AR124117A2 - Agentes inductores de la apoptosis que pueden usarse para tratar el cáncer y las enfermedades inmunes y autoinmunes - Google Patents
Agentes inductores de la apoptosis que pueden usarse para tratar el cáncer y las enfermedades inmunes y autoinmunesInfo
- Publication number
- AR124117A2 AR124117A2 ARP210103216A ARP210103216A AR124117A2 AR 124117 A2 AR124117 A2 AR 124117A2 AR P210103216 A ARP210103216 A AR P210103216A AR P210103216 A ARP210103216 A AR P210103216A AR 124117 A2 AR124117 A2 AR 124117A2
- Authority
- AR
- Argentina
- Prior art keywords
- group
- nhc
- cr6r7
- independently selected
- alkyl
- Prior art date
Links
- 208000023275 Autoimmune disease Diseases 0.000 title 1
- 206010028980 Neoplasm Diseases 0.000 title 1
- 201000011510 cancer Diseases 0.000 title 1
- 208000026278 immune system disease Diseases 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 11
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 11
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 11
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 11
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 8
- 229910052739 hydrogen Inorganic materials 0.000 abstract 8
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 7
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 7
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 6
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 6
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 abstract 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 6
- 229910006074 SO2NH2 Inorganic materials 0.000 abstract 6
- 229910052794 bromium Inorganic materials 0.000 abstract 6
- 229910052799 carbon Inorganic materials 0.000 abstract 6
- 125000000623 heterocyclic group Chemical group 0.000 abstract 6
- 229910052740 iodine Inorganic materials 0.000 abstract 6
- 125000001424 substituent group Chemical group 0.000 abstract 6
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 5
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 5
- 125000003118 aryl group Chemical group 0.000 abstract 5
- 229910052801 chlorine Inorganic materials 0.000 abstract 5
- 229910052731 fluorine Inorganic materials 0.000 abstract 5
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 abstract 4
- 101100240521 Caenorhabditis elegans nhr-16 gene Proteins 0.000 abstract 4
- 101100516554 Caenorhabditis elegans nhr-5 gene Proteins 0.000 abstract 4
- 101100516572 Caenorhabditis elegans nhr-8 gene Proteins 0.000 abstract 4
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 4
- 125000005843 halogen group Chemical group 0.000 abstract 3
- 125000001072 heteroaryl group Chemical group 0.000 abstract 3
- 125000004366 heterocycloalkenyl group Chemical group 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- 102000010565 Apoptosis Regulatory Proteins Human genes 0.000 abstract 2
- 108010063104 Apoptosis Regulatory Proteins Proteins 0.000 abstract 2
