CN102036990B - 新型酪氨酸激酶抑制剂 - Google Patents
新型酪氨酸激酶抑制剂 Download PDFInfo
- Publication number
- CN102036990B CN102036990B CN200980118256.XA CN200980118256A CN102036990B CN 102036990 B CN102036990 B CN 102036990B CN 200980118256 A CN200980118256 A CN 200980118256A CN 102036990 B CN102036990 B CN 102036990B
- Authority
- CN
- China
- Prior art keywords
- oxo
- dihydropyridin
- dihydroimidazo
- ethyl
- mmol
- 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 C[C@@](CC1=CC=CCC1)*(C=C)C(C=C*1=C)=C(C2=*c3cc(CC(CCC*4CCCC4)C4O)c4cc3*2C)C1=O Chemical compound C[C@@](CC1=CC=CCC1)*(C=C)C(C=C*1=C)=C(C2=*c3cc(CC(CCC*4CCCC4)C4O)c4cc3*2C)C1=O 0.000 description 19
- COLPYVAVNIYJMT-UHFFFAOYSA-N CC(Cc([s]cc1)c1Cl)NC(C=CN1)=C(c2nc3cc(C(N(CCN4CCCC4)C4)=O)c4cc3[nH]2)C1=O Chemical compound CC(Cc([s]cc1)c1Cl)NC(C=CN1)=C(c2nc3cc(C(N(CCN4CCCC4)C4)=O)c4cc3[nH]2)C1=O COLPYVAVNIYJMT-UHFFFAOYSA-N 0.000 description 1
- JKSJCZONSZZHGB-UHFFFAOYSA-N CC(Cc1c(C)cc[s]1)N Chemical compound CC(Cc1c(C)cc[s]1)N JKSJCZONSZZHGB-UHFFFAOYSA-N 0.000 description 1
- TZBHTUUTVCEESP-UHFFFAOYSA-N CC(Cc1c[s]cc1)NC(C=CN1)=C(c2nc(cc(CN(CCCN3CCCC3)C3=O)c3c3)c3[nH]2)C1=O Chemical compound CC(Cc1c[s]cc1)NC(C=CN1)=C(c2nc(cc(CN(CCCN3CCCC3)C3=O)c3c3)c3[nH]2)C1=O TZBHTUUTVCEESP-UHFFFAOYSA-N 0.000 description 1
- QRKUZIJZPXXCCA-UHFFFAOYSA-N CC(Cc1cc(cccc2)c2[s]1)NC(C=CN1)=C(c2nc(cc(CN(CCCN3CCCC3)C3=O)c3c3)c3[nH]2)C1=O Chemical compound CC(Cc1cc(cccc2)c2[s]1)NC(C=CN1)=C(c2nc(cc(CN(CCCN3CCCC3)C3=O)c3c3)c3[nH]2)C1=O QRKUZIJZPXXCCA-UHFFFAOYSA-N 0.000 description 1
- IDUAQSPIDXGMKI-UHFFFAOYSA-N CC(Cc1ccc[o]1)N Chemical compound CC(Cc1ccc[o]1)N IDUAQSPIDXGMKI-UHFFFAOYSA-N 0.000 description 1
- JDBOVXMUOFVGPL-UHFFFAOYSA-N CCC(Cc1ccc[s]1)NC(C=CN1)=C(c2nc(cc(CN(CCCN3CCCC3)C3=O)c3c3)c3[nH]2)C1=O Chemical compound CCC(Cc1ccc[s]1)NC(C=CN1)=C(c2nc(cc(CN(CCCN3CCCC3)C3=O)c3c3)c3[nH]2)C1=O JDBOVXMUOFVGPL-UHFFFAOYSA-N 0.000 description 1
- RIKLCXOBWUKNRH-UHFFFAOYSA-N CCC(Cc1ccc[s]1)NC(C=CN1)=C(c2nc(cc(c(C(N3CCCN4CCCC4)=O)c4)C3=O)c4[nH]2)C1=O Chemical compound CCC(Cc1ccc[s]1)NC(C=CN1)=C(c2nc(cc(c(C(N3CCCN4CCCC4)=O)c4)C3=O)c4[nH]2)C1=O RIKLCXOBWUKNRH-UHFFFAOYSA-N 0.000 description 1
- GRGGAFFKKODMSY-HMTLIYDFSA-N CCCC(CN1CCCC1)CN(Cc(c1c2)cc3c2[nH]c(C(C(NC=C2)=O)=C2N[C@@H](C)Cc2c(C)cc[s]2)n3)C1=O Chemical compound CCCC(CN1CCCC1)CN(Cc(c1c2)cc3c2[nH]c(C(C(NC=C2)=O)=C2N[C@@H](C)Cc2c(C)cc[s]2)n3)C1=O GRGGAFFKKODMSY-HMTLIYDFSA-N 0.000 description 1
- KAQKKYYTGLMYKH-UHFFFAOYSA-N CN(C)CCN(C(c(c1c2)cc3c2nc(C(C(NC=C2)=O)=C2Cl)[nH]3)=O)C1=O Chemical compound CN(C)CCN(C(c(c1c2)cc3c2nc(C(C(NC=C2)=O)=C2Cl)[nH]3)=O)C1=O KAQKKYYTGLMYKH-UHFFFAOYSA-N 0.000 description 1
