PA8568201A1 - Terapias de combinacion para tratar celulas deficientes en metiltioadenosina-fosforilasa - Google Patents
Terapias de combinacion para tratar celulas deficientes en metiltioadenosina-fosforilasaInfo
- Publication number
- PA8568201A1 PA8568201A1 PA20038568201A PA8568201A PA8568201A1 PA 8568201 A1 PA8568201 A1 PA 8568201A1 PA 20038568201 A PA20038568201 A PA 20038568201A PA 8568201 A PA8568201 A PA 8568201A PA 8568201 A1 PA8568201 A1 PA 8568201A1
- Authority
- PA
- Panama
- Prior art keywords
- combination therapies
- mtap
- deficient cells
- methyltioadenosine
- syndro
- Prior art date
Links
- 238000002648 combination therapy Methods 0.000 title abstract 3
- 230000002950 deficient Effects 0.000 title abstract 2
- 102100034187 S-methyl-5'-thioadenosine phosphorylase Human genes 0.000 abstract 3
- 101710136206 S-methyl-5'-thioadenosine phosphorylase Proteins 0.000 abstract 3
- 230000001147 anti-toxic effect Effects 0.000 abstract 2
- 239000000758 substrate Substances 0.000 abstract 2
- 239000003440 toxic substance Substances 0.000 abstract 2
- 101001138523 Homo sapiens Inosine 5'-monophosphate cyclohydrolase Proteins 0.000 abstract 1
- 102100020796 Inosine 5'-monophosphate cyclohydrolase Human genes 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 230000004663 cell proliferation Effects 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 239000002243 precursor Substances 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
Classifications
-
- 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
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
- A61K31/513—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
-
- 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
- A61K31/52—Purines, e.g. adenine
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Molecular Biology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Enzymes And Modification Thereof (AREA)
Abstract
LA PRESENTE INVENCION SE REFIERE A TERAPIAS DE COMBINACION PARA TRATAR TRASTORNOS DE PROLIFERACION CELULAR ASOCIADOS CON CELULAS DEFICIENTES EN METILTIOADENOSINAFOSFORILASA ("MTAP") EN UN ANIMAL MAMIFERO. LAS TERAPIAS DE COMBINACION DESTRUYEN SELECTIVAMENTE LAS CELULAS MTAP-DEFICIENTES POR ADMINISTRACION DE UN INHIBIDOR DE LA SINTESIS DE INOSINATO DE NOVO Y ADMINISTRANDO UN AGENTE ANTI-TOXICO, EN DONDE LOS INHIBIDORES DE LA SINTESIS DE INOSINATO DE NOVO SON INHIBIDORES DE GLICINAMIDARIBONUCLEOTIDO-FORMILTRASFERASA ("GARFT") Y/O AMINOINIDAZOLCARBOXIMIDARIBONUCLEOTIDO-FORMILTRANSFERASA ("AICARFT"), Y EL AGENTE ANTI-TOXICO ES UN SUSTRATO DE MTAP (P.EJ., METILTIOADENOSINA O "MTA"), UN PRECURSOR DE MTA, UN ANALOGO DE UN PRECURSOR DE MTA O UN PROFARMACO DE UN SUSTRATO DE MTAP.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US36164502P | 2002-03-04 | 2002-03-04 | |
| US43227502P | 2002-12-09 | 2002-12-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PA8568201A1 true PA8568201A1 (es) | 2003-11-12 |
Family
ID=27791683
