SI2769980T1 - Derivati pirazolokinolina kot inhibitorji PDE9 - Google Patents

Derivati pirazolokinolina kot inhibitorji PDE9

Info

Publication number
SI2769980T1
SI2769980T1 SI201230501A SI201230501A SI2769980T1 SI 2769980 T1 SI2769980 T1 SI 2769980T1 SI 201230501 A SI201230501 A SI 201230501A SI 201230501 A SI201230501 A SI 201230501A SI 2769980 T1 SI2769980 T1 SI 2769980T1
Authority
SI
Slovenia
Prior art keywords
pde9 inhibitors
pyrazoloquinoline derivative
pyrazoloquinoline
derivative
pde9
Prior art date
Application number
SI201230501A
Other languages
English (en)
Inventor
Yoshihiko Norimine
Kunitoshi Takeda
Koji Hagiwara
Yuichi Suzuki
Yuki Ishihara
Nobuaki Sato
Original Assignee
Eisai R&D Management Co., 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 Eisai R&D Management Co., Ltd. filed Critical Eisai R&D Management Co., Ltd.
Publication of SI2769980T1 publication Critical patent/SI2769980T1/sl

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
    • A61K31/435Heterocyclic 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
    • A61K31/437Heterocyclic 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 five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
SI201230501A 2011-10-07 2012-10-04 Derivati pirazolokinolina kot inhibitorji PDE9 SI2769980T1 (sl)

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
US201161544860P 2011-10-07 2011-10-07
US201161550623P 2011-10-24 2011-10-24
US201161558110P 2011-11-10 2011-11-10
US201161580903P 2011-12-28 2011-12-28
EP12837953.4A EP2769980B1 (en) 2011-10-07 2012-10-04 Pyrazoloquinoline derivative as pde9 inhibitors
PCT/JP2012/075748 WO2013051639A1 (ja) 2011-10-07 2012-10-04 ピラゾロキノリン誘導体

Publications (1)

Publication Number Publication Date
SI2769980T1 true SI2769980T1 (sl) 2016-08-31

Family

ID=48043792

Family Applications (1)

Application Number Title Priority Date Filing Date
SI201230501A SI2769980T1 (sl) 2011-10-07 2012-10-04 Derivati pirazolokinolina kot inhibitorji PDE9

Country Status (33)

