AU2016276806B9 - Tricyclic derivative compound, method for preparing same, and pharmaceutical composition comprising same - Google Patents

Tricyclic derivative compound, method for preparing same, and pharmaceutical composition comprising same Download PDF

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Publication number
AU2016276806B9
AU2016276806B9 AU2016276806A AU2016276806A AU2016276806B9 AU 2016276806 B9 AU2016276806 B9 AU 2016276806B9 AU 2016276806 A AU2016276806 A AU 2016276806A AU 2016276806 A AU2016276806 A AU 2016276806A AU 2016276806 B9 AU2016276806 B9 AU 2016276806B9
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AU
Australia
Prior art keywords
methyl
naphthyridin
piperazin
oxo
hexahydrobenzo
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AU2016276806A
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English (en)
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AU2016276806A1 (en
AU2016276806B2 (en
Inventor
Kwangwoo Chun
Eun Sung Jang
Bo-Young Joe
Eun Seon Kim
Jeong-Min Kim
Hanchang LEE
Hyunho Lee
Hyeongchan OH
Jiseon PARK
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Onconic Therapeutics Inc
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Onconic Therapeutics Inc
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Publication of AU2016276806A1 publication Critical patent/AU2016276806A1/en
Publication of AU2016276806B2 publication Critical patent/AU2016276806B2/en
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Publication of AU2016276806B9 publication Critical patent/AU2016276806B9/en
Assigned to ONCONIC THERAPEUTICS INC. reassignment ONCONIC THERAPEUTICS INC. Request for Assignment Assignors: JE IL PHARMACEUTICAL CO., LTD.
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Classifications

    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4375Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
    • 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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • 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
    • C07D401/06Heterocyclic 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
    • 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

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Neurosurgery (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
AU2016276806A 2015-06-09 2016-06-03 Tricyclic derivative compound, method for preparing same, and pharmaceutical composition comprising same Active AU2016276806B9 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
KR10-2015-0081021 2015-06-09
KR20150081021 2015-06-09
PCT/KR2016/005911 WO2016200101A2 (ko) 2015-06-09 2016-06-03 트리사이클릭 유도체 화합물, 이의 제조방법 및 이를 포함하는 약학적 조성물

Publications (3)

Publication Number Publication Date
AU2016276806A1 AU2016276806A1 (en) 2018-01-04
AU2016276806B2 AU2016276806B2 (en) 2019-02-14
AU2016276806B9 true AU2016276806B9 (en) 2019-02-21

Family

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Family Applications (1)

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AU2016276806A Active AU2016276806B9 (en) 2015-06-09 2016-06-03 Tricyclic derivative compound, method for preparing same, and pharmaceutical composition comprising same

Country Status (21)

Country Link
US (1) US10464919B2 (https=)
EP (1) EP3312177B1 (https=)
JP (2) JP2018521033A (https=)
KR (1) KR101837047B1 (https=)
CN (1) CN107849040B (https=)
AU (1) AU2016276806B9 (https=)
BR (1) BR112017026392B1 (https=)
CA (1) CA2990277C (https=)
CL (1) CL2017003138A1 (https=)
DK (1) DK3312177T3 (https=)
ES (1) ES2870203T3 (https=)
MX (1) MX375707B (https=)
MY (1) MY194590A (https=)
NZ (1) NZ738187A (https=)
PH (1) PH12017502228B1 (https=)
PL (1) PL3312177T3 (https=)
PT (1) PT3312177T (https=)
RU (1) RU2715413C2 (https=)
SA (1) SA517390509B1 (https=)
WO (1) WO2016200101A2 (https=)
ZA (1) ZA201708663B (https=)

