MA31036B1 - Inhibiteurs non nucleosidiques de la transcriptase inverse - Google Patents
Inhibiteurs non nucleosidiques de la transcriptase inverseInfo
- Publication number
- MA31036B1 MA31036B1 MA32059A MA32059A MA31036B1 MA 31036 B1 MA31036 B1 MA 31036B1 MA 32059 A MA32059 A MA 32059A MA 32059 A MA32059 A MA 32059A MA 31036 B1 MA31036 B1 MA 31036B1
- Authority
- MA
- Morocco
- Prior art keywords
- compounds
- reverse transcriptase
- hiv
- prophylaxis
- formula
- Prior art date
Links
- 102100034343 Integrase Human genes 0.000 title 1
- 108010092799 RNA-directed DNA polymerase Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- 238000011321 prophylaxis Methods 0.000 abstract 2
- 238000011282 treatment Methods 0.000 abstract 2
- 208000030507 AIDS Diseases 0.000 abstract 1
- 102000004163 DNA-directed RNA polymerases Human genes 0.000 abstract 1
- 108090000626 DNA-directed RNA polymerases Proteins 0.000 abstract 1
- 208000031886 HIV Infections Diseases 0.000 abstract 1
- 108010078851 HIV Reverse Transcriptase Proteins 0.000 abstract 1
- 208000037357 HIV infectious disease Diseases 0.000 abstract 1
- 239000003242 anti bacterial agent Substances 0.000 abstract 1
- 229940088710 antibiotic agent Drugs 0.000 abstract 1
- 239000003443 antiviral agent Substances 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 208000033519 human immunodeficiency virus infectious disease Diseases 0.000 abstract 1
- 239000002955 immunomodulating agent Substances 0.000 abstract 1
- 229940121354 immunomodulator Drugs 0.000 abstract 1
- 239000004615 ingredient Substances 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 229940042443 other antivirals in atc Drugs 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 239000003419 rna directed dna polymerase inhibitor Substances 0.000 abstract 1
- 229960005486 vaccine Drugs 0.000 abstract 1
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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4192—1,2,3-Triazoles
-
- 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
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/16—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems
- C07D249/18—Benzotriazoles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Virology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Communicable Diseases (AREA)
- Epidemiology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Oncology (AREA)
- AIDS & HIV (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Steroid Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