Country Link
US (2) US8563565B2 (sl)
EP (1) EP2769980B1 (sl)
JP (1) JP5546693B2 (sl)
KR (1) KR101943680B1 (sl)
CN (1) CN103930423B (sl)
AR (1) AR088235A1 (sl)
AU (1) AU2012319549B2 (sl)
BR (1) BR112014007912B1 (sl)
CA (1) CA2861795C (sl)
CL (1) CL2014000821A1 (sl)
CO (1) CO6910200A2 (sl)
CY (1) CY1117427T1 (sl)
DK (1) DK2769980T3 (sl)
ES (1) ES2568015T3 (sl)
HK (1) HK1199018A1 (sl)
HR (1) HRP20160273T1 (sl)
HU (1) HUE028555T2 (sl)
IL (1) IL231650A (sl)
IN (1) IN2014CN02463A (sl)
JO (1) JO3116B1 (sl)
ME (1) ME02394B (sl)
MX (1) MX358149B (sl)
MY (1) MY167698A (sl)
PE (1) PE20141557A1 (sl)
PL (1) PL2769980T3 (sl)
RS (1) RS54702B1 (sl)
RU (1) RU2605096C2 (sl)
SG (1) SG11201400717QA (sl)
SI (1) SI2769980T1 (sl)
SM (1) SMT201600108B (sl)
TW (1) TWI562993B (sl)
WO (1) WO2013051639A1 (sl)
ZA (1) ZA201402439B (sl)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SG11201502728WA (en) 2011-10-10 2015-05-28 Lundbeck & Co As H Pde9i with imidazo pyrazinone backbone
SG11201507897SA (en) * 2013-04-05 2015-11-27 Eisai R&D Man Co Ltd Salt of pyrazoloquinoline derivative, and crystal thereof
CN105189496B (zh) * 2013-04-05 2017-03-29 卫材R&D管理有限公司 吡啶基吡唑并喹啉化合物
GB201406486D0 (en) 2014-04-10 2014-05-28 Redx Pharma Ltd Antibacterial compounds
WO2016021192A1 (en) * 2014-08-08 2016-02-11 Eisai R&D Management Co., Ltd. Process for production of (s)-(tetrahydrofuran-3-yl)hydrazine
PT3865484T (pt) 2015-07-07 2024-01-30 H Lundbeck As Inibidor da pde9 com esqueleto de imidazo pirazinona para tratamento de doenças periféricas
WO2017046606A1 (en) * 2015-09-18 2017-03-23 Redx Pharma Plc Antibacterial compounds
CN107056690A (zh) * 2017-03-22 2017-08-18 上海康鹏科技有限公司 一种6‑溴吡啶‑3‑甲醛的制备方法
BR112019023557A2 (pt) 2017-06-01 2020-06-02 Eisai R&D Management Co., Ltd. Composição farmacêutica compreendendo inibidor de pde9
MX2019013397A (es) * 2017-06-01 2020-02-07 Eisai R&D Man Co Ltd Agente terapeutico para enfermedad con cuerpos de lewy que contiene derivado de pirazoloquinolina.
JP7177772B2 (ja) * 2017-06-01 2022-11-24 エーザイ・アール・アンド・ディー・マネジメント株式会社 ピラゾロキノリン誘導体とメマンチンの併用による認知症治療剤
ES2980131T3 (es) * 2017-06-01 2024-09-30 Eisai R&D Man Co Ltd Agente terapéutico para la demencia que combina derivado de pirazoloquinolina y donepezilo
CN111630042A (zh) 2018-01-23 2020-09-04 巴斯夫欧洲公司 吡啶衍生物的卤化
SI3801526T1 (sl) 2018-05-25 2024-05-31 Cardurion Pharmaceuticals, Inc. Monohidratne in kristalinične oblike 6-((3s, 4s)-4-metil-1-(pirimidin-2-ilmetil)pirolidin-3-il)-3-tetrahidropiran-4- il-7h-imidazo (1.5 - a) pirazin-8-ona
EP3843737A4 (en) * 2018-08-31 2022-06-01 Imara Inc. PDE9 INHIBITORS FOR THE TREATMENT OF SICKLE CELL DISEASE
CA3122183A1 (en) * 2018-12-13 2020-06-18 Intervet International B.V. Process for preparing 1-[(3r,4s)-4-cyanotetrahydropyran-3-yl]-3-[(2-fluoro-6-methoxy-4-pyridyl)amino]p yrazole-4-carboxamide
EP3965770A4 (en) 2019-05-09 2023-01-18 The Feinstein Institutes for Medical Research COMPOUNDS FOR USE IN THE SYNTHESIS OF PEPTIDOMIMETICS
CA3139109A1 (en) 2019-05-09 2020-11-12 The Feinstein Institutes For Medical Research Hmgb1 antagonist
AU2020270125A1 (en) 2019-05-09 2021-11-25 The Feinstein Institutes For Medical Research Thiosemicarbazates and uses thereof
US11883461B2 (en) 2019-05-09 2024-01-30 The Feinstein Institutes For Medical Research HMGB1 antagonist treatment of severe sepsis
WO2021150613A1 (en) 2020-01-20 2021-07-29 Incyte Corporation Spiro compounds as inhibitors of kras
US20210355121A1 (en) * 2020-04-16 2021-11-18 Incyte Corporation Fused tricyclic kras inhibitors
US11739102B2 (en) 2020-05-13 2023-08-29 Incyte Corporation Fused pyrimidine compounds as KRAS inhibitors
MX2022016551A (es) 2020-06-30 2023-02-01 Bayer Ag Heteroariloxipiridinas sustituidas, asi como sus sales y su uso como principios activos herbicidas.
US11999752B2 (en) 2020-08-28 2024-06-04 Incyte Corporation Vinyl imidazole compounds as inhibitors of KRAS
WO2022072783A1 (en) 2020-10-02 2022-04-07 Incyte Corporation Bicyclic dione compounds as inhibitors of kras
US12077539B2 (en) 2021-03-22 2024-09-03 Incyte Corporation Imidazole and triazole KRAS inhibitors
WO2023049697A1 (en) 2021-09-21 2023-03-30 Incyte Corporation Hetero-tricyclic compounds as inhibitors of kras
WO2023056421A1 (en) 2021-10-01 2023-04-06 Incyte Corporation Pyrazoloquinoline kras inhibitors
KR20240101561A (ko) 2021-10-14 2024-07-02 인사이트 코포레이션 Kras의 저해제로서의 퀴놀린 화합물

