TN2016000188A1 - Derives de purines 2,6-substitues et leur utilisation dans le traitement de troubles proliferatifs. - Google Patents
Derives de purines 2,6-substitues et leur utilisation dans le traitement de troubles proliferatifs.Info
- Publication number
- TN2016000188A1 TN2016000188A1 TN2016000188A TN2016000188A TN2016000188A1 TN 2016000188 A1 TN2016000188 A1 TN 2016000188A1 TN 2016000188 A TN2016000188 A TN 2016000188A TN 2016000188 A TN2016000188 A TN 2016000188A TN 2016000188 A1 TN2016000188 A1 TN 2016000188A1
- Authority
- TN
- Tunisia
- Prior art keywords
- sup
- treatment
- purine derivatives
- proliferative disorders
- substituted purine
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
- C07D473/16—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two nitrogen atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—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
- A61K31/52—Purines, e.g. adenine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5386—1,4-Oxazines, e.g. morpholine spiro-condensed or forming part of bridged ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
- C07D473/18—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 one oxygen and one nitrogen atom, e.g. guanine
-
- 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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
La présente invention concerne des composés de formule<br /> ( I) ou leurs sel pharmaceutiquement acceptables , formule dans laquelle Q,G,le noyau A , le noyau B, R<sup>1 ,</sup> R<sup>2,</sup> R<sup>3,</sup> R<sup>4,</sup> R<sup>5,</sup> R<sup>6,</sup> R<sup>7,</sup> R<sup>8,</sup> R<sup>9,</sup> R<sup>10,</sup> R<sup>11,</sup> R<sup>12,</sup> R<sup>13,</sup> R<sup>14,</sup> R<sup>15,</sup> R<sup>16,</sup> R<sup>17,</sup> R<sup>18,</sup> R<sup>19,</sup> R<sup>20,</sup> R<sup>21,</sup> R<sup>22,</sup> R<sup>23,</sup> R<sup>24 </sup>et m répondent aux définitions figurant dans le présent mémoire. Les dérivés de purine nouveaux sont utiles dans le traitement d'une croissance cellulaire anormale , telle que le cancer , chez des mammifères . Des formes de réalisations supplémentaires concernant des compositions pharmaceutiques contenant les composés et des procédés d'utilisation des composés et compositions dans le traitement d'une croissance cellulaire anormale chez les mammifères
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361907322P | 2013-11-21 | 2013-11-21 | |
| PCT/IB2014/065935 WO2015075598A1 (fr) | 2013-11-21 | 2014-11-10 | Dérivés de purine substitués en positions 2 et 6, et leur utilisation dans le traitement des désordres prolifératifs |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TN2016000188A1 true TN2016000188A1 (fr) | 2017-10-06 |
Family
ID=52004011
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TN2016000188A TN2016000188A1 (fr) | 2013-11-21 | 2014-11-10 | Derives de purines 2,6-substitues et leur utilisation dans le traitement de troubles proliferatifs. |
Country Status (39)
| Country | Link |
|---|---|
| US (1) | US9290496B2 (fr) |
