JP5560496B2 - Cdk阻害剤としてのピロロピリミジン化合物 - Google Patents
Cdk阻害剤としてのピロロピリミジン化合物 Download PDFInfo
- Publication number
- JP5560496B2 JP5560496B2 JP2011523425A JP2011523425A JP5560496B2 JP 5560496 B2 JP5560496 B2 JP 5560496B2 JP 2011523425 A JP2011523425 A JP 2011523425A JP 2011523425 A JP2011523425 A JP 2011523425A JP 5560496 B2 JP5560496 B2 JP 5560496B2
- Authority
- JP
- Japan
- Prior art keywords
- cyclopentyl
- pyrrolo
- carboxylic acid
- pyrimidine
- ylamino
- 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.)
- Active
Links
- 0 *Cc1ccc(Nc2ncc(cc(C#N)[n]3C4CCCC4)c3n2)nc1 Chemical compound *Cc1ccc(Nc2ncc(cc(C#N)[n]3C4CCCC4)c3n2)nc1 0.000 description 1
- BMBFWSJTQOPTEI-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CCN1c(cc1)nnc1Nc1ncc(cc(C(N(C)C)=O)[n]2C3CCCC3)c2n1)=O Chemical compound CC(C)(C)OC(N(CC1)CCN1c(cc1)nnc1Nc1ncc(cc(C(N(C)C)=O)[n]2C3CCCC3)c2n1)=O BMBFWSJTQOPTEI-UHFFFAOYSA-N 0.000 description 1
- GCQNLBPDVDSOAK-UHFFFAOYSA-N CC(C)(C)OC(NC(CC1)CN1c(cc1)cnc1N)=O Chemical compound CC(C)(C)OC(NC(CC1)CN1c(cc1)cnc1N)=O GCQNLBPDVDSOAK-UHFFFAOYSA-N 0.000 description 1
- FMQFHFZPWFOGON-UHFFFAOYSA-N CC(C1)NCCN1c1ccc(Nc2ncc(cc(C#N)[n]3C4CCCC4)c3n2)nc1 Chemical compound CC(C1)NCCN1c1ccc(Nc2ncc(cc(C#N)[n]3C4CCCC4)c3n2)nc1 FMQFHFZPWFOGON-UHFFFAOYSA-N 0.000 description 1
- SGBLGMZZKLPXCW-UHFFFAOYSA-N CN(C)C(CC1)CCN1c(cc1)cnc1Nc1ncc(cc(C(N(C)C)=O)[n]2C3CCCC3)c2n1 Chemical compound CN(C)C(CC1)CCN1c(cc1)cnc1Nc1ncc(cc(C(N(C)C)=O)[n]2C3CCCC3)c2n1 SGBLGMZZKLPXCW-UHFFFAOYSA-N 0.000 description 1
- KBWFQCHPVFOJEU-UHFFFAOYSA-N CN(C)C(c1cc2cnc(Nc(cc3)ncc3C(O)=O)nc2[n]1C1CCCC1)=O Chemical compound CN(C)C(c1cc2cnc(Nc(cc3)ncc3C(O)=O)nc2[n]1C1CCCC1)=O KBWFQCHPVFOJEU-UHFFFAOYSA-N 0.000 description 1
- UKSSOERBIHXEIJ-UHFFFAOYSA-N CN(C)C(c1cc2cnc(Nc(cc3)ncc3N(CC3)CCN3C(N3CCCCC3)=O)nc2[n]1C1CCCC1)=O Chemical compound CN(C)C(c1cc2cnc(Nc(cc3)ncc3N(CC3)CCN3C(N3CCCCC3)=O)nc2[n]1C1CCCC1)=O UKSSOERBIHXEIJ-UHFFFAOYSA-N 0.000 description 1
- KOQPLGGYAJCOQR-UHFFFAOYSA-N CN(C)C(c1cc2cnc(Nc(cc3)ncc3N(CC3)CCN3C(N3CCOCC3)=O)nc2[n]1C1CCCC1)=O Chemical compound CN(C)C(c1cc2cnc(Nc(cc3)ncc3N(CC3)CCN3C(N3CCOCC3)=O)nc2[n]1C1CCCC1)=O KOQPLGGYAJCOQR-UHFFFAOYSA-N 0.000 description 1
- WCCRZTMTXBWQTH-UHFFFAOYSA-N CN(C)C(c1cc2cnc(Nc(cc3)ncc3N3CCN(CC(CO)O)CC3)nc2[n]1C1CCCC1)=O Chemical compound CN(C)C(c1cc2cnc(Nc(cc3)ncc3N3CCN(CC(CO)O)CC3)nc2[n]1C1CCCC1)=O WCCRZTMTXBWQTH-UHFFFAOYSA-N 0.000 description 1
- UFZLZSPDJSRERW-UHFFFAOYSA-N CN(C)C(c1cc2cnc(Nc(cc3)ncc3N3CCN(CC(N)=O)CC3)nc2[n]1C1CCCC1)=O Chemical compound CN(C)C(c1cc2cnc(Nc(cc3)ncc3N3CCN(CC(N)=O)CC3)nc2[n]1C1CCCC1)=O UFZLZSPDJSRERW-UHFFFAOYSA-N 0.000 description 1
- LXCZVGKSFJMLRO-UHFFFAOYSA-N OC(c([n](C1CCCC1)c1n2)cc1cnc2Cl)=O Chemical compound OC(c([n](C1CCCC1)c1n2)cc1cnc2Cl)=O LXCZVGKSFJMLRO-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
- 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
- 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
- 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
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
-
- 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
-
- 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
- C07D487/08—Bridged 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Rheumatology (AREA)
- Hospice & Palliative Care (AREA)
- Pain & Pain Management (AREA)
- Hematology (AREA)
- Psychiatry (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US9103708P | 2008-08-22 | 2008-08-22 | |
| US61/091,037 | 2008-08-22 | ||
| PCT/EP2009/060793 WO2010020675A1 (en) | 2008-08-22 | 2009-08-20 | Pyrrolopyrimidine compounds as cdk inhibitors |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014016933A Division JP5882371B2 (ja) | 2008-08-22 | 2014-01-31 | Cdk阻害剤としてのピロロピリミジン化合物 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2012500785A JP2012500785A (ja) | 2012-01-12 |
| JP2012500785A5 JP2012500785A5 (enExample) | 2012-09-27 |
| JP5560496B2 true JP5560496B2 (ja) | 2014-07-30 |
Family
ID=41171100
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011523425A Active JP5560496B2 (ja) | 2008-08-22 | 2009-08-20 | Cdk阻害剤としてのピロロピリミジン化合物 |
| JP2014016933A Active JP5882371B2 (ja) | 2008-08-22 | 2014-01-31 | Cdk阻害剤としてのピロロピリミジン化合物 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014016933A Active JP5882371B2 (ja) | 2008-08-22 | 2014-01-31 | Cdk阻害剤としてのピロロピリミジン化合物 |
Country Status (48)
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2014129361A (ja) * | 2008-08-22 | 2014-07-10 | Novartis Ag | Cdk阻害剤としてのピロロピリミジン化合物 |
Families Citing this family (242)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20120100100A1 (en) | 2009-05-13 | 2012-04-26 | Sharpless Norman E | Cyclin dependent kinase inhibitors and methods of use |
| UY33227A (es) | 2010-02-19 | 2011-09-30 | Novartis Ag | Compuestos de pirrolopirimidina como inhibidores de la cdk4/6 |
| UY33226A (es) * | 2010-02-19 | 2011-09-30 | Novartis Ag | Compuestos de pirrolopirimidina deuterada como inhibidores de la cdk4/6 |
| ES2689177T3 (es) | 2010-04-13 | 2018-11-08 | Novartis Ag | Combinación que comprende un inhibidor de cinasa 4 dependiente de ciclina o cinasa dependiente de ciclina (CDK4/6) y un inhibidor de mTOR para tratar cáncer |
| JP5959516B2 (ja) | 2010-08-18 | 2016-08-02 | ライフ テクノロジーズ コーポレーション | 電気化学的検出装置のためのマイクロウェルの化学コーティング法 |
| MX379532B (es) | 2010-10-25 | 2025-03-10 | G1 Therapeutics Inc | Inhibidores de cdk. |
| US8691830B2 (en) | 2010-10-25 | 2014-04-08 | G1 Therapeutics, Inc. | CDK inhibitors |
| US20120115878A1 (en) * | 2010-11-10 | 2012-05-10 | John Vincent Calienni | Salt(s) of 7-cyclopentyl-2-(5-piperazin-1-yl-pyridin-2-ylamino)-7h-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid dimethylamide and processes of making thereof |
