JP2008506714A - オーロラキナーゼインヒビターとして有用なチエノピリミジン - Google Patents
オーロラキナーゼインヒビターとして有用なチエノピリミジン Download PDFInfo
- Publication number
- JP2008506714A JP2008506714A JP2007521708A JP2007521708A JP2008506714A JP 2008506714 A JP2008506714 A JP 2008506714A JP 2007521708 A JP2007521708 A JP 2007521708A JP 2007521708 A JP2007521708 A JP 2007521708A JP 2008506714 A JP2008506714 A JP 2008506714A
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- JP
- Japan
- Prior art keywords
- alkyl
- aryl
- heteroaryl
- compound
- hydrogen
- 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.)
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- 0 C*c1ccc(CCC*N2CCCC2)cc1 Chemical compound C*c1ccc(CCC*N2CCCC2)cc1 0.000 description 28
- PCSWDVSHDHQYSA-UHFFFAOYSA-N CN1C(NCCc2cnc(NC(Nc3cccc(C(F)(F)F)c3)=O)[s]2)=C2SC(S(C)(=O)=O)=CC2=NC1 Chemical compound CN1C(NCCc2cnc(NC(Nc3cccc(C(F)(F)F)c3)=O)[s]2)=C2SC(S(C)(=O)=O)=CC2=NC1 PCSWDVSHDHQYSA-UHFFFAOYSA-N 0.000 description 1
- AZPMALJVBUIZFS-UHFFFAOYSA-N CNc1ncnc2c1[s]cc2 Chemical compound CNc1ncnc2c1[s]cc2 AZPMALJVBUIZFS-UHFFFAOYSA-N 0.000 description 1
- RUICZHLJQSXMFL-UHFFFAOYSA-N CNc1ncnc2c1cc[s]2 Chemical compound CNc1ncnc2c1cc[s]2 RUICZHLJQSXMFL-UHFFFAOYSA-N 0.000 description 1
- XTSLBDJQPAYELB-UHFFFAOYSA-N CS(c1cccc(I)c1)(=O)=O Chemical compound CS(c1cccc(I)c1)(=O)=O XTSLBDJQPAYELB-UHFFFAOYSA-N 0.000 description 1
- ULKWBVNMJZUEBD-UHFFFAOYSA-N Cc(cc1)ccc1C(N(C)C)=O Chemical compound Cc(cc1)ccc1C(N(C)C)=O ULKWBVNMJZUEBD-UHFFFAOYSA-N 0.000 description 1
- XOODLNRDHSTOQJ-UHFFFAOYSA-N Cc(cc1)cnc1I Chemical compound Cc(cc1)cnc1I XOODLNRDHSTOQJ-UHFFFAOYSA-N 0.000 description 1
- SZQCPPRPWDXLMM-UHFFFAOYSA-N Cc1c[n](C)nc1 Chemical compound Cc1c[n](C)nc1 SZQCPPRPWDXLMM-UHFFFAOYSA-N 0.000 description 1
- AODCJVRLFOJIQX-UHFFFAOYSA-N Cc1c[n](CCN2CCCCC2)nn1 Chemical compound Cc1c[n](CCN2CCCCC2)nn1 AODCJVRLFOJIQX-UHFFFAOYSA-N 0.000 description 1
- QEPCSAOHBQEUCL-UHFFFAOYSA-N Cc1c[n](CCN2CCOCC2)cn1 Chemical compound Cc1c[n](CCN2CCOCC2)cn1 QEPCSAOHBQEUCL-UHFFFAOYSA-N 0.000 description 1
- CFBMMPPHOBSVEC-UHFFFAOYSA-N Cc1c[n](CCN2CCOCC2)nc1 Chemical compound Cc1c[n](CCN2CCOCC2)nc1 CFBMMPPHOBSVEC-UHFFFAOYSA-N 0.000 description 1
- WGRPQCFFBRDZFV-UHFFFAOYSA-N Cc1cc(C(N)=O)ccc1 Chemical compound Cc1cc(C(N)=O)ccc1 WGRPQCFFBRDZFV-UHFFFAOYSA-N 0.000 description 1
- HMTSWYPNXFHGEP-UHFFFAOYSA-N Cc1ccc(CN)cc1 Chemical compound Cc1ccc(CN)cc1 HMTSWYPNXFHGEP-UHFFFAOYSA-N 0.000 description 1
- JBZFWJJJLREXJO-UHFFFAOYSA-N Cc1ccc(CN2CCOCC2)cc1 Chemical compound Cc1ccc(CN2CCOCC2)cc1 JBZFWJJJLREXJO-UHFFFAOYSA-N 0.000 description 1
- UJPXOHXMJDQRLY-UHFFFAOYSA-N Cc1ccc(CNCCO)cc1 Chemical compound Cc1ccc(CNCCO)cc1 UJPXOHXMJDQRLY-UHFFFAOYSA-N 0.000 description 1
- KMTDMTZBNYGUNX-UHFFFAOYSA-N Cc1ccc(CO)cc1 Chemical compound Cc1ccc(CO)cc1 KMTDMTZBNYGUNX-UHFFFAOYSA-N 0.000 description 1