L'INVENTION CONCERNE DES COMPOSÉS DE FORMULE I: (I), QUI CONSISTENT EN DES INHIBITEURS DE LA TRANSCRIPTASE INVERSE DU VIH, Q, R2, R3, R6, T1, T2, ET T3 ÉTANT DÉFINIS DANS LE PRÉSENT DOCUMENT. LES COMPOSÉS DE FORMULE I, ET LES SELS ET PROMÉDICAMENTS DE CEUX-CI ACCEPTABLES SUR LE PLAN PHARMACEUTIQUE, SONT UTILES DANS L'INHIBITION DE LA TRANSCRIPTASE INVERSE DU VIH, DANS LA PROPHYLAXIE ET LE TRAITEMENT D'INFECTION PAR LE VIH ET DANS LA PROPHYLAXIE, LE RETARDEMENT DE L'APPARITION OU DE LA PROGRESSION, ET LE TRAITEMENT DU SIDA. LES COMPOSÉS ET LEURS SELS PEUVENT ÊTRE UTILISÉS COMME INGRÉDIENTS DANS DES COMPOSITIONS PHARMACEUTIQUES, FACULTATIVEMENT COMBINÉS À D'AUTRES ANTIVIRAUX, IMMUNOMODULATEURS, ANTIBIOTIQUES OU VACCINS.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US87462906P | 2006-12-13 | 2006-12-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA31036B1 true MA31036B1 (fr) | 2009-12-01 |
Family
ID=39277099
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA32059A MA31036B1 (fr) | 2006-12-13 | 2009-06-30 | Inhibiteurs non nucleosidiques de la transcriptase inverse |
Country Status (29)
| Country | Link |
|---|---|
| US (2) | US7781454B2 (fr) |
| EP (1) | EP2121638B1 (fr) |
| JP (1) | JP5123949B2 (fr) |
| KR (1) | KR20090087481A (fr) |
| CN (1) | CN101558050A (fr) |
| AR (1) | AR064199A1 (fr) |
| AU (1) | AU2007334598B2 (fr) |
| BR (1) | BRPI0720196A2 (fr) |
| CA (1) | CA2673093A1 (fr) |
| CL (1) | CL2007003594A1 (fr) |
| CR (1) | CR10843A (fr) |
| DO (1) | DOP2009000138A (fr) |
| EA (1) | EA200970572A1 (fr) |
| EC (1) | ECSP099373A (fr) |
| GE (1) | GEP20115320B (fr) |
| GT (1) | GT200900158A (fr) |
| HN (1) | HN2009001160A (fr) |
| IL (1) | IL199103A0 (fr) |
| MA (1) | MA31036B1 (fr) |
| MX (1) | MX2009006285A (fr) |
| NI (1) | NI200900103A (fr) |
| NO (1) | NO20092636L (fr) |
| NZ (1) | NZ577637A (fr) |
| PE (1) | PE20081448A1 (fr) |
| SV (1) | SV2009003294A (fr) |
| TN (1) | TN2009000243A1 (fr) |
| TW (1) | TW200831085A (fr) |
| WO (2) | WO2008076225A2 (fr) |
| ZA (1) | ZA200903395B (fr) |
Families Citing this family (51)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0420722D0 (en) | 2004-09-17 | 2004-10-20 | Addex Pharmaceuticals Sa | Novel allosteric modulators |
| TWI417095B (zh) | 2006-03-15 | 2013-12-01 | Janssen Pharmaceuticals Inc | １，４-二取代之３-氰基-吡啶酮衍生物及其作為ｍＧｌｕＲ２-受體之正向異位性調節劑之用途 |
| TW200831085A (en) * | 2006-12-13 | 2008-08-01 | Merck & Co Inc | Non-nucleoside reverse transcriptase inhibitors |
| TW200900065A (en) | 2007-03-07 | 2009-01-01 | Janssen Pharmaceutica Nv | 3-cyano-4-(4-pyridinyloxy-phenyl)-pyridin-2-one derivatives |
| TW200845978A (en) | 2007-03-07 | 2008-12-01 | Janssen Pharmaceutica Nv | 3-cyano-4-(4-tetrahydropyran-phenyl)-pyridin-2-one derivatives |
| JP5433579B2 (ja) | 2007-09-14 | 2014-03-05 | ジャンセン ファーマシューティカルズ， インコーポレイテッド． | １，３−二置換−４−フェニル−１ｈ−ピリジン−２−オン |
| TW200922566A (en) | 2007-09-14 | 2009-06-01 | Ortho Mcneil Janssen Pharm | 1,3 disubstituted 4-(aryl-X-phenyl)-1H-pyridin-2-ones |
| RS51660B (en) | 2007-09-14 | 2011-10-31 | Ortho-Mcneil-Janssen Pharmaceuticals Inc. | 1`, 3`-DISUPSTITUATED-4-PHENYL-3,4,5,6-TETRAHYDRO-2H, 1`H- [1,4`] BIPYRIDINYL-2`-ONE |
| CN101861316B (zh) | 2007-11-14 | 2013-08-21 | 奥梅-杨森制药有限公司 | 咪唑并[1,2-a]吡啶衍生物及其作为MGLUR2受体的正变构调节剂的用途 |