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2426734C2 (ru) * 2003-10-03 2011-08-20 Зм Инновейтив Пропертиз Компани Пиразолопиридины и их аналоги
US20060035920A1 (en) * 2004-05-28 2006-02-16 Millennium Pharmaceuticals, Inc. Chk-1 inhibitors
CA2622605A1 (en) * 2005-09-15 2007-03-22 Aska Pharmaceutical Co., Ltd. Heterocycle compound, and production process and application thereof
JP2009184924A (ja) 2006-05-31 2009-08-20 Eisai R & D Management Co Ltd 生物学的試薬用化合物
WO2008072779A1 (ja) * 2006-12-13 2008-06-19 Aska Pharmaceutical Co., Ltd. キノキサリン誘導体
JP4579346B2 (ja) 2007-05-11 2010-11-10 ファイザー・インク アミノ複素環式化合物
UA105362C2 (en) 2008-04-02 2014-05-12 Бьорингер Ингельхайм Интернациональ Гмбх 1-heterocyclyl-1, 5-dihydro-pyrazolo [3, 4-d] pyrimidin-4-one derivatives and their use as pde9a modulators
AU2010219598A1 (en) * 2009-03-05 2011-09-22 Astellas Pharma Inc. Quinoxaline compounds
ES2460019T3 (es) 2009-03-31 2014-05-13 Boehringer Ingelheim International Gmbh Derivados de 1-heterociclil-1,5-dihidro-pirazolo[3,4-d]pirimidin-4-ona y su uso como moduladores de PDE9A
US8880976B2 (en) 2009-09-25 2014-11-04 Stmicroelectronics, Inc. Method and apparatus for encoding LBA information into the parity of a LDPC system
SI2615089T1 (sl) 2010-09-07 2016-08-31 Astellas Pharma Inc. Spojine pirazolokinolina
JP6042060B2 (ja) * 2011-09-26 2016-12-14 サノフイ ピラゾロキノリノン誘導体、その調製および治療上の使用

Also Published As

Publication number Publication date
BR112014007912A2 (pt) 2017-04-04
EP2769980B1 (en) 2016-02-03
MX2014003800A (es) 2014-07-28
KR101943680B1 (ko) 2019-01-29
AU2012319549B2 (en) 2016-07-28
CA2861795A1 (en) 2013-04-11
RU2014112931A (ru) 2015-11-20
MX358149B (es) 2018-08-07
CY1117427T1 (el) 2017-04-26
AR088235A1 (es) 2014-05-21
IL231650A0 (en) 2014-05-28
HRP20160273T1 (hr) 2016-04-08
TWI562993B (en) 2016-12-21
ES2568015T3 (es) 2016-04-27
NZ622594A (en) 2015-06-26
PL2769980T3 (pl) 2016-07-29
PE20141557A1 (es) 2014-11-15
AU2012319549A1 (en) 2014-04-24
US20130143907A1 (en) 2013-06-06
CO6910200A2 (es) 2014-03-31
RU2605096C2 (ru) 2016-12-20
KR20140082684A (ko) 2014-07-02
DK2769980T3 (en) 2016-04-11
BR112014007912B1 (pt) 2022-06-07
IN2014CN02463A (sl) 2015-06-19
ZA201402439B (en) 2015-03-25
SG11201400717QA (en) 2014-06-27
CA2861795C (en) 2018-12-04
HUE028555T2 (en) 2016-12-28
IL231650A (en) 2016-05-31
TW201321379A (zh) 2013-06-01
CN103930423A (zh) 2014-07-16
JPWO2013051639A1 (ja) 2015-03-30
WO2013051639A1 (ja) 2013-04-11
SMT201600108B (it) 2016-04-29
JP5546693B2 (ja) 2014-07-09
RS54702B1 (en) 2016-08-31
EP2769980A1 (en) 2014-08-27
US8563565B2 (en) 2013-10-22
JO3116B1 (ar) 2017-09-20
US20130296352A1 (en) 2013-11-07
CN103930423B (zh) 2015-09-16
EP2769980A4 (en) 2015-02-25
HK1199018A1 (zh) 2015-06-19
MY167698A (en) 2018-09-21
CL2014000821A1 (es) 2014-07-25
ME02394B (me) 2016-09-20

Similar Documents

Publication Publication Date Title
IL273079B (en) Heterocycloamines as pi3k inhibitors
HK1199018A1 (zh) 作為 抑制劑的吡唑並喹啉衍生物
EP2683693A4 (en) ROR-GAMMA-T INHIBITORS
IL228707A0 (en) History of tetrahydroquinolines used as bromodomain inhibitors
EP2785183A4 (en) TRIAZOLOPYRIDINONE PDE10 INHIBITORS
AP3529A (en) Hydroxymethylaryl-substituted pyrrolotriazines as alk1 inhibitors
PL2588457T3 (pl) Pochodne pirazolochinolinowe jako inhibitory dna-pk
ZA201308697B (en) Hydroxymethylaryl-substituted pyprolotriazines as alk1 inhibitors
GB201120474D0 (en) Inhibitors