AR108926A1 - Moduladores de cot y sus métodos de uso - Google Patents
Moduladores de cot y sus métodos de usoInfo
- Publication number
- AR108926A1 AR108926A1 ARP170101815A ARP170101815A AR108926A1 AR 108926 A1 AR108926 A1 AR 108926A1 AR P170101815 A ARP170101815 A AR P170101815A AR P170101815 A ARP170101815 A AR P170101815A AR 108926 A1 AR108926 A1 AR 108926A1
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- Prior art keywords
- alkyl
- heterocyclyl
- heteroaryl
- cycloalkyl
- aryl
- Prior art date
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- 238000000034 method Methods 0.000 title abstract 2
- 125000006545 (C1-C9) alkyl group Chemical group 0.000 abstract 50
- 125000000623 heterocyclic group Chemical group 0.000 abstract 47
- 125000001072 heteroaryl group Chemical group 0.000 abstract 45
- 125000003118 aryl group Chemical group 0.000 abstract 41
- 125000006647 (C3-C15) cycloalkyl group Chemical group 0.000 abstract 37
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 29
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 26
- 125000006648 (C1-C8) haloalkyl group Chemical group 0.000 abstract 22
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 9
- 239000001257 hydrogen Substances 0.000 abstract 9
- 229910052739 hydrogen Inorganic materials 0.000 abstract 9
- 125000000217 alkyl group Chemical group 0.000 abstract 8
- 125000000304 alkynyl group Chemical group 0.000 abstract 7
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 7
- -1 C1−9-thio alkyl Chemical group 0.000 abstract 6
- 150000002431 hydrogen Chemical group 0.000 abstract 6
- 125000001475 halogen functional group Chemical group 0.000 abstract 5
- 125000003342 alkenyl group Chemical group 0.000 abstract 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 4
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 125000004043 oxo group Chemical group O=* 0.000 abstract 3
- 125000000041 C6-C10 aryl group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000001188 haloalkyl group Chemical group 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 125000000464 thioxo group Chemical group S=* 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 208000024770 Thyroid neoplasm Diseases 0.000 abstract 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 201000002510 thyroid cancer Diseases 0.000 abstract 1
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- 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
