AR127308A1 - Inhibidores ras - Google Patents

Inhibidores ras

Info

Publication number
AR127308A1
AR127308A1 ARP220102737A ARP220102737A AR127308A1 AR 127308 A1 AR127308 A1 AR 127308A1 AR P220102737 A ARP220102737 A AR P220102737A AR P220102737 A ARP220102737 A AR P220102737A AR 127308 A1 AR127308 A1 AR 127308A1
Authority
AR
Argentina
Prior art keywords
optionally substituted
membered
compound
pharmaceutically acceptable
acceptable salt
Prior art date
Application number
ARP220102737A
Other languages
English (en)
Inventor
Andreas Buckl
G Leslie Burnett
James Cregg
Anne V Edwards
Adrian L Gill
John E Knox
Elena S Koltun
Yang Liu
Christopher Semko
Original Assignee
Revolution Medicines Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Revolution Medicines Inc filed Critical Revolution Medicines Inc
Publication of AR127308A1 publication Critical patent/AR127308A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/62Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being a protein, peptide or polyamino acid
    • A61K47/64Drug-peptide, drug-protein or drug-polyamino acid conjugates, i.e. the modifying agent being a peptide, protein or polyamino acid which is covalently bonded or complexed to a therapeutically active agent
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/05Isotopically modified compounds, e.g. labelled

Abstract

La invención caracteriza compuestos macrocíclicos y composiciones farmacéuticas y sus complejos proteínicos, capaces de inhibir las proteínas Ras y sus usos en el tratamiento de cánceres. Reivindicación 1: Un compuesto, o una sal farmacéuticamente aceptable de este, que tiene la estructura de la fórmula (1) en donde A es heterocicloalquileno de 3 a 6 miembros opcionalmente sustituido, cicloalquileno de 3 a 6 miembros opcionalmente sustituido, arileno de 6 miembros opcionalmente sustituido o heteroarileno de 5 a 10 miembros opcionalmente sustituido; cada uno de X¹, X² y X³ se selecciona independientemente de CH₂, CHF, CF₂, C=O u O; m es 1 o 2; n es 0 o 1; R¹ es hidrógeno, heteroalquilo C₁-C₆ opcionalmente sustituido o heterocicloalquilo de 3 a 10 miembros opcionalmente sustituido; R² es alquilo C₁-C₆ opcionalmente sustituido; y R³ es alquilo C₁-C₆ opcionalmente sustituido, heteroalquilo C₁-C₆ opcionalmente sustituido, cicloalquilo de 3 a 6 miembros opcionalmente sustituido o heterocicloalquilo opcionalmente sustituido, y donde cada hidrógeno se enriquece opcionalmente, de manera independiente, isotópicamente por deuterio. Reivindicación 26: Un compuesto, o una sal farmacéuticamente aceptable de este, que tiene la estructura de un compuesto de la Tabla 1 o la Tabla 2. Reivindicación 27: Una composición farmacéutica que comprende un compuesto, o una sal farmacéuticamente aceptable de este, de cualquiera de las reivindicaciones 1 a 26, y un excipiente farmacéuticamente aceptable. Reivindicación 33: Un método para la inhibición de una proteína Ras en una célula, donde el método comprende poner en contacto a la célula con una cantidad eficaz de un compuesto o una sal farmacéuticamente aceptable de este, de cualquiera de las reivindicaciones 1 a 26, o una composición farmacéutica de la reivindicación 27.
ARP220102737A 2021-10-08 2022-10-06 Inhibidores ras AR127308A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US202163254013P 2021-10-08 2021-10-08

Publications (1)

Publication Number Publication Date
AR127308A1 true AR127308A1 (es) 2024-01-10

Family

ID=84044950

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP220102737A AR127308A1 (es) 2021-10-08 2022-10-06 Inhibidores ras

Country Status (5)

Country Link
US (1) US20230303591A1 (es)
AR (1) AR127308A1 (es)
CA (1) CA3234100A1 (es)
TW (1) TW202315616A (es)
WO (1) WO2023060253A1 (es)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023240263A1 (en) 2022-06-10 2023-12-14 Revolution Medicines, Inc. Macrocyclic ras inhibitors
CN116376844B (zh) * 2023-05-31 2023-08-11 四川大学华西医院 包含shp2 sh2结构域的靶向her2阳性肿瘤的car-t及制备方法和应用

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