| CA2818046A1 (en) | 2010-11-17 | 2012-05-24 | The University Of North Carolina At Chapel Hill | Protection of renal tissues from ischemia through inhibition of the proliferative kinases cdk4 and cdk6 |
| PE20140471A1 (es) * | 2011-01-04 | 2014-04-13 | Novartis Ag | Moduladores de la via del complemento y usos de los mismos |
| AU2014259534B2 (en) * | 2011-01-04 | 2016-05-19 | Novartis Ag | Indole compounds or analogues thereof useful for the treatment of age-related macular degeneration (AMD) |
| PH12013502697A1 (en) * | 2011-07-01 | 2014-02-10 | Novartis Ag | Combination therapy comprising a cdk4/6 inhibitor and a pi3k inhibitor for use in the treatment of cancer |
| RU2014103250A (ru) * | 2011-07-01 | 2015-08-10 | Новартис Аг | Комбинированная терапия |
| WO2013059634A1 (en) | 2011-10-20 | 2013-04-25 | The Regents Of The University Of California | Use of cdk9 inhibitors to reduce cartilage degradation |
| US9194840B2 (en) | 2012-01-19 | 2015-11-24 | Life Technologies Corporation | Sensor arrays and methods for making same |
| WO2013148748A1 (en) * | 2012-03-29 | 2013-10-03 | Francis Xavier Tavares | Lactam kinase inhibitors |
| CA2870019C (en) | 2012-04-26 | 2020-08-18 | Francis Xavier Tavares | Synthesis of lactams |
| ES2710491T3 (es) | 2012-06-28 | 2019-04-25 | Novartis Ag | Moduladores de la vía del complemento y sus usos |
| CN104640855B (zh) | 2012-06-28 | 2017-08-29 | 诺华股份有限公司 | 补体途经调节剂及其用途 |
| ES2647124T3 (es) | 2012-06-28 | 2017-12-19 | Novartis Ag | Derivados de pirrolidina y su uso como moduladores de la ruta del complemento |
| WO2014002052A1 (en) | 2012-06-28 | 2014-01-03 | Novartis Ag | Pyrrolidine derivatives and their use as complement pathway modulators |
| US9388199B2 (en) | 2012-06-28 | 2016-07-12 | Novartis Ag | Pyrrolidine derivatives and their use as complement pathway modulators |
| AU2013288319A1 (en) | 2012-07-12 | 2015-02-05 | Novartis Ag | Complement pathway modulators and uses thereof |
| AR091876A1 (es) * | 2012-07-26 | 2015-03-04 | Novartis Ag | Combinaciones farmaceuticas para el tratamiento de enfermedades proliferativas |
| CA2880764C (en) | 2012-08-03 | 2022-08-30 | Foundation Medicine, Inc. | Human papilloma virus as predictor of cancer prognosis |
| EP2742940B1 (en) | 2012-12-13 | 2017-07-26 | IP Gesellschaft für Management mbH | Fumarate salt of (R)-3-(6-(4-methylphenyl)-pyridin-3-yloxy)-l-aza-bicyclo-[2.2.2]octane for adminstration once daily, twice daily or thrice daily |
| US9867825B2 (en) * | 2012-12-20 | 2018-01-16 | Novartis Ag | Pharmaceutical combination comprising binimetinib |
| US20140199728A1 (en) | 2013-01-14 | 2014-07-17 | Amgen Inc. | Methods of using cell-cycle inhibitors to modulate one or more properties of a cell culture |
| EP3327144B1 (en) | 2013-02-25 | 2020-03-25 | Novartis AG | Novel androgen receptor mutation |
| CN105189481A (zh) | 2013-03-13 | 2015-12-23 | 艾伯维公司 | 吡啶cdk9激酶抑制剂 |
| MX2015012386A (es) | 2013-03-13 | 2016-02-03 | Abbvie Inc | Inhibidores de la cinasa cdk9. |
| CA2903538A1 (en) | 2013-03-14 | 2014-10-02 | Abbvie Inc. | Pyrrolopyrimindine cdk9 kinase inhibitors |
| BR112015023356A2 (pt) | 2013-03-14 | 2017-07-18 | Abbvie Inc | inibidores de quinase pirrol[2,3-b]piridina cdk9 |
| UY35419A (es) | 2013-03-14 | 2014-10-31 | Abbvie Inc | Inhibidores de cdk9 quinasa de pirrolo (2,3- b) piridina |
| US20140271460A1 (en) | 2013-03-15 | 2014-09-18 | G1 Therapeutics, Inc. | Highly Active Anti-Neoplastic and Anti-Proliferative Agents |
| WO2014144596A2 (en) * | 2013-03-15 | 2014-09-18 | G1 Therapeutics, Inc. | Transient protection of hematopoietic stem and progenitor cells against ionizing radiation |
| CN105473140B (zh) | 2013-03-15 | 2018-04-10 | G1治疗公司 | 在化学疗法期间对正常细胞的瞬时保护 |
| CA2907704C (en) | 2013-03-21 | 2023-01-10 | Giordano Caponigro | Combination therapy for reversing b-raf inhibitor resistance comprising a second inhibitor based on genetic alterations |
| EP2986740B1 (en) | 2013-04-16 | 2020-01-15 | Memorial Sloan-Kettering Cancer Center | Companion diagnostic for cdk4 inhibitors |
| CN105828822B (zh) * | 2013-08-14 | 2019-10-18 | 诺华股份有限公司 | 用于治疗癌症的组合疗法 |
| JP6479812B2 (ja) * | 2013-08-28 | 2019-03-06 | ノバルティス アーゲー | 細胞増殖性疾患を治療するためのalk阻害剤とcdk阻害剤との組合せ |
| WO2015048312A1 (en) | 2013-09-26 | 2015-04-02 | Costim Pharmaceuticals Inc. | Methods for treating hematologic cancers |
| TW201605857A (zh) * | 2013-10-03 | 2016-02-16 | 赫孚孟拉羅股份公司 | Cdk8之醫療性抑制劑及其用途 |
| US20160257688A1 (en) * | 2013-10-24 | 2016-09-08 | Francis Xavier Tavares | Process for Synthesis of Lactams |
| AU2014354821A1 (en) * | 2013-11-27 | 2016-05-26 | Novartis Ag | Combination therapy comprising an inhibitor of JAK, CDK and PIM |
| US9476853B2 (en) | 2013-12-10 | 2016-10-25 | Life Technologies Corporation | System and method for forming microwells |
| WO2015095840A1 (en) * | 2013-12-20 | 2015-06-25 | Biomed Valley Discoveries, Inc. | Cancer treatments using combinations of cdk and erk inhibitors |
| CN105848656B (zh) | 2013-12-23 | 2019-10-25 | 诺华股份有限公司 | 药物组合 |
| CN105848682A (zh) * | 2013-12-23 | 2016-08-10 | 诺华股份有限公司 | 药物组合 |
| KR101787680B1 (ko) * | 2013-12-31 | 2017-10-19 | 수안주 파마 코포레이션 리미티드 | 키나아제 억제제 및 이의 용도 |
| US9949976B2 (en) | 2013-12-31 | 2018-04-24 | Xuanzhu Pharma Co., Ltd. | Kinase inhibitor and use thereof |
| JOP20200094A1 (ar) | 2014-01-24 | 2017-06-16 | Dana Farber Cancer Inst Inc | جزيئات جسم مضاد لـ pd-1 واستخداماتها |
| JOP20200096A1 (ar) | 2014-01-31 | 2017-06-16 | Children’S Medical Center Corp | جزيئات جسم مضاد لـ tim-3 واستخداماتها |
| KR20240110004A (ko) | 2014-03-14 | 2024-07-12 | 노파르티스 아게 | Lag-3에 대한 항체 분자 및 그의 용도 |
| AU2015240465B2 (en) | 2014-04-04 | 2020-02-27 | Del Mar Pharmaceuticals | Use of dianhydrogalactitol and analogs or derivatives thereof to treat non-small-cell carcinoma of the lung and ovarian cancer |
| WO2015160986A2 (en) | 2014-04-16 | 2015-10-22 | Infinity Pharmaceuticals, Inc. | Combination therapies |
