AR077446A1 - Derivados de 2,3-dihidro-1h-imidazo(1,2-a) pirimidin-5-ona. su preparacion y su utilizacion farmaceutica - Google Patents
Derivados de 2,3-dihidro-1h-imidazo(1,2-a) pirimidin-5-ona. su preparacion y su utilizacion farmaceuticaInfo
- Publication number
- AR077446A1 AR077446A1 ARP100102346A ARP100102346A AR077446A1 AR 077446 A1 AR077446 A1 AR 077446A1 AR P100102346 A ARP100102346 A AR P100102346A AR P100102346 A ARP100102346 A AR P100102346A AR 077446 A1 AR077446 A1 AR 077446A1
- Authority
- AR
- Argentina
- Prior art keywords
- radical
- radicals
- alkyl
- optionally substituted
- chosen
- Prior art date
Links
- 125000003545 alkoxy group Chemical group 0.000 abstract 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 6
- 125000005843 halogen group Chemical group 0.000 abstract 5
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 3
- 229910052757 nitrogen Inorganic materials 0.000 abstract 3
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 3
- 229910052760 oxygen Inorganic materials 0.000 abstract 3
- 229910052717 sulfur Inorganic materials 0.000 abstract 3
- 125000004414 alkyl thio group Chemical group 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 2
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 2
- 239000011707 mineral Substances 0.000 abstract 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- TUJKJAMUKRIRHC-UHFFFAOYSA-N hydroxyl Chemical compound [OH] TUJKJAMUKRIRHC-UHFFFAOYSA-N 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 150000007522 mineralic acids Chemical class 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 150000007524 organic acids Chemical class 0.000 abstract 1
- 235000005985 organic acids Nutrition 0.000 abstract 1
- 150000007530 organic bases Chemical class 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 230000026731 phosphorylation Effects 0.000 abstract 1
- 238000006366 phosphorylation reaction Methods 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 0.000 abstract 1
Classifications
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- 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
- A61K31/535—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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
- A61P33/06—Antimalarials
-
- 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
- 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
- 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
- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- 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
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Obesity (AREA)
- Gastroenterology & Hepatology (AREA)
- Neurology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Como medicamentos principalmente como inhibidores de fosforilacion de AKT(PKB). Reivindicacion 1: Productos de formula (1) en la que R1 representa un radical -L-arilo o -L-heteroarilo, tal que L representa: bien un radical alquilo lineal o ramificado C1-6 y opcionalmente sustituido con un radical hidroxilo, bien un grupo CO, bien un grupo L'-X donde L' representa un radical alquilo lineal o ramificado C1-6 y X un átomo de oxígeno o de azufre; estando los radicales arilo y heteroarilo eventualmente sustituidos con uno o varios radicales idénticos o diferentes elegidos entre los átomos de halogeno y los radicales