- GNFLFHZJXXFDRA-UHFFFAOYSA-N Cc1ccc[n]1C Chemical compound Cc1ccc[n]1C GNFLFHZJXXFDRA-UHFFFAOYSA-N 0.000 description 1
- HNOQHUVQEAQMFT-UHFFFAOYSA-N Cc1ncnc2c1[s]cc2 Chemical compound Cc1ncnc2c1[s]cc2 HNOQHUVQEAQMFT-UHFFFAOYSA-N 0.000 description 1
- GKVSTMSWKDNXAQ-UHFFFAOYSA-N I[IH]c1cccc(CN2CCOCC2)c1 Chemical compound I[IH]c1cccc(CN2CCOCC2)c1 GKVSTMSWKDNXAQ-UHFFFAOYSA-N 0.000 description 1
- KFGMIELEORXLFO-UHFFFAOYSA-N O=C(Nc1ncc(CCNc2ncnc3c2[s]c(-c2c[n](CCN4CCOCC4)nn2)c3)[s]1)Nc1cccc(C(F)(F)F)c1 Chemical compound O=C(Nc1ncc(CCNc2ncnc3c2[s]c(-c2c[n](CCN4CCOCC4)nn2)c3)[s]1)Nc1cccc(C(F)(F)F)c1 KFGMIELEORXLFO-UHFFFAOYSA-N 0.000 description 1
- SELBNGIRQTXDTJ-UHFFFAOYSA-N O=C(c1c(-c2ccccc2)[o]cn1)Nc1ccc(CCNc2ncnc3c2[s]cc3)cc1 Chemical compound O=C(c1c(-c2ccccc2)[o]cn1)Nc1ccc(CCNc2ncnc3c2[s]cc3)cc1 SELBNGIRQTXDTJ-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
-
- 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
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- 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
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- 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
- 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
- A61P37/04—Immunostimulants
-
- 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
- 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
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- 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
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- 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)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Biomedical Technology (AREA)
- Hematology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Transplantation (AREA)
- Cardiology (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Psychiatry (AREA)
- Gastroenterology & Hepatology (AREA)
- Hospice & Palliative Care (AREA)
- Pain & Pain Management (AREA)
- Heart & Thoracic Surgery (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Obesity (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US58871804P | 2004-07-16 | 2004-07-16 | |
| US63256804P | 2004-12-01 | 2004-12-01 | |
| PCT/US2005/025340 WO2006036266A1 (en) | 2004-07-16 | 2005-07-15 | Thienopyrimidines useful as aurora kinase inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2008506714A true JP2008506714A (ja) | 2008-03-06 |
| JP2008506714A5 JP2008506714A5 (enExample) | 2008-08-14 |
Family
ID=35527256
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007521708A Pending JP2008506714A (ja) | 2004-07-16 | 2005-07-15 | オーロラキナーゼインヒビターとして有用なチエノピリミジン |
Country Status (14)
| Country | Link |
|---|---|
| US (2) | US7601725B2 (enExample) |
| EP (1) | EP1768984B1 (enExample) |
| JP (1) | JP2008506714A (enExample) |
| KR (1) | KR20070057792A (enExample) |
| AT (1) | ATE485300T1 (enExample) |