| WO2015161285A1 (en) | 2014-04-17 | 2015-10-22 | G1 Therapeutics, Inc. | Tricyclic lactams for use in the protection of hematopoietic stem and progenitor cells against ionizing radiation |
| KR101864589B1 (ko) * | 2014-05-28 | 2018-07-04 | 상하이 포천 파마슈티컬 씨오 엘티디 | 특정한 단백질 키나아제 억제제 |
| CN105294737B (zh) * | 2014-07-26 | 2019-02-12 | 广东东阳光药业有限公司 | Cdk类小分子抑制剂的化合物及其用途 |
| EP3191098A4 (en) | 2014-09-12 | 2018-04-25 | G1 Therapeutics, Inc. | Combinations and dosing regimes to treat rb-positive tumors |
| WO2016040848A1 (en) | 2014-09-12 | 2016-03-17 | G1 Therapeutics, Inc. | Treatment of rb-negative tumors using topoisomerase inhibitors in combination with cyclin dependent kinase 4/6 inhibitors |
| ES2771926T3 (es) | 2014-09-13 | 2020-07-07 | Novartis Ag | Terapias de combinación |
| JP2017535528A (ja) | 2014-10-03 | 2017-11-30 | ノバルティス アーゲー | 組み合わせ治療 |
| MA41044A (fr) | 2014-10-08 | 2017-08-15 | Novartis Ag | Compositions et procédés d'utilisation pour une réponse immunitaire accrue et traitement contre le cancer |
| EP3206749B1 (en) | 2014-10-14 | 2021-09-08 | The Regents of the University of California | The cdk9 and brd4 inhibitors flavopiridol and jq1 to inhibit cartilage inflammation |
| US9988452B2 (en) | 2014-10-14 | 2018-06-05 | Novartis Ag | Antibody molecules to PD-L1 and uses thereof |
| PT3218005T (pt) | 2014-11-12 | 2023-04-11 | Seagen Inc | Compostos que interagem com glicano e métodos de uso |
| US10138250B2 (en) | 2014-12-12 | 2018-11-27 | Crystal Pharmatech Co., Ltd. | Salt of pyrrolo[2,3-D]pyrimidine compound and novel polymorph of salt |
| US9994579B2 (en) | 2014-12-12 | 2018-06-12 | Crystal Pharmatech Co., Ltd. | Salt of pyrrolo[2,3-D]pyrimidine compound and novel polymorph of salt |
| CN105111215B (zh) * | 2014-12-12 | 2019-06-18 | 苏州晶云药物科技股份有限公司 | 一种周期蛋白依赖性激酶抑制剂的晶型及其制备方法 |
| WO2016126889A1 (en) * | 2015-02-03 | 2016-08-11 | G1 Therapeutics, Inc. | Cdk4/6 inhibitor dosage formulations for the protection of hematopoietic stem and progenitor cells during chemotherapy |
| JP6692826B2 (ja) | 2015-03-10 | 2020-05-13 | アドゥロ バイオテック,インク. | 「インターフェロン遺伝子刺激因子」依存性シグナル伝達の活性化のための組成物及び方法 |
| EP3273959A1 (en) | 2015-03-25 | 2018-01-31 | Novartis Ag | Pharmaceutical combinations |
| SI3283058T1 (sl) | 2015-04-16 | 2023-03-31 | Novartis Ag | Tableta ribocikliba |
| 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 |
| TWI696617B (zh) | 2015-04-28 | 2020-06-21 | 大陸商上海復尚慧創醫藥研究有限公司 | 特定蛋白質激酶抑制劑 |
| RU2695337C2 (ru) | 2015-05-29 | 2019-07-23 | Тейдзин Фарма Лимитед | ПРОИЗВОДНОЕ ПИРИДО[3,4-d]ПИРИМИДИНА И ЕГО ФАРМАЦЕВТИЧЕСКИ ПРИЕМЛЕМАЯ СОЛЬ |
| CN105037236B (zh) * | 2015-06-04 | 2017-07-28 | 苏州明锐医药科技有限公司 | 瑞博西尼中间体及其制备方法 |
| CN106336412A (zh) * | 2015-07-10 | 2017-01-18 | 南开大学 | 作为cdk4/6抑制剂的2-(n-氧化芳环-2基氨基)-吡咯并嘧啶及嘌呤类化合物 |
| CN106699785A (zh) * | 2015-07-13 | 2017-05-24 | 南开大学 | 作为CDK4/6抑制剂的2-(N-氧化吡啶-2基氨基)-吡啶并[2,3-d]嘧啶-7-酮类化合物 |
| CN105130992B (zh) * | 2015-07-16 | 2018-02-09 | 苏州大学 | 具有激酶抑制活性的含氮杂环化合物、制备方法和用途 |
| WO2017019894A1 (en) | 2015-07-29 | 2017-02-02 | Novartis Ag | Combination therapies comprising antibody molecules to lag-3 |
| CN108025051B (zh) | 2015-07-29 | 2021-12-24 | 诺华股份有限公司 | 包含抗pd-1抗体分子的联合疗法 |
| EP3878465A1 (en) | 2015-07-29 | 2021-09-15 | Novartis AG | Combination therapies comprising antibody molecules to tim-3 |
| EP3340986A1 (en) | 2015-08-28 | 2018-07-04 | Novartis AG | A pharmaceutical combination comprising the pi3k inhibitor alpelisib and the cdk4/6 inhibitor ribociclib, and the use thereof in the treatment/prevention of cancer |
| WO2017037576A1 (en) | 2015-08-28 | 2017-03-09 | Novartis Ag | Pharmaceutical combinations comprising (a) the cyclin dependent kinase 4/6 (cdk4/6) inhibitor lee011 (=ribociclib), and (b) the epidermal growth factor receptor (egfr) inhibitor erlotinib, for the treatment or prevention of cancer |
| WO2017037574A1 (en) | 2015-08-28 | 2017-03-09 | Novartis Ag | Combinations of the cdk4/6 inhibitor lee011 and the mek1/2 inhibitor trametinib, optionally further comprising the pi3k inhibitor byl719 to treat cancer |
| WO2017037587A1 (en) | 2015-08-28 | 2017-03-09 | Novartis Ag | Combination of ribociclib and dabrafenib for treating or preventing cancer |
| EP3156406A1 (en) | 2015-10-14 | 2017-04-19 | ratiopharm GmbH | Crystalline forms of ribociclib free base |
| RU2018119085A (ru) | 2015-11-02 | 2019-12-04 | Новартис Аг | Схема введения ингибитора фосфатидилинозитол-3-киназы |
| HRP20220436T1 (hr) | 2015-11-03 | 2022-05-27 | Janssen Biotech, Inc. | Protutijela koja se specifično vežu na pd-1 i njihove uporabe |
| JP7066613B2 (ja) | 2015-11-12 | 2022-05-13 | シージェン インコーポレイテッド | グリカン相互作用化合物および使用方法 |
| CN106749259B (zh) * | 2015-11-19 | 2019-02-01 | 华东师范大学 | 一种环戊基嘧啶并吡咯类化合物的合成方法 |
| CN106831780A (zh) * | 2015-12-03 | 2017-06-13 | 南开大学 | 具有cdk4/6和hdac抑制活性的新型杂环衍生物 |
| CA3007671A1 (en) | 2015-12-17 | 2017-06-22 | Novartis Ag | Antibody molecules to pd-1 and uses thereof |
| CN105541863B (zh) * | 2016-02-16 | 2017-09-05 | 安纳康科学股份有限公司 | 噻吩[2,3‑c]吡啶衍生物及其作为CDK激酶抑制剂的用途 |
| WO2017156263A1 (en) | 2016-03-09 | 2017-09-14 | Memorial Sloan-Kettering Cancer Center | Enigma and cdh18 as companion diagnostics for cdk4 inhibitors |
| US11077110B2 (en) | 2016-03-18 | 2021-08-03 | Tufts Medical Center | Compositions and methods for treating and preventing metabolic disorders |
| CN108884101B (zh) * | 2016-03-25 | 2020-07-24 | 正大天晴药业集团股份有限公司 | 取代的吡咯并嘧啶类cdk抑制剂、包含其的药物组合物以及它们的用途 |
| CN107266451B (zh) * | 2016-04-07 | 2021-12-31 | 上海医药工业研究院 | 瑞布昔利布中间体的制备方法 |
| WO2017185031A1 (en) * | 2016-04-22 | 2017-10-26 | Dana-Farber Cancer Institute, Inc. | Degradation of cyclin-dependent kinase 4/6 (cdk4/6) by conjugation of cdk4/6 inhibitors with e3 ligase ligand and methods of use |
