NO20073959L - Kinazolinderivat, fremgangsmate for fremstilling og anvendelse derav for inhibering av vekst av kreftceller - Google Patents
Kinazolinderivat, fremgangsmate for fremstilling og anvendelse derav for inhibering av vekst av kreftcellerInfo
- Publication number
- NO20073959L NO20073959L NO20073959A NO20073959A NO20073959L NO 20073959 L NO20073959 L NO 20073959L NO 20073959 A NO20073959 A NO 20073959A NO 20073959 A NO20073959 A NO 20073959A NO 20073959 L NO20073959 L NO 20073959L
- Authority
- NO
- Norway
- Prior art keywords
- preparation
- quinazoline derivative
- cancer cell
- cell growth
- inhibiting cancer
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
- C07D239/94—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Abstract
Oppfinnelsen angår kinazolinderivat og et farmasøytisk akseptabelt salt derav for inhibering av vekst av cancerceller, en fremgangsmåte for fremstilling av kinazolinderivatet og et farmasøytisk preparat omfattende dette som en aktiv ingrediens.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR20040114839 | 2004-12-29 | ||
KR1020050111724A KR100735639B1 (ko) | 2004-12-29 | 2005-11-22 | 암세포 성장 억제 효과를 갖는 퀴나졸린 유도체 및 이의제조방법 |
PCT/KR2005/004395 WO2006071017A1 (en) | 2004-12-29 | 2005-12-20 | Quinazoline derivatives for inhibiting cancer cell growth and method for the preparation thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
NO20073959L true NO20073959L (no) | 2007-09-27 |
Family
ID=36615106
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO20073959A NO20073959L (no) | 2004-12-29 | 2007-07-27 | Kinazolinderivat, fremgangsmate for fremstilling og anvendelse derav for inhibering av vekst av kreftceller |
Country Status (15)
Country | Link |
---|---|
US (1) | US8003658B2 (no) |
EP (1) | EP1844022B1 (no) |
JP (1) | JP4914372B2 (no) |
KR (2) | KR100735639B1 (no) |
CN (1) | CN101094840B (no) |
AU (1) | AU2005320472B2 (no) |
BR (1) | BRPI0519474A2 (no) |
CA (1) | CA2592286C (no) |
ES (1) | ES2427445T3 (no) |
IL (1) | IL183583A (no) |
MX (1) | MX2007007458A (no) |
NO (1) | NO20073959L (no) |
NZ (1) | NZ556773A (no) |
RU (1) | RU2362773C2 (no) |
WO (1) | WO2006071017A1 (no) |
Families Citing this family (49)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7501427B2 (en) | 2003-08-14 | 2009-03-10 | Array Biopharma, Inc. | Quinazoline analogs as receptor tyrosine kinase inhibitors |
KR101028952B1 (ko) | 2003-08-14 | 2011-04-12 | 어레이 바이오파마 인크. | 수용체 티로신 키나아제 억제제로서의 퀴나졸린 유사체 |
JP2008542356A (ja) * | 2005-06-03 | 2008-11-27 | ファイザー・プロダクツ・インク | 異常な細胞増殖の治療用の二環式誘導体 |
CA2755268C (en) | 2005-11-15 | 2013-12-31 | Array Biopharma, Inc. | Erbb inhibitors |
CN101003514A (zh) * | 2006-01-20 | 2007-07-25 | 上海艾力斯医药科技有限公司 | 喹唑啉衍生物、其制备方法及用途 |
KR100929146B1 (ko) * | 2006-06-28 | 2009-12-01 | 한미약품 주식회사 | 암세포 성장 억제 효과를 갖는 퀴나졸린 유도체 |
JP2010502743A (ja) * | 2006-09-11 | 2010-01-28 | キュリス,インコーポレイテッド | 抗増殖薬剤としての多機能性低分子 |
MX2009002585A (es) * | 2006-09-11 | 2009-08-24 | Curis Inc | Inhibidores e egfr a base de quinolina que contienen porcion de enlace de zinc. |
US7547781B2 (en) | 2006-09-11 | 2009-06-16 | Curis, Inc. | Quinazoline based EGFR inhibitors containing a zinc binding moiety |
CN101245050A (zh) * | 2007-02-14 | 2008-08-20 | 上海艾力斯医药科技有限公司 | 4-苯胺喹唑啉衍生物的盐 |
US8163923B2 (en) | 2007-03-14 | 2012-04-24 | Advenchen Laboratories, Llc | Spiro substituted compounds as angiogenesis inhibitors |