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- BSCVBWJNWZTZAQ-LURJTMIESA-N C[C@@H](Cc(c(C)c1F)ccc1F)N Chemical compound C[C@@H](Cc(c(C)c1F)ccc1F)N BSCVBWJNWZTZAQ-LURJTMIESA-N 0.000 description 1
- GSAJGOBYFQZCPA-HNNXBMFYSA-N C[C@@H](Cc(c(C)c1F)ccc1F)NC(C=CN1)=C(c2nc(cc(c(CN3CCN(C)C)c4)C3=O)c4[nH]2)C1=O Chemical compound C[C@@H](Cc(c(C)c1F)ccc1F)NC(C=CN1)=C(c2nc(cc(c(CN3CCN(C)C)c4)C3=O)c4[nH]2)C1=O GSAJGOBYFQZCPA-HNNXBMFYSA-N 0.000 description 1
- JKSJCZONSZZHGB-ZETCQYMHSA-N C[C@@H](Cc1c(C)cc[s]1)N Chemical compound C[C@@H](Cc1c(C)cc[s]1)N JKSJCZONSZZHGB-ZETCQYMHSA-N 0.000 description 1
- FPTQXZXPSPFFSP-SSDOTTSWSA-N C[C@H](Cc(cccc1)c1Cl)O Chemical compound C[C@H](Cc(cccc1)c1Cl)O FPTQXZXPSPFFSP-SSDOTTSWSA-N 0.000 description 1
- NIOGDCDTKPQEAT-UHFFFAOYSA-N Cc(cc(cc1)F)c1Cl Chemical compound Cc(cc(cc1)F)c1Cl NIOGDCDTKPQEAT-UHFFFAOYSA-N 0.000 description 1
- ITVUQDYLWWAIPM-UHFFFAOYSA-N O=C(c1c2cc3nc(C(C(NC=C4)=O)=C4Cl)[nH]c3c1)N(CCCC1CCCCC1)C2=O Chemical compound O=C(c1c2cc3nc(C(C(NC=C4)=O)=C4Cl)[nH]c3c1)N(CCCC1CCCCC1)C2=O ITVUQDYLWWAIPM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C07D401/14—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 three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/10—Anti-acne agents
-
- 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
-
- 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
- A61K31/435—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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Dermatology (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US3803208P | 2008-03-19 | 2008-03-19 | |
| US61/038,032 | 2008-03-19 | ||
| PCT/US2009/001691 WO2009117097A1 (en) | 2008-03-19 | 2009-03-18 | Novel tyrosine kinase inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN102036990A CN102036990A (zh) | 2011-04-27 |
| CN102036990B true CN102036990B (zh) | 2015-09-30 |
Family
ID=40814009
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN200980118256.XA Expired - Fee Related CN102036990B (zh) | 2008-03-19 | 2009-03-18 | 新型酪氨酸激酶抑制剂 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US8815906B2 (https=) |
| EP (2) | EP2966076A1 (https=) |
| JP (2) | JP5628145B2 (https=) |
| CN (1) | CN102036990B (https=) |
| AU (1) | AU2009226153B2 (https=) |
| CA (1) | CA2718872C (https=) |
| DK (1) | DK2262807T3 (https=) |
| MX (1) | MX2010010272A (https=) |
| WO (1) | WO2009117097A1 (https=) |
Families Citing this family (41)
