BR0111438A - Análogos de ácido barbitúrico como agentes terapeuticos - Google Patents
Análogos de ácido barbitúrico como agentes terapeuticosInfo
- Publication number
- BR0111438A BR0111438A BR0111438-7A BR0111438A BR0111438A BR 0111438 A BR0111438 A BR 0111438A BR 0111438 A BR0111438 A BR 0111438A BR 0111438 A BR0111438 A BR 0111438A
- Authority
- BR
- Brazil
- Prior art keywords
- barbituric acid
- therapeutic agents
- acid analogues
- inhibit
- hif
- Prior art date
Links
- 150000007656 barbituric acids Chemical class 0.000 title abstract 2
- 239000003814 drug Substances 0.000 title 1
- 229940124597 therapeutic agent Drugs 0.000 title 1
- 102100032742 Histone-lysine N-methyltransferase SETD2 Human genes 0.000 abstract 3
- 101000654725 Homo sapiens Histone-lysine N-methyltransferase SETD2 Proteins 0.000 abstract 3
- 208000005623 Carcinogenesis Diseases 0.000 abstract 2
- 206010028980 Neoplasm Diseases 0.000 abstract 2
- 230000033115 angiogenesis Effects 0.000 abstract 2
- 201000011510 cancer Diseases 0.000 abstract 2
- 230000036952 cancer formation Effects 0.000 abstract 2
- 231100000504 carcinogenesis Toxicity 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 230000000694 effects Effects 0.000 abstract 2
- 230000002062 proliferating effect Effects 0.000 abstract 2
- 238000000338 in vitro Methods 0.000 abstract 1
- 238000001727 in vivo Methods 0.000 abstract 1
- 230000003993 interaction Effects 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
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
- C07D403/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
- A61K31/515—Barbituric acids; Derivatives thereof, e.g. sodium pentobarbital
-
- 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
- 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
- A61K31/522—Purines, e.g. adenine having oxo groups directly attached to the heterocyclic ring, e.g. hypoxanthine, guanine, acyclovir
-
- 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
- A61K31/525—Isoalloxazines, e.g. riboflavins, vitamin B2
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/60—Three or more oxygen or sulfur atoms
- C07D239/62—Barbituric acids
-
- 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
- C07D405/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D409/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
- C07D473/04—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms
- C07D473/06—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
- C07D473/04—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms
- C07D473/06—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3
- C07D473/08—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3 with methyl radicals in positions 1 and 3, e.g. theophylline
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
"ANáLOGOS DE áCIDO BARBITúRICO COMO AGENTES TERAPEUTICOS". A presente invenção se refere a análogos de ácido barbitúricos os quais inibem a atividade de HIF-1 (por exemplo, a interação entre o HIFl<244> e p300) e, dessa forma, inibem a angiogênese, tumorigênese e condições proliferativas tal como câncer. A presente invenção também se refere a composições farmacêuticas compreendendo tais compostos e ao uso de tais compostos e composições, in vitro e in vivo, para inibir a atividade de HIF-1 e inibir a angiogênese, tumorigênese e condições proliferativas tal como câncer.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0013655.6A GB0013655D0 (en) | 2000-06-05 | 2000-06-05 | Therapeutic compounds |
| PCT/GB2001/002468 WO2001093841A2 (en) | 2000-06-05 | 2001-06-05 | Barbituric acid analogs as therapeutic agents |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BR0111438A true BR0111438A (pt) | 2003-06-17 |
Family
ID=9893008
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BR0111438-7A BR0111438A (pt) | 2000-06-05 | 2001-06-05 | Análogos de ácido barbitúrico como agentes terapeuticos |
Country Status (14)
| Country | Link |
|---|---|
| US (2) | US20030229108A1 (pt) |
