PE20080527A1 - Derivado de pirimidina como inhibidor de la fosfatidilinositol 3-quinasa (pi3k) - Google Patents
Derivado de pirimidina como inhibidor de la fosfatidilinositol 3-quinasa (pi3k)Info
- Publication number
- PE20080527A1 PE20080527A1 PE2007001059A PE2007001059A PE20080527A1 PE 20080527 A1 PE20080527 A1 PE 20080527A1 PE 2007001059 A PE2007001059 A PE 2007001059A PE 2007001059 A PE2007001059 A PE 2007001059A PE 20080527 A1 PE20080527 A1 PE 20080527A1
- Authority
- PE
- Peru
- Prior art keywords
- pi3k
- phosphatidylinositol
- kinase
- pyridin
- dihydro
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- 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
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (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)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
SE REFIERE A COMPUESTOS DERIVADOS DE PIRIMIDINA DE FORMULA (I) DONDE X ES UN ENLACE SIMPLE, -CO-, -SO2-, -CS- O -CH2-; Y ES UN ENLACE SIMPLE, BENCENO, PIRIDINA, PIRAZOL, TIAZOL, ENTRE OTROS; Z ES H, ALQUILO(C1-C6), ETINILO, HALOGENO, ENTRE OTROS; m ES 1 O 2; R1 ES UN COMPUESTO DE FORMULA (R1a), (R1b1), (R1c1), ENTRE OTROS, DONDE T ES ALQUILO(C1-C6), HALOGENO, O-HALOGENOALQUILO(C1-C6), CN, ENTRE OTROS; n ES DE 0 A 5. SON COMPUESTOS PREFERIDOS: 4-(3-METOXI-FENIL)-2-MORFOLIN-4-IL-7-PIRIDIN-4-IL-6,7-DIHIDRO-5H-PIRROLO[2,3-d]PIRIMIDINA, 4-(3-METOXI-FENIL)-2-MORFOLIN-4-IL-7-PIRIDIN-3-IL-6,7-DIHIDRO-5H-PIRROLO[2,3-d]PIRIMIDINA, 5-[4-(3-METOXI-FENIL)-2-MORFOLIN-4-IL-5,6-DIHIDRO-PIRROLO[2,3-d]PIRIMIDIN-7-IL]-PIRIDIN-2-OL, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA FOSFATIDILINOSITOL 3-QUINASA (PI3K) SIENDO UTILES EN EL TRATAMIENTO DE ENFERMEDADES PROLIFERATIVAS TALES COMO EL CANCER
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006216108 | 2006-08-08 | ||
JP2007118631 | 2007-04-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20080527A1 true PE20080527A1 (es) | 2008-07-09 |
Family
ID=39032956
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2007001059A PE20080527A1 (es) | 2006-08-08 | 2007-08-08 | Derivado de pirimidina como inhibidor de la fosfatidilinositol 3-quinasa (pi3k) |
Country Status (26)
Country | Link |
---|---|
US (1) | US8022205B2 (es) |
EP (1) | EP2050749B1 (es) |
JP (1) | JP4450857B2 (es) |
KR (1) | KR101435692B1 (es) |
AR (1) | AR062292A1 (es) |
AU (1) | AU2007282535B9 (es) |
BR (1) | BRPI0714908B8 (es) |
CA (1) | CA2659604C (es) |
CL (1) | CL2007002316A1 (es) |
CY (1) | CY1119882T1 (es) |
DK (1) | DK2050749T3 (es) |
ES (1) | ES2657635T3 (es) |
HU (1) | HUE035116T2 (es) |
IL (1) | IL196601A (es) |
LT (1) | LT2050749T (es) |
MX (1) | MX2009001451A (es) |
MY (1) | MY145385A (es) |
NO (1) | NO342978B1 (es) |
NZ (1) | NZ575274A (es) |
PE (1) | PE20080527A1 (es) |
PL (1) | PL2050749T3 (es) |
PT (1) | PT2050749T (es) |
RU (1) | RU2448109C2 (es) |
SI (1) | SI2050749T1 (es) |
TW (1) | TWI394758B (es) |
WO (1) | WO2008018426A1 (es) |
