CL2022000110A1 - Inhibidores de parp1 - Google Patents

Inhibidores de parp1

Info

Publication number
CL2022000110A1
CL2022000110A1 CL2022000110A CL2022000110A CL2022000110A1 CL 2022000110 A1 CL2022000110 A1 CL 2022000110A1 CL 2022000110 A CL2022000110 A CL 2022000110A CL 2022000110 A CL2022000110 A CL 2022000110A CL 2022000110 A1 CL2022000110 A1 CL 2022000110A1
Authority
CL
Chile
Prior art keywords
parp1 inhibitors
parp1
inhibitors
medicine
formula
Prior art date
Application number
CL2022000110A
Other languages
English (en)
Inventor
Martin John Packer
Jeffrey Wallace Johannes
Sudhir Mahadeo Hande
Sebastien Louis Degorce
Original Assignee
Astrazeneca Ab
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 Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of CL2022000110A1 publication Critical patent/CL2022000110A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • 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
    • 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
    • A61K31/4965Non-condensed pyrazines
    • A61K31/497Non-condensed pyrazines containing further heterocyclic 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
    • A61K31/495Heterocyclic 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
    • A61K31/498Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
    • 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
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • 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
    • C07D401/12Heterocyclic 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 chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • 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
    • C07D401/14Heterocyclic 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 three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

La presente invención se refiere a compuestos de azaquinolona de fórmula (I), y a su uso en medicina.
CL2022000110A 2019-07-19 2022-01-17 Inhibidores de parp1 CL2022000110A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201962876065P 2019-07-19 2019-07-19

Publications (1)

Publication Number Publication Date
CL2022000110A1 true CL2022000110A1 (es) 2022-09-20

Family

ID=71728735

Family Applications (1)

Application Number Title Priority Date Filing Date
CL2022000110A CL2022000110A1 (es) 2019-07-19 2022-01-17 Inhibidores de parp1

Country Status (21)

Country Link
US (2) US11325906B2 (es)
EP (1) EP3999506A1 (es)
JP (1) JP2022541483A (es)
KR (1) KR20220035941A (es)
CN (1) CN114144413A (es)
AR (1) AR119424A1 (es)
AU (1) AU2020318599B2 (es)
BR (1) BR112022000534A2 (es)
CA (1) CA3145644A1 (es)
CL (1) CL2022000110A1 (es)
CO (1) CO2022001590A2 (es)
CR (1) CR20220070A (es)
DO (1) DOP2022000006A (es)
EC (1) ECSP22012826A (es)
IL (1) IL289534A (es)
JO (1) JOP20220008A1 (es)
MX (1) MX2022000711A (es)
PE (1) PE20221339A1 (es)
TW (1) TWI837403B (es)
UY (1) UY38793A (es)
WO (1) WO2021013735A1 (es)

