MA39043B1 - Dérivés de purine substitués en positions 2 et 6, et leur utilisation dans le traitement des désordres prolifératifs - Google Patents
Dérivés de purine substitués en positions 2 et 6, et leur utilisation dans le traitement des désordres prolifératifsInfo
- Publication number
- MA39043B1 MA39043B1 MA39043A MA39043A MA39043B1 MA 39043 B1 MA39043 B1 MA 39043B1 MA 39043 A MA39043 A MA 39043A MA 39043 A MA39043 A MA 39043A MA 39043 B1 MA39043 B1 MA 39043B1
- Authority
- MA
- Morocco
- Prior art keywords
- treatment
- purine derivatives
- positions
- proliferative disorders
- derivatives substituted
- 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
Abstract
L'invention concerne des composés de formule (i) ou leur sels pharmaceutiquement acceptables, formule dans laquelle q, g, le cycle a, le cycle b, r1, r2, r3, r4, r5, r5a, r6, r7, r8, r9, r10, r11, r12, r13, r14, r15, r16, r17, r18, r19, r20, r21, r22, r23, r24 et m sont tels que définis dans la description. Ces nouveaux dérivés de purine sont utiles dans le traitement d'une croissance cellulaire anormale, telle que le cancer, chez les mammifères. D'autres modes de réalisation concernent des compositions pharmaceutiques contenant ces composés, ainsi que des procédés d'utilisation de ces 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 (2)
Publication Number | Publication Date |
---|---|
MA39043A1 MA39043A1 (fr) | 2018-01-31 |
MA39043B1 true MA39043B1 (fr) | 2018-09-28 |
Family
ID=52004011
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA39043A MA39043B1 (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 |
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 (1) | 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 (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB201311891D0 (en) | 2013-07-03 | 2013-08-14 | Glaxosmithkline Ip Dev Ltd | Novel compound |
GB201311888D0 (en) | 2013-07-03 | 2013-08-14 | Glaxosmithkline Ip Dev Ltd | Novel compounds |
CN104311573B (zh) | 2013-09-18 | 2017-12-15 | 北京韩美药品有限公司 | 抑制btk和/或jak3激酶活性的化合物 |
BR112017024163A2 (pt) * | 2015-05-12 | 2018-07-17 | Kalyra Pharmaceuticals Inc | compostos bicíclicos |
JP2019533652A (ja) * | 2016-09-30 | 2019-11-21 | エスアールアイ インターナショナルSRI International | がんを処置するための二重clk/cdk1阻害剤 |
EP3541389A1 (fr) | 2016-11-16 | 2019-09-25 | 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 |
JP2020505327A (ja) | 2016-12-23 | 2020-02-20 | アルビナス・オペレーションズ・インコーポレイテッドArvinas Operations, Inc. | Egfrタンパク質分解標的化キメラ分子およびその関連する使用方法 |
CA3056030A1 (fr) | 2017-03-10 | 2018-09-13 | Pfizer Inc. | Nouveaux derives imidazo[4,5-c]quinoleine utilises en tant qu'inhibiteurs de lrrk2 |
CN111201226B (zh) | 2017-03-10 | 2022-07-22 | 辉瑞大药厂 | 环状被取代的咪唑并[4,5-c]喹啉衍生物 |
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 |
WO2020175968A1 (fr) * | 2019-02-28 | 2020-09-03 | 주식회사 보로노이 | Dérivé hétéroaryle contenant de l'azote et composition pharmaceutique le comprenant en tant que principe actif |
KR20230015944A (ko) * | 2020-05-20 | 2023-01-31 | 티와이케이 메디슨즈, 인코포레이티드 | Ret 키나아제 억제제로 사용되는 화합물 및 이의 용도 |
US20230131465A1 (en) | 2021-09-14 | 2023-04-27 | 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 |
CA2102780C (fr) | 1991-05-10 | 2007-01-09 | Alfred P. Spada | Composes de type bis-monoaryle, aryle bicyclique et (ou) heteroaryle inhibant l'activite de tyrosine kinase des recepteurs de l'egf et (ou) du pdgf |
NZ243082A (en) | 1991-06-28 | 1995-02-24 | Ici Plc | 4-anilino-quinazoline derivatives; pharmaceutical compositions, preparatory processes, and use thereof |
