AR084226A1 - Derivados de bencimidazol-amidas, composiciones farmaceuticas que los contienen y uso de los mismos para tratar enfermedades inflamatorias asociadas con el dolor - Google Patents
Derivados de bencimidazol-amidas, composiciones farmaceuticas que los contienen y uso de los mismos para tratar enfermedades inflamatorias asociadas con el dolorInfo
- Publication number
- AR084226A1 AR084226A1 ARP110104608A ARP110104608A AR084226A1 AR 084226 A1 AR084226 A1 AR 084226A1 AR P110104608 A ARP110104608 A AR P110104608A AR P110104608 A ARP110104608 A AR P110104608A AR 084226 A1 AR084226 A1 AR 084226A1
- Authority
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- Argentina
- Prior art keywords
- alkyl
- optionally substituted
- groups
- last
- substituents selected
- Prior art date
Links
- 208000027866 inflammatory disease Diseases 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 59
- 125000000217 alkyl group Chemical group 0.000 abstract 30
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 27
- 125000001153 fluoro group Chemical group F* 0.000 abstract 27
- 125000001424 substituent group Chemical group 0.000 abstract 20
- 125000005843 halogen group Chemical group 0.000 abstract 13
- 125000000304 alkynyl group Chemical group 0.000 abstract 9
- 125000003118 aryl group Chemical group 0.000 abstract 7
- 125000001072 heteroaryl group Chemical group 0.000 abstract 7
- -1 -OH Chemical group 0.000 abstract 5
- 239000012634 fragment Substances 0.000 abstract 5
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 5
- 229910052739 hydrogen Inorganic materials 0.000 abstract 5
- 239000001257 hydrogen Substances 0.000 abstract 5
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 5
- 125000006568 (C4-C7) heterocycloalkyl group Chemical group 0.000 abstract 4
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 3
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- 125000006555 (C3-C5) cycloalkyl group Chemical group 0.000 abstract 2
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 125000006526 (C1-C2) alkyl group Chemical group 0.000 abstract 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 abstract 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 abstract 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 208000035389 Ring chromosome 6 syndrome Diseases 0.000 abstract 1
- 125000002877 alkyl aryl group Chemical group 0.000 abstract 1
- 125000002393 azetidinyl group Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000002993 cycloalkylene group Chemical group 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000003386 piperidinyl group Chemical group 0.000 abstract 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D235/30—Nitrogen atoms not forming part of a nitro radical
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- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
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- A—HUMAN NECESSITIES
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- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A61P19/00—Drugs for skeletal disorders
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- A61P25/00—Drugs for disorders of the nervous system
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
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- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
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- 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
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- 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
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- C07D401/14—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 three or more hetero rings
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- 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
- C07D403/04—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 directly linked by a ring-member-to-ring-member bond
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- 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
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- 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
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- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
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- 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
