AR099890A1 - Inhibidores de histona demetilasas - Google Patents
Inhibidores de histona demetilasasInfo
- Publication number
- AR099890A1 AR099890A1 ARP150100947A ARP150100947A AR099890A1 AR 099890 A1 AR099890 A1 AR 099890A1 AR P150100947 A ARP150100947 A AR P150100947A AR P150100947 A ARP150100947 A AR P150100947A AR 099890 A1 AR099890 A1 AR 099890A1
- Authority
- AR
- Argentina
- Prior art keywords
- cycloalkyl
- aryl
- heteroaryl
- alkynyl
- alkenyl
- Prior art date
Links
- 108010033040 Histones Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 21
- 125000003118 aryl group Chemical group 0.000 abstract 20
- 125000001072 heteroaryl group Chemical group 0.000 abstract 20
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 abstract 16
- 125000000304 alkynyl group Chemical group 0.000 abstract 14
- 125000003342 alkenyl group Chemical group 0.000 abstract 12
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 abstract 11
- 125000000217 alkyl group Chemical group 0.000 abstract 11
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 11
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 10
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 abstract 10
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 abstract 9
- 125000003709 fluoroalkyl group Chemical group 0.000 abstract 9
- 229910052736 halogen Inorganic materials 0.000 abstract 9
- 150000002367 halogens Chemical class 0.000 abstract 9
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 7
- 229910052739 hydrogen Inorganic materials 0.000 abstract 7
- 239000001257 hydrogen Substances 0.000 abstract 7
- 125000004043 oxo group Chemical group O=* 0.000 abstract 7
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 6
- 125000004104 aryloxy group Chemical group 0.000 abstract 5
- 125000005553 heteroaryloxy group Chemical group 0.000 abstract 5
- 125000004122 cyclic group Chemical group 0.000 abstract 4
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 125000004432 carbon atom Chemical group C* 0.000 abstract 3
- 150000002431 hydrogen Chemical class 0.000 abstract 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 2
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 125000002947 alkylene group Chemical group 0.000 abstract 2
- 125000002993 cycloalkylene group Chemical group 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 125000005010 perfluoroalkyl group Chemical group 0.000 abstract 2
- 125000003003 spiro group Chemical group 0.000 abstract 2
- 125000003107 substituted aryl group Chemical group 0.000 abstract 2
- 238000006467 substitution reaction Methods 0.000 abstract 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 1
- 125000002733 (C1-C6) fluoroalkyl group Chemical group 0.000 abstract 1
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 1
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 abstract 1
- 101100203602 Hypocrea jecorina (strain QM6a) sor7 gene Proteins 0.000 abstract 1
- 150000001336 alkenes Chemical class 0.000 abstract 1
- 150000001345 alkine derivatives Chemical class 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 125000005429 oxyalkyl group Chemical group 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
Classifications
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- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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 to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/79—Acids; Esters
