JP5600111B2 - TRKキナーゼ阻害剤としての置換ピラゾロ[1,5−a]ピリミジン化合物 - Google Patents
TRKキナーゼ阻害剤としての置換ピラゾロ[1,5−a]ピリミジン化合物 Download PDFInfo
- Publication number
- JP5600111B2 JP5600111B2 JP2011533303A JP2011533303A JP5600111B2 JP 5600111 B2 JP5600111 B2 JP 5600111B2 JP 2011533303 A JP2011533303 A JP 2011533303A JP 2011533303 A JP2011533303 A JP 2011533303A JP 5600111 B2 JP5600111 B2 JP 5600111B2
- Authority
- JP
- Japan
- Prior art keywords
- pyrrolidin
- pyrazolo
- pyrimidin
- alkyl
- difluorophenyl
- 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*1CCN(C)C(*)(*)CC1 Chemical compound C*1CCN(C)C(*)(*)CC1 0.000 description 3
- YHBJBVSIEWTKMO-QGZVFWFLSA-N CC(C)(C(Nc(cn[n]1cc2)c1nc2N(CCC1)[C@H]1c(cc(cc1)F)c1F)=O)NC Chemical compound CC(C)(C(Nc(cn[n]1cc2)c1nc2N(CCC1)[C@H]1c(cc(cc1)F)c1F)=O)NC YHBJBVSIEWTKMO-QGZVFWFLSA-N 0.000 description 1
- SSULIMRGZQKFMY-QGZVFWFLSA-N CC(C)C(Nc(cn[n]1cc2)c1nc2N(CCC1)[C@H]1c(cc(cc1)F)c1F)=O Chemical compound CC(C)C(Nc(cn[n]1cc2)c1nc2N(CCC1)[C@H]1c(cc(cc1)F)c1F)=O SSULIMRGZQKFMY-QGZVFWFLSA-N 0.000 description 1
- KTHSAJOEFMMLBZ-QGZVFWFLSA-N CC(C1)(CN1C(Nc(cn[n]1cc2)c1nc2N(CCC1)[C@H]1c(cc(cc1)F)c1F)=O)O Chemical compound CC(C1)(CN1C(Nc(cn[n]1cc2)c1nc2N(CCC1)[C@H]1c(cc(cc1)F)c1F)=O)O KTHSAJOEFMMLBZ-QGZVFWFLSA-N 0.000 description 1
- VDXGZMWESOKUJV-UHFFFAOYSA-N CC(CCC1)(c2cccc(F)c2)N1c(cc[n]1nc2)nc1c2NC(N(C1)CC1O)=O Chemical compound CC(CCC1)(c2cccc(F)c2)N1c(cc[n]1nc2)nc1c2NC(N(C1)CC1O)=O VDXGZMWESOKUJV-UHFFFAOYSA-N 0.000 description 1
- FYDGKZRDCFWKFG-UHFFFAOYSA-N CC1(c2cc(F)ccc2F)N(C)CCOC1 Chemical compound CC1(c2cc(F)ccc2F)N(C)CCOC1 FYDGKZRDCFWKFG-UHFFFAOYSA-N 0.000 description 1
- DTHIWCDBGPDFSF-UHFFFAOYSA-N CCC(C)(C)[n]1ncnc1 Chemical compound CCC(C)(C)[n]1ncnc1 DTHIWCDBGPDFSF-UHFFFAOYSA-N 0.000 description 1
- BJHSCJQTERBIFM-LJQANCHMSA-N CN(CC1)CCN1C(Nc(cn[n]1cc2)c1nc2N(CCC1)[C@H]1c(cc(cc1)F)c1F)=O Chemical compound CN(CC1)CCN1C(Nc(cn[n]1cc2)c1nc2N(CCC1)[C@H]1c(cc(cc1)F)c1F)=O BJHSCJQTERBIFM-LJQANCHMSA-N 0.000 description 1
- GJSJPIXDLWUTPT-UHFFFAOYSA-N CN(CCOC1)C1c(cccc1)c1OC Chemical compound CN(CCOC1)C1c(cccc1)c1OC GJSJPIXDLWUTPT-UHFFFAOYSA-N 0.000 description 1
- SRHMXXVBGJNPAA-UHFFFAOYSA-N CN(CCOC1)C1c1cc(F)ccc1 Chemical compound CN(CCOC1)C1c1cc(F)ccc1 SRHMXXVBGJNPAA-UHFFFAOYSA-N 0.000 description 1
- YXLFQBXQTPAAIH-UHFFFAOYSA-N CN(CCOC1)C1c1cc(F)ccc1[F]C Chemical compound CN(CCOC1)C1c1cc(F)ccc1[F]C YXLFQBXQTPAAIH-UHFFFAOYSA-N 0.000 description 1
- OIYANYVIFQBNMS-UHFFFAOYSA-N CN(CCOC1)C1c1ccccc1 Chemical compound CN(CCOC1)C1c1ccccc1 OIYANYVIFQBNMS-UHFFFAOYSA-N 0.000 description 1
- LGBFIQSNYNDORW-UHFFFAOYSA-N CN(CCOC1)C1c1cnccc1 Chemical compound CN(CCOC1)C1c1cnccc1 LGBFIQSNYNDORW-UHFFFAOYSA-N 0.000 description 1
- QUIAAVXELSDZCI-HTAPYJJXSA-N C[C@@H](CN(CC1)C(Nc(cn[n]2cc3)c2nc3N(CCC2)[C@H]2c(cc(cc2)F)c2F)=O)N1C(OC(C)(C)C)=O Chemical compound C[C@@H](CN(CC1)C(Nc(cn[n]2cc3)c2nc3N(CCC2)[C@H]2c(cc(cc2)F)c2F)=O)N1C(OC(C)(C)C)=O QUIAAVXELSDZCI-HTAPYJJXSA-N 0.000 description 1