| EP (1) | EP1305026B1 (pt) |
| JP (1) | JP2003535123A (pt) |
| CN (1) | CN1433312A (pt) |
| AT (1) | ATE431149T1 (pt) |
| AU (1) | AU2001260504A1 (pt) |
| BR (1) | BR0111438A (pt) |
| CA (1) | CA2410311C (pt) |
| DE (1) | DE60138709D1 (pt) |
| GB (1) | GB0013655D0 (pt) |
| IL (1) | IL153014A0 (pt) |
| NZ (1) | NZ522779A (pt) |
| WO (1) | WO2001093841A2 (pt) |
| ZA (1) | ZA200209439B (pt) |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2384428A (en) * | 2002-01-29 | 2003-07-30 | Thromb X Nv | Inhibitors of HIF |
| US7288546B1 (en) * | 2003-02-20 | 2007-10-30 | University Of Central Florida | Method and compound for inhibition of cell death |
| AU2003225668A1 (en) * | 2002-03-01 | 2003-09-16 | Pintex Pharmaceutical, Inc. | Pin1-modulating compounds and methods of use thereof |
| GB0206711D0 (en) | 2002-03-21 | 2002-05-01 | Isis Innovation | HIF Inhibitor |
| GB2386892A (en) * | 2002-03-28 | 2003-10-01 | Pantherix Ltd | Carboxy containing (phenyl-/heterocyclyl-)methylene substituted azole & azine derivatives and their therapeutic use as antibacterials |
| GB2387172A (en) * | 2002-03-28 | 2003-10-08 | Pantherix Ltd | [(Aryl-/arylthio-)aryl]methylene substituted azole & azine derivatives and their therapeutic use as antibacterials |
| ES2527068T3 (es) | 2002-10-23 | 2015-01-19 | University Of Utah Research Foundation | Análisis de fusión de amplicones con colorantes de saturación |
| EP1651226B1 (en) | 2003-07-11 | 2010-02-24 | Proteologics, Inc. | Ubiquitin ligase inhibitors and methods related thereto |
| US9657347B2 (en) | 2004-04-20 | 2017-05-23 | University of Utah Research Foundation and BioFire Defense, LLC | Nucleic acid melting analysis with saturation dyes |
| CN101083998A (zh) * | 2004-11-22 | 2007-12-05 | 王者制药研究发展有限公司 | 用腺苷a3受体激动剂强化治疗hif-1介导的病症 |
| WO2009065897A2 (en) * | 2007-11-21 | 2009-05-28 | Vib Vzw | Inhibitors of malt1 proteolytic activity and uses thereof |
| KR100965726B1 (ko) * | 2007-11-23 | 2010-06-24 | 재단법인서울대학교산학협력재단 | 피리미딘-2,4,6-트라이온 유도체를 함유하는 Hsp90억제제 및 이를 이용한 항암제 |
| CA2723233C (en) * | 2008-05-08 | 2017-06-13 | Nova Southeastern University | Specific inhibitors for vascular endothelial growth factor receptors |
| WO2010018458A2 (en) * | 2008-08-12 | 2010-02-18 | Crystalgenomics, Inc. | Phenol derivatives and methods of use thereof |
| US8304421B2 (en) * | 2008-09-30 | 2012-11-06 | Vanderbilt University | Indole compounds and their use as radiation sensitizing agents and chemotherapeutic agents |
| WO2012065139A2 (en) * | 2010-11-11 | 2012-05-18 | Board Of Regents, The University Of Texas System | Entpd5 inhibitors |
| US9878998B2 (en) * | 2011-08-18 | 2018-01-30 | Nuhope Llc | Barbiturate and thiobarbiturate compounds for use in cancer therapy |
| CN103917529B (zh) | 2011-11-11 | 2016-08-17 | 辉瑞大药厂 | 2-硫代嘧啶酮类 |
| US9873674B2 (en) * | 2012-09-21 | 2018-01-23 | Cornell University | C-Rel inhibitors and uses thereof |
| WO2014105957A1 (en) | 2012-12-28 | 2014-07-03 | Board Of Trustees University Of Arkansas | Indole compounds for use in treating inflammation and cancer |
| AU2014254078A1 (en) | 2013-04-19 | 2015-10-15 | Bioventures, Llc | Combretastatin analogs |
| CA2910063A1 (en) * | 2013-04-23 | 2014-10-30 | The Board Of Trustees Of The University Of Arkansas | Polymerase, endonuclease, and helicase inhibitors and methods of using thereof |
| WO2015048531A1 (en) * | 2013-09-26 | 2015-04-02 | Beth Israel Deaconess Medical Center, Inc. | Inhibition of sgk1 in the treatment of heart conditions |
| US9145374B2 (en) * | 2013-11-20 | 2015-09-29 | National Tsing Hua University | Shikimate pathway inhibitors and the use thereof |
| WO2015147204A1 (ja) * | 2014-03-27 | 2015-10-01 | 国立大学法人京都大学 | 血管新生増殖因子を阻害する医薬組成物 |
| CA2940694A1 (en) | 2014-03-31 | 2015-10-08 | Board Of Trustees Of The University Of Arkansas | Disubstituted triazole analogs |
| WO2015195951A1 (en) * | 2014-06-18 | 2015-12-23 | University Of Pittsburgh - Of The Commonwealth System Of Higher Education | Combination therapy to enhance the anticancer efficacy of platinum drugs |
