AU2009284098B2 - Pyrrolopyrimidine compounds as CDK inhibitors - Google Patents
Pyrrolopyrimidine compounds as CDK inhibitors Download PDFInfo
- Publication number
- AU2009284098B2 AU2009284098B2 AU2009284098A AU2009284098A AU2009284098B2 AU 2009284098 B2 AU2009284098 B2 AU 2009284098B2 AU 2009284098 A AU2009284098 A AU 2009284098A AU 2009284098 A AU2009284098 A AU 2009284098A AU 2009284098 B2 AU2009284098 B2 AU 2009284098B2
- Authority
- AU
- Australia
- Prior art keywords
- cyclopentyl
- pyrrolo
- carboxylic acid
- ylamino
- pyrimidine
- 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, expires
Links
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)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Neurology (AREA)
- Oncology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Hospice & Palliative Care (AREA)
- Hematology (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (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 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2009284098A1 AU2009284098A1 (en) | 2010-02-25 |
| AU2009284098B2 true AU2009284098B2 (en) | 2012-03-29 |
Family
ID=41171100
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2009284098A Active 2032-10-23 AU2009284098B2 (en) | 2008-08-22 | 2009-08-20 | Pyrrolopyrimidine compounds as CDK inhibitors |
Country Status (48)
Families Citing this family (245)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2522346T3 (es) * | 2008-08-22 | 2014-11-14 | Novartis Ag | Compuestos de pirrolopirimidina como inhibidores de CDK |
| EP3718560A3 (en) | 2009-05-13 | 2020-12-09 | The University of North Carolina at Chapel Hill | Cyclin dependent kinase inhibitors and methods of use |
| 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 |
| US20130035336A1 (en) * | 2010-04-13 | 2013-02-07 | Novartis Ag | Combination comprising a cyclin dependent kinase 4 or cyclin dependent kinase (cdk4/6) inhibitor for treating cancer |
| WO2012024500A1 (en) | 2010-08-18 | 2012-02-23 | Life Technologies Corporation | Chemical coating of microwell for electrochemical detection device |
| US8691830B2 (en) | 2010-10-25 | 2014-04-08 | G1 Therapeutics, Inc. | CDK inhibitors |
| HRP20161092T1 (hr) * | 2010-10-25 | 2016-10-21 | G1 Therapeutics, Inc. | Cdk inhibitori |
| 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 |
| US9808461B2 (en) | 2010-11-17 | 2017-11-07 | The University Of North Carolina At Chapel Hill | Protection of renal tissues from ischemia through inhibition of the proliferative kinases CDK4 and CDK6 |
| WO2012093101A1 (en) * | 2011-01-04 | 2012-07-12 | Novartis Ag | Indole compounds or analogues thereof useful for the treatment of age-related macular degeneration (amd) |
| 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) |
| ES2610931T3 (es) * | 2011-07-01 | 2017-05-04 | Novartis Ag | Terapia de combinación |
| JP5832647B2 (ja) | 2011-07-01 | 2015-12-16 | ノバルティス アーゲー | がんの治療における使用のためのcdk4/6阻害剤およびpi3k阻害剤を含む併用療法 |
| US9498471B2 (en) | 2011-10-20 | 2016-11-22 | 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 |
| CA2868966C (en) * | 2012-03-29 | 2021-01-26 | Francis Xavier Tavares | Lactam kinase inhibitors |
| US10202392B2 (en) | 2012-04-26 | 2019-02-12 | Francis Xavier Tavares | Synthesis of lactams |
| JP6155332B2 (ja) | 2012-06-28 | 2017-06-28 | ノバルティス アーゲー | ピロリジン誘導体、および補体経路調節因子としてのその使用 |
| JP6209605B2 (ja) | 2012-06-28 | 2017-10-04 | ノバルティス アーゲー | ピロリジン誘導体、および補体経路調節因子としてのその使用 |
| JP6273274B2 (ja) | 2012-06-28 | 2018-01-31 | ノバルティス アーゲー | 補体経路モジュレーターおよびその使用 |
| WO2014002052A1 (en) | 2012-06-28 | 2014-01-03 | Novartis Ag | Pyrrolidine derivatives and their use as complement pathway modulators |
| ES2712190T3 (es) | 2012-06-28 | 2019-05-09 | Novartis Ag | Moduladores de la vía del complemento y sus usos |
| EA201590200A1 (ru) | 2012-07-12 | 2015-08-31 | Новартис Аг | Модуляторы пути активации комплемента и их применение |
| AR091876A1 (es) * | 2012-07-26 | 2015-03-04 | Novartis Ag | Combinaciones farmaceuticas para el tratamiento de enfermedades proliferativas |
