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PE20241625A1 - Combinaciones farmaceuticas de inhibidores de sos1 para tratar o prevenir cancer - Google Patents

Combinaciones farmaceuticas de inhibidores de sos1 para tratar o prevenir cancer

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Publication number
PE20241625A1
PE20241625A1 PE2023002105A PE2023002105A PE20241625A1 PE 20241625 A1 PE20241625 A1 PE 20241625A1 PE 2023002105 A PE2023002105 A PE 2023002105A PE 2023002105 A PE2023002105 A PE 2023002105A PE 20241625 A1 PE20241625 A1 PE 20241625A1
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PE
Peru
Prior art keywords
substituted
inhibitor
unsubstituted
ring
unsubstituted alkyl
Prior art date
Application number
PE2023002105A
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English (en)
Inventor
Mandar Ramesh Bhonde
Sukanya Patra
Venkata P Palle
Rajender Kumar Kamboj
Original Assignee
Lupin Ltd
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Filing date
Publication date
Application filed by Lupin Ltd filed Critical Lupin Ltd
Publication of PE20241625A1 publication Critical patent/PE20241625A1/es

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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/337Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having four-membered rings, e.g. taxol
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    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
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    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404Indoles, e.g. pindolol
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    • A61K31/41Heterocyclic 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
    • A61K31/4151,2-Diazoles
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4402Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 2, e.g. pheniramine, bisacodyl
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    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non 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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    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4545Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
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    • A61K31/435Heterocyclic 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
    • A61K31/47Quinolines; Isoquinolines
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    • A61K31/435Heterocyclic 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4738Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4745Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
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    • A61K31/495Heterocyclic 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
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/4965Non-condensed pyrazines
    • A61K31/497Non-condensed pyrazines containing further heterocyclic rings
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    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/517Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
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    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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    • A61K31/53Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
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    • A61K31/535Heterocyclic 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
    • A61K31/53751,4-Oxazines, e.g. morpholine
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    • A61K31/7028Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages
    • A61K31/7034Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin
    • A61K31/704Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin attached to a condensed carbocyclic ring system, e.g. sennosides, thiocolchicosides, escin, daunorubicin
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    • A61K31/7052Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
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  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
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  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Referido a una combinacion farmaceutica que comprende un inhibidor de SOS1 de formula I o formula II, su forma tautomerica, su estereoisomero, o su sal farmaceuticamente aceptable, y al menos un principio activo adicional seleccionado de un inhibidor de KRAS tal como un inhibidor de KRAS G12C y un inhibidor de KRASG12D, entre otros, y agentes quimioterapeuticos, tales como gemcitabina, doxorrubicina, entre otros. En donde el inhibidor de SOS1 de formula (I), el anillo A se selecciona entre arilo, heteroarilo y heterociclilo; el anillo B se selecciona entre un anillo carbociclico de 5 o 6 miembros sustituido o no sustituido y un anillo 5 heterociclico de 5 o 6 miembros sustituido o no sustituido; R1 se selecciona entre H, alquilo sustituido o no sustituido y cicloalquilo sustituido o no sustituido; R2 y R3 se seleccionan independientemente entre H, halogeno, ciano, entre otros; R4 se selecciona entre halogeno, ciano, -NReRf, entre otros; n es 0, 1, 2 o 3; y el inhibidor de SOS1 de formula (II), en la que el anillo A se selecciona entre arilo, heteroarilo y heterociclilo; "----" es un enlace simple o un enlace doble; X e Y se seleccionan independientemente entre C, O y NRC; R1 se selecciona entre H y alquilo sustituido o no sustituido; R2 se selecciona entre H, halogeno, alquilo y cicloalquilo; R3 se selecciona entre -OR6, -NRaRb, alquilo sustituido o no sustituido, entre otros; R4 se selecciona entre oxo y alquilo sustituido o no sustituido; R5 se selecciona entre halogeno, ciano, -NRcRd, alquilo sustituido o no sustituido, entre otros; m es 0, 1, 2 o 3; n es 0, 1, 2, 3 o 4. Un compuesto seleccionado es (R)-4-((1-(3-(1,1-difluoro-2-hidroxi-2-metilpropil)-2-fluorofenil)etil)amino)-2,6,8,8-tetrametil-6,8-dihidro-7H-pirrolo[2,3-g]quinazolin-7-ona (Compuesto 1). Tambien se la preparacion de dichos compuestos, compuestos intermedios, y su uso para tratar y/o prevenir el cancer.
PE2023002105A 2021-01-19 2022-01-19 Combinaciones farmaceuticas de inhibidores de sos1 para tratar o prevenir cancer PE20241625A1 (es)

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IN202121002487 2021-01-19
PCT/IB2022/050415 WO2022157629A1 (en) 2021-01-19 2022-01-19 Pharmaceutical combinations of sos1 inhibitors for treating and/or preventing cancer

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EP (1) EP4281078A1 (es)
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KR (1) KR20230137368A (es)
CN (1) CN116723843A (es)
AU (1) AU2022210517A1 (es)
CA (1) CA3203205A1 (es)
CL (1) CL2023002071A1 (es)
CO (1) CO2023010777A2 (es)
CR (1) CR20230402A (es)
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PE (1) PE20241625A1 (es)
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ZA (1) ZA202307014B (es)

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