AR064430A1 - Derivados indolicos con anillo unido en las posiciones 5,6 . composiciones farmaceuticas y uso de los mismos. - Google Patents
Derivados indolicos con anillo unido en las posiciones 5,6 . composiciones farmaceuticas y uso de los mismos.Info
- Publication number
- AR064430A1 AR064430A1 ARP070105707A ARP070105707A AR064430A1 AR 064430 A1 AR064430 A1 AR 064430A1 AR P070105707 A ARP070105707 A AR P070105707A AR P070105707 A ARP070105707 A AR P070105707A AR 064430 A1 AR064430 A1 AR 064430A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- cycloalkyl
- heterocycloalkyl
- aryl
- heteroaryl
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 21
- 125000003118 aryl group Chemical group 0.000 abstract 18
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 13
- 125000001072 heteroaryl group Chemical group 0.000 abstract 13
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 12
- 125000001475 halogen functional group Chemical group 0.000 abstract 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 10
- 125000004366 heterocycloalkenyl group Chemical group 0.000 abstract 9
- -1 -OR9 Chemical group 0.000 abstract 8
- 125000003342 alkenyl group Chemical group 0.000 abstract 8
- 125000000304 alkynyl group Chemical group 0.000 abstract 8
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 8
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 8
- 125000001188 haloalkyl group Chemical group 0.000 abstract 7
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 7
- 125000001424 substituent group Chemical group 0.000 abstract 7
- 125000004432 carbon atom Chemical group C* 0.000 abstract 4
- 125000006163 5-membered heteroaryl group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000002433 cyclopentenyl group Chemical group C1(=CCCC1)* 0.000 abstract 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
-
- 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
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Virology (AREA)
- Public Health (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Composiciones farmacéuticas que los contienen. Reivindicacion 1: Un compuesto que presenta la formula (1), o una sale, un solvato, éster o profármaco del mismo aceptables para uso farmacéutico, donde el anillo Z de la formula (1) es ciclopentilo, ciclopentenilo, heterocicloalquilo de 5 miembros, heterocicloalquenilo de 5 miembros o un anillo heteroarilo de 5 miembros, donde el anillo Z puede estar: (i) sustituido opcionalmente en uno o más átomos de carbono anulares con sustituyentes, que son iguales o diferentes, y que se seleccionan de alquilo, arilo, heteroarilo, halo, haloalquilo, hidroxialquilo, hidroxi, -CN, -C(O)R8, -C(O)OR9, -C(O)N(R9)2, -[C(R12)2]q-OR9, -[C(R12)2]q-N(R9)2, -NHC(O)R8, -NHSO2R11, -S(O)pR11 o -SO2N(R9)2; y/o (ii) sustituido opcionalmente en un átomo de nitrogeno anular con sustituyentes, que son