AR049389A1 - Imidazoles sustituidos, composiciones que los contienen, procedimiento de preparacion y su uso - Google Patents
Imidazoles sustituidos, composiciones que los contienen, procedimiento de preparacion y su usoInfo
- Publication number
- AR049389A1 AR049389A1 ARP050102268A ARP050102268A AR049389A1 AR 049389 A1 AR049389 A1 AR 049389A1 AR P050102268 A ARP050102268 A AR P050102268A AR P050102268 A ARP050102268 A AR P050102268A AR 049389 A1 AR049389 A1 AR 049389A1
- Authority
- AR
- Argentina
- Prior art keywords
- substituted
- alkylene
- heteroaryl
- aryl
- group
- Prior art date
Links
Classifications
-
- 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
- C07D231/56—Benzopyrazoles; Hydrogenated benzopyrazoles
-
- 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
- A61P17/06—Antipsoriatics
-
- 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
-
- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
- 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
-
- 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
- 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
- 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
-
- 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
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Diabetes (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Hematology (AREA)
- Ophthalmology & Optometry (AREA)
- Hospice & Palliative Care (AREA)
- Oncology (AREA)
- Obesity (AREA)
- Endocrinology (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
La presente se refiere en particular a indazoles sustituidos específicos que presentan una actividad inhibidora de quinasas, que tienen una actividad terapéutica, en particular en oncología. Reivindicacion 1: Producto que responde a la formula (1), en la cual 1) A se selecciona del grupo constituido por: H, arilo, heteroarilo, arilo sustituido, y heteroarilo sustituido; 2) Ar se selecciona del grupo constituido por: arilo, heteroarilo, arilo sustituido, y heteroarilo sustituido; 3) L se selecciona del grupo constituido por: enlace, CO, NH, CO-NH, NH-CO, NH-SO, NH-SO2, NH-CO-NH-SO2, SO2NH, NH-CH2, CH2-NH, CH2-CO-NH, NH-CO-CH2, NH-CH2-CO, CO-CH2-NH, NH-CO-NH, NH-CS-NH, NH-CO-O, O-CO-NH, CH2-NH-CO-NH, y NH-CO-NH-CH2; 4) M se selecciona del grupo cosntituido por enlace, CO, NH, CO-NH, CS-NH, NH-CO, NH-SO, NH-SO2, CO-NH-SO2, NH-CH2, CH2-CO-NH, NH-CO-CH2, NH-CH2-CO, y CO-CH2-NH; 5) R3 se selecciona independientemente del grupo constituido por H, alquilo, alquileno, alquinilo, arilo, heteroarilo, cicloalquilo, heterociclilo, alquilo sustituido, alquileno sustituido, alquinilo sustituido, arilo sustituido, heteroarilo sustituido, cicloalquilo sustituido, heterociclilo sustituido, alquileno, alquileno sustituido, y alquinilo sustituido; 6) R4, R5 y R7 se seleccionan independientemente del grupo cosntituido por: H, halogeno; R2, CN, O(R2), OC(O)(R2), OC(O)N(R2)(R1), OS(O2)(R2), N(R2)(R1), N=C(R2)(R1), N(R2)C(O)(R1), N(R2)C(O)O(R1), N(R6)C(O)N(R2)(R1), N(R6)C(S)N(R2)(R1), N(R2)S(O2)(R1), C(O)(R2), C(O)O(R2), C(O)N(R2)(R1), C(=N(R1))(R2), C(=N(OR1))(R2), S(R2), S(O)(R2), S(O2)(R2), S(O2)O(R2), S(O2)N(R2)(R1); en el cual cada R2, R1, R6 se selecciona independientemente del grupo constituido por H, alquilo, alquileno, alquinilo, arilo, heteroarilo, cicloalquilo, heterociclilo, alquilo sustituido, alquileno sustituido, alquinilo sustituido, arilo sustituido, heteroarilo sustituido, cicloalquilo sustituido, heterociclilo sustituido, alquileno, alquileno sustituido, y alquinilo sustituido; en el cual, cuando R2 y R1 están simultáneamente presentes en uno de los R4, R5 y R7, pueden estar unidos entre si para formar un ciclo.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0406042A FR2871158A1 (fr) | 2004-06-04 | 2004-06-04 | Indazoles substitues, compositions les contenant, procede de fabrication et utilisation |
