AR056210A1 - 4-(3-aminopirazol)pirimidina para uso como inhibidores de tirosina-quinasa - Google Patents
4-(3-aminopirazol)pirimidina para uso como inhibidores de tirosina-quinasaInfo
- Publication number
- AR056210A1 AR056210A1 ARP060104713A ARP060104713A AR056210A1 AR 056210 A1 AR056210 A1 AR 056210A1 AR P060104713 A ARP060104713 A AR P060104713A AR P060104713 A ARP060104713 A AR P060104713A AR 056210 A1 AR056210 A1 AR 056210A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- carbamoyl
- amino
- sulfamoyl
- heterocyclyl
- Prior art date
Links
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 title 1
- 229940043355 kinase inhibitor Drugs 0.000 title 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 47
- -1 hydroxy, amino, mercapto Chemical group 0.000 abstract 27
- 229910052757 nitrogen Inorganic materials 0.000 abstract 23
- 125000000623 heterocyclic group Chemical group 0.000 abstract 11
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 7
- 229910052799 carbon Inorganic materials 0.000 abstract 7
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 6
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 6
- 125000001589 carboacyl group Chemical group 0.000 abstract 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 6
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 6
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 5
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 abstract 5
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 5
- 125000005236 alkanoylamino group Chemical group 0.000 abstract 5
- 125000000217 alkyl group Chemical group 0.000 abstract 5
- 125000004452 carbocyclyl group Chemical group 0.000 abstract 5
- 125000001475 halogen functional group Chemical group 0.000 abstract 5
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 abstract 4
- 125000004423 acyloxy group Chemical group 0.000 abstract 4
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 2
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 abstract 2
- 150000002431 hydrogen Chemical group 0.000 abstract 2
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 abstract 2
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004656 alkyl sulfonylamino group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 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
- C07D403/14—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 three or more hetero 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
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (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)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Reivindicacion 1: Un compuesto caracterizado porque es de formula (1), o una sal aceptable para uso farmacéutico del mismo, donde: R1 se selecciona entre hidrogeno, hidroxi, amino, mercapto, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alcoxi C1-6, alcanoiloxi C1-6, N-(alquil C1-6)amino, N,N-(alquil C1-6)2amino, alcanoilamino C1-6, alquilsulfonilamino C1-6, carbociclilo de entre 3 y 5 miembros o heterociclilo de entre 3 y 5 miembros; donde R1 puede estar opcionalmente substituido sobre carbono con uno o más R6; y donde si dicho heterociclilo contiene una porcion -NH- ese nitrogeno puede estar opcionalmente substituido con un grupo seleccionado entre R7; R2 y R3 se seleccionan en forma independiente entre hidrogeno, halo, nitro, ciano, hidroxi, amino, carboxi, carbamoilo, mercapto, sulfamoilo, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alcoxi C1-6, alcanoilo C1-6, alcanoiloxi