BR112017012402A2 - derivados de 2,4-dioxo-quinazolina-6-sulfonamida como inibidores de parg - Google Patents

derivados de 2,4-dioxo-quinazolina-6-sulfonamida como inibidores de parg

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Publication number
BR112017012402A2
BR112017012402A2 BR112017012402A BR112017012402A BR112017012402A2 BR 112017012402 A2 BR112017012402 A2 BR 112017012402A2 BR 112017012402 A BR112017012402 A BR 112017012402A BR 112017012402 A BR112017012402 A BR 112017012402A BR 112017012402 A2 BR112017012402 A2 BR 112017012402A2
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Prior art keywords
quinazoline
dioxo
parg
sulfonamide derivatives
parg inhibitors
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BR112017012402A
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English (en)
Inventor
E Mcgonagle Alison
Jordan Allan
Waszkowycz Bohdan
Hutton Colin
Waddell Ian
R Hitchin James
Mary Smith Kate
M Hamilton Niall
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Cancer Research Tech Ltd
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Application filed by Cancer Research Tech Ltd filed Critical Cancer Research Tech Ltd
Publication of BR112017012402A2 publication Critical patent/BR112017012402A2/pt

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    • C07ORGANIC CHEMISTRY
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    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72Quinazolines; Hydrogenated quinazolines
    • C07D239/95Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in positions 2 and 4
    • C07D239/96Two oxygen atoms
    • 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
    • A61K31/495Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D215/20Oxygen atoms
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    • C07D217/00Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
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    • C07D217/00Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/22Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems 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 carbon atoms of the nitrogen-containing ring
    • C07D217/24Oxygen atoms
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D237/00Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/26Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings condensed with carbocyclic rings or ring systems
    • C07D237/30Phthalazines
    • C07D237/32Phthalazines with oxygen atoms directly attached to carbon atoms of the nitrogen-containing ring
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    • C07D239/70Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72Quinazolines; Hydrogenated quinazolines
    • C07D239/86Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
    • C07D239/88Oxygen atoms
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    • C07DHETEROCYCLIC COMPOUNDS
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    • C07D239/72Quinazolines; Hydrogenated quinazolines
    • C07D239/86Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
    • C07D239/88Oxygen atoms
    • C07D239/90Oxygen atoms with acyclic radicals attached in position 2 or 3
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    • C07ORGANIC CHEMISTRY
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    • C07D239/72Quinazolines; Hydrogenated quinazolines
    • C07D239/86Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
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    • C07D239/91Oxygen atoms with aryl or aralkyl radicals attached in position 2 or 3
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    • C07ORGANIC CHEMISTRY
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    • C07D241/38Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with only hydrogen or carbon atoms directly attached to the ring nitrogen atoms
    • C07D241/40Benzopyrazines
    • C07D241/44Benzopyrazines 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 carbon atoms of the hetero ring
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    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/06Heterocyclic 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 linked by a carbon chain containing only aliphatic carbon atoms
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    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
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    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems

Abstract

a presente invenção refere-se a compostos de fórmula i que funcionam como inibidores de atividade enzimática de parg (poli adp-ribose glico-hidrolase): (i) em que r1a, r1b, r1c, r1d, r1e, w, x1, x2, x3, x4, x5, x6, x7, c são, cada um, conforme definidos no presente documento. a presente invenção também se refere a processos para a preparação desses compostos, a composições farmacêuticas que compreendem os mesmos, e a seu uso no tratamento de distúrbios proliferativos, tais como câncer, assim como outras doenças ou condições em que a atividade de parg está implicada.
BR112017012402A 2014-12-12 2015-12-11 derivados de 2,4-dioxo-quinazolina-6-sulfonamida como inibidores de parg BR112017012402A2 (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB201422098 2014-12-12
PCT/GB2015/053883 WO2016092326A1 (en) 2014-12-12 2015-12-11 2,4-dioxo-quinazoline-6-sulfonamide derivatives as inhibitors of parg

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BR112017012402A2 true BR112017012402A2 (pt) 2017-12-26