| MX387648B (es) | 2016-05-07 | 2025-03-18 | Fochon Pharmaceuticals Ltd | Derivados de heteroarilo tieno[3,2-d]pirimidina-6-carboxamida de la fórmula (ii) que presentan actividad inhibitoria sobre cinasa cdk4/6. |
| WO2017211245A1 (zh) * | 2016-06-06 | 2017-12-14 | 深圳市塔吉瑞生物医药有限公司 | 一种取代的吡咯并嘧啶化合物及其应用 |
| CN109311848B (zh) | 2016-06-07 | 2022-02-01 | 北京加科思新药研发有限公司 | 可用作shp2抑制剂的新型杂环衍生物 |
| WO2018005533A1 (en) | 2016-07-01 | 2018-01-04 | G1 Therapeutics, Inc. | Antiproliferative pyrimidine-based compounds |
| JP7106462B2 (ja) | 2016-07-01 | 2022-07-26 | ジー1 セラピューティクス, インコーポレイテッド | N-(ヘテロアリール)-ピロロ[3,2-d]ピリミジン-2-アミンの合成 |
| JP2019520379A (ja) * | 2016-07-01 | 2019-07-18 | ジー1 セラピューティクス, インコーポレイテッド | ピリミジン系の抗増殖剤 |
| WO2018005863A1 (en) | 2016-07-01 | 2018-01-04 | G1 Therapeutics, Inc. | Pyrimidine-based compounds for the treatment of cancer |
| US11098077B2 (en) | 2016-07-05 | 2021-08-24 | Chinook Therapeutics, Inc. | Locked nucleic acid cyclic dinucleotide compounds and uses thereof |
| AU2017315357B2 (en) | 2016-08-23 | 2022-12-01 | Eisai R&D Management Co., Ltd. | Combination therapies for the treatment of hepatocellular carcinoma |
| WO2018051280A1 (en) * | 2016-09-15 | 2018-03-22 | Dr. Reddy’S Laboratories Limited | Process for preparation of ribociclib, its acid addition salts |
| KR102341660B1 (ko) | 2016-09-19 | 2021-12-23 | 노파르티스 아게 | Raf 억제제 및 erk 억제제를 포함하는 치료적 조합 |
| WO2018060833A1 (en) | 2016-09-27 | 2018-04-05 | Novartis Ag | Dosage regimen for alpha-isoform selective phosphatidylinositol 3-kinase inhibitor alpelisib |
| BR112019005526A2 (pt) | 2016-10-20 | 2019-06-18 | Pfizer | agentes antiproliferativos para tratamento de pah |
| WO2018081211A1 (en) * | 2016-10-26 | 2018-05-03 | Li George Y | Deuterated 7-cyclopentyl-n, n-dimethyl-2-((5-(piperazin-1-yl)pyridin-2-yl)amino)-7h-pyrrolo[2,3-d]pyrimdine-6-carboxamide |
| US11865176B2 (en) | 2016-11-08 | 2024-01-09 | Dana-Farber Cancer Institute, Inc. | Compositions and methods of modulating anti-tumor immunity |
| US11401330B2 (en) | 2016-11-17 | 2022-08-02 | Seagen Inc. | Glycan-interacting compounds and methods of use |
| WO2018094227A1 (en) * | 2016-11-17 | 2018-05-24 | The University Of North Carolina At Chapel Hill | Alkyl pyrrolopyrimidine analogs and methods of making and using same |
| CN109996800B (zh) | 2016-11-28 | 2021-11-19 | 帝人制药株式会社 | 吡啶并[3,4-d]嘧啶衍生物或其溶剂合物的晶体 |
| SI3546458T1 (sl) | 2016-11-28 | 2021-03-31 | Teijin Pharma Limited | Derivati ((piridin-2-il)-amino)pirido(3,4-d)pirimidina in ((piridazin-3-il)amino)pirido(3,4-d)pirimidina kot zaviralci CDK4/6 za zdravljenje npr. revmatoidnega artritisa, arterioskleroze, pljučne fibroze, možganske kapi ali raka |
| CA3045465A1 (en) | 2016-12-05 | 2018-06-14 | G1 Therapeutics, Inc. | Preservation of immune response during chemotherapy regimens |
| EA201991622A1 (ru) | 2017-01-06 | 2020-01-23 | Г1 Терапьютикс, Инк. | Комплексная терапия для лечения рака |
| WO2018140730A1 (en) | 2017-01-27 | 2018-08-02 | Signalrx Pharmaceuticals, Inc. | Thienopyranones and furanopyranones as kinase, bromodomain, and checkpoint inhibitors |
| US11395821B2 (en) | 2017-01-30 | 2022-07-26 | G1 Therapeutics, Inc. | Treatment of EGFR-driven cancer with fewer side effects |
| WO2018160909A1 (en) | 2017-03-03 | 2018-09-07 | Siamab Therapeutics, Inc. | Glycan-interacting compounds and methods of use |
| IL269357B2 (en) | 2017-03-16 | 2024-10-01 | Eisai R&D Man Co Ltd | A combination of ER? inhibitor and CDK 4/6 inhibitor for use in a method of treating breast cancer |
| SMT202400385T1 (it) | 2017-03-23 | 2024-11-15 | Jacobio Pharmaceuticals Co Ltd | Nuovi derivati eterociclici utili come inibitori di shp2 |
| UY37695A (es) | 2017-04-28 | 2018-11-30 | Novartis Ag | Compuesto dinucleótido cíclico bis 2’-5’-rr-(3’f-a)(3’f-a) y usos del mismo |
| ES2952265T3 (es) | 2017-05-02 | 2023-10-30 | Novartis Ag | Terapia combinada que comprende un inhibidor de Raf y trametinib |
| CN106946880B (zh) * | 2017-05-06 | 2019-04-26 | 南京焕然生物科技有限公司 | 一种制备瑞博西尼中间体的方法 |
| CN107118215B (zh) * | 2017-05-06 | 2019-04-05 | 上海耀大生物科技有限公司 | 一种治疗乳腺癌药物瑞博西尼中间体的制备方法 |
| CN107267481A (zh) * | 2017-05-09 | 2017-10-20 | 上海交通大学医学院附属新华医院 | Cdk5抗原表位肽及其应用 |
| CN108929324A (zh) * | 2017-05-22 | 2018-12-04 | 南开大学 | 新型1,1-环丙基二酰胺衍生物的制备与应用 |
| CN108929312A (zh) * | 2017-05-22 | 2018-12-04 | 南开大学 | 具有cdk或hdac抑制活性的新型苯并杂环联嘧啶抑制剂 |
| TW201906818A (zh) * | 2017-05-31 | 2019-02-16 | 美商511製藥公司 | 新穎氘取代之正子發射斷層掃描(pet)顯影劑及其藥理應用 |
| WO2018218633A1 (en) | 2017-06-02 | 2018-12-06 | Beijing Percans Oncology Co. Ltd. | Combination therapies for treating cancers |
| WO2018237173A1 (en) | 2017-06-22 | 2018-12-27 | Novartis Ag | Antibody molecules to cd73 and uses thereof |
| CN110913861B (zh) | 2017-06-29 | 2024-01-09 | G1治疗公司 | G1t38的形态学形式及其制造方法 |
| WO2019026006A1 (en) | 2017-08-03 | 2019-02-07 | Novartis Ag | THERAPEUTIC ASSOCIATION OF THIRD GENERATION EGFR TYROSINE KINASE INHIBITOR AND CYCLIN D KINASE INHIBITOR |
| CA3073936A1 (en) | 2017-08-25 | 2019-02-28 | Sicor - Societa Italiana Corticosteroidi S.R.L. | Ribociclib salts and solid state forms thereof |
| CN119162314A (zh) | 2017-08-31 | 2024-12-20 | 诺华股份有限公司 | 选择针对癌症患者的治疗的方法 |
| US11286259B2 (en) | 2017-09-29 | 2022-03-29 | Hangzhou Solipharma Co., Ltd. | Co-crystals of ribociclib and co-crystals of ribociclib monosuccinate, preparation method therefor, compositions thereof, and uses thereof |
| US11440912B2 (en) | 2017-10-27 | 2022-09-13 | Fresenius Kabi Oncology Ltd | Process for the preparation of ribociclib and its salts |
| US11179365B2 (en) | 2017-11-16 | 2021-11-23 | Novartis Ag | Pharmaceutical combination comprising LSZ102 and ribociclib |
| MX2020004756A (es) | 2017-11-16 | 2020-08-20 | Novartis Ag | Terapias de combinacion. |
| JP7569688B2 (ja) * | 2017-12-22 | 2024-10-18 | ハイバーセル,インコーポレイテッド | ホスファチジルイノシトールリン酸キナーゼ阻害剤としてのアミノピリジン誘導体 |