C1-6, N-(alquil C1-6)amino, N,N-(alquil C1-6)2amino, alcanoilamino C1-6, N-(alquil C1-6)carbamoilo, N,N- (alquil C1-6)2carbamoilo, alquil C1-6S(O)a donde a es entre 0 y 2, alcoxicarbonilo C1-6, N-(alquil C1-6)sulfamoilo, N,N-(alquil C1-6)2sulfamoilo, (alquil C1-6)2N-S(O)2-NH-, (alquil C1-6)NH-S(O)2-NH-, NH2-S(O)2-NH-, (alquil C1-6)2N-S(O)2-N(alquil C1- 6)-, (alquil C1-6)NH-S(O)2-N(alquil C1-6)-, NH2-S(O)2-N(alquil C1-6)-, N-(alquil C1-6)-N-(alquil C1-6sulfonil)amino, alquilsulfonilamino C1-6, carbociclil-R19- o heterociclil-R21-; donde R2 y R3 en forma independiente entre sí pueden estar opcionalmente substituidos sobre carbono con uno o más R8; y donde si dicho heterociclilo contiene una porcion -NH- ese nitrogeno puede estar opcionalmente substituido con un grupo seleccionado entre R9; R4 se selecciona entre ciano, carboxi, carbamoilo, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alcanoilo C1-6, N-(alquil C1-6)carbamoilo, N,N-(alquil C1-6)2carbamoilo, alcoxicarbonilo C1-6, carbociclilo o heterociclilo; donde R4 puede estar opcionalmente substituido sobre carbono con uno o más R10; y donde si dicho heterociclilo contiene una porcion -NH- ese nitrogeno puede estar opcionalmente substituido con un grupo seleccionado entre R11; R5 se selecciona entre halo, nitro, ciano, hidroxi, amino, carboxi, carbamoilo, mercapto, sulfamoilo, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alcoxi C1-6, alcanoilo C1-6, alcanoiloxi C1-6, N-(alquil C1-6)amino, N,N-(alquil C1-6)2amino, alcanoilamino C1-6, N-(alquil C1-6)carbamoilo, N,N-(alquil C1-6)2carbamoilo, alquil C1- 6S(O)a donde a es entre 0 y 2, alcoxicarbonilo, N-(alquil C1-6)sulfamoilo, N,N-(alquil C1-6)2sulfamoilo, alquilsulfonilamino C1-6, carbociclilo o heterociclilo; donde R5 puede estar opcionalmente substituido sobre carbono con uno o más R12; y donde si dicho heterociclilo contiene una porcion -NH- ese nitrogeno puede estar opcionalmente substituido con un grupo seleccionado entre R13; n = 0, 1, 2 o 3; donde los valores de R5 pueden ser iguales o diferentes; R6, R8, R10 y R12 se seleccionan en forma independiente entre halo, nitro, ciano, hidroxi, amino, carboxi, carbamoilo, mercapto, sulfamoilo, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alcoxi C1-6, alcanoilo C1-6, alcanoiloxi C1-6, N-(alquil C1-6)amino, N,N-(alquil C1-6)2amino, alcanoilamino C1-6, N-(alquil C1-6)carbamoilo, N,N-(alquil C1-6)2carbamoilo, alquil C1-6S(O)a donde a es entre 0 y 2, alcoxicarbonilo C1-6, N-(alquil C1-6)sulfamoilo, N,N-(alquil C1-6)2sulfamoilo, alquilsulfonilamino C1-6, carbociclilo o heterociclilo; donde R6, R8, R10 y R12 en forma independiente entre sí pueden estar opcionalmente substituidos sobre carbono con uno o más R14; y donde si dicho heterociclilo contiene una porcion -NH- ese nitrogeno puede estar opcionalmente substituido con un grupo seleccionado entre R15; R7, R9, R11, R13 y R15 se seleccionan en forma independiente entre alquilo C1-6, alcanoilo C1-6, alquilsulfonilo C1-6, alcoxicarbonilo C1-6, carbamoilo, N-(alquil C1-6)carbamoilo, N,N-(alquil C1- 6)2carbamoilo, bencilo, benciloxicarbonilo, benzoilo y fenilsulfonilo; donde R7, R9, R11, R13 y R15 en forma independiente entre sí pueden estar opcionalmente substituido sobre carbono con uno o más R16; R14 y R16 se seleccionan en forma independiente entre halo, nitro, ciano, hidroxi, amino, carboxi, carbamoilo, mercapto, sulfamoilo, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alcoxi C1-6, alcanoilo C1-6, alcanoiloxi C1-6, N-(alquil