| WO2014022830A2 (en) | 2012-08-03 | 2014-02-06 | Foundation Medicine, Inc. | Human papilloma virus as predictor of cancer prognosis |
| EP3251673A1 (en) | 2012-12-13 | 2017-12-06 | IP Gesellschaft für Management mbH | Combination therapy comprising a cdk4/6 inhibitor and a pi3k inhibitor for use in the treatment of cancer |
| WO2014097125A1 (en) | 2012-12-20 | 2014-06-26 | Novartis Ag | Pharmaceutical combination comprising binimetinib |
| WO2014109858A1 (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 |
| CN105143463A (zh) | 2013-02-25 | 2015-12-09 | 诺华股份有限公司 | 新的雄激素受体突变 |
| JP2016512559A (ja) | 2013-03-13 | 2016-04-28 | アッヴィ・インコーポレイテッド | Cdk9キナーゼ阻害薬 |
| EP2970200A1 (en) | 2013-03-13 | 2016-01-20 | Abbvie Inc. | Pyridine cdk9 kinase inhibitors |
| CA2903538A1 (en) * | 2013-03-14 | 2014-10-02 | Abbvie Inc. | Pyrrolopyrimindine cdk9 kinase inhibitors |
| JP2016514113A (ja) | 2013-03-14 | 2016-05-19 | アッヴィ・インコーポレイテッド | ピロロ[2,3−b]ピリジンcdk9キナーゼ阻害剤 |
| UY35419A (es) | 2013-03-14 | 2014-10-31 | Abbvie Inc | Inhibidores de cdk9 quinasa de pirrolo (2,3- b) piridina |
| WO2014144326A1 (en) | 2013-03-15 | 2014-09-18 | G1 Therapeutics, Inc. | Transient protection of normal cells during chemotherapy |
| CN105407723A (zh) * | 2013-03-15 | 2016-03-16 | G1治疗公司 | 高效的抗赘生剂和抗增生剂 |
| WO2014144596A2 (en) * | 2013-03-15 | 2014-09-18 | G1 Therapeutics, Inc. | Transient protection of hematopoietic stem and progenitor cells against ionizing radiation |
| PT2976106T (pt) | 2013-03-21 | 2021-05-26 | Array Biopharma Inc | Terapia de combinação que compreende um inibidor de b-raf e um segundo inibidor |
| AU2014253932B2 (en) | 2013-04-16 | 2020-04-30 | Memorial Sloan-Kettering Cancer Center | Companion diagnostic for CDK4 inhibitors |
| MX378263B (es) * | 2013-08-14 | 2025-03-10 | Novartis Ag | Terapia de combinación para el tratamiento del cáncer. |
| 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 |
| EP3757130A1 (en) | 2013-09-26 | 2020-12-30 | Costim Pharmaceuticals Inc. | Methods for treating hematologic cancers |
| AR097894A1 (es) * | 2013-10-03 | 2016-04-20 | Hoffmann La Roche | Inhibidores terapéuticos de cdk8 o uso de los mismos |
| WO2015061407A1 (en) * | 2013-10-24 | 2015-04-30 | Francis Xavier Tavares | Process for synthesis of lactams |
| WO2015081083A1 (en) * | 2013-11-27 | 2015-06-04 | 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 |
| AU2014368927B2 (en) * | 2013-12-20 | 2018-10-25 | Biomed Valley Discoveries, Inc. | Cancer treatments using combinations of CDK and ERK inhibitors |
| EP3086787B1 (en) * | 2013-12-23 | 2021-01-20 | Novartis AG | Pharmaceutical combinations |
| MX2016008362A (es) * | 2013-12-23 | 2016-09-08 | Novartis Ag | Combinaciones farmaceuticas. |
| US9949976B2 (en) | 2013-12-31 | 2018-04-24 | Xuanzhu Pharma Co., Ltd. | Kinase inhibitor and use thereof |
| HUE039504T2 (hu) * | 2013-12-31 | 2019-01-28 | Xuanzhu Pharma Co Ltd | Kináz inhibitor és alkalmazása |
| 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 |
| ME03558B (me) | 2014-03-14 | 2020-07-20 | Novartis Ag | Molekuli anti-lag-3 antiтela i njihove upotrebe |
| WO2015154064A2 (en) | 2014-04-04 | 2015-10-08 | Del Mar Pharmaceuticals | Use of dianhydrogalactitol and analogs or derivatives thereof to treat non-small-cell carcinoma of the lung and ovarian cancer |
| US20150320754A1 (en) | 2014-04-16 | 2015-11-12 | Infinity Pharmaceuticals, Inc. | Combination therapies |
| US20150297606A1 (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 |
| DK3149008T3 (en) * | 2014-05-28 | 2019-04-01 | Shanghai Fochon Pharmaceutical Co Ltd | Specific protein kinase inhibitors |
| 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 |
| WO2016040858A1 (en) | 2014-09-12 | 2016-03-17 | 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 |
| KR20170060042A (ko) | 2014-09-13 | 2017-05-31 | 노파르티스 아게 | Alk 억제제의 조합 요법 |
| EA201790737A1 (ru) | 2014-10-03 | 2017-08-31 | Новартис Аг | Комбинированная терапия |
| 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 |