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KR101775356B1 (ko) 2015-07-06 2017-09-06 재단법인 아산사회복지재단 Parp 및 탄키라제 동시 저해제에 대한 감수성 결정 방법
CN109689654A (zh) 2016-07-11 2019-04-26 拜耳医药股份有限公司 7-取代的1-吡啶基-萘啶-3-甲酰胺类及其用途
JOP20190045A1 (ar) 2016-09-14 2019-03-14 Bayer Ag مركبات أميد حمض 1- أريل-نفثيريدين-3-كربوكسيليك مستبدلة في الموضع 7 واستخدامها.
CN108727377A (zh) * 2017-04-14 2018-11-02 四川大学 3-氰基吡唑并[1,5-a]嘧啶衍生物及其制备方法和用途
WO2019134985A1 (en) 2018-01-08 2019-07-11 F. Hoffmann-La Roche Ag Octahydropyrido[1,2-alpha]pyrazines as magl inhibitors
US20220110936A1 (en) * 2019-02-02 2022-04-14 Shanghai Institute Of Organic Chemistry, Chinese Academy Of Sciences Pharmaceutical composition for treatment of neurodegenerative diseases or diseases caused by abnormality of rna binding protein and applications thereof
EP3953360B1 (en) * 2019-04-09 2024-02-28 F. Hoffmann-La Roche AG Heterocyclic compounds as inhibitors of monoacylglycerol lipase (magl)
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MX2022001200A (es) * 2019-07-29 2022-02-21 Jeil Pharmaceutical Co Ltd Metodo para el tratamiento de accidente cerebrovascular usando un derivado triciclico.
US20220324899A1 (en) * 2019-08-14 2022-10-13 Metro International Biotech, Llc Compounds and compositions for differential modulation of nicotinamide adenine dinucleotide
IL326597A (en) 2019-10-07 2026-04-01 Contineum Therapeutics Inc Muscarinic M1 acetylcholine receptor antagonists
AU2020372682A1 (en) * 2019-10-31 2022-06-09 Jd Bioscience Inc. Tricyclic compound and pharmaceutical use thereof
US11752149B2 (en) 2019-12-02 2023-09-12 Pipeline Therapeutics, Inc. Muscarinic acetylcholine M1 receptor antagonists
US11795158B2 (en) 2020-06-25 2023-10-24 Astrazeneca Ab Chemical compounds
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US11591331B2 (en) 2021-04-19 2023-02-28 Xinthera, Inc. PARP1 inhibitors and uses thereof
EP4328224A4 (en) * 2021-04-22 2025-06-18 Wigen Biomedicine Technology (Shanghai) Co., Ltd. PARP INHIBITOR WITH PIPERAZINE STRUCTURE, MANUFACTURING METHOD THEREOF AND PHARMACEUTICAL USE THEREOF
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
CN115702156A (zh) * 2021-04-23 2023-02-14 南京明德新药研发有限公司 吡啶酰胺类化合物
EP4342470A4 (en) * 2021-05-18 2025-04-30 Onconic Therapeutics Inc. THERAPEUTIC AGENT FOR PARP INHIBITOR-RESISTANT CANCER
MX2023013624A (es) * 2021-05-18 2023-11-30 Onconic Therapeutics Inc Forma cristalina del compuesto derivado triciclico, metodo para preparar la misma y composicion farmaceutica que comprende la misma.
MA63136A1 (fr) * 2021-05-18 2024-06-28 Onconic Therapeutics Inc. Agent thérapeutique contre le cancer résistant à un inhibiteur de parp
WO2023011608A1 (zh) * 2021-08-05 2023-02-09 上海枢境生物科技有限公司 含三并环类衍生物调节剂、其制备方法和应用
AU2022334408A1 (en) 2021-08-27 2024-02-15 Impact Therapeutics (Shanghai), Inc. Substituted tricyclic compounds as parp inhibitors and use thereof
CN118119618A (zh) * 2021-09-09 2024-05-31 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
KR102867210B1 (ko) 2021-10-01 2025-10-14 신테라, 인크. 아제티딘 및 피롤리딘 parp1 저해제, 및 이의 용도
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
US20250163022A1 (en) * 2021-12-22 2025-05-22 Synnovation Therapeutics, Inc. Parp1 inhibitors
KR20240134366A (ko) * 2022-01-13 2024-09-09 에이스랜드 테라퓨틱스 (홍콩) 리미티드 피페라진 고리 함유 유도체, 이의 약학적으로 허용 가능한 염, 이의 제조방법 및 용도
CN120081844A (zh) 2022-01-21 2025-06-03 新特拉有限公司 Parp1抑制剂及其用途
CN119013279A (zh) * 2022-03-11 2024-11-22 上海瑛派药业有限公司 作为parp抑制剂的取代的三环类化合物及其应用
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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
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Also Published As

Publication number Publication date
CN107849040B (zh) 2021-04-06
ZA201708663B (en) 2019-04-24
JP2018521033A (ja) 2018-08-02
MX2017016013A (es) 2018-04-20
JP2019163287A (ja) 2019-09-26
ES2870203T3 (es) 2021-10-26
SA517390509B1 (ar) 2021-06-02
DK3312177T3 (da) 2021-07-05
BR112017026392B1 (pt) 2023-12-26
PH12017502228B1 (en) 2022-08-03
BR112017026392A2 (https=) 2018-08-21
RU2017146130A (ru) 2019-07-16
CA2990277A1 (en) 2016-12-15
KR20160144916A (ko) 2016-12-19
EP3312177B1 (en) 2021-04-14
EP3312177A4 (en) 2018-12-05
AU2016276806A1 (en) 2018-01-04
CL2017003138A1 (es) 2018-06-15
NZ738187A (en) 2019-03-29
RU2715413C2 (ru) 2020-02-28
MY194590A (en) 2022-12-05
MX375707B (es) 2025-03-06
WO2016200101A3 (ko) 2017-02-02
PL3312177T3 (pl) 2021-11-02
US20180162834A1 (en) 2018-06-14
JP6806969B2 (ja) 2021-01-06
CN107849040A (zh) 2018-03-27
AU2016276806B2 (en) 2019-02-14
CA2990277C (en) 2021-10-26
RU2017146130A3 (https=) 2019-07-17
US10464919B2 (en) 2019-11-05
EP3312177A2 (en) 2018-04-25
PT3312177T (pt) 2021-05-17
KR101837047B1 (ko) 2018-03-09
PH12017502228A1 (en) 2018-06-11
WO2016200101A2 (ko) 2016-12-15

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