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/44—Radicals substituted by doubly-bound oxygen, sulfur, or nitrogen atoms, or by two such atoms singly-bound to the same carbon atom
- C07D213/46—Oxygen atoms
- C07D213/48—Aldehydo radicals
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/56—Amides
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- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members 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 to ring carbon atoms
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- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
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- 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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- C07D417/12—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 linked by a chain containing hetero atoms as chain links
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Abstract
Reivindicación 1: Un compuesto de la fórmula (1) en donde Q se selecciona CO₂H, -CH=NR¹², -W, -CHR²⁰NR²¹R¹³, -CH=O y -CH(OR¹⁷)₂; A se selecciona de -C(R²ᵃ)₂C(O)-, -C(R²)₂C(R²)₂C(O)-, -Z-cicloalquileno C₃₋₁₀, -Z-heterociclileno, -Z-heteroarileno y -Z-arileno, cuyos -Z-cicloalquileno, -Z-heterociclileno, -Z-heteroarileno y -Z-arileno pueden estar opcionalmente sustituidos con uno o varios R³ y pueden formar una estructura cíclica o heterocíclica con Y, en donde dicha estructura cíclica o heterocíclica formada con Y se fusiona opcionalmente con un grupo arilo o heteroarilo opcionalmente sustituido; Z se selecciona de alquileno C₁₋₄, alqueneno C₂₋₅, alquineno C₂₋₅, heterociclileno y cicloalquileno C₃₋₆; cada M se selecciona, de modo independiente, CH o N; Y se selecciona de -H, -NR⁶R⁷, -OR⁷, alquilo C₁₋₈, alquenilo C₂₋₈, alquinilo C₂₋₈, cicloalquilo C₃₋₁₀, heterociclilo, heteroarilo y arilo, cuyos alquilo, alquenilo, alquinilo, cicloalquilo, heterociclilo, heteroarilo y arilo pueden estar opcionalmente sustituidos con uno o varios R³; R¹ se selecciona de -H, alquilo C₁₋₈, alquenilo C₂₋₈, alquinilo C₂₋₈, cicloalquilo C₃₋₁₀, cuyos alquilo, alquenilo, alquinilo y cicloalquilo pueden estar opcionalmente sustituidos con uno o varios seleccionados de -OH, arilo, alcoxi C₁₋₆, heteroarilo, ariloxi, heteroariloxi, -NR⁶R⁷, F y cicloalquilo C₃₋₆; o con mayor preferencia, se selecciona de -H y alquilo C₁₋₄; o con -A-Y forma un nitrógeno que contiene grupo heterocíclico opcionalmente sustituido donde la sustitución opcional puede ser alquilo C₁₋₈, alquenilo C₂₋₈, alquinilo C₂₋₈, cicloalquilo C₃₋₁₀, alcoxi C₁₋₆, hidroxialquilo C₁₋₆, arilo, -C(=O)NR⁶R⁷, -NR⁶R⁷, -OH y halógeno, cuyos alquilo, alquenilo, alquinilo, cicloalquilo y arilo pueden estar opcionalmente sustituidos con uno o varios seleccionados de -OH, arilo, alcoxi C₁₋₆, heteroarilo, ariloxi, heteroariloxi, -NR⁶R⁷, F y cicloalquilo C₃₋₆; o dicho nitrógeno que contiene grupo heterocíclico opcionalmente sustituido formado con -A-Y se fusiona opcionalmente con un grupo arilo o heteroarilo opcionalmente sustituido; o con R¹⁸ forma un nitrógeno que contiene grupo heterocíclico opcionalmente sustituido donde la sustitución opcional puede ser alquilo C₁₋₈, alquenilo C₂₋₈, alquinilo C₂₋₈ o cicloalquilo C₃₋₁₀, cuyos alquilo, alquenilo, alquinilo y cicloalquilo pueden estar opcionalmente sustituidos con uno o varios seleccionados de -OH, arilo, alcoxi C₁₋₆, heteroarilo, ariloxi, heteroariloxi, -NR⁶R⁷, F