| CA3000633C (en) | 2014-10-14 | 2023-10-03 | The Regents Of The University Of California | Use of cdk9 and brd4 inhibitors to inhibit inflammation |
| MX389663B (es) | 2014-10-14 | 2025-03-20 | Novartis Ag | Moleculas de anticuerpo que se unen a pd-l1 y usos de las mismas. |
| IL278574B2 (en) | 2014-11-12 | 2024-11-01 | Seagen Inc | Glycan-interacting compounds and methods of use |
| EP3231805B1 (en) * | 2014-12-12 | 2020-03-04 | Crystal Pharmatech Co. Ltd. | Salt of pyrrolo[2,3-d]pyrimidine compound and novel polymorph of salt |
| 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 |
| 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 |
| US20160220569A1 (en) * | 2015-02-03 | 2016-08-04 | G1 Therapeutics, Inc. | CDK4/6 Inhibitor Dosage Formulations For The Protection Of Hematopoietic Stem And Progenitor Cells During Chemotherapy |
| US10449211B2 (en) | 2015-03-10 | 2019-10-22 | Aduro Biotech, Inc. | Compositions and methods for activating “stimulator of interferon gene”—dependent signalling |
| JP2018509448A (ja) | 2015-03-25 | 2018-04-05 | ノバルティス アーゲー | 組合せ医薬 |
| JP2018514523A (ja) | 2015-04-16 | 2018-06-07 | ノバルティス アーゲー | リボシクリブ錠剤 |
| 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 |
| KR102601320B1 (ko) | 2015-05-29 | 2023-11-10 | 데이진 화-마 가부시키가이샤 | 피리도[3,4-d]피리미딘 유도체 및 그 약학적으로 허용되는 염 |
| 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 |
| US20180222982A1 (en) | 2015-07-29 | 2018-08-09 | Novartis Ag | Combination therapies comprising antibody molecules to pd-1 |
| EP3878465A1 (en) | 2015-07-29 | 2021-09-15 | Novartis AG | Combination therapies comprising antibody molecules to tim-3 |
| DK3317301T3 (da) | 2015-07-29 | 2021-06-28 | Immutep Sas | Kombinationsterapier omfattende antistofmolekyler mod lag-3 |
| CN108348522A (zh) | 2015-08-28 | 2018-07-31 | 诺华股份有限公司 | 含(a)周期素依赖性激酶4/6(cdk4/6)抑制剂lee011(=ribociclib)和(b)表皮生长因子受体(egfr)抑制剂厄洛替尼的药物组合,用于治疗或预防癌症 |
| WO2017037587A1 (en) | 2015-08-28 | 2017-03-09 | Novartis Ag | Combination of ribociclib and dabrafenib for treating or preventing cancer |
| EP3340991A1 (en) | 2015-08-28 | 2018-07-04 | 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 |
| CN108348514A (zh) | 2015-08-28 | 2018-07-31 | 诺华股份有限公司 | 含pi3k抑制剂alpelisib和cdk4/6抑制剂ribociclib的药物组合以及其在治疗/预防癌症中的应用 |
| EP3156406A1 (en) | 2015-10-14 | 2017-04-19 | ratiopharm GmbH | Crystalline forms of ribociclib free base |
| CN108472289A (zh) | 2015-11-02 | 2018-08-31 | 诺华股份有限公司 | 磷脂酰肌醇3-激酶抑制剂的给药方案 |
| SI3370768T1 (sl) | 2015-11-03 | 2022-04-29 | Janssen Biotech, Inc. | Protitelesa, ki se specifično vežejo na PD-1, in njihove uporabe |
| WO2017083582A1 (en) | 2015-11-12 | 2017-05-18 | Siamab Therapeutics, Inc. | Glycan-interacting compounds and methods of use |
| 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 |
| EP3389712B1 (en) | 2015-12-17 | 2024-04-10 | 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 |
| US10570141B2 (en) | 2016-03-25 | 2020-02-25 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Substituted pyrrolopyrimidine CDK inhibitor, pharmaceutical composition containing same and use thereof |
| 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 |
| US10865204B2 (en) | 2016-04-22 | 2020-12-15 | 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 |
| AU2017262155B2 (en) | 2016-05-07 | 2021-03-11 | Fochon Pharmaceuticals, Ltd. | Certain protein kinase inhibitors |
| CN108290899B (zh) * | 2016-06-06 | 2020-09-18 | 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 |
| EA202092442A3 (ru) | 2016-06-07 | 2021-08-31 | Джакобио Фармасьютикалс Ко., Лтд. | Новые гетероциклические производные, применимые в качестве ингибиторов shp2 |
| EA201990189A1 (ru) | 2016-07-01 | 2019-06-28 | Г1 Терапьютикс, Инк. | Синтез n-(гетероарил)пирроло[3,2-d]пиримидин-2-аминов |
| WO2018005863A1 (en) | 2016-07-01 | 2018-01-04 | G1 Therapeutics, Inc. | Pyrimidine-based compounds for the treatment of cancer |
| KR20190025943A (ko) | 2016-07-01 | 2019-03-12 | 쥐원 쎄라퓨틱스, 인크. | 피리미딘-기재 항증식제 |
| WO2018005533A1 (en) | 2016-07-01 | 2018-01-04 | G1 Therapeutics, Inc. | Antiproliferative pyrimidine-based compounds |