| EP (1) | EP3071570B1 (fr) |
| JP (2) | JP6166845B2 (fr) |
| KR (1) | KR101919672B1 (fr) |
| CN (1) | CN105916853B (fr) |
| AP (1) | AP2016009219A0 (fr) |
| AR (1) | AR098492A1 (fr) |
| AU (1) | AU2014351433B2 (fr) |
| CA (1) | CA2931034C (fr) |
| CL (1) | CL2016001151A1 (fr) |
| CR (1) | CR20160236A (fr) |
| CU (1) | CU24402B1 (fr) |
| CY (1) | CY1120478T1 (fr) |
| DK (1) | DK3071570T3 (fr) |
| DO (1) | DOP2016000115A (fr) |
| EA (1) | EA029842B1 (fr) |
| ES (1) | ES2681799T3 (fr) |
| GE (2) | GEP20186878B (fr) |
| GT (1) | GT201600091A (fr) |
| HR (1) | HRP20181036T1 (fr) |
| HU (1) | HUE039858T2 (fr) |
| IL (1) | IL245698B (fr) |
| LT (1) | LT3071570T (fr) |
| MA (1) | MA39043B1 (fr) |
| MD (1) | MD20160053A2 (fr) |
| MX (1) | MX2016006397A (fr) |
| MY (1) | MY184433A (fr) |
| NI (1) | NI201600072A (fr) |
| PE (1) | PE20160885A1 (fr) |
| PH (1) | PH12016500911A1 (fr) |
| PL (1) | PL3071570T3 (fr) |
| PT (1) | PT3071570T (fr) |
| RS (1) | RS57537B1 (fr) |
| SI (1) | SI3071570T1 (fr) |
| TN (1) | TN2016000188A1 (fr) |
| TW (1) | TWI538913B (fr) |
| UA (1) | UA115388C2 (fr) |
| UY (1) | UY35845A (fr) |
| WO (1) | WO2015075598A1 (fr) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB201311888D0 (en) | 2013-07-03 | 2013-08-14 | Glaxosmithkline Ip Dev Ltd | Novel compounds |
| GB201311891D0 (en) | 2013-07-03 | 2013-08-14 | Glaxosmithkline Ip Dev Ltd | Novel compound |
| CA2924362C (fr) * | 2013-09-18 | 2018-12-18 | Beijing Hanmi Pharmaceutical Co., Ltd. | Compose inhibiteur d'activites de kinase de btk et/ou de jak3 |
| US20180228907A1 (en) | 2014-04-14 | 2018-08-16 | Arvinas, Inc. | Cereblon ligands and bifunctional compounds comprising the same |
| US20180201614A1 (en) * | 2015-05-12 | 2018-07-19 | Kalyra Pharmaceuticals, Inc. | Bicyclic compounds |
| CN109937039A (zh) * | 2016-09-30 | 2019-06-25 | 斯坦福国际研究院 | 用于癌症治疗的双重clk/cdk1抑制剂 |
| WO2018091999A1 (fr) | 2016-11-16 | 2018-05-24 | Pfizer Inc. | Combinaison d'un inhibiteur de t790m de l'egfr et d'un inhibiteur de cdk dans le traitement du cancer du poumon non à petites cellules |
| BR112019012682A2 (pt) | 2016-12-23 | 2019-12-17 | Arvinas Operations Inc | moléculas quiméricas visando a proteólise de egfr e métodos associados de uso |
| CN111051304B (zh) | 2017-03-10 | 2022-12-27 | 辉瑞大药厂 | 作为LRRK2抑制剂的咪唑并[4,5-c]喹啉衍生物 |
| CA3056027A1 (fr) | 2017-03-10 | 2018-09-13 | Pfizer Inc. | Derives d'imidazo [4,5-c] quinoleine substitues cycliques |
| WO2019241896A1 (fr) | 2018-06-22 | 2019-12-26 | The Royal Institution For The Advancement Of Learning/Mcgill University | Composés de purine et procédé pour letraitement du cancer |
| KR20200105631A (ko) * | 2019-02-28 | 2020-09-08 | 보로노이바이오 주식회사 | N을 포함하는 헤테로아릴 유도체 및 이를 유효성분으로 포함하는 약학적 조성물 |
| KR102841446B1 (ko) * | 2020-05-20 | 2025-07-31 | 티와이케이 메디슨즈, 인코포레이티드 | Ret 키나아제 억제제로 사용되는 화합물 및 이의 용도 |
| US12115157B2 (en) | 2021-09-14 | 2024-10-15 | Boehringer Ingelheim International Gmbh | 3-phenoxyazetidin-1-yl-heteroaryl pyrrolidine derivatives and the use thereof as medicament |