US8148532B2 (en) * | 2007-03-14 | 2012-04-03 | Guoqing Paul Chen | Spiro substituted compounds as angiogenesis inhibitors |
US20120065201A1 (en) * | 2007-03-28 | 2012-03-15 | Pharmacyclics, Inc. | Inhibitors of bruton's tyrosine kinase |
US20120101113A1 (en) | 2007-03-28 | 2012-04-26 | Pharmacyclics, Inc. | Inhibitors of bruton's tyrosine kinase |
PT2154967E (pt) | 2007-04-16 | 2014-06-05 | Hutchison Medipharma Entpr Ltd | Derivados de pirimidina |
KR101397523B1 (ko) * | 2007-04-27 | 2014-05-30 | 한미약품 주식회사 | 다중저해제로서의 퀴나졸린 유도체 |
CN101348466B (zh) * | 2007-07-20 | 2012-06-20 | 江苏艾力斯生物医药有限公司 | N-{4-[3-氯-4-(3-氟-苄氧基)-苯胺基]-喹唑啉-6-基}-丙烯酰胺的制备方法 |
CN101357905B (zh) * | 2007-08-01 | 2012-06-20 | 江苏艾力斯生物医药有限公司 | 4-[3-氯-4-(3-氟-苄氧基)-苯胺基]-6-取代胺基-喹唑啉衍生物的制备方法 |
CN101544609A (zh) * | 2008-03-25 | 2009-09-30 | 上海艾力斯医药科技有限公司 | 4-苯胺喹唑啉衍生物的结晶形式 |
US7829574B2 (en) | 2008-05-09 | 2010-11-09 | Hutchison Medipharma Enterprises Limited | Substituted quinazoline compounds and their use in treating angiogenesis-related diseases |
CN101584696A (zh) | 2008-05-21 | 2009-11-25 | 上海艾力斯医药科技有限公司 | 包含喹唑啉衍生物的组合物及制备方法、用途 |
US8426430B2 (en) * | 2008-06-30 | 2013-04-23 | Hutchison Medipharma Enterprises Limited | Quinazoline derivatives |
US7737157B2 (en) | 2008-08-29 | 2010-06-15 | Hutchison Medipharma Enterprises Limited | Pyrimidine compounds |
ITMI20082336A1 (it) * | 2008-12-29 | 2010-06-30 | Univ Parma | Composti inibitori irreversibili di egfr con attivita' antiproliferativa |
US8575203B2 (en) | 2010-04-21 | 2013-11-05 | Boehringer Ingelheim International Gmbh | Chemical compounds |
CA2800913C (en) | 2010-06-03 | 2019-07-23 | Pharmacyclics, Inc. | The use of inhibitors of bruton's tyrosine kinase (btk) |
CN102311438A (zh) * | 2010-06-30 | 2012-01-11 | 和记黄埔医药(上海)有限公司 | 喹唑啉化合物 |
CN102906086B (zh) * | 2010-06-30 | 2014-02-12 | 和记黄埔医药(上海)有限公司 | 喹唑啉化合物 |
CN102485735B (zh) * | 2010-12-02 | 2014-09-24 | 东莞南方医大代谢医学研发有限公司 | 6-果糖氨-4-芳胺基喹唑啉衍生物及其用途 |
US9138436B2 (en) | 2011-07-13 | 2015-09-22 | Pharmacyclics Llc | Inhibitors of Bruton's tyrosine kinase |
JP6437820B2 (ja) | 2011-07-27 | 2018-12-12 | シャンハイ ファーマシューティカルズ ホールディング カンパニー,リミティド | キナゾリン誘導体、その製造方法、中間体、組成物及びその適用 |
US8377946B1 (en) | 2011-12-30 | 2013-02-19 | Pharmacyclics, Inc. | Pyrazolo[3,4-d]pyrimidine and pyrrolo[2,3-d]pyrimidine compounds as kinase inhibitors |
WO2013143057A1 (zh) * | 2012-03-26 | 2013-10-03 | 中国科学院福建物质结构研究所 | 喹唑啉衍生物及用途 |
CN103360382B (zh) * | 2012-03-26 | 2016-04-27 | 中国科学院福建物质结构研究所 | 喹唑啉衍生物及其用途 |
BR112015001690A2 (pt) | 2012-07-24 | 2017-11-07 | Pharmacyclics Inc | mutações associadas com a resistência a inibidores da tirosina quinase de bruton (btk) |
CN103102315B (zh) * | 2012-11-01 | 2016-01-20 | 云南大学 | 一种喹唑啉类芳基脲及其制备方法和用途 |
CN102942561A (zh) * | 2012-11-06 | 2013-02-27 | 深圳海王药业有限公司 | 4-氨基喹唑啉杂环化合物及其用途 |
CN103275018B (zh) * | 2013-04-26 | 2016-03-02 | 浙江工业大学 | 4-[3-氯-4-取代苯胺基]-6-取代甲酰氨基喹唑啉类化合物及制备和应用 |
CN103288758B (zh) * | 2013-05-16 | 2015-01-21 | 苏州明锐医药科技有限公司 | 一种达克米替尼的制备方法 |
CA2925124A1 (en) | 2013-09-30 | 2015-04-02 | Pharmacyclics Llc | Inhibitors of bruton's tyrosine kinase |
CN103570692A (zh) * | 2013-10-31 | 2014-02-12 | 浙江大学 | 含吖丙啶环侧链的喹唑啉衍生物及制备和应用 |
WO2015120821A1 (zh) * | 2014-02-17 | 2015-08-20 | 江苏恩华络康药物研发有限公司 | 一类水溶性丙泊酚衍生物及其用途 |
US10239851B2 (en) | 2014-02-17 | 2019-03-26 | Qingeng Li | Carboxylic acid derivatives and use thereof in the preparation of prodrugs |