| JP5269087B2 (ja) | 2007-11-16 | 2013-08-21 | ギリアード サイエンシス インコーポレーテッド | ヒト免疫不全ウイルス複製のインヒビター |
| WO2009067166A2 (fr) * | 2007-11-20 | 2009-05-28 | Merck & Co., Inc. | Inhibiteurs non-nucléosidiques de la transcriptase inverse |
| WO2009117278A2 (fr) * | 2008-03-20 | 2009-09-24 | Merck & Co., Inc. | Procédés de préparation d'éthers de biaryle substitués par un (amino-pyrazolopyridinyl)méthoxy |
| RU2510396C2 (ru) | 2008-09-02 | 2014-03-27 | Янссен Фармасьютикалз, Инк. | 3-азабицикло[3.1.0]гексильные производные в качестве модуляторов метаботропных глутаматных рецепторов |
| US8697689B2 (en) | 2008-10-16 | 2014-04-15 | Janssen Pharmaceuticals, Inc. | Indole and benzomorpholine derivatives as modulators of metabotropic glutamate receptors |
| RU2512283C2 (ru) | 2008-11-28 | 2014-04-10 | Янссен Фармасьютикалз, Инк. | Производные индола и бензоксазина в качестве модуляторов метаботропных глутаматных рецепторов |
| MY153912A (en) | 2009-05-12 | 2015-04-15 | Janssen Pharmaceuticals Inc | 1, 2, 4,-triazolo[4,3-a[pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors |
| MY153913A (en) | 2009-05-12 | 2015-04-15 | Janssen Pharmaceuticals Inc | 7-aryl-1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors |
| ME01573B (me) | 2009-05-12 | 2014-09-20 | Addex Pharma Sa | DERIVATI 1,2,4-TRIAZOLO[4,3-a]PIRIDINA I NJIHOVA UPOTREBA U TRETMANU ILI PREVENCIJI NEUROLOŠKIH I PSIHIJATRIJSKIH POREMEĆAJA |
| US20120232062A1 (en) * | 2009-10-20 | 2012-09-13 | Eiger Biopharmaceuticals, Inc. | Azaindazoles to treat flaviviridae virus infection |
| GEP20156368B (en) | 2010-03-30 | 2015-09-25 | Merck Canada Inc | Non-nucleoside reverse transcriptase inhibitors |
| WO2012062759A1 (fr) | 2010-11-08 | 2012-05-18 | Janssen Pharmaceuticals, Inc. | Dérivés 1,2,4-triazolo[4,3-a]pyridine et leur utilisation en tant que modulateurs allostériques positifs des récepteurs mglur2 |
| CN103261195B (zh) | 2010-11-08 | 2015-09-02 | 杨森制药公司 | 1,2,4-三唑并[4,3-a]吡啶衍生物及其作为MGLUR2受体的正变构调节剂的用途 |
| CA2814996C (fr) | 2010-11-08 | 2019-10-01 | Janssen Pharmaceuticals, Inc. | Derives de 1,2,4-triazolo[4,3-a]pyridine et leur utilisation en tant que modulateurs allosteriques positifs des recepteurs mglur2 |
| WO2012078416A2 (fr) * | 2010-12-06 | 2012-06-14 | Rfs Pharma, Llc | Promédicaments monophosphatés de dapd et leurs analogues |
| EP2744481A4 (fr) * | 2011-08-16 | 2015-07-01 | Merck Sharp & Dohme | Utilisation de matrice inorganique et de combinaisons de polymères organiques pour la préparation de dispersions amorphes stables |
| US9328138B2 (en) | 2011-11-15 | 2016-05-03 | Msd Italia S.R.L. | HCV NS3 protease inhibitors |
| PT2861566T (pt) | 2012-06-13 | 2017-02-08 | Hoffmann La Roche | Novos diazaspirocicloalcanos e azaspirocicloalcanos |
| UA116547C2 (uk) | 2012-09-25 | 2018-04-10 | Ф. Хоффманн-Ля Рош Аг | Біциклічні похідні |
| JO3470B1 (ar) | 2012-10-08 | 2020-07-05 | Merck Sharp & Dohme | مشتقات 5- فينوكسي-3h-بيريميدين-4-أون واستخدامها كمثبطات ناسخ عكسي ل hiv |
