AR114972A1 - Compuestos - Google Patents

Compuestos

Info

Publication number
AR114972A1
AR114972A1 ARP190101711A ARP190101711A AR114972A1 AR 114972 A1 AR114972 A1 AR 114972A1 AR P190101711 A ARP190101711 A AR P190101711A AR P190101711 A ARP190101711 A AR P190101711A AR 114972 A1 AR114972 A1 AR 114972A1
Authority
AR
Argentina
Prior art keywords
optionally substituted
hydroxy
phenyl
groups
heteroaryl
Prior art date
Application number
ARP190101711A
Other languages
English (en)
Inventor
Scott Raymond Walker
Bozikis Ylva Elisabet Bergman
Paul Anthony Stupple
Michelle Ang Camerino
Catherine Fae Hemley
Richard Charles Foitzik
Benjamin Joseph Morrow
Helen Rachel Lagiakos
Original Assignee
Ctxt Pty Ltd
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 Ctxt Pty Ltd filed Critical Ctxt Pty Ltd
Publication of AR114972A1 publication Critical patent/AR114972A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D261/00Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/20Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings condensed with carbocyclic rings or ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A61K31/41Heterocyclic 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
    • A61K31/42Oxazoles
    • A61K31/423Oxazoles condensed with carbocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A61K31/41Heterocyclic 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
    • A61K31/4245Oxadiazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A61K31/41Heterocyclic 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
    • A61K31/425Thiazoles
    • A61K31/428Thiazoles condensed with carbocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/10Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic 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
    • C07D417/02Heterocyclic 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
    • C07D417/12Heterocyclic 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Peptides Or Proteins (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Un compuesto de fórmula (1), o una sal farmacéutica del mismo. Reivindicación 1: Un compuesto de fórmula (1), o una sal farmacéuticamente aceptable del mismo, para su uso en un método de terapia, en donde: R¹, R², R³ y R⁴ se seleccionan independientemente entre: (i) H; (ii) alquilo C₁₋₃, opcionalmente sustituido con: hidroxi, alcoxi C₁₋₂, opcionalmente sustituido con uno o más grupos flúor, NH₂, fenilo, heteroarilo C₅₋₆, alquilcarbamoílo C₁₋₄, acilamido, o uno o más grupos flúor; (iii) alcoxi C₁₋₃, opcionalmente sustituido con cicloalquilo C₃₋₆ o con uno o más grupos flúor; (iv) cicloalquilo C₃₋₆; (v) halo; (vi) CORC, donde RC se selecciona entre NRN¹RN², donde RN¹ y RN² se seleccionan independientemente entre H y metilo; (vii) ciano, NH₂ o NO₂; y (viii) fenilo o heteroarilo C₅₋₆, opcionalmente sustituido con metilo, ciano, hidroxi o metoxi; Ar es un grupo fenilo, naftilo o heteroarilo C₅₋₁₀, estando estos grupos opcionalmente sustituidos con uno o más grupos seleccionados entre: (i) alquilo C₁₋₄, opcionalmente sustituido con hidroxi, alcoxi C₁₋₂, NH₂, alquilcarbamoílo C₁₋₄, o con uno o más grupos flúor; (ii) cicloalquilo C₃₋₆; (iii) hidroxi; ciano; NRN³RN⁴, donde RN³ y RN⁴ se seleccionan independientemente entre H y metilo; o acilamido; (iv) halo; (v) alcoxi C₁₋₃, opcionalmente sustituido con hidroxi, C(O)NH₂, cicloalquilo C₃₋₆, fenilo, heteroarilo C₅₋₆, o con uno o más grupos flúor; (vi) fenoxi, opcionalmente sustituido con flúor; (vii) fenilo o heteroarilo C₅₋₆; (viii) SF₅ o SO₂CH₃; (ix) -(CH₂)ₙ-Y-, donde Y es O ó CH₂, y n es 2 ó 3; o (x) alquil C₁₋₄ éster.
ARP190101711A 2018-06-20 2019-06-21 Compuestos AR114972A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB1810092.5A GB201810092D0 (en) 2018-06-20 2018-06-20 Compounds