| AU (1) | AU2005290226A1 (enExample) |
| BR (1) | BRPI0513405A (enExample) |
| CA (1) | CA2573999A1 (enExample) |
| DE (1) | DE602005024274D1 (enExample) |
| IL (1) | IL180722A0 (enExample) |
| MX (1) | MX2007000631A (enExample) |
| NZ (1) | NZ552751A (enExample) |
| SG (1) | SG156650A1 (enExample) |
| WO (1) | WO2006036266A1 (enExample) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009113637A1 (ja) * | 2008-03-12 | 2009-09-17 | 東ソー株式会社 | 新規なチアゾール誘導体、チアゾール誘導体固定化マトリックス、及びそれらの製造方法 |
| JP2009244252A (ja) * | 2008-03-13 | 2009-10-22 | Sagami Chem Res Center | 新規なチアゾール誘導体固定化マトリックス、及びその製造方法 |
| JP2010159239A (ja) * | 2008-03-12 | 2010-07-22 | Sagami Chemical Research Institute | 新規なチアゾール誘導体、及びその製造方法 |
| JP2016501192A (ja) * | 2012-11-20 | 2016-01-18 | ケイテーベー ツモルフォルシュングスゲゼルシャフト ミット ベシュレンクテル ハフツング | プロテインキナーゼ阻害剤としてのチオエーテル誘導体 |
| WO2016199761A1 (ja) * | 2015-06-08 | 2016-12-15 | 石原産業株式会社 | ジフルオロメチレン化合物 |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2573538C (en) | 2004-07-30 | 2014-11-25 | Methylgene Inc. | Inhibitors of vegf receptor and hgf receptor signaling |
| ES2473341T3 (es) | 2005-05-20 | 2014-07-04 | Methylgene Inc | Inhibidores de la se�alizaci�n del receptor del VEGF y del receptor del HGF |
| JP5148499B2 (ja) | 2005-05-20 | 2013-02-20 | メチルジーン インコーポレイテッド | Vegf受容体およびhgf受容体シグナル伝達の阻害剤 |
| US8119655B2 (en) | 2005-10-07 | 2012-02-21 | Takeda Pharmaceutical Company Limited | Kinase inhibitors |
| CA2645583A1 (en) * | 2006-03-20 | 2007-09-27 | F. Hoffman-La Roche Ag | Methods of inhibiting btk and syk protein kinases |
| SG158147A1 (en) | 2006-10-09 | 2010-01-29 | Takeda Pharmaceutical | Kinase inhibitors |
| NZ582349A (en) * | 2007-06-29 | 2012-06-29 | Sunesis Pharmaceuticals Inc | Heterocyclic compounds useful as raf kinase inhibitors |
| EP2014663A1 (de) * | 2007-07-12 | 2009-01-14 | Bayer Schering Pharma AG | Thienopyrimidylamine als Modulatoren des EP2-Rezeptors |
| WO2009109035A1 (en) | 2008-03-05 | 2009-09-11 | Methylgene Inc. | Inhibitors of protein tyrosine kinase activity |
| EP2265618A2 (en) * | 2008-03-14 | 2010-12-29 | Sunesis Pharmaceuticals, Inc. | Aurora kinase inhibitors |
| CA2719579C (en) * | 2008-03-25 | 2020-07-21 | Sunesis Pharmaceuticals, Inc. | Methods of chemotype evolution |
| KR101667822B1 (ko) * | 2008-04-30 | 2016-10-19 | 내셔날 헬스 리서치 인스티튜트 | 오로라 키나아제 저해제용 접합 2고리 피리미딘 화합물 |
| US20100063047A1 (en) * | 2008-09-10 | 2010-03-11 | Kalypsys, Inc. | Aminopyrimidine inhibitors of histamine receptors for the treatment of disease |
| EP2331530B8 (en) * | 2008-09-26 | 2013-12-25 | National Health Research Institutes | Fused multicyclic compounds as protein kinase inhibitors |
| ES2468391T3 (es) | 2008-12-22 | 2014-06-16 | Millennium Pharmaceuticals, Inc. | Combinación de inhibidores de cinasas Aurora y anticuerpos anti-CD20 |