| US11098077B2 (en) | 2016-07-05 | 2021-08-24 | Chinook Therapeutics, Inc. | Locked nucleic acid cyclic dinucleotide compounds and uses thereof |
| IL264950B2 (en) | 2016-08-23 | 2024-01-01 | Eisai R&D Man Co Ltd | Combined treatments for the treatment of malignant liver cell carcinoma |
| WO2018051280A1 (en) * | 2016-09-15 | 2018-03-22 | Dr. Reddy’S Laboratories Limited | Process for preparation of ribociclib, its acid addition salts |
| CA3037456A1 (en) | 2016-09-19 | 2018-03-22 | Novartis Ag | Therapeutic combinations comprising a raf inhibitor and a erk inhibitor |
| 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 |
| AU2017359333B2 (en) | 2016-11-08 | 2024-03-21 | Dana-Farber Cancer Institute, Inc. | Compositions and methods of modulating anti-tumor immunity |
| CN110177553A (zh) | 2016-11-17 | 2019-08-27 | 北卡罗来纳大学教堂山分校 | 烷基吡咯并嘧啶类似物及其制备和使用方法 |
| WO2018094143A1 (en) | 2016-11-17 | 2018-05-24 | Siamab Therapeutics, Inc. | Glycan-interacting compounds and methods of use |
| ES2852123T3 (es) | 2016-11-28 | 2021-09-13 | Teijin Pharma Ltd | Derivados de ((piridin-2-il)-amino)pirido[3,4-d]pirimidina y ((piridazin-3-il)-amino)pirido[3,4-d]pirimidina como inhibidores de CDK4/6 para tratar p. ej. artritis reumatoide, arteriosclerosis, fibrosis pulmonar, infarto cerebral o cáncer |
| RS63004B1 (sr) | 2016-11-28 | 2022-03-31 | Teijin Pharma Ltd | Kristal pirido[3, 4-d]pirimidin derivata ili njegov solvat |
| WO2018106729A1 (en) | 2016-12-05 | 2018-06-14 | G1 Therapeutics, Inc. | Preservation of immune response during chemotherapy regimens |
| EP3565558B1 (en) | 2017-01-06 | 2023-12-06 | G1 Therapeutics, Inc. | Combination therapy with a serd compound and a cdk4/6 inhibitor for the treatment of cancer |
| JP2020506904A (ja) * | 2017-01-27 | 2020-03-05 | シグナルアールエックス ファーマシューティカルズ,インコーポレイテッド | キナーゼ、ブロモドメイン及びチェックポイント阻害剤としてのチエノピラノン及びフラノピラノン |
| US11395821B2 (en) | 2017-01-30 | 2022-07-26 | G1 Therapeutics, Inc. | Treatment of EGFR-driven cancer with fewer side effects |
| KR20240044544A (ko) | 2017-03-03 | 2024-04-04 | 씨젠 인크. | 글리칸-상호작용 화합물 및 사용 방법 |
| CN110636862A (zh) | 2017-03-16 | 2019-12-31 | 卫材 R&D 管理有限公司 | 用于治疗乳腺癌的组合疗法 |
| KR102317480B1 (ko) | 2017-03-23 | 2021-10-25 | 자코바이오 파마슈티칼스 컴퍼니 리미티드 | Shp2 억제제로서 유용한 신규한 헤테로환형 유도체 |
| 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 |
| IL270224B1 (en) | 2017-05-02 | 2024-04-01 | Novartis Ag | Combination therapy employing trametinib and a defined raf inhibitor |
| 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 |
| WO2019006393A1 (en) | 2017-06-29 | 2019-01-03 | G1 Therapeutics, Inc. | Morphic forms of git38 and methods of manufacture thereof |
| CN110996962A (zh) | 2017-08-03 | 2020-04-10 | 诺华股份有限公司 | 第三代egfr酪氨酸激酶抑制剂和周期素d激酶抑制剂的治疗组合 |
| 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 |
| WO2019062854A1 (zh) * | 2017-09-29 | 2019-04-04 | 杭州领业医药科技有限公司 | 瑞博西林的共晶和瑞博西林单琥珀酸盐的共晶、其制备方法、组合物和用途 |
| AU2018354972B2 (en) * | 2017-10-27 | 2021-07-08 | Fresenius Kabi Oncology Ltd. | An improved process for the preparation of ribociclib and its salts |
| AU2018368731A1 (en) | 2017-11-16 | 2020-05-14 | Novartis Ag | Combination therapies |
| JP2021503448A (ja) | 2017-11-16 | 2021-02-12 | ノバルティス アーゲー | Lsz102及びリボシクリブを含む医薬組合せ |
| US11111250B2 (en) | 2017-12-22 | 2021-09-07 | Shilpa Meicare Limited | Polymorphs of Ribociclib mono succinate |
| US11667651B2 (en) * | 2017-12-22 | 2023-06-06 | Hibercell, Inc. | Aminopyridine derivatives as phosphatidylinositol phosphate kinase inhibitors |
| US10519136B2 (en) | 2017-12-29 | 2019-12-31 | 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 |
| WO2019136451A1 (en) | 2018-01-08 | 2019-07-11 | G1 Therapeutics, Inc. | G1t38 superior dosage regimes |
| US12398209B2 (en) | 2018-01-22 | 2025-08-26 | Janssen Biotech, Inc. | Methods of treating cancers with antagonistic anti-PD-1 antibodies |
| CA3088381A1 (en) * | 2018-01-29 | 2019-08-01 | Beta Pharma, Inc. | 2h-indazole derivatives as cdk4 and cdk6 inhibitors and therapeutic uses thereof |