| EP3255042B1 (en) | 2015-02-04 | 2020-12-30 | Beyondbio Inc. | Heterocyclic compound and pharmaceutical composition comprising same |
| MA42035A (fr) | 2015-05-05 | 2018-03-14 | Pfizer | 2-thiopyrimidinones |
| KR102260995B1 (ko) * | 2018-11-28 | 2021-06-04 | 국립암센터 | Plk1의 활성 억제제를 유효성분으로 포함하는 암 예방 또는 치료용 약학적 조성물 |
| WO2020205646A2 (en) * | 2019-03-29 | 2020-10-08 | Board Of Regents, The University Of Texas System | Small molecule parg inhibitors and methods of use thereof |
| GB202202297D0 (en) | 2022-02-21 | 2022-04-06 | Verona Pharma Plc | Formulation production process |
| TW202506117A (zh) | 2023-06-26 | 2025-02-16 | 英商維羅納製藥Plc公司 | 顆粒組成物 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3331687A (en) * | 1962-09-24 | 1967-07-18 | Render Belipa G M B H Fa | Electrophotographic material |
| DE2042663A1 (de) * | 1970-08-28 | 1972-03-02 | Agfa-Gevaert Ag, 5090 Leverkusen | Photographisches Trockenkopierverfahren |
| PL77134B1 (pt) * | 1971-12-29 | 1975-02-28 | ||
| US3819595A (en) * | 1972-09-05 | 1974-06-25 | Dow Chemical Co | Nucleation of normally crystalline vinylidene chloride polymers |
| SU1129202A1 (ru) * | 1981-09-08 | 1984-12-15 | Предприятие П/Я Г-4740 | Способ получени 2-арилиденкарбонильных соединений |
| JPS6229570A (ja) * | 1985-07-29 | 1987-02-07 | Kanegafuchi Chem Ind Co Ltd | 3,5−ジイソプロピルベンジリデン複素環式化合物 |
| JPH0196628A (ja) * | 1987-10-08 | 1989-04-14 | Idemitsu Kosan Co Ltd | 有機非線型光学材料 |
| US5141943A (en) * | 1990-04-12 | 1992-08-25 | Brown University Research Foundation | 5-benzyl barbiturate derivatives |
| AU6087894A (en) * | 1993-01-14 | 1994-08-15 | Cell Therapeutics, Inc. | Acetal or ketal substituted therapeutic compounds |
| JPH1048824A (ja) * | 1996-07-31 | 1998-02-20 | Toyobo Co Ltd | 光重合性組成物、それを用いた感光性原版およびその露光方法 |
| WO2000013708A1 (en) * | 1998-09-04 | 2000-03-16 | Viropharma Incorporated | Methods for treating or preventing viral infections and associated diseases |
| WO2000074725A1 (en) * | 1999-06-04 | 2000-12-14 | Dana-Farber Cancer Institute, Inc. | Identification of compounds that modify transcriptional responses to hypoxia |
-
2000
- 2000-06-05 GB GBGB0013655.6A patent/GB0013655D0/en not_active Ceased
-
2001
- 2001-06-05 CN CN01810729A patent/CN1433312A/zh active Pending
- 2001-06-05 DE DE60138709T patent/DE60138709D1/de not_active Expired - Fee Related
- 2001-06-05 AU AU2001260504A patent/AU2001260504A1/en not_active Abandoned
- 2001-06-05 AT AT01934202T patent/ATE431149T1/de not_active IP Right Cessation
- 2001-06-05 WO PCT/GB2001/002468 patent/WO2001093841A2/en not_active Ceased
- 2001-06-05 IL IL15301401A patent/IL153014A0/xx unknown
- 2001-06-05 US US10/297,203 patent/US20030229108A1/en not_active Abandoned
- 2001-06-05 NZ NZ522779A patent/NZ522779A/en unknown
- 2001-06-05 BR BR0111438-7A patent/BR0111438A/pt not_active Application Discontinuation
- 2001-06-05 EP EP01934202A patent/EP1305026B1/en not_active Expired - Lifetime
- 2001-06-05 JP JP2002501414A patent/JP2003535123A/ja active Pending
- 2001-06-05 CA CA002410311A patent/CA2410311C/en not_active Expired - Fee Related
-
2002
- 2002-11-20 ZA ZA200209439A patent/ZA200209439B/en unknown
-
2008
- 2008-01-16 US US12/015,208 patent/US20080113993A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| US20030229108A1 (en) | 2003-12-11 |
| DE60138709D1 (de) | 2009-06-25 |
| CA2410311A1 (en) | 2001-12-13 |
| CN1433312A (zh) | 2003-07-30 |
| CA2410311C (en) | 2009-12-29 |
| AU2001260504A1 (en) | 2001-12-17 |
| ZA200209439B (en) | 2003-11-20 |
| NZ522779A (en) | 2004-08-27 |
| US20080113993A1 (en) | 2008-05-15 |
| EP1305026A2 (en) | 2003-05-02 |
| WO2001093841A2 (en) | 2001-12-13 |
| GB0013655D0 (en) | 2000-07-26 |
| JP2003535123A (ja) | 2003-11-25 |
| EP1305026B1 (en) | 2009-05-13 |
| ATE431149T1 (de) | 2009-05-15 |
| WO2001093841A3 (en) | 2002-06-06 |
| IL153014A0 (en) | 2003-06-24 |
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