Publications (1)

Publication Number Publication Date
AR114972A1 true AR114972A1 (es) 2020-11-11

Family

ID=63042663

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP190101711A AR114972A1 (es) 2018-06-20 2019-06-21 Compuestos

Country Status (39)

Country Link
US (2) US20200039945A1 (es)
EP (2) EP3810602B1 (es)
JP (1) JP2021529738A (es)
KR (1) KR20210022655A (es)
CN (1) CN112334466A (es)
AR (1) AR114972A1 (es)
AU (1) AU2019289888A1 (es)
BR (1) BR112020025869A2 (es)
CA (1) CA3101238A1 (es)
CL (1) CL2020003219A1 (es)
CO (1) CO2020014586A2 (es)
CR (1) CR20210032A (es)
CU (1) CU20200096A7 (es)
DK (1) DK3810602T3 (es)
DO (1) DOP2020000249A (es)
EA (1) EA202092451A1 (es)
EC (1) ECSP20075270A (es)
ES (1) ES2967983T3 (es)
FI (1) FI3810602T3 (es)
GB (1) GB201810092D0 (es)
GE (1) GEP20227403B (es)
HR (1) HRP20231467T1 (es)
HU (1) HUE064744T2 (es)
IL (1) IL279554A (es)
LT (1) LT3810602T (es)
MA (1) MA52948B1 (es)
MD (1) MD3810602T2 (es)
MX (1) MX2020012723A (es)
NI (1) NI202000092A (es)
PE (1) PE20210181A1 (es)
PH (1) PH12020500673A1 (es)
PL (1) PL3810602T3 (es)
PT (1) PT3810602T (es)
RS (1) RS64932B1 (es)
SG (1) SG11202010450VA (es)
SI (1) SI3810602T1 (es)
TW (1) TWI826471B (es)
UY (1) UY38270A (es)
WO (1) WO2019243491A1 (es)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3471271A1 (en) 2017-10-16 2019-04-17 Acoustical Beauty Improved convolutions of digital signals using a bit requirement optimization of a target digital signal
MX2021016085A (es) * 2019-06-18 2022-04-20 Pfizer Derivados de benzisoxazol sulfonamida.
AU2020295006B2 (en) * 2019-06-19 2023-11-09 Ctxt Pty Ltd Cycloalkyl and heterocycloalkyl benzisoxazole sulfonamide derivatives
EP3999490A4 (en) 2019-07-12 2023-03-08 Canopy Growth Corporation CANNABINOID DERIVATIVES
MX2023000735A (es) 2020-07-15 2023-02-13 Pfizer Metodos y combinaciones de inhibidor de kat6 para el tratamiento del cancer.
KR20240012434A (ko) * 2021-05-21 2024-01-29 오리진 온콜로지 리미티드 Kat6a 저해제로서의 융합된 이속사졸릴 화합물
EP4368620A1 (en) * 2021-07-05 2024-05-15 Hangzhou Innogate Pharma Co., Ltd. Compound serving as kat6 inhibitor
EP4385989A1 (en) 2021-08-10 2024-06-19 Jiangsu Hengrui Pharmaceuticals Co., Ltd. Sulfonamide derivative, preparation method therefor and medical use thereof
KR20240109267A (ko) * 2021-11-16 2024-07-10 인실리코 메디신 아이피 리미티드 리신 아세틸트랜스퍼라제 6a (kat6a) 억제제 및 그의 용도
WO2023114710A1 (en) * 2021-12-13 2023-06-22 Aurigene Oncology Limited Fused benzoisoxazolyl compounds as kat6a inhibitors
TW202400593A (zh) 2022-03-28 2024-01-01 美商艾索司特瑞克斯公司 Myst家族離胺酸乙醯轉移酶之抑制劑
WO2023245150A1 (en) * 2022-06-16 2023-12-21 Prelude Therapeutics Incorporated Kat6 targeting compounds with ubiquitin ligase binding moiety
WO2024023703A1 (en) 2022-07-29 2024-02-01 Pfizer Inc. Dosing regimens comprising a kat6 inhibitor for the treatment of cancer