| BR112020015431A2 (pt) | 2018-02-15 | 2020-12-08 | Nuvation Bio Inc. | Compostos heterocíclicos como inibidores de quinase |
| 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 |
| TWI869346B (zh) | 2018-05-30 | 2025-01-11 | 瑞士商諾華公司 | Entpd2抗體、組合療法、及使用該等抗體和組合療法之方法 |
| IL279152B2 (en) | 2018-06-05 | 2024-09-01 | Crinetics Pharmaceuticals Inc | Melanocortin subtype-2 receptor 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 |
| SG11202100429TA (en) | 2018-07-27 | 2021-02-25 | California Inst Of Techn | Cdk inhibitors and uses thereof |
| WO2020036852A1 (en) | 2018-08-13 | 2020-02-20 | Beijing Percans Oncology Co. Ltd. | Biomarkers for cancer therapy |
| KR20210049847A (ko) | 2018-08-24 | 2021-05-06 | 쥐원 쎄라퓨틱스, 인크. | 1,4-디아자스피로[5.5]운데칸-3-온의 개선된 합성 |
| AU2019338032A1 (en) * | 2018-09-13 | 2021-05-20 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Salts of substituted pyrrolopyrimidine CDK inhibitor, crystal and use thereof |
| WO2020063760A1 (en) | 2018-09-26 | 2020-04-02 | 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 |
| CN117105933A (zh) | 2018-10-31 | 2023-11-24 | 吉利德科学公司 | 具有hpk1抑制活性的取代的6-氮杂苯并咪唑化合物 |
| MX2021005047A (es) | 2018-10-31 | 2021-09-08 | Gilead Sciences Inc | Compuestos de 6-azabenzimidazol sustituidos como inhibidores de hpk1. |
| WO2020128972A1 (en) | 2018-12-20 | 2020-06-25 | 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 |
| WO2020140052A1 (en) * | 2018-12-28 | 2020-07-02 | Spv Therapeutics Inc. | Cyclin-dependent kinase inhibitors |
| EP3902805A4 (en) | 2018-12-28 | 2023-03-01 | SPV Therapeutics Inc. | CYCLINE-DEPENDENT KINASE INHIBITORS |
| AU2020211071A1 (en) | 2019-01-23 | 2021-07-15 | Novartis Ag | New crystalline forms of a succinate salt of 7-Cyclopentyl-2-(5-piperazin-1-yl-pyridin-2-ylamino)-7H-pyrrolo[2,3-d]pyrimidine -6-carboxylic acid dimethylamide |
| MX2021009563A (es) | 2019-02-12 | 2021-09-08 | Novartis Ag | Combinacion farmaceutica que comprende tno155 y ribociclib. |
| ES3032659T3 (en) | 2019-02-15 | 2025-07-23 | Novartis Ag | 3-(1-oxo-5-(piperidin-4-yl)isoindolin-2-yl)piperidine-2,6-dione derivatives and uses thereof |
| ES2982474T3 (es) | 2019-02-15 | 2024-10-16 | Novartis Ag | Derivados de 3-(1-oxoisoindolin-2-il)piperidin-1,6-diona sustituidos y usos de estos |
| TW202521536A (zh) | 2019-05-05 | 2025-06-01 | 美商基尼特奇公司 | Cdk抑制劑 |
| WO2020225827A1 (en) | 2019-05-08 | 2020-11-12 | Mylan Laboratories Limited | Novel polymorphs of ribociclib succinate |
| EP4563150A3 (en) | 2019-05-13 | 2025-07-23 | 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 |
| UY38700A (es) | 2019-05-20 | 2020-12-31 | Novartis Ag | Conjugados de anticuerpo-fármaco inhibidores de mcl-1 y sus métodos de uso |
| TWI826690B (zh) | 2019-05-23 | 2023-12-21 | 美商基利科學股份有限公司 | 經取代之烯吲哚酮化物及其用途 |
| JP7595593B2 (ja) * | 2019-06-04 | 2024-12-06 | ステップ ファーマ エス.エー.エス | 増殖性疾患の治療のための、ヒトctps1阻害剤としてのn-(5-(6-エトキシピラジン-2-イル)ピリジン-2-イル)-4-(2-(メチルスルホンアミド)ピリミジン-4-イル)テトラヒドロ-2h-ピラン-4-カルボキサミド誘導体及び関連化合物 |
| 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 |
| EP4021450B1 (en) | 2019-08-26 | 2025-11-05 | Arvinas Operations, Inc. | Methods of treating breast cancer with tetrahydronaphthalene derivatives as estrogen receptor degraders |
| WO2021038590A1 (en) | 2019-08-30 | 2021-03-04 | Mylan Laboratories Limited | Novel polymorph of ribociclib succinate |
| US20220348651A1 (en) | 2019-09-18 | 2022-11-03 | 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 |
| IL293940A (en) | 2019-12-16 | 2022-08-01 | Lunella Biotech Inc | Selective cancer drugs cdk4/6 inhibitors |
| CA3164619A1 (en) | 2019-12-16 | 2021-06-24 | Lunella Biotech, Inc. | Selective cdk4/6 inhibitor cancer therapeutics |
| DK4077307T3 (da) | 2019-12-18 | 2025-05-26 | Crinetics Pharmaceuticals Inc | Gem-disubstituerede piperidinmelanocortin subtype-2-receptor- (mc2r)-antagonister og anvendelser deraf |
| MX2022007759A (es) | 2019-12-20 | 2022-07-19 | Novartis Ag | Combinacion del anticuerpo anti tim-3 mbg453 y anticuerpo anti tgf-beta nis793, con o sin decitabina o el anticuerpo anti pd-1 spartalizumab, para el tratamiento de mielofibrosis y sindrome mielodisplasico. |