Families Citing this family (69)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MX2009006613A (es) * | 2006-12-21 | 2009-07-02 | Nerviano Medical Sciences Srl | Derivados de pirazolo-quinazolina sustituidos, proceso para su preparacion y su uso como inhibidores de cinasa. |
CL2009000241A1 (es) * | 2008-02-07 | 2010-09-03 | Chugai Pharmaceutical Co Ltd | Compuestos derivados de 5-(2-morfolin-4-il-7h-pirrolo[2,3-d]pirimidin-4-il)pirimidin-2-ilamina; proceso de preparacion; composicion farmaceutica; y uso de los compuestos para tratar o prevenir una enfermedad proliferativa tal como el cancer. |
US8822513B2 (en) | 2010-03-01 | 2014-09-02 | Gtx, Inc. | Compounds for treatment of cancer |
US9447049B2 (en) | 2010-03-01 | 2016-09-20 | University Of Tennessee Research Foundation | Compounds for treatment of cancer |
ES2629927T3 (es) * | 2008-06-16 | 2017-08-16 | University Of Tennessee Research Foundation | Compuesto para el tratamiento del cáncer |
US9029408B2 (en) | 2008-06-16 | 2015-05-12 | Gtx, Inc. | Compounds for treatment of cancer |
CN102089308A (zh) * | 2008-07-07 | 2011-06-08 | 艾科睿控股公司 | Pi3k亚型选择性抑制剂 |
TWI378933B (en) | 2008-10-14 | 2012-12-11 | Daiichi Sankyo Co Ltd | Morpholinopurine derivatives |
GB2465405A (en) * | 2008-11-10 | 2010-05-19 | Univ Basel | Triazine, pyrimidine and pyridine analogues and their use in therapy |
JP5877064B2 (ja) * | 2008-11-11 | 2016-03-02 | エックスカバリー ホールディング カンパニー エルエルシー | PI3K/mTORキナーゼ阻害剤 |
PE20120305A1 (es) * | 2008-12-19 | 2012-04-09 | Abbott Lab | Compuestos heterociclicos derivados de benzotiazol y tetrahidroquinolina como inhbidores de bcl-2 y bcl-xl |
NZ595372A (en) | 2009-03-27 | 2013-11-29 | Vetdc Inc | Pyrimidinyl and 1,3,5-triazinyl benzimidazole sulfonamides and their use in cancer therapy |
WO2010114494A1 (en) * | 2009-04-03 | 2010-10-07 | S*Bio Pte Ltd | 8-substituted-2-morpholino purines for use as pi3k and/or mtor inhibitors in the treatment of proliferative disorders |
SI2442809T1 (sl) | 2009-06-17 | 2017-01-31 | Vertex Pharmaceuticals Incorporated | Inhibitorji replikacije virusov gripe |
SI2448938T1 (sl) | 2009-06-29 | 2014-08-29 | Incyte Corporation Experimental Station | Pirimidinoni kot zaviralci pi3k |
DK3072890T3 (en) | 2009-07-07 | 2019-02-11 | Mei Pharma Inc | Pyrimidinyl and 1,3,5-triazinylbenzimidazoles and their use in cancer therapy |
RU2595718C2 (ru) * | 2009-09-09 | 2016-08-27 | Селджен Авиломикс Рисерч,Инк. | Ингибиторы pi3-киназы и их применение |
WO2011075643A1 (en) | 2009-12-18 | 2011-06-23 | Incyte Corporation | Substituted heteroaryl fused derivatives as pi3k inhibitors |
WO2011109059A1 (en) | 2010-03-01 | 2011-09-09 | Gtx, Inc. | Compounds for treatment of cancer |
US8912178B2 (en) | 2010-05-19 | 2014-12-16 | Xcovery Holdings Company, LLC | mTOR selective kinase inhibitors |
JP5961187B2 (ja) | 2010-12-20 | 2016-08-02 | インサイト・ホールディングス・コーポレイションIncyte Holdings Corporation | Pi3k阻害剤としてのn−(1−(置換フェニル)エチル)−9h−プリン−6−アミン |
KR20130116358A (ko) * | 2011-02-09 | 2013-10-23 | 에프. 호프만-라 로슈 아게 | Pi3 키나아제 억제제로서 헤테로사이클릭 화합물 |