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Abstract
La presente descripción se refiere en general a compuestos derivados de quinazolina como moduladores de Cot (cancer Osaka thyroid) y sus métodos de uso y su fabricación. Reivindicación 1: Un compuesto de la fórmula (1), en donde R¹ es alquilo C₁₋₉, cicloalquilo C₃₋₁₅, heterociclilo, heteroarilo o arilo C₆₋₁₀; en donde cada alquilo C₁₋₉, cicloalquilo C₃₋₁₅, heterociclilo, heteroarilo y arilo C₆₋₁₀ puede estar opcionalmente sustituido con uno a cuatro Z¹; R² es hidrógeno, -C(O)-R⁷, -C(O)O-R⁷, -C(O)N(R⁷)₂ o alquilo C₁₋₉; R³ es heterociclilo o heteroarilo; en donde cada heterociclilo o heteroarilo está opcionalmente sustituido con uno a cuatro Z³; R⁴ es arilo, heterociclilo o heteroarilo; en donde cada arilo, heterociclilo o heteroarilo está opcionalmente sustituido con uno a cuatro Z⁴; R⁵ es hidrógeno, halo, ciano, -NO₂, -O-R⁷, -N(R⁸)(R⁹), -S(O)-R⁷, -S(O)₂R⁷, -S(O)₂N(R⁷)₂, -C(O)R⁷, -OC(O)-R⁷, -C(O)O-R⁷, -OC(O)O-R⁷, -OC(O)N(R¹⁰)(R¹¹), -C(O)N(R⁷)₂, -N(R⁷)C(O)(R⁷), alquilo C₁₋₉, alquenilo C₂₋₆, alquinilo C₂₋₆, alquil C₁₋₉-tio, haloalquilo C₁₋₆, cicloalquilo C₃₋₁₅, arilo, heterociclilo o heteroarilo; en donde cada alquilo C₁₋₉, alquenilo C₂₋₆, alquinilo C₂₋₆, alquil C₁₋₉-tio, haloalquilo C₁₋₆, cicloalquilo C₃₋₁₅, arilo, heterociclilo y heteroarilo puede estar opcionalmente sustituido con uno a cuatro Z⁵; R⁶ es hidrógeno, -C(O)-R⁷, -C(O)O-R⁷, -C(O)N(R⁷)₂, alquilo C₁₋₉, alquenilo C₂₋₆, alquinilo C₂₋₆, haloalquilo C₁₋₆, cicloalquilo C₃₋₁₅, arilo, heterociclilo o heteroarilo; en donde cada alquilo C₁₋₉, alquenilo C₂₋₆, alquinilo C₂₋₆, haloalquilo C₁₋₆, cicloalquilo C₃₋₁₅, arilo, heterociclilo y heteroarilo puede estar opcionalmente sustituido con uno a cuatro Z⁶; cada R⁷ es, de modo independiente, hidrógeno, alquilo C₁₋₉, alquenilo C₂₋₆, alquinilo C₂₋₆, haloalquilo C₁₋₆, cicloalquilo C₃₋₁₅, arilo, heterociclilo o heteroarilo; en donde cada alquilo C₁₋₉, alquenilo C₂₋₆, alquinilo C₂₋₆, haloalquilo C₁₋₆, cicloalquilo C₃₋₁₅, arilo, heterociclilo y heteroarilo puede estar opcionalmente sustituido con uno a cuatro Z⁷; R⁸ y R⁹ en cada aparición son, de modo independiente, hidrógeno, -S(O)₂R¹⁰, -C(O)-R¹⁰, -C(O)O-R¹⁰, -C(O)N(R¹⁰)(R¹¹), alquilo C₁₋₉, alquenilo C₂₋₆, alquinilo C₂₋₆, haloalquilo C₁₋₆, cicloalquilo C₃₋₁₅, arilo, heterociclilo o heteroarilo; en donde cada alquilo C₁₋₉, alquenilo C₂₋₆, alquinilo C₂₋₆, haloalquilo C₁₋₆, cicloalquilo