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|---|---|---|---|---|
| MX2010010272A (es) * | 2008-03-19 | 2011-05-25 | Chembridge Corp | Nuevos inhibidores de tirosina quinasa. |
| US9249147B2 (en) * | 2008-03-19 | 2016-02-02 | Chembridge Corporation | Tyrosine kinase inhibitors |
| WO2011049625A1 (en) | 2009-10-20 | 2011-04-28 | Mansour Samadpour | Method for aflatoxin screening of products |
| NZ599830A (en) | 2009-11-05 | 2014-08-29 | Rhizen Pharmaceuticals Sa | Novel kinase modulators |
| ME03376B (me) | 2010-05-20 | 2020-01-20 | Array Biopharma Inc | Makrociklička jedinjenja kао inhibiтori trk kinaze |
| WO2012037155A2 (en) | 2010-09-13 | 2012-03-22 | Gtx, Inc. | Tyrosine kinase inhibitors |
| PH12013502240B1 (en) | 2011-05-04 | 2018-06-27 | Rhizen Pharmaceuticals Sa | Novel compounds as modulators of protein kinase |
| EP2779833A4 (en) * | 2011-11-14 | 2015-03-18 | Tesaro Inc | MODULATION OF SPECIFIC TYROSINE KINASES |
| CA2871237A1 (en) | 2012-04-24 | 2013-10-31 | Chugai Seiyaku Kabushiki Kaisha | Benzamide derivative |
| AR090835A1 (es) | 2012-04-24 | 2014-12-10 | Chugai Pharmaceutical Co Ltd | Derivados de quinazolindiona |
| RS56494B1 (sr) | 2012-07-04 | 2018-01-31 | Rhizen Pharmaceuticals S A | Selektivni inhibitori pi3k delta |
| MX2015011428A (es) | 2013-03-06 | 2016-02-03 | Genentech Inc | Metodos para tratar y prevenir la resistencia a los farmacos para el cancer. |
| CN104109168B (zh) * | 2013-04-20 | 2017-02-15 | 山东轩竹医药科技有限公司 | 四并环激酶抑制剂 |
| WO2015054465A1 (en) | 2013-10-11 | 2015-04-16 | Alios Biopharma, Inc. | Substituted nucleosides, nucleotides and analogs thereof |
| US10005739B2 (en) | 2013-10-23 | 2018-06-26 | Chugai Seiyaku Kabushiki Kaisha | Quinazolinone and isoquinolinone derivative |
| US11045468B2 (en) * | 2014-02-04 | 2021-06-29 | Astellas Pharma Inc. | Pharmaceutical composition comprising diamino heterocyclic carboxamide compound as active ingredient |
| EP3131903A4 (en) * | 2014-04-17 | 2018-05-02 | Amgen Inc. | Polymorphic forms and co-crystals of a c-met inhibitor |
| CN107073121A (zh) | 2014-06-13 | 2017-08-18 | 基因泰克公司 | 治疗及预防癌症药物抗性的方法 |
| US20180044350A1 (en) * | 2015-03-10 | 2018-02-15 | Pottayil Govindan Nair Sasikumar | Therapeutic cyclic compounds as immunomodulators |
| US10087191B2 (en) | 2015-06-16 | 2018-10-02 | Jiangsu Hengrui Medicine Co., Ltd. | Piperidine derivative and preparation method and pharmaceutical use thereof |
| BR112018000808A2 (pt) | 2015-07-16 | 2018-09-04 | Array Biopharma Inc | compostos de pirazolo[1,5-a]piridina substituída como inibidores de ret cinase |
