MA31151B1 - Inhibiteurs de mapk/erk kinase - Google Patents
Inhibiteurs de mapk/erk kinaseInfo
- Publication number
- MA31151B1 MA31151B1 MA32088A MA32088A MA31151B1 MA 31151 B1 MA31151 B1 MA 31151B1 MA 32088 A MA32088 A MA 32088A MA 32088 A MA32088 A MA 32088A MA 31151 B1 MA31151 B1 MA 31151B1
- Authority
- MA
- Morocco
- Prior art keywords
- mapk
- kinase inhibitors
- compounds
- erk kinase
- manufacture
- 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
-
- 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)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Urology & Nephrology (AREA)
- Epidemiology (AREA)
- Communicable Diseases (AREA)
- Transplantation (AREA)
- Vascular Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pain & Pain Management (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Oncology (AREA)
- Dermatology (AREA)
- Tropical Medicine & Parasitology (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)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
L'invention concerne des composés de la formule suivante prévus pour une utilisation avec la mek (i), les variables étant telles que définies ici. De même, l'invention concerne des compositions pharmaceutiques, des nécessaires et des articles de fabrication comprenant ces composés. Des procédés et des intermédiaires utiles dans la fabrication des composés ; et des procédés d'utilisation desdits composés.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US87091306P | 2006-12-20 | 2006-12-20 | |
PCT/US2007/087913 WO2008079814A2 (fr) | 2006-12-20 | 2007-12-18 | Inhibiteurs de mapk/erk kinase |
Publications (1)
Publication Number | Publication Date |
---|---|
MA31151B1 true MA31151B1 (fr) | 2010-02-01 |
Family
ID=39462025
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA32088A MA31151B1 (fr) | 2006-12-20 | 2009-07-10 | Inhibiteurs de mapk/erk kinase |
Country Status (35)
Country | Link |
---|---|
US (4) | US8030317B2 (fr) |
EP (1) | EP2125810B1 (fr) |
JP (1) | JP5513127B2 (fr) |
KR (1) | KR101488467B1 (fr) |
CN (1) | CN101679411B (fr) |
AR (1) | AR064640A1 (fr) |
AU (1) | AU2007337003B2 (fr) |
BR (1) | BRPI0720525B8 (fr) |
CA (1) | CA2673647C (fr) |
CL (1) | CL2007003742A1 (fr) |
CO (1) | CO6230984A2 (fr) |
CR (1) | CR10937A (fr) |
DK (1) | DK2125810T3 (fr) |
EA (1) | EA016312B1 (fr) |
EC (1) | ECSP099529A (fr) |
ES (1) | ES2430966T3 (fr) |
GE (1) | GEP20125511B (fr) |
HR (1) | HRP20130684T1 (fr) |
IL (1) | IL199362A (fr) |
JO (1) | JO2985B1 (fr) |
MA (1) | MA31151B1 (fr) |
MX (1) | MX2009006675A (fr) |
MY (1) | MY157871A (fr) |
NO (1) | NO342270B1 (fr) |
NZ (1) | NZ578310A (fr) |
PE (1) | PE20090071A1 (fr) |
PL (1) | PL2125810T3 (fr) |
PT (1) | PT2125810E (fr) |
RS (1) | RS52887B (fr) |
SI (1) | SI2125810T1 (fr) |
TN (1) | TN2009000249A1 (fr) |
TW (1) | TWI396538B (fr) |
UA (1) | UA98479C2 (fr) |
WO (1) | WO2008079814A2 (fr) |
ZA (1) | ZA200904682B (fr) |
Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1790649A1 (fr) * | 2005-11-21 | 2007-05-30 | Sanofi-Aventis | Dérivés de pyrimidone substitués bicycliques |
TW200800997A (en) * | 2006-03-22 | 2008-01-01 | Astrazeneca Ab | Chemical compounds |
NZ577047A (en) * | 2006-10-23 | 2011-02-25 | Takeda Pharmaceutical | Mapk/erk kinase inhibitors |
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 |
EP2150544B1 (fr) * | 2007-03-19 | 2016-01-13 | Takeda Pharmaceutical Company Limited | Inhibiteurs de mapk/erk kinase |