C1-6)amino, N,N-(alquil C1-6)2amino, alcanoilamino C1-6, N-(alquil C1-6)carbamoilo, N,N-(alquil C1-6)2carbamoilo, alquil C1-6S(O)a donde a es entre 0 y 2, alcoxicarbonilo C1-6, N-(alquil C1-6)sulfamoilo, N,N-(alquil C1-6)2sulfamoilo, alquilsulfonilamino C1-6, carbociclilo o heterociclilo; donde R14 y R16 en forma independiente entre sí pueden estar opcionalmente substituidos sobre carbono con uno o más R17; y donde si dicho heterociclilo contiene una porcion -NH- ese nitrogeno puede estar opcionalmente substituido con un grupo seleccionado entre R18; R17 se selecciona entre halo, nitro, ciano, hidroxi, trifluorometoxi, trifluorometilo, amino, carboxi, carbamoilo, mercapto, sulfamoilo, metilo, etilo, metoxi, etoxi, acetilo, acetoxi, metilamino, etilamino, dimetilamino, dietilamino, N-metil-N-etilamino, acetilamino, N-metilcarbamoilo, N-etilcarbamoilo, N,N-dimetilcarbamoilo, N,N-dietilcarbamoilo, N-metil-N-etilcarbamoilo, metiltio, etiltio, metilsulfinilo, etilsulfinilo, mesilo, etilsulfonilo, metoxicarbonilo, etoxicarbonilo, N-metilsulfamoilo, N-etilsulfamoilo, N,N-dimetilsulfamoilo, N,N-dietilsulfamoilo o N-metil-N-etilsulfamoilo; y R19 y R21 se seleccionan en forma independiente entre un enlace directo, -O-, -N(R22)-, -C(O)-, - N(R23)C(O)-, -C(O)N(R24)-, -S(O)s-, -SO2N(R25)- o -N(R26)SO2-; donde R22, R23, R24, R25 y R26 se seleccionan en forma independiente entre hidrogeno o alquilo C1-6 y s es 0-2; y R18 se selecciona entre alquilo C1-6, alcanoilo C1-6, alquilsulfonilo C1- 6, alcoxicarbonilo C1-6, carbamoilo, N-(alquil C1-6)carbamoilo, N,N-(alquil C1-6)2carbamoilo, bencilo, benciloxicarbonilo, benzoilo y fenilsulfonilo.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US73129905P | 2005-10-28 | 2005-10-28 | |
| US80306106P | 2006-05-24 | 2006-05-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR056210A1 true AR056210A1 (es) | 2007-09-26 |
Family
ID=37575154
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP060104713A AR056210A1 (es) | 2005-10-28 | 2006-10-27 | 4-(3-aminopirazol)pirimidina para uso como inhibidores de tirosina-quinasa |
Country Status (22)
| Country | Link |
|---|---|
| US (3) | US20080287475A1 (es) |
| EP (2) | EP1945631B8 (es) |
| JP (1) | JP2009513615A (es) |
| KR (1) | KR20080063846A (es) |
| AR (1) | AR056210A1 (es) |
| AU (1) | AU2006307657B2 (es) |
| BR (1) | BRPI0618011A2 (es) |
| CA (1) | CA2626375A1 (es) |
| DK (1) | DK1945631T3 (es) |
| EC (1) | ECSP088450A (es) |
| ES (1) | ES2391783T3 (es) |
| HR (1) | HRP20120824T1 (es) |
| IL (1) | IL190935A0 (es) |
| MX (1) | MX2008005398A (es) |
| NO (1) | NO20081893L (es) |
| NZ (1) | NZ567584A (es) |
| PL (1) | PL1945631T3 (es) |
| PT (1) | PT1945631E (es) |
| RU (1) | RU2463302C2 (es) |
| TW (1) | TW200800963A (es) |
| UY (1) | UY29886A1 (es) |
| WO (1) | WO2007049041A1 (es) |
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| JP4377583B2 (ja) * | 2000-12-05 | 2009-12-02 | バーテックス ファーマシューティカルズ インコーポレイテッド | C−junn末端キナーゼ(jnk)および他のタンパク質キナーゼのインヒビター |
| DK2383268T3 (en) | 2005-02-04 | 2015-09-14 | Astrazeneca Ab | PYRAZOLYLAMINOPYRIDINDERIVATER useful as kinase inhibitors |
| KR101362621B1 (ko) | 2005-02-16 | 2014-02-13 | 아스트라제네카 아베 | 화합물 |
| AU2006248780B2 (en) * | 2005-05-16 | 2010-06-03 | Astrazeneca Ab | Pyrazolylaminopyrimidine derivatives useful as tyrosine kinase inhibitors |
| EP1945631B8 (en) * | 2005-10-28 | 2013-01-02 | AstraZeneca AB | 4- (3-aminopyrazole) pyrimidine derivatives for use as tyrosine kinase inhibitors in the treatment of cancer |