| MA43416A (fr) | 2015-12-11 | 2018-10-17 | Regeneron Pharma | Méthodes pour ralentir ou empêcher la croissance de tumeurs résistantes au blocage de l'egfr et/ou d'erbb3 |
| TWI704148B (zh) | 2016-10-10 | 2020-09-11 | 美商亞雷生物製藥股份有限公司 | 作為ret激酶抑制劑之經取代吡唑并[1,5-a]吡啶化合物 |
| TWI752098B (zh) | 2016-10-10 | 2022-01-11 | 美商亞雷生物製藥股份有限公司 | 作為ret激酶抑制劑之經取代吡唑并[1,5-a]吡啶化合物 |
| WO2018136661A1 (en) | 2017-01-18 | 2018-07-26 | Andrews Steven W | SUBSTITUTED PYRAZOLO[1,5-a]PYRAZINE COMPOUNDS AS RET KINASE INHIBITORS |
| WO2018136663A1 (en) | 2017-01-18 | 2018-07-26 | Array Biopharma, Inc. | Ret inhibitors |
| JOP20190213A1 (ar) | 2017-03-16 | 2019-09-16 | Array Biopharma Inc | مركبات حلقية ضخمة كمثبطات لكيناز ros1 |
| US10513515B2 (en) | 2017-08-25 | 2019-12-24 | Biotheryx, Inc. | Ether compounds and uses thereof |
| TWI876442B (zh) | 2017-10-10 | 2025-03-11 | 美商絡速藥業公司 | 6-(2-羥基-2-甲基丙氧基)-4-(6-(6-((6-甲氧基吡啶-3-基)甲基)-3,6-二氮雜雙環[3.1.1]庚-3-基)吡啶-3-基)吡唑并[1,5-a]吡啶-3-甲腈之調配物 |
| TWI791053B (zh) | 2017-10-10 | 2023-02-01 | 美商亞雷生物製藥股份有限公司 | 6-(2-羥基-2-甲基丙氧基)-4-(6-(6-((6-甲氧基吡啶-3-基)甲基)-3,6-二氮雜雙環[3.1.1]庚-3-基)吡啶-3-基)吡唑并[1,5-a]吡啶-3-甲腈之結晶形式及其醫藥組合物 |
| EP3740490A1 (en) | 2018-01-18 | 2020-11-25 | Array Biopharma, Inc. | Substituted pyrazolo[3,4-d]pyrimidine compounds as ret kinase inhibitors |
| JP7060694B2 (ja) | 2018-01-18 | 2022-04-26 | アレイ バイオファーマ インコーポレイテッド | Retキナーゼ阻害剤としての置換ピロロ[2,3-d]ピリミジン化合物 |
| US11472802B2 (en) | 2018-01-18 | 2022-10-18 | Array Biopharma Inc. | Substituted pyrazolyl[4,3-c]pyridine compounds as RET kinase inhibitors |
| CA3106239A1 (en) | 2018-07-27 | 2020-01-30 | Biotheryx, Inc. | Bifunctional compounds as cdk modulators |
| CN112996794A (zh) | 2018-09-10 | 2021-06-18 | 阿雷生物药品公司 | 作为ret激酶抑制剂的稠合杂环化合物 |
| EA202192575A1 (ru) | 2019-03-21 | 2022-01-14 | Онксео | Соединения dbait в сочетании с ингибиторами киназ для лечения рака |
| CN114761006A (zh) | 2019-11-08 | 2022-07-15 | Inserm(法国国家健康医学研究院) | 对激酶抑制剂产生耐药性的癌症的治疗方法 |
| WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
| WO2021222150A2 (en) | 2020-04-28 | 2021-11-04 | Anwita Biosciences, Inc. | Interleukin-2 polypeptides and fusion proteins thereof, and their pharmaceutical compositions and therapeutic applications |
| TW202216676A (zh) | 2020-07-06 | 2022-05-01 | 美商塔朵根公司 | 用於心理疾病或心理強化的有益苯并噻吩組合物 |
| CN116209657A (zh) | 2020-08-06 | 2023-06-02 | 泰科根公司 | 用于精神障碍或增强的2-氨基茚满化合物 |
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| WO2008021369A2 (en) * | 2006-08-14 | 2008-02-21 | Chembridge Research Laboratories, Inc. | Tricyclic compounds and its use as tyrosine kinase modulators |