y cicloalquilo C₃₋₆; R² se selecciona de -H, alquilo C₁₋₈, alquenilo C₂₋₈, alquinilo C₂₋₈ y cicloalquilo C₃₋₁₀, cuyos alquilo, alquenilo, alquinilo y cicloalquilo pueden estar opcionalmente sustituidos con uno o varios seleccionados de -OH, arilo, alcoxi C₁₋₆, heteroarilo, ariloxi, heteroariloxi, F y cicloalquilo C₃₋₆, -Z-heterociclilo, -Z-arilo, -Z-heteroarilo, -Z-NR⁶R⁷, -Z-C(=O)-NR⁶R⁷, -Z-NR⁶-C(=O)-R⁷, -Z-C(=O)-R⁷, -Z-OR⁷, halógeno, -Z-SR⁷, -Z-SOR⁷, -Z-SO₂R⁷, -Z-SO₂NR⁶R⁷ y -Z-COOR⁷; de modo alternativo, R² puede formar una estructura cíclica o heterocíclica con otros R², R¹, R¹⁸ o Y; R²ᵃ se selecciona de -H, alquilo C₁₋₈, alquenilo C₂₋₈, alquinilo C₂₋₈ y cicloalquilo C₃₋₁₀, cuyos alquilo, alquenilo, alquinilo y cicloalquilo pueden estar opcionalmente sustituidos con uno o varios seleccionados de -OH, arilo, alcoxi C₁₋₆, heteroarilo, ariloxi, heteroariloxi, F y cicloalquilo C₃₋₆, -Z-heterociclilo, -Z-arilo, -Z-heteroarilo, -Z-NR⁶R⁷, -Z-C(=O)-NR⁶R⁷, -Z-NR⁶-C(=O)-R⁷, -Z-NR⁶-C(=O)-OR⁷, -Z-C(=O)-OR⁷, -Z-OR⁷, halógeno, -Z-SR⁷, -Z-SOR⁷, -Z-SO₂R⁷, -Z-SO₂NR⁶R⁷ y -Z-COOR⁷; siempre que los dos grupos R²ᵃ son ambos no hidrógeno o uno de R²ᵃ forma un anillo con R¹ o R¹⁸; cada R³ se selecciona, de modo independiente, de alquilo C₁₋₆, fluoroalquilo C₁₋₄, hidroxialquilo C₁₋₄, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₁₀, -Z-heterociclilo, -Z-arilo, -Z-heteroarilo, -Z-NR⁶R⁷, -Z-C(=O)-NR⁶R⁷, -Z-NR⁶-C(=O)-R⁷, -Z-NR⁶-C(=O)-OR⁷, -Z-C(=O)-R⁷, -Z-OR⁷, halógeno, -Z-SR⁷, -Z-SOR⁷, -Z-SO₂R⁷, -Z-SO₂NR⁶R⁷ y -Z-COOR⁷, en donde cualquier heterociclilo puede estar sustituido con uno o varios R⁴ y en donde cualquier heteroarilo y cualquier arilo puede estar sustituido con uno o varios R⁵; Z se selecciona de un enlace simple, alquileno C₁₋₄, heterociclileno y cicloalquileno C₃₋₆; cada R⁴ se selecciona, de modo independiente, de alquilo C₁₋₆, fluoroalquilo C₁₋₄, hidroxialquilo C₁₋₄, alcoxi C₁₋₄, cicloalquilo C₃₋₁₀, NR⁶R⁷, C(=O)-NR⁶R⁷, NR⁶-C(=O)-R⁷, Z-C(=O)-R⁷, -Z-C(=O)-H, OR⁷, halógeno, SR⁷, SOR⁷, SO₂R⁷, SO₂NR⁶R⁷ y COOR⁷ y -OH; cada R⁵ se selecciona, de modo independiente, de alquilo C₁₋₆, fluoroalquilo C₁₋₄, hidroxialquilo C₁₋₄, alcoxi C₁₋₄, cicloalquilo C₃₋₆, -Z-C(=O)-NR⁶R⁷, -Z-NR⁶-C(=O)-R⁷, -Z-C(=O)-R⁷, -Z-C(=O)OR⁷, -Z-NR⁶C(=O)OR⁷, OR⁷, -CN y halógeno; cada uno de R⁶ y R⁷ se selecciona, de modo independiente, de hidrógeno, donde opcionalmente no son ambos hidrógeno, alquilo C₁₋₈, fluoroalquilo C₁₋₄, perfluoroalquilo C₁₋₄, hidroxialquilo C₁₋₄, alquenilo C₂₋₈, alquinilo C₂₋₈, cicloalquilo C₃₋₁₀, -Z-heterociclilo, -Z-heteroarilo y -Z-arilo, cuyos alquilo, alquenilo, alquinilo, cicloalquilo, heterociclilo, heteroarilo y arilo pueden estar opcionalmente sustituidos con uno o varios R⁸ seleccionados de modo independiente; o, de modo alternativo, R⁶ y R⁷ pueden formar, junto con el átomo de N al que están unidos, un anillo N-heterocíclico opcionalmente sustituido con uno o varios R⁸ seleccionados de modo independiente; cada R⁸ se selecciona, de modo independiente, de alquilo C₁₋₆, fluoroalquilo C₁₋₄, hidroxialquilo C₁₋₄, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₁₀, -Z-heterociclilo, -Z-heteroarilo, -Z-arilo, -Z-NR¹⁰R¹¹, -Z-C(=O)-NR¹⁰R¹¹, -Z-OR⁹, halógeno, -CN, -Z-SR⁹, -Z-SOR⁹, -Z-SO₂R⁹ y -Z-COOR⁹, cuyos alquilo, alquenilo, alquinilo, cicloalquilo, heterocíclicos, heteroarilo y arilo pueden estar opcionalmente sustituidos con uno o varios seleccionados de alquilo