- 102100026596 Bcl-2-like protein 1 Human genes 0.000 abstract 2
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical group [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 2
- 125000004429 atom Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 150000001924 cycloalkanes Chemical class 0.000 abstract 2
- 150000001925 cycloalkenes Chemical class 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 150000002390 heteroarenes Chemical class 0.000 abstract 2
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 1
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 1
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 abstract 1
- 101001043818 Mus musculus Interleukin-31 receptor subunit alpha Proteins 0.000 abstract 1
- 101100160255 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) YLR154C-H gene Proteins 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 229910052805 deuterium Inorganic materials 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 125000005549 heteroarylene group Chemical group 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—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
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/541—Non-condensed thiazines containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- 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
- C07D487/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/08—Bridged systems
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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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- Chemical & Material Sciences (AREA)
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- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Compuestos que inhiben la actividad de las proteínas antiapoptóticas Bcl-xL, composiciones que contienen dichos compuestos y métodos para tratar enfermedades en las que se expresan las proteínas antiapoptóticas Bcl-xL. Reivindicación 1: Un compuesto caracterizado porque es de la fórmula (1) o una sal aceptable para terapia del mismo, donde X es heteroarilo; donde el heteroarilo representado por X está opcionalmente sustituido con uno, dos, tres, o cuatro R⁴; Y¹ es fenileno o C₅₋₆ heteroarileno; opcionalmente fusionado a uno o dos anillos seleccionados entre el grupo que consiste en C₃₋₈ cicloalcano, C₃₋₈ cicloalqueno, benceno, C₅₋₆ heteroareno, C₃₋₈ heterocicloalcano, y C₃₋₈ heterocicloalqueno; donde Y¹ está opcionalmente sustituido con uno, dos, tres, o cuatro sustituyentes seleccionados en forma independiente entre el grupo que consiste en R⁵, OR⁵, SR⁵, S(O)R⁵, SO₂R⁵, C(O)R⁵, CO(O)R⁵, OC(O)R⁵, OC(O)OR⁵, NH₂, NHR⁵, N(R⁵)₂, NHC(O)R⁵, NR⁵C(O)R⁵, NHS(O)₂R⁵, NR⁵S(O)₂R⁵, NHC(O)OR⁵, NR⁵C(O)OR⁵, NHC(O)NH₂, NHC(O)NHR⁵, NHC(O)N(R⁵)₂, NR⁵C(O)NHR⁵, NR⁵C(O)N(R⁵)₂, C(O)NH₂, C(O)NHR⁵, C(O)N(R⁵)₂, C(O)NHOH, C(O)NHOR⁵, C(O)NHSO₂R⁵, C(O)NR⁵SO₂R⁵, SO₂NH₂, SO₂NHR⁵, SO₂N(R⁵)₂, CO(O)H, C(O)H, OH, CN, N₅, NO₂, F, Cl, Br