- BYOPZUKUWITKOE-LJQANCHMSA-N Cc1c(C(Nc(cn[n]2cc3)c2nc3N(CCC2)[C@H]2c(cc(cc2)F)c2F)=O)nccc1 Chemical compound Cc1c(C(Nc(cn[n]2cc3)c2nc3N(CCC2)[C@H]2c(cc(cc2)F)c2F)=O)nccc1 BYOPZUKUWITKOE-LJQANCHMSA-N 0.000 description 1
- MLUHWYZNTZXEFX-HXUWFJFHSA-N Cc1cccc(C(Nc(cn[n]2cc3)c2nc3N(CCC2)[C@H]2c(cc(cc2)F)c2F)=O)n1 Chemical compound Cc1cccc(C(Nc(cn[n]2cc3)c2nc3N(CCC2)[C@H]2c(cc(cc2)F)c2F)=O)n1 MLUHWYZNTZXEFX-HXUWFJFHSA-N 0.000 description 1
- NCXSNNVYILYEBC-SNVBAGLBSA-N Fc(cc1[C@@H]2NCCC2)ccc1F Chemical compound Fc(cc1[C@@H]2NCCC2)ccc1F NCXSNNVYILYEBC-SNVBAGLBSA-N 0.000 description 1
- PDIREONSOPXOGN-GOSISDBHSA-N O=C(Nc(cn[n]1cc2)c1nc2N(CCC1)[C@H]1c(cc(cc1)F)c1Cl)N1CCOCC1 Chemical compound O=C(Nc(cn[n]1cc2)c1nc2N(CCC1)[C@H]1c(cc(cc1)F)c1Cl)N1CCOCC1 PDIREONSOPXOGN-GOSISDBHSA-N 0.000 description 1
- CDIBLDMRAYKSQO-HXUWFJFHSA-N O=C(Nc(cn[n]1cc2)c1nc2N(CCC1)[C@H]1c(cc(cc1)F)c1F)Nc1ccccc1 Chemical compound O=C(Nc(cn[n]1cc2)c1nc2N(CCC1)[C@H]1c(cc(cc1)F)c1F)Nc1ccccc1 CDIBLDMRAYKSQO-HXUWFJFHSA-N 0.000 description 1
- IPFJWILEQTTXKZ-LJQANCHMSA-N O=C(c(nc1)ccc1Cl)Nc(cn[n]1cc2)c1nc2N(CCC1)[C@H]1c(cc(cc1)F)c1F Chemical compound O=C(c(nc1)ccc1Cl)Nc(cn[n]1cc2)c1nc2N(CCC1)[C@H]1c(cc(cc1)F)c1F IPFJWILEQTTXKZ-LJQANCHMSA-N 0.000 description 1
- OHIHEIPCEBOBSX-LJQANCHMSA-N O=C(c1ncccc1)Nc(cn[n]1cc2)c1nc2N(CCC1)[C@H]1c1cccc(F)c1 Chemical compound O=C(c1ncccc1)Nc(cn[n]1cc2)c1nc2N(CCC1)[C@H]1c1cccc(F)c1 OHIHEIPCEBOBSX-LJQANCHMSA-N 0.000 description 1
- HPMCYSIXHLNHGW-XPKAQORNSA-N OC(CC1)CN1C(C(Nc(cn[n]1cc2)c1nc2N(CCC1)[C@H]1c(cc(cc1)F)c1F)=O)=O Chemical compound OC(CC1)CN1C(C(Nc(cn[n]1cc2)c1nc2N(CCC1)[C@H]1c(cc(cc1)F)c1F)=O)=O HPMCYSIXHLNHGW-XPKAQORNSA-N 0.000 description 1
- AWZMRQLNTJDDRU-MRXNPFEDSA-N OC1(CC1)C(Nc(cn[n]1cc2)c1nc2N(CCC1)[C@H]1c(cc(cc1)F)c1F)=O Chemical compound OC1(CC1)C(Nc(cn[n]1cc2)c1nc2N(CCC1)[C@H]1c(cc(cc1)F)c1F)=O AWZMRQLNTJDDRU-MRXNPFEDSA-N 0.000 description 1
- ZUWQIFRIICXNQB-DNVCBOLYSA-N O[C@H](CCC1)CN1C(Nc(cn[n]1cc2)c1nc2N(CCC1)[C@H]1c1cc(F)ccc1C(F)F)=O Chemical compound O[C@H](CCC1)CN1C(Nc(cn[n]1cc2)c1nc2N(CCC1)[C@H]1c1cc(F)ccc1C(F)F)=O ZUWQIFRIICXNQB-DNVCBOLYSA-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
- 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
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
-
- 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]
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
- C07D519/02—Ergot alkaloids of the cyclic peptide type
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Nutrition Science (AREA)
- Physiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10761608P | 2008-10-22 | 2008-10-22 | |
| US61/107,616 | 2008-10-22 | ||