C₁₋₄, fluoroalquilo C₁₋₄, hidroxialquilo C₁₋₄, cicloalquilo C₃₋₆, -Z-heterociclilo, -Z-heteroarilo, -Z-arilo, -Z-NR¹⁰R¹¹, -Z-C(=O)-NR¹⁰R¹¹, -Z-OR⁹, halógeno, -CN, -Z-SR⁹, -Z-SOR⁹, -Z-SO₂R⁹ y -Z-COOR⁹; en donde cualquier heterociclilo puede también estar sustituido con uno o varios R⁴ como se definió con anterioridad y en donde cualquier heteroarilo y cualquier arilo también puede estar sustituido con uno o varios R⁵ como se definió con anterioridad; cada R⁹ se selecciona, de modo independiente, de -H, alquilo C₁₋₈, fluoroalquilo C₁₋₄, hidroxialquilo C₁₋₄, alquenilo C₂₋₈, alquinilo C₂₋₈, cicloalquilo C₃₋₁₀, -Z-heterociclilo, -Z-arilo y -Z-heteroarilo, en donde cualquier heterociclilo puede estar sustituido con uno o varios R⁴ como se definió con anterioridad y en donde cualquier heteroarilo y cualquier arilo puede estar sustituido con uno o varios R⁵ como se definió con anterioridad; cada uno de R¹⁰ y R¹¹ se selecciona, de modo independiente, de -H, alquilo C₁₋₆, fluoroalquilo C₁₋₄, hidroxialquilo C₁₋₄, alquenilo C₂₋₈, alquinilo C₂₋₈, cicloalquilo C₃₋₁₀, heterociclilo, heteroarilo y arilo, en donde cualquier heterociclilo puede estar sustituido con uno o varios R⁴ como se definió con anterioridad y en donde cualquier heteroarilo y cualquier arilo puede estar sustituido con uno o varios R⁵ como se definió con anterioridad, o, de modo alternativo, R¹⁰ y R¹¹ pueden formar, junto con el átomo de N al que están unidos, un anillo N-heterocíclico opcionalmente de 5 a 7 miembros, opcionalmente sustituido con uno o varios R⁴ como se definió con anterioridad; cuando Q es -CH=NR¹², R¹² se selecciona de alquilo C₁₋₁₀, alquenilo C₂₋₁₀, alquinilo C₂₋₁₀, cicloalquilo C₃₋₁₀, -Z-heterociclilo, -Z-arilo, -Z-heteroarilo, -Z-NR⁶R⁷, -Z-C(=O)-NR⁶R⁷, -Z-NR⁶-C(=O)-R⁷, -Z-C(=O)-R⁷, -Z-OR⁷, halógeno, -Z-SR⁷, -Z-SOR⁷, -Z-SO₂R⁷ y -Z-COOR⁷, cuyos alquilo, alquenilo, alquinilo, cicloalquilo, heterociclilo, heteroarilo y arilo pueden estar opcionalmente sustituidos con uno o varios R³; cuando Q es -CHR²⁰NR²¹R¹³, R¹³ se selecciona de hidrógeno, -C(O)R⁷, -C(O)C(O)R⁷, -C(O)C(O)OR⁷, alquilo C₁₋₈, fluoroalquilo C₁₋₄, perfluoroalquilo C₁₋₄, hidroxialquilo C₁₋₄, alquenilo C₂₋₈, alquinilo C₂₋₈, cicloalquilo C₃₋₁₀, -Z-heterociclilo, -Z-arilo y -Z-heteroarilo, cuyos alquilo, alquenilo, alquinilo, cicloalquilo, heterociclilo, arilo y heteroarilo pueden estar opcionalmente sustituidos con uno o varios seleccionados de modo independiente R⁸ o es -CR¹⁴R¹⁵-NR⁶R⁷, -CR¹⁴R¹⁵CN o -CR¹⁴R¹⁵OR⁷, en donde cada uno de R¹⁴ y R¹⁵ se selecciona, de modo independiente, de -H, alquilo C₁₋₈, alquenilo C₂₋₈, alquinilo C₂₋₈, cicloalquilo C₃₋₁₀, heterociclilo, heteroarilo y arilo y en donde R¹⁴ y R¹⁵ junto con el átomo de carbono interviniente pueden designar un anillo cicloalquilo C₃₋₁₀ o cicloalquenilo C₅₋₁₀, cuyos alquilo, alquenilo, alquinilo, cicloalquilo (anillo), anillo cicloalquenilo, heterociclilo, heteroarilo y arilo pueden estar opcionalmente sustituidos con uno o varios R³; R²⁰ y R²¹ son hidrógeno o forman juntos un grupo a 1,3-diaza-C₅₋₇-cicIoalqu-2-ilo que está N-sustituido con R¹⁶ y opcionalmente también sustituido con uno o varios R⁶ y que opcionalmente contiene uno o dos grupos oxo; un grupo 1,3-tiaza-C₅₋₇-cicloalqu-2-ilo que está N-sustituido con R¹⁶ y opcionalmente también sustituido con uno o varios R³ y que opcionalmente contiene uno o dos grupos oxo; un grupo 1,3-oxaza-C₅₋₇-cicloalqu-2-ilo que está