| CN103848826A (zh) * | 2012-11-30 | 2014-06-11 | 南京大学 | 一类含苯并三氮唑结构的1,3,4-恶二唑类衍生物的制法与用途 |
| CN103848827A (zh) * | 2012-11-30 | 2014-06-11 | 南京大学 | 一种含苯并三氮唑类衍生物在抗癌药物中的应用 |
| AR095079A1 (es) | 2013-03-12 | 2015-09-16 | Hoffmann La Roche | Derivados de octahidro-pirrolo[3,4-c]-pirrol y piridina-fenilo |
| JO3368B1 (ar) | 2013-06-04 | 2019-03-13 | Janssen Pharmaceutica Nv | مركبات 6، 7- ثاني هيدرو بيرازولو [5،1-a] بيرازين- 4 (5 يد)- اون واستخدامها بصفة منظمات تفارغية سلبية لمستقبلات ميجلور 2 |
| JO3367B1 (ar) | 2013-09-06 | 2019-03-13 | Janssen Pharmaceutica Nv | مركبات 2،1، 4- ثلاثي زولو [3،4-a] بيريدين واستخدامها بصفة منظمات تفارغية موجبة لمستقبلات ميجلور 2 |
| DK3074400T3 (en) | 2013-11-26 | 2018-01-15 | Hoffmann La Roche | Octahydro-cyclobuta [1,2-c; 3,4-c '] dipyrrole derivatives as autotaxin inhibitors |
| KR102502485B1 (ko) | 2014-01-21 | 2023-02-21 | 얀센 파마슈티카 엔.브이. | 대사 조절형 글루탐산 작동성 수용체 제2아형의 양성 알로스테릭 조절제 또는 오르토스테릭 작동제를 포함하는 조합 및 그 용도 |
| UA121965C2 (uk) | 2014-01-21 | 2020-08-25 | Янссен Фармацевтика Нв | Комбінації, які містять позитивні алостеричні модулятори або ортостеричні агоністи метаботропного глутаматергічного рецептора 2 підтипу, та їх застосування |
| MA50635A (fr) | 2014-03-26 | 2020-08-12 | Hoffmann La Roche | Nouveaux composés bicycliques comme inhibiteurs de la production d'autotaxin (atx) et de l'acide lysophosphatidique |
| UA119347C2 (uk) | 2014-03-26 | 2019-06-10 | Ф. Хоффманн-Ля Рош Аг | Конденсовані [1,4]діазепінові сполуки як інгібітори продукції аутотаксину (atх) та лізофосфатидилової кислоти (lpa) |
| BR112016022722B8 (pt) | 2014-04-01 | 2023-11-21 | Merck Sharp & Dohme | Composto, composição farmacêutica que o comprende e uso do mesmo |
| MA41898A (fr) | 2015-04-10 | 2018-02-13 | Hoffmann La Roche | Dérivés de quinazolinone bicyclique |
| KR20180043837A (ko) | 2015-09-04 | 2018-04-30 | 에프. 호프만-라 로슈 아게 | 페녹시메틸 유도체 |
| CA2983782A1 (fr) | 2015-09-24 | 2017-03-30 | F. Hoffmann-La Roche Ag | Composes bicycliques utilises en tant qu'inhibiteurs d'atx |
| WO2017050791A1 (fr) | 2015-09-24 | 2017-03-30 | F. Hoffmann-La Roche Ag | Nouveaux composés bicycliques utilisés en tant qu'inhibiteurs doubles d'atx/ca |
| CN107922412B (zh) | 2015-09-24 | 2021-02-23 | 豪夫迈·罗氏有限公司 | 作为atx抑制剂的二环化合物 |
| CA2984585A1 (fr) | 2015-09-24 | 2017-03-30 | F. Hoffmann-La Roche Ag | Nouveaux composes bicycliques utilises en tant qu'inhibiteurs doubles d'atx/ca |
| CN105906482B (zh) * | 2016-05-19 | 2019-02-12 | 江苏优嘉植物保护有限公司 | 一种利用2,5-二氯酚醚制备2,5-二氯苯酚的方法 |
| JP7090099B2 (ja) | 2017-03-16 | 2022-06-23 | エフ．ホフマン－ラ ロシュ アーゲー | Ａｔｘインヒビターとしての新規二環式化合物 |
| CR20190423A (es) | 2017-03-16 | 2019-11-01 | Hoffmann La Roche | Nuevos compuestos biciclícos como inhibidores dobles de atx/ca |
| CA3143436A1 (fr) | 2019-06-21 | 2020-12-24 | Ascendis Pharma A/S | Conjugues de composes azotes heteroaromatiques donneurs de paires d'electrons p |