Publications (1)
Publication Number | Publication Date |
---|---|
AR049389A1 true AR049389A1 (es) | 2006-07-26 |
Family
ID=34946329
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP050102268A AR049389A1 (es) | 2004-06-04 | 2005-06-02 | Imidazoles sustituidos, composiciones que los contienen, procedimiento de preparacion y su uso |
Country Status (22)
Country | Link |
---|---|
US (1) | US7517902B2 (es) |
EP (1) | EP1765813A1 (es) |
JP (1) | JP2008501669A (es) |
KR (1) | KR20070043769A (es) |
CN (1) | CN1980918A (es) |
AR (1) | AR049389A1 (es) |
AU (1) | AU2005259139B2 (es) |
BR (1) | BRPI0510777A (es) |
CA (1) | CA2567744A1 (es) |
CR (1) | CR8767A (es) |
EA (1) | EA012702B1 (es) |
EC (1) | ECSP067046A (es) |
FR (1) | FR2871158A1 (es) |
IL (1) | IL179595A0 (es) |
MA (1) | MA28664B1 (es) |
MX (1) | MXPA06013954A (es) |
NO (1) | NO20066050L (es) |
TN (1) | TNSN06384A1 (es) |
TW (1) | TW200610756A (es) |
UY (1) | UY28941A1 (es) |
WO (1) | WO2006003276A1 (es) |
ZA (1) | ZA200610040B (es) |
Families Citing this family (38)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PE20061119A1 (es) * | 2005-01-19 | 2006-11-27 | Aventis Pharma Sa | PIRAZOLO PIRIDINAS SUSTITUIDAS COMO INHIBIDORES DE CINASAS FAK, KDR Y Tie |
FR2889526B1 (fr) * | 2005-08-04 | 2012-02-17 | Aventis Pharma Sa | 7-aza-indazoles substitues, compositions les contenant, procede de fabrication et utilisation |
US8119655B2 (en) | 2005-10-07 | 2012-02-21 | Takeda Pharmaceutical Company Limited | Kinase inhibitors |
DE102006005179A1 (de) * | 2006-02-06 | 2007-08-09 | Merck Patent Gmbh | Aminoindazolderivate |
EP2223925A1 (en) * | 2006-10-09 | 2010-09-01 | Takeda Pharmaceutical Company Limited | Kinase inhibitors |
GEP20135728B (en) * | 2006-10-09 | 2013-01-25 | Takeda Pharmaceuticals Co | Kinase inhibitors |
EP2120932B1 (en) * | 2006-12-20 | 2014-07-09 | Nerviano Medical Sciences S.r.l. | Indazole derivatives as kinase inhibitors for the treatment of cancer |
PT2176231T (pt) | 2007-07-20 | 2016-12-09 | Nerviano Medical Sciences Srl | Derivados de indazol substituídos activos como inibidores de quinases |
KR101061599B1 (ko) * | 2008-12-05 | 2011-09-02 | 한국과학기술연구원 | 비정상 세포 성장 질환의 치료를 위한 단백질 키나아제 저해제인 신규 인다졸 유도체, 이의 약학적으로 허용가능한염 및 이를 유효성분으로 함유하는 약학적 조성물 |
US9180127B2 (en) | 2009-12-29 | 2015-11-10 | Dana-Farber Cancer Institute, Inc. | Type II Raf kinase inhibitors |
AU2011227643A1 (en) * | 2010-03-16 | 2012-09-20 | Dana-Farber Cancer Institute, Inc. | Indazole compounds and their uses |
CA2856291C (en) | 2011-11-17 | 2020-08-11 | Dana-Farber Cancer Institute, Inc. | Inhibitors of c-jun-n-terminal kinase (jnk) |
KR20130077390A (ko) * | 2011-12-29 | 2013-07-09 | 제이더블유중외제약 주식회사 | 단백질 키나아제 저해활성을 가지는 6-아미노-3-카복스아미도인다졸 유도체 |
EP2909194A1 (en) | 2012-10-18 | 2015-08-26 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinase 7 (cdk7) |
USRE48175E1 (en) | 2012-10-19 | 2020-08-25 | Dana-Farber Cancer Institute, Inc. | Hydrophobically tagged small molecules as inducers of protein degradation |
US10000483B2 (en) | 2012-10-19 | 2018-06-19 | Dana-Farber Cancer Institute, Inc. | Bone marrow on X chromosome kinase (BMX) inhibitors and uses thereof |
WO2015058126A1 (en) | 2013-10-18 | 2015-04-23 | Syros Pharmaceuticals, Inc. | Heteroaromatic compounds useful for the treatment of prolferative diseases |