C₃₋₁₅, arilo, heterociclilo o heteroarilo puede estar opcionalmente sustituido con uno a cuatro Z⁸; R¹⁰ y R¹¹ en cada aparición son, de modo independiente, hidrógeno, alquilo C₁₋₉, alquenilo C₂₋₆, alquinilo C₂₋₆, haloalquilo C₁₋₆, cicloalquilo C₃₋₁₅, arilo, heterociclilo o heteroarilo, en donde cada alquilo C₁₋₉, alquenilo C₂₋₆, alquinilo C₂₋₆, haloalquilo C₁₋₆, cicloalquilo C₃₋₁₅, arilo, heterociclilo y heteroarilo está opcionalmente sustituido con uno a cuatro Z¹ᵇ; cada Z¹, Z³, Z⁴, Z⁵, Z⁶, Z⁷ y Z⁸ es, de modo independiente, hidrógeno, oxo, halo, -NO₂, -N₃, ciano, tioxo, alquilo C₁₋₉, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₁₅, haloalquilo C₁₋₈, arilo, heteroarilo, heterociclilo, -O-R¹², -C(O)-R¹², -C(O)O-R¹², -C(O)-N(R¹³)(R¹⁴), -N(R¹³)(R¹⁴), -N(R¹³)₂(R¹⁴)⁺, -N(R¹²)C(O)-R¹², -N(R¹²)C(O)O-R¹², -N(R¹²)C(O)N(R¹³)(R¹⁴), -N(R¹²)S(O)₂(R¹²), -NR¹²S(O)₂N(R¹³)(R¹⁴), -NR¹²S(O)₂O(R¹²), -OC(O)R¹², -OC(O)-N(R¹³)(R¹⁴), -P(O)(OR¹²)₂, -OP(O)(OR¹²)₂, -CH₂P(O)(OR¹²)₂, -OCH₂P(O)(OR¹²)₂, -C(O)OCH₂P(O)(OR¹²)₂, -P(O)(R¹²)(OR¹²), -OP(O)(R¹²)(OR¹²), -CH₂P(O)(R¹²)(OR¹²), -OCH₂P(O)(R¹²)(OR¹²), -C(O)OCH₂P(O)(R¹²)(OR¹²), -P(O)(N(R¹²)₂)₂, -OP(O)(N(R¹²)₂)₂, -CH₂P(O)(N(R¹²)₂)₂, -OCH₂P(O)(N(R¹²)₂)₂, -C(O)OCH₂P(O)(N(R¹²)₂)₂, -P(O)(N(R¹²)₂)(OR¹²), OP(O)(N(R¹²)₂)(OR¹²), CH₂P(O)(N(R¹²)₂)(OR¹²), -OCH₂P(O)(N(R¹²)₂)(OR¹²), -C(O)OCH₂P(O)(N(R¹²)₂)(OR¹²), -P(O)(R¹²)(N(R¹²)₂), -OP(O)(R¹²)(N(R¹²)₂), -CH₂P(O)(R¹²)(N(R¹²)₂), -OCH₂P(O)(R¹²)(N(R¹²)₂), -C(O)OCH₂P(O)(R¹²)(N(R¹²)₂), -Si(R¹²)₃, -S-R¹², -S(O)R¹², -S(O)(NH)R¹², -S(O)₂R¹² o -S(O)₂N(R¹³)(R¹⁴); en donde cualquier alquilo, alquenilo, alquinilo, cicloalquilo, haloalquilo, arilo, heteroarilo o heterociclilo está opcionalmente sustituido con uno a cuatro grupos Z¹ᵃ; cada Z¹ᵃ es, de modo independiente, oxo, halo, tioxo, -NO₂, ciano, -N₃, alquilo C₁₋₉, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₁₅, haloalquilo C₁₋₈, arilo, heteroarilo, heterociclilo, -O-R¹², -C(O)R¹², -C(O)O-R¹², -C(O)N(R¹³)(R¹⁴), -N(R¹³)(R¹⁴), -N(R¹³)₂(R¹⁴)⁺, -N(R¹²)-C(O)R¹², -N(R¹²)C(O)O(R¹²), -N(R¹²)C(O)N(R¹³)(R¹⁴), -N(R¹²)S(O)₂(R¹²), N(R¹²)S(O)₂-N(R¹³)(R¹⁴), -N(R¹²)S(O)₂O(R¹²), -OC(O)R¹², -OC(O)OR¹², -OC(O)-N(R¹³)(R¹⁴), -Si(R¹²)₃, -S-R¹², -S(O)R¹², -S(O)(NH)R¹², -S(O)₂R¹² o -S(O)₂N(R¹³)(R¹⁴); en donde cualquier alquenilo, alquinilo, cicloalquilo, arilo, heteroarilo o heterociclilo está opcionalmente sustituido con uno a cuatro grupos Z¹ᵇ; cada R¹² es, de modo independiente, hidrógeno, alquilo