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US (1) US10239843B2 (pt)
EP (1) EP3230273A1 (pt)
JP (1) JP2017537137A (pt)
KR (1) KR20170093967A (pt)
CN (1) CN107207467A (pt)
AU (1) AU2015359082A1 (pt)
BR (1) BR112017012402A2 (pt)
CA (1) CA2969296A1 (pt)
IL (1) IL252575A0 (pt)
MA (1) MA41140A (pt)
MX (1) MX2017007478A (pt)
RU (1) RU2017124425A (pt)
SG (1) SG11201704686UA (pt)
WO (1) WO2016092326A1 (pt)
ZA (1) ZA201704382B (pt)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MA41179A (fr) 2014-12-19 2017-10-24 Cancer Research Tech Ltd Composés inhibiteurs de parg
US9624219B2 (en) 2015-04-21 2017-04-18 Glaxosmithkline Intellectual Property Development Limited Compound (S) and (R)-N-(2-fluoropyridin-4-yl)-3-methyl-2-(5-methyl-2,4-dioxo-1,2-dihydropyrido[3,4-d]pyrimidin-3(4H)-yl)butanamide and use
AU2021410926A1 (en) 2020-12-24 2023-06-29 Modulus Discovery, Inc. Tetrahydrothienopyrimidinesulfonamide compounds
WO2023057394A1 (en) 2021-10-04 2023-04-13 Forx Therapeutics Ag N,n-dimethyl-4-(7-(n-(1-methylcyclopropyl)sulfamoyl)-imidazo[1,5-a]pyridin-5-yl)piperazine-1-carboxamide derivatives and the corresponding pyrazolo[1,5-a]pyridine derivatives as parg inhibitors for the treatment of cancer
AU2022359801A1 (en) 2021-10-04 2024-02-01 Forx Therapeutics Ag Parg inhibitory compounds
WO2023154913A1 (en) * 2022-02-14 2023-08-17 Arase Therapeutics Inc. Inhibitors of parg
WO2023165571A1 (zh) * 2022-03-04 2023-09-07 上海璎黎药业有限公司 一种含五元杂芳环结构化合物、其药物组合物及应用
WO2023175185A1 (en) 2022-03-17 2023-09-21 Forx Therapeutics Ag 2,4-dioxo-1,4-dihydroquinazoline derivatives as parg inhibitors for the treatment of cancer
WO2023175184A1 (en) 2022-03-17 2023-09-21 Forx Therapeutics Ag 2,4-dioxo-1,4-dihydroquinazoline derivatives as parg inhibitors for the treatment of cancer
WO2023208092A1 (en) * 2022-04-28 2023-11-02 Danatlas Pharmaceuticals Co., Ltd. Tricyclic heterocyclic derivatives, compositions and uses thereof
WO2023224998A1 (en) * 2022-05-17 2023-11-23 858 Therapeutics, Inc. Inhibitors of parg
US11939335B2 (en) 2022-05-17 2024-03-26 858 Therapeutics, Inc. Substituted imidazo[1,2-a]quinazolines and imidazo [1,2-a]pyrido[4,3-e]pyrimidines as inhibitors of PARG
WO2024017306A1 (zh) * 2022-07-19 2024-01-25 苏州信诺维医药科技股份有限公司 含硫杂芳环化合物、其药物组合物及其用途
EP4311829A1 (en) 2022-07-28 2024-01-31 Nodus Oncology Limited Substituted bicyclic heteroaryl sulfonamide derivatives for the treatment of cancer
WO2024074497A1 (en) 2022-10-03 2024-04-11 Forx Therapeutics Ag Parg inhibitory compound