ES2608967T3 (es) | 2011-03-28 | 2017-04-17 | Mei Pharma, Inc. | (Aralquilamino sustituido en alfa y heteroarilalquilamino)pirimidinil y 1,3,5-triazinil benzimidazoles, composiciones farmacéuticas que los contienen, y estos compuestos para usar en el tratamiento de enfermedades proliferativas |
BR112014000115A2 (pt) * | 2011-07-05 | 2016-10-04 | Vertex Pharma | processos e intermediários para a produção de azaindóis, e suas formas sólidas |
UA118010C2 (uk) | 2011-08-01 | 2018-11-12 | Вертекс Фармасьютікалз Інкорпорейтед | Інгібітори реплікації вірусів грипу |
DK3196202T3 (da) | 2011-09-02 | 2019-05-13 | Incyte Holdings Corp | Heterocyclylaminer som pi3k-inhibitorer |
US20130123255A1 (en) * | 2011-11-10 | 2013-05-16 | Chugai Seiyaku Kabushiki Kaisha | Combination of a pi3k inhibitor and a mek inhibitor |
US9376715B2 (en) | 2011-12-09 | 2016-06-28 | Roche Molecular Systems, Inc | Methods for detecting mutations in the catalytic subunit of the phosphoinositol-3 kinase (PIK3CA) gene |
AR090548A1 (es) | 2012-04-02 | 2014-11-19 | Incyte Corp | Azaheterociclobencilaminas biciclicas como inhibidores de pi3k |
CN104349779A (zh) | 2012-05-16 | 2015-02-11 | 诺华股份有限公司 | Pi-3激酶抑制剂的剂量方案 |
CN103450204B (zh) * | 2012-05-31 | 2016-08-17 | 中国科学院上海药物研究所 | 吡咯[2,1-f][1,2,4]并三嗪类化合物,其制备方法及用途 |
AU2013284570B2 (en) | 2012-07-02 | 2016-04-14 | Taiho Pharmaceutical Co., Ltd. | Antitumor effect potentiator composed of imidazooxazine compound |
WO2014022728A1 (en) | 2012-08-02 | 2014-02-06 | Endo Pharmaceuticals, Inc | Substituted 5 - (quinazolin - 2 - yl) pyrimidin- 2 -amine derivatives useful as pi3k/mtor inhibitors for the treatment of cancer |
US20150258127A1 (en) | 2012-10-31 | 2015-09-17 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for preventing antiphospholipid syndrome (aps) |
AU2013337717B2 (en) * | 2012-11-01 | 2018-10-25 | Infinity Pharmaceuticals, Inc. | Treatment of cancers using PI3 kinase isoform modulators |
CN103588792B (zh) * | 2013-03-04 | 2016-03-23 | 中国科学院上海药物研究所 | 吡啶并嘧啶或嘧啶并嘧啶类化合物、其制备方法、药物组合物及其用途 |
US9242969B2 (en) | 2013-03-14 | 2016-01-26 | Novartis Ag | Biaryl amide compounds as kinase inhibitors |
US9296727B2 (en) | 2013-10-07 | 2016-03-29 | Vertex Pharmaceuticals Incorporated | Methods of regioselective synthesis of 2,4-disubstituted pyrimidines |
SG11201602446VA (en) * | 2013-10-16 | 2016-05-30 | Shanghai Yingli Pharm Co Ltd | Fused heterocyclic compound, preparation method therefor, pharmaceutical composition, and uses thereof |
SI3068782T1 (sl) | 2013-11-13 | 2018-10-30 | Vertex Pharmaceuticals Incorporated | Postopki za pripravo inhibitorjev v replikacije virusov gripe |
EP4012049A3 (en) | 2014-04-04 | 2022-08-24 | Crown Bioscience, Inc. (Taicang) | Methods for determining responsiveness to mek/erk inhibitors |
WO2015155624A1 (en) | 2014-04-10 | 2015-10-15 | Pfizer Inc. | Dihydropyrrolopyrimidine derivatives |
US10077277B2 (en) | 2014-06-11 | 2018-09-18 | Incyte Corporation | Bicyclic heteroarylaminoalkyl phenyl derivatives as PI3K inhibitors |
