AR086096A1 - Derivados de nucleosidos 2’-ciano sustituidos y metodos de uso de los mismos para el tratamiento de enfermedades virales - Google Patents
Derivados de nucleosidos 2’-ciano sustituidos y metodos de uso de los mismos para el tratamiento de enfermedades viralesInfo
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- AR086096A1 AR086096A1 ARP120101283A ARP120101283A AR086096A1 AR 086096 A1 AR086096 A1 AR 086096A1 AR P120101283 A ARP120101283 A AR P120101283A AR P120101283 A ARP120101283 A AR P120101283A AR 086096 A1 AR086096 A1 AR 086096A1
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- Prior art keywords
- group
- alkyl
- alkylene
- haloalkyl
- membered
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- 201000010099 disease Diseases 0.000 title 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title 1
- 230000003612 virological effect Effects 0.000 title 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 23
- 125000002947 alkylene group Chemical group 0.000 abstract 21
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 20
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 17
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 15
- 125000005843 halogen group Chemical group 0.000 abstract 14
- 125000001072 heteroaryl group Chemical group 0.000 abstract 14
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 13
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 13
- 125000000041 C6-C10 aryl group Chemical group 0.000 abstract 13
- 125000006568 (C4-C7) heterocycloalkyl group Chemical group 0.000 abstract 7
- 125000002619 bicyclic group Chemical group 0.000 abstract 7
- 125000002950 monocyclic group Chemical group 0.000 abstract 7
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- 125000003358 C2-C20 alkenyl group Chemical group 0.000 abstract 2
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 125000002795 guanidino group Chemical group C(N)(=N)N* 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 1
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 abstract 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 1
- KDCGOANMDULRCW-UHFFFAOYSA-N Purine Natural products N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 abstract 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 239000003937 drug carrier Substances 0.000 abstract 1
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- IGFXRKMLLMBKSA-UHFFFAOYSA-N purine Chemical compound N1=C[N]C2=NC=NC2=C1 IGFXRKMLLMBKSA-UHFFFAOYSA-N 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
Classifications
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- A—HUMAN NECESSITIES
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/7056—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing five-membered rings with nitrogen as a ring hetero atom
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
- A61K31/7068—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K31/00—Medicinal preparations containing organic active ingredients
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- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
- A61K31/7076—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines containing purines, e.g. adenosine, adenylic acid
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
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- 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
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- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/06—Pyrimidine radicals
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- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/06—Pyrimidine radicals
- C07H19/10—Pyrimidine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
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- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
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- C07H19/06—Pyrimidine radicals
- C07H19/10—Pyrimidine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