| ES3032933T3 (en) | 2019-12-23 | 2025-07-29 | 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 |
| CN114245753A (zh) * | 2020-03-27 | 2022-03-25 | 江苏康宁杰瑞生物制药有限公司 | 用于肿瘤治疗的抗her2抗体与cdk抑制剂的组合 |
| JP2023525100A (ja) | 2020-05-12 | 2023-06-14 | ノバルティス アーゲー | Craf阻害剤を含む治療的組み合わせ |
| 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 |
| EP4140997A4 (en) * | 2020-05-12 | 2023-09-06 | Suzhou Alphama Biotechnology Co., Ltd. | PYRIDINE ACETAMIDE DERIVATIVE AS CDK INHIBITOR, PREPARATION METHOD AND USE THEREOF |
| AU2021273744A1 (en) | 2020-05-19 | 2022-12-08 | Pharmacosmos Holding A/S | Cyclin-dependent kinase inhibiting compounds for the treatment of medical disorders |
| KR20230023661A (ko) * | 2020-06-11 | 2023-02-17 | 루넬라 바이오테크 인코포레이티드 | 선택적 cdk4/6 억제제 암 치료제 |
| US10988479B1 (en) | 2020-06-15 | 2021-04-27 | G1 Therapeutics, Inc. | Morphic forms of trilaciclib and methods of manufacture thereof |
| MX2022015852A (es) | 2020-06-23 | 2023-01-24 | Novartis Ag | Regimen de dosificacion que comprende derivados de 3-(1-oxoisoindolin-2-il)piperidina-2,6-diona. |
| EP4188549A1 (en) | 2020-08-03 | 2023-06-07 | Novartis AG | Heteroaryl substituted 3-(1-oxoisoindolin-2-yl)piperidine-2,6-dione derivatives and uses thereof |
| 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 |
| US20240042051A1 (en) | 2020-11-24 | 2024-02-08 | Francesca Rocchetti | Mcl-1 inhibitor antibody-drug conjugates and methods of use |
| PE20240225A1 (es) | 2020-11-24 | 2024-02-16 | Novartis Ag | Anticuerpos anti-cd48, conjugados de anticuerpo-farmaco, y usos de los mismos |
| 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 |
| AU2022218128A1 (en) | 2021-02-02 | 2023-08-17 | Les Laboratoires Servier | Selective bcl-xl protac compounds and methods of use |
| US12280046B2 (en) | 2021-03-19 | 2025-04-22 | Crinetics Pharmaceuticals, Inc. | Melanocortin subtype-2 receptor (MC2R) antagonist for the treatment of disease |
| 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 |
| EP4333847A1 (en) | 2021-05-05 | 2024-03-13 | Novartis AG | Compounds and compositions for the treatment of mpnst |
| AR125874A1 (es) | 2021-05-18 | 2023-08-23 | Novartis Ag | Terapias de combinación |
| TW202320795A (zh) | 2021-07-26 | 2023-06-01 | 美商凱爾科迪股份有限公司 | 使用1-(4-{[4-(二甲胺基)哌啶-1-基]羰基}苯基)-3-[4-(4,6-二嗎啉-4-基-1,3,5-三-2-基)苯基]脲治療癌症之方法 |
| 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 |
| US12275738B2 (en) | 2022-04-08 | 2025-04-15 | Biolexis Therapeutics, Inc. | CDK9 inhibitors |
| EP4504709A1 (en) * | 2022-04-08 | 2025-02-12 | Biolexis Therapeutics, Inc. | Cdk9 inhibitors |
| US20250339547A1 (en) | 2022-05-20 | 2025-11-06 | Novartis Ag | Met bcl-xl inhibitor antibody-drug conjugates and methods of use thereof |
| EP4525925A1 (en) | 2022-05-20 | 2025-03-26 | Novartis AG | Epha2 bcl-xl inhibitor antibody-drug conjugates and methods of use thereof |
| TWI866427B (zh) | 2022-08-31 | 2024-12-11 | 美商亞文納營運公司 | 雌激素受體降解劑之給藥方案 |
| 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 |
| WO2024189481A1 (en) | 2023-03-10 | 2024-09-19 | 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 |
| WO2025219830A1 (en) | 2024-04-15 | 2025-10-23 | Novartis Ag | Pharmaceutical compositions of ribociclib |
| WO2025235331A1 (en) * | 2024-05-07 | 2025-11-13 | Nikang Therapeutics, Inc. | Bifunctional compounds containing pyrazolopyrimidine derivatives for degrading certain cyclin-dependent kinase via ubiquitin proteasome pathway |
| 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 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007140222A2 (en) * | 2006-05-26 | 2007-12-06 | Novartis Ag | Pyrrolopyrimidine compounds and their uses |
Family Cites Families (39)
| 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 |
| WO1998004689A1 (en) | 1995-07-31 | 1998-02-05 | Urocor, Inc. | Biomarkers and targets for diagnosis, prognosis and management of prostate disease |