| PCT/US2009/061519 WO2010048314A1 (en) | 2008-10-22 | 2009-10-21 | SUBSTITUTED PYRAZOLO[1,5-a]PYRIMIDINE COMPOUNDS AS TRK KINASE INHIBITORS |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014134304A Division JP5832597B2 (ja) | 2008-10-22 | 2014-06-30 | TRKキナーゼ阻害剤としての置換ピラゾロ[1,5−a]ピリミジン化合物 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2012506446A JP2012506446A (ja) | 2012-03-15 |
| JP2012506446A5 JP2012506446A5 (enExample) | 2012-12-06 |
| JP5600111B2 true JP5600111B2 (ja) | 2014-10-01 |
Family
ID=41328903
Family Applications (5)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011533303A Active JP5600111B2 (ja) | 2008-10-22 | 2009-10-21 | TRKキナーゼ阻害剤としての置換ピラゾロ[1,5−a]ピリミジン化合物 |
| JP2014134304A Expired - Fee Related JP5832597B2 (ja) | 2008-10-22 | 2014-06-30 | TRKキナーゼ阻害剤としての置換ピラゾロ[1,5−a]ピリミジン化合物 |
| JP2015170033A Active JP6105008B2 (ja) | 2008-10-22 | 2015-08-31 | TRKキナーゼ阻害剤としての置換ピラゾロ[1,5−a]ピリミジン化合物 |
| JP2016182689A Expired - Fee Related JP6431512B2 (ja) | 2008-10-22 | 2016-09-20 | TRKキナーゼ阻害剤としての置換ピラゾロ[1,5−a]ピリミジン化合物 |
| JP2018207330A Active JP6788649B2 (ja) | 2008-10-22 | 2018-11-02 | TRKキナーゼ阻害剤としての置換ピラゾロ[1,5−a]ピリミジン化合物 |
Family Applications After (4)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014134304A Expired - Fee Related JP5832597B2 (ja) | 2008-10-22 | 2014-06-30 | TRKキナーゼ阻害剤としての置換ピラゾロ[1,5−a]ピリミジン化合物 |
| JP2015170033A Active JP6105008B2 (ja) | 2008-10-22 | 2015-08-31 | TRKキナーゼ阻害剤としての置換ピラゾロ[1,5−a]ピリミジン化合物 |
| JP2016182689A Expired - Fee Related JP6431512B2 (ja) | 2008-10-22 | 2016-09-20 | TRKキナーゼ阻害剤としての置換ピラゾロ[1,5−a]ピリミジン化合物 |
| JP2018207330A Active JP6788649B2 (ja) | 2008-10-22 | 2018-11-02 | TRKキナーゼ阻害剤としての置換ピラゾロ[1,5−a]ピリミジン化合物 |
Country Status (38)
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2015214590A (ja) * | 2008-10-22 | 2015-12-03 | アレイ バイオファーマ、インコーポレイテッド | TRKキナーゼ阻害剤としての置換ピラゾロ[1,5−a]ピリミジン化合物 |
Families Citing this family (140)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK2350075T3 (da) | 2008-09-22 | 2014-05-26 | Array Biopharma Inc | Substituerede imidazo[1,2b]pyridazinforbindelser som trk-kinase-inhibitorer |
| AR077468A1 (es) | 2009-07-09 | 2011-08-31 | Array Biopharma Inc | Compuestos de pirazolo (1,5 -a) pirimidina sustituidos como inhibidores de trk- quinasa |
| TWI619713B (zh) | 2010-04-21 | 2018-04-01 | 普雷辛肯公司 | 用於激酶調節的化合物和方法及其適應症 |
| RU2735545C2 (ru) * | 2010-05-20 | 2020-11-03 | Эррэй Биофарма Инк. | Макроциклические соединения в качестве ингибиторов киназы trk |
| UY33597A (es) | 2010-09-09 | 2012-04-30 | Irm Llc | Compuestos y composiciones como inhibidores de la trk |
| WO2012034095A1 (en) * | 2010-09-09 | 2012-03-15 | Irm Llc | Compounds and compositions as trk inhibitors |
| KR20140014184A (ko) * | 2011-02-25 | 2014-02-05 | 아이알엠 엘엘씨 | Trk 억제제로서의 화합물 및 조성물 |
| MY173181A (en) * | 2011-05-13 | 2020-01-02 | Array Biopharma Inc | Pyrrolidinyl urea, pyrrolidinyl thiourea and pyrrolidinyl guanidine compounds as trka kinase inhibitors |