| WO2019123364A1 (en) | 2017-12-22 | 2019-06-27 | Shilpa Medicare Limited | Novel polymorphs of ribociclib mono succinate |
| WO2019133864A1 (en) * | 2017-12-29 | 2019-07-04 | Accutar Biotechnology | DUAL INHIBITORS OF PARP1 and CDK |
| CN107936029B (zh) * | 2018-01-08 | 2020-06-30 | 南京奇可药业有限公司 | 一种合成瑞博西尼的方法 |
| PE20210121A1 (es) | 2018-01-08 | 2021-01-19 | G1 Therapeutics Inc | Regimenes de dosificacion superior de g1t38 |
| US12398209B2 (en) | 2018-01-22 | 2025-08-26 | Janssen Biotech, Inc. | Methods of treating cancers with antagonistic anti-PD-1 antibodies |
| TW201940166A (zh) * | 2018-01-29 | 2019-10-16 | 美商貝達醫藥公司 | 作為cdk4及cdk6抑制劑之2h-吲唑衍生物及其治療用途 |
| CA3089592A1 (en) | 2018-02-15 | 2019-08-22 | Nuvation Bio Inc. | Heterocyclic compounds as kinase inhibitors |
| WO2019167068A1 (en) | 2018-03-01 | 2019-09-06 | Cipla Limited | Novel polymorphs of ribociclib succinate |
| WO2019195959A1 (en) | 2018-04-08 | 2019-10-17 | Cothera Biosciences, Inc. | Combination therapy for cancers with braf mutation |
| CA3043066A1 (en) | 2018-05-14 | 2019-11-14 | Apotex Inc. | Processes for the preparation of ribociclib and intermediates thereof |
| WO2019222521A1 (en) * | 2018-05-16 | 2019-11-21 | G1 Therapeutics, Inc. | Cdk inhibitors for the treatment of neoplastic disorders |
| CN108558745A (zh) * | 2018-05-17 | 2018-09-21 | 苏州莱克施德药业有限公司 | 一种帕博西林中间体的合成方法 |
| AR126019A1 (es) | 2018-05-30 | 2023-09-06 | Novartis Ag | Anticuerpos frente a entpd2, terapias de combinación y métodos de uso de los anticuerpos y las terapias de combinación |
| SG11202012071TA (en) | 2018-06-05 | 2021-01-28 | Crinetics Pharmaceuticals Inc | Melanocortin subtype-2 receptor (mc2r) antagonists and uses thereof |
| AR116109A1 (es) | 2018-07-10 | 2021-03-31 | Novartis Ag | Derivados de 3-(5-amino-1-oxoisoindolin-2-il)piperidina-2,6-diona y usos de los mismos |
| AU2019310595B2 (en) | 2018-07-27 | 2022-11-24 | 1200 Pharma Llc | CDK inhibitors and uses thereof |
| AU2019321289B2 (en) | 2018-08-13 | 2025-01-23 | Beijing Percans Oncology Co. Ltd. | Biomarkers for cancer therapy |
| CN120817904A (zh) | 2018-08-24 | 2025-10-21 | 法码科思莫斯有限公司 | 1,4-二氮杂螺[5.5]十一烷-3-酮改进的合成 |
| WO2020052627A1 (zh) * | 2018-09-13 | 2020-03-19 | 正大天晴药业集团股份有限公司 | 取代的吡咯并嘧啶类cdk抑制剂的盐及其结晶和用途 |
| US20210393623A1 (en) | 2018-09-26 | 2021-12-23 | Jacobio Pharmaceuticals Co., Ltd. | Novel Heterocyclic Derivatives Useful as SHP2 Inhibitors |
| WO2020084389A1 (en) | 2018-10-23 | 2020-04-30 | Lupin Limited | Ribociclib intermediate and process for preparation thereof |
| CA3117556A1 (en) | 2018-10-31 | 2020-05-07 | Gilead Sciences, Inc. | Substituted 6-azabenzimidazole compounds as hpk1 inhibitors |
| TWI721624B (zh) | 2018-10-31 | 2021-03-11 | 美商基利科學股份有限公司 | 經取代之6-氮雜苯并咪唑化合物 |
| AU2019402189B2 (en) | 2018-12-20 | 2023-04-13 | Novartis Ag | Dosing regimen and pharmaceutical combination comprising 3-(1-oxoisoindolin-2-yl)piperidine-2,6-dione derivatives |
| CN109400612A (zh) * | 2018-12-24 | 2019-03-01 | 重庆三圣实业股份有限公司 | 一种瑞博西尼的制备方法及其产品和用途 |
| WO2020140054A1 (en) | 2018-12-28 | 2020-07-02 | Spv Therapeutics Inc. | Cyclin-dependent kinase inhibitors |
| US20220056037A1 (en) * | 2018-12-28 | 2022-02-24 | Spv Therapeutics Inc. | Cyclin-dependent kinase inhibitors |
| CN113316471A (zh) | 2019-01-23 | 2021-08-27 | 诺华股份有限公司 | 7-环戊基-2-(5-哌嗪-1-基-吡啶-2-基氨基)-7H-吡咯并[2,3-d]嘧啶-6-羧酸二甲基酰胺的琥珀酸盐的新的结晶形式 |
| CN113382731A (zh) | 2019-02-12 | 2021-09-10 | 诺华股份有限公司 | 包含tno155和瑞博西尼的药物组合 |
| CN113329792B (zh) | 2019-02-15 | 2024-06-28 | 诺华股份有限公司 | 取代的3-(1-氧代异吲哚啉-2-基)哌啶-2,6-二酮衍生物及其用途 |
| BR112021015783A2 (pt) | 2019-02-15 | 2021-10-05 | Novartis Ag | Derivados de 3-(1-oxo-5-(piperidin-4-il)isoindolin-2-il)piperidina-2,6-diona e usos dos mesmos |
| CN114364675A (zh) | 2019-05-05 | 2022-04-15 | 上海齐鲁锐格医药研发有限公司 | Cdk抑制剂 |
| WO2020225827A1 (en) | 2019-05-08 | 2020-11-12 | Mylan Laboratories Limited | Novel polymorphs of ribociclib succinate |
| EP3969449B1 (en) | 2019-05-13 | 2025-02-12 | Novartis AG | New crystalline forms of n-(3-(2-(2-hydroxyethoxy)-6-morpholinopyridin-4-yl)-4-methvlphenyl)-2(trifluoromethyl)isonicotinamide as raf inhibitors for the treatment of cancer |
| CN114728076A (zh) | 2019-05-20 | 2022-07-08 | 诺华股份有限公司 | Mcl-1抑制剂抗体-药物缀合物及使用方法 |
| EP3972695A1 (en) | 2019-05-23 | 2022-03-30 | Gilead Sciences, Inc. | Substituted exo-methylene-oxindoles which are hpk1/map4k1 inhibitors |
| CN114008039B (zh) * | 2019-06-04 | 2024-01-16 | 斯泰普制药股份公司 | 作为人ctps1抑制剂用于治疗增殖性疾病的化合物 |
| TW202112767A (zh) | 2019-06-17 | 2021-04-01 | 美商佩特拉製藥公司 | 作為磷脂酸肌醇磷酸激酶抑制劑之胺基吡啶衍生物 |
| CN112094272A (zh) | 2019-06-18 | 2020-12-18 | 北京睿熙生物科技有限公司 | Cdk激酶抑制剂 |
| IL290789B2 (en) | 2019-08-26 | 2025-09-01 | Arvinas Operations Inc | Methods for treating breast cancer with a history of tetrahydronaphthalene as estrogen receptor-disrupting agents |
| WO2021038590A1 (en) | 2019-08-30 | 2021-03-04 | Mylan Laboratories Limited | Novel polymorph of ribociclib succinate |
| EP4031578A1 (en) | 2019-09-18 | 2022-07-27 | Novartis AG | Entpd2 antibodies, combination therapies, and methods of using the antibodies and combination therapies |
| EP4054583A4 (en) * | 2019-11-07 | 2023-10-25 | Crinetics Pharmaceuticals, Inc. | MELANOCORTIN SUBTYPE 2 RECEPTOR (MC2R) ANTAGONISTS AND THEIR USES |
| BR112022011758A2 (pt) * | 2019-12-16 | 2022-08-30 | Lunella Biotech Inc | Terapêutica de câncer inibidor de cdk4/6 seletivo |
| KR20220113986A (ko) | 2019-12-16 | 2022-08-17 | 루넬라 바이오테크 인코포레이티드 | 선택적 cdk 4/6 억제제 암 치료제 |
| AU2020406350A1 (en) | 2019-12-20 | 2022-08-11 | Novartis Ag | Uses of anti-TGF-beta antibodies and checkpoint inhibitors for the treatment of proliferative diseases |
| EP4603142A3 (en) | 2019-12-23 | 2025-08-27 | Crinetics Pharmaceuticals, Inc. | Spirocyclic piperidine melanocortin subtype-2 receptor (mc2r) antagonists and uses thereof |