Families Citing this family (71)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2022532342A (ja) 2019-05-14 2022-07-14 ニューベイション・バイオ・インコーポレイテッド 抗がん核内ホルモン受容体標的化化合物
EP4058464A1 (en) 2019-11-13 2022-09-21 Nuvation Bio Inc. Anti-cancer nuclear hormone receptor-targeting compounds
US11795158B2 (en) 2020-06-25 2023-10-24 Astrazeneca Ab Chemical compounds
TW202228693A (zh) * 2020-10-08 2022-08-01 瑞典商阿斯特捷利康公司 用於治療癌症之組合療法
IL301921A (en) 2020-10-09 2023-06-01 Daiichi Sankyo Co Ltd Combining an antibody-drug conjugate and a selective 1PARP inhibitor
MX2023011241A (es) 2021-03-23 2023-10-03 Nuvation Bio Inc Compuestos dirigidos a receptores de hormonas nucleares contra el cancer.
JP2024514223A (ja) * 2021-04-19 2024-03-28 シンセラ, インコーポレイテッド Parp1阻害薬及びその使用
CN117279916A (zh) * 2021-04-22 2023-12-22 微境生物医药科技(上海)有限公司 含哌嗪结构的parp抑制剂、其制备方法及医药用途
TW202309026A (zh) * 2021-04-23 2023-03-01 大陸商上海翰森生物醫藥科技有限公司 雜環類衍生物抑制劑、其製備方法和應用
WO2022222966A1 (zh) * 2021-04-23 2022-10-27 成都百裕制药股份有限公司 一种选择性parp1抑制剂及其应用
CN115232121B (zh) * 2021-04-23 2023-08-29 成都百裕制药股份有限公司 吡啶衍生物及其在医药上的应用
TW202304911A (zh) * 2021-04-23 2023-02-01 大陸商南京明德新藥研發有限公司 吡啶醯胺類化合物
EP4334314A1 (en) * 2021-05-03 2024-03-13 Nuvation Bio Inc. Anti-cancer nuclear hormone receptor-targeting compounds
CA3219248A1 (en) * 2021-05-18 2022-11-24 Hyun Ju Cha Parp inhibitor-resistant cancer therapeutic agent
KR20240012437A (ko) 2021-05-24 2024-01-29 지앙수 헨그루이 파마슈티컬스 컴퍼니 리미티드 질소 함유 헤테로사이클릭 화합물, 이의 제조 방법 및 의학에서 이의 응용
IL309388A (en) * 2021-06-16 2024-02-01 Repare Therapeutics Inc Combining ATR inhibitors and PARP inhibitors for cancer treatment
WO2022271547A1 (en) 2021-06-21 2022-12-29 Tesaro, Inc. Combination treatment of cancer with a parp inhibitor and a lipophilic statin
WO2023036285A1 (zh) * 2021-09-09 2023-03-16 南京奥利墨斯医药科技有限公司 一种杂芳环类化合物及其应用
WO2023046034A1 (zh) * 2021-09-22 2023-03-30 明慧医药(杭州)有限公司 一种含氮杂环化合物、其制备方法、其中间体及其应用
WO2023046158A1 (zh) * 2021-09-26 2023-03-30 张文燕 氮杂喹啉酮类化合物及其医药用途
WO2023046149A1 (zh) * 2021-09-26 2023-03-30 张文燕 喹喔啉类化合物及其医药用途
WO2023051812A1 (zh) 2021-09-30 2023-04-06 海思科医药集团股份有限公司 含氮杂环衍生物parp抑制剂及其用途
CN118019740A (zh) * 2021-09-30 2024-05-10 海思科医药集团股份有限公司 杂芳基衍生物parp抑制剂及其用途
CN118043323A (zh) 2021-09-30 2024-05-14 西藏海思科制药有限公司 双环衍生物parp抑制剂及其用途
IL311376A (en) * 2021-10-01 2024-05-01 Xinthera Inc AZETIDINE AND PYRROLIDINE PARP1 INHIBITORS AND USES
WO2023061406A1 (zh) * 2021-10-12 2023-04-20 微境生物医药科技(上海)有限公司 含三并环结构的parp抑制剂、及其制备方法和医药用途
CA3235698A1 (en) 2021-10-22 2023-04-27 Yao Li Parp-1 degradation agent and use thereof
CA3238116A1 (en) 2021-11-18 2023-05-25 Matthew Simon SUNG Combination of antibody-drug conjugate and parp1 selective inhibitor
AU2022390101A1 (en) 2021-11-19 2024-06-06 Kangbaida (Sichuan) Biotechnology Co., Ltd. Selective parp1 inhibitor and application thereof
WO2023096915A1 (en) * 2021-11-24 2023-06-01 Slap Pharmaceuticals Llc Multicyclic compounds
CA3241338A1 (en) * 2021-12-17 2023-06-22 Yongqi Deng Parp inhibitor, pharmaceutical composition comprising same, and use thereof
CA3242082A1 (en) * 2021-12-21 2023-06-29 Astrazeneca Ab Methods of treating brain tumours and neuroblastomas
TW202332438A (zh) * 2021-12-22 2023-08-16 美商思諾維新醫藥公司 Parp1抑制劑
WO2023133413A1 (en) * 2022-01-07 2023-07-13 Slap Pharmaceuticals Llc Multicyclic compounds