| CN114031619A (zh) * | 2021-12-17 | 2022-02-11 | 山东汇海医药化工有限公司 | 一种图卡替尼中间体的制备方法 |
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| AR057455A1 (es) | 2005-07-22 | 2007-12-05 | Merck & Co Inc | Inhibidores de la transcriptasa reversa de vih y composicion farmaceutica |
| ATE503744T1 (de) | 2006-08-16 | 2011-04-15 | Hoffmann La Roche | Nicht-nukleosidische reverse-transkriptase-hemmer |
| CN101535298A (zh) * | 2006-11-16 | 2009-09-16 | 弗·哈夫曼-拉罗切有限公司 | 取代的4-咪唑类化合物 |
| TW200831085A (en) * | 2006-12-13 | 2008-08-01 | Merck & Co Inc | Non-nucleoside reverse transcriptase inhibitors |
-
2007
- 2007-12-05 TW TW096146405A patent/TW200831085A/zh unknown
- 2007-12-06 WO PCT/US2007/025012 patent/WO2008076225A2/fr active Application Filing
- 2007-12-06 KR KR1020097012312A patent/KR20090087481A/ko not_active Application Discontinuation
- 2007-12-06 WO PCT/US2007/024974 patent/WO2008076223A1/fr active Application Filing
- 2007-12-06 BR BRPI0720196-6A patent/BRPI0720196A2/pt not_active IP Right Cessation
- 2007-12-06 EP EP07862604.1A patent/EP2121638B1/fr active Active
- 2007-12-06 EA EA200970572A patent/EA200970572A1/ru unknown
- 2007-12-06 JP JP2009538427A patent/JP5123949B2/ja not_active Expired - Fee Related
- 2007-12-06 MX MX2009006285A patent/MX2009006285A/es active IP Right Grant
- 2007-12-06 NZ NZ577637A patent/NZ577637A/en not_active IP Right Cessation
- 2007-12-06 CN CNA2007800464165A patent/CN101558050A/zh active Pending
- 2007-12-06 GE GEAP200711359A patent/GEP20115320B/en unknown
- 2007-12-06 US US11/999,686 patent/US7781454B2/en active Active
- 2007-12-06 CA CA002673093A patent/CA2673093A1/fr not_active Abandoned
- 2007-12-06 AU AU2007334598A patent/AU2007334598B2/en not_active Ceased
- 2007-12-07 AR ARP070105499A patent/AR064199A1/es not_active Application Discontinuation
- 2007-12-10 PE PE2007001749A patent/PE20081448A1/es not_active Application Discontinuation
- 2007-12-11 CL CL200703594A patent/CL2007003594A1/es unknown
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2009
- 2009-05-18 ZA ZA200903395A patent/ZA200903395B/xx unknown
- 2009-05-28 NI NI200900103A patent/NI200900103A/es unknown
- 2009-06-01 EC EC2009009373A patent/ECSP099373A/es unknown
- 2009-06-02 IL IL199103A patent/IL199103A0/en unknown
- 2009-06-08 CR CR10843A patent/CR10843A/es unknown
- 2009-06-09 GT GT200900158A patent/GT200900158A/es unknown
- 2009-06-09 HN HN2009001160A patent/HN2009001160A/es unknown
- 2009-06-10 SV SV2009003294A patent/SV2009003294A/es unknown
- 2009-06-12 DO DO2009000138A patent/DOP2009000138A/es unknown
- 2009-06-12 TN TNP2009000243A patent/TN2009000243A1/fr unknown
- 2009-06-30 MA MA32059A patent/MA31036B1/fr unknown
- 2009-07-10 NO NO20092636A patent/NO20092636L/no not_active Application Discontinuation
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2010
- 2010-07-20 US US12/839,807 patent/US20100286192A1/en not_active Abandoned
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