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PA20038568201A PA8568201A1 (es) | 2002-03-04 | 2003-02-28 | Terapias de combinacion para tratar celulas deficientes en metiltioadenosina-fosforilasa |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US20040043959A1 (es) |
| EP (1) | EP1482977A1 (es) |
| KR (1) | KR20040091089A (es) |
| AR (1) | AR038863A1 (es) |
| AU (1) | AU2003206019A1 (es) |
| BR (1) | BR0308222A (es) |
| CA (1) | CA2477422A1 (es) |
| IL (1) | IL163776A0 (es) |
| NO (1) | NO20044191L (es) |
| PA (1) | PA8568201A1 (es) |
| PE (1) | PE20030907A1 (es) |
| TW (1) | TW200304380A (es) |
| UY (1) | UY27692A1 (es) |
| WO (1) | WO2003074083A1 (es) |
Families Citing this family (60)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2004113328A1 (en) * | 2003-06-25 | 2004-12-29 | Pfizer Inc. | Convergent asymmetric synthesis route to produce a key intermediate towards the synthesis of a garft inhibitor |
| JP2005292087A (ja) * | 2004-04-05 | 2005-10-20 | Shionogi & Co Ltd | 5’−デオキシ−5’−メチルチオアデノシンに対する抗体 |
| US7981902B2 (en) * | 2006-06-28 | 2011-07-19 | Duquesne University Of The Holy Ghost | Substituted pyrrolo[2,3-d]pyrimidines for selectively targeting tumor cells with FR type receptors |
| WO2009032057A2 (en) * | 2007-08-29 | 2009-03-12 | Adam Lubin | Method for the selective therapy of disease |
| US8193182B2 (en) | 2008-01-04 | 2012-06-05 | Intellikine, Inc. | Substituted isoquinolin-1(2H)-ones, and methods of use thereof |
| DK2240451T3 (da) | 2008-01-04 | 2017-11-20 | Intellikine Llc | Isoquinolinonderivater substitueret med en purin, der er anvendelig som pi3k-inhibitorer |
| WO2010036380A1 (en) | 2008-09-26 | 2010-04-01 | Intellikine, Inc. | Heterocyclic kinase inhibitors |
| EP2427195B1 (en) | 2009-05-07 | 2019-05-01 | Intellikine, LLC | Heterocyclic compounds and uses thereof |
| US9725479B2 (en) * | 2010-04-22 | 2017-08-08 | Ionis Pharmaceuticals, Inc. | 5′-end derivatives |
| EP2571357B1 (en) | 2010-05-21 | 2016-07-06 | Infinity Pharmaceuticals, Inc. | Chemical compounds, compositions and methods for kinase modulation |
| WO2012064973A2 (en) | 2010-11-10 | 2012-05-18 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| BR112013013668A2 (pt) | 2010-12-03 | 2016-09-06 | Epizyme Inc | moduladores 7-deazapurina de histona metiltransferase, e métodos de uso dos mesmos |
| RU2606514C2 (ru) | 2010-12-03 | 2017-01-10 | Эпизайм, Инк. | Замещенные пуриновые и 7-деазапуриновые соединения |
| DK2663309T3 (en) | 2011-01-10 | 2017-06-19 | Infinity Pharmaceuticals Inc | METHODS FOR PRODUCING ISOQUINOLINONES AND SOLID FORMS OF ISOQUINOLINONES |
| KR20140063605A (ko) | 2011-07-19 | 2014-05-27 | 인피니티 파마슈티칼스, 인코포레이티드 | 헤테로사이클릭 화합물 및 그의 용도 |
| US8969363B2 (en) | 2011-07-19 | 2015-03-03 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| AR091790A1 (es) | 2011-08-29 | 2015-03-04 | Infinity Pharmaceuticals Inc | Derivados de isoquinolin-1-ona y sus usos |
| WO2013062943A1 (en) * | 2011-10-24 | 2013-05-02 | Glaxosmithkline Intellectual Property Development Limited | New compounds |