| WO2013088257A1 (en) * | 2011-12-12 | 2013-06-20 | Dr. Reddy's Laboratories Ltd. | Substituted heterocyclic compounds as tropomyosin receptor kinase a (trka) inhibitors |
| CN104302649B (zh) * | 2012-03-09 | 2017-06-23 | 莱西肯医药有限公司 | 基于吡唑并[1,5‑a]嘧啶的化合物、包含它们的组合物及其使用方法 |
| US9809578B2 (en) | 2012-11-13 | 2017-11-07 | Array Biopharma Inc. | Pyrazolyl urea, thiourea, guanidine and cyanoguanidine compounds as trkA kinase inhibitors |
| US9822118B2 (en) | 2012-11-13 | 2017-11-21 | Array Biopharma Inc. | Bicyclic heteroaryl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors |
| WO2014078325A1 (en) | 2012-11-13 | 2014-05-22 | Array Biopharma Inc. | N-(monocyclic aryl),n'-pyrazolyl-urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors |
| WO2014078328A1 (en) * | 2012-11-13 | 2014-05-22 | Array Biopharma Inc. | N-bicyclic aryl,n'-pyrazolyl urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors |
| WO2014078331A1 (en) | 2012-11-13 | 2014-05-22 | Array Biopharma Inc. | N-(arylalkyl)-n'-pyrazolyl-urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors |
| EP2922844B1 (en) | 2012-11-13 | 2018-01-10 | Array Biopharma, Inc. | N-pyrrolidinyl, n'-pyrazolyl- urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors |
| WO2014078378A1 (en) | 2012-11-13 | 2014-05-22 | Array Biopharma Inc. | Pyrrolidinyl urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors |
| US9790178B2 (en) | 2012-11-13 | 2017-10-17 | Array Biopharma Inc. | Pyrrolidinyl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors |
| EP2920166B1 (en) | 2012-11-13 | 2016-11-02 | Array Biopharma, Inc. | Bicyclic urea, thiourea, guanidine and cyanoguanidine compounds useful for the treatment of pain |
| US9981959B2 (en) | 2012-11-13 | 2018-05-29 | Array Biopharma Inc. | Thiazolyl and oxazolyl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors |
| CA2897200C (en) | 2013-01-14 | 2021-07-06 | Incyte Corporation | Bicyclic aromatic carboxamide compounds useful as pim kinase inhibitors |
| PE20191245A1 (es) | 2013-01-15 | 2019-09-18 | Incyte Holdings Corp | Compuestos de tiazolcarboxamidas y piridinacarboxamida utiles como inhibidores de quinasa pim |
| CN105658653A (zh) | 2013-08-23 | 2016-06-08 | 因赛特公司 | 可用作pim激酶抑制剂的呋喃并-和噻吩并-吡啶甲酰胺化合物 |
| TW201542550A (zh) * | 2013-09-06 | 2015-11-16 | Lexicon Pharmaceuticals Inc | 吡唑并[1,5-a]嘧啶基化合物、包含彼之組合物以及使用彼之方法 |
| HRP20191283T1 (hr) | 2014-01-24 | 2019-10-18 | Turning Point Therapeutics, Inc. | Diaril makrocikli kao modulatori protein kinaze |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2015214590A (ja) * | 2008-10-22 | 2015-12-03 | アレイ バイオファーマ、インコーポレイテッド | TRKキナーゼ阻害剤としての置換ピラゾロ[1,5−a]ピリミジン化合物 |
| JP2019034961A (ja) * | 2008-10-22 | 2019-03-07 | アレイ バイオファーマ、インコーポレイテッド | TRKキナーゼ阻害剤としての置換ピラゾロ[1,5−a]ピリミジン化合物 |
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