US5587458A (en) | 1991-10-07 | 1996-12-24 | Aronex Pharmaceuticals, Inc. | Anti-erbB-2 antibodies, combinations thereof, and therapeutic and diagnostic uses thereof |
AU661533B2 (en) | 1992-01-20 | 1995-07-27 | Astrazeneca Ab | Quinazoline derivatives |
WO1993016185A2 (fr) | 1992-02-06 | 1993-08-19 | Creative Biomolecules, Inc. | Proteine de liaison biosynthetique pour marqueur de cancer |
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 |
ATE198326T1 (de) | 1995-04-20 | 2001-01-15 | Pfizer | Arylsulfonamido-substituierte hydroxamsäure derivate als inhibitoren von mmp und tnf |
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 |
ES2183905T3 (es) | 1995-12-20 | 2003-04-01 | Hoffmann La Roche | Inhibidores de metaloproteasa de matriz. |
GB9603095D0 (en) | 1996-02-14 | 1996-04-10 | Zeneca Ltd | Quinazoline derivatives |
ES2169355T3 (es) | 1996-03-05 | 2002-07-01 | Astrazeneca Ab | Derivados de 4-anilinoquinazolina. |
JP4386967B2 (ja) | 1996-07-13 | 2009-12-16 | グラクソ、グループ、リミテッド | プロテインチロシンキナーゼ阻害剤としての縮合複素環式化合物 |
HRP970371A2 (en) | 1996-07-13 | 1998-08-31 | Kathryn Jane Smith | Heterocyclic compounds |
WO1998002437A1 (fr) | 1996-07-13 | 1998-01-22 | Glaxo Group Limited | Composes heteroaromatiques bicycliques en tant qu'inhibiteurs de la proteine tyrosine kinase |
IL127567A0 (en) | 1996-07-18 | 1999-10-28 | Pfizer | Phosphinate based inhibitors of matrix metalloproteases |
US5866702A (en) | 1996-08-02 | 1999-02-02 | Cv Therapeutics, Incorporation | Purine inhibitors of cyclin dependent kinase 2 |
US6790958B2 (en) | 1996-08-02 | 2004-09-14 | Robert T. Lum | Purine inhibitors of cyclin dependent kinase 2 & IKBA |
US6794390B2 (en) | 1996-08-02 | 2004-09-21 | Cv Therapeutics, Inc. | Purine inhibitors of cyclin dependent kinase 2 & ikappabalpha |
CA2264284A1 (fr) | 1996-08-23 | 1998-02-26 | Ralph P. Robinson | Derives de l'acide arylsulfonylamino hydroxamique |
ES2224277T3 (es) | 1997-01-06 | 2005-03-01 | Pfizer Inc. | Derivados de sulfonas ciclicas. |
TR199901849T2 (xx) | 1997-02-03 | 2000-02-21 | Pfizer Products Inc. | Arils�lfonilamino hidroksamik asit t�revleri. |
WO1998034915A1 (fr) | 1997-02-07 | 1998-08-13 | Pfizer Inc. | Derives du n-hxdroxy-beta-sulfonyl-propionamide et leur utilisation comme inhibiteurs des metalloproteases matrices |
IL131123A0 (en) | 1997-02-11 | 2001-01-28 | Pfizer | Arylsulfonyl hydroxamic acid derivatives |
ATE292623T1 (de) | 1997-05-07 | 2005-04-15 | Sugen Inc | 2-indolinonderivate als modulatoren der proteinkinase-ativität |
CA2291709A1 (fr) | 1997-05-30 | 1998-12-03 | 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. |
AU744939B2 (en) | 1997-09-26 | 2002-03-07 | Merck & Co., Inc. | Novel angiogenesis inhibitors |
EA005889B1 (ru) | 1997-11-11 | 2005-06-30 | Пфайзер Продактс Инк. | Производные тиенопиримидина и тиенопиридина, полезные в качестве противораковых агентов |
GB9725782D0 (en) | 1997-12-05 | 1998-02-04 | Pfizer Ltd | Therapeutic agents |
RS49779B (sr) | 1998-01-12 | 2008-06-05 | Glaxo Group Limited, | Biciklična heteroaromatična jedinjenja kao inhibitori protein tirozin kinaze |
GB9800575D0 (en) | 1998-01-12 | 1998-03-11 | Glaxo Group Ltd | Heterocyclic compounds |
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 |
EP2020408B1 (fr) | 1998-05-29 | 2013-06-26 | Sugen, Inc. | Dérivé de 2-indolinone substitutée par un pyrrole en tant qu'inhibiteurs de protéine kinase |
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 |