CA2927920A1 (en) | 2013-10-18 | 2015-04-23 | Dana-Farber Cancer Institute, Inc. | Polycyclic inhibitors of cyclin-dependent kinase 7 (cdk7) |
US10231965B2 (en) | 2014-02-20 | 2019-03-19 | Ignyta, Inc. | Molecules for administration to ROS1 mutant cancer cells |
US10017477B2 (en) | 2014-04-23 | 2018-07-10 | Dana-Farber Cancer Institute, Inc. | Janus kinase inhibitors and uses thereof |
US9862688B2 (en) | 2014-04-23 | 2018-01-09 | Dana-Farber Cancer Institute, Inc. | Hydrophobically tagged janus kinase inhibitors and uses thereof |
JP6744309B2 (ja) | 2014-12-02 | 2020-08-19 | イグニタ,インコーポレイテッド | 神経芽細胞腫の治療のための併用 |
US10336707B2 (en) | 2014-12-16 | 2019-07-02 | Eudendron S.R.L. | Heterocyclic derivatives modulating activity of certain protein kinases |
US10870651B2 (en) | 2014-12-23 | 2020-12-22 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinase 7 (CDK7) |
CN106032359B (zh) * | 2015-03-09 | 2018-07-20 | 复旦大学 | 吲唑类化合物及其制备方法和用途 |
CA2978518C (en) | 2015-03-27 | 2023-11-21 | Nathanael S. Gray | Inhibitors of cyclin-dependent kinases |
US10702527B2 (en) | 2015-06-12 | 2020-07-07 | Dana-Farber Cancer Institute, Inc. | Combination therapy of transcription inhibitors and kinase inhibitors |
JP7028766B2 (ja) | 2015-09-09 | 2022-03-02 | ダナ-ファーバー キャンサー インスティテュート, インコーポレイテッド | サイクリン依存性キナーゼの阻害剤 |
US10869864B2 (en) | 2015-12-18 | 2020-12-22 | Ignyta, Inc. | Combinations for the treatment of cancer |
JOP20190053A1 (ar) | 2016-09-23 | 2019-03-21 | Novartis Ag | مركبات أزا إندازول للاستخدام في إصابات الأوتار و/ أو الرباط |
TWI651308B (zh) | 2016-09-23 | 2019-02-21 | 瑞士商諾華公司 | 用於肌腱及/或韌帶傷害之吲唑化合物 |
CA3050770C (en) * | 2016-12-07 | 2023-09-12 | Nanjing Xin Shi Dai Meditech Co. Ltd. | Compounds and pharmaceutical compositions for modulating sgk activity, and methods thereof |
CN110913842A (zh) | 2017-07-19 | 2020-03-24 | 伊尼塔公司 | 包括恩曲替尼的药物组合物 |
WO2019018562A1 (en) | 2017-07-19 | 2019-01-24 | Ideaya Biosciences, Inc. | AMIDO COMPOUND AS MODULATORS OF AHR |
EP3697390A1 (en) | 2017-10-17 | 2020-08-26 | Ignyta, Inc. | Pharmaceutical compositions and dosage forms |
CN109134451A (zh) * | 2018-09-10 | 2019-01-04 | 遵义医学院 | 1,3-二取代脲类与硫脲类衍生物及其应用 |
WO2020210828A1 (en) * | 2019-04-12 | 2020-10-15 | Hibercell, Inc. | (aza)indazolyl-aryl sulfonamide and related compounds and their use in treating medical conditions |
CN114276297A (zh) * | 2020-10-15 | 2022-04-05 | 兰州大学 | 一种1h-吲唑vegfr-2激酶抑制剂及其制备与应用 |
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US2971842A (en) * | 1956-03-21 | 1961-02-14 | Gen Aniline & Film Corp | Light sensitive layers for photomechanical reproduction |
NZ517759A (en) | 1999-09-17 | 2004-04-30 | Abbott Gmbh & Co | Kinase inhibitors as therapeutic agents |
JPWO2002100833A1 (ja) * | 2001-06-12 | 2004-09-24 | 住友製薬株式会社 | Rhoキナーゼ阻害剤 |
FR2827861B1 (fr) * | 2001-07-27 | 2004-04-02 | Aventis Pharma Sa | Derives des indazoles ou des indoles, leur utilisation en medecine humaine et plus particulierement en cancerologie |
US20030187026A1 (en) * | 2001-12-13 | 2003-10-02 | Qun Li | Kinase inhibitors |
WO2003051847A1 (en) * | 2001-12-19 | 2003-06-26 | Smithkline Beecham P.L.C. | (1-h-indazol-3-yl) -amide derivatives as gsk-3 inhibitors |
FR2836915B1 (fr) | 2002-03-11 | 2008-01-11 | Aventis Pharma Sa | Derives d'aminoindazoles, procede de preparation et intermediaires de ce procede a titre de medicaments et compositions pharmaceutiques les renfermant |
WO2003097610A1 (en) * | 2002-05-17 | 2003-11-27 | Pharmacia Italia S.P.A. | Aminoindazole derivatives active as kinase inhibitors, process for their preparation and pharmaceutical compositions comprising them |