N-sustituido con R¹⁶ y opcionalmente también sustituido con uno o varios R⁶ y que opcionalmente contiene uno o dos grupos oxo, en donde en todas las tres instancias, dos R³ en el mismo átomo de carbono pueden formar juntos un grupo espiro; cuando Q es W, W se selecciona de un grupo 1,3-diaza-C₅₋₇-cicloalqu-2-ilo que está N-sustituido con R¹⁶ y opcionalmente también sustituido con uno o varios R³ y que opcionalmente contiene uno o dos grupos oxo; un grupo 1,3-tiaza-C₅₋₇-cicloalqu-2-ilo que está N-sustituido con R¹⁶ y opcionalmente también sustituido con uno o varios R³ y que opcionalmente contiene uno o dos grupos oxo; un grupo 1,3-oxaza-C₅₋₇-cicloalqu-2-ilo que está N-sustituido con R¹⁶ y opcionalmente también sustituido con uno o varios R⁶ y que opcionalmente contiene uno o dos grupos oxo, en donde en todas las tres instancias, dos R³ en el mismo átomo de carbono pueden formar juntos un grupo espiro; R¹⁶ se selecciona de hidrógeno, -C(O)R⁷, -C(O)C(O)R⁷, -C(O)C(O)OR⁷ y -C(O)C(O)NR⁶R⁷; cuando Q es -CH(OR¹⁷)₂, cada R¹⁷ es, de modo independiente, R³ o en donde dos sustituyentes de R¹⁷ junto con el -O-CH(-)-O- interviniente pueden formar un heterociclilo opcionalmente sustituido con uno o varios R³ y que contienen hasta dos grupos oxo; R¹⁸ se selecciona de hidrógeno, alquilo C₁₋₆, fluoroalquilo C₁₋₆, hidroxialquilo C₁₋₆, alquenilo C₂₋₇, alquinilo C₂₋₇, cicloalquilo C₃₋₇, oxialquilo C₃₋₇ y pueden formar una estructura cíclica o heterocíclica con A, Y o R¹; uno de sus isómeros o una mezcla de sus isómeros o una de sus sales o solvatos o profármacos farmacéuticamente aceptables.
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IT1403156B1 (it) * | 2010-12-01 | 2013-10-04 | Università Degli Studi Di Torino | Inibitori di fosfatidilinositol 3-chinasi, relative composizioni ed usi. |
EP2772490B1 (en) * | 2011-10-27 | 2016-04-06 | Astellas Pharma Inc. | Aminoalkyl-substituted n-thienyl benzamide derivative |
CN102585150B (zh) * | 2012-02-01 | 2013-09-04 | 嘉兴学院 | 织物涂饰用阴离子水性聚氨酯分散体的制备方法 |
WO2013129435A1 (ja) * | 2012-02-28 | 2013-09-06 | 協和発酵キリン株式会社 | 縮環チオフェン誘導体 |
PL2903968T3 (pl) * | 2012-10-02 | 2017-05-31 | Gilead Sciences, Inc. | Inhibitory demetylaz histonowych |
JP6514117B2 (ja) * | 2013-02-27 | 2019-05-15 | エピセラピューティクス アーペーエス | ヒストン脱メチル化酵素の阻害剤 |
CN103436254B (zh) * | 2013-08-19 | 2014-10-08 | 中国科学院合肥物质科学研究院 | 一种功能化多元氮杂环荧光探针、其制备方法及其用途 |
-
2015
- 2015-03-30 WO PCT/US2015/023407 patent/WO2015153498A1/en active Application Filing
- 2015-03-30 AU AU2015241022A patent/AU2015241022A1/en not_active Abandoned
- 2015-03-30 JP JP2016559901A patent/JP2017512804A/ja active Pending
- 2015-03-30 TW TW104110270A patent/TW201625535A/zh unknown
- 2015-03-30 AR ARP150100947A patent/AR099890A1/es unknown
- 2015-03-30 EP EP15715631.6A patent/EP3126345A1/en not_active Withdrawn
- 2015-03-30 US US15/129,351 patent/US20170369444A1/en not_active Abandoned
- 2015-03-30 CA CA2943824A patent/CA2943824A1/en not_active Abandoned
-
2018
- 2018-02-09 AU AU2018200982A patent/AU2018200982A1/en not_active Abandoned
Also Published As
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EP3126345A1 (en) | 2017-02-08 |
TW201625535A (en) | 2016-07-16 |
US20170369444A1 (en) | 2017-12-28 |
JP2017512804A (ja) | 2017-05-25 |
WO2015153498A1 (en) | 2015-10-08 |
CA2943824A1 (en) | 2015-10-08 |
AU2015241022A1 (en) | 2016-10-27 |
AU2018200982A1 (en) | 2018-03-01 |
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