PH12017501538B1 (en) | 2015-02-27 | 2024-02-14 | Incyte Holdings Corp | Salts of p13k inhibitor and processes for their preparation |
CN107428779A (zh) | 2015-02-27 | 2017-12-01 | 大鹏药品工业株式会社 | 咪唑并噁嗪晶体、含有所述晶体的药物组合物和制备所述晶体的方法 |
WO2016183060A1 (en) | 2015-05-11 | 2016-11-17 | Incyte Corporation | Process for the synthesis of a phosphoinositide 3-kinase inhibitor |
WO2016183063A1 (en) | 2015-05-11 | 2016-11-17 | Incyte Corporation | Crystalline forms of a pi3k inhibitor |
WO2016183120A1 (en) | 2015-05-13 | 2016-11-17 | Vertex Pharmaceuticals Incorporated | Inhibitors of influenza viruses replication |
JP6704416B2 (ja) | 2015-05-13 | 2020-06-03 | 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Vertex Pharmaceuticals Incorporated | インフルエンザウイルスの複製の阻害剤を調製する方法 |
JP6616244B2 (ja) * | 2015-05-29 | 2019-12-04 | 北興化学工業株式会社 | 新規なヒドロキシフェニルボロン酸エステルとその製造方法、およびヒドロキシビフェニル化合物の製造法 |
US11883404B2 (en) | 2016-03-04 | 2024-01-30 | Taiho Pharmaceuticals Co., Ltd. | Preparation and composition for treatment of malignant tumors |
PT3458067T (pt) * | 2016-05-18 | 2021-04-07 | Univ Basel | Tratamento de distúrbios neurológicos |
EP3481829B1 (en) | 2016-07-08 | 2021-04-07 | H. Hoffnabb-La Roche Ag | Fused pyrimidine derivatives |
CN109311877B (zh) | 2016-07-14 | 2021-05-28 | 豪夫迈·罗氏有限公司 | 稠合嘧啶衍生物 |
IT201600092469A1 (it) * | 2016-09-14 | 2018-03-14 | Lundbeck Pharmaceuticals Italy S P A | Processo per la produzione di Blonanserina |
WO2018051306A1 (en) | 2016-09-19 | 2018-03-22 | Novartis Ag | Therapeutic combinations comprising a raf inhibitor and a erk inhibitor |
US10647721B2 (en) | 2016-10-04 | 2020-05-12 | Hoffmann-La Roche Inc. | Bicyclic heteroaryl derivatives |
FI3618875T3 (fi) | 2017-05-02 | 2023-07-04 | Novartis Ag | Raf-inhibiittoria ja trametinibia käsittävä yhdistelmähoito |
CA3063976A1 (en) | 2017-05-23 | 2018-11-29 | Mei Pharma, Inc. | Combination therapy |
RU2020109775A (ru) | 2017-08-14 | 2021-09-16 | Мей Фарма, Инк. | Комплексная терапия |
WO2019101984A1 (en) | 2017-11-27 | 2019-05-31 | F. Hoffmann-La Roche Ag | Pyrimidine derivatives |
SG11202011680YA (en) | 2018-06-01 | 2020-12-30 | Incyte Corp | Dosing regimen for the treatment of pi3k related disorders |
MX2021013817A (es) | 2019-05-13 | 2021-12-14 | Novartis Ag | Nuevas formas cristalinas de n-(3-(2-(2-hidroxietoxi)-6-morfolinop iridin-4-il)-4-metilfenil)-2-(trifluorometil)isonicotinamida como inhibidores de raf para el tratamiento del cancer. |
WO2021247862A1 (en) * | 2020-06-03 | 2021-12-09 | Yumanity Therapeutics, Inc. | Bicyclic heteroarenes and methods of their use |
TW202220661A (zh) | 2020-08-07 | 2022-06-01 | 德商柏林化學股份公司 | 包含pi3k抑制劑之經改良醫藥調配物 |
WO2022214691A1 (en) | 2021-04-09 | 2022-10-13 | Immunic Ag | Deuterated dhodh inhibitors |
WO2023107603A1 (en) * | 2021-12-08 | 2023-06-15 | Kineta, Inc. | Pyrimidines and methods of their use |
CN118946360A (zh) * | 2021-12-08 | 2024-11-12 | 奇尼塔公司 | 双环杂芳烃及其使用方法 |
WO2024023766A1 (en) | 2022-07-28 | 2024-02-01 | Berlin-Chemie Ag | P13k inhibitor combination therapy |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH08325268A (ja) | 1986-02-24 | 1996-12-10 | Mitsui Petrochem Ind Ltd | ピロロ〔3,4−d〕ピリミジン誘導体 |