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9624482D0 (en) 1995-12-18 1997-01-15 Zeneca Phaema S A Chemical compounds
IL125686A (en) 1996-02-13 2002-11-10 Zeneca Ltd Quinazoline derivatives, processes for their preparation, pharmaceutical preparations containing them and their use in the manufacture of a drug with an anti-angiogenic effect and / or an effect of reducing vascular permeability
WO1997032856A1 (en) 1996-03-05 1997-09-12 Zeneca Limited 4-anilinoquinazoline derivatives
GB9718972D0 (en) 1996-09-25 1997-11-12 Zeneca Ltd Chemical compounds
NZ337750A (en) 1997-02-12 2001-08-31 Univ Michigan Protein markers for lung cancer and use thereof
GB9714249D0 (en) 1997-07-08 1997-09-10 Angiogene Pharm Ltd Vascular damaging agents
GB9900334D0 (en) 1999-01-07 1999-02-24 Angiogene Pharm Ltd Tricylic vascular damaging agents
GB9900752D0 (en) 1999-01-15 1999-03-03 Angiogene Pharm Ltd Benzimidazole vascular damaging agents
CZ303692B6 (cs) 1999-02-10 2013-03-13 Astrazeneca Ab Chinazolinové deriváty jako inhibitory angiogeneze
IL149034A0 (en) 1999-11-05 2002-11-10 Astrazeneca Ab Quinazoline derivatives as vegf inhibitors
MXPA02008021A (es) 2000-02-15 2004-04-05 Sugen Inc Indolinonas sustituidas con pirroles inhibidoras de proteinquinasas.
IL152682A0 (en) 2000-05-31 2003-06-24 Astrazeneca Ab Indole derivatives with vascular damaging activity
UA73993C2 (uk) 2000-06-06 2005-10-17 Астразенека Аб Хіназолінові похідні для лікування пухлин та фармацевтична композиція
RU2003103603A (ru) 2000-07-07 2004-08-20 Энджиоджен Фармасьютикалз Лимитед (Gb) Производные колхинола в качестве ингибиторов ангиогенеза
WO2002004434A1 (en) 2000-07-07 2002-01-17 Angiogene Pharmaceuticals Limited Colchinol derivatives as vascular damaging agents
WO2010079443A1 (en) * 2009-01-12 2010-07-15 Pfizer Limited Sulfonamide derivatives
US9493429B2 (en) * 2013-03-15 2016-11-15 Genentech, Inc. Substituted benzoxazoles and methods of use thereof
MX2016013913A (es) * 2014-04-23 2016-11-15 Mitsubishi Tanabe Pharma Corp Compuesto heterociclico biciclico o triciclico novedoso.
GB201510019D0 (en) 2015-06-09 2015-07-22 Cancer Therapeutics Crc Pty Ltd Compounds
WO2018102419A1 (en) * 2016-11-29 2018-06-07 Epizyme, Inc. Compounds containing a sulfonic group as kat inhibitors
MX2021016085A (es) * 2019-06-18 2022-04-20 Pfizer Derivados de benzisoxazol sulfonamida.