| JP4291696B2 (ja) * | 2002-01-22 | 2009-07-08 | ワーナー−ランバート カンパニー リミテッド ライアビリティー カンパニー | 2−(ピリジン−2−イルアミノ)−ピリド[2,3−d]ピリミジン−7−オン |
| RU2301233C2 (ru) | 2002-03-07 | 2007-06-20 | Ф.Хоффманн-Ля Рош Аг | Бициклические пиридины и пиримидины в качестве ингибиторов киназы р38 |
| JP4881558B2 (ja) | 2002-09-04 | 2012-02-22 | シェーリング コーポレイション | サイクリン依存性キナーゼインヒビターとしてのピラゾロピリミジン |
| WO2004065378A1 (en) * | 2003-01-17 | 2004-08-05 | Warner-Lambert Company Llc | 2-aminopyridine substituted heterocycles as inhibitors of cellular proliferation |
| CN1878773A (zh) | 2003-09-05 | 2006-12-13 | 神经能质公司 | 作为crf1受体配位体的杂芳基稠合的吡啶,吡嗪及嘧啶 |
| WO2005023761A2 (en) | 2003-09-11 | 2005-03-17 | Kemia, Inc. | Cytokine inhibitors |
| US7319102B1 (en) | 2003-12-09 | 2008-01-15 | The Procter & Gamble Company | Pyrrolo[2,3-d]pyrimidine cytokine inhibitors |
| PL1713806T3 (pl) * | 2004-02-14 | 2013-09-30 | Irm Llc | Związki i kompozycje jako inhibitory kinaz białkowych |
| US20070270588A1 (en) | 2004-03-05 | 2007-11-22 | Taisho Pharmaceutical Co., Ltd. | Pyrrolopyrimidine Derivatives |
| WO2005107760A1 (en) | 2004-04-30 | 2005-11-17 | Irm Llc | Compounds and compositions as inducers of keratinocyte differentiation |
| JP2008506761A (ja) | 2004-07-22 | 2008-03-06 | アステックス、セラピューティックス、リミテッド | プロテインキナーゼ阻害剤としてのチアゾールおよびイソチアゾール誘導体 |
| WO2006042102A2 (en) | 2004-10-05 | 2006-04-20 | Neurogen Corporation | Pyrrolo-pyridine, pyrrolo-pyrimidine and related heterocyclic compounds |
| CA2577588C (en) | 2004-10-29 | 2013-09-10 | 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 |
| AU2006205851A1 (en) * | 2005-01-14 | 2006-07-20 | Janssen Pharmaceutica N.V. | 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 |
| GB0526246D0 (en) | 2005-12-22 | 2006-02-01 | Novartis Ag | Organic compounds |
| AU2006331765A1 (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 |
| CA2646429A1 (en) | 2006-03-09 | 2007-09-13 | Pharmacopeia, Inc. | 8-heteroarylpurine mnk2 inhibitors for treating metabolic disorders |
| US7998978B2 (en) | 2006-05-01 | 2011-08-16 | Pfizer Inc. | Substituted 2-amino-fused heterocyclic compounds |
| US8841312B2 (en) * | 2007-12-19 | 2014-09-23 | Amgen Inc. | Fused pyridine, pyrimidine and triazine compounds as cell cycle inhibitors |
| CN101981036B (zh) * | 2008-02-06 | 2013-09-04 | 诺瓦提斯公司 | 吡咯并[2,3-d]嘧啶及其作为酪氨酸激酶抑制剂的用途 |
| ES2522346T3 (es) * | 2008-08-22 | 2014-11-14 | Novartis Ag | Compuestos de pirrolopirimidina como inhibidores de CDK |
| GB0819105D0 (en) | 2008-10-17 | 2008-11-26 | Chroma Therapeutics Ltd | Pyrrolo-pyrimidine compounds |
| 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 |
| US20130035336A1 (en) | 2010-04-13 | 2013-02-07 | Novartis Ag | Combination comprising a cyclin dependent kinase 4 or cyclin dependent kinase (cdk4/6) inhibitor for treating cancer |
-
2009
- 2009-08-20 ES ES09782051.8T patent/ES2522346T3/es active Active
- 2009-08-20 CN CN200980141314.0A patent/CN102186856B/zh active Active
- 2009-08-20 AU AU2009284098A patent/AU2009284098B2/en active Active
- 2009-08-20 HR HRP20141018AT patent/HRP20141018T1/hr unknown
- 2009-08-20 GE GEAP200912114A patent/GEP20135785B/en unknown
- 2009-08-20 RS RSP20140536 patent/RS53574B1/sr unknown
- 2009-08-20 NZ NZ591176A patent/NZ591176A/xx unknown
- 2009-08-20 EP EP09782051.8A patent/EP2331547B1/en active Active
- 2009-08-20 PL PL09782051T patent/PL2331547T3/pl unknown
- 2009-08-20 EA EA201100355A patent/EA019094B1/ru active Protection Beyond IP Right Term
- 2009-08-20 DK DK09782051.8T patent/DK2331547T3/da active
- 2009-08-20 PT PT97820518T patent/PT2331547E/pt unknown
- 2009-08-20 KR KR1020117006436A patent/KR101353857B1/ko active Active
- 2009-08-20 ME MEP-2011-25A patent/ME01282B/me unknown
- 2009-08-20 PE PE2011000180A patent/PE20110419A1/es active IP Right Grant
- 2009-08-20 CN CN201410068898.6A patent/CN103788100A/zh active Pending
- 2009-08-20 MY MYPI20110681 patent/MY150560A/en unknown
- 2009-08-20 SI SI200931040T patent/SI2331547T1/sl unknown
- 2009-08-20 WO PCT/EP2009/060793 patent/WO2010020675A1/en not_active Ceased
- 2009-08-20 JO JO2009319A patent/JO2924B1/en active
