UY39199A - Nuevos inhibidores macrocíclicos de la quinasa de lrrk2 - Google Patents

Nuevos inhibidores macrocíclicos de la quinasa de lrrk2

Info

Publication number
UY39199A
UY39199A UY0001039199A UY39199A UY39199A UY 39199 A UY39199 A UY 39199A UY 0001039199 A UY0001039199 A UY 0001039199A UY 39199 A UY39199 A UY 39199A UY 39199 A UY39199 A UY 39199A
Authority
UY
Uruguay
Prior art keywords
lrrk2 kinase
novel macrocyclic
macrocyclic inhibitors
inhibitors
novel
Prior art date
Application number
UY0001039199A
Other languages
English (en)
Inventor
Lamotte Yann
Denis Alexis
Petra Marcella Blom
Christopher Gaétan Housseman
Daugan Alain
DUMOULIN Audrey
Laugeois Maxime
FAUCHER Nicolas
Botez Iuliana
Tiran Arnaud Le
CHRISTENSEN Kenneth
Original Assignee
Servier Lab
Oncodesign Sa
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 Servier Lab, Oncodesign Sa filed Critical Servier Lab
Publication of UY39199A publication Critical patent/UY39199A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/12Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
    • C07D498/16Peri-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
    • A61K31/41Heterocyclic 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
    • A61K31/4151,2-Diazoles
    • A61K31/41621,2-Diazoles condensed with heterocyclic ring systems
    • 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
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16Anti-Parkinson drugs
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/08Bridged systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/12Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
    • C07D498/18Bridged systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/12Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains three hetero rings
    • C07D513/18Bridged systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Neurosurgery (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Public Health (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Psychiatry (AREA)
  • Hospice & Palliative Care (AREA)
  • Epidemiology (AREA)
  • Psychology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)

Abstract

Compuestos de fórmula (I): en donde R, X1, X2, X3, Z1, Z2, Z3, A y Ra son como se han definido en la descripción. Medicamentos.
UY0001039199A 2020-05-06 2021-05-06 Nuevos inhibidores macrocíclicos de la quinasa de lrrk2 UY39199A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP20315236 2020-05-06
EP21305112 2021-01-28

Publications (1)

Publication Number Publication Date
UY39199A true UY39199A (es) 2021-11-30

Family

ID=75746649

Family Applications (1)

Application Number Title Priority Date Filing Date
UY0001039199A UY39199A (es) 2020-05-06 2021-05-06 Nuevos inhibidores macrocíclicos de la quinasa de lrrk2

Country Status (18)

Country Link
US (1) US20230357269A1 (es)
EP (1) EP4146658A1 (es)
JP (1) JP2023523863A (es)
KR (1) KR20230006560A (es)
CN (1) CN115996932A (es)
AU (1) AU2021267691A1 (es)
BR (1) BR112022022511A2 (es)
CA (1) CA3182162A1 (es)
CL (1) CL2022003070A1 (es)
CO (1) CO2022015871A2 (es)
CR (1) CR20220561A (es)
DO (1) DOP2022000242A (es)
IL (1) IL297867A (es)
MX (1) MX2022013861A (es)
PE (1) PE20230612A1 (es)
TW (1) TW202208379A (es)
UY (1) UY39199A (es)
WO (1) WO2021224320A1 (es)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2021226208A2 (en) 2020-05-05 2021-11-11 Nuvalent, Inc. Heteroaromatic macrocyclic ether chemotherapeutic agents
CA3205986A1 (en) 2020-12-30 2022-07-07 Tyra Biosciences, Inc. Indazole compounds as kinase inhibitors
TW202304935A (zh) * 2021-03-18 2023-02-01 法商施維雅藥廠 新穎的巨環lrrk2激酶抑制劑
KR20240087788A (ko) 2021-10-01 2024-06-19 뉴베일런트, 아이엔씨. 헤테로방향족 매크로사이클릭 에테르 화합물의 고체 형태, 약학 조성물 및 제조
CN117425660A (zh) * 2022-05-18 2024-01-19 上海翊石医药科技有限公司 一种芳杂环类化合物及其中间体、药物组合物和用途
WO2023240140A1 (en) * 2022-06-08 2023-12-14 Blossomhill Therapeutics, Inc. Indazole macrocycles and their use

