NO20092692L - MAPK/ERK kinaseinhibitorer - Google Patents
MAPK/ERK kinaseinhibitorerInfo
- Publication number
- NO20092692L NO20092692L NO20092692A NO20092692A NO20092692L NO 20092692 L NO20092692 L NO 20092692L NO 20092692 A NO20092692 A NO 20092692A NO 20092692 A NO20092692 A NO 20092692A NO 20092692 L NO20092692 L NO 20092692L
- Authority
- NO
- Norway
- Prior art keywords
- mapk
- kinase inhibitors
- erk kinase
- compounds
- erk
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4375—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- 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
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Epidemiology (AREA)
- Urology & Nephrology (AREA)
- Transplantation (AREA)
- Cardiology (AREA)
- Communicable Diseases (AREA)
- Tropical Medicine & Parasitology (AREA)
- Vascular Medicine (AREA)
- Pain & Pain Management (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Oncology (AREA)
- Dermatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Forbindelse med følgende formel er tilveiebrakt for anvendelse med MEK: hvori variablene er som definert heri. Også tilveiebrakt er farmasøytiske sammensetninger, kitt og fremstilte artikler som innbefatter slike forbindelser; fremgangsmåter og intermediater anvendelige for fremstilling av forbindelsene; og fremgangsmåter for anvendelse av nevnte forbindelser.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US87091306P | 2006-12-20 | 2006-12-20 | |
PCT/US2007/087913 WO2008079814A2 (en) | 2006-12-20 | 2007-12-18 | Mapk/erk kinase inhibitors |
Publications (2)
Publication Number | Publication Date |
---|---|
NO20092692L true NO20092692L (no) | 2009-09-16 |
NO342270B1 NO342270B1 (no) | 2018-04-30 |
Family
ID=39462025
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO20092692A NO342270B1 (no) | 2006-12-20 | 2009-07-15 | MAPK/ERK-kinaseinhibitorer, farmasøytiske sammensetninger inneholdende slike og anvendelse |
Country Status (35)
Country | Link |
---|---|
US (4) | US8030317B2 (no) |
EP (1) | EP2125810B1 (no) |
JP (1) | JP5513127B2 (no) |
KR (1) | KR101488467B1 (no) |
CN (1) | CN101679411B (no) |
AR (1) | AR064640A1 (no) |
AU (1) | AU2007337003B2 (no) |
BR (1) | BRPI0720525B8 (no) |
CA (1) | CA2673647C (no) |
CL (1) | CL2007003742A1 (no) |
CO (1) | CO6230984A2 (no) |
CR (1) | CR10937A (no) |
DK (1) | DK2125810T3 (no) |
EA (1) | EA016312B1 (no) |
EC (1) | ECSP099529A (no) |
ES (1) | ES2430966T3 (no) |
GE (1) | GEP20125511B (no) |
HR (1) | HRP20130684T1 (no) |
IL (1) | IL199362A (no) |
JO (1) | JO2985B1 (no) |
MA (1) | MA31151B1 (no) |
MX (1) | MX2009006675A (no) |
MY (1) | MY157871A (no) |
NO (1) | NO342270B1 (no) |
NZ (1) | NZ578310A (no) |
PE (1) | PE20090071A1 (no) |
PL (1) | PL2125810T3 (no) |
PT (1) | PT2125810E (no) |
RS (1) | RS52887B (no) |
SI (1) | SI2125810T1 (no) |
TN (1) | TN2009000249A1 (no) |
TW (1) | TWI396538B (no) |
UA (1) | UA98479C2 (no) |
WO (1) | WO2008079814A2 (no) |
ZA (1) | ZA200904682B (no) |
Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1790649A1 (en) * | 2005-11-21 | 2007-05-30 | Sanofi-Aventis | Substituted bicyclic pyrimidone derivatives |
TW200800997A (en) * | 2006-03-22 | 2008-01-01 | Astrazeneca Ab | Chemical compounds |
JP5249939B2 (ja) * | 2006-10-23 | 2013-07-31 | 武田薬品工業株式会社 | Mapk/erkキナーゼ阻害剤 |
JO2985B1 (ar) * | 2006-12-20 | 2016-09-05 | Takeda Pharmaceuticals Co | مثبطات كينازmapk/erk |
SA08280783B1 (ar) * | 2007-01-11 | 2011-04-24 | استرازينيكا ايه بي | مشتقات بيريدوبيريميدين كمثبطات pde4 |
US8063066B2 (en) * | 2007-03-19 | 2011-11-22 | Takeda Pharmaceutical Company Limited | MAPK/ERK kinase inhibitors |
CA2705452C (en) * | 2007-11-12 | 2016-05-31 | Takeda Pharmaceutical Company Limited | Mapk/erk kinase inhibitors |
US20090246198A1 (en) * | 2008-03-31 | 2009-10-01 | Takeda Pharmaceutical Company Limited | Mapk/erk kinase inhibitors and methods of use thereof |
CA2742785A1 (en) * | 2008-11-18 | 2010-05-27 | Takeda Pharmaceutical Company Limited | Process for making (r) -3-(2,3-dihydroxypropyl)-6-fluoro-5-(2-flouro-4-iodophenylamino)-8-methylpyrido[2,3-d]pyrimidine-4,7(3h,8h)-dione and intermediates thereof |
JP2013532627A (ja) | 2010-07-01 | 2013-08-19 | 武田薬品工業株式会社 | cMET阻害剤とHGFおよび/またはcMETに対する抗体との組み合わせ |
TWI505828B (zh) * | 2010-12-20 | 2015-11-01 | 葛蘭素史克智慧財產(第二)有限公司 | 新穎醫藥組成物 |
UY34114A (es) | 2011-06-03 | 2013-01-03 | Millennium Pharm Inc | Combinación de inhibidores de mek e inhibidores selectivos de la quiinasa aurora a |
SG11201405356QA (en) | 2012-03-01 | 2014-11-27 | Array Biopharma Inc | Serine/threonine kinase inhibitors |
WO2013144923A1 (en) | 2012-03-30 | 2013-10-03 | Takeda Pharmaceutical Company Limited | Administration of a raf inhibitor and a mek inhibitor in the treatment of melanoma |
WO2015192761A1 (zh) * | 2014-06-17 | 2015-12-23 | 辰欣药业股份有限公司 | 作为mTOR/PI3K抑制剂的吡啶并[1,2-a]嘧啶酮类似物 |
WO2016009306A1 (en) * | 2014-07-15 | 2016-01-21 | Lupin Limited | Heterocyclyl compounds as mek inhibitors |
KR101671404B1 (ko) * | 2014-09-02 | 2016-11-02 | 한국원자력의학원 | 항암 효과, 방사선 병용치료 효과 및 당뇨병 치료 효과를 갖는 피리미딘 유도체 및 이의 의학적 용도 |
JP2016155776A (ja) * | 2015-02-24 | 2016-09-01 | 学校法人兵庫医科大学 | 抗腫瘍効果増強剤および抗腫瘍剤 |
CN111201225B (zh) * | 2017-06-23 | 2021-11-05 | 基石药业 | 作为mek抑制剂的类香豆素环类化合物及其应用 |
GB201713975D0 (en) | 2017-08-31 | 2017-10-18 | Macrophage Pharma Ltd | Medical use |
US20220144819A1 (en) | 2018-11-20 | 2022-05-12 | Nflection Therapeutics, Inc. | Naphthyridinone-aniline compounds for treatment of dermal disorders |
TWI825637B (zh) * | 2021-03-31 | 2023-12-11 | 美商輝瑞股份有限公司 | 啶-1,6(2h,7h)-二酮 |
CN117779203B (zh) * | 2024-02-28 | 2024-05-31 | 西北工业大学 | 一种n-苄基-2-甲基-4-硝基苯胺单晶及其制备方法和应用 |
Family Cites Families (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5430148A (en) | 1992-03-31 | 1995-07-04 | Agouron Pharmaceuticals, Inc. | Antiproliferative quinazolines |
IL117923A (en) | 1995-05-03 | 2000-06-01 | Warner Lambert Co | Anti-cancer pharmaceutical compositions containing polysubstituted pyrido¬2,3-d¾pyrimidine derivatives and certain such novel compounds |