y I; L¹ se selecciona entre el grupo que consiste en (CR⁶R⁷)q, (CR⁶R⁷)ₛ-O-(CR⁶R⁷)ʳ, (CR⁶R⁷)ₛC(O)-(CR⁶R⁷)ʳ, (CR⁶R⁷)ₛ-S-(CR⁶R⁷)ʳ, (CR⁶R⁷)ₛ-S(O)₂-(CR⁶R⁷)ʳ, (CR⁶R⁷)ₛ-NR⁶AC(O)-(CR⁶R⁷)ʳ, (CR⁶R⁷)ₛ-C(O)NR⁶A-(CR⁶R⁷)ʳ, (CR⁶R⁷)ₛ-NR⁶A-(CR⁶R⁷)ʳ, (CR⁶R⁷)ₛ-S(O)₂NR⁶A-(CR⁶R⁷)ʳ, y (CR⁶R⁷)ₛNR⁶AS(O)₂-(CR⁶R⁷)ʳ; Y² es C₈₋₁₄ cicloalquilo, C₈₋₁₄ cicloalquenilo, C₈₋₁₄ heterocicloalquilo, o C₈₋₁₄ heterocicloalquenilo; opcionalmente fusionado a uno o dos anillos seleccionados entre el grupo que consiste en C₃₋₈ cicloalcano, C₃₋₈ cicloalqueno, benceno, C₅₋₆ heteroareno, C₃₋₈ heterocicloalcano, y C₃₋₈ heterocicloalqueno; donde Y² está opcionalmente sustituido con uno, dos, tres, cuatro, o cinco sustituyentes seleccionados en forma independiente entre el grupo que consiste en R⁸, OR⁸, SR⁸, S(O)R⁸, SO₂R⁸, C(O)R⁸, CO(O)R⁸, OC(O)R⁸, OC(O)OR⁸, NH₂, NHR⁸, N(R⁸)₂, NHC(O)R⁸, NR⁸C(O)R⁸, NHS(O)₂R⁸, NR⁸S(O)₂R⁸, NHC(O)OR⁸, NR⁸C(O)OR⁸, NHC(O)NH₂, NHC(O)NHR⁸, NHC(O)N(R⁸)₂, NR⁸C(O)NHR⁸, NR⁸C(O)N(R⁸)₂, C(O)NH₂, C(O)NHR⁸, C(O)N(R⁸)₂, C(O)NHOH, C(O)NHOR⁸, C(O)NHSO₂R⁸, C(O)NR⁸SO₂R⁸, SO₂NH₂, SO₂NHR⁸, SO₂N(R⁸)₂, CO(O)H, C(O)H, OH, CN, N₃, NO₂, F, Cl, Br y I; Z¹ se selecciona entre el grupo que consiste en C(O)OR⁹, C(O)NR¹⁰R¹¹, C(O)R¹¹, NR¹⁰C(O)R¹¹, NR¹⁰C(O)NR¹⁰R¹¹, OC(O)NR¹⁰R¹¹, NR¹⁰C(O)OR⁹, C(=NOR¹⁰)NR¹⁰R¹¹, NR¹⁰C(=NCN)NR¹⁰R¹¹, NR¹⁰S(O)₂NR¹⁰R¹¹, S(O)₂R⁹, S(O)₂NR¹⁰R¹¹, N(R¹⁰)S(O)₂R¹¹, NR¹⁰C(=NR¹¹)NR¹⁰R¹¹, C(=S)NR¹⁰R¹¹, C(=NR¹⁰)NR¹⁰R¹¹, halógeno, NO₂, y CN; o Z¹ se selecciona entre el grupo que consiste en los compuestos del grupo de fórmulas (2); R¹, en cada caso, se selecciona en forma independiente entre el grupo que consiste en halo, C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ alquinilo, y C₁₋₆ haloalquilo; R², en cada caso, se selecciona en forma independiente entre el grupo que consiste en deuterio, halo, C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ alquinilo, y C₁₋₆ haloalquilo; dos R² que se unen al mismo átomo de carbono, junto con dicho átomo de carbono, forman opcionalmente un anillo seleccionado entre el grupo que consiste en heterocicloalquilo, heterocicloalquenilo, cicloalquilo, y cicloalquenilo; R³, en cada caso, se selecciona en forma independiente entre el grupo que consiste en halo, C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ alquinilo, y C₁₋₆ haloalquilo; R⁴, en cada caso, se selecciona en forma independiente entre el grupo que consiste en NR¹²R¹³, OR¹², CN, NO₂, halógeno, C(O)OR¹², C(O)NR¹²R¹³, NR¹²C(O)R¹³, NR¹²S(O)₂R¹⁴, NR¹²S(O)R¹⁴, S(O)₂R¹⁴, S(O)R¹⁴ y R¹⁴; R⁵, en cada caso, se selecciona en forma independiente entre el grupo que consiste en C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ alquinilo, C₁₋₆ haloalquilo, C₁₋₆ hidroxialquilo, arilo, heterociclilo, cicloalquilo, y cicloalquenilo; R⁶A se selecciona en forma independiente entre el grupo que consiste en