| CN103012428A (zh) | 2013-01-08 | 2013-04-03 | 中国药科大学 | 4-(五元杂环并嘧啶/吡啶取代)氨基-1H-3-吡唑甲酰胺类CDK/Aurora双重抑制剂及其用途 |
| US10335494B2 (en) | 2013-12-06 | 2019-07-02 | Millennium Pharmaceuticals, Inc. | Combination of aurora kinase inhibitors and anti-CD30 antibodies |
| FR3015483B1 (fr) * | 2013-12-23 | 2016-01-01 | Servier Lab | Nouveaux derives de thienopyrimidine, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| WO2017015316A1 (en) | 2015-07-21 | 2017-01-26 | Millennium Pharmaceuticals, Inc. | Administration of aurora kinase inhibitor and chemotherapeutic agents |
| GB201705263D0 (en) * | 2017-03-31 | 2017-05-17 | Probiodrug Ag | Novel inhibitors |
| US11874276B2 (en) | 2018-04-05 | 2024-01-16 | Dana-Farber Cancer Institute, Inc. | STING levels as a biomarker for cancer immunotherapy |
| WO2020049208A1 (es) | 2018-09-09 | 2020-03-12 | Fundacio Privada Institut De Recerca De La Sida - Caixa | Aurora cinasa como diana para tratar, prevenir o curar una infección por vih o sida |
| WO2021041532A1 (en) | 2019-08-26 | 2021-03-04 | Dana-Farber Cancer Institute, Inc. | Use of heparin to promote type 1 interferon signaling |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61286373A (ja) * | 1985-06-14 | 1986-12-16 | Sankyo Co Ltd | フエノキシアルキルアミン誘導体、その製法および殺虫殺ダニ剤 |
| WO1997009316A1 (en) * | 1995-09-04 | 1997-03-13 | Novartis Ag | 4-[2-(pyrimidin-4-oxy- or 4-ylamino)-ethyl]-phenyl-oximes |
| US6133271A (en) * | 1998-11-19 | 2000-10-17 | Cell Pathways, Inc. | Method for inhibiting neoplastic cells and related conditions by exposure thienopyrimidine derivatives |
| WO2002051849A1 (en) * | 2000-12-26 | 2002-07-04 | Daiichi Pharmaceutical Co., Ltd. | Cdk4 inhibitors |
| US6503914B1 (en) * | 2000-10-23 | 2003-01-07 | Board Of Regents, The University Of Texas System | Thienopyrimidine-based inhibitors of the Src family |
| WO2003055890A1 (en) * | 2001-12-21 | 2003-07-10 | Bayer Pharmaceuticals Corporation | Thienopyrimidine derivative compounds as inhibitors of prolylpeptidase, inducers of apoptosis and cancer treatment agents |
Family Cites Families (70)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1570494A (en) | 1975-11-28 | 1980-07-02 | Ici Ltd | Thienopyrimidine derivatives and their use as pesticides |
| ZA782648B (en) | 1977-05-23 | 1979-06-27 | Ici Australia Ltd | The prevention,control or eradication of infestations of ixodid ticks |
| JPH0720943B2 (ja) | 1988-08-19 | 1995-03-08 | 宇部興産株式会社 | アミノピリミジン誘導体、その製法及び殺虫・殺菌剤 |
| US5141941A (en) | 1988-11-21 | 1992-08-25 | Ube Industries, Ltd. | Aralkylamine derivatives, and fungicides containing the same |
| US5124333A (en) | 1989-08-02 | 1992-06-23 | Ube Industries, Ltd. | Aminopyrimidine derivatives and harmful organisms preventive agent |
| JPH0717638B2 (ja) | 1989-08-02 | 1995-03-01 | 宇部興産株式会社 | アミノピリミジン誘導体、その製造方法及び殺虫、殺菌剤 |
| JPH075569B2 (ja) | 1989-08-02 | 1995-01-25 | 宇部興産株式会社 | アラルキルアミン誘導体、その製法及び殺菌、殺虫剤 |