Also Published As

Publication number Publication date
PH12020500673A1 (en) 2021-05-31
PE20210181A1 (es) 2021-01-29
KR20210022655A (ko) 2021-03-03
DOP2020000249A (es) 2021-02-28
HRP20231467T1 (hr) 2024-03-01
JP2021529738A (ja) 2021-11-04
PT3810602T (pt) 2024-01-03
ES2967983T3 (es) 2024-05-06
CR20210032A (es) 2021-02-11
HUE064744T2 (hu) 2024-04-28
FI3810602T3 (fi) 2023-12-21
DK3810602T3 (da) 2023-12-11
RS64932B1 (sr) 2023-12-29
US20220153710A1 (en) 2022-05-19
CL2020003219A1 (es) 2021-06-11
EP4335439A3 (en) 2024-05-15
MA52948B1 (fr) 2024-02-29
EA202092451A1 (ru) 2021-03-16
EP3810602A1 (en) 2021-04-28
TWI826471B (zh) 2023-12-21
UY38270A (es) 2020-01-31
TW202016103A (zh) 2020-05-01
MD3810602T2 (ro) 2024-03-31
US20200039945A1 (en) 2020-02-06
LT3810602T (lt) 2024-01-25
WO2019243491A1 (en) 2019-12-26
EP3810602B1 (en) 2023-11-01
ECSP20075270A (es) 2021-02-26
CU20200096A7 (es) 2021-08-06
IL279554A (en) 2021-01-31
CO2020014586A2 (es) 2021-03-08
SI3810602T1 (sl) 2024-02-29
MA52948A (fr) 2021-04-28
CA3101238A1 (en) 2019-12-26
GEP20227403B (en) 2022-08-10
CN112334466A (zh) 2021-02-05
MX2020012723A (es) 2021-05-14
EP4335439A2 (en) 2024-03-13
SG11202010450VA (en) 2021-01-28
BR112020025869A2 (pt) 2021-03-23
NI202000092A (es) 2021-03-23
AU2019289888A1 (en) 2020-11-12
GB201810092D0 (en) 2018-08-08
PL3810602T3 (pl) 2024-03-04

Similar Documents

Publication Publication Date Title
AR114972A1 (es) Compuestos
AR112797A1 (es) Inhibidores de kras g12c y métodos para utilizarlos
AR116939A1 (es) 2-amino-n-heteroaril-nicotinamidas como inhibidores de nav1.8
AR121044A1 (es) Inhibidores de egfr
PE20191532A1 (es) Compuestos heterociclicos como inmunomoduladores
AR119424A1 (es) Derivados de 3-oxo-4h-quinoxalina y oxo-1h-naftiridina como inhibidores de parp
AR088175A1 (es) 3-pirimidin-4-il-oxazolidin-2-onas utiles para tratar cancer y composiciones farmaceuticas que las contienen
AR093818A1 (es) Compuesto de 1-(bencil sustituido)piperazina sustituida
AR110922A1 (es) Compuestos inhibidores del vih
AR104176A1 (es) Inhibidores de ido (indolamina-2,3-dioxigenasa)
AR104362A1 (es) Dihidropiridoisoquinolinonas y composiciones farmacéuticas de las mismas para el tratamiento de trastornos inflamatorios
AR106865A1 (es) Piridinas sustituidas y métodos de uso
AR094668A1 (es) Amidas como moduladores de canales de sodio
AR099228A1 (es) Inhibidores macrocíclicos de fxia que tienen grupos heterocíclicos
AR099177A1 (es) Determinadas (2s)-n-[(1s)-1-ciano-2-feniletil]-1,4-oxazepan-2-carboxamidas como inhibidores de dipeptidil peptidasa 1
AR120896A1 (es) COMPUESTO DE PIRIDAZINIL-TIAZOLCARBOXAMIDA COMO INHIBIDORES DE DGKz
AR094452A1 (es) COMPUESTOS HETEROCÍCLICOS SUSTITUIDOS CON AMIDA ÚTILES COMO MODULADORES DE LAS RESPUESTAS DE IL-12, IL-23 Y/O INFa
PE20212070A1 (es) Moduladores de trex1
RU2013116924A (ru) N1/n2-лактамные ингибиторы ацетил-коа-карбоксилаз
AR098522A1 (es) Compuesto de triazolo-piridina
AR119010A1 (es) Compuestos, composiciones y métodos de uso
AR104880A1 (es) MODULADORES DE ROR GAMMA (RORg)
AR107428A1 (es) COMPUESTOS DE ISOXAZOL DE ÁCIDO HIDROXÁMICO COMO INHIBIDORES DE LpxC
AR104963A1 (es) Derivados de 2-(pirazolopiridin-3-il)pirimidina como inhibidores de jak
AR106297A1 (es) Compuestos macrocíclicos modificados como inhibidores selectivos de la quinasa cdk9