iguales o diferentes, y que se seleccionan de alquilo, arilo, haloalquilo, heteroarilo, hidroxialquilo, -C(O)R8, -C(O)OR9, -C(O)N(R9)2, -[C(R12)2]r-OR9, - [C(R12)2]r-N(R9)2, -NHC(O)R8, -NHSO2R11, -S(O)pR11 y -SO2N(R9)2; R1 es una union, -[C(R12)2]r-, -[C(R12)2]r-O-[C(R12)2]q-, -[C(R12)2]r-N(R9)-[C(R12)2]q-, -[C(R12)2]q-CH=CH-[C(R12)2]q-, -[C(R12)2]q-C:::C-[C(R12)2]q- o -[C(R12)2]q-SO2-[C(R12)2]q-; R2 es -C(O)R9, -C(O)OR9, -C(O)OCH2OR9, -C(O)N(R9)2, -[C(R12)2]q-C(O)OR9, -[C(R12)2]q-C(O)N(R9)2, -[C(R12)2]q-C(O)N(R9)C=N(R9)2, -[C(R12)2]q-arilo, -[C(R12)2]q-cicloalquilo, -[C(R12)2]q-cicloalquenilo, -[C(R12)2]q-heterocicloalquilo, -[C(R12)2]q- heteroarilo, -[C(R12)2]q-heterocicloalquenilo, -[C(R12)2]q-C(O)N(R9)SOR11, -[C(R12)2]q-C(O)N(R9)SO2R11, -[C(R12)2]q-C(O)N(R9)SO2N(R9)2, alquilo, grupo de formulas (2), donde un grupo arilo, cicloalquilo, cicloalquenilo, heterocicloalquilo, heterocicloalquenilo o heteroarilo puede estar opcionalmente sustituido con hasta 4 sustituyentes, que se seleccionan cada uno de manera independiente de alquilo, alquenilo, alquinilo, arilo, -[C(R12)2]q-cicloalquilo, -[C(R12)2]q-cicloalquenilo, - [C(R12)2]q-heterocicloalquilo, -[C(R12)2]q-heterocicloalquenilo, -[C(R12)2]q-heteroarilo, -[C(R12)2]q-haloalquilo, -[C(R12)2]q-hidroxialquilo, halo, hidroxi, -OR9, -CN, -[C(R12)2]q-C(O)R8, -[C(R12)2]q-C(O)OR9, -[C(R12)2)q-C(O)N(R9)2, -[C(R12)2]q- OR9, -[C(R12)2]q-N(R9)2, -[C(R12)2]q-NHC(O)R8, -[C(R12)2]q-NR8C(O)N(R9)2, -[C(R12)2]q-NHSO2R11, -[C(R12)2]q-S(O)pR11, -[C(R12)2]q-SO2N(R9)2 y -SO2N(R9)C(O)N(R9)2; R3 es H, -[C(R12)2]q-alquilo, -[C(R12)2]q-arilo, -[C(R12)2]q-cicloalquilo, -[C(R12)2]q- cicloalquenilo, -[C(R12)2]q-heterocicloalquilo, -[C(R12)2]q-heteroarilo o -[C(R12)2]q-heterocicloalquenilo, grupo de formulas (3) donde un grupo arilo, cicloalquilo, cicloalquenilo, heterocicloalquilo, heterocicloalquenilo o heteroarilo puede estar opcionalmente sustituido con hasta 3 sustituyentes, que son iguales o diferentes, y se seleccionan de alquilo, arilo, heteroaril-, halo, haloalquilo, hidroxialquilo, hidroxi, CN, -C(O)R8, -C(O)OR9, -C(O)N(R9)2, -[C(R12)2]q-OR9, -[C(R12)2]q-N(R9)2, - NHC(O)R8, -NHSO2R11, -S(O)pR11 o -SO2N(R9)2; R4 y R7 son cada uno, de manera independiente, H, alquilo, alquenilo, alquinilo, arilo, -[C(R12)2]q-cicloalquilo, -[C(R12)2]q-cicloalquenilo, -[C(R12)2]q-heterocicloalquilo, -[C(R12)2]q- heterocicloalquenilo, -[C(R12)2]q-heteroarilo, -[C(R12)2]q-haloalquilo, -[C(R12)2]q-hidroxialquilo, halo, hidroxi, -OR9, -CN, -[C(R12)2]q-C(O)R8, -[C(R12)2]q-C(O)OR9, -[C(R12)2)q-C(O)N(R9)2, -[C(R12)2]q-OR9, -[C(R12)2]q-N(R9)2, -[C(R12)2]q-NHC(O)R8, -[C(R12)2]q-NR8C(O)N(R9)2, -[C(R12)2]q-NHSO2R11, -[C(R12)2]q-S(O)pR11, -[C(R12)2]q-SO2N(R9)2 o -SO2N(R9)C(O)N(R9)2; cada aparicion de R8 es de manera independiente