ES2456966T3 (es) * | 2007-11-12 | 2014-04-24 | Takeda Pharmaceutical Company Limited | Inhibidores de MAPK/ERK cinasa |
WO2009146034A2 (fr) * | 2008-03-31 | 2009-12-03 | Takeda Pharmaceutical Company Limited | Inhibiteurs de kinases mapk/erk et procédés d’utilisation de ceux-ci |
US20100125138A1 (en) * | 2008-11-18 | 2010-05-20 | 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 |
US20130315895A1 (en) | 2010-07-01 | 2013-11-28 | Takeda Pharmaceutical Company Limited | COMBINATION OF A cMET INHIBITOR AND AN ANTIBODY TO HGF AND/OR cMET |
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 |
TW201316991A (zh) | 2011-06-03 | 2013-05-01 | Millennium Pharm Inc | Mek抑制劑與奧諾拉(aurora)a激酶選擇性抑制劑之組合 |
PT2820009T (pt) | 2012-03-01 | 2018-04-12 | Array Biopharma Inc | Inibidores de serina/treonina quinases |
US20150126533A1 (en) * | 2012-03-30 | 2015-05-07 | Takeda Pharmaceutical Company Limited | Administration of a raf inhibitor and a mek inhibitor in the treatment of melanoma |
US9868737B2 (en) * | 2014-06-17 | 2018-01-16 | Cisen Pharmaceutical Co., Ltd. | Pyridino[1,2-A]pyrimidone analogue used as MTOR/P13K inhibitor |
WO2016009306A1 (fr) * | 2014-07-15 | 2016-01-21 | Lupin Limited | Composés hétérocyclyles utilisés comme inhibiteurs de mek |
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 |
BR112019027292A2 (pt) | 2017-06-23 | 2020-07-21 | Cstone Pharmaceuticals | composto cíclico semelhante a cumarina como inibidor de mek e uso do mesmo |
GB201713975D0 (en) | 2017-08-31 | 2017-10-18 | Macrophage Pharma Ltd | Medical use |
MA55144A (fr) * | 2018-11-20 | 2021-09-29 | Nflection Therapeutics Inc | Composés naphthyridinone-aniline destinés au traitement d'affections de la peau |
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 |
BR9916904A (pt) | 1999-01-13 | 2001-10-30 | Warner Lambert Co | Benzo heterociclos e seu uso como inibidores demek |
YU50402A (sh) | 2000-01-25 | 2005-11-28 | Warner-Lambert Company | Pirido(2,3-d)pirimidin-2,7-diaminski inhibitori kinaze |
EE05450B1 (et) | 2000-07-19 | 2011-08-15 | Warner-Lambert Company | 4-jodofenlaminobenshdroksaamhapete oksgeenitud estrid, nende kristallvormid ja farmatseutilised kompositsioonid ning kasutamine |
MXPA03003612A (es) | 2000-10-23 | 2003-06-19 | Smithkline Beecham Corp | Compuestos novedosos. |
US6825180B2 (en) | 2001-05-18 | 2004-11-30 | Cell Therapeutics, Inc. | Pyridopyrimidine compounds and their uses |
CN101486682B (zh) | 2002-03-13 | 2013-08-14 | 阵列生物制药公司 | 作为mek抑制剂的n3烷基化苯并咪唑衍生物 |
DOP2003000614A (es) | 2002-03-13 | 2009-09-30 | Array Biopharma Inc | Derivados de bencimidazol n3 alquilado como inhibidores de mek (n3 alkylated benzimidazole |
WO2004104003A1 (fr) * | 2003-05-23 | 2004-12-02 | Zentaris Gmbh | Nouvelles pyridopyrazines et leur utilisation en tant que modulateurs de kinases |
AU2003277715A1 (en) | 2003-07-03 | 2005-01-21 | Sunghag Koo | Ferment ginseng oil |
CA2532067C (fr) * | 2003-07-24 | 2010-12-21 | Stephen Douglas Barrett | Benzimidazoles n-methyle-substitues |
US7371750B2 (en) * | 2003-07-29 | 2008-05-13 | Irm Llc | Compounds and compositions as protein kinase inhibitors |
NZ547481A (en) | 2003-11-19 | 2009-12-24 | Array Biopharma Inc | Heterocyclic inhibitors of mek and methods of use thereof |
US7378423B2 (en) * | 2004-06-11 | 2008-05-27 | Japan Tobacco Inc. | Pyrimidine compound and medical use thereof |
WO2005121142A1 (fr) | 2004-06-11 | 2005-12-22 | Japan Tobacco Inc. | Dérivés de 5-amino-2,4,7-trioxo-3,4,7,8-tétrahydro-2h-pyrido’2,3-d! pyrimidine et composés apparentés pour le traitement du cancer |