C₁₋₉, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₁₅, arilo, heteroarilo o heterociclilo, en donde cualquier alquilo, alquenilo, alquinilo, cicloalquilo, arilo, heteroarilo o heterociclilo está opcionalmente sustituido con uno a cuatro grupos Z¹ᵇ; R¹³ y R¹⁴ en cada aparición son cada uno, de modo independiente, hidrógeno, alquilo C₁₋₉, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₁₅, arilo, heteroarilo o heterociclilo; en donde cualquier alquilo, alquenilo, alquinilo, cicloalquilo, arilo, heteroarilo o heterociclilo está opcionalmente sustituido con uno a cuatro grupos Z¹ᵇ o R¹³ y R¹⁴ junto con el nitrógeno al que están unidos forman un heterociclilo, en donde dicho heterociclilo está opcionalmente sustituido con uno a cuatro grupos Z¹ᵇ; cada Z¹ᵇ es, de modo independiente, oxo, tioxo, hidroxi, halo, -NO₂, -N₃, ciano, alquilo C₁₋₉, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₁₅, haloalquilo C₁₋₈, arilo, heteroarilo, heterociclilo, -O(alquilo C₁₋₉), -O(alquenilo C₂₋₆), -O(alquinilo C₂₋₆), -O(cicloalquilo C₃₋₁₅), -O(haloalquilo C₁₋₈), -O(arilo), -O(heteroarilo), -O(heterociclilo), -NH₂, -NH(alquilo C₁₋₉), -NH(alquenilo C₂₋₆), -NH(alquinilo C₂₋₆), -NH(cicloalquilo C₃₋₁₅), -NH(haloalquilo C₁₋₈), -NH(arilo), -NH(heteroarilo), -NH(heterociclilo), -N(alquilo C₁₋₉)₂, -N(cicloalquilo C₃₋₁₅)₂, -N(alquenilo C₂₋₆)₂, -N(alquinilo C₂₋₆)₂, -N(cicloalquilo C₃₋₁₅)₂, -N(haloalquilo C₁₋₈)₂, -N(arilo)₂, -N(heteroarilo)₂, -N(heterociclilo)₂, -N(alquil C₁₋₉)(cicloalquilo C₃₋₁₅), -N(alquil C₁₋₉)(alquenilo C₂₋₆), -N(alquil C₁₋₉)(alquinilo C₂₋₆), -N(alquil C₁₋₉)(cicloalquilo C₃₋₁₅), -N(alquil C₁₋₉)(haloalquilo C₁₋₈), -N(alquil C₁₋₉)(arilo), -N(alquil C₁₋₉)(heteroarilo), -N(alquil C₁₋₉)(heterociclilo), -C(O)(alquilo C₁₋₉), -C(O)(alquenilo C₂₋₆), -C(O)(alquinilo C₂₋₆), -C(O)(cicloalquilo C₃₋₁₅), -C(O)(haloalquilo C₁₋₈), -C(O)(arilo), -C(O)(heteroarilo), -C(O)(heterociclilo), -C(O)O(alquilo C₁₋₉), -C(O)O(alquenilo C₂₋₆), -C(O)O(alquinilo C₂₋₆), -C(O)O(cicloalquilo C₃₋₁₅), -C(O)O(haloalquilo C₁₋₈), -C(O)O(arilo), -C(O)O(heteroarilo), -C(O)O(heterociclilo), -C(O)NH₂, -C(O)NH(alquilo C₁₋₉), -C(O)NH(alquenilo C₂₋₆), -C(O)NH(alquinilo C₂₋₆), -C(O)NH(cicloalquilo C₃₋₁₅), -C(O)NH(haloalquilo C₁₋₈), -C(O)NH(arilo), -C(O)NH(heteroarilo), -C(O)NH(heterociclilo), -C(O)N(alquilo C₁₋₉)₂, -C(O)N(cicloalquilo C₃₋₁₅)₂, -C(O)N(alquenilo C₂₋₆)₂, -C(O)N(alquinilo C₂₋₆)₂, -C(O)N(cicloalquilo C₃₋₁₅)₂, -C(O)N(haloalquilo