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
UA113186C2 (xx) * 2011-09-30 2016-12-26 Макроциклічні інгібітори lrrk2 кінази
EP3035800B1 (en) * 2013-08-22 2019-10-09 Merck Sharp & Dohme Corp. Compounds inhibiting leucine-rich repeat kinase enzyme activity
ES2717510T3 (es) 2014-09-17 2019-06-21 Oncodesign Sa Inhibidores macrocíclicos de cinasa LRRK2
WO2018006931A1 (en) 2016-07-04 2018-01-11 Telefonaktiebolaget Lm Ericsson (Publ) Pipelined analog-to-digital converter
WO2018137618A1 (en) 2017-01-25 2018-08-02 Glaxosmithkline Intellectual Property Development Limited Compounds for inhibiting lrrk2 kinase activity
WO2018155916A2 (ko) 2017-02-22 2018-08-30 재단법인 대구경북첨단의료산업진흥재단 피롤로-피리미딘 유도체 화합물, 이의 제조방법 및 이를 유효성분으로 함유하는 단백질 키나아제 관련 질환의 예방 또는 치료용 약학적 조성물
WO2018163066A1 (en) 2017-03-10 2018-09-13 Pfizer Inc. Novel imidazo[4,5-c]quinoline derivatives as lrrk2 inhibitors
WO2018217946A1 (en) 2017-05-24 2018-11-29 Denali Therapeutics Inc. Compounds, compositions and methods
CN110891954A (zh) 2017-07-14 2020-03-17 葛兰素史密斯克莱知识产权发展有限公司 富含亮氨酸的重复激酶2的抑制剂
WO2019074809A1 (en) 2017-10-11 2019-04-18 Merck Sharp & Dohme Corp. INDAZOLYL-SPIRO [2.2] PENTANE-CARBONITRILE DERIVATIVES AS LRRK2 INHIBITORS, PHARMACEUTICAL COMPOSITIONS AND USES THEREOF
CN111433208B (zh) 2017-12-05 2023-06-30 奥斯考泰克公司 作为lrrk2抑制剂的吡咯并(吡唑并)嘧啶衍生物
US20210261553A1 (en) 2018-05-15 2021-08-26 E-Scape Bio, Inc. Fused tetrazoles as lrrk2 inhibitors
WO2019241540A1 (en) * 2018-06-15 2019-12-19 Samumed, Llc Indazole containing macrocycles and therapeutic uses thereof
TWI833770B (zh) 2018-06-27 2024-03-01 美商Ionis製藥公司 用於減少 lrrk2 表現之化合物及方法

Also Published As

Publication number Publication date
PE20230612A1 (es) 2023-04-13
CL2022003070A1 (es) 2023-07-07
JP2023523863A (ja) 2023-06-07
TW202208379A (zh) 2022-03-01
CN115996932A (zh) 2023-04-21
WO2021224320A1 (en) 2021-11-11
BR112022022511A2 (pt) 2022-12-13
CO2022015871A2 (es) 2022-12-30
DOP2022000242A (es) 2023-07-31
CR20220561A (es) 2023-02-17
US20230357269A1 (en) 2023-11-09
KR20230006560A (ko) 2023-01-10
AU2021267691A1 (en) 2022-12-08
CA3182162A1 (en) 2021-11-11
EP4146658A1 (en) 2023-03-15
IL297867A (en) 2023-01-01
MX2022013861A (es) 2023-02-22

Similar Documents

Publication Publication Date Title
CL2022003070A1 (es) Nuevos inhibidores macrocíclicos de la quinasa de lrrk2
CY1121867T1 (el) Αναστολεις jak2 και alk2 και μεθοδοι για τη χρηση τους
PH12021500015A1 (en) New heterocyclic compounds as monoacylglycerol lipase inhibitors
PH12018502513A1 (en) Sulfonamide compound or salt thereof
BR112021017620A2 (pt) Compostos macrocíclicos
CO6620025A2 (es) Inhibidores de la tirosina -quinasa de bruton
ATE469154T1 (de) Pyrazolopyrimidine als zellzyklus-kinasehemmer
UY29826A1 (es) Derivados de pirimidina, sales farmaceuticamente aceptables, esteres de los mismos hidrolisables in vivo, procesos de preparacion y aplicaciones
DOP2010000191A (es) Derivados bis-(sulfonilamino)
UY39680A (es) Nuevos inhibidores macrocíclicos de la quinasa de lrrk2
UA108240C2 (uk) Похідні гексафторізопропілкарбамату, їх одержання і їх терапевтичне застосування
MX2012007060A (es) Compuesto heterociclico conteniendo nitrogeno y fungicida para el uso en agricultura y jardineria.
MX2022002976A (es) Inhibidores selectivos de jak1.
UY30371A1 (es) Compuestos quimicos
ECSP089019A (es) Inhibidores de sulfonamida tricíclicos, fusionados del gama secretasa
WO2011143772A9 (en) Inhibitors of hiv replication
EA200900397A1 (ru) Новые соединения диосметина, способ их получения и фармацевтические композиции, которые их содержат
NZ603186A (en) Fluorescent carbapenems
CY1119402T1 (el) Παραγωγα κινολινης ως αντιβακτηριακοι παραγοντες
PH12020550253A1 (en) Bicyclic compounds for use as rip1 kinase inhibitors
CR11057A (es) Nuevos compuestos heterociclicos nitrogenados, su preparacion y su utilizacion como medicamentos antibacterianos
BR112022001125A2 (pt) Compostos macrocíclicos como agonistas de sting, seus métodos e seus usos
WO2011100838A9 (en) Derivatives of l-plienyl-1.5-diliydio-benzo[b] [1.4]diazepine-2.4-dione as inhibitors of hiv replication
MA32560B1 (fr) Nouveaux derives tricycliques, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
ECSP077378A (es) Isoxazoles sustituidos como fungicidas