| WO2021133886A1 (en) | 2019-12-23 | 2021-07-01 | Accutar Biotechnology | Combinations of estrogen receptor degraders and cyclin-dependent kinase inhibitors for treating cancer |
| US20230118053A1 (en) * | 2020-03-27 | 2023-04-20 | Jiangsu Alphamab Biopharmaceuticals Co., Ltd. | Combination of anti-her2 antibody and cdk inhibitior for tumor treatment |
| US20240000789A1 (en) | 2020-05-12 | 2024-01-04 | Novartis Ag | Therapeutic combinations comprising a craf inhibitor |
| WO2021227906A1 (zh) * | 2020-05-12 | 2021-11-18 | 苏州阿尔脉生物科技有限公司 | 一种作为cdk抑制剂的吡啶乙酰胺类衍生物、其制备方法及用途 |
| CN113149996B (zh) * | 2020-05-12 | 2022-12-20 | 苏州阿尔脉生物科技有限公司 | 一种作为cdk9抑制剂的多环酰胺类衍生物、其制备方法及用途 |
| EP4652997A2 (en) | 2020-05-19 | 2025-11-26 | Pharmacosmos Holding A/s | Cyclin-dependent kinase inhibiting compounds for the treatment of medical disorders |
| EP4165046B1 (en) * | 2020-06-11 | 2025-09-17 | Lunella Biotech, Inc. | Selective cdk4/6 inhibitor cancer therapeutics |
| US10988479B1 (en) | 2020-06-15 | 2021-04-27 | G1 Therapeutics, Inc. | Morphic forms of trilaciclib and methods of manufacture thereof |
| CA3182346A1 (en) | 2020-06-23 | 2021-12-30 | Novartis Ag | Dosing regimen comprising 3-(1-oxoisoindolin-2-yl)piperidine-2,6-dione derivatives |
| JP2023536164A (ja) | 2020-08-03 | 2023-08-23 | ノバルティス アーゲー | ヘテロアリール置換3-(1-オキソイソインドリン-2-イル)ピペリジン-2,6-ジオン誘導体及びその使用 |
| CN112375081B (zh) * | 2020-11-23 | 2022-04-12 | 中国医学科学院医药生物技术研究所 | 具有抑制CDK4、6或9活性的吡咯[2,3-d]嘧啶衍生物及其制备方法和应用 |
| MX2023006010A (es) | 2020-11-24 | 2023-06-08 | Novartis Ag | Anticuerpos anti-cd48, conjugados de anticuerpo-farmaco, y usos de los mismos. |
| KR20230138444A (ko) | 2020-11-24 | 2023-10-05 | 노파르티스 아게 | Mcl-1 억제제 항체-약물 접합체 및 사용 방법 |
| WO2022162122A1 (en) | 2021-01-29 | 2022-08-04 | Biotx.Ai Gmbh | Genetically verified netosis inhibitor for use in the treatment of a sars-cov2 infection |
| IL304891A (en) | 2021-02-02 | 2023-10-01 | Servier Lab | Selective Protech BCL-XL compounds and methods of use |
| JP2024510260A (ja) | 2021-03-19 | 2024-03-06 | クリネティックス ファーマシューティカルズ,インク. | 疾患の治療のためのメラノコルチンサブタイプ-2受容体(mc2r)アンタゴニスト |
| EP4313987A2 (en) | 2021-04-01 | 2024-02-07 | KRKA, d.d., Novo mesto | Process for the preparation of ribociclib and pharmaceutically acceptable salts thereof |
| TW202304979A (zh) | 2021-04-07 | 2023-02-01 | 瑞士商諾華公司 | 抗TGFβ抗體及其他治療劑用於治療增殖性疾病之用途 |
| CN117177752A (zh) | 2021-05-05 | 2023-12-05 | 诺华股份有限公司 | 用于治疗mpnst的化合物和组合物 |
| AR125874A1 (es) | 2021-05-18 | 2023-08-23 | Novartis Ag | Terapias de combinación |
| AU2022320615B2 (en) | 2021-07-26 | 2025-08-21 | Celcuity Inc. | 1-(4-{[4-(dimethylamino)piperidin-1-yl]carbonyl}phenyl)-3-[4-(4,6-dimorpholin-4-yl-1,3,5-triazin-2-yl)phenyl]urea (gedatolisib) and its combinations for use in the treatment of cancer |
| KR20240041340A (ko) * | 2021-07-27 | 2024-03-29 | 보로노이 주식회사 | 피롤로피리미딘 유도체 화합물 및 이의 용도 |
| TWI848533B (zh) | 2022-01-25 | 2024-07-11 | 瑞士商諾華公司 | 瑞博西尼藥物組成物 |
| CN114456180B (zh) * | 2022-02-18 | 2023-07-25 | 贵州大学 | 用于治疗和/或预防恶性肿瘤的化合物及药物制剂和应用 |
| AU2023248394A1 (en) * | 2022-04-08 | 2024-10-31 | Baerenkraft Therapeutics, Llc | Cdk9 inhibitors |
| AU2023250538A1 (en) * | 2022-04-08 | 2024-10-31 | Baerenkraft Therapeutics, Llc | Cdk9 inhibitors |
| IL317103A (en) | 2022-05-20 | 2025-01-01 | Novartis Ag | Antibody-drug conjugates of MET inhibitor BCL-XL and methods of using them |
| EP4525925A1 (en) | 2022-05-20 | 2025-03-26 | Novartis AG | Epha2 bcl-xl inhibitor antibody-drug conjugates and methods of use thereof |
| IL319242A (en) | 2022-08-31 | 2025-04-01 | Arvinas Operations Inc | Estrogen Receptor Blocker Dosage Regimen |
| EP4605088A1 (en) * | 2022-10-21 | 2025-08-27 | Novartis AG | Molecular glue degrader compounds and uses thereof |
| EP4615431A1 (en) | 2022-11-11 | 2025-09-17 | Astrazeneca AB | Combination therapies for the treatment of cancer |
| EP4626890A1 (en) | 2022-12-01 | 2025-10-08 | KRKA, d.d., Novo mesto | Ribociclib salts and formulations thereof |
| AU2024234194A1 (en) | 2023-03-10 | 2025-08-07 | Novartis Ag | Panras inhibitor antibody-drug conjugates and methods of use thereof |
| TW202508595A (zh) | 2023-05-04 | 2025-03-01 | 美商銳新醫藥公司 | 用於ras相關疾病或病症之組合療法 |
| TW202508598A (zh) | 2023-05-05 | 2025-03-01 | 瑞典商阿斯特捷利康公司 | 癌症療法 |
| WO2024235844A1 (en) | 2023-05-12 | 2024-11-21 | Institut National de la Santé et de la Recherche Médicale | Methods of preventing on-target genotoxicity induced by nucleases |
| WO2025034702A1 (en) | 2023-08-07 | 2025-02-13 | Revolution Medicines, Inc. | Rmc-6291 for use in the treatment of ras protein-related disease or disorder |
| CN117069663B (zh) * | 2023-08-31 | 2023-12-26 | 四川维亚本苑生物科技有限公司 | 一种瑞博西尼中间体v的合成方法及瑞博西尼的合成方法 |
| WO2025051337A1 (en) | 2023-09-06 | 2025-03-13 | Afyx Development A/S | Compositions and methods for treating and preventing oral cancer |
| WO2025080628A1 (en) * | 2023-10-10 | 2025-04-17 | Biolexis Therapeutics, Inc. | Bifunctional protac and molecular glue compounds and methods of use thereof |
| WO2025080946A2 (en) | 2023-10-12 | 2025-04-17 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2025111450A1 (en) | 2023-11-22 | 2025-05-30 | Les Laboratoires Servier | Anti-cd74 antibody-drug conjugates and methods of use thereof |
| WO2025171296A1 (en) | 2024-02-09 | 2025-08-14 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2025217307A1 (en) | 2024-04-09 | 2025-10-16 | Revolution Medicines, Inc. | Methods for predicting response to a ras(on) inhibitor and combination therapies |
| WO2025215536A1 (en) | 2024-04-10 | 2025-10-16 | Novartis Ag | Macrocyclic panras inhibitors for the treatment of cancer |
| US20250319032A1 (en) | 2024-04-15 | 2025-10-16 | Novartis Ag | Pharmaceutical compositions of ribociclib |
| WO2025240847A1 (en) | 2024-05-17 | 2025-11-20 | Revolution Medicines, Inc. | Ras inhibitors |