C₁₋₈)₂, -C(O)N(arilo)₂, -C(O)N(heteroarilo)₂, -C(O)N(heterociclilo)₂, -NHC(O)(alquilo C₁₋₉), -NHC(O)(alquenilo C₂₋₆), -NHC(O)(alquinilo C₂₋₆), -NHC(O)(cicloalquilo C₃₋₁₅), -NHC(O)(haloalquilo C₁₋₈), -NHC(O)(arilo), -NHC(O)(heteroarilo), -NHC(O)(heterociclilo), -NHC(O)O(alquilo C₁₋₉), -NHC(O)O(alquenilo C₂₋₆), -NHC(O)O(alquinilo C₂₋₆), -NHC(O)O(cicloalquilo C₃₋₁₅), -NHC(O)O(haloalquilo C₁₋₈), -NHC(O)O(arilo), -NHC(O)O(heteroarilo), -NHC(O)O(heterociclilo), -NHC(O)NH(alquilo C₁₋₉), -NHC(O)NH(alquenilo C₂₋₆), -NHC(O)NH(alquinilo C₂₋₆), -NHC(O)NH(cicloalquilo C₃₋₁₅), -NHC(O)NH(haloalquilo C₁₋₈), -NHC(O)NH(arilo), -NHC(O)NH(heteroarilo), -NHC(O)NH(heterociclilo), -SH, -S(alquilo C₁₋₉), -S(alquenilo C₂₋₆), -S(alquinilo C₂₋₆), -S(cicloalquilo C₃₋₁₅), -S(haloalquilo C₁₋₈), -S(arilo), -S(heteroarilo), -S(heterociclilo), -NHS(O)(alquilo C₁₋₉), -N(alquilo C₁₋₉)(S(O)(alquilo C₁₋₉), -S(O)N(alquilo C₁₋₉)₂, -S(O)(alquilo C₁₋₉), -S(O)(NH)(alquilo C₁₋₉), -S(O)(alquenilo C₂₋₆), -S(O)(alquinilo C₂₋₆), -S(O)(cicloalquilo C₃₋₁₅), -S(O)(haloalquilo C₁₋₈), -S(O)(arilo), -S(O)(heteroarilo), -S(O)(heterociclilo), -S(O)₂(alquilo C₁₋₉), -S(O)₂(alquenilo C₂₋₆), -S(O)₂(alquinilo C₂₋₆), -S(O)₂(cicloalquilo C₃₋₁₅), -S(O)₂(haloalquilo C₁₋₈), -S(O)₂(arilo), -S(O)₂(heteroarilo), -S(O)₂(heterociclilo), -S(O)₂NH(alquilo C₁₋₉) o -S(O)₂N(alquilo C₁₋₉)₂; en donde cualquier alquilo, cicloalquilo, arilo, heteroarilo o heterociclilo está opcionalmente sustituido con uno a cuatro halo, alquilo C₁₋₉, haloalquilo C₁₋₈, -OH, -NH₂, -NH(alquilo C₁₋₉), -NH(cicloalquilo C₃₋₁₅), -NH(haloalquilo C₁₋₈), -NH(arilo), -NH(heteroarilo), -NH(heterociclilo), -N(alquilo C₁₋₉)₂, -N(cicloalquilo C₃₋₁₅)₂, -NHC(O)(cicloalquilo C₃₋₁₅), -NHC(O)(haloalquilo C₁₋₈), -NHC(O)(arilo), -NHC(O)(heteroarilo), -NHC(O)(heterociclilo), -NHC(O)O(alquilo C₁₋₉), -NHC(O)O(alquinilo C₂₋₆), -NHC(O)O(cicloalquilo C₃₋₁₅), -NHC(O)O(haloalquilo C₁₋₈), -NHC(O)O(arilo), -NHC(O)O(heteroarilo), -NHC(O)O(heterociclilo), -NHC(O)NH(alquilo C₁₋₉), -S(O)(NH)(alquilo C₁₋₉), S(O)₂(alquilo C₁₋₉), -S(O)₂(cicloalquilo C₃₋₁₅), -S(O)₂(haloalquilo C₁₋₈), -S(O)₂(arilo), -S(O)₂(heteroarilo), -S(O)₂(heterociclilo), -S(O)₂NH(alquilo C₁₋₉), -S(O)₂N(alquilo C₁₋₉)₂, -O(cicloalquilo C₃₋₁₅), -O(haloalquilo C₁₋₈), -O(arilo), -O(heteroarilo), -O(heterociclilo) u -O(alquilo C₁₋₉); m es 0, 1 ó 2; o una de sus sales, estereoisómeros, mezcla de estereoisómeros o análogos farmacéuticamente aceptables.
