PE20050700A1 - SAL DE ISETIONATO DE 6-ACETIL-8-CICLOPENTIL-5-METIL-2-(5-PIPERAZIN-1-IL-PIRIDIN-2-ILAMINO)-8H-PIRIDO[2,3-d]PIRIMIDIN-7-ONA COMO INHIBIDOR SELECTIVO DE CDK4 - Google Patents
SAL DE ISETIONATO DE 6-ACETIL-8-CICLOPENTIL-5-METIL-2-(5-PIPERAZIN-1-IL-PIRIDIN-2-ILAMINO)-8H-PIRIDO[2,3-d]PIRIMIDIN-7-ONA COMO INHIBIDOR SELECTIVO DE CDK4Info
- Publication number
- PE20050700A1 PE20050700A1 PE2004000652A PE2004000652A PE20050700A1 PE 20050700 A1 PE20050700 A1 PE 20050700A1 PE 2004000652 A PE2004000652 A PE 2004000652A PE 2004000652 A PE2004000652 A PE 2004000652A PE 20050700 A1 PE20050700 A1 PE 20050700A1
- Authority
- PE
- Peru
- Prior art keywords
- pyridin
- ilamine
- salt
- cyclopentil
- ona
- Prior art date
Links
- SUMDYPCJJOFFON-UHFFFAOYSA-N isethionic acid Chemical class OCCS(O)(=O)=O SUMDYPCJJOFFON-UHFFFAOYSA-N 0.000 title abstract 4
- 102000013701 Cyclin-Dependent Kinase 4 Human genes 0.000 title abstract 2
- 108010025464 Cyclin-Dependent Kinase 4 Proteins 0.000 title abstract 2
- 229940124639 Selective inhibitor Drugs 0.000 title 1
- 239000000203 mixture Substances 0.000 abstract 3
- 239000002904 solvent Substances 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 238000001237 Raman spectrum Methods 0.000 abstract 1
- 230000001419 dependent effect Effects 0.000 abstract 1
- 238000001938 differential scanning calorimetry curve Methods 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 230000002757 inflammatory effect Effects 0.000 abstract 1
- 229940045996 isethionic acid Drugs 0.000 abstract 1
- 229940043355 kinase inhibitor Drugs 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- JTJMJGYZQZDUJJ-UHFFFAOYSA-N phencyclidine Chemical compound C1CCCCN1C1(C=2C=CC=CC=2)CCCCC1 JTJMJGYZQZDUJJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 abstract 1
- 238000000634 powder X-ray diffraction Methods 0.000 abstract 1
- 230000002062 proliferating effect Effects 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Diabetes (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Rheumatology (AREA)
- Cardiology (AREA)
- Endocrinology (AREA)
- Neurology (AREA)
- Vascular Medicine (AREA)
- Virology (AREA)
- Hematology (AREA)
- Transplantation (AREA)
- Biomedical Technology (AREA)
- Emergency Medicine (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Obesity (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Reproductive Health (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