Family Cites Families (97)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8607683D0 (en) | 1986-03-27 | 1986-04-30 | Ici Plc | Anti-tumor agents |
| GB8827305D0 (en) | 1988-11-23 | 1988-12-29 | British Bio Technology | Compounds |
| DE69222637T2 (de) | 1991-05-10 | 1998-02-26 | Rhone Poulenc Rorer Int | Bis mono- und bicyclische aryl- und heteroarylderivate mit inhibierender wirkung auf die egf und/oder pdgf-rezeptor tyrosinkinase |
| NZ243082A (en) | 1991-06-28 | 1995-02-24 | Ici Plc | 4-anilino-quinazoline derivatives; pharmaceutical compositions, preparatory processes, and use thereof |
| FI941572L (fi) | 1991-10-07 | 1994-05-27 | Oncologix Inc | Anti-erbB-2-monoklonaalisten vasta-aineiden yhdistelmä ja käyttömenetelmä |
| AU661533B2 (en) | 1992-01-20 | 1995-07-27 | Astrazeneca Ab | Quinazoline derivatives |
| ATE295420T1 (de) | 1992-02-06 | 2005-05-15 | Chiron Corp | Marker für krebs und biosynthetisches bindeprotein dafür |
| US6177401B1 (en) | 1992-11-13 | 2001-01-23 | Max-Planck-Gesellschaft Zur Forderung Der Wissenschaften | Use of organic compounds for the inhibition of Flk-1 mediated vasculogenesis and angiogenesis |
| GB9323290D0 (en) | 1992-12-10 | 1994-01-05 | Zeneca Ltd | Quinazoline derivatives |
| US5455258A (en) | 1993-01-06 | 1995-10-03 | Ciba-Geigy Corporation | Arylsulfonamido-substituted hydroxamic acids |
| GB9314884D0 (en) | 1993-07-19 | 1993-09-01 | Zeneca Ltd | Tricyclic derivatives |
| GB9314893D0 (en) | 1993-07-19 | 1993-09-01 | Zeneca Ltd | Quinazoline derivatives |
| IL112248A0 (en) | 1994-01-25 | 1995-03-30 | Warner Lambert Co | Tricyclic heteroaromatic compounds and pharmaceutical compositions containing them |
| GB9510757D0 (en) | 1994-09-19 | 1995-07-19 | Wellcome Found | Therapeuticaly active compounds |
| GB9424233D0 (en) | 1994-11-30 | 1995-01-18 | Zeneca Ltd | Quinazoline derivatives |
| US5863949A (en) | 1995-03-08 | 1999-01-26 | Pfizer Inc | Arylsulfonylamino hydroxamic acid derivatives |
| US5861510A (en) | 1995-04-20 | 1999-01-19 | Pfizer Inc | Arylsulfonyl hydroxamic acid derivatives as MMP and TNF inhibitors |
| US5880141A (en) | 1995-06-07 | 1999-03-09 | Sugen, Inc. | Benzylidene-Z-indoline compounds for the treatment of disease |
| GB9520822D0 (en) | 1995-10-11 | 1995-12-13 | Wellcome Found | Therapeutically active compounds |
| GB9624482D0 (en) | 1995-12-18 | 1997-01-15 | Zeneca Phaema S A | Chemical compounds |
| PT780386E (pt) | 1995-12-20 | 2003-02-28 | Hoffmann La Roche | Inibidores de metaloprotease de matriz |
| GB9603095D0 (en) | 1996-02-14 | 1996-04-10 | Zeneca Ltd | Quinazoline derivatives |
| AU719327B2 (en) | 1996-03-05 | 2000-05-04 | Astrazeneca Ab | 4-anilinoquinazoline derivatives |
| PT912559E (pt) | 1996-07-13 | 2003-03-31 | Glaxo Group Ltd | Compostos heterociclicos fundidos como inibidores de proteina tirosina quinase |
| HRP970371A2 (en) | 1996-07-13 | 1998-08-31 | Kathryn Jane Smith | Heterocyclic compounds |
| CA2260058A1 (fr) | 1996-07-13 | 1998-01-22 | Kathryn Jane Smith | Composes heteroaromatiques bicycliques en tant qu'inhibiteurs de la proteine tyrosine kinase |