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| SG145744A1 (en) | 2003-08-19 | 2008-09-29 | Wyeth Corp | Process for the preparation of 4-amino-3- quinolinecarbonitriles |
| EP1881981A1 (en) | 2005-05-18 | 2008-01-30 | Wyeth | 4, 6-diamino-[1,7] naphthyridine-3-carbonitrile inhibitors of tpl2 kinase and methods of making and using the same |
| JP2008540656A (ja) * | 2005-05-18 | 2008-11-20 | ワイス | Tpl2キナーゼの3−シアノキノリン阻害物質ならびにそれを製造および使用する方法 |
| MX2008012482A (es) | 2006-03-31 | 2008-10-10 | Abbott Lab | Compuestos de indazol. |
| US20130059851A1 (en) | 2010-03-09 | 2013-03-07 | Dana-Farber Cancer Institute, Inc. | Methods of Diagnosing and Treating Cancer in Patients Having or Developing Resistance to a First Cancer Therapy |
| IN2015DN03795A (es) | 2012-10-24 | 2015-10-02 | Inserm Inst Nat De La Santé Et De La Rech Médicale | |
| US9815818B2 (en) | 2015-07-06 | 2017-11-14 | Gilead Sciences, Inc. | Cot modulators and methods of use thereof |
| EP3456717B1 (en) | 2015-07-06 | 2021-03-17 | Gilead Sciences, Inc. | 4,6-diamino-quinoline-3-carbonitrile derivative as cancer osaka thyroid (cot) modulator for treating inflammatory disease |
| EP3478674B1 (en) | 2016-06-30 | 2020-05-13 | Gilead Sciences, Inc. | 4,6-diaminoquinazolines as cot modulators and methods of use thereof |
-
2017
- 2017-06-27 EP EP17735754.8A patent/EP3478674B1/en active Active
- 2017-06-27 WO PCT/US2017/039418 patent/WO2018005435A1/en not_active Ceased
- 2017-06-27 US US15/634,314 patent/US10059695B2/en active Active
- 2017-06-27 CA CA3029457A patent/CA3029457A1/en active Pending
- 2017-06-27 AU AU2017289158A patent/AU2017289158C1/en active Active
- 2017-06-27 JP JP2018568417A patent/JP6776378B2/ja active Active
- 2017-06-27 ES ES17735754T patent/ES2800339T3/es active Active
- 2017-06-29 TW TW106121722A patent/TWI644910B/zh active
- 2017-06-29 TW TW107138228A patent/TWI680126B/zh active
- 2017-06-30 AR ARP170101815A patent/AR108926A1/es unknown
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2018
- 2018-07-25 US US16/045,518 patent/US10577352B2/en active Active
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2020
- 2020-02-20 JP JP2020027397A patent/JP2020073614A/ja not_active Withdrawn
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| JP2020073614A (ja) | 2020-05-14 |
| AU2017289158C1 (en) | 2020-07-23 |
| US10059695B2 (en) | 2018-08-28 |
| TWI644910B (zh) | 2018-12-21 |
| NZ749172A (en) | 2020-07-31 |
| AU2017289158A1 (en) | 2019-01-03 |
| ES2800339T3 (es) | 2020-12-29 |
| TWI680126B (zh) | 2019-12-21 |
| EP3478674B1 (en) | 2020-05-13 |
| US20190016705A1 (en) | 2019-01-17 |
| CA3029457A1 (en) | 2018-01-04 |
| EP3478674A1 (en) | 2019-05-08 |
| AU2017289158B2 (en) | 2019-12-19 |
| TW201805281A (zh) | 2018-02-16 |
| JP2019519580A (ja) | 2019-07-11 |
| US10577352B2 (en) | 2020-03-03 |
| JP6776378B2 (ja) | 2020-10-28 |
| TW201920151A (zh) | 2019-06-01 |
| WO2018005435A1 (en) | 2018-01-04 |
| US20180002316A1 (en) | 2018-01-04 |
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