US9885086B2 (en) | 2014-03-20 | 2018-02-06 | Pharmacyclics Llc | Phospholipase C gamma 2 and resistance associated mutations |
KR102139496B1 (ko) | 2014-12-15 | 2020-07-30 | 더 리젠츠 오브 더 유니버시티 오브 미시간 | Egfr 및 pi3k의 소분자 억제제 |
CN106117182B (zh) * | 2016-06-20 | 2019-08-30 | 中国药科大学 | 喹唑啉-n-苯乙基四氢异喹啉类化合物及其制备方法和应用 |
JP2020023441A (ja) * | 2016-11-02 | 2020-02-13 | 国立大学法人九州大学 | Egfr阻害及び腫瘍治療に有用な新規化合物 |
AU2019340598A1 (en) * | 2018-09-14 | 2021-03-18 | Hanmi Pharmaceutical Co., Ltd. | Crystalline forms of a quinazole compound and its hydrochloride salts |
CN117295716A (zh) | 2020-12-22 | 2023-12-26 | 麦克尼斯迪克治疗有限公司 | 作为egfr和/或pi3k抑制剂的取代氨基苄基杂芳基化合物 |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9323290D0 (en) | 1992-12-10 | 1994-01-05 | Zeneca Ltd | Quinazoline derivatives |
GB9603095D0 (en) * | 1996-02-14 | 1996-04-10 | Zeneca Ltd | Quinazoline derivatives |
TW436485B (en) | 1997-08-01 | 2001-05-28 | American Cyanamid Co | Substituted quinazoline derivatives |
SI20582A (sl) * | 2000-05-05 | 2001-12-31 | Univerza V Ljubljani | Novi inhibitorji trombina, njihova priprava in uporaba |
OA12291A (en) | 2000-06-22 | 2004-03-18 | Pfizer Prod Inc | Substituted bicyclic derivatives for the treatmentof abnormal cell growth. |
US20020082270A1 (en) * | 2000-08-26 | 2002-06-27 | Frank Himmelsbach | Aminoquinazolines which inhibit signal transduction mediated by tyrosine kinases |
WO2002068396A1 (en) * | 2001-02-26 | 2002-09-06 | Mcgill University | Combi-molecules having signal transduction inhibitory properties and dna damaging properties |
PE20040945A1 (es) * | 2003-02-05 | 2004-12-14 | Warner Lambert Co | Preparacion de quinazolinas substituidas |
ES2374553T3 (es) | 2004-05-06 | 2012-02-17 | Warner-Lambert Company Llc | 4-fenilamino-quinazolin-6-il-amidas. |
-
2005
- 2005-11-22 KR KR1020050111724A patent/KR100735639B1/ko active IP Right Grant
- 2005-12-20 MX MX2007007458A patent/MX2007007458A/es active IP Right Grant
- 2005-12-20 BR BRPI0519474-1A patent/BRPI0519474A2/pt not_active IP Right Cessation
- 2005-12-20 JP JP2007549242A patent/JP4914372B2/ja not_active Expired - Fee Related
- 2005-12-20 AU AU2005320472A patent/AU2005320472B2/en not_active Ceased
- 2005-12-20 RU RU2007128920/04A patent/RU2362773C2/ru not_active IP Right Cessation
- 2005-12-20 WO PCT/KR2005/004395 patent/WO2006071017A1/en active Application Filing
- 2005-12-20 US US11/722,096 patent/US8003658B2/en not_active Expired - Fee Related
- 2005-12-20 NZ NZ556773A patent/NZ556773A/en not_active IP Right Cessation
- 2005-12-20 EP EP05819138.8A patent/EP1844022B1/en not_active Not-in-force
- 2005-12-20 CA CA2592286A patent/CA2592286C/en not_active Expired - Fee Related
- 2005-12-20 CN CN2005800455133A patent/CN101094840B/zh not_active Expired - Fee Related
- 2005-12-20 ES ES05819138T patent/ES2427445T3/es active Active
- 2005-12-22 KR KR1020050127660A patent/KR100658891B1/ko active IP Right Grant
-
2007
- 2007-05-31 IL IL183583A patent/IL183583A/en not_active IP Right Cessation
- 2007-07-27 NO NO20073959A patent/NO20073959L/no unknown
Also Published As
Publication number | Publication date |
---|---|
NZ556773A (en) | 2010-10-29 |
KR100658891B1 (ko) | 2006-12-15 |
EP1844022A1 (en) | 2007-10-17 |
MX2007007458A (es) | 2007-08-15 |
CN101094840A (zh) | 2007-12-26 |
RU2362773C2 (ru) | 2009-07-27 |
WO2006071017A1 (en) | 2006-07-06 |
EP1844022B1 (en) | 2013-08-14 |
KR100735639B1 (ko) | 2007-07-04 |