EP1144385B1 (en) | 1999-01-13 | 2005-08-17 | Warner-Lambert Company Llc | Benzoheterocycles and their use as mek inhibitors |
WO2001055147A1 (en) | 2000-01-25 | 2001-08-02 | Warner-Lambert Company | PYRIDO[2,3-d]PYRIMIDINE-2,7-DIAMINE KINASE INHIBITORS |
BRPI0112584B8 (pt) | 2000-07-19 | 2021-05-25 | Warner Lambert Co | ésteres oxigenados de derivados de ácido benzidroxâmico de 4-iodofenilamino, composição farmacêutica e combinação |
NZ524806A (en) | 2000-10-23 | 2006-03-31 | Smithkline Beecham Corp | Tri-substituted 8H-pyrido[2,3-d]pyrimidin-7-one compounds |
US6825180B2 (en) | 2001-05-18 | 2004-11-30 | Cell Therapeutics, Inc. | Pyridopyrimidine compounds and their uses |
EP1482932B1 (en) | 2002-03-13 | 2009-11-25 | Array Biopharma, Inc. | N3 alkylated benzimidazole derivatives as mek inhibitors |
AU2003220202A1 (en) | 2002-03-13 | 2003-09-29 | Array Biopharma, Inc | N3 alkylated benzimidazole derivatives as mek inhibitors |
RU2330851C9 (ru) * | 2003-05-23 | 2008-10-20 | Центарис Гмбх | ПИРИДО[2,3-b]ПИРАЗИНОВЫЕ ПРОИЗВОДНЫЕ, ЛЕКАРСТВЕННОЕ СРЕДСТВО ДЛЯ ЛЕЧЕНИЯ ЗАБОЛЕВАНИЯ ИЛИ НАРУШЕНИЯ, КОТОРЫЕ ОБУСЛОВЛЕНЫ НЕПРАВИЛЬНО НАПРАВЛЕННЫМИ ПРОЦЕССАМИ КЛЕТОЧНОЙ СИГНАЛЬНОЙ ТРАНСДУКЦИИ, СПОСОБ ПОЛУЧЕНИЯ ЛЕКАРСТВЕННОГО СРЕДСТВА |
WO2005002351A2 (en) | 2003-07-03 | 2005-01-13 | Sunghag Koo | Ferment ginseng oil |
MXPA06000921A (es) | 2003-07-24 | 2006-03-30 | Warner Lambert Co | Derivados de benzamidazoles como inhibidores de mek. |
WO2005011597A2 (en) | 2003-07-29 | 2005-02-10 | Irm Llc | Compounds and compositions as protein kinase inhibitors |
US7485643B2 (en) | 2003-11-19 | 2009-02-03 | Array Biopharma Inc. | Bicyclic inhibitors of MEK and methods of use thereof |
CN101912400B (zh) | 2004-06-11 | 2013-06-26 | 日本烟草产业株式会社 | 用于治疗癌症的5-氨基-2,4,7-三氧代-3,4,7,8-四氢-2H-吡啶并[2,3-d]嘧啶衍生物和相关化合物 |
US7378423B2 (en) * | 2004-06-11 | 2008-05-27 | Japan Tobacco Inc. | Pyrimidine compound and medical use thereof |
DE102004054215A1 (de) | 2004-11-10 | 2006-05-11 | Merck Patent Gmbh | Pyridopyrimidinonderivate |
ATE443063T1 (de) | 2004-12-01 | 2009-10-15 | Merck Serono Sa | Ä1,2,4ütriazoloä4,3-aüpyridin-derivative zur behandlung hyperproliferativer erkrankungen |
US20100056516A1 (en) | 2006-07-17 | 2010-03-04 | Williams Peter D | 1-hydroxy naphthyridine compounds as anti-hiv agents |
JP5249939B2 (ja) * | 2006-10-23 | 2013-07-31 | 武田薬品工業株式会社 | Mapk/erkキナーゼ阻害剤 |
WO2008055842A1 (en) | 2006-11-09 | 2008-05-15 | F. Hoffmann-La Roche Ag | Substituted 6-phenyl-pyrido [2,3-d] pyrimidin-7-one derivatives as kinase inhibitors and methods for using the same |
JO2985B1 (ar) * | 2006-12-20 | 2016-09-05 | Takeda Pharmaceuticals Co | مثبطات كينازmapk/erk |
CA2705452C (en) * | 2007-11-12 | 2016-05-31 | Takeda Pharmaceutical Company Limited | Mapk/erk kinase inhibitors |
US20090246198A1 (en) * | 2008-03-31 | 2009-10-01 | Takeda Pharmaceutical Company Limited | Mapk/erk kinase inhibitors and methods of use thereof |