hidrógeno, C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ alquinilo, y C₁₋₆ haloalquilo; R⁶ y R⁷, en cada caso, se seleccionan en forma independiente entre sí entre el grupo que consiste en hidrógeno, R¹⁵, OR¹⁵, SR¹⁵, S(O)R¹⁵, SO₂R¹⁵, C(O)R¹⁵, CO(O)R¹⁵, OC(O)R¹⁵, OC(O)OR¹⁵, NH₂, NHR¹⁵, N(R¹⁵)₂, NHC(O)R¹⁵, NR¹⁵C(O)R¹⁵, NHS(O)₂R¹⁵, NR¹⁵S(O)₂R¹⁵, NHC(O)OR¹⁵, NR¹⁵C(O)OR¹⁵, NHC(O)NH₂, NHC(O)NHR¹⁵, NHC(O)N(R¹⁵)₂, NR¹⁵C(O)NHR¹⁵, NR¹⁵C(O)N(R¹⁵)₂, C(O)NH₂, C(O)NHR¹⁵, C(O)N(R¹⁵)₂, C(O)NHOH, C(O)NHOR¹⁵, C(O)NHSO₂R¹⁵, C(O)NR¹⁵SO₂R¹⁵, SO₂NH₂, SO₂NHR¹⁵, SO₂N(R¹⁵)₂, CO(O)H, C(O)H, OH, CN, N₃, NO₂, F, Cl, Br y I; R⁸, en cada caso, se selecciona en forma independiente entre el grupo que consiste en C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ alquinilo, C₁₋₆ haloalquilo, arilo, heterociclilo, cicloalquilo, y cicloalquenilo; donde R⁸ C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ alquinilo, y C₁₋₆ haloalquilo están opcionalmente sustituidos con uno, dos, tres, cuatro, cinco, o seis sustituyentes seleccionados en forma independiente entre el grupo que consiste en R¹⁶, OR¹⁶, SR¹⁶, S(O)R¹⁶, SO₂R¹⁶, C(O)R¹⁶, CO(O)R¹⁶, OC(O)R¹⁶, OC(O)OR¹⁶, NH₂, NHR¹⁶, N(R¹⁶)₂, NHC(O)R¹⁶, NR¹⁶C(O)R¹⁶, NHS(O)₂R¹⁶, NR¹⁶S(O)₂R¹⁶, NHC(O)OR¹⁶, NR¹⁶C(O)OR¹⁶, NHC(O)NH₂, NHC(O)NHR¹⁶, NHC(O)N(R¹⁶)₂, NR¹⁶C(O)NHR¹⁶, NR¹⁶C(O)N(R¹⁶)₂, C(O)NH₂, C(O)NHR¹⁶, C(O)N(R¹⁶)₂, C(O)NHOH, C(O)NHOR¹⁶, C(O)NHSO₂R¹⁶, C(O)NR¹⁶SO₂R¹⁶, SO₂NH₂, SO₂NHR¹⁶, SO₂N(R¹⁶)₂, CO(O)H, C(O)H, OH, CN, N₃, NO₂, F, Cl, Br y I; donde R⁸ arilo, heterociclilo, cicloalquilo, y cicloalquenilo están opcionalmente sustituidos con uno, dos o tres sustituyentes seleccionados en forma independiente entre el grupo que consiste en C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ alquinilo, C₁₋₆ haloalquilo, NH₂, C(O)NH₂, SO₂NH₂, C(O)H, (O), OH, CN, NO₂, OCF₃, OCF₂CF₃, F, Cl, Br y I; R⁹ se selecciona entre el grupo que consiste en C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ alquinilo, C₁₋₆ haloalquilo, cicloalquilo, fenilo y (CH₂)₁₋₄-fenilo; y R¹⁰ y R¹¹, en cada caso, se seleccionan en forma independiente entre sí entre el grupo que consiste en hidrógeno, C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ alquinilo, C₃₋₆ cicloalquilo, C₁₋₆ haloalquilo, fenilo y (CH₂)₁₋₄-fenilo; o R¹⁰ y R¹¹, o R¹⁰ y R⁹, junto con el átomo al cual están unidos se combinan para formar un heterociclilo; Rᵏ, en cada caso, se selecciona en forma independiente entre el grupo que consiste en C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ alquinilo, C₃₋₇ heterocicloalquilo, C₃₋₇ cicloalquilo y C₁₋₆ haloalquilo; R¹² y R¹³, en cada caso, se seleccionan en forma independiente entre sí entre el grupo que consiste en hidrógeno, C₁₋₄ alquilo, C₂₋₄ alquenilo, C₂₋₄ alquinilo, C₁₋₄ haloalquilo y (CH₂)₁₋₄ fenilo; R¹⁴, en cada caso, se selecciona en forma independiente entre el grupo que consiste en C₁₋₄ alquilo, C₂₋₄ alquenilo, C₂₋₄ alquinilo y C₁₋₄ haloalquilo; R¹² y R¹³, o R¹² y R¹⁴, en cada caso, junto con el átomo al cual están unidos, se combinan opcionalmente para formar un heterociclilo; R¹⁵, en cada caso, se selecciona en forma independiente entre el grupo que consiste en C₁₋₄ alquilo, C₂₋₄ alquenilo, C₂₋₄ alquinilo, C₁₋₄ haloalquilo, C₁₋₄ hidroxialquilo, arilo, heterociclilo, cicloalquilo, y cicloalquenilo; donde R¹⁵ C₁₋₄ alquilo, C₂₋₄ alquenilo, C₂₋₄ alquinilo, C₁₋₄ haloalquilo, y C₁₋₄ hidroxialquilo están opcionalmente sustituidos con uno, dos o tres sustituyentes seleccionados en forma independiente entre el grupo que consiste en O-(C₁₋₄ alquilo), NH₂, C(O)NH₂, SO₂NH₂, C(O)H, C(O)OH, (O), OH, CN, NO₂, OCF₃, OCF₂CF₃, F, Cl, Br y I; R¹⁶, en cada caso, se selecciona en forma independiente entre el grupo que consiste en C₁₋₄ alquilo, C₂₋₄ alquenilo, C₂₋₄ alquinilo, C₁₋₄ haloalquilo, C₁₋₄ hidroxialquilo, arilo, heterocicloalquilo, heterocicloalquenilo, heteroarilo, cicloalquilo, y cicloalquenilo; donde R¹⁶ C₁₋₄ alquilo, C₂₋₄ alquenilo, C₂₋₄ alquinilo, C₁₋₄ haloalquilo, y C₁₋₄ hidroxialquilo están opcionalmente sustituidos con un sustituyente seleccionado en forma independiente entre el grupo que consiste en OCH₃, OCH₂CH₂OCH₃, y OCH₂CH₂NHCH₃; q es 1, 2, ó 3; s es 0, 1, 2, ó 3; r es 0, 1, 2, ó 3; donde la suma de s y r es 0, 1, ó 2; m es 0, 1, 2, ó 3; n es 0, 1, 2, 3, 4, 5, ó 6; y p es 0, 1, ó 2.
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| CN (1) | CN103987711B (es) |
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| CA2970161A1 (en) * | 2014-12-09 | 2016-06-16 | Abbvie Inc. | Bcl-xl inhibitory compounds and antibody drug conjugates including the same |
| US10195213B2 (en) | 2015-03-13 | 2019-02-05 | Unity Biotechnology, Inc. | Chemical entities that kill senescent cells for use in treating age-related disease |
| CR20180614A (es) * | 2016-06-08 | 2019-07-29 | Abbvie Inc | Conjugados de anticuerpo y fármaco anti-egfr |
| AU2017277534A1 (en) * | 2016-06-08 | 2019-01-03 | Abbvie Inc. | Anti-EGFR antibody drug conjugates |
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| CN108261414B (zh) * | 2018-01-11 | 2019-09-06 | 广西师范大学 | 一种治疗肺癌的药物组合物 |
| AR119494A1 (es) * | 2019-07-29 | 2021-12-22 | Servier Lab | DERIVADOS DE 6,7-DIHIDRO-5H-PIRIDO[2,3-c]PIRIDAZIN-8-ILO, COMPOSICIONES FARMACÉUTICAS QUE LOS CONTIENEN Y SUS USOS COMO AGENTES PROAPOPTÓTICOS |
| WO2022117697A1 (en) * | 2020-12-03 | 2022-06-09 | Enyo Pharma | Pyrrole-type compounds and uses thereof for treating viral infections |
| JP2025516358A (ja) | 2022-05-06 | 2025-05-27 | ツリーライン バイオサイエンシズ インコーポレイテッド | テトラヒドロイソキノリンヘテロ二官能性bcl-xl分解剤 |
| CA3251489A1 (en) | 2022-05-06 | 2023-11-09 | Treeline Biosciences, Inc. | BCL-XL HETEROBFUNCTIONAL TETRAHYDROISOQUINOLINE DEGRADING AGENTS |
| AU2023264537A1 (en) | 2022-05-06 | 2024-11-14 | Treeline Biosciences, Inc. | Tetrahydroisoquinoline heterobifunctional bcl-xl degraders |