| JPH03173872A (ja) | 1989-09-14 | 1991-07-29 | Ube Ind Ltd | アミノピリミジン誘導体、その製造方法及び殺虫・殺菌剤 |
| EP0424125A3 (en) | 1989-10-18 | 1991-10-09 | Ube Industries, Ltd. | Aralkylamine derivatives, preparation method thereof and fungicides containing the same |
| DE4008726A1 (de) | 1990-03-19 | 1991-09-26 | Basf Ag | Thieno(2,3-d)pyrimidinderivate |
| EP0452002A3 (en) | 1990-03-30 | 1992-02-26 | Dowelanco | Thienopyrimidine derivatives |
| JPH04164072A (ja) | 1990-10-26 | 1992-06-09 | Ube Ind Ltd | オキシピリミジン誘導体、その製法及び有害生物防除剤 |
| JP2762430B2 (ja) | 1991-01-18 | 1998-06-04 | 宇部興産株式会社 | アラルキルアミノピリミジン類の製法 |
| US5227387A (en) | 1991-09-03 | 1993-07-13 | Dowelanco | Quinoline nematicidal method |
| DE4131924A1 (de) | 1991-09-25 | 1993-07-08 | Hoechst Ag | Substituierte 4-alkoxypyrimidine, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel |
| US5187168A (en) | 1991-10-24 | 1993-02-16 | American Home Products Corporation | Substituted quinazolines as angiotensin II antagonists |
| JPH0710712A (ja) | 1993-06-25 | 1995-01-13 | Ube Ind Ltd | 花卉園芸用殺菌剤 |
| IL112249A (en) | 1994-01-25 | 2001-11-25 | Warner Lambert Co | Pharmaceutical compositions containing di and tricyclic pyrimidine derivatives for inhibiting tyrosine kinases of the epidermal growth factor receptor family and some new such compounds |
| US5654307A (en) | 1994-01-25 | 1997-08-05 | Warner-Lambert Company | Bicyclic compounds capable of inhibiting tyrosine kinases of the epidermal growth factor receptor family |
| GB9424676D0 (en) | 1994-12-07 | 1995-02-01 | Sandoz Ltd | Organic compounds |
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009113637A1 (ja) * | 2008-03-12 | 2009-09-17 | 東ソー株式会社 | 新規なチアゾール誘導体、チアゾール誘導体固定化マトリックス、及びそれらの製造方法 |
| JP2010159239A (ja) * | 2008-03-12 | 2010-07-22 | Sagami Chemical Research Institute | 新規なチアゾール誘導体、及びその製造方法 |
| JP2009244252A (ja) * | 2008-03-13 | 2009-10-22 | Sagami Chem Res Center | 新規なチアゾール誘導体固定化マトリックス、及びその製造方法 |
| JP2016501192A (ja) * | 2012-11-20 | 2016-01-18 | ケイテーベー ツモルフォルシュングスゲゼルシャフト ミット ベシュレンクテル ハフツング | プロテインキナーゼ阻害剤としてのチオエーテル誘導体 |
| WO2016199761A1 (ja) * | 2015-06-08 | 2016-12-15 | 石原産業株式会社 | ジフルオロメチレン化合物 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1768984B1 (en) | 2010-10-20 |
| IL180722A0 (en) | 2007-06-03 |
| DE602005024274D1 (de) | 2010-12-02 |
| WO2006036266A1 (en) | 2006-04-06 |
| US20100179123A1 (en) | 2010-07-15 |
| ATE485300T1 (de) | 2010-11-15 |
| CA2573999A1 (en) | 2006-04-06 |
| SG156650A1 (en) | 2009-11-26 |
| US20060035908A1 (en) | 2006-02-16 |
| EP1768984A1 (en) | 2007-04-04 |
| MX2007000631A (es) | 2007-03-30 |
| KR20070057792A (ko) | 2007-06-07 |
| BRPI0513405A (pt) | 2008-05-06 |
| AU2005290226A1 (en) | 2006-04-06 |
| US7601725B2 (en) | 2009-10-13 |
| NZ552751A (en) | 2010-11-26 |
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