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- 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
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- 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
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- 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
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- 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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Abstract
Reivindicación 1: Un compuesto caracterizado porque tiene la fórmula (1) en la que R1 representa halo, OH, -CN, alquilo C1-3, alquinilo C2-6, O-alquilo C1-3, estando estos tres últimos grupos opcionalmente sustituidos con uno o más sustituyentes seleccionados de fluoro, -CN, =O, OH, -OCH3, -OCF3; R2 representa halo, -CN, alquilo C1-3, O-alquilo C1-3, estando estos dos últimos grupos opcionalmente sustituidos con uno o más sustituyentes seleccionados de fluoro, -CN, =O, OH, -OCH3, -OCF3; R3 y R4 representan independientemente hidrógeno, halo, -CN, alquilo C1-3, O-alquilo C1-3, estando estos dos últimos grupos opcionalmente sustituidos con uno o más sustituyentes seleccionados de fluoro, -CN, =O, OH, -OCH3, -OCF3; Ra, Rb representan independientemente hidrógeno, alquilo C1-3 opcionalmente sustituido con uno o más átomos de fluoro, o ambos junto con el átomo de carbono al que están unidos, forman un anillo de cicloalquileno C3-7, o un anillo de heterocicloalquileno de 4 - 6 miembros, estando estos dos últimos anillos opcionalmente sustituidos con uno o más átomos de flúor; W representa -C(O)-, -S(O)-, -S(O)2-, -C(O)O-, C(O)NRd- y estos grupos están unidos al nitrógeno del resto -NH- mediante un átomo de carbono o de azufre; Rd representa hidrógeno, alquilo C1-3; M representa alquilo C1-8, alquinilo C2-8, cicloalquil C3-8-alquilo C0-4, (heterocicloalquil de 4 - 10 miembros)-alquil C0-4-, estando estos cuatro últimos grupos opcionalmente sustituidos con uno o más grupos seleccionados de fluoro, -OH, =O, -CN, -NH2, alquilo C1-3, -NH(alquil C1-3), -N(alquil C1-3)2, azetidinilo, pirrolidinilo, piperidinilo, -O-alquilo C1-3 [y estos siete últimos grupos alquilo pueden estar sustituidos con uno o más sustituyentes seleccionados de fluoro, OH, -CN, O-alquilo C1-2 (y este último grupo alquilo está opcionalmente sustituido con uno o más átomos de flúor)], arilo, heteroarilo [estando estos dos últimos grupos opcionalmente sustituidos con uno o más sustituyentes seleccionados de halo, OH, -CN, alquilo C1-3, O-alquilo C1-3 (estando estos dos últimos grupos alquilo opcionalmente sustituidos con uno o más átomos de flúor)], o arilo, heteroarilo, estando estos dos últimos grupos opcionalmente sustituidos con uno o más sustituyentes seleccionados de halo, -OH, -CN, -NH2, arilo, heteroarilo [estando estos dos últimos grupos opcionalmente sustituidos con uno o más sustituyentes seleccionados de halo, OH, -CN, alquilo C1-3, -O-alquilo C1-3 (estando estos dos últimos grupos alquilo opcionalmente sustituidos con uno o más átomos de flúor)], alquilo C1-7, alquinilo C2-7, cicloalquilo C3-7, heterocicloalquilo de 4 - 7 miembros, -NH(alquil C1-3), -N(alquil C1-3)2, -O-alquilo C1-3, -O-alquil C0-2-arilo, -S-alquilo C1-3, (estando estos últimos grupos alquilo, alquinilo, heterocicloalquilo, arilo o cicloalquilo, opcionalmente sustituidos con uno o más sustituyentes seleccionados de fluoro, -CN, =O, -NH2, -NH(alquil C1-3), -N(alquil C1-3)2, -OH, -O-alquilo C1-3)]; R6 representa hidrógeno, alquilo C1-5, alquinilo C3-6, (heterocicloalquil de 4 - 7 miembros)-alquilo C0-2 o cicloalquil C3-7-alquilo C0-2 [estando estos cuatro últimos grupos opcionalmente sustituidos con uno o más sustituyentes seleccionados de fluoro, -CN, =O, -C(O)-NH2, -C(O)-NH(alquil C1-3), -C(O)-N(alquil C1-3)2, alquilo C1-3 opcionalmente sustituido con OH o fluoro, -OH, -NH2, -O-alquilo C1-3, -NH(alquil C1-3), -N(alquil C1-3)2]; R7 y R9 representan independientemente hidrógeno, halo, -CN, alquilo C1-5, cicloalquil C3-5-alquil C0-2-, alquil C1-5-O-, cicloalquil C3-5-alquil C0-2-O- (y en estos cuatro últimos grupos los fragmentos alquilo y cicloalquilo están opcionalmente sustituidos con uno o más sustituyentes seleccionados de fluoro, -CN, =O, OH, -O-alquilo C1-3 o con uno o más grupos alquilo