| US8940742B2 (en) | 2012-04-10 | 2015-01-27 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| US8828998B2 (en) | 2012-06-25 | 2014-09-09 | Infinity Pharmaceuticals, Inc. | Treatment of lupus, fibrotic conditions, and inflammatory myopathies and other disorders using PI3 kinase inhibitors |
| WO2014026198A1 (en) | 2012-08-10 | 2014-02-13 | Epizyme, Inc. | Inhibitors of protein methyltransferase dot1l and methods of use thereof |
| AU2013312319B2 (en) | 2012-09-06 | 2018-04-19 | Epizyme, Inc. | Method of treating leukemia |
| KR102229478B1 (ko) | 2012-11-01 | 2021-03-18 | 인피니티 파마슈티칼스, 인코포레이티드 | Pi3 키나아제 동형단백질 조절인자를 사용하는 암의 치료 |
| CN103073606B (zh) * | 2013-02-05 | 2016-05-18 | 中国医药研究开发中心有限公司 | 5’-s-(4,4’-二甲氧基三苯甲基)-2’-脱氧肌苷的合成与制备方法 |
| US9481667B2 (en) | 2013-03-15 | 2016-11-01 | Infinity Pharmaceuticals, Inc. | Salts and solid forms of isoquinolinones and composition comprising and methods of using the same |
| JP2016517426A (ja) | 2013-03-15 | 2016-06-16 | エピザイム,インコーポレイティド | 置換プリン化合物の合成方法 |
| US9751888B2 (en) | 2013-10-04 | 2017-09-05 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| PL3052485T3 (pl) | 2013-10-04 | 2022-02-28 | Infinity Pharmaceuticals, Inc. | Związki heterocykliczne i ich zastosowania |
| CA2943075C (en) | 2014-03-19 | 2023-02-28 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds for use in the treatment of pi3k-gamma mediated disorders |
| US20150320755A1 (en) | 2014-04-16 | 2015-11-12 | Infinity Pharmaceuticals, Inc. | Combination therapies |
| US10654884B2 (en) | 2014-04-25 | 2020-05-19 | Boehringer Ingelheim International Gmbh | Purine derivatives as CD73 inhibitors for the treatment of cancer |
| WO2016054491A1 (en) | 2014-10-03 | 2016-04-07 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| JPWO2016056606A1 (ja) * | 2014-10-07 | 2017-07-20 | 国立大学法人京都大学 | ベンゾイソチアゾロピリミジン誘導体またはその塩、およびウイルス感染阻害剤ならびに医薬品 |
| TWI791251B (zh) * | 2015-08-26 | 2023-02-01 | 比利時商健生藥品公司 | 使用作為prmt5抑制劑之新穎經6-6雙環芳香環取代之核苷類似物 |
| NZ740616A (en) | 2015-09-14 | 2023-05-26 | Infinity Pharmaceuticals Inc | Solid forms of isoquinolinone derivatives, process of making, compositions comprising, and methods of using the same |
| US10898504B2 (en) | 2016-03-10 | 2021-01-26 | Janssen Pharmaceutica Nv | Substituted nucleoside analogues for use as PRMT5 inhibitors |
| WO2017153186A1 (en) | 2016-03-10 | 2017-09-14 | Janssen Pharmaceutica Nv | Substituted nucleoside analogues for use as prmt5 inhibitors |
| WO2017161116A1 (en) | 2016-03-17 | 2017-09-21 | Infinity Pharmaceuticals, Inc. | Isotopologues of isoquinolinone and quinazolinone compounds and uses thereof as pi3k kinase inhibitors |
| CA2969295A1 (en) * | 2016-06-06 | 2017-12-06 | Pfizer Inc. | Substituted carbonucleoside derivatives, and use thereof as a prmt5 inhibitor |
| WO2017214269A1 (en) | 2016-06-08 | 2017-12-14 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| IL263680B2 (en) | 2016-06-24 | 2025-10-01 | Infinity Pharmaceuticals Inc | PI3K inhibitors for use in combination with a second therapeutic agent for the treatment, management or prevention of cancer |