| ATE217315T1 (de) | 1996-07-18 | 2002-05-15 | Pfizer | Matrix metalloprotease-inhibitoren auf basis von phosphinsäuren |
| US6790958B2 (en) | 1996-08-02 | 2004-09-14 | Robert T. Lum | Purine inhibitors of cyclin dependent kinase 2 & IKBA |
| US5866702A (en) | 1996-08-02 | 1999-02-02 | Cv Therapeutics, Incorporation | Purine inhibitors of cyclin dependent kinase 2 |
| US6794390B2 (en) | 1996-08-02 | 2004-09-21 | Cv Therapeutics, Inc. | Purine inhibitors of cyclin dependent kinase 2 & ikappabalpha |
| EP0922030A1 (fr) | 1996-08-23 | 1999-06-16 | Pfizer Inc. | Derives de l'acide arylsulfonylamino hydroxamique |
| BR9714266A (pt) | 1997-01-06 | 2000-04-18 | Pfizer | Derivados de sulfona cìclicos. |
| IL131042A0 (en) | 1997-02-03 | 2001-01-28 | Pfizer Prod Inc | Arylsulfonylamino hydroxamic acid derivatives |
| BR9807824A (pt) | 1997-02-07 | 2000-03-08 | Pfizer | Derivados de n-hidróxi-beta-sulfonil-propionamida e seu uso como inibidores de metaloproteinases de matriz |
| WO1998034918A1 (fr) | 1997-02-11 | 1998-08-13 | Pfizer Inc. | Derives de l'acide arylsulfonylhydroxamique |
| WO1998050356A1 (fr) | 1997-05-07 | 1998-11-12 | Sugen, Inc. | Derives de 2-indolinone utilises en tant que modulateurs de l'activite de la proteine kinase |
| EP0984692A4 (fr) | 1997-05-30 | 2001-02-21 | Merck & Co Inc | Nouveaux inhibiteurs d'angiogenese |
| AU735127B2 (en) | 1997-08-07 | 2001-06-28 | Regents Of The University Of California, The | Purine inhibitor of protein kinases, G proteins and polymerases |
| ES2289791T3 (es) | 1997-08-22 | 2008-02-01 | Astrazeneca Ab | Derivados de oxindolilquinazolina como inhibidores de la angiogenesis. |
| WO1999016755A1 (fr) | 1997-09-26 | 1999-04-08 | Merck & Co., Inc. | Nouveaux inhibiteurs de l'angiogenese |
| KR100446363B1 (ko) | 1997-11-11 | 2004-09-01 | 화이자 프로덕츠 인코포레이티드 | 항암제로 유용한 티에노피리미딘 및 티에노피리딘 유도체 |
| GB9725782D0 (en) | 1997-12-05 | 1998-02-04 | Pfizer Ltd | Therapeutic agents |
| GB9800575D0 (en) | 1998-01-12 | 1998-03-11 | Glaxo Group Ltd | Heterocyclic compounds |
| RS49779B (sr) | 1998-01-12 | 2008-06-05 | Glaxo Group Limited, | Biciklična heteroaromatična jedinjenja kao inhibitori protein tirozin kinaze |
| GB9801690D0 (en) | 1998-01-27 | 1998-03-25 | Pfizer Ltd | Therapeutic agents |
| PA8469501A1 (es) | 1998-04-10 | 2000-09-29 | Pfizer Prod Inc | Hidroxamidas del acido (4-arilsulfonilamino)-tetrahidropiran-4-carboxilico |
| PA8469401A1 (es) | 1998-04-10 | 2000-05-24 | Pfizer Prod Inc | Derivados biciclicos del acido hidroxamico |
| EA005032B1 (ru) | 1998-05-29 | 2004-10-28 | Сьюджен, Инк. | Пирролзамещенные 2-индолиноны (варианты), фармацевтическая композиция (варианты), способ модулирования каталитической активности протеинкиназы, способ лечения или профилактики нарушения в организме, связанного с протеинкиназой |
| US6232320B1 (en) | 1998-06-04 | 2001-05-15 | Abbott Laboratories | Cell adhesion-inhibiting antiinflammatory compounds |
| JP3270834B2 (ja) | 1999-01-27 | 2002-04-02 | ファイザー・プロダクツ・インク | 抗がん剤として有用なヘテロ芳香族二環式誘導体 |