SE REFIERE A UNA SAL MONO-ISETIONATO DE 6-ACETIL-8-CICLOPENTIL-5-METIL-2-(5-PIPERAZIN-1-IL-PIRIDIN-2-ILAMINO)-8H-PIRIDO[2,3-d]PIRIMIDIN-7-ONA, QUE PUEDE PRESENTARSE COMO LOS POLIMORFOS DE FORMA A, B Y D, DONDE CADA UNO PUEDE DISTINGUIRSE POR SU PERFIL DE PXRD, ESPECTRO RAMAN Y TERMOGRAMA DSC. TAMBIEN SE REFIERE A METODOS DE PREPARACION DE LA SAL DE ISETIONATO, QUE COMPRENDE EN COMBINAR UNA SOLUCION DE ACIDO ISETIONICO Y UN PRIMER DISOLVENTE A UNA MEZCLA ACUOSA DEL COMPUESTO, PARA PRODUCIR UNA PRIMERA MEZCLA, TAMBIEN INCLUYE LIOFILIZAR LA MEZCLA PARA DAR UNA SAL AMORFA QUE POSTERIORMENTE SE COMBINARA CON UN SEGUNDO DISOLVENTE PARA PRODUCIR UNA SEGUNDA MEZCLA QUE INCLUYE LA SAL DE ISETRIONATO CRISTALINA, Y OPCIONALMENTE CALENTAR Y/O REFRIGERAR, EL PRIMER Y SEGUNDO DISOLVENTE PUEDEN SER LOS MISMOS, Y SON MISCIBLES EN AGUA COMO METANOL, ETANOL U OTROS ALCOHOLES. TAMBIEN SE REFIERE A UNA COMPOSICION FARMACEUTICA QUE LOS CONTIENE, ESTE COMPUESTO ES UN INHIBIDOR DE QUINASA SELECTIVA DEPENDIENTE DE CICLINA 4 (CDK4) Y ES UTIL PARA TRATAR ENFERMEDADES INFLAMATORIAS Y PROLIFERATIVAS DE CELULAS ANORMALES TALES COMO EL CANCER Y REESTENOSIS
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US48635103P | 2003-07-11 | 2003-07-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20050700A1 true PE20050700A1 (es) | 2005-10-18 |
Family
ID=34062121
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2004000652A PE20050700A1 (es) | 2003-07-11 | 2004-07-07 | SAL DE ISETIONATO DE 6-ACETIL-8-CICLOPENTIL-5-METIL-2-(5-PIPERAZIN-1-IL-PIRIDIN-2-ILAMINO)-8H-PIRIDO[2,3-d]PIRIMIDIN-7-ONA COMO INHIBIDOR SELECTIVO DE CDK4 |
Country Status (31)
| Country | Link |
|---|---|
| US (2) | US7345171B2 (es) |
| EP (1) | EP1648889B1 (es) |
| JP (1) | JP4053073B2 (es) |
| KR (1) | KR100816945B1 (es) |
| CN (1) | CN1835951B (es) |
| AR (1) | AR045898A1 (es) |
| AT (1) | ATE412650T1 (es) |
| AU (1) | AU2004255934B2 (es) |
| BR (1) | BRPI0412516A (es) |
| CA (1) | CA2532049C (es) |
| CL (1) | CL2004001701A1 (es) |
| CY (1) | CY1108589T1 (es) |
| DE (1) | DE602004017474D1 (es) |
| DK (1) | DK1648889T3 (es) |
| ES (1) | ES2313016T3 (es) |
| GT (1) | GT200400130A (es) |
| IL (1) | IL173034A (es) |
| MX (1) | MXPA06000484A (es) |
| NL (1) | NL1026624C2 (es) |
| NO (1) | NO335100B1 (es) |
| NZ (1) | NZ544609A (es) |
| PA (1) | PA8606501A1 (es) |
| PE (1) | PE20050700A1 (es) |
| PL (1) | PL1648889T3 (es) |
| PT (1) | PT1648889E (es) |
| RU (1) | RU2317296C2 (es) |
| SI (1) | SI1648889T1 (es) |
| TW (1) | TWI288750B (es) |
| UY (1) | UY28404A1 (es) |
| WO (1) | WO2005005426A1 (es) |
| ZA (1) | ZA200600230B (es) |
Families Citing this family (127)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GEP20063909B (en) | 2002-01-22 | 2006-08-25 | Warner Lambert Co | 2-(PYRIDIN-2-YLAMINO)-PYRIDO[2,3d] PYRIMIDIN-7-ONES |
| EP1740184A1 (en) * | 2004-03-30 | 2007-01-10 | Pfizer Products Incorporated | Combinations of signal transduction inhibitors |