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- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
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- C07H19/20—Purine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
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- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/16—Purine radicals
- C07H19/20—Purine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
- C07H19/207—Purine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids the phosphoric or polyphosphoric acids being esterified by a further hydroxylic compound, e.g. flavine adenine dinucleotide or nicotinamide-adenine dinucleotide
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- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/16—Purine radicals
- C07H19/20—Purine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
- C07H19/213—Purine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids containing cyclic phosphate
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Abstract
Reivindicación 1: Un compuesto que tiene la estructura de fórmula (1) o una sal farmacéuticamente aceptable del mismo, en la que: X es O, S o CH2; B es una base de purina o pirimidina natural o no natural, o B se selecciona entre uno de los restos del grupo de fórmulas (2); Y es N o -C(R19)-; R1 es H, o un resto del grupo de fórmulas (3); R2 es H, o el resto de fórmula (4), o R1 y R2 se unen para formar un compuesto del grupo de fórmulas (5); R3 es alquilo C1-6, haloalquilo C1-6, hidroxialquilo C1-6, alquenilo C2-6, alquinilo C2-6 o cicloalquilo C3-7; cada uno de R4, R5, R7 y R8 es independientemente H, alquilo C1-6, haloalquilo C1-6, hidroxialquilo C1-6, halo, -OR20, -SR20 o -N(R20)2; cada uno de R6, R9, R10, R11 se selecciona independientemente entre H, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-7, heteroarilo monocíclico de 5 ó 6 miembros, heteroarilo bicíclico de 9 ó 10 miembros, halo, -OR20, -SR20, -S(O)R20, -S(O)2R20, -S(O)2N(R20)2, -NHC(O)OR20, -NHC(O)N(R20)2, haloalquilo C1-6, hidroxialquilo C1-6, -O-(haloalquilo C1-6), -CN, -NO2, -N(R20)2, -NH(alquileno C1-6)-(heteroarilo monocíclico de 5 ó 6 miembros), -NH(alquileno C1-6)-(heteroarilo bicíclico de 9 ó 10 miembros), -C(O)R20, -C(O)OR20, -C(O)N(R20)2 y -NHC(O)R20, en la que dicho grupo alquenilo C2-6 y dicho grupo alquinilo C2-6 pueden estar opcionalmente sustituidos con un grupo halo; R12 es H o -(alquileno C1-6)-T-R21; R13 es H o -(alquileno C1-6)-T-R21, o R12 y R13 pueden unirse para formar un grupo alquileno C2-4 entre los átomos de oxígeno a los que R12 y R13 están unidos, en la que dicho grupo alquileno C2-4 está sustituido con al menos un grupo arilo C6-10; R14 es H, arilo C6-10, heteroarilo monocíclico de 5 ó 6 miembros o heteroarilo bicíclico de 9 ó 10 miembros, en la que dicho grupo arilo C6-10, dicho grupo heteroarilo monocíclico de 5 ó 6 miembros y dicho grupo heteroarilo bicíclico de 9 ó 10 miembros puede estar opcionalmente sustituido con R22; R15 es H, alquilo C1-6, cicloalquilo C3-7, fenilo o bencilo, en la que dicho alquilo C1-6 puede estar opcionalmente sustituido con un grupo seleccionado entre halo, -OR20, -SR20, guanidino, -N(R20)2, -C(O)OR20, -C(O)N(R20)2, -NHC(O)R20, heteroarilo monocíclico de 5 ó 6 miembros y heteroarilo bicíclico de 9 ó 10 miembros, y en la que dicho grupo fenilo y dicho grupo bencilo pueden estar opcionalmente sustituidos con hasta 2 grupos, cada uno seleccionado independientemente entre alquilo C1-6, halo y -OR20; R16 es H, alquilo C1-6, cicloalquilo C3-7, fenilo o bencilo, en la que dicho alquilo C1-6 puede estar opcionalmente sustituido con un grupo seleccionado entre halo, -OR20, -SR20, guanidino, -N(R20)2, -C(O)OR20, -C(O)N(R20)2, -NHC(O)R20, heteroarilo monocíclico de 5 ó 6 miembros y heteroarilo bicíclico de 9 ó 10 miembros, y en la que dicho grupo fenilo y dicho grupo bencilo pueden estar opcionalmente sustituidos con hasta 2 grupos, cada uno seleccionado independientemente entre