WO2023134647A1 (zh) * 2022-01-13 2023-07-20 优领医药科技(香港)有限公司 含哌嗪并环类衍生物、其药学上可接受的盐及其制备方法和应用
WO2023138541A1 (zh) * 2022-01-20 2023-07-27 微境生物医药科技(上海)有限公司 吡啶酰胺类parp抑制剂、及其制备方法和医药用途
WO2023141290A1 (en) 2022-01-21 2023-07-27 Xinthera, Inc. Parp1 inhibitors and uses thereof
WO2023146957A1 (en) * 2022-01-27 2023-08-03 Xinthera, Inc. Parp1 inhibitors and uses thereof
WO2023146960A1 (en) * 2022-01-28 2023-08-03 Xinthera, Inc. Parp1 inhibitors and uses thereof
TW202348252A (zh) 2022-02-16 2023-12-16 英商梅迪繆思有限公司 用治療性結合分子治療癌症的組合療法
WO2023165501A1 (zh) * 2022-03-01 2023-09-07 杭州领业医药科技有限公司 Azd5305的晶型及其制备方法和用途
WO2023178035A1 (en) * 2022-03-14 2023-09-21 Slap Pharmaceuticals Llc Multicyclic compounds
WO2023194530A1 (en) 2022-04-07 2023-10-12 Astrazeneca Ab Combination therapy for treating cancer
WO2023194528A1 (en) 2022-04-07 2023-10-12 Astrazeneca Ab Combination therapy for treating cancer
WO2023194525A1 (en) 2022-04-07 2023-10-12 Astrazeneca Ab Combination therapy for treating cancer
WO2023201338A1 (en) 2022-04-15 2023-10-19 Ideaya Biosciences, Inc. Combination therapy comprising a mat2a inhibitor and a parp inhibitor
WO2023207284A1 (en) * 2022-04-28 2023-11-02 Ningbo Newbay Technology Development Co., Ltd Piperazine derivatives as parp1 inhibitiors
TW202400596A (zh) 2022-04-28 2024-01-01 美商辛瑟拉股份有限公司 三環parp1抑制劑及其用途
WO2023207283A1 (en) * 2022-04-28 2023-11-02 Ningbo Newbay Technology Development Co., Ltd Compounds as parp1 inhibitiors
WO2023217045A1 (zh) * 2022-05-07 2023-11-16 南京明德新药研发有限公司 选择性抑制parp1的氟代喹喔啉酮衍生物
WO2023227052A1 (zh) * 2022-05-25 2023-11-30 西藏海思科制药有限公司 双环衍生物parp抑制剂及其用途
WO2023242302A1 (en) 2022-06-15 2023-12-21 Astrazeneca Ab Combination therapy for treating cancer
CN115919859B (zh) * 2022-07-14 2024-01-05 四川海思科制药有限公司 一种杂芳基衍生物的药物组合物及其在医药上的应用
TW202408509A (zh) * 2022-07-14 2024-03-01 大陸商西藏海思科製藥有限公司 雜芳基衍生物的藥物組合物及其在醫藥上的應用
CN115232129B (zh) * 2022-08-18 2023-12-01 上海闻耐医药科技有限公司 一种parp1选择性抑制剂及其制备方法和用途
WO2024041608A1 (zh) * 2022-08-24 2024-02-29 四川海思科制药有限公司 一种杂芳基衍生物parp抑制剂的晶体形式及其用途
WO2024041605A1 (zh) * 2022-08-24 2024-02-29 四川海思科制药有限公司 一种杂芳基衍生物parp抑制剂药学上可接受的盐及其用途
WO2024041643A1 (zh) * 2022-08-25 2024-02-29 江苏恒瑞医药股份有限公司 稠合三环类化合物、其制备方法及其在医药上的应用
WO2024046420A1 (zh) * 2022-08-31 2024-03-07 江苏恒瑞医药股份有限公司 稠合二环类化合物、其制备方法及其在医药上的应用
CN117658983A (zh) * 2022-09-01 2024-03-08 浙江文达医药科技有限公司 选择性parp1抑制剂
CN118119629A (zh) * 2022-09-30 2024-05-31 中国医药研究开发中心有限公司 含氮杂环类化合物及其医药用途
TW202415658A (zh) * 2022-09-30 2024-04-16 大陸商中國醫藥研究開發中心有限公司 含氮雜環類化合物及其醫藥用途
US20240174669A1 (en) * 2022-10-06 2024-05-30 Xinthera, Inc. Crystalline forms of a parp1 inhibitor
WO2024083218A1 (zh) * 2022-10-20 2024-04-25 成都赜灵生物医药科技有限公司 取代四氢吡啶类化合物及其用途
CN117917407A (zh) * 2022-10-20 2024-04-23 成都赜灵生物医药科技有限公司 并杂环类化合物及其用途
WO2024083211A1 (zh) * 2022-10-20 2024-04-25 成都赜灵生物医药科技有限公司 并杂环类氘代化合物及其用途
WO2024083204A1 (zh) * 2022-10-21 2024-04-25 上海翰森生物医药科技有限公司 杂环类衍生物抑制剂的盐、晶型及其制备方法和应用
WO2024097775A1 (en) * 2022-11-02 2024-05-10 Nuvation Bio Inc. Anti-cancer nuclear hormone receptor-targeting compounds
WO2024099386A1 (zh) * 2022-11-10 2024-05-16 正大天晴药业集团股份有限公司 稠合双环化合物
WO2024109871A1 (zh) * 2022-11-23 2024-05-30 江苏恒瑞医药股份有限公司 一种含氮杂环类化合物的可药用盐、晶型及制备方法
WO2024121753A1 (en) 2022-12-06 2024-06-13 Astrazeneca Ab Polq inhibitors