| UA71945C2 (en) | 1999-01-27 | 2005-01-17 | Pfizer Prod Inc | Substituted bicyclic derivatives being used as anticancer agents |
| JP4044839B2 (ja) | 2000-06-22 | 2008-02-06 | ファイザー・プロダクツ・インク | 異常細胞増殖を治療するための置換2環式誘導体 |
| EP1317450B1 (fr) | 2000-09-15 | 2006-11-22 | Vertex Pharmaceuticals Incorporated | Composes de pyrazole utiles comme inhibiteurs de proteine kinase |
| AR042586A1 (es) | 2001-02-15 | 2005-06-29 | Sugen Inc | 3-(4-amidopirrol-2-ilmetiliden)-2-indolinona como inhibidores de la protein quinasa; sus composiciones farmaceuticas; un metodo para la modulacion de la actividad catalitica de la proteinquinasa; un metodo para tratar o prevenir una afeccion relacionada con la proteinquinasa |
| WO2002072549A1 (fr) | 2001-03-12 | 2002-09-19 | Millennium Pharmaceuticals, Inc. | Heterocycles fonctionnalises en tant que modulateurs de la fonction du recepteur de chimiokines et procedes de mise en oeuvre |
| WO2003009852A1 (fr) | 2001-07-24 | 2003-02-06 | Merck & Co., Inc. | Inhibiteurs de tyrosine kinase |
| CA2463563A1 (fr) | 2001-10-12 | 2003-04-17 | Irm Llc | Squelettes d'inhibiteurs de kinase et leurs methodes de preparation |
| US20060009642A1 (en) | 2001-10-12 | 2006-01-12 | Irm Llc, A Delaware Limited Liability Company | Methods for the synthesis of substituted purines |
| US6949644B2 (en) | 2001-10-12 | 2005-09-27 | Irm Llc | Methods for the synthesis of substituted purines |
| EP1556053A4 (fr) | 2002-10-31 | 2006-04-19 | Amgen Inc | Agents anti-inflammatoires |
| US20070161582A1 (en) | 2003-08-08 | 2007-07-12 | Dusan Mijikovic | Pharmaceutical compositions and methods for metabolic modulation |
| WO2005016268A2 (fr) | 2003-08-08 | 2005-02-24 | Mitochroma Research, Inc. | Compositions alimentaires et procedes pour moduler un metabolisme |
| SG145748A1 (en) | 2003-08-15 | 2008-09-29 | Irm Llc | 6-substituted anilino purines as rtk inhibitors |
| US20060029642A1 (en) | 2004-08-03 | 2006-02-09 | Dusan Miljkovic | Methods and compositions for improved chromium complexes |
| GB0420719D0 (en) | 2004-09-17 | 2004-10-20 | Addex Pharmaceuticals Sa | Novel allosteric modulators |
| FR2876583B1 (fr) | 2004-10-15 | 2007-04-13 | Centre Nat Rech Scient Cnrse | Utilisation de derives de purines pour la fabrication de medicaments pour le traitement de la mucoviscidose et de maladies liees a un defaut d'adressage des proteines dans les cellules |
| GB0502573D0 (en) | 2005-02-08 | 2005-03-16 | Topotarget As | Therapeutic compounds |
| GB0526246D0 (en) | 2005-12-22 | 2006-02-01 | Novartis Ag | Organic compounds |
| US20070253896A1 (en) | 2006-02-07 | 2007-11-01 | Conforma Therapeutics Corporation | 7,9-Dihydro-Purin-8-One and Related Analogs as HSP90-Inhibitors |
| EP2008210A1 (fr) | 2006-03-15 | 2008-12-31 | Csir | Modulation de l'activite phosphoryl transferase de la glutamine synthetase |
| ES2402907T3 (es) | 2006-10-19 | 2013-05-10 | Genzyme Corporation | Roscovitina para el tratamiento de ciertas enfermedades quísticas |