Family Cites Families (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1157858A (en) * 1979-12-03 1983-11-29 Ikuo Ueda Quinazoline derivatives
DE19927415A1 (de) 1999-06-16 2000-12-21 Bayer Ag Indolinylharnstoffderivate
PE20010306A1 (es) 1999-07-02 2001-03-29 Agouron Pharma Compuestos de indazol y composiciones farmaceuticas que los contienen utiles para la inhibicion de proteina kinasa
US6566372B1 (en) 1999-08-27 2003-05-20 Ligand Pharmaceuticals Incorporated Bicyclic androgen and progesterone receptor modulator compounds and methods
TW200303304A (en) * 2002-02-18 2003-09-01 Astrazeneca Ab Chemical compounds
US7009052B2 (en) * 2003-03-20 2006-03-07 Warner Lambert Company Llc Sulfonamide derivatives
GB0322722D0 (en) 2003-09-27 2003-10-29 Glaxo Group Ltd Compounds
US20070049593A1 (en) 2004-02-24 2007-03-01 Japan Tobacco Inc. Tetracyclic fused heterocyclic compound and use thereof as HCV polymerase inhibitor
PT1719773E (pt) 2004-02-24 2009-06-03 Japan Tobacco Inc Compostos heterotetracíclicos fundidos e a sua utilização como inibidores da polimerase do hcv
WO2007014226A2 (en) * 2005-07-26 2007-02-01 The Board Of Trustees Of The University Of Illinois Compounds for the treatment of neurodegeneration and stroke
DK1979314T3 (da) 2006-01-24 2013-02-04 Lilly Co Eli Indolsulfonamidmodulatorer af progesteronreceptorer
EP1998777A1 (en) * 2006-03-20 2008-12-10 F. Hoffmann-La Roche AG Methods of inhibiting btk and syk protein kinases
WO2009047255A1 (en) * 2007-10-09 2009-04-16 Ucb Pharma, S.A. Heterobicyclic compounds as histamine h4-receptor antagonists
CA2728098A1 (en) 2008-07-17 2010-01-21 Asahi Kasei Pharma Corporation Pyrazole-containing tricyclic compounds as_antagonits of an ep1 receptor
CN101429191B (zh) 2008-11-03 2012-05-23 中国药科大学 取代的四氢异喹啉衍生物的用途
US8846935B2 (en) 2010-05-07 2014-09-30 Glaxosmithkline Llc Indazoles
WO2011140442A1 (en) 2010-05-07 2011-11-10 Glaxo Group Limited Amino-quinolines as kinase inhibitors
US8946260B2 (en) * 2010-09-16 2015-02-03 Novartis Ag 17α-hydroxylase/C17,20-lyase inhibitors
US8623889B2 (en) * 2010-12-17 2014-01-07 Genentech, Inc. Substituted 6,6-fused nitrogenous heterocyclic compounds and uses thereof
EP2471363A1 (de) * 2010-12-30 2012-07-04 Bayer CropScience AG Verwendung von Aryl-, Heteroaryl- und Benzylsulfonamidocarbonsäuren, -carbonsäureestern, -carbonsäureamiden und -carbonitrilen oder deren Salze zur Steigerung der Stresstoleranz in Pflanzen
WO2013027168A1 (en) * 2011-08-22 2013-02-28 Pfizer Inc. Novel heterocyclic compounds as bromodomain inhibitors
WO2013067300A1 (en) 2011-11-04 2013-05-10 Glaxosmithkline Intellectual Property (No. 2) Limited Method of treatment
JP2014106019A (ja) 2012-11-26 2014-06-09 Stack Electronics Co Ltd プローブ
EA201591220A1 (ru) 2012-12-27 2016-01-29 Дрексел Юниверсити Новые противовирусные агенты против инфекции вирусом гепатита в
MA41179A (fr) 2014-12-19 2017-10-24 Cancer Research Tech Ltd Composés inhibiteurs de parg

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CN107207467A (zh) 2017-09-26
CA2969296A1 (en) 2016-06-16
MA41140A (fr) 2017-10-17
ZA201704382B (en) 2019-09-25
KR20170093967A (ko) 2017-08-16
IL252575A0 (en) 2017-07-31
US10239843B2 (en) 2019-03-26
JP2017537137A (ja) 2017-12-14
SG11201704686UA (en) 2017-07-28
RU2017124425A (ru) 2019-01-14
EP3230273A1 (en) 2017-10-18
US20180016242A1 (en) 2018-01-18
MX2017007478A (es) 2018-05-04
AU2015359082A1 (en) 2017-06-29
WO2016092326A1 (en) 2016-06-16

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