CN101094840B (zh) | 2012-10-31 |
BRPI0519474A2 (pt) | 2009-01-27 |
AU2005320472B2 (en) | 2009-02-26 |
IL183583A (en) | 2015-11-30 |
JP2008525522A (ja) | 2008-07-17 |
IL183583A0 (en) | 2007-09-20 |
US20080009509A1 (en) | 2008-01-10 |
CA2592286A1 (en) | 2006-07-06 |
ES2427445T3 (es) | 2013-10-30 |
KR20060076186A (ko) | 2006-07-04 |
RU2007128920A (ru) | 2009-02-10 |
JP4914372B2 (ja) | 2012-04-11 |
KR20060076210A (ko) | 2006-07-04 |
AU2005320472A1 (en) | 2006-07-06 |
EP1844022A4 (en) | 2009-10-28 |
CA2592286C (en) | 2012-05-29 |
US8003658B2 (en) | 2011-08-23 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
NO20073959L (no) | Kinazolinderivat, fremgangsmate for fremstilling og anvendelse derav for inhibering av vekst av kreftceller | |
DK2324008T3 (da) | Diarylpyrazol som protein kinase inhibitorer | |
EA201070167A1 (ru) | Замещенные производные индазола, активные как ингибиторы киназы | |
TW200833693A (en) | Substituted pyrazolo-quinazoline derivatives, process for their preparation and their use as kinase inhibitors | |
EA200970595A1 (ru) | Производные замещенных индазолов, активные в качестве ингибиторов киназ | |
WO2009071480A3 (en) | Substituted dihydropteridin-6-one derivatives, process for their preparation and their use as kinase inhibitors | |
IS8132A (is) | Pýrósóló-kínasólín afleiður, aðferð við framleiðslu þeirra og notkun sem kínasa hindrar | |
WO2005005414A3 (en) | Pyrazolyl-indole derivatives active as kinase inhibitors, process for their preparation and pharmaceutical compositions comprising them | |
AU2003244632A1 (en) | Bicyclo-pyrazoles active as kinase inhibitors, process for their preparation and pharmaceutical compositions comprising them | |
AU2003227741A1 (en) | Aminoindazole derivatives active as kinase inhibitors, process for their preparation and pharmaceutical compositions comprising them | |
BRPI0415288A (pt) | composto, composição farmacêutica, método para tratar ou prevenir doenças, e, método para preparar o composto | |
BRPI0413427A (pt) | derivados de piridilpirrol ativos como inibidores da cinase | |
RS52169B (en) | STABLE LAKVINIMOD PREPARATIONS | |
ATE514699T1 (de) | Substituierte pyrrolopyrazolderivate als kinaseinhibitoren | |
WO2008150118A3 (en) | Novel amide derivative for inhibiting the growth of cancer cells | |
NO20082088L (no) | Azetidiner som MEK-inhibitorer for behandling av proliferative sykdommer | |
NO20071617L (no) | Indozolonderivater som 11B-HSD1-inhibitorer | |
AU2003244649A1 (en) | Bicyclo-pyrazoles active as kinase inhibitors, process for their preparation and pharmaceutical compositions comprising them | |
UA97348C2 (en) | HETEROCYCLIC NF-kB INHIBITORS | |
WO2005014572A8 (en) | Pyrimidylpyrrole derivatives active as kinase inhibitors | |
WO2009032843A3 (en) | Deuterated ethambutols and their use | |
UA102219C2 (ru) | Замещенные пиразолохиназолиновые производные, способ их получения и их применения как ингибиторов киназы | |
EA201000889A1 (ru) | Тризамещенные пиперидины в качестве ингибиторов ренина | |
WO2007052167A3 (en) | Stable composition for a pharmaceutical formulation containing olanzapine | |
CU23596A3 (es) | Derivados de pirazol-quinazolina y proceso para su preparación |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
CREP | Change of representative |
Representative=s name: TANDBERGS PATENTKONTOR AS, POSTBOKS |
|
RE | Reestablishment of rights (par. 72 patents act) |