CA2413424C (fr) | 2000-06-22 | 2007-10-02 | Pfizer Products Inc. | Derives bicycliques substitues destines au traitement de la croissance cellulaire anormale |
JP4922539B2 (ja) | 2000-09-15 | 2012-04-25 | バーテックス ファーマシューティカルズ インコーポレイテッド | プロテインキナーゼインヒビターとして有用なピラゾール化合物 |
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 |
US20060009642A1 (en) | 2001-10-12 | 2006-01-12 | Irm Llc, A Delaware Limited Liability Company | Methods for the synthesis of substituted purines |
CA2463563A1 (fr) | 2001-10-12 | 2003-04-17 | Irm Llc | Squelettes d'inhibiteurs de kinase et leurs methodes de preparation |
US6949644B2 (en) | 2001-10-12 | 2005-09-27 | Irm Llc | Methods for the synthesis of substituted purines |
AU2003270701B2 (en) | 2002-10-31 | 2009-11-12 | Amgen Inc. | Antiinflammation agents |
WO2005020892A2 (fr) | 2003-08-08 | 2005-03-10 | Mitochroma Research, Inc. | Compositions pharmaceutiques et procedes de modulation metabolique |
WO2005016268A2 (fr) | 2003-08-08 | 2005-02-24 | Mitochroma Research, Inc. | Compositions alimentaires et procedes pour moduler un metabolisme |
EP1656378A4 (fr) | 2003-08-15 | 2011-05-11 | Irm Llc | Composes et compositions inhibiteurs de l'activite du recepteur tyrosine kinase |
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 |
WO2008051502A1 (fr) | 2006-10-19 | 2008-05-02 | Genzyme Corporation | Dérives de purine pour traitement de maladies cystiques |
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 |
EA200900983A1 (ru) * | 2007-01-26 | 2010-02-26 | Айрм Ллк | Соединения и композиции в качестве ингибиторов киназы |
CA2683016A1 (fr) * | 2007-03-07 | 2008-09-12 | Boehringer Ingelheim International Gmbh | Nouveaux composes |
EA201000201A1 (ru) | 2007-08-10 | 2010-12-30 | ГЛАКСОСМИТКЛАЙН ЭлЭлСи | Азотсодержащие бициклические химические вещества для лечения вирусных инфекций |
BRPI0818578A2 (pt) | 2007-10-17 | 2015-07-21 | Novartis Ag | Derivados de purina como ligantes receptores de adenosina a1 |
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 |
TW201024298A (en) * | 2008-09-23 | 2010-07-01 | Palau Pharma Sa | (R)-3-(N,N-dimethylamino)pyrrolidine derivatives |
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 |
WO2010129053A2 (fr) * | 2009-05-05 | 2010-11-11 | Dana Farber Cancer Institute | 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 |
US9139592B2 (en) | 2010-06-14 | 2015-09-22 | Trt Pharma Inc. | Modulators of Nrf2 and uses thereof |
WO2011163424A2 (fr) | 2010-06-22 | 2011-12-29 | 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 |
JP5956999B2 (ja) * | 2010-11-01 | 2016-07-27 | セルジーン アヴィロミクス リサーチ, インコーポレイテッド | ヘテロアリール化合物およびその使用 |
EP2637502B1 (fr) * | 2010-11-10 | 2018-01-10 | Celgene CAR LLC | Inhibiteurs d'egfr sélectifs d'un mutant et leurs utilisations |
CA2832504C (fr) * | 2011-05-04 | 2019-10-01 | Ariad Pharmaceuticals, Inc. | Composes permettant d'inhiber la proliferation cellulaire dans les cancers induits par l'egfr |
US8762299B1 (en) | 2011-06-27 | 2014-06-24 | Google Inc. | Customized predictive analytical model training |
MD20140023A2 (ro) | 2011-09-22 | 2014-06-30 | Pfizer Inc. | Derivaţi de pirolpirimidină şi purină |
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 |
BR112015023020A2 (pt) | 2013-03-14 | 2017-07-18 | Pfizer | combinação de inibidor de egfr t790m e inibidor de egfr para o tratamento de câncer pulmonar de células não-pequenas |
US10884952B2 (en) | 2016-09-30 | 2021-01-05 | Intel Corporation | Enforcing memory operand types using protection keys |
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