| US12084462B2 (en) | 2016-09-14 | 2024-09-10 | Janssen Pharmaceutica Nv | Spiro bicyclic inhibitors of menin-MLL interaction |
| LT3512857T (lt) | 2016-09-14 | 2021-04-12 | Janssen Pharmaceutica Nv | Menin-mll sąveikos spirobicikliniai inhibitoriai |
| US10611778B2 (en) | 2016-09-14 | 2020-04-07 | Janssen Pharmaceutica Nv | Fused bicyclic inhibitors of menin-MLL interaction |
| WO2018065365A1 (en) | 2016-10-03 | 2018-04-12 | Janssen Pharmaceutica Nv | Novel monocyclic and bicyclic ring system substituted carbanucleoside analogues for use as prmt5 inhibitors |
| EP3519413A1 (en) * | 2016-10-03 | 2019-08-07 | Janssen Pharmaceutica NV | Novel monocyclic and bicyclic ring system substituted carbanucleoside analogues for use as prmt5 inhibitors |
| MX391405B (es) | 2016-12-15 | 2025-03-21 | Janssen Pharmaceutica Nv | Inhibidores de azepano de la interacción menina-mll. |
| PE20191359A1 (es) | 2017-02-27 | 2019-10-01 | Janssen Pharmaceutica Nv | Uso de biomarcadores en la identificacion de pacientes con cancer que seran sensibles al tratamiento con un inhibidor de prmt5 |
| MX2020005944A (es) | 2017-12-08 | 2020-08-24 | Janssen Pharmaceutica Nv | Analogos espirobiciclicos novedosos. |
| US11396517B1 (en) | 2017-12-20 | 2022-07-26 | Janssen Pharmaceutica Nv | Exo-aza spiro inhibitors of menin-MLL interaction |
| CN109369758B (zh) * | 2018-11-02 | 2021-04-13 | 哈尔滨商业大学 | 5′-(6-氯烟酰酯)-3′-脱氧腺苷的合成方法及其应用 |
| CN109111445B (zh) * | 2018-11-02 | 2020-12-18 | 哈尔滨商业大学 | 5’-呋喃甲酰酯-3’-脱氧腺苷的合成方法及应用 |
| WO2020190073A1 (ko) * | 2019-03-20 | 2020-09-24 | 한국화학연구원 | 신규한 아졸로피리미딘 헤테로고리 화합물을 유효 성분으로 함유하는 약제학적 조성물 |
| TW202112375A (zh) | 2019-06-06 | 2021-04-01 | 比利時商健生藥品公司 | 使用prmt5抑制劑治療癌症之方法 |
| JOP20210327A1 (ar) | 2019-06-12 | 2023-01-30 | Janssen Pharmaceutica Nv | مركبات وسيطة سبيرو ثنائية الحلقة جديدة |
| UA129208C2 (uk) | 2019-12-19 | 2025-02-05 | Янссен Фармацевтика Нв | Заміщені спіропохідні з прямим ланцюгом |
| CN116406271B (zh) * | 2020-07-14 | 2024-09-24 | 南京再明医药有限公司 | 双环类化合物 |
| LV15670B (lv) * | 2021-03-10 | 2023-11-20 | Latvijas Organiskās Sintēzes Institūts | Jauni adenozilmerkaptāna atvasinājumi kā vīrusu m-RNS kapinga metiltransferāžu inhibitori |
| US20240208944A1 (en) * | 2021-04-19 | 2024-06-27 | Emory University | Quinazoline Derivatives, Pharmaceutical Compositions, and Therapeutic Uses Related to Nox Inhibition |
| CN113603721B (zh) * | 2021-06-21 | 2023-12-01 | 重庆文理学院 | 一种合成saicar的方法 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4683195A (en) * | 1986-01-30 | 1987-07-28 | Cetus Corporation | Process for amplifying, detecting, and/or-cloning nucleic acid sequences |
| US4683202A (en) * | 1985-03-28 | 1987-07-28 | Cetus Corporation | Process for amplifying nucleic acid sequences |
| GB8625019D0 (en) * | 1986-10-18 | 1986-11-19 | Wellcome Found | Compounds |