| WO2007044813A1 (en) * | 2005-10-07 | 2007-04-19 | Exelixis, Inc. | PYRIDOPYRIMIDINONE INHIBITORS OF PI3Kα |
| JP5480503B2 (ja) * | 2005-10-07 | 2014-04-23 | エクセリクシス, インク. | PI3Kαのピリドピリミジノン型阻害剤 |
| RU2009108006A (ru) * | 2006-09-08 | 2010-10-20 | Пфайзер Продактс Инк. (Us) | Синтез 2-(пиридин-2-иламино)-пиридо[2, 3-d]пиримидин-7-онов |
| PL2074122T3 (pl) | 2006-09-15 | 2011-10-31 | Pfizer Prod Inc | Związki pirydo(2,3-D)pirymidynonowe i ich zastosowanie jako inhibitory PI3 |
| WO2008063888A2 (en) | 2006-11-22 | 2008-05-29 | Plexxikon, Inc. | Compounds modulating c-fms and/or c-kit activity and uses therefor |
| CA2672898A1 (en) * | 2006-12-14 | 2008-06-26 | Panacea Pharmaceuticals, Inc. | Methods of neuroprotection by cyclin-dependent kinase inhibition |
| WO2009061345A2 (en) * | 2007-11-07 | 2009-05-14 | Cornell Research Foundation, Inc. | Targeting cdk4 and cdk6 in cancer therapy |
| AU2008343932B2 (en) * | 2007-12-19 | 2013-08-15 | Amgen Inc. | Fused pyridine, pyrimidine and triazine compounds as cell cycle inhibitors |
| ATE531372T1 (de) * | 2008-04-07 | 2011-11-15 | Amgen Inc | Gem-disubstituierte und spirocyclische aminopyridine/pyrimidine als zellcyclus- inhibitoren |
| AU2009298367A1 (en) * | 2008-10-01 | 2010-04-08 | The University Of North Carolina At Chapel Hill | Hematopoietic protection against chemotherapeutic compounds using selective cyclin-dependent kinase 4/6 inhibitors |
| AU2009310352A1 (en) * | 2008-10-01 | 2010-05-06 | The University Of North Carolina At Chapel Hill | Hematopoietic protection against ionizing radiation using selective cyclin-dependent kinase 4/6 inhibitors |
| PA8852901A1 (es) | 2008-12-22 | 2010-07-27 | Lilly Co Eli | Inhibidores de proteina cinasa |
| EA022924B1 (ru) | 2009-04-03 | 2016-03-31 | Ф.Хоффманн-Ля Рош Аг | ТВЁРДАЯ ФОРМА {3-[5-(4-ХЛОРФЕНИЛ)-1Н-ПИРРОЛО[2,3-b]ПИРИДИН-3-КАРБОНИЛ]-2,4-ДИФТОРФЕНИЛ}АМИДА ПРОПАН-1-СУЛЬФОНОВОЙ КИСЛОТЫ И ЕЁ ПРИМЕНЕНИЕ |
| EP3025724B1 (en) | 2009-05-13 | 2018-07-11 | The University of North Carolina At Chapel Hill | Cyclin dependent kinase inhibitors and methods of use |
| NZ629615A (en) | 2009-11-06 | 2016-01-29 | Plexxikon Inc | Compounds and methods for kinase modulation, and indications therefor |
| PH12012501361A1 (en) | 2009-12-31 | 2012-10-22 | Centro Nac De Investigaciones Oncologicas Cnio | Tricyclic compounds for use as kinase inhibitors |
| TWI510487B (zh) | 2010-04-21 | 2015-12-01 | Plexxikon Inc | 用於激酶調節的化合物和方法及其適應症 |
| US8691830B2 (en) | 2010-10-25 | 2014-04-08 | G1 Therapeutics, Inc. | CDK inhibitors |
| CN103501789A (zh) * | 2010-11-17 | 2014-01-08 | 北卡罗来纳大学查珀尔希尔分校 | 通过抑制增殖性激酶cdk4和cdk6保护肾组织免于局部缺血 |