H, alquilo, alquenilo, alquinilo, -[C(R12)2]q-arilo, -[C(R12)2]q-cicloalquilo, - [C(R12)2]q-cicloalquenilo, -[C(R12)2]q-heterocicloalquilo, -[C(R12)2]q-heterocicloalquenilo, -[C(R12)2]q-heteroarilo, haloalquilo o hidroxialquilo; cada aparicion de R9 es de manera independiente H, alquilo, alquenilo, alquinilo, -[C(R12)2]q-arilo, - [C(R12)2]q-cicloalquilo, -[C(R12)2]q-cicloalquenilo, -[C(R12)2]q-heterocicloalquilo, -[C(R12)2]q-heterocicloalquenilo, -[C(R12)2]q-heteroarilo, haloalquilo o hidroxialquilo; R10 es H, cicloalquilo, cicloalquenilo, heterocicloalquilo, heterocicloalquenilo, arilo, heteroarilo, donde un grupo cicloalquilo, cicloalquenilo, heterocicloalquilo, heterocicloalquenilo, arilo o heteroarilo puede estar sustituido de modo opcional e independiente con hasta 4 sustituyentes, que se seleccionan cada uno de manera independiente de H, alquilo, alquenilo, alquinilo, arilo, -[C(R12)2]q-cicloalquilo, -[C(R12)2]q-cicloalquenilo, -[C(R12)2]q-heterocicloalquilo, -[C(R12)2]q-heterocicloalquenilo, -[C(R12)2]q-heteroarilo, -[C(R12)2]q- haloalquilo, -[C(R12)2]q-hidroxialquilo, halo, hidroxi, -OR9, -CN, -[C(R12)2]q-C(O)R8, -[C(R12)2]q-C(O)OR9, -[C(R12)2]q-C(O)N(R9)2, -[C(R12)2]q-OR9, -[C(R12)2]q-N(R9)2, -[C(R12)2]q-NHC(O)R8, -[C(R12)2]q-NR8C(O)N(R9)2, -[C(R12)2]q-NHSO2R11, - [C(R12)2]q-S(O)pR11, -[C(R12)2]q-SO2N(R9)2 y -SO2N(R9)C(O)N(R9)2, de modo tal que cuando R1 es una union, R10 no es H; cada aparicion de R11 es de manera independiente alquilo, arilo, cicloalquilo, cicloalquenilo, heterocicloalquilo, heterocicloalquenilo, heteroarilo, haloalquilo, hidroxi o hidroxialquilo, donde un grupo cicloalquilo, cicloalquenilo, heterocicloalquilo, heterocicloalquenilo, arilo o heteroarilo puede estar sustituido de modo opcional e independiente con hasta 4 sustituyentes, que se seleccionan cada uno de manera independiente de -H, alquilo, alquenilo, alquinilo, arilo, -[C(R12)2]q-cicloalquilo, -[C(R12)2]q-cicloalquenilo, -[C(R12)2]q-heterocicloalquilo, -[C(R12)2]q-heterocicloalquenilo, -[C(R12)2]q- heteroarilo, -[C(R12)2]q-haloalquilo, -[C(R12)2]q-hidroxialquilo, halo, hidroxi, -OR9, -CN, -[C(R12)2]q-C(O)R8, -[C(R12)2]q-C(O)OR9, -[C(R12)2]q-C(O)N(R9)2, -[C(R12)2]q-OR9, -[C(R12)2]q-N(R9)2, -[C(R12)2]q-NHC(O)R8, -[C(R12)2]q-NR8C(O)N(R9)2, - [C(R12)2]q-NHSO2alquilo, -[C(R12)2]q-NHSO2cicloalquilo, -[C(R12)2]q-NHSO2arilo, -[C(R12)2]q-SO2N(R9)2 y -SO2N(R9)C(O)N(R9)2; cada aparicion de R12 es de manera independiente H, halo, -N(R9)2, -OR9, alquilo, cicloalquilo, cicloalquenilo, heterocicloalquilo o heterocicloalquenilo, donde un grupo cicloalquilo, cicloalquenilo, heterocicloalquilo o heterocicloalquenilo puede estar sustituido de modo opcional e independiente con hasta 4 sustituyentes, cada uno de manera independiente de alquilo, halo, haloalquilo, hidroxialquilo, hidroxi, -CN, -C(O)alquilo, -C(O)Oalquilo, -C(O)NHalquilo, -C(O)N(alquilo)2, -O-alquilo, -NH2, -NH(alquilo), -N(alquilo)2, -NHC(O)alquilo, -NHSO2aIquilo -SO2alquiIo o -SO2NH-alquilo, o dos grupos R12, junto con los átomos de carbono a los que están unidos, en conjunto forman un grupo cicloalquilo, heterocicloalquilo o C=O; cada aparicion de R20 es de manera independiente H, alquilo, arilo, cicloalquilo, heterocicloalquilo o heteroarilo, o ambos grupos R20 y los átomos de carbono a los que están unidos, en conjunto forman un grupo cicloalquilo, cicloheteroalquilo, arilo o heteroarilo, donde un grupo cicloalquilo, cicloheteroalquilo, arilo o heteroarilo puede estar sustituido con hasta 4 grupos, que se seleccionan cada uno de manera independiente de alquilo, alquenilo, alquinilo, halo, hidroxi, -OR9, -CN, -[C(R12)2]q-cicloalquilo, -[C(R12)2]q-cicloalquenilo, -[C(R12)2]q-heterocicloalquilo, -[C(R12)2]q-heterocicloalquenilo, - [C(R12)2]q-haloalquilo, -[C(R12)2]q-hidroxialquilo, -[C(R12)2]q-C(O)R8, -[C(R12)2]q-C(O)OR9, -[C(R12)2]q-C(O)N(R9)2, -[C(R12)2]q-OR9, -[C(R12)2]q-N(R9)2, -[C(R12)2]q-NHC(O)R8, -[C(R12)2]q-NR8C(O)N(R9)2, -[C(R12)2]q-NHSO2R11, -[C(R12)2]q-S(O)pR11, - [C(R12)2]q-SO2N(R9)2 y -SO2N(R9)C(O)N(R9)2; cada aparicion de R30 es de manera independiente H, alquilo, alquenilo, alquinilo, arilo, -[C(R12)2]q-cicloalquilo, -[C(R12)2]q-cicloalquenilo, -[C(R12)2]q-heterocicloalquilo, -[C(R12)2]q- heterocicloalquenilo, -[C(R12)2]q-heteroarilo, -[C(R12)2]q-haloalquilo, -[C(R12)2]q-hidroxialquilo, halo, hidroxi, -OR9, -CN, -[C(R12)2]q-C(O)R8, -[C(R12)2]q-C(O)OR9, -[C(R12)2]q-C(O)N(R9)2, -[C(R12)2]q-OR9, -[C(R12)2]q-N(R9)2, -[C(R12)2]q-NHC(O)R8, -[C(R12)2]q-NR8C(O)N(R9)2, -[C(R12)2]q-NHSO2R11, -[C(R12)2]q-S(O)pR11, -[C(R12)2]q-SO2N(R9)2 o -SO2N(R9)C(O)N(R9)2, o dos grupos adyacentes R30, junto con los átomos de carbono a los que están unidos, en conjunto forman un anillo de 3 a 7 miembros seleccionado de arilo, cicloalquilo, heteroarilo y heterocicloalquilo; cada aparicion de p es de manera independiente 0, 1 o 2; cada aparicion de q es de manera independiente un numero entero en el rango de 0 a 4; y cada aparicion de r es de manera independiente un numero entero en el rango de 1 a 4.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US87659606P | 2006-12-22 | 2006-12-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR064430A1 true AR064430A1 (es) | 2009-04-01 |
Family
ID=39944141
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP070105707A AR064430A1 (es) | 2006-12-22 | 2007-12-18 | Derivados indolicos con anillo unido en las posiciones 5,6 . composiciones farmaceuticas y uso de los mismos. |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US8268803B2 (es) |
| EP (1) | EP2081922B1 (es) |
| JP (1) | JP5055377B2 (es) |
| CN (1) | CN101611025A (es) |
| AR (1) | AR064430A1 (es) |
| AT (1) | ATE543808T1 (es) |
| CA (1) | CA2674831A1 (es) |
| CL (1) | CL2007003684A1 (es) |
| MX (1) | MX2009006877A (es) |
| PE (1) | PE20081658A1 (es) |
| TW (1) | TW200833684A (es) |