| EP3838903B1 (en) | 2005-12-13 | 2023-11-22 | Incyte Holdings Corporation | Pyrrolo[2,3-d]pyrimidine derivative as janus kinase inhibitor |
| KR101435231B1 (ko) | 2006-08-24 | 2014-10-02 | 아스트라제네카 아베 | 증식성 질환의 치료에 유용한 모르폴리노 피리미딘 유도체 |
| WO2008061370A1 (en) * | 2006-11-24 | 2008-05-29 | Mcmaster University | Diagnostic method to detect endometriosis |
| WO2008129255A1 (en) * | 2007-04-18 | 2008-10-30 | Astrazeneca Ab | 5-aminopyrazol-3-yl-3h-imidazo [4,5-b] pyridine derivatives and their use for the treatment of cancer |
| WO2008135786A1 (en) * | 2007-05-04 | 2008-11-13 | Astrazeneca Ab | Amino-thiazolyl- pyrimidine derivatives and their use for the treatment of cancer |
| UA99459C2 (en) * | 2007-05-04 | 2012-08-27 | Астразенека Аб | 9-(pyrazol-3-yl)- 9h-purine-2-amine and 3-(pyraz0l-3-yl)-3h-imidazo[4,5-b]pyridin-5-amine derivatives and their use for the treatment of cancer |
| CN101932582B (zh) | 2007-06-13 | 2013-09-25 | 因塞特公司 | 詹纳斯激酶抑制剂(R)-3-(4-(7H-吡咯并[2,3-d]嘧啶-4-基)-1H-吡唑-1-基)-3-环戊基丙腈的盐 |
| US8138183B2 (en) | 2007-07-09 | 2012-03-20 | Astrazeneca Ab | Morpholino pyrimidine derivatives used in diseases linked to mTOR kinase and/or PI3K |
| WO2009007753A2 (en) * | 2007-07-11 | 2009-01-15 | Astrazeneca Ab | 4- (3-aminopyrazole) -pyrimidine derivativee and their use as tyrosine kinase inhibitors for the treatment of cancer |
| WO2009013545A2 (en) * | 2007-07-26 | 2009-01-29 | Astrazeneca Ab | Chemical compounds |
| TW200906818A (en) * | 2007-07-31 | 2009-02-16 | Astrazeneca Ab | Chemical compounds |
| KR101580482B1 (ko) | 2007-11-16 | 2015-12-28 | 인사이트 홀딩스 코포레이션 | 야누스 키나제 억제제로서의 4-피라졸릴-n-아릴피리미딘-2-아민 및 4-피라졸릴-n-헤테로아릴피리미딘-2-아민 |
| WO2009095712A2 (en) * | 2008-01-29 | 2009-08-06 | Astrazeneca Ab | Chemical compounds |
| AU2009259026B2 (en) * | 2008-06-11 | 2012-10-04 | Astrazeneca Ab | Tricyclic 2,4-diamin0-L,3,5-triazine derivatives useful for the treatment of cancer and myeloproliferative disorders |
| WO2010020810A1 (en) * | 2008-08-19 | 2010-02-25 | Astrazeneca Ab | 2-(imidaz0lylamin0)-pyridine derivatives and their use as jak kinase inhibitors |
| CN102227422A (zh) * | 2008-09-30 | 2011-10-26 | 阿斯利康(瑞典)有限公司 | 杂环jak激酶抑制剂 |
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| RS59632B1 (sr) | 2009-05-22 | 2020-01-31 | Incyte Holdings Corp | 3-[4-(7h-pirolo[2,3-d]pirimidin-4-il)-1h-pirazol-1-il]oktan- ili heptan-nitril kao jak inhibitori |
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| NZ567584A (en) | 2011-08-26 |
| BRPI0618011A2 (pt) | 2011-08-16 |
| EP1945631B8 (en) | 2013-01-02 |
| AU2006307657A1 (en) | 2007-05-03 |
| PT1945631E (pt) | 2012-10-15 |
| DK1945631T3 (da) | 2012-10-22 |
| US20100160325A1 (en) | 2010-06-24 |
| MX2008005398A (es) | 2008-09-24 |
| WO2007049041A1 (en) | 2007-05-03 |
| KR20080063846A (ko) | 2008-07-07 |
| IL190935A0 (en) | 2009-09-22 |
| WO2007049041A8 (en) | 2012-11-01 |
| EP2388259A1 (en) | 2011-11-23 |
| RU2008120848A (ru) | 2009-12-10 |
| RU2463302C2 (ru) | 2012-10-10 |
| HRP20120824T1 (hr) | 2012-11-30 |
| EP1945631B1 (en) | 2012-08-08 |
| US8088784B2 (en) | 2012-01-03 |
| TW200800963A (en) | 2008-01-01 |
| ES2391783T3 (es) | 2012-11-29 |
| CA2626375A1 (en) | 2007-05-03 |
| UY29886A1 (es) | 2007-05-31 |
| US20080287475A1 (en) | 2008-11-20 |
| EP1945631A1 (en) | 2008-07-23 |
| ECSP088450A (es) | 2008-06-30 |
| NO20081893L (no) | 2008-05-20 |
| PL1945631T3 (pl) | 2012-12-31 |
| AU2006307657B2 (en) | 2010-10-28 |
| US20120071480A1 (en) | 2012-03-22 |
| JP2009513615A (ja) | 2009-04-02 |
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