- 2009-08-20 US US13/060,154 patent/US8685980B2/en active Active
- 2009-08-20 UA UAA201102052A patent/UA103628C2/ru unknown
- 2009-08-20 EP EP13197275.4A patent/EP2716643A1/en not_active Withdrawn
- 2009-08-20 KR KR1020137031722A patent/KR20130140222A/ko not_active Ceased
- 2009-08-20 BR BRPI0917791-4A patent/BRPI0917791B1/pt active IP Right Grant
- 2009-08-20 CA CA2734802A patent/CA2734802C/en active Active
- 2009-08-20 JP JP2011523425A patent/JP5560496B2/ja active Active
- 2009-08-20 MX MX2011001879A patent/MX2011001879A/es active IP Right Grant
- 2009-08-21 AR ARP090103233A patent/AR073116A1/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 UY UY0001038935A patent/UY38935A/es not_active Application Discontinuation
- 2009-08-21 TW TW98128319A patent/TWI468409B/zh active
-
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 DO DO2011000057A patent/DOP2011000057A/es unknown
- 2011-02-21 NI NI201100042A patent/NI201100042A/es unknown
- 2011-02-21 CU CU2011000040A patent/CU24062B1/es active IP Right Grant
- 2011-02-22 CR CR20110101A patent/CR20110101A/es unknown
- 2011-02-22 EC EC2011010843A patent/ECSP11010843A/es unknown
- 2011-02-22 HN HN2011000542A patent/HN2011000542A/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 LU LU00048C patent/LUC00048I2/fr unknown
- 2017-11-09 NL NL300909C patent/NL300909I2/nl 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
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007140222A2 (en) * | 2006-05-26 | 2007-12-06 | Novartis Ag | Pyrrolopyrimidine compounds and their uses |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AU2009284098B2 (en) | Pyrrolopyrimidine compounds as CDK inhibitors | |
| AU2008333136B2 (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 |
|---|---|---|---|
| DA2 | Applications for amendment section 104 |
Free format text: THE NATURE OF THE AMENDMENT IS: AMEND THE NAME OF THE INVENTOR TO READ BESONG, GILBERT; BRAIN, CHRISTOPHER THOMAS; BROOKS, CLINTON A.; CONGREVE, MILES STUART; DAGOSTIN, CLAUDIO; HE, GUO; HOU, YING; HOWARD, STEVEN; LI, YUE; LU, YIPIN; MORTENSON, PAUL; SMITH, TROY; SUNG, MOO; WOODHEAD, STEVEN; WRONA, WOJCIECH AND BAHARAT, LAGU. |
|
| DA3 | Amendments made section 104 |
Free format text: THE NATURE OF THE AMENDMENT IS: AMEND THE NAME OF THE INVENTOR TO READ BESONG, GILBERT; BRAIN, CHRISTOPHER THOMAS; BROOKS, CLINTON A.; CONGREVE, MILES STUART; DAGOSTIN, CLAUDIO; HE, GUO; HOU, YING; HOWARD, STEVEN; LI, YUE; LU, YIPIN; MORTENSON, PAUL; SMITH, TROY; SUNG, MOO; WOODHEAD, STEVEN; WRONA, WOJCIECH AND LAGU, BAHARAT |
|
| DA2 | Applications for amendment section 104 |
Free format text: THE NATURE OF THE AMENDMENT IS: AMEND THE NAME OF THE INVENTOR TO READ ESONG, GILBERT; BRAIN, CHRISTOPHER THOMAS; BROOKS, CLINTON A.; CONGREVE, MILES STUART; DAGOSTIN, CLAUDIO; HE, GUO; HOU, YING; HOWARD, STEVEN; LI, YUE; LU, YIPIN; MORTENSON, PAUL; SMITH, TROY; SUNG, MOO; WOODHEAD, STEVEN; WRONA, WOJCIECH AND LAGU, BHARAT . |
|
| TH | Corrigenda |
Free format text: IN VOL 26 , NO 37 , PAGE(S) 4869 UNDER THE HEADING AMENDMENTS - AMENDMENTS MADE DELETE ALL REFERENCE TO 2009284098 |
|
| DA3 | Amendments made section 104 |
Free format text: THE NATURE OF THE AMENDMENT IS: AMEND THE NAME OF THE INVENTOR TO READ BESONG, GILBERT; BRAIN, CHRISTOPHER THOMAS; BROOKS, CLINTON A.; CONGREVE, MILES STUART; DAGOSTIN, CLAUDIO; HE, GUO; HOU, YING; HOWARD, STEVEN; LI, YUE; LU, YIPIN; MORTENSON, PAUL; SMITH, TROY; SUNG, MOO; WOODHEAD, STEVEN; WRONA, WOJCIECH AND LAGU, BHARAT |
|
| FGA | Letters patent sealed or granted (standard patent) | ||
| NC | Extension of term for standard patent requested (sect. 70) |
Free format text: PRODUCT NAME: KISQALI RIBOCICLIB Filing date: 20171023 |
|
| NDA | Extension of term for standard patent accepted (sect.70) |
Free format text: PRODUCT NAME: KISQALI RIBOCICLIB Filing date: 20171023 |
|
| NDB | Extension of term for standard patent granted (sect.76) |
Free format text: PRODUCT NAME: KISQALI RIBOCICLIB Filing date: 20171023 Extension date: 20321023 |