| WO2012098387A1 (en) | 2011-01-18 | 2012-07-26 | Centro Nacional De Investigaciones Oncológicas (Cnio) | 6, 7-ring-fused triazolo [4, 3 - b] pyridazine derivatives as pim inhibitors |
| SI2672967T1 (sl) | 2011-02-07 | 2018-12-31 | Plexxikon Inc. | Spojine in postopki za kinazno modulacijo in indikacije zanjo |
| WO2012129344A1 (en) | 2011-03-23 | 2012-09-27 | Amgen Inc. | Fused tricyclic dual inhibitors of cdk 4/6 and flt3 |
| EP2721686B1 (en) | 2011-06-17 | 2018-11-28 | NantEnergy, Inc. | Ionic liquid containing sulfonate ions |
| WO2013148748A1 (en) | 2012-03-29 | 2013-10-03 | Francis Xavier Tavares | Lactam kinase inhibitors |
| US9150570B2 (en) | 2012-05-31 | 2015-10-06 | Plexxikon Inc. | Synthesis of heterocyclic compounds |
| EP2958916B1 (en) * | 2013-02-21 | 2018-09-12 | Pfizer Inc | Solid forms of a selective cdk4/6 inhibitor |
| CA2904054A1 (en) * | 2013-03-15 | 2014-09-25 | Concert Pharmaceuticals, Inc. | Deuterated palbociclib |
| 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 |
| WO2014203129A1 (en) | 2013-06-19 | 2014-12-24 | Olema Pharmaceuticals, Inc. | Combinations of benzopyran compounds, compositions and uses thereof |
| US20150297608A1 (en) | 2014-04-17 | 2015-10-22 | G1 Therapeutics, Inc. | Tricyclic Lactams for Use as Anti-Neoplastic and Anti-Proliferative Agents |
| JP6631616B2 (ja) * | 2014-07-26 | 2020-01-15 | ノース・アンド・サウス・ブラザー・ファーマシー・インベストメント・カンパニー・リミテッド | CDK阻害剤としての2−アミノ−ピリド[2,3−d]ピリミジン−7(8H)−オン誘導体及びその使用 |
| EP3174878A4 (en) * | 2014-07-31 | 2017-12-27 | Sun Pharmaceutical Industries Limited | A process for the preparation of palbociclib |
| WO2016024249A1 (en) * | 2014-08-14 | 2016-02-18 | Sun Pharmaceutical Industries Limited | Crystalline forms of palbociclib |
| 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 |
| WO2016040858A1 (en) | 2014-09-12 | 2016-03-17 | G1 Therapeutics, Inc. | Combinations and dosing regimes to treat rb-positive tumors |
| CN105622638B (zh) * | 2014-10-29 | 2018-10-02 | 广州必贝特医药技术有限公司 | 嘧啶或吡啶并吡啶酮类化合物及其制备方法和应用 |
| WO2016066420A1 (en) * | 2014-10-29 | 2016-05-06 | Sandoz Ag | Crystalline forms of palbociclib monohydrochloride |
| CN105616419A (zh) * | 2014-11-07 | 2016-06-01 | 江苏豪森药业集团有限公司 | 含有细胞周期蛋白抑制剂固体分散体的药物组合物及其制备方法 |
| CN105616418A (zh) * | 2014-11-07 | 2016-06-01 | 江苏豪森药业集团有限公司 | 含有细胞周期蛋白抑制剂的药物制剂及其制备方法 |
| CA2967595A1 (en) | 2014-11-12 | 2016-05-19 | Siamab Therapeutics, Inc. | Glycan-interacting compounds and methods of use |
| WO2016090257A1 (en) * | 2014-12-05 | 2016-06-09 | Crystal Pharmatech Inc. | Salts and crystalline forms of 6-acetyl-8-cyclopentyl-5-methyl-2((5-(piperazin-1-yl)pyridin-2-yl)amino)pyrido[2,3-d] pyrimidin-7(8h)-one (palbociclib) |