C1-3 que están opcionalmente sustituidos con uno o más átomos de flúor); L representa -NH2, -NHR10, -NR10R11, o un grupo heterocicloalquilo de 4 - 10 miembros que está unido al bencimidazol a través de un átomo de nitrógeno y que puede estar opcionalmente anillado con un fenilo o con un anillo heteroarilo de 5 ó 6 miembros y que está opcionalmente sustituido con uno o más sustituyentes R12; R10 y R11 representan independientemente alquilo C1-7, alquinilo C3-6, cicloalquil C3-7-alquil C0-4- o heterocicloalquil C4-7-alquil C0-4- [estando estos cuatro últimos grupos opcionalmente sustituidos con uno o más grupos seleccionados de fluoro, -OH, NH2, -C(O)NH2, -CN, =O, alquilo C1-3, -NH(alquil C1-3), -N(alquil C1-3)2, -O-alquilo C1-5, -O-cicloalquilo C3-6, -O-heterocicloalquilo C4-6, -S-alquilo C1-3, -S(O)alquilo C1-3, -S(O)2-alquilo C1-3 (estando estos nueve últimos grupos opcionalmente sustituidos con uno o más sustituyentes seleccionados de fluoro, -CF3, -CHF2, -CH2F, -CH3)], o aril-alquil C0-4, heteroaril-alquil C0-4- [estando estos dos últimos grupos opcionalmente sustituidos con uno o más sustituyentes seleccionados de halo, -OH, -NH2, -CN, alquilo C1-3, cicloalquilo C3-5, alquil C1-3-O-, cicloalquil C3-5-O- (estando estos cuatro últimos grupos opcionalmente sustituidos con uno o más átomos de flúor)]; cada R12 representa independientemente halo, -OH, -NH2, =O, -CN, -C(=O)-NH2, alquilo C1-4, cicloalquil C3-5-alquil C0-2-, heterocicloalquil C4-5-alquil C0-2-, alquil C1-4-O-, alquil C1-3-C(=O)-, -C(O)-NH(alquil C1-3), -C(=O)-N(alquil C1-3)2 [estando estos siete últimos grupos opcionalmente sustituidos con uno ó más grupos seleccionados de: fluoro, -OH, oxo, -NH2, -CN, alquilo C1-3, -NH(alquil C1-3), -N(alquil C1-3)2, -O-alquilo C1-3, -O-cicloalquilo C3-5 (estando estos cinco últimos grupos opcionalmente sustituidos con uno o más sustituyentes seleccionados de fluoro, -CF3, -CHF2, -CH2F)], o aril-alquil C0-4-, heteroaril-alquil C0-4- [estando estos dos últimos grupos opcionalmente sustituidos con uno o más sustituyentes seleccionados de halo, -OH, -CN, alquilo C1-3, cicloalquilo C3-5, alquil C1-3-O-, cicloalquil C3-5-O- (estando estos cuatro últimos grupos opcionalmente sustituidos con uno o más átomos de flúor)]; A representa alquilo C1-8, alquinilo C3-8, aril-alquil C0-3-, cicloalquil C3-8-alquil C0-3, (heterocicloalquil de 4 - 7 miembros)-alquil C0-3-, heteroaril-alquil C0-3, y en estos seis últimos grupos los fragmentos alquil-, alquinil-, cicloalquil- y heterocicloalquil- están opcionalmente sustituidos con uno o más sustituyentes seleccionados de R14 y los fragmentos arilo y heteroarilo están opcionalmente sustituidos con uno o más sustituyentes seleccionados de R15; cada R14 representa independientemente fluoro, -OH, -CN, =O, -NH2, -NH(alquil C1-3), -N(alquil C1-3)2, -O-alquilo C1-6, alquilo C1-6 [y en estos cuatro últimos grupos los fragmentos alquilo están opcionalmente sustituidos con uno o más sustituyentes seleccionados de fluoro, -CN, =O, -NH2, -NH(alquil C1-3), N(alquil C1-3)2, -OH, -O-alquilo C1-3] o arilo, heteroarilo [estando estos dos últimos grupos opcionalmente sustituidos con uno o más sustituyentes seleccionados de halo, OH, -CN, alquilo C1-3, O-alquilo C1-3 (estando estos dos últimos grupos alquilo opcionalmente sustituidos con uno o más átomos de flúor)]; cada R15 representa independientemente halo, -OH, -CN, -NH2, -NH(alquil C1-3), -N(alquil C1-3)2, -O-alquilo C1-3 [y en estos tres últimos grupos los fragmentos alquilo están opcionalmente sustituidos con uno o más sustituyentes seleccionados de fluoro, -CN, =O, -NH2, -NH(alquil C1-3), N(alquil C1-3)2, -OH, -O-alquilo C1-3] o arilo, heteroarilo [estando estos dos últimos grupos opcionalmente sustituidos con uno o más sustituyentes seleccionados de halo, OH, -CN, alquilo C1-3, O-alquilo C1-3 (estando estos dos últimos grupos alquilo opcionalmente sustituidos con uno o más átomos de flúor)] o alquilo C1-7, alquinilo C2-7, cicloalquilo C3-7, heterocicloalquilo de 4 - 7 miembros [estando estos últimos grupos alquilo, alquinilo, heterocicloalquilo o cicloalquilo opcionalmente sustituidos con uno o más sustituyentes seleccionados de fluoro, -CN, =O, -NH2, -NH(alquil C1-3), N(alquil C1-3)2, -OH, O-alquilo C1-3]; o una de sus sales, particularmente una de sus sales fisiológicamente aceptables.