| WO2008057402A2 (fr) | 2006-11-02 | 2008-05-15 | Cytovia, Inc. | N-aryl-isoxazolopyrimidin-4-amines et composés associés servant d'activateurs de caspases et d'inducteurs d'apoptose et leur utilisation |
| KR20090112732A (ko) | 2007-01-26 | 2009-10-28 | 아이알엠 엘엘씨 | 플라스모듐 관련 질환의 치료를 위한 키나제 억제제로서의 퓨린 화합물 및 조성물 |
| US8404674B2 (en) * | 2007-03-07 | 2013-03-26 | Boehringer Ingelheim International Gmbh | Substituted 9H-purin-2-YL compounds, compositions thereof and uses thereof |
| BRPI0814939A2 (pt) | 2007-08-10 | 2015-01-27 | Glaxosmithkline Llc | Entidade química, composição farmacêutica, e, método para tratar uma infecção viral em um mamífero. |
| US20100197914A1 (en) | 2007-10-17 | 2010-08-05 | Robin Alec Fairhurst | Purine Derivatives as Adenosine Al Receptor Ligands |
| US9089572B2 (en) | 2008-01-17 | 2015-07-28 | California Institute Of Technology | Inhibitors of p97 |
| EP2312945A4 (fr) | 2008-08-13 | 2012-05-09 | Merck Sharp & Dohme | Dérivés de purine pour le traitement de la maladie d alzheimer |
| WO2010034740A1 (fr) * | 2008-09-23 | 2010-04-01 | Palau Pharma, S.A. | Dérivés (r)-3-(n,n-diméthylamino)pyrrolidine |
| PE20100362A1 (es) | 2008-10-30 | 2010-05-27 | Irm Llc | Derivados de purina que expanden las celulas madre hematopoyeticas |
| US8426428B2 (en) * | 2008-12-05 | 2013-04-23 | Principia Biopharma, Inc. | EGFR kinase knockdown via electrophilically enhanced inhibitors |
| WO2010118367A2 (fr) | 2009-04-10 | 2010-10-14 | Progenics Pharmaceuticals, Inc. | Pyrimidines antivirales |
| EP2440559B1 (fr) * | 2009-05-05 | 2018-01-10 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs d'egfr et procédés de traitement de troubles |
| FR2945747A1 (fr) * | 2009-05-25 | 2010-11-26 | Centre Nat Rech Scient | Composition pharmaceutique antitumorale comprenant un inhibiteur de cdks et un inhibiteur de la croissance cellulaire |
| TW201111385A (en) | 2009-08-27 | 2011-04-01 | Biocryst Pharm Inc | Heterocyclic compounds as janus kinase inhibitors |
| WO2011156889A1 (fr) | 2010-06-14 | 2011-12-22 | Trt Pharma Inc. | Nouveaux modulateurs de la nrf2 et leurs utilisations |
| EP2585464A2 (fr) | 2010-06-22 | 2013-05-01 | University Of Central Florida Research Foundation, Inc. | Analogues d'acide 2-(9h-purin-9-yl)acétique substitués en tant qu'inhibiteurs de stat3 |
| AU2011315831B2 (en) * | 2010-10-14 | 2015-01-22 | Takeda Pharmaceutical Company Limited | Methods for inhibiting cell proliferation in EGFR-driven cancers |
| WO2012061303A1 (fr) * | 2010-11-01 | 2012-05-10 | Avila Therapeutics, Inc. | Composés hétéroaryle et leurs utilisations |
| WO2012064706A1 (fr) * | 2010-11-10 | 2012-05-18 | Avila Therapeutics, Inc. | Inhibiteurs d'egfr sélectifs d'un mutant et leurs utilisations |
| EA201391626A1 (ru) * | 2011-05-04 | 2014-03-31 | Ариад Фармасьютикалз, Инк. | Соединения для ингибирования клеточной пролиферации в egfr-стимулированных типах рака |
| US8762299B1 (en) | 2011-06-27 | 2014-06-24 | Google Inc. | Customized predictive analytical model training |