| WO2016092442A1 (en) * | 2014-12-08 | 2016-06-16 | Sun Pharmaceutical Industries Limited | Processes for the preparation of crystalline forms of palbociclib acetate |
| CN105732615B (zh) * | 2014-12-31 | 2018-05-01 | 山东轩竹医药科技有限公司 | Cdk激酶抑制剂 |
| SI3255046T1 (sl) * | 2015-02-03 | 2020-02-28 | Jiangsu Hengrui Medicine Co., Ltd. | Hidroksietil sulfonat zaviralca od ciklina odvisne protein-kinaze, njegova kristalinična oblika in postopek priprave le-teh |
| CZ201589A3 (cs) | 2015-02-11 | 2016-08-24 | Zentiva, K.S. | Pevné formy soli Palbociclibu |
| AR104068A1 (es) | 2015-03-26 | 2017-06-21 | Hoffmann La Roche | Combinaciones de un compuesto inhibidor de fosfoinosítido 3-cinasa y un compuesto inhibidor de cdk4/6 para el tratamiento del cáncer |
| WO2016156070A1 (en) | 2015-04-02 | 2016-10-06 | Sandoz Ag | Modified particles of palbociclib |
| EP3078663A1 (en) | 2015-04-09 | 2016-10-12 | Sandoz Ag | Modified particles of palbociclib |
| CN104910149A (zh) * | 2015-04-28 | 2015-09-16 | 上海百奇医药科技有限公司 | 一种Palbociclib制备方法 |
| CN106117199A (zh) * | 2015-05-04 | 2016-11-16 | 江苏恒瑞医药股份有限公司 | 一种细胞周期蛋白依赖性激酶抑制剂的二羟乙基磺酸盐、其结晶形式及其制备方法 |
| RU2695337C2 (ru) * | 2015-05-29 | 2019-07-23 | Тейдзин Фарма Лимитед | ПРОИЗВОДНОЕ ПИРИДО[3,4-d]ПИРИМИДИНА И ЕГО ФАРМАЦЕВТИЧЕСКИ ПРИЕМЛЕМАЯ СОЛЬ |
| HUE047477T2 (hu) * | 2015-06-04 | 2020-04-28 | Pfizer | Palbociclib szilárd dózisformái |
| CN106317053A (zh) * | 2015-06-29 | 2017-01-11 | 北大方正集团有限公司 | 一种帕博昔布晶型a的制备方法 |
| SI3331881T1 (sl) | 2015-08-05 | 2019-08-30 | Ratiopharm Gmbh | Nova kristalna oblika in adukti palbocikliba in matanojske kisline |
| CN105085517B (zh) * | 2015-08-06 | 2016-11-23 | 天津华洛康生物科技有限公司 | 一种结晶型帕博西尼游离碱水合物及其制备方法 |
| CN106474129A (zh) * | 2015-09-01 | 2017-03-08 | 上海方楠生物科技有限公司 | 一种帕博西林或其药学上可接受的盐与药用辅料的组合物及其制备方法 |
| HU230962B1 (hu) | 2015-10-28 | 2019-06-28 | Egis Gyógyszergyár Zrt. | Palbociclib sók |
| 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 |
| CN105418603A (zh) * | 2015-11-17 | 2016-03-23 | 重庆莱美药业股份有限公司 | 一种高纯度帕布昔利布及其反应中间体的制备方法 |
| CN106800554A (zh) * | 2015-11-26 | 2017-06-06 | 上海科胜药物研发有限公司 | 一种帕博西尼二盐酸盐的晶型及其制备方法 |
| CN106800553A (zh) * | 2015-11-26 | 2017-06-06 | 上海科胜药物研发有限公司 | 一种帕博西尼二羟乙基磺酸盐的晶型 |
| CN105541832A (zh) * | 2015-12-15 | 2016-05-04 | 南京艾德凯腾生物医药有限责任公司 | 一种羟乙基磺酸盐帕布昔利布的制备方法 |
| WO2017130219A1 (en) | 2016-01-25 | 2017-08-03 | Mylan Laboratories Limited | Amorphous solid dispersion of palbociclib |
| WO2017145054A1 (en) | 2016-02-24 | 2017-08-31 | Lupin Limited | Modified particles of crystalline palbociclib free base and process for the preparation thereof |
| CN107137409A (zh) * | 2016-03-01 | 2017-09-08 | 江苏恒瑞医药股份有限公司 | 一种cdk4/6抑制剂与雌激素受体拮抗剂联合在制备治疗乳腺癌的药物中的用途 |
| CN107137408A (zh) * | 2016-03-01 | 2017-09-08 | 江苏恒瑞医药股份有限公司 | 一种cdk4/6抑制剂与芳香化酶抑制剂联合在制备治疗乳腺癌的药物中的用途 |