CA2742785A1 (en) | 2008-11-18 | 2010-05-27 | Takeda Pharmaceutical Company Limited | Process for making (r) -3-(2,3-dihydroxypropyl)-6-fluoro-5-(2-flouro-4-iodophenylamino)-8-methylpyrido[2,3-d]pyrimidine-4,7(3h,8h)-dione and intermediates thereof |
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2007
- 2007-12-17 JO JOP/2007/0555A patent/JO2985B1/ar active
- 2007-12-18 NZ NZ578310A patent/NZ578310A/en unknown
- 2007-12-18 US US11/958,999 patent/US8030317B2/en active Active
- 2007-12-18 SI SI200731281T patent/SI2125810T1/sl unknown
- 2007-12-18 JP JP2009543137A patent/JP5513127B2/ja active Active
- 2007-12-18 CN CN2007800503244A patent/CN101679411B/zh active Active
- 2007-12-18 BR BRPI0720525A patent/BRPI0720525B8/pt active IP Right Grant
- 2007-12-18 GE GEAP200711376A patent/GEP20125511B/en unknown
- 2007-12-18 PL PL07869422T patent/PL2125810T3/pl unknown
- 2007-12-18 EP EP07869422.1A patent/EP2125810B1/en active Active
- 2007-12-18 ES ES07869422T patent/ES2430966T3/es active Active
- 2007-12-18 KR KR20097015218A patent/KR101488467B1/ko active IP Right Grant
- 2007-12-18 AU AU2007337003A patent/AU2007337003B2/en active Active
- 2007-12-18 ZA ZA200904682A patent/ZA200904682B/xx unknown
- 2007-12-18 CA CA2673647A patent/CA2673647C/en active Active
- 2007-12-18 US US12/520,247 patent/US8293901B2/en active Active
- 2007-12-18 EA EA200970605A patent/EA016312B1/ru unknown
- 2007-12-18 UA UAA200907471A patent/UA98479C2/ru unknown
- 2007-12-18 WO PCT/US2007/087913 patent/WO2008079814A2/en active Application Filing
- 2007-12-18 MY MYPI20092545A patent/MY157871A/en unknown
- 2007-12-18 DK DK07869422.1T patent/DK2125810T3/da active
- 2007-12-18 PT PT78694221T patent/PT2125810E/pt unknown
- 2007-12-18 MX MX2009006675A patent/MX2009006675A/es active IP Right Grant
- 2007-12-18 RS RS20130315A patent/RS52887B/en unknown
- 2007-12-20 TW TW096149026A patent/TWI396538B/zh active
- 2007-12-20 CL CL200703742A patent/CL2007003742A1/es unknown
- 2007-12-20 AR ARP070105806A patent/AR064640A1/es active IP Right Grant
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2008
- 2008-01-02 PE PE2008000065A patent/PE20090071A1/es active IP Right Grant
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2009
- 2009-06-15 IL IL199362A patent/IL199362A/en active IP Right Grant
- 2009-06-17 TN TNP2009000249A patent/TN2009000249A1/fr unknown
- 2009-07-10 MA MA32088A patent/MA31151B1/fr unknown
- 2009-07-15 NO NO20092692A patent/NO342270B1/no unknown
- 2009-07-17 CO CO09074721A patent/CO6230984A2/es active IP Right Grant
- 2009-07-17 CR CR10937A patent/CR10937A/es unknown
- 2009-07-21 EC EC2009009529A patent/ECSP099529A/es unknown
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2010
- 2010-10-07 US US12/900,350 patent/US20110065733A1/en not_active Abandoned
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2012
- 2012-04-18 US US13/450,064 patent/US8470837B2/en active Active
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2013
- 2013-07-22 HR HRP20130684TT patent/HRP20130684T1/hr unknown
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