hidroxilo, CN, nitro, -COOH, -COOalk, -NRxRy, -CONRxRy, -NRxCORy, -NRxCO2Rz, CORy, alcoxi, fenoxi, alquiltio, alquilo, cicloalquilo y heterocicloalquilo; estando estos ultimos radicales alcoxi, fenoxi, alquiltio, alquilo y heterocicloalquilo ellos mismos sustituidos opcionalmente con uno o varios radicales idénticos o diferentes elegidos entre los átomos de halogeno y NRvRw; pudiendo contener además los radicales heterocicloalquilo y heteroarilo un radical oxo; R2 representa un átomo de hidrogeno o un radical alquilo; R3 representa un radical alquilo opcionalmente sustituido con uno o varios átomos de halogeno; R4 representa un átomo de hidrogeno o un átomo de halogeno; siendo NRxRy tal que Rx representa un átomo de hidrogeno o un radical alquilo y Ry representa un átomo de hidrogeno, un radical cicloalquilo o un radical alquilo sustituido opcionalmente con uno o varios radicales idénticos o diferentes elegidos entre los radicales hidroxilo, alcoxi, NRvRw y heterocicloalquilo; bien Rx y Ry forman con el átomo de nitrogeno al que están unidos un radical cíclico que comprende de 3 a 10 eslabones y opcionalmente uno o varios heteroátomos más elegido(s) entre O, S, NH y N-alquilo, estando este radical cíclico sustituido opcionalmente; siendo NRvRw tal que Rv representa un átomo de hidrogeno o un radical alquilo y Rw representa un átomo de hidrogeno, un radical cicloalquilo o un radical alquilo sustituido opcionalmente con uno o varios radicales idénticos o diferentes elegidos entre los radicales hidroxilo, alcoxi y heterocicloalquilo; bien Rv y Rw forman con el átomo de nitrogeno al que están unidos un radical cíclico que comprende de 3 a 10 eslabones y opcionalmente uno o varios heteroátomos más elegido(s) entre O, S, NH y N-alquilo, estando este radical cíclico sustituido opcionalmente; estando los radicales cíclicos que pueden formar Rx y Ry o Rv y Rw respectivamente con el átomo de nitrogeno al que están unidos, sustituidos opcionalmente con uno o varios radicales idénticos o diferentes elegidos entre los átomos de halogeno, los radicales alquilo, hidroxilo, oxo, alcoxi, NH2; NHalk y N(alk)2; Rz representa los valores de Ry con la excepcion de hidrogeno; eligiéndose Rx, Ry y Rz en los radicales -NRxCORy, -CORy y NRxCO2Rz entre los significados indicados anteriormente para Rx, Ry, y Rz; siendo todos los radicales alquilo (alk), alcoxi y alquiltio anteriores lineales o ramificados y comprendiendo de 1 a 6 átomos de carbono, estando dichos productos de formula (1) en todas las formas isomeras racémicas, enantiomeras y diastereoisomeras posibles, así como las sales de adicion con los ácidos minerales y orgánicos o con las bases minerales y orgánicas de dichos productos de formula (1).
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0903236A FR2947550B1 (fr) | 2009-07-02 | 2009-07-02 | Nouveaux derives de 2,3-dihydro-1h-imidazo{1,2-a}pyrimidin-5-one, leur preparation et leur utilisation pharmaceutique comme inhibiteurs de phosphorylation d'akt (pkb) |
| US24109709P | 2009-09-10 | 2009-09-10 | |
| FR0957067A FR2951173B1 (fr) | 2009-10-09 | 2009-10-09 | Nouveaux derives de 2,3-dihydro-1h-imidazo{1,2-a}pyrimidin-5-one, leur preparation et leur utilisation pharmaceutique comme inhibiteurs de phosphorylation d'akt(pkb) |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR077446A1 true AR077446A1 (es) | 2011-08-31 |
Family
ID=43127464