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| US8586604B2 (en) | 2010-08-20 | 2013-11-19 | Boehringer Ingelheim International Gmbh | Inhibitors of the microsomal prostaglandin E2 synthase-1 |
| US8759537B2 (en) | 2010-08-20 | 2014-06-24 | Boehringer Ingelheim International Gmbh | 3H-imidazo [4, 5-C] pyridine-6-carboxamides as anti-inflammatory agents |
| US8674113B2 (en) | 2010-12-10 | 2014-03-18 | Boehringer Ingelheim International Gmbh | Compounds |
| US8486968B2 (en) | 2010-12-10 | 2013-07-16 | Boehringer Ingelheim International Gmbh | Compounds |
| US8466186B2 (en) | 2010-12-10 | 2013-06-18 | Boehringer Ingelheim International Gmbh | Compounds |
-
2011
- 2011-12-08 US US13/314,561 patent/US8674113B2/en not_active Expired - Fee Related
- 2011-12-08 UY UY0001033779A patent/UY33779A/es not_active Application Discontinuation
- 2011-12-09 CN CN2011800659456A patent/CN103402987A/zh active Pending
- 2011-12-09 PH PH1/2013/501175A patent/PH12013501175A1/en unknown
- 2011-12-09 BR BR112013014314A patent/BR112013014314A2/pt not_active IP Right Cessation
- 2011-12-09 EP EP11791593.4A patent/EP2649051A1/en not_active Withdrawn
- 2011-12-09 KR KR1020137014659A patent/KR20130143076A/ko not_active Withdrawn
- 2011-12-09 NZ NZ610312A patent/NZ610312A/en not_active IP Right Cessation
- 2011-12-09 EA EA201300684A patent/EA201300684A1/ru unknown
- 2011-12-09 CA CA2820838A patent/CA2820838A1/en not_active Abandoned
- 2011-12-09 MX MX2013006083A patent/MX2013006083A/es not_active Application Discontinuation
- 2011-12-09 AU AU2011340482A patent/AU2011340482A1/en not_active Abandoned
- 2011-12-09 JP JP2013542551A patent/JP5808820B2/ja not_active Expired - Fee Related
- 2011-12-09 WO PCT/EP2011/072257 patent/WO2012076673A1/en not_active Ceased
- 2011-12-12 AR ARP110104608A patent/AR084226A1/es unknown
-
2013
- 2013-05-13 IL IL226328A patent/IL226328A0/en unknown
- 2013-06-07 CL CL2013001654A patent/CL2013001654A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| IL226328A0 (en) | 2013-07-31 |
| JP2014502281A (ja) | 2014-01-30 |
| CN103402987A (zh) | 2013-11-20 |
| EP2649051A1 (en) | 2013-10-16 |
| NZ610312A (en) | 2015-11-27 |
| UY33779A (es) | 2012-07-31 |
| CL2013001654A1 (es) | 2014-03-28 |
| US8674113B2 (en) | 2014-03-18 |
| CA2820838A1 (en) | 2012-06-14 |
| US20120149676A1 (en) | 2012-06-14 |
| JP5808820B2 (ja) | 2015-11-10 |
| KR20130143076A (ko) | 2013-12-30 |
| EA201300684A1 (ru) | 2013-12-30 |
| WO2012076673A1 (en) | 2012-06-14 |
| BR112013014314A2 (pt) | 2016-09-27 |
| PH12013501175A1 (en) | 2017-08-23 |
| AU2011340482A1 (en) | 2013-05-30 |
| MX2013006083A (es) | 2013-07-02 |
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