| WO2017172734A1 (en) * | 2016-03-29 | 2017-10-05 | Mayo Foundation For Medical Education And Research | Treating cancer metastasis |
| US10449195B2 (en) | 2016-03-29 | 2019-10-22 | Shenzhen Pharmacin Co., Ltd. | Pharmaceutical formulation of palbociclib and a preparation method thereof |
| WO2018001270A1 (en) * | 2016-06-30 | 2018-01-04 | Noratech Pharmaceuticals, Inc. | Palbociclib prodrugs and composition thereof |
| WO2018005863A1 (en) | 2016-07-01 | 2018-01-04 | G1 Therapeutics, Inc. | Pyrimidine-based compounds for the treatment of cancer |
| EP3481825A1 (en) | 2016-07-07 | 2019-05-15 | Plantex Ltd. | Solid state forms of palbociclib dimesylate |
| PE20190475A1 (es) | 2016-08-15 | 2019-04-04 | Pfizer | Inhibidores de cdk2/4/6 |
| WO2018065999A1 (en) | 2016-10-07 | 2018-04-12 | Mylan Laboratories Limited | Novel polymorph of an intermediate for palbociclib synthesis |
| WO2018073574A1 (en) | 2016-10-20 | 2018-04-26 | Cipla Limited | Polymorphic forms of palbociclib |
| RU2019111887A (ru) | 2016-10-20 | 2020-11-20 | Пфайзер Инк. | Антипролиферативные средства для лечения лаг |
| WO2018091999A1 (en) | 2016-11-16 | 2018-05-24 | Pfizer Inc. | Combination of an egfr t790m inhibitor and a cdk inhibitor for the treatment of non-small cell lung cancer |
| US11401330B2 (en) | 2016-11-17 | 2022-08-02 | Seagen Inc. | Glycan-interacting compounds and methods of use |
| HRP20220065T1 (hr) * | 2016-11-28 | 2022-04-15 | Teijin Pharma Limited | Kristal derivata pirido[3,4-d]pirimidina ili njegov solvat |
| CA3048057A1 (en) | 2017-01-06 | 2018-07-12 | G1 Therapeutics, Inc. | Combination therapy for the treatment of cancer |
| CA3054939A1 (en) | 2017-03-03 | 2018-09-07 | Seattle Genetics, Inc. | Glycan-interacting compounds and methods of use |
| EP3612230A4 (en) * | 2017-04-21 | 2020-12-16 | Alnova Pharmaceuticals, Ltd. | PALBOCICLIB COMPOSITIONS AND RELATED METHODS |
| ES2988261T3 (es) | 2017-06-29 | 2024-11-19 | G1 Therapeutics Inc | Formas mórficas de GIT38 y métodos de fabricación de las mismas |
| EA202090402A1 (ru) | 2017-07-28 | 2020-05-19 | Синтон Б.В. | Фармацевтическая композиция, содержащая пальбоциклиб |
| CN111989099A (zh) | 2018-01-29 | 2020-11-24 | 贝塔制药有限公司 | 作为cdk4和cdk6抑制剂的2h-吲唑衍生物及其治疗用途 |
| EP3749654B1 (en) | 2018-02-06 | 2025-04-23 | The Board of Trustees of the University of Illinois | Substituted benzothiophene analogs as selective estrogen receptor degraders |
| WO2019166928A1 (en) | 2018-02-27 | 2019-09-06 | Pfizer Inc. | Combination of a cyclin dependent kinase inhibitor and a bet-bromodomain inhibitor |
| AU2019269159A1 (en) | 2018-05-14 | 2020-11-19 | Pfizer Inc. | Oral solution formulation |