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP100102346A AR077446A1 (es) | 2009-07-02 | 2010-07-01 | Derivados de 2,3-dihidro-1h-imidazo(1,2-a) pirimidin-5-ona. su preparacion y su utilizacion farmaceutica |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US8828997B2 (es) |
| EP (1) | EP2448939B1 (es) |
| JP (1) | JP5663571B2 (es) |
| KR (1) | KR101745028B1 (es) |
| CN (1) | CN102482285B (es) |
| AR (1) | AR077446A1 (es) |
| AU (1) | AU2010267814B2 (es) |
| BR (1) | BRPI1015949A2 (es) |
| CA (1) | CA2767051C (es) |
| CY (1) | CY1119442T1 (es) |
| DK (1) | DK2448939T3 (es) |
| ES (1) | ES2627428T3 (es) |
| HR (1) | HRP20170827T1 (es) |
| HU (1) | HUE034503T2 (es) |
| IL (1) | IL217294A (es) |
| LT (1) | LT2448939T (es) |
| MX (1) | MX2012000097A (es) |
| PL (1) | PL2448939T3 (es) |
| PT (1) | PT2448939T (es) |
| RU (1) | RU2554868C2 (es) |
| SG (2) | SG177421A1 (es) |
| SI (1) | SI2448939T1 (es) |
| TW (1) | TWI458730B (es) |
| UY (1) | UY32753A (es) |
| WO (1) | WO2011001112A1 (es) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK2655375T3 (en) * | 2010-12-23 | 2015-03-09 | Sanofi Sa | PYRIMIDINON DERIVATIVES, PREPARATION AND PHARMACEUTICAL USE THEREOF |
| FR2969612B1 (fr) * | 2010-12-23 | 2013-02-08 | Sanofi Aventis | Nouveaux derives de 2,3-dihydro-1h-imidazo{1,2-a}pyrimidin-5-one, leur preparation et leur utilisation pharmaceutique |
| ES2661510T3 (es) | 2011-12-15 | 2018-04-02 | Novartis Ag | Uso de inhibidores de la actividad o función de PI3K |
| FR2992316A1 (fr) * | 2012-06-22 | 2013-12-27 | Sanofi Sa | Derives de pyrimidinones, leur preparation et leur application en therapeutique |
| FR2992314B1 (fr) | 2012-06-22 | 2015-10-16 | Sanofi Sa | Nouveaux derives de 2,3-dihydro-1h-imidazo{1,2-a}pyrimidin-5-one et 1,2,3,4-tetrahydro-pyrimido{1,2-a}pyrimidin-6-one comportant une morpholine substituee, leur preparation et leur utilisation pharmaceutique |
| KR102572178B1 (ko) * | 2015-01-23 | 2023-08-28 | 글락소스미스클라인 인털렉츄얼 프로퍼티 디벨로프먼트 리미티드 | 피라졸로[3,4-d]피리미딘 유도체 및 리슈마니아증의 치료를 위한 그의 용도 |
| CN108137599B (zh) * | 2015-08-07 | 2020-10-27 | 葛兰素史密斯克莱知识产权发展有限公司 | 化合物 |
| JP2019086340A (ja) * | 2017-11-02 | 2019-06-06 | シスメックス株式会社 | 細胞検出方法および細胞検出システム |
| WO2022093820A1 (en) * | 2020-10-28 | 2022-05-05 | Genentech, Inc. | Substituted morpholine compounds |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5888381A (ja) * | 1981-11-24 | 1983-05-26 | Ube Ind Ltd | イミダゾピリミジン類 |
| US20020077327A1 (en) * | 1999-09-23 | 2002-06-20 | Neurocrine Biosciences, Inc. | Gonadotropin-releasing hormone receptor antagonists and methods relating thereto |
| MY125533A (en) * | 1999-12-06 | 2006-08-30 | Bristol Myers Squibb Co | Heterocyclic dihydropyrimidine compounds |
| AU3042601A (en) | 2000-01-24 | 2001-07-31 | Thrombogenix Pty Ltd | Therapeutic morpholino-substituted compounds |
| EP1184384A1 (en) * | 2000-09-01 | 2002-03-06 | Sanofi-Synthelabo | 1-(Alkyl), 1-((heteroaryl)alkyl) and 1-((aryl)alkyl)-7-pyridin-4-ylimidazo(1,2a)pyrimidin-5(1H)-one derivatives |
| ATE269333T1 (de) * | 2000-09-01 | 2004-07-15 | Sanofi Synthelabo | 2-pyridinyl-6,7,8,9-tetrahydropyrimido(1,2- a)pyrimidin-4-on- und 7-pyridinyl-2,3- dihydroimidazo(1,2-a)pyrimidin-5 1honderivate |
| GB0119865D0 (en) | 2001-08-14 | 2001-10-10 | Cancer Res Campaign Tech | DNA-PK inhibitors |
| CN1247585C (zh) * | 2001-09-21 | 2006-03-29 | 赛诺菲安万特 | 取代的2－吡啶基－6,7,8,9－四氢嘧啶并[1,2－a]嘧啶－4－酮及7－吡啶基－2,3－二氢咪唑并[1,2－a]嘧啶－5(1h)酮衍生物 |
