase inhibitor containing the same |
| DE10223917A1 (de) | 2002-05-29 | 2003-12-11 | Bayer Cropscience Ag | Pyrazolopyrimidine |
| ES2285164T3 (es) * | 2002-09-04 | 2007-11-16 | Schering Corporation | Pirazolopirimidinas como inhibidores de quinasas dependientes de ciclina. |
| US7119200B2 (en) * | 2002-09-04 | 2006-10-10 | Schering Corporation | Pyrazolopyrimidines as cyclin dependent kinase inhibitors |
| JP2004277337A (ja) * | 2003-03-14 | 2004-10-07 | Sumitomo Pharmaceut Co Ltd | ピラゾロ[1,5−a]ピリミジン誘導体 |
| US20070179161A1 (en) * | 2003-03-31 | 2007-08-02 | Vernalis (Cambridge) Limited. | Pyrazolopyrimidine compounds and their use in medicine |
| US20070060595A1 (en) * | 2003-10-10 | 2007-03-15 | Toshio Yoshizawa | Novel fused heterocyclic compound and use thereof |
-
2004
- 2004-02-11 US US10/776,988 patent/US7119200B2/en not_active Expired - Lifetime
-
2005
- 2005-02-05 TW TW094104016A patent/TWI393566B/zh not_active IP Right Cessation
- 2005-02-08 DK DK05722809.0T patent/DK1720882T3/da active
- 2005-02-08 AU AU2005212409A patent/AU2005212409C1/en not_active Expired
- 2005-02-08 JP JP2006553181A patent/JP4845743B2/ja not_active Expired - Lifetime
- 2005-02-08 BR BRPI0507644A patent/BRPI0507644B8/pt not_active IP Right Cessation
- 2005-02-08 NZ NZ590480A patent/NZ590480A/en not_active IP Right Cessation
- 2005-02-08 CA CA2555345A patent/CA2555345C/en not_active Expired - Lifetime
- 2005-02-08 WO PCT/US2005/003859 patent/WO2005077954A2/en not_active Ceased
- 2005-02-08 AT AT05722809T patent/ATE494287T1/de active
- 2005-02-08 RU RU2006132288/04A patent/RU2414472C9/ru active
- 2005-02-08 ES ES05722809T patent/ES2359410T3/es not_active Expired - Lifetime
- 2005-02-08 EP EP05722809A patent/EP1720882B1/en not_active Expired - Lifetime
- 2005-02-08 DE DE602005025733T patent/DE602005025733D1/de not_active Expired - Lifetime
- 2005-02-08 MY MYPI20050514A patent/MY149044A/en unknown
- 2005-02-08 KR KR1020067016132A patent/KR101196498B1/ko not_active Expired - Lifetime
- 2005-02-08 CN CN2005800122934A patent/CN1946725B/zh not_active Expired - Lifetime
- 2005-02-08 HR HR20110245T patent/HRP20110245T1/hr unknown
- 2005-02-08 SI SI200531260T patent/SI1720882T1/sl unknown
- 2005-02-08 PL PL05722809T patent/PL1720882T3/pl unknown
- 2005-02-10 AR ARP050100483A patent/AR047543A1/es active IP Right Grant
- 2005-02-10 PE PE2005000156A patent/PE20050774A1/es active IP Right Grant
-
2006
- 2006-03-31 US US11/396,079 patent/US20070054925A1/en not_active Abandoned
- 2006-08-03 IL IL177283A patent/IL177283A/en active IP Right Grant
- 2006-08-07 ZA ZA200606573A patent/ZA200606573B/xx unknown
- 2006-09-08 NO NO20064046A patent/NO337520B1/no unknown
-
2010
- 2010-07-09 JP JP2010157338A patent/JP2010215675A/ja not_active Withdrawn
-
2011
- 2011-04-05 CY CY20111100349T patent/CY1112400T1/el unknown
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4864097A (https=) * | 1971-12-09 | 1973-09-05 | ||
| JPS6157587A (ja) * | 1984-08-29 | 1986-03-24 | Shionogi & Co Ltd | 縮合複素環誘導体および抗潰瘍剤 |
| US5602137A (en) * | 1993-06-10 | 1997-02-11 | Beiersdorf-Lilly Gmbh | Pyrimidine compounds and their use as pharmaceuticals |
| JP2006502163A (ja) * | 2002-09-04 | 2006-01-19 | シェーリング コーポレイション | サイクリン依存性キナーゼインヒビターとしてのピラゾロピリミジン |
| JP2006519226A (ja) * | 2003-02-28 | 2006-08-24 | 帝人ファーマ株式会社 | ピラゾロ[1,5−a]ピリミジン誘導体 |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010215675A (ja) * | 2004-02-11 | 2010-09-30 | Schering Corp | サイクリン依存性キナーゼインヒビターとしてのピラゾロピリミジン誘導体 |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP4845743B2 (ja) | サイクリン依存性キナーゼインヒビターとしてのピラゾロピリミジン誘導体 | |