| JP2025522588A (ja) * | 2022-06-24 | 2025-07-15 | 南京瑞初医▲薬▼有限公司 | ベンゾチアゾール化合物及びその適用 |
| JP2025522589A (ja) * | 2022-06-24 | 2025-07-15 | 南京瑞初医▲薬▼有限公司 | エステル類化合物及びその適用 |
| WO2025101571A1 (en) | 2023-11-07 | 2025-05-15 | Treeline Biosciences, Inc. | Tetrahydroisoquinoline heterobifunctional bcl-x l degraders |
| WO2025101575A1 (en) | 2023-11-07 | 2025-05-15 | Treeline Biosciences, Inc. | Tetrahydroisoquinoline heterobifunctional bcl-x l degraders |
| TW202527930A (zh) | 2023-11-07 | 2025-07-16 | 美商樹線生物科學公司 | 四氫異喹啉異雙功能bcl-xl降解劑 |
| WO2025130875A1 (zh) * | 2023-12-18 | 2025-06-26 | 南京瑞初医药有限公司 | 氮杂环化合物及其应用 |
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| US8940737B2 (en) | 2011-10-14 | 2015-01-27 | Abbvie Inc. | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
| CN103987711B (zh) | 2011-10-14 | 2016-08-24 | 艾伯维公司 | 作为用于治疗癌症和免疫性和自身免疫性疾病的凋亡诱导剂的8-氨基甲酰基-2-(2,3-二取代吡啶-6-基)-1,2,3,4-四氢异喹啉衍生物 |
| EP2882439B1 (en) | 2012-08-13 | 2018-04-11 | AbbVie Inc. | Apoptosis-inducing agents |
| CN104768581A (zh) | 2012-09-07 | 2015-07-08 | 吉宁特有限公司 | II型抗CD20抗体与选择性Bcl-2抑制剂的组合治疗 |
-
2012
- 2012-10-11 CN CN201280061275.5A patent/CN103987711B/zh active Active
- 2012-10-11 US US13/649,900 patent/US8889675B2/en active Active
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2014
- 2014-11-17 US US14/543,817 patent/US9227963B2/en active Active
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2015
- 2015-12-07 US US14/961,748 patent/US9844547B2/en active Active
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2016
- 2016-11-10 SM SM201600406T patent/SMT201600406B/it unknown
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2017
- 2017-11-03 US US15/803,568 patent/US20180140595A1/en not_active Abandoned
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2019
- 2019-09-20 US US16/578,229 patent/US20200253954A1/en not_active Abandoned
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2020
- 2020-09-16 US US17/022,693 patent/US11786519B2/en active Active
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- 2021-11-19 AR ARP210103216A patent/AR124117A2/es not_active Application Discontinuation
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| Publication number | Publication date |
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| US20200253954A1 (en) | 2020-08-13 |
| US20160158218A1 (en) | 2016-06-09 |
| US8889675B2 (en) | 2014-11-18 |
| CN103987711A (zh) | 2014-08-13 |
| CN103987711B (zh) | 2016-08-24 |
| US20170296531A9 (en) | 2017-10-19 |
| US11786519B2 (en) | 2023-10-17 |
| US20210228565A1 (en) | 2021-07-29 |
| US9844547B2 (en) | 2017-12-19 |
| US20130096120A1 (en) | 2013-04-18 |
| US20180140595A1 (en) | 2018-05-24 |
| US9227963B2 (en) | 2016-01-05 |
| US20150072978A1 (en) | 2015-03-12 |
| SMT201600406B (it) | 2017-01-10 |
| US20240285611A1 (en) | 2024-08-29 |
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