| CN120441576B (zh) * | 2025-07-08 | 2025-09-26 | 山东大学 | 一种靶向cdk4/6的化合物及其衍生的放射性示踪剂 |
| CN120483984B (zh) * | 2025-07-09 | 2025-10-10 | 山东大学 | 一种靶向cdk4/6的分子影像探针标记前体、探针及其制备方法与应用 |
Family Cites Families (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4666828A (en) | 1984-08-15 | 1987-05-19 | The General Hospital Corporation | Test for Huntington's disease |
| US4683202A (en) | 1985-03-28 | 1987-07-28 | Cetus Corporation | Process for amplifying nucleic acid sequences |
| US4801531A (en) | 1985-04-17 | 1989-01-31 | Biotechnology Research Partners, Ltd. | Apo AI/CIII genomic polymorphisms predictive of atherosclerosis |
| US5272057A (en) | 1988-10-14 | 1993-12-21 | Georgetown University | Method of detecting a predisposition to cancer by the use of restriction fragment length polymorphism of the gene for human poly (ADP-ribose) polymerase |
| US5192659A (en) | 1989-08-25 | 1993-03-09 | Genetype Ag | Intron sequence analysis method for detection of adjacent and remote locus alleles as haplotypes |
| US6218529B1 (en) | 1995-07-31 | 2001-04-17 | Urocor, Inc. | Biomarkers and targets for diagnosis, prognosis and management of prostate, breast and bladder cancer |
| CA2262403C (en) | 1995-07-31 | 2011-09-20 | Urocor, Inc. | Biomarkers and targets for diagnosis, prognosis and management of prostate disease |
| KR20060111716A (ko) * | 2002-01-22 | 2006-10-27 | 워너-램버트 캄파니 엘엘씨 | 2-(피리딘-2-일아미노)-피리도[2,3-d]피리미딘-7-온 |
| JP4187657B2 (ja) | 2002-03-07 | 2008-11-26 | エフ.ホフマン−ラ ロシュ アーゲー | p38キナーゼインヒビターとしての二環式ピリジン及びピリミジン |
| CA2497440C (en) | 2002-09-04 | 2011-03-22 | Schering Corporation | Pyrazolopyrimidines as cyclin-dependent kinase inhibitors |
| MXPA05007503A (es) * | 2003-01-17 | 2005-09-21 | Warner Lambert Co | Heterociclicos 2-aminopiridina sustituidos como inhibidores de proliferacion celular. |
| JP2007504271A (ja) | 2003-09-05 | 2007-03-01 | ニューロジェン・コーポレーション | Crf1受容体リガンドである、ヘテロアリール縮合ピリジン類、ピラジン類及びピリミジン類 |
| CN102060806A (zh) | 2003-09-11 | 2011-05-18 | iTherX药品公司 | 细胞因子抑制剂 |
| US7319102B1 (en) | 2003-12-09 | 2008-01-15 | The Procter & Gamble Company | Pyrrolo[2,3-d]pyrimidine cytokine inhibitors |
| CN1918158B (zh) * | 2004-02-14 | 2011-03-02 | Irm责任有限公司 | 作为蛋白激酶抑制剂的化合物和组合物 |
| CA2556946A1 (en) | 2004-03-05 | 2005-09-15 | Taisho Pharmaceutical Co., Ltd. | Pyrrolopyrimidine derivatives |
| WO2005107760A1 (en) | 2004-04-30 | 2005-11-17 | Irm Llc | Compounds and compositions as inducers of keratinocyte differentiation |
| US20080167309A1 (en) | 2004-07-22 | 2008-07-10 | Astex Therapeutics, Ltd. | Pharmaceutical Compounds |
| WO2006042102A2 (en) | 2004-10-05 | 2006-04-20 | Neurogen Corporation | Pyrrolo-pyridine, pyrrolo-pyrimidine and related heterocyclic compounds |
| WO2006045828A1 (en) | 2004-10-29 | 2006-05-04 | Tibotec Pharmaceuticals Ltd. | Hiv inhibiting bicyclic pyrimidine derivatives |
| US7521446B2 (en) | 2005-01-13 | 2009-04-21 | Signal Pharmaceuticals, Llc | Haloaryl substituted aminopurines, compositions thereof, and methods of treatment therewith |
| US7723340B2 (en) | 2005-01-13 | 2010-05-25 | Signal Pharmaceuticals, Llc | Haloaryl substituted aminopurines, compositions thereof, and methods of treatment therewith |
| US7947695B2 (en) * | 2005-01-14 | 2011-05-24 | Janssen Pharmaceutica Nv | 5-membered annelated heterocyclic pyrimidines as kinase inhibitors |
| WO2006091737A1 (en) * | 2005-02-24 | 2006-08-31 | Kemia, Inc. | Modulators of gsk-3 activity |
| JP2006241089A (ja) | 2005-03-04 | 2006-09-14 | Astellas Pharma Inc | ピロロピリミジン誘導体またはその塩 |
| US20070225304A1 (en) | 2005-09-06 | 2007-09-27 | Pharmacopeia Drug Discovery, Inc. | Aminopurine derivatives for treating neurodegenerative diseases |
| GB0520164D0 (en) | 2005-10-04 | 2005-11-09 | Novartis Ag | Organic compounds |
| WO2007058990A2 (en) | 2005-11-14 | 2007-05-24 | Kemia, Inc. | Therapy using cytokine inhibitors |
| CA2631777A1 (en) | 2005-12-22 | 2007-07-05 | Wyeth | Substituted isoquinoline-1,3(2h,4h)-diones, 1-thioxo-1,4-dihydro-2h-isoquinoline-3-ones and 1,4-dihydro-3(2h)-isoquinolones and use thereof as kinase inhibitor |
| GB0526246D0 (en) | 2005-12-22 | 2006-02-01 | Novartis Ag | Organic compounds |
| MX2008011525A (es) | 2006-03-09 | 2008-09-18 | Pharmacopeia Inc | Inhibidores de mnk2 de 8-heteroarilpurina para el tratamiento de trastornos metabolicos. |
| WO2007125405A2 (en) | 2006-05-01 | 2007-11-08 | Pfizer Products Inc. | Substituted 2-amino-fused heterocyclic compounds |
| TWI398252B (zh) | 2006-05-26 | 2013-06-11 | Novartis Ag | 吡咯并嘧啶化合物及其用途 |
| CA2709202C (en) * | 2007-12-19 | 2013-04-23 | Amgen Inc. | Fused pyridine, pyrimidine and triazine compounds as cell cycle inhibitors |
| MX2010008719A (es) * | 2008-02-06 | 2010-09-24 | Novartis Ag | Pirrolo [2,-d] piridinas y usos de las mismas como inhibidores de cinasa de tirosina. |
| NZ591176A (en) * | 2008-08-22 | 2012-11-30 | Novartis Ag | Pyrrolopyrimidine compounds as cdk inhibitors |
| GB0819105D0 (en) | 2008-10-17 | 2008-11-26 | Chroma Therapeutics Ltd | Pyrrolo-pyrimidine compounds |
| UY33226A (es) | 2010-02-19 | 2011-09-30 | Novartis Ag | Compuestos de pirrolopirimidina deuterada como inhibidores de la cdk4/6 |
| UY33227A (es) | 2010-02-19 | 2011-09-30 | Novartis Ag | Compuestos de pirrolopirimidina como inhibidores de la cdk4/6 |
| ES2689177T3 (es) | 2010-04-13 | 2018-11-08 | Novartis Ag | Combinación que comprende un inhibidor de cinasa 4 dependiente de ciclina o cinasa dependiente de ciclina (CDK4/6) y un inhibidor de mTOR para tratar cáncer |
-
2009
- 2009-08-20 NZ NZ591176A patent/NZ591176A/xx unknown
- 2009-08-20 GE GEAP200912114A patent/GEP20135785B/en unknown
- 2009-08-20 US US13/060,154 patent/US8685980B2/en active Active
- 2009-08-20 DK DK09782051.8T patent/DK2331547T3/da active
- 2009-08-20 JP JP2011523425A patent/JP5560496B2/ja active Active
- 2009-08-20 ME MEP-2011-25A patent/ME01282B/me unknown