WO1987004928A1 (en) | 1986-02-24 | 1987-08-27 | Mitsui Petrochemical Industries, Ltd. | Agents for treating neurophathy |
ATE139232T1 (de) * | 1989-10-11 | 1996-06-15 | Teijin Ltd | Bizyklische pyrimidinderivate, verfahren zu deren herstellung und diese enthaltende pharmazeutische zusammensetzung |
TW574214B (en) * | 1994-06-08 | 2004-02-01 | Pfizer | Corticotropin releasing factor antagonists |
NZ524806A (en) * | 2000-10-23 | 2006-03-31 | Smithkline Beecham Corp | Tri-substituted 8H-pyrido[2,3-d]pyrimidin-7-one compounds |
WO2004043367A2 (en) | 2002-11-06 | 2004-05-27 | Bristol-Myers Squibb Company | Fused heterocyclic compounds and use thereof |
MXPA05005477A (es) | 2002-11-21 | 2005-07-25 | Chiron Corp | Pirimidinas 2,4,6-trisustituidas como inhibidores de fosfotidilinositol (pi) 3-cinasa y su uso en el tratamiento del cancer. |
WO2004099209A1 (en) * | 2003-05-05 | 2004-11-18 | F. Hoffmann-La-Roche Ag | Fused pyrimidine derivatives with crf activity |
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2007
- 2007-08-07 SI SI200731994T patent/SI2050749T1/en unknown
- 2007-08-07 WO PCT/JP2007/065396 patent/WO2008018426A1/ja active Search and Examination
- 2007-08-07 KR KR1020097002650A patent/KR101435692B1/ko active Active
- 2007-08-07 BR BRPI0714908A patent/BRPI0714908B8/pt active IP Right Grant
- 2007-08-07 NZ NZ575274A patent/NZ575274A/en unknown
- 2007-08-07 DK DK07792065.0T patent/DK2050749T3/en active
- 2007-08-07 HU HUE07792065A patent/HUE035116T2/hu unknown
- 2007-08-07 AU AU2007282535A patent/AU2007282535B9/en active Active
- 2007-08-07 MX MX2009001451A patent/MX2009001451A/es active IP Right Grant
- 2007-08-07 LT LTEP07792065.0T patent/LT2050749T/lt unknown
- 2007-08-07 CA CA2659604A patent/CA2659604C/en active Active
- 2007-08-07 PL PL07792065T patent/PL2050749T3/pl unknown
- 2007-08-07 EP EP07792065.0A patent/EP2050749B1/en active Active
- 2007-08-07 US US12/376,039 patent/US8022205B2/en active Active
- 2007-08-07 JP JP2008528817A patent/JP4450857B2/ja active Active
- 2007-08-07 PT PT77920650T patent/PT2050749T/pt unknown
- 2007-08-07 MY MYPI20090459A patent/MY145385A/en unknown
- 2007-08-07 ES ES07792065T patent/ES2657635T3/es active Active
- 2007-08-07 RU RU2009108328/04A patent/RU2448109C2/ru active
- 2007-08-08 AR ARP070103510A patent/AR062292A1/es active IP Right Grant
- 2007-08-08 PE PE2007001059A patent/PE20080527A1/es active IP Right Grant
- 2007-08-08 TW TW096129165A patent/TWI394758B/zh active
- 2007-08-08 CL CL200702316A patent/CL2007002316A1/es unknown
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2008
- 2008-10-28 NO NO20084533A patent/NO342978B1/no unknown
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2009
- 2009-01-20 IL IL196601A patent/IL196601A/en active IP Right Grant
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2017
- 2017-12-28 CY CY20171101353T patent/CY1119882T1/el unknown
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