| JP4881558B2 (ja) | サイクリン依存性キナーゼインヒビターとしてのピラゾロピリミジン | |
| JP4799864B2 (ja) | サイクリン依存性キナーゼインヒビターとしてのイミダゾピラジン | |
| JP4571969B2 (ja) | キナーゼインヒビターとしてのピラゾロトリアジン | |
| JP4925226B2 (ja) | サイクリン依存性キナーゼインヒビターとしての新規ピラゾロピリミジン | |
| JP4845379B2 (ja) | サイクリン依存性キナーゼインヒビターとしてのイミダゾピリジン | |
| JP4790265B2 (ja) | サイクリン依存性キナーゼインヒビターとしての新規ピラゾロピリミジン | |
| US8673924B2 (en) | Substituted pyrazolo[1,5-a]pyrimidines as cyclin dependent kinase inhibitors | |
| JP2006502184A5 (https=) | ||
| JP2006503838A (ja) | サイクリン依存性キナーゼインヒビターとしての新規イミダゾピラジン | |
| JP2011074088A (ja) | サイクリン依存性キナーゼインヒビターとしてのピラゾロピリミジン | |
| JP2006502161A (ja) | サイクリン依存性キナーゼインヒビターとしてのピラゾロピリミジン | |
| JP2010180234A (ja) | サイクリン依存性キナーゼインヒビターとしてのピラゾロピリミジン | |
| JP4845380B2 (ja) | サイクリン依存性キナーゼインヒビターとしてのピラゾロピリミジン | |
| US7161003B1 (en) | Pyrazolopyrimidines as cyclin dependent kinase inhibitors | |
| MXPA06009245A (en) | Pyrazolopyrimidine-derivatives as cyclin dependent kinase inhibitors |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20071226 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20100709 |
|
| A871 | Explanation of circumstances concerning accelerated examination |
Free format text: JAPANESE INTERMEDIATE CODE: A871 Effective date: 20100709 |
|
| A975 | Report on accelerated examination |
Free format text: JAPANESE INTERMEDIATE CODE: A971005 Effective date: 20100729 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A132 Effective date: 20100806 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20101108 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20101115 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20101202 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20101209 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20110502 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20110817 |
|
| A911 | Transfer to examiner for re-examination before appeal (zenchi) |
Free format text: JAPANESE INTERMEDIATE CODE: A911 Effective date: 20110830 |
|
| 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: 20110922 |
|
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20111011 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20141021 Year of fee payment: 3 |
|
| R150 | Certificate of patent or registration of utility model |
Ref document number: 4845743 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20141021 Year of fee payment: 3 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20141021 Year of fee payment: 3 |
|
| R154 | Certificate of patent or utility model (reissue) |
Free format text: JAPANESE INTERMEDIATE CODE: R154 |
|
| S111 | Request for change of ownership or part of ownership |
Free format text: JAPANESE INTERMEDIATE CODE: R313115 |
|
| S531 | Written request for registration of change of domicile |
Free format text: JAPANESE INTERMEDIATE CODE: R313531 |
|
| S533 | Written request for registration of change of name |
Free format text: JAPANESE INTERMEDIATE CODE: R313533 |
|
| S531 | Written request for registration of change of domicile |
Free format text: JAPANESE INTERMEDIATE CODE: R313531 |
|
| S533 | Written request for registration of change of name |
Free format text: JAPANESE INTERMEDIATE CODE: R313533 |
|
| R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
| R370 | Written measure of declining of transfer procedure |
Free format text: JAPANESE INTERMEDIATE CODE: R370 |
|
| 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 |
|
| S111 | Request for change of ownership or part of ownership |
Free format text: JAPANESE INTERMEDIATE CODE: R313115 |
|
| R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| EXPY | Cancellation because of completion of term |