| UA110259C2 (uk) * | 2011-09-22 | 2015-12-10 | Пфайзер Інк. | Похідні піролопіримідину і пурину |
| CN103159742B (zh) | 2011-12-16 | 2015-08-12 | 北京韩美药品有限公司 | 5-氯嘧啶类化合物及其作为egfr酪氨酸激酶抑制剂的应用 |
| WO2013106792A1 (fr) | 2012-01-13 | 2013-07-18 | Acea Biosciences Inc. | Composés hétérocycliques et utilisations en tant qu'agents anticancéreux |
| EP2968336A2 (fr) | 2013-03-14 | 2016-01-20 | Pfizer Inc. | Combinaison d'un inhibiteur de l'egfr t790m et d'un inhibiteur de l'egfr dans le traitement d'un cancer du poumon non à petites cellules |
| US10884952B2 (en) | 2016-09-30 | 2021-01-05 | Intel Corporation | Enforcing memory operand types using protection keys |
-
2014
- 2014-10-11 UA UAA201605505A patent/UA115388C2/uk unknown
- 2014-11-10 MA MA39043A patent/MA39043B1/fr unknown
- 2014-11-10 EP EP14806447.0A patent/EP3071570B1/fr active Active
- 2014-11-10 LT LTEP14806447.0T patent/LT3071570T/lt unknown
- 2014-11-10 ES ES14806447.0T patent/ES2681799T3/es active Active
- 2014-11-10 SI SI201430806T patent/SI3071570T1/sl unknown
- 2014-11-10 HU HUE14806447A patent/HUE039858T2/hu unknown
- 2014-11-10 PE PE2016000650A patent/PE20160885A1/es unknown
- 2014-11-10 WO PCT/IB2014/065935 patent/WO2015075598A1/fr not_active Ceased
- 2014-11-10 DK DK14806447.0T patent/DK3071570T3/en active
- 2014-11-10 GE GEAP201414151A patent/GEP20186878B/en unknown
- 2014-11-10 PL PL14806447T patent/PL3071570T3/pl unknown
- 2014-11-10 EA EA201600337A patent/EA029842B1/ru not_active IP Right Cessation
- 2014-11-10 HR HRP20181036TT patent/HRP20181036T1/hr unknown
- 2014-11-10 JP JP2016532623A patent/JP6166845B2/ja not_active Expired - Fee Related
- 2014-11-10 CU CU2016000073A patent/CU24402B1/es unknown
- 2014-11-10 MY MYPI2016701796A patent/MY184433A/en unknown
- 2014-11-10 TN TN2016000188A patent/TN2016000188A1/fr unknown
- 2014-11-10 AP AP2016009219A patent/AP2016009219A0/en unknown
- 2014-11-10 CN CN201480073530.7A patent/CN105916853B/zh not_active Expired - Fee Related
- 2014-11-10 PT PT148064470T patent/PT3071570T/pt unknown
- 2014-11-10 RS RS20180909A patent/RS57537B1/sr unknown
- 2014-11-10 GE GEAP201814151A patent/GEAP201814151A/en unknown
- 2014-11-10 AU AU2014351433A patent/AU2014351433B2/en not_active Ceased
- 2014-11-10 KR KR1020167016053A patent/KR101919672B1/ko not_active Expired - Fee Related
- 2014-11-10 MD MDA20160053A patent/MD20160053A2/ro not_active Application Discontinuation
- 2014-11-10 MX MX2016006397A patent/MX2016006397A/es unknown
- 2014-11-10 CA CA2931034A patent/CA2931034C/fr active Active
- 2014-11-19 UY UY0001035845A patent/UY35845A/es not_active Application Discontinuation
- 2014-11-20 TW TW103140297A patent/TWI538913B/zh not_active IP Right Cessation
- 2014-11-20 AR ARP140104368A patent/AR098492A1/es unknown
- 2014-11-20 US US14/548,749 patent/US9290496B2/en active Active
-
2016
- 2016-05-13 CL CL2016001151A patent/CL2016001151A1/es unknown
- 2016-05-17 PH PH12016500911A patent/PH12016500911A1/en unknown
- 2016-05-18 IL IL24569816A patent/IL245698B/en active IP Right Grant
- 2016-05-19 DO DO2016000115A patent/DOP2016000115A/es unknown