| JP2021532139A (ja) | 2018-07-23 | 2021-11-25 | エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト | Pi3k阻害剤であるgdc−0077による癌の治療方法 |
| CN112839657B (zh) | 2018-08-24 | 2025-07-25 | 法码科思莫斯控股有限公司 | 1,4-二氮杂螺[5.5]十一烷-3-酮改进的合成 |
| JP6952747B2 (ja) | 2018-09-18 | 2021-10-20 | ファイザー・インク | がん処置のためのTGFβ阻害剤およびCDK阻害剤の組合せ |
| JP2022504388A (ja) | 2018-10-08 | 2022-01-13 | エフ・ホフマン-ラ・ロシュ・アクチェンゲゼルシャフト | Pi3kアルファ阻害剤およびメトホルミンを用いたがんの処置方法 |
| US11424484B2 (en) | 2019-01-24 | 2022-08-23 | Octet Scientific, Inc. | Zinc battery electrolyte additive |
| US20220125777A1 (en) | 2019-02-01 | 2022-04-28 | Pfizer Inc. | Combination of a cdk inhibitor and a pim inhibitor |
| JP2022534889A (ja) | 2019-05-24 | 2022-08-04 | ファイザー・インコーポレイテッド | Cdk阻害剤を使用した組合せ療法 |
| WO2020240360A1 (en) | 2019-05-24 | 2020-12-03 | Pfizer Inc. | Combination therapies using cdk inhibitors |
| 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 |
| CN110143948B (zh) * | 2019-06-21 | 2021-05-14 | 上海博悦生物科技有限公司 | Cdk4/6抑制剂、其药物组合物、制备方法及应用 |
| KR20220054347A (ko) | 2019-08-26 | 2022-05-02 | 아비나스 오퍼레이션스, 인코포레이티드 | 에스트로겐 수용체 분해제로서의 테트라히드로나프탈렌 유도체로 유방암을 치료하는 방법 |
| TW202133857A (zh) | 2019-12-03 | 2021-09-16 | 美商建南德克公司 | 用於乳癌治療之組合療法 |
| TW202146017A (zh) | 2020-03-05 | 2021-12-16 | 美商輝瑞股份有限公司 | 間變性淋巴瘤激酶抑制劑及周期蛋白依賴型激酶抑制劑之組合 |
| US10988479B1 (en) | 2020-06-15 | 2021-04-27 | G1 Therapeutics, Inc. | Morphic forms of trilaciclib and methods of manufacture thereof |
| PT4181920T (pt) | 2020-07-15 | 2025-11-04 | Ctxt Pty Ltd | Inibidor de kat6 e combinações para o tratamento do cancro da mama |
| JP2022020583A (ja) | 2020-07-20 | 2022-02-01 | ファイザー・インク | 併用療法 |
| WO2022063119A1 (zh) * | 2020-09-24 | 2022-03-31 | 南京济群医药科技股份有限公司 | 一种羟乙磺酸哌柏西利的组合物及药物 |
| CN114306245A (zh) | 2020-09-29 | 2022-04-12 | 深圳市药欣生物科技有限公司 | 无定形固体分散体的药物组合物及其制备方法 |
| WO2022091001A1 (en) | 2020-10-29 | 2022-05-05 | Pfizer Ireland Pharmaceuticals | Process for preparation of palbociclib |
| WO2022123419A1 (en) | 2020-12-08 | 2022-06-16 | Pfizer Inc. | Treatment of luminal subtypes of hr-positive, her2-negative early breast cancer with palbociclib |
| CN113845520A (zh) * | 2021-09-09 | 2021-12-28 | 安徽皓元药业有限公司 | 一种帕布昔利布乳清酸盐及其制备方法 |
| US20240398832A1 (en) | 2021-12-10 | 2024-12-05 | Eli Lilly And Company | Cdk4 and 6 inhibitor in combination with fulvestrant for the treatment of hormone receptor-positive, human epidermal growth factor receptor 2-negative advanced or metastatic breast cancer in patients previously treated with a cdk4 and 6 inhibitor |
| US20250049802A1 (en) | 2021-12-14 | 2025-02-13 | Pfizer Inc. | Combination therapies and uses for treating cancer |