DE102004054215A1 (de) | 2004-11-10 | 2006-05-11 | Merck Patent Gmbh | Pyridopyrimidinonderivate |
ES2330872T3 (es) | 2004-12-01 | 2009-12-16 | Merck Serono Sa | Derivados de (1,2,4)triazolo(4,3-a)piridina para el tratamiento de enfermedades hiperproliferativas. |
EP2044068A4 (fr) | 2006-07-17 | 2010-07-21 | Merck Sharp & Dohme | Composés de 1-hydroxy naphtyridine en tant qu'agents anti-vih |
NZ577047A (en) * | 2006-10-23 | 2011-02-25 | Takeda Pharmaceutical | Mapk/erk kinase inhibitors |
WO2008055842A1 (fr) | 2006-11-09 | 2008-05-15 | F. Hoffmann-La Roche Ag | Dérivés de 6-phényl-pyrido [2,3-d] pyrimidine-7-one substitués utilisés comme inhibiteurs de la kinase et méthodes d'utilisation de ceux-ci |
JO2985B1 (ar) * | 2006-12-20 | 2016-09-05 | Takeda Pharmaceuticals Co | مثبطات كينازmapk/erk |
ES2456966T3 (es) * | 2007-11-12 | 2014-04-24 | Takeda Pharmaceutical Company Limited | Inhibidores de MAPK/ERK cinasa |
WO2009146034A2 (fr) * | 2008-03-31 | 2009-12-03 | Takeda Pharmaceutical Company Limited | Inhibiteurs de kinases mapk/erk et procédés d’utilisation de ceux-ci |
US20100125138A1 (en) * | 2008-11-18 | 2010-05-20 | 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 |
-
2007
- 2007-12-17 JO JOP/2007/0555A patent/JO2985B1/ar active
- 2007-12-18 PT PT78694221T patent/PT2125810E/pt unknown
- 2007-12-18 EA EA200970605A patent/EA016312B1/ru unknown
- 2007-12-18 RS RS20130315A patent/RS52887B/en unknown
- 2007-12-18 ZA ZA200904682A patent/ZA200904682B/xx unknown
- 2007-12-18 EP EP07869422.1A patent/EP2125810B1/fr active Active
- 2007-12-18 KR KR20097015218A patent/KR101488467B1/ko active IP Right Grant
- 2007-12-18 MY MYPI20092545A patent/MY157871A/en unknown
- 2007-12-18 GE GEAP200711376A patent/GEP20125511B/en unknown
- 2007-12-18 AU AU2007337003A patent/AU2007337003B2/en active Active
- 2007-12-18 ES ES07869422T patent/ES2430966T3/es active Active
- 2007-12-18 MX MX2009006675A patent/MX2009006675A/es active IP Right Grant
- 2007-12-18 CA CA2673647A patent/CA2673647C/fr 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 DK DK07869422.1T patent/DK2125810T3/da active
- 2007-12-18 US US11/958,999 patent/US8030317B2/en active Active
- 2007-12-18 WO PCT/US2007/087913 patent/WO2008079814A2/fr active Application Filing
- 2007-12-18 UA UAA200907471A patent/UA98479C2/ru unknown
- 2007-12-18 JP JP2009543137A patent/JP5513127B2/ja active Active
- 2007-12-18 US US12/520,247 patent/US8293901B2/en active Active
- 2007-12-18 PL PL07869422T patent/PL2125810T3/pl unknown
- 2007-12-18 NZ NZ578310A patent/NZ578310A/en unknown
- 2007-12-18 SI SI200731281T patent/SI2125810T1/sl unknown
- 2007-12-20 AR ARP070105806A patent/AR064640A1/es active IP Right Grant
- 2007-12-20 TW TW096149026A patent/TWI396538B/zh active
- 2007-12-20 CL CL200703742A patent/CL2007003742A1/es unknown
-
2008
- 2008-01-02 PE PE2008000065A patent/PE20090071A1/es active IP Right Grant
-
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 CR CR10937A patent/CR10937A/es unknown
- 2009-07-17 CO CO09074721A patent/CO6230984A2/es active IP Right Grant
- 2009-07-21 EC EC2009009529A patent/ECSP099529A/es unknown
-
2010
- 2010-10-07 US US12/900,350 patent/US20110065733A1/en not_active Abandoned
-
2012
- 2012-04-18 US US13/450,064 patent/US8470837B2/en active Active
-
2013
- 2013-07-22 HR HRP20130684TT patent/HRP20130684T1/hr unknown
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