alquilo C1-6, halo y -OR20; R17 es H, alquilo C1-20, alquenilo C2-20, -(alquileno C1-3)m-cicloalquilo C3-7, -(alquileno C1-3)m-arilo C6-10 o adamantilo, en la que dicho grupo alquilo C1-20, dicho grupo alquenilo C2-20, dicho grupo arilo C6-10 y dicho grupo adamantilo pueden estar opcionalmente sustituidos con hasta tres grupos, cada uno seleccionado independientemente entre halo, -OR20, -C(O)OR20, CN, NO2, haloalquilo C1-6, hidroxialquilo C1-6, cicloalquilo C3-7, arilo C6-10, heteroarilo monocíclico de 5 ó 6 miembros, heteroarilo bicíclico de 9 ó 10 miembros, -N(R20)2, -C(O)N(R20)2, -SR20, -S(O)R20, -S(O)2R20, -S(O)2N(R20)2, -NHC(O)R20, -NHC(O)OR20 y -NHC(O)N(R20)2; y R18 es H, alquilo C1-6, cicloalquilo C3-7, -(alquileno C1-3)m-arilo C6-10, heteroarilo monocíclico de 5 ó 6 miembros, heteroarilo bicíclico de 9 ó 10 miembros o un resto de fórmula (6), en la que dicho grupo arilo C6-10, dicho grupo heteroarilo monocíclico de 5 ó 6 miembros y dicho grupo heteroarilo bicíclico de 9 ó 10 miembros pueden estar opcionalmente sustituidos con hasta cinco grupos, cada uno seleccionado independientemente entre alquilo C1-6, alquenilo C2-6, alquinilo C2-6, halo, -OR20, -SR20, haloalquilo C1-6, hidroxialquilo C1-6, -O-(haloalquilo C1-6), -CN, -NO2, -N(R20)2, -C(O)OR20, -C(O)N(R20)2 y -NHC(O)R20; R19 es H, alquilo C1-6, haloalquilo C1-6, hidroxialquilo C1-6, halo, -OR20, -SR20, N(R20)2, cicloalquilo C3-7, arilo C6-10, heteroarilo monocíclico de 5 ó 6 miembros o heteroarilo bicíclico de 9 ó 10 miembros; cada aparición de R20 es independientemente H, alquilo C1-10, haloalquilo C1-6, hidroxialquilo C1-6, -(alquileno C1-3)m-(cicloalquilo C3-7), -(alquileno C1-3)m-(arilo C6-10), -(alquileno C1-3)m-(heterocicloalquilo de 4 a 7 miembros), -(alquileno C1-3)m-(heteroarilo monocíclico de 5 ó 6 miembros) o -(alquileno C1-3)m-(heteroarilo bicíclico de 9 ó 10 miembros), en la que dicho grupo cicloalquilo C3-7, dicho grupo arilo C6-10, dicho grupo heterocicloalquilo de 4 a 7 miembros, dicho -(grupo heteroarilo monocíclico de 5 ó 6 miembros) o dicho grupo heteroarilo bicíclico de 9 ó 10 miembros puede estar opcionalmente sustituido con R26; cada aparición de R21 es independientemente H, alquilo C1-6, haloalquilo C1-6, hidroxialquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-7, cicloalquenilo C3-7, heteroarilo monocíclico de 5 ó 6 miembros, heteroarilo bicíclico de 9 ó 10 miembros, -OR20, -O-(haloalquilo C1-6) o -N(R20)2, en la que dicho grupo alquenilo C2-6, dicho grupo alquinilo C2-6, dicho grupo cicloalquilo C3-7, dicho grupo cicloalquenilo C3-7, dicho grupo arilo C6-10, dicho grupo heteroarilo monocíclico de 5 ó 6 miembros y dicho grupo heteroarilo bicíclico de 9 ó 10 miembros pueden estar opcionalmente sustituidos con hasta cinco grupos, cada uno seleccionado independientemente entre alquilo C1-6, alquenilo C2-6, alquinilo C2-6, halo, -OR20, -SR20, haloalquilo C1-6, hidroxialquilo C1-6, -O-(haloalquilo C1-6), -CN, -NO2, -N(R20)2, -C(O)R20, -C(O)OR20, -C(O)N(R20)2 y -NHC(O)R20; R22 representa de uno a cinco grupos de sustituyentes, cada uno seleccionado independientemente entre alquilo C1-6, halo, -OR20, -SR20, haloalquilo C1-6, hidroxialquilo C1-6, -O-(haloalquilo C1-6), -CN, -NO2, -N(R20)2, -C(O)OR20, -C(O)N(R20)2 y -NHC(O)R20, o dos grupos R22 cualesquiera en los átomos de carbono adyacentes del anillo pueden combinarse para formar -O-R23-O-; R23 es -[C(R24)2]n-; cada aparición de R24 es independientemente H o alquilo C1-6; cada aparición de R25 es independientemente H, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-7, -(alquileno C1-3)m-(arilo C6-10), heterocicloalquilo de 4 a 7 miembros, heteroarilo monocíclico de 5 ó 6 miembros o heteroarilo bicíclico de 9 ó 10 miembros, en la que dicho grupo alquilo C1-6, dicho grupo alquenilo C2-6, dicho grupo alquinilo C2-6, dicho grupo cicloalquilo C3-7, dicho grupo arilo C6-10, dicho grupo heterocicloalquilo de 4 a 7 miembros, dicho -(grupo heteroarilo monocíclico de 5 ó 6 miembros) o