| WO2023114264A1 (en) | 2021-12-15 | 2023-06-22 | Eli Lilly And Company | Combination for treatment of high-risk metastatic hormone-sensitive prostate cancer |
| CN114195784A (zh) * | 2021-12-29 | 2022-03-18 | 斯坦德标准技术研究(湖北)有限公司 | 帕博西尼有关物质及其制备方法和应用 |
| EP4302755B1 (en) | 2022-07-07 | 2025-08-20 | Lotus Pharmaceutical Co., Ltd. | Palbociclib formulation containing an amino acid |
| EP4302832A1 (en) | 2022-07-07 | 2024-01-10 | Lotus Pharmaceutical Co., Ltd. | Palbociclib formulation containing glucono delta lactone |
| CN119604288A (zh) | 2022-07-29 | 2025-03-11 | 辉瑞大药厂 | 用于治疗癌症的包含kat6抑制剂的给药方案 |
| TW202539669A (zh) | 2022-08-31 | 2025-10-16 | 美商亞文納營運公司 | 雌激素受體降解劑之給藥方案 |
| TWI863667B (zh) | 2022-11-02 | 2024-11-21 | 美商佩特拉製藥公司 | 用於治療疾病之磷酸肌醇3-激酶(pi3k)異位色烯酮抑制劑 |
| WO2024133726A1 (en) | 2022-12-22 | 2024-06-27 | Synthon B.V. | Pharmaceutical composition comprising palbociclib |
| WO2024132652A1 (en) | 2022-12-22 | 2024-06-27 | Synthon B.V. | Pharmaceutical composition comprising palbociclib |
| CN120981721A (zh) | 2023-03-30 | 2025-11-18 | 辉瑞大药厂 | Kat6a作为用kat6a抑制剂治疗的预测性生物标志物和相关治疗方法 |
| WO2024201340A1 (en) | 2023-03-30 | 2024-10-03 | Pfizer Inc. | Kat6a as a predictive biomarker for treatment of breast cancer with a cdk4 inhibitor and an antiestrogen and methods of treatment thereof |
| WO2025122470A1 (en) | 2023-12-04 | 2025-06-12 | Genentech, Inc. | Combination therapies for treatment of breast cancer |
| WO2025202854A1 (en) | 2024-03-27 | 2025-10-02 | Pfizer Inc. | Cdk4 inhibitors and combinations with cdk2 inhibitors or further agents for use in the treatment of cancer |
| WO2026025013A2 (en) | 2024-07-26 | 2026-01-29 | Pfizer Inc. | Combination therapy using cdk4 inhibitors for cancer treatments |
Family Cites Families (9)
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| YU66502A (sh) * | 2000-03-06 | 2005-09-19 | Warner-Lambert Company | 5-alkilpirido(2,3-d)pirimidini, inhibitori tirozinkinaza |
| US6720332B2 (en) * | 2000-09-01 | 2004-04-13 | Smithkline Beecham Corporation | Oxindole derivatives |
| EP1463730B1 (en) * | 2001-12-17 | 2006-04-19 | SmithKline Beecham Corporation | Pyrazolopyridazine derivatives |
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| WO2004032882A2 (en) * | 2002-10-10 | 2004-04-22 | Smithkline Beecham Corporation | Chemical compounds |
| ATE411302T1 (de) * | 2002-11-22 | 2008-10-15 | Smithkline Beecham Corp | Thiazolidin-4-ones um hyak3 proteinen zu hemmen |
| ATE433967T1 (de) * | 2003-01-17 | 2009-07-15 | Warner Lambert Co | 2-aminopyridin-substituierteheterocyclen als inhibitoren der zellulären proliferation |
| WO2004076414A2 (en) * | 2003-02-27 | 2004-09-10 | Smithkline Beecham Corporation | Novel compounds |
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