- 2016-05-20 NI NI201600072A patent/NI201600072A/es unknown
- 2016-05-20 CR CR20160236A patent/CR20160236A/es unknown
- 2016-05-20 GT GT201600091A patent/GT201600091A/es unknown
-
2017
- 2017-06-23 JP JP2017122759A patent/JP2017214390A/ja active Pending
-
2018
- 2018-07-25 CY CY20181100779T patent/CY1120478T1/el unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| TN2016000188A1 (fr) | Derives de purines 2,6-substitues et leur utilisation dans le traitement de troubles proliferatifs. | |
| MA41134B1 (fr) | Composés substitués de 5-amino-6h-thiazolo[4,5-d]pyrimidine-2,7-dione pour le traitement et la prophylaxie des infections virales | |
| MA38391A1 (fr) | Dérivés de pyridinyl et triazolone pyridinyl de fusion | |
| MA40225B1 (fr) | Composés dihydroisoquinolinone substitués | |
| MA38138A1 (fr) | Dérivés inédits de quinolone | |
| MA45920A (fr) | Inhibiteurs de pyridopyrimidinone cdk2/4/6 | |
| MA40111A1 (fr) | Dérivés du tétrahydronaphtalène inhibant la protéine mcl-1 | |
| MA37405A1 (fr) | Composés hétérocyclyle | |
| MA38175A1 (fr) | Lactames fusionnés à un aryle et hétéroaryle | |
| MA54653B1 (fr) | Modulateurs du récepteur de cxcr7 pipéridine | |
| MA38287A1 (fr) | Nouveaux dérivés aminopyrazine pour le traitement ou la prévention du cancer | |
| TN2014000115A1 (fr) | Derives de pyrrolopyrimidines et de purines | |
| MA42230B1 (fr) | Dérivés bicycliques, leur procédé de préparation, et compositions pharmaceutiques les contenant | |
| MA39211B1 (fr) | Composés tricycliques comme agents anti-cancers | |
| MA42231B1 (fr) | Nouveaux dérivés d'hydroxyacide, leur procédé de préparation, et compositions pharmaceutiques les contenant | |
| MA38323A1 (fr) | Dérivés pyrimidone et leur utilisation dans le traitement, l'amélioration ou la prévention d'une maladie virale | |
| MA32351B1 (fr) | Derives d'aminodihydrothiazine a titre d'inhibiteurs de bace pour le traitement de la maladie d'alzheimer | |
| PH12017502257A1 (en) | Compositions and methods of use of phorbol esters | |
| MA46038A (fr) | Composés de sulfonimidoylpurinone substitués dans la position 7 pour le traitement et la prophylaxie d'infection virale | |
| MA38315B1 (fr) | Composés tétracycliques substitués par un hétérocycle et procédés pour les utiliser pour le traitement de maladies virales | |
| MA38240A1 (fr) | Nouveaux composes dimeres substitues antagonistes de l'iap utiles pour le traitement du cancer, de preference des tumeurs solides | |
| MA38260A1 (fr) | Nouveaux dérivés de cyclohexyl et quinuclidinyl carbamate ayant une activité d'agoniste adrénergique beta2 et une activité d'antagoniste muscarinique m3 | |
| MA38009A1 (fr) | Composes d'azaindoline substitues qui ont une activite inhibitrice de la proteine d'apoptose pour leurs utilisations dans le traitement et/ou la prophylaxie du cancer | |
| MA39229A1 (fr) | Pyrrolidines, térahydrofuranes et cyclopentanes substitués utiles en tant qu'antagonistes des récepteurs des orexines | |
| MA39926B1 (fr) | Dérivés de dihétérocycle liés à cycloalkyle |