dicho grupo heteroarilo bicíclico de 9 ó 10 miembros puede estar opcionalmente sustituido con R26; o dos grupos R25, junto con el átomo de nitrógeno común al que están unidos, se unen para formar un grupo heterocicloalquilo de 4 a 7 miembros; R26 representa de uno a cinco grupos de sustituyentes, cada uno seleccionado independientemente entre alquilo C1-6, alquenilo C2-6, alquinilo C2-6, halo, -OR27, -SR27, haloalquilo C1-6, hidroxialquilo C1-6, -O-(haloalquilo C1-6), -CN, -NO2, -N(R27)2, -C(O)OR27, -C(O)N(R27)2 y -NHC(O)R27; cada aparición de R27 es independientemente H, alquilo C1-6, haloalquilo C1-6, hidroxialquilo C1-6, -(alquileno C1-3)m-(cicloalquilo C3-7), -(alquileno C1-3)m-(arilo C6-10), -(alquileno C1-3)m-(heterocicloalquilo de 4 a 7 miembros), -(alquileno C1-3)m-(heteroarilo monocíclico de 5 ó 6 miembros) o -(alquileno C1-3)m-(heteroarilo bicíclico de 9 ó 10 miembros); R28 es H, alquilo C1-6, haloalquilo C1-6, hidroxialquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-7, cicloalquenilo C3-7, heteroarilo monocíclico de 5 ó 6 miembros, heteroarilo bicíclico de 9 ó 10 miembros, -OR20, -O-(haloalquilo C1-6) o -N(R20)2, en la que dicho grupo alquenilo C2-6, dicho grupo alquinilo C2-6, dicho grupo cicloalquilo C3-7, dicho grupo cicloalquenilo C3-7, dicho grupo arilo C6-10, dicho grupo heteroarilo monocíclico de 5 ó 6 miembros y dicho grupo heteroarilo bicíclico de 9 ó 10 miembros pueden estar opcionalmente sustituidos con hasta cinco grupos, cada uno seleccionado independientemente entre alquilo C1-6, alquenilo C2-6, alquinilo C2-6, halo, -OR20, -SR20, haloalquilo C1-6, hidroxialquilo C1-6, -O-(haloalquilo C1-6), -CN, -NO2, -N(R20)2, -C(O)R20, -C(O)OR20, -C(O)N(R20)2 y -NHC(O)R20; cada aparición de R29 es independientemente H, alquilo C1-6, haloalquilo C1-6, hidroxialquilo C1-6, -(alquileno C1-3)m-(cicloalquilo C3-7), -(alquileno C1-3)m-(arilo C6-10), -(alquileno C1-3)m-(heterocicloalquilo de 4 a 7 miembros), -(alquileno C1-3)m-(heteroarilo monocíclico de 5 ó 6 miembros) o -(alquileno C1-3)m-(heteroarilo bicíclico de 9 ó 10 miembros), en la que dicho grupo cicloalquilo C3-7, dicho grupo arilo C6-10, dicho grupo heterocicloalquilo de 4 a 7 miembros, dicho -(grupo heteroarilo monocíclico de 5 ó 6 miembros) o dicho grupo heteroarilo bicíclico de 9 ó 10 miembros puede estar opcionalmente sustituido con R26; cada aparición de T es independientemente -S-, -O-, -SC(O)-, -SC(S)-, -OC(O)- y -OC(S)-; cada aparición de m es independientemente 0 ó 1; y cada aparición de n es independientemente 1 ó 2.Reivindicación 16: Una composición farmacéutica que comprende una cantidad eficaz del compuesto de cualquiera de las reivindicaciones 1 a 15, o una sal farmacéuticamente aceptable del mismo, y un vehículo farmacéuticamente aceptable. Reivindicación 20: Un método para tratar a un paciente infectado con VHC que comprende el paso de administrar una cantidad de (i) el compuesto de acuerdo con cualquiera de las reivindicaciones de 1 a 15, o una sal farmacéuticamente aceptable del mismo, o
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- 2012-04-11 WO PCT/US2012/033028 patent/WO2012142093A2/en not_active Ceased
- 2012-04-11 US US14/111,688 patent/US9150603B2/en active Active
- 2012-04-11 AU AU2012242978A patent/AU2012242978A1/en not_active Abandoned
- 2012-04-11 EP EP12770821.2A patent/EP2696679B1/en not_active Not-in-force
- 2012-04-13 TW TW101113292A patent/TW201247694A/zh unknown
- 2012-04-13 AR ARP120101283A patent/AR086096A1/es not_active Application Discontinuation
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| EP2696679A2 (en) | 2014-02-19 |
| US20140161770A1 (en) | 2014-06-12 |
| CA2832449A1 (en) | 2012-10-18 |
| TW201247694A (en) | 2012-12-01 |
| JP2014511875A (ja) | 2014-05-19 |
| EP2696679A4 (en) | 2015-06-10 |
| EP2696679B1 (en) | 2017-08-02 |
| US9150603B2 (en) | 2015-10-06 |
| WO2012142093A3 (en) | 2013-02-07 |
| AU2012242978A1 (en) | 2013-10-24 |
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