| WO (1) | WO2008136815A2 (es) |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20110104109A1 (en) * | 2005-07-13 | 2011-05-05 | Frank Bennett | Tetracyclic indole derivatives and their use for treating or preventing viral infections |
| JP5055377B2 (ja) | 2006-12-22 | 2012-10-24 | シェーリング コーポレイション | [5,6−環]環形成インドール誘導体およびその使用方法 |
| AU2007339382B2 (en) | 2006-12-22 | 2013-05-02 | Merck Sharp & Dohme Llc | 4,5-ring annulated indole derivatives for treating or preventing of HCV and related viral infections |
| CA2673254C (en) | 2006-12-22 | 2013-09-10 | Schering Corporation | 4,5-ring annulated indole derivatives for treating or preventing of hcv and related viral infections |
| JP5272008B2 (ja) * | 2007-08-29 | 2013-08-28 | メルク・シャープ・アンド・ドーム・コーポレーション | 置換インドール誘導体およびその使用の方法 |
| WO2009032125A1 (en) * | 2007-08-29 | 2009-03-12 | Schering Corporation | 2,3-substituted azaindole derivatives for treating viral infections |
| JP5416708B2 (ja) * | 2007-11-16 | 2014-02-12 | メルク・シャープ・アンド・ドーム・コーポレーション | 3−アミノスルホニル置換インドール誘導体およびそれらの使用方法 |
| US8765757B2 (en) * | 2007-11-16 | 2014-07-01 | Merck Sharp & Dohme Corp. | 3-heterocyclic substituted indole derivatives and methods of use thereof |
| AR072088A1 (es) * | 2008-06-13 | 2010-08-04 | Schering Corp | Derivados de indol triciclicos y sus metodos de uso |
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2007
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- 2007-12-17 WO PCT/US2007/025757 patent/WO2008136815A2/en not_active Ceased
- 2007-12-17 AT AT07870161T patent/ATE543808T1/de active
- 2007-12-17 CN CNA200780051694XA patent/CN101611025A/zh active Pending
- 2007-12-17 CA CA002674831A patent/CA2674831A1/en not_active Abandoned
- 2007-12-17 US US12/519,975 patent/US8268803B2/en active Active
- 2007-12-17 MX MX2009006877A patent/MX2009006877A/es unknown
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- 2007-12-18 CL CL200703684A patent/CL2007003684A1/es unknown
- 2007-12-18 AR ARP070105707A patent/AR064430A1/es not_active Application Discontinuation
- 2007-12-18 TW TW096148485A patent/TW200833684A/zh unknown
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2008
- 2008-01-02 PE PE2008000044A patent/PE20081658A1/es not_active Application Discontinuation
Also Published As
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| US20100322901A1 (en) | 2010-12-23 |
| WO2008136815A2 (en) | 2008-11-13 |
| CN101611025A (zh) | 2009-12-23 |
| EP2081922A2 (en) | 2009-07-29 |
| MX2009006877A (es) | 2009-09-28 |
| JP2010513491A (ja) | 2010-04-30 |
| EP2081922B1 (en) | 2012-02-01 |
| WO2008136815A3 (en) | 2009-05-22 |
| CL2007003684A1 (es) | 2008-07-18 |
| ATE543808T1 (de) | 2012-02-15 |
| TW200833684A (en) | 2008-08-16 |
| US8268803B2 (en) | 2012-09-18 |
| CA2674831A1 (en) | 2008-11-13 |
| JP5055377B2 (ja) | 2012-10-24 |
| PE20081658A1 (es) | 2008-10-24 |
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