EP1545515A1 (en) | 2002-08-12 | 2005-06-29 | Sugen, Inc. | 3-pyrrolyl-pyridopyrazoles and 3-pyrrolyl-indazoles as novel kinase inhibitors |
PL374946A1 (en) | 2002-09-05 | 2005-11-14 | Aventis Pharma S.A. | Novel aminoindazole derivatives as medicines and pharmaceutical compositions containing same |
WO2004062662A1 (fr) * | 2002-12-12 | 2004-07-29 | Aventis Pharma S.A. | Derives d'aminoindazoles et leur utilisation comme inhibiteurs de kinases |
ES2346538T3 (es) * | 2003-05-22 | 2010-10-18 | Abbott Laboratories | Inhibidores de quinasa de tipo indazol, benzisoxazol y benzisotiazol. |
AU2004259012C1 (en) | 2003-07-23 | 2012-08-02 | Exelixis, Inc. | Anaplastic lymphoma kinase modulators and methods of use |
MXPA06013250A (es) | 2004-05-14 | 2007-02-28 | Abbott Lab | Inhibidores de quinasa como agentes terapeuticos. |
PE20061119A1 (es) | 2005-01-19 | 2006-11-27 | Aventis Pharma Sa | PIRAZOLO PIRIDINAS SUSTITUIDAS COMO INHIBIDORES DE CINASAS FAK, KDR Y Tie |
CN101223141A (zh) | 2005-03-10 | 2008-07-16 | Cgi药品股份有限公司 | 特定取代的酰胺,其制备方法和使用方法 |
-
2004
- 2004-06-04 FR FR0406042A patent/FR2871158A1/fr not_active Withdrawn
-
2005
- 2005-06-01 ZA ZA200610040A patent/ZA200610040B/xx unknown
- 2005-06-01 KR KR1020077000131A patent/KR20070043769A/ko not_active Application Discontinuation
- 2005-06-01 BR BRPI0510777-6A patent/BRPI0510777A/pt not_active IP Right Cessation
- 2005-06-01 CN CNA2005800226007A patent/CN1980918A/zh active Pending
- 2005-06-01 JP JP2007514025A patent/JP2008501669A/ja active Pending
- 2005-06-01 AU AU2005259139A patent/AU2005259139B2/en not_active Ceased
- 2005-06-01 EA EA200602241A patent/EA012702B1/ru not_active IP Right Cessation
- 2005-06-01 CA CA002567744A patent/CA2567744A1/fr not_active Abandoned
- 2005-06-01 EP EP05775644A patent/EP1765813A1/fr not_active Withdrawn
- 2005-06-01 WO PCT/FR2005/001335 patent/WO2006003276A1/fr active Application Filing
- 2005-06-01 MX MXPA06013954A patent/MXPA06013954A/es active IP Right Grant
- 2005-06-02 AR ARP050102268A patent/AR049389A1/es unknown
- 2005-06-03 TW TW094118279A patent/TW200610756A/zh unknown
- 2005-06-03 UY UY28941A patent/UY28941A1/es unknown
-
2006
- 2006-11-23 CR CR8767A patent/CR8767A/es not_active Application Discontinuation
- 2006-11-24 TN TNP2006000384A patent/TNSN06384A1/fr unknown
- 2006-11-26 IL IL179595A patent/IL179595A0/en unknown
- 2006-11-30 EC EC2006007046A patent/ECSP067046A/es unknown
- 2006-12-04 US US11/566,382 patent/US7517902B2/en not_active Expired - Fee Related
- 2006-12-14 MA MA29532A patent/MA28664B1/fr unknown
- 2006-12-28 NO NO20066050A patent/NO20066050L/no not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
UY28941A1 (es) | 2005-12-30 |
WO2006003276A1 (fr) | 2006-01-12 |
TW200610756A (en) | 2006-04-01 |
BRPI0510777A (pt) | 2007-11-20 |
US20070161626A1 (en) | 2007-07-12 |
AU2005259139B2 (en) | 2011-09-08 |
ZA200610040B (en) | 2008-02-27 |
MXPA06013954A (es) | 2007-03-15 |
ECSP067046A (es) | 2006-12-29 |
CN1980918A (zh) | 2007-06-13 |
EA012702B1 (ru) | 2009-12-30 |
IL179595A0 (en) | 2007-05-15 |
US7517902B2 (en) | 2009-04-14 |
EA200602241A1 (ru) | 2007-04-27 |
NO20066050L (no) | 2007-02-05 |
TNSN06384A1 (fr) | 2008-02-22 |
CA2567744A1 (fr) | 2006-01-12 |
CR8767A (es) | 2007-08-28 |
MA28664B1 (fr) | 2007-06-01 |
FR2871158A1 (fr) | 2005-12-09 |
JP2008501669A (ja) | 2008-01-24 |
KR20070043769A (ko) | 2007-04-25 |
AU2005259139A1 (en) | 2006-01-12 |
EP1765813A1 (fr) | 2007-03-28 |
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