| WO2008022747A1 (en) * | 2006-08-21 | 2008-02-28 | F. Hoffmann-La Roche Ag | Tricyclic lactam derivatives, their manufacture and use as pharmaceutical agents |
| CN101160312A (zh) * | 2005-04-14 | 2008-04-09 | 霍夫曼-拉罗奇有限公司 | 三环吡咯衍生物、它们的制备和作为药剂的应用 |
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| EP1648455A4 (en) | 2003-07-23 | 2009-03-04 | Exelixis Inc | MODULATORS OF ALK PROTEIN (ANAPLASTIC LYMPHOMA KINASE) AND METHODS OF USE |
| CN101208093A (zh) * | 2005-04-27 | 2008-06-25 | 阿斯利康(瑞典)有限公司 | 吡唑-嘧啶衍生物在治疗疼痛中的用途 |
| US20080062003A1 (en) * | 2006-08-07 | 2008-03-13 | Christian Paetz | Wireless controllable power control device molded into a power cable |
| MX2010010272A (es) * | 2008-03-19 | 2011-05-25 | Chembridge Corp | Nuevos inhibidores de tirosina quinasa. |
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2009
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- 2009-03-18 WO PCT/US2009/001691 patent/WO2009117097A1/en not_active Ceased
- 2009-03-18 US US12/922,891 patent/US8815906B2/en not_active Expired - Fee Related
- 2009-03-18 JP JP2011500801A patent/JP5628145B2/ja not_active Expired - Fee Related
- 2009-03-18 DK DK09721981.0T patent/DK2262807T3/en active
- 2009-03-18 EP EP15177176.3A patent/EP2966076A1/en not_active Withdrawn
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Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101160312A (zh) * | 2005-04-14 | 2008-04-09 | 霍夫曼-拉罗奇有限公司 | 三环吡咯衍生物、它们的制备和作为药剂的应用 |
| WO2008021369A2 (en) * | 2006-08-14 | 2008-02-21 | Chembridge Research Laboratories, Inc. | Tricyclic compounds and its use as tyrosine kinase modulators |
| WO2008022747A1 (en) * | 2006-08-21 | 2008-02-28 | F. Hoffmann-La Roche Ag | Tricyclic lactam derivatives, their manufacture and use as pharmaceutical agents |
Also Published As
| Publication number | Publication date |
|---|---|
| US8815906B2 (en) | 2014-08-26 |
| CA2718872C (en) | 2016-09-13 |
| JP2011515397A (ja) | 2011-05-19 |
| MX2010010272A (es) | 2011-05-25 |
| JP2013082744A (ja) | 2013-05-09 |
| CN102036990A (zh) | 2011-04-27 |
| US20130053376A1 (en) | 2013-02-28 |
| EP2966076A1 (en) | 2016-01-13 |
| EP2262807A1 (en) | 2010-12-22 |
| DK2262807T3 (en) | 2015-11-30 |
| AU2009226153B2 (en) | 2014-02-20 |
| CA2718872A1 (en) | 2009-09-24 |
| AU2009226153A1 (en) | 2009-09-24 |
| EP2262807B1 (en) | 2015-08-12 |
| WO2009117097A1 (en) | 2009-09-24 |
| JP5628145B2 (ja) | 2014-11-19 |
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