MX2018000471A - Moduladores de proteolisis basados en alanina y metodos de uso asociados. - Google Patents

Moduladores de proteolisis basados en alanina y metodos de uso asociados.

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Publication number
MX2018000471A
MX2018000471A MX2018000471A MX2018000471A MX2018000471A MX 2018000471 A MX2018000471 A MX 2018000471A MX 2018000471 A MX2018000471 A MX 2018000471A MX 2018000471 A MX2018000471 A MX 2018000471A MX 2018000471 A MX2018000471 A MX 2018000471A
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Mexico
Prior art keywords
compounds
binds
inhibition
polypeptides
proteolysis
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Application number
MX2018000471A
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English (en)
Inventor
Qian Yimin
Dong Hanqing
Berlin Michael
P Crew Andrew
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Arvinas Inc
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Publication date
Application filed by Arvinas Inc filed Critical Arvinas Inc
Publication of MX2018000471A publication Critical patent/MX2018000471A/es

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    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/10Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
    • C07D207/16Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • 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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    • A61K31/41Heterocyclic 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
    • A61K31/41641,3-Diazoles
    • A61K31/41781,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • 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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    • A61K31/44Non 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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    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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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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    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
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    • A61K47/55Medicinal 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 an organic compound the modifying agent being also a pharmacologically or therapeutically active agent, i.e. the entire conjugate being a codrug, i.e. a dimer, oligomer or polymer of pharmacologically or therapeutically active compounds
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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
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  • Engineering & Computer Science (AREA)
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  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Immunology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Investigating Or Analysing Biological Materials (AREA)

Abstract

La descripción se refiere a inhibidores de compuestos de enlace a Proteínas de Apoptosis (TAPs), incluyendo compuestos funcionales que comprenden los mismos, que encuentran utilidad como moduladores de la ubiquitinación dirigida, especialmente inhibidores de una variedad de polipéptidos y otras proteínas que se degradan y/o de otra manera se inhiben por los compuestos bifuncionales de acuerdo con la presente invención. En particular, la descripción proporciona compuestos, que contienen en un extremo un ligando que se enlaza a la IAP E3 ubiquitina-ligasa y en el otro extremo una porción que se enlaz a una proteína objetivo tal que la proteína objetivo se pone en proximidad con la ubiquitina ligasa para llevar a cabo la degradación (e inhibición) de esa proteínas. Se pueden sintetizar compuestos que muestren una amplia gama de actividades farmacológicas consistentes con la degradación/inhibición de los polipéptidos dirigidos de casi cualquier tipo.
MX2018000471A 2015-07-13 2016-07-13 Moduladores de proteolisis basados en alanina y metodos de uso asociados. MX2018000471A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201562192056P 2015-07-13 2015-07-13
PCT/US2016/042155 WO2017011590A1 (en) 2015-07-13 2016-07-13 Alanine-based modulators of proteolysis and associated methods of use

Publications (1)

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MX2018000471A true MX2018000471A (es) 2018-04-10

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MX2018000471A MX2018000471A (es) 2015-07-13 2016-07-13 Moduladores de proteolisis basados en alanina y metodos de uso asociados.

Country Status (10)

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US (2) US20170037004A1 (es)
EP (1) EP3322986A4 (es)
KR (1) KR20180029061A (es)
AU (1) AU2016294450A1 (es)
BR (1) BR112017028269A2 (es)
CA (1) CA2988436A1 (es)
HK (1) HK1255697A1 (es)
MX (1) MX2018000471A (es)
RU (1) RU2018105094A (es)
WO (1) WO2017011590A1 (es)

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US11510920B2 (en) 2016-10-28 2022-11-29 Icahn School Of Medicine At Mount Sinai Compositions and methods for treating EZH2-mediated cancer
US11541051B2 (en) 2016-12-08 2023-01-03 Icahn School Of Medicine At Mount Sinai Compositions and methods for treating CDK4/6-mediated cancer

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