| SG52739A1 (en) * | 1992-12-16 | 1998-09-28 | Agouron Pharma | Antiproliferative substituted 5-thiapyrimidinone and 5-selenopyrimidinone compounds |
| US5945427A (en) * | 1995-06-07 | 1999-08-31 | Agouron Pharmaceuticals, Inc. | Antiproliferative substituted 5-thiapyrimidinone and 5-selenopyrimidinone compounds |
| US5594139A (en) * | 1993-01-29 | 1997-01-14 | Agouron Pharmaceuticals, Inc. | Processes for preparing antiproliferative garft-inhibiting compounds |
| ATE201877T1 (de) * | 1993-01-29 | 2001-06-15 | Agouron Pharma | Kondensierte heterocyclische glutaminsäurederivate als antiproliferative mittel |
| US5942393A (en) * | 1993-12-29 | 1999-08-24 | The Regents Of The University Of California | Method for the detection of the presence or absence of methylthioadenosine phosphorylase (MTASE) in a cell sample by detection of the presence or absence of MTASE encoding nucleic acid in the cell sample |
| US5840505A (en) * | 1993-12-29 | 1998-11-24 | The Regents Of The University Of California | Method for inhibiting adenylosuccinate synthetase activity in methylthioadenosine phosphorylase deficient cells |
| US5608082A (en) * | 1994-07-28 | 1997-03-04 | Agouron Pharmaceuticals, Inc. | Compounds useful as antiproliferative agents and GARFT inhibitors |
| ATE242253T1 (de) * | 1994-07-28 | 2003-06-15 | Agouron Pharma | Verbindungen die als antiproliferierende mittel und garft inhibitoren verwendbar sind |
-
2003
- 2003-02-14 US US10/367,366 patent/US20040043959A1/en not_active Abandoned
- 2003-02-17 AU AU2003206019A patent/AU2003206019A1/en not_active Abandoned
- 2003-02-17 BR BR0308222-9A patent/BR0308222A/pt not_active Application Discontinuation
- 2003-02-17 KR KR10-2004-7013707A patent/KR20040091089A/ko not_active Ceased
- 2003-02-17 EP EP03702902A patent/EP1482977A1/en not_active Withdrawn
- 2003-02-17 CA CA002477422A patent/CA2477422A1/en not_active Abandoned
- 2003-02-17 WO PCT/IB2003/000615 patent/WO2003074083A1/en not_active Ceased
- 2003-02-17 IL IL17377603A patent/IL163776A0/xx unknown
- 2003-02-28 PE PE2003000205A patent/PE20030907A1/es not_active Application Discontinuation
- 2003-02-28 UY UY27692A patent/UY27692A1/es not_active Application Discontinuation
- 2003-02-28 PA PA20038568201A patent/PA8568201A1/es unknown
- 2003-03-03 AR ARP030100700A patent/AR038863A1/es not_active Application Discontinuation
- 2003-03-03 TW TW092104399A patent/TW200304380A/zh unknown
-
2004
- 2004-09-30 NO NO20044191A patent/NO20044191L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| PE20030907A1 (es) | 2003-10-29 |
| AR038863A1 (es) | 2005-02-02 |
| TW200304380A (en) | 2003-10-01 |
| CA2477422A1 (en) | 2003-09-12 |
| EP1482977A1 (en) | 2004-12-08 |
| UY27692A1 (es) | 2003-10-31 |
| IL163776A0 (en) | 2005-12-18 |
| NO20044191L (no) | 2004-09-30 |
| BR0308222A (pt) | 2005-02-09 |
| WO2003074083A1 (en) | 2003-09-12 |
| US20040043959A1 (en) | 2004-03-04 |
| AU2003206019A1 (en) | 2003-09-16 |
| KR20040091089A (ko) | 2004-10-27 |
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