| EP1340761A1 (en) | 2002-02-28 | 2003-09-03 | Sanofi-Synthelabo | Substituted 2-pyridinyl-6,7,8,9-tetrahydropyrimido[1,2-a]pyrimidin-4-one and 7-pyridinyl-2,3-dihydroimidazo[1,2-a]pyrimidin-5(1H)one derivatives |
| EP1340759A1 (en) * | 2002-02-28 | 2003-09-03 | Sanofi-Synthelabo | 1-[alkyl], 1-[(heteroaryl)alkyl] and 1-[(aryl)alkyl]-7-(pyrimidin-4-yl)-imidazo[1,2-a]pyrimidin-5(1H)-one derivatives |
| AU2003221500B9 (en) * | 2002-02-28 | 2008-11-20 | Mitsubishi Pharma Corporation | Heteroaryl substituted 2-pyridinyl and 2-pyrimidinyl -6,7,8,9-tetrahydropyrimido[1,2-a] pyrimidin-4-one derivatives |
| WO2004016607A1 (en) | 2002-08-16 | 2004-02-26 | Kinacia Pty Ltd. | Inhibition of phosphoinositide 3-kinase beta |
| CN1898243A (zh) * | 2003-12-23 | 2007-01-17 | 诺瓦提斯公司 | 二环杂环类p－38激酶抑制剂 |
| AR053358A1 (es) | 2005-04-15 | 2007-05-02 | Cancer Rec Tech Ltd | Inhibidores de adn - pk |
| EP1895997A2 (en) * | 2005-05-26 | 2008-03-12 | Kudos Pharmaceuticals Ltd | Use of dna-pk inhibition to sensitise atm deficient cancers to dna-damaging cancer therapies |
| WO2008064244A2 (en) | 2006-11-20 | 2008-05-29 | The Trustees Of Columbia University In The City Of New York | Phosphoinositide modulation for the treatment of neurodegenerative diseases |
| WO2008148074A2 (en) * | 2007-05-24 | 2008-12-04 | Research Foundation Of State University Of New York | Inhibitors of mtor and methods of treatment using same |
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2010
- 2010-07-01 US US13/381,571 patent/US8828997B2/en not_active Expired - Fee Related
- 2010-07-01 HU HUE10742012A patent/HUE034503T2/en unknown
- 2010-07-01 BR BRPI1015949A patent/BRPI1015949A2/pt not_active IP Right Cessation
- 2010-07-01 SI SI201031451A patent/SI2448939T1/sl unknown
- 2010-07-01 LT LTEP10742012.7T patent/LT2448939T/lt unknown
- 2010-07-01 PT PT107420127T patent/PT2448939T/pt unknown
- 2010-07-01 ES ES10742012.7T patent/ES2627428T3/es active Active
- 2010-07-01 HR HRP20170827TT patent/HRP20170827T1/hr unknown
- 2010-07-01 KR KR1020127002797A patent/KR101745028B1/ko not_active Expired - Fee Related
- 2010-07-01 DK DK10742012.7T patent/DK2448939T3/en active
- 2010-07-01 CN CN201080039104.3A patent/CN102482285B/zh not_active Expired - Fee Related
- 2010-07-01 EP EP10742012.7A patent/EP2448939B1/fr not_active Not-in-force
- 2010-07-01 AU AU2010267814A patent/AU2010267814B2/en not_active Ceased
- 2010-07-01 CA CA2767051A patent/CA2767051C/fr not_active Expired - Fee Related
- 2010-07-01 WO PCT/FR2010/051373 patent/WO2011001112A1/fr not_active Ceased
- 2010-07-01 SG SG2011097227A patent/SG177421A1/en unknown
- 2010-07-01 JP JP2012518118A patent/JP5663571B2/ja not_active Expired - Fee Related
- 2010-07-01 PL PL10742012T patent/PL2448939T3/pl unknown
- 2010-07-01 AR ARP100102346A patent/AR077446A1/es unknown
- 2010-07-01 MX MX2012000097A patent/MX2012000097A/es active IP Right Grant
- 2010-07-01 RU RU2012103460/04A patent/RU2554868C2/ru not_active IP Right Cessation
- 2010-07-01 SG SG10201403138WA patent/SG10201403138WA/en unknown
- 2010-07-02 UY UY0001032753A patent/UY32753A/es not_active Application Discontinuation
- 2010-07-02 TW TW099121898A patent/TWI458730B/zh not_active IP Right Cessation
-
2011
- 2011-12-29 IL IL217294A patent/IL217294A/en not_active IP Right Cessation
-
2017
- 2017-05-31 CY CY20171100567T patent/CY1119442T1/el unknown
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