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002503943A (ja) 1994-08-12 2002-02-05 ミリアド・ジェネティックス・インコーポレイテッド 17q−連鎖乳癌および卵巣癌感受性遺伝子におけるイン・ビボ突然変異および多形性
WO1996005307A2 (en) 1994-08-12 1996-02-22 Myriad Genetics, Inc. 17q-LINKED BREAST AND OVARIAN CANCER SUSCEPTIBILITY GENE
AUPS137402A0 (en) * 2002-03-26 2002-05-09 Fujisawa Pharmaceutical Co., Ltd. Novel tricyclic compounds
GB2415430B (en) 2003-03-12 2006-07-12 Kudos Pharm Ltd Phthalazinone derivatives
EP1687277B1 (en) 2003-11-20 2018-04-04 Janssen Pharmaceutica NV 6-alkenyl and 6-phenylalkyl substituted 2-quinolinones and 2-quinoxalinones as poly(adp-ribose) polymerase inhibitors
UA89618C2 (ru) 2003-12-05 2010-02-25 Янссен Фармацевтика Н.В. 6-замещенные 2-хинолиноны и 2-хиноксалиноны как ингибиторы поли(адф-рибоза)полимеразы
AU2004299183B2 (en) 2003-12-10 2010-09-23 Janssen Pharmaceutica N.V. Substituted 6-cyclohexylalkyl substituted 2-quinolinones and 2-quinoxalinones as poly(ADP-ribose) polymerase inhibitors
MX2007002318A (es) 2004-08-26 2007-04-17 Kudos Pharm Ltd Derivados de ftalazinona substituidos con 4-heteroarilmetilo.
DK2134691T3 (da) 2007-03-08 2012-05-07 Janssen Pharmaceutica Nv Quinolinonderivativer som parp- og tank-inhibitorer
ES2448870T3 (es) * 2007-10-26 2014-03-17 Janssen Pharmaceutica, N.V. Derivados de quinolina como inhibidores de PARP
UY31603A1 (es) 2008-01-23 2009-08-31 Derivados de ftalazinona
US7928105B2 (en) * 2009-01-23 2011-04-19 Takeda Pharmaceutical Company Limited Substituted 6a,7,8,9-tetrahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-6(5H)-ones
US8541417B2 (en) * 2009-07-30 2013-09-24 Takeda Pharmaceutical Company Limited Poly (ADP-ribose) polymerase (PARP) inhibitors
WO2016200101A2 (ko) * 2015-06-09 2016-12-15 제일약품주식회사 트리사이클릭 유도체 화합물, 이의 제조방법 및 이를 포함하는 약학적 조성물

Also Published As

Publication number Publication date
PE20221339A1 (es) 2022-09-13
US11325906B2 (en) 2022-05-10
AR119424A1 (es) 2021-12-15
EP3999506A1 (en) 2022-05-25
US20210040084A1 (en) 2021-02-11
TWI837403B (zh) 2024-04-01
CR20220070A (es) 2022-03-21
KR20220035941A (ko) 2022-03-22
AU2020318599A1 (en) 2022-03-10
CN114144413A (zh) 2022-03-04
CA3145644A1 (en) 2021-01-28
WO2021013735A1 (en) 2021-01-28
DOP2022000006A (es) 2022-03-15
TW202116750A (zh) 2021-05-01
ECSP22012826A (es) 2022-03-31
AU2020318599B2 (en) 2023-09-07
JP2022541483A (ja) 2022-09-26
US20220227768A1 (en) 2022-07-21
BR112022000534A2 (pt) 2022-05-10
CO2022001590A2 (es) 2022-03-18
UY38793A (es) 2021-02-26
IL289534A (en) 2022-03-01
JOP20220008A1 (ar) 2023-01-30
MX2022000711A (es) 2022-02-23

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