- 2009-08-20 ES ES09782051.8T patent/ES2522346T3/es active Active
- 2009-08-20 CA CA2734802A patent/CA2734802C/en active Active
- 2009-08-20 PE PE2011000180A patent/PE20110419A1/es active IP Right Grant
- 2009-08-20 PL PL09782051T patent/PL2331547T3/pl unknown
- 2009-08-20 KR KR1020117006436A patent/KR101353857B1/ko active Active
- 2009-08-20 RS RSP20140536 patent/RS53574B1/sr unknown
- 2009-08-20 KR KR1020137031722A patent/KR20130140222A/ko not_active Ceased
- 2009-08-20 AU AU2009284098A patent/AU2009284098B2/en active Active
- 2009-08-20 SI SI200931040T patent/SI2331547T1/sl unknown
- 2009-08-20 JO JO2009319A patent/JO2924B1/en active
- 2009-08-20 MY MYPI20110681 patent/MY150560A/en unknown
- 2009-08-20 CN CN201410068898.6A patent/CN103788100A/zh active Pending
- 2009-08-20 EP EP13197275.4A patent/EP2716643A1/en not_active Withdrawn
- 2009-08-20 CN CN200980141314.0A patent/CN102186856B/zh active Active
- 2009-08-20 EP EP09782051.8A patent/EP2331547B1/en active Active
- 2009-08-20 HR HRP20141018AT patent/HRP20141018T1/hr unknown
- 2009-08-20 MX MX2011001879A patent/MX2011001879A/es active IP Right Grant
- 2009-08-20 UA UAA201102052A patent/UA103628C2/ru unknown
- 2009-08-20 WO PCT/EP2009/060793 patent/WO2010020675A1/en not_active Ceased
- 2009-08-20 EA EA201100355A patent/EA019094B1/ru active Protection Beyond IP Right Term
- 2009-08-20 PT PT97820518T patent/PT2331547E/pt unknown
- 2009-08-20 BR BRPI0917791-4A patent/BRPI0917791B1/pt active IP Right Grant
- 2009-08-21 TW TW98128319A patent/TWI468409B/zh active
- 2009-08-21 UY UY0001038935A patent/UY38935A/es not_active Application Discontinuation
- 2009-08-21 UY UY0001032067A patent/UY32067A/es active IP Right Grant
- 2009-08-21 US US12/545,322 patent/US8415355B2/en active Active
- 2009-08-21 AR ARP090103233A patent/AR073116A1/es not_active Application Discontinuation
-
2011
- 2011-02-04 TN TN2011000062A patent/TN2011000062A1/fr unknown
- 2011-02-08 ZA ZA2011/00994A patent/ZA201100994B/en unknown
- 2011-02-10 IL IL211164A patent/IL211164A/en active Protection Beyond IP Right Term
- 2011-02-11 CL CL2011000306A patent/CL2011000306A1/es unknown
- 2011-02-11 MA MA33606A patent/MA32555B1/fr unknown
- 2011-02-21 CU CU2011000040A patent/CU24062B1/es active IP Right Grant
- 2011-02-21 DO DO2011000057A patent/DOP2011000057A/es unknown
- 2011-02-21 NI NI201100042A patent/NI201100042A/es unknown
- 2011-02-22 HN HN2011000542A patent/HN2011000542A/es unknown
- 2011-02-22 CR CR20110101A patent/CR20110101A/es unknown
- 2011-02-22 EC EC2011010843A patent/ECSP11010843A/es unknown
- 2011-02-23 CO CO11022224A patent/CO6341561A2/es not_active Application Discontinuation
-
2013
- 2013-03-06 US US13/786,955 patent/US8962630B2/en active Active
-
2014
- 2014-01-17 US US14/158,358 patent/US9416136B2/en active Active
- 2014-01-31 JP JP2014016933A patent/JP5882371B2/ja active Active
- 2014-10-30 CY CY20141100895T patent/CY1115703T1/el unknown
-
2015
- 2015-01-20 SM SM201500017T patent/SMT201500017B/xx unknown
-
2016
- 2016-08-08 US US15/231,005 patent/US20170183352A1/en not_active Abandoned
-
2017
- 2017-11-09 NL NL300909C patent/NL300909I2/nl unknown
- 2017-11-09 LU LU00048C patent/LUC00048I2/fr unknown
- 2017-11-13 NO NO2017059C patent/NO2017059I1/no unknown
- 2017-11-23 LT LTPA2017039C patent/LTC2331547I2/lt unknown
- 2017-12-01 CY CY2017042C patent/CY2017042I2/el unknown
- 2017-12-06 HU HUS1700051C patent/HUS1700051I1/hu unknown
- 2017-12-15 FR FR17C1059C patent/FR17C1059I2/fr active Active
-
2018
- 2018-02-01 US US15/886,014 patent/US20180155351A1/en not_active Abandoned
- 2018-05-16 AR ARP180101294A patent/AR111763A2/es not_active Application Discontinuation
-
2020
- 2020-09-16 US US17/023,041 patent/US20210253578A1/en not_active Abandoned
-
2022
- 2022-12-21 US US18/069,646 patent/US20240043428A1/en not_active Abandoned
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2014129361A (ja) * | 2008-08-22 | 2014-07-10 | Novartis Ag | Cdk阻害剤としてのピロロピリミジン化合物 |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5560496B2 (ja) | Cdk阻害剤としてのピロロピリミジン化合物 | |
| US7576085B2 (en) | Imidazopyrazines as cyclin dependent kinase inhibitors | |
| WO2009071701A1 (en) | Pyrazole derivatives and use thereof as inhibitors of cyclin dependent kinases | |
| HK1193406A (en) | Pyrrolopyrimidine compounds and their uses | |
| HK1156625B (en) | Pyrrolopyrimidine compounds as cdk inhibitors |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20120802 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20130514 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20130516 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20130814 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20130821 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20130904 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20131001 |
|
| RD03 | Notification of appointment of power of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7423 Effective date: 20140123 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20140131 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20140307 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20140409 |
|
| A911 | Transfer to examiner for re-examination before appeal (zenchi) |
Free format text: JAPANESE INTERMEDIATE CODE: A911 Effective date: 20140414 |
|
| 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: 20140513 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20140522 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20140522 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A821 Effective date: 20140522 |
|
| R150 | Certificate of patent or registration of utility model |
Ref document number: 5560496 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| 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 |