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EA201990851A1 - NEW CARBANUCLEOSIDE ANALOGUES REPLACED BY MONOCYCLIC AND BICYCLIC RING SYSTEM FOR USE AS PRMT5 INHIBITORS - Google Patents

NEW CARBANUCLEOSIDE ANALOGUES REPLACED BY MONOCYCLIC AND BICYCLIC RING SYSTEM FOR USE AS PRMT5 INHIBITORS

Info

Publication number
EA201990851A1
EA201990851A1 EA201990851A EA201990851A EA201990851A1 EA 201990851 A1 EA201990851 A1 EA 201990851A1 EA 201990851 A EA201990851 A EA 201990851A EA 201990851 A EA201990851 A EA 201990851A EA 201990851 A1 EA201990851 A1 EA 201990851A1
Authority
EA
Eurasian Patent Office
Prior art keywords
monocyclic
ring system
bicyclic ring
new
prmt5 inhibitors
Prior art date
Application number
EA201990851A
Other languages
Russian (ru)
Inventor
Тонгфей Ву
Дирк Бремер
Лейс Беке
Ан Буккс
Гастон Станислас Марселла Дилс
Эдвард Чарльз Лосон
Ливен Мерпул
Винет Панде
Маркус Корнелис Бернардус Катарина Параде
Вим Берт Грит Схепенс
Вэймэй Сунь
Йоханнес Вильхельмус Йохн Ф. Тюринг
Марсель Вьейевуа
Original Assignee
Янссен Фармацевтика Нв
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 Янссен Фармацевтика Нв filed Critical Янссен Фармацевтика Нв
Publication of EA201990851A1 publication Critical patent/EA201990851A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • 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
    • A61P37/00Drugs for immunological or allergic disorders
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Immunology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Настоящее изобретение относится к новым аналогам карбануклеозида, замещенным моноциклической и бициклической кольцевой системой, формулы (I)где переменные имеют значения, определенные в формуле изобретения. Соединения согласно настоящему изобретению являются пригодными в качестве ингибиторов PRMT5. Кроме того, настоящее изобретение относится к фармацевтическим композициям, содержащим указанные соединения в качестве активного ингредиента, а также к применению указанных соединений в качестве лекарственного препарата.The present invention relates to new analogues of carbanucleoside substituted by a monocyclic and bicyclic ring system, formula (I) where the variables have the meanings defined in the claims. The compounds of the present invention are useful as PRMT5 inhibitors. In addition, the present invention relates to pharmaceutical compositions containing said compounds as an active ingredient, and also to the use of said compounds as a medicine.

EA201990851A 2017-02-24 2017-10-02 NEW CARBANUCLEOSIDE ANALOGUES REPLACED BY MONOCYCLIC AND BICYCLIC RING SYSTEM FOR USE AS PRMT5 INHIBITORS EA201990851A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP17157785 2017-02-24
PCT/EP2017/074983 WO2018065365A1 (en) 2016-10-03 2017-10-02 Novel monocyclic and bicyclic ring system substituted carbanucleoside analogues for use as prmt5 inhibitors

Publications (1)

Publication Number Publication Date
EA201990851A1 true EA201990851A1 (en) 2019-09-30

Family

ID=58158964

Family Applications (1)

Application Number Title Priority Date Filing Date
EA201990851A EA201990851A1 (en) 2017-02-24 2017-10-02 NEW CARBANUCLEOSIDE ANALOGUES REPLACED BY MONOCYCLIC AND BICYCLIC RING SYSTEM FOR USE AS PRMT5 INHIBITORS

Country Status (2)

Country Link
EA (1) EA201990851A1 (en)
WO (1) WO2018065365A1 (en)

Families Citing this family (30)

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UA123637C2 (en) 2016-03-10 2021-05-05 Янссен Фармацевтика Нв SUBSTITUTED NUCLEOSIDE ANALOGUES FOR USE AS PRMT5 INHIBITORS
US11098062B2 (en) 2016-10-03 2021-08-24 Janssen Pharmaceutica Nv Monocyclic and bicyclic ring system substituted carbanucleoside analogues for use as PRMT5 inhibitors
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ES2978117T3 (en) 2017-12-08 2024-09-05 Janssen Pharmaceutica Nv New spirobicyclic analogues
PE20211444A1 (en) * 2017-12-13 2021-08-05 Lupin Ltd BICYCLE HETEROCYCLIC COMPONENTS REPLACED AS PRMT5 INHIBITORS
US10711007B2 (en) 2018-03-14 2020-07-14 Prelude Therapeutics Incorporated Selective inhibitors of protein arginine methyltransferase 5 (PRMT5)
DK3765461T3 (en) 2018-03-14 2023-11-20 Prelude Therapeutics Inc SELECTIVE PROTEIN ARGININE METHYL TRANSFERASE 5 (PRMT5) INHIBITORS
AU2019317549A1 (en) * 2018-08-07 2021-02-25 Msd International Gmbh PRMT5 inhibitors
EP3833669A4 (en) * 2018-08-07 2022-05-11 Merck Sharp & Dohme Corp. PRMT5 INHIBITORS
GB201819621D0 (en) 2018-11-30 2019-01-16 Sumitomo Chemical Co Photoactive compound
EP3947387B1 (en) * 2019-03-25 2024-10-23 California Institute Of Technology Prmt5 inhibitors and uses thereof
BR112021019465A8 (en) 2019-04-02 2022-06-07 Aligos Therapeutics Inc Compounds that target prmt5
EP3947390A4 (en) * 2019-04-03 2022-11-30 Mitokinin, Inc. COMPOSITIONS AND METHOD OF USE THEREOF FOR TREATING NEURODEGENERATIVE AND MITOCHONDRIAL DISEASE
KR20220016194A (en) * 2019-05-30 2022-02-08 앤젝스 파마수티컬, 인크. Heterocyclic compounds as PRMT5 inhibitors
TW202112375A (en) 2019-06-06 2021-04-01 比利時商健生藥品公司 Methods of treating cancer using prmt5 inhibitors
ES2967457T3 (en) 2019-06-10 2024-04-30 Lupin Ltd PRMT5 inhibitors
AU2020290672A1 (en) 2019-06-12 2022-02-10 Janssen Pharmaceutica Nv Novel spirobicyclic intermediates
JP2022553077A (en) * 2019-10-21 2022-12-21 アクセント・セラピューティクス・インコーポレイテッド METTL3 modulator
PE20221154A1 (en) * 2019-10-22 2022-07-18 Lupin Ltd PHARMACEUTICAL COMBINATION OF PRMT5 INHIBITORS
MX2022006735A (en) 2019-12-03 2022-07-21 Lupin Ltd Substituted nucleoside analogs as prmt5 inhibitors.
WO2021202480A1 (en) * 2020-04-01 2021-10-07 Aligos Therapeutics, Inc. Compounds targeting prmt5
US20240101589A1 (en) * 2020-10-08 2024-03-28 Strom Therapeutics Limited Inhibitors of mettl3
WO2024229406A1 (en) 2023-05-04 2024-11-07 Revolution Medicines, Inc. Combination therapy for a ras related disease or disorder
US20250049810A1 (en) 2023-08-07 2025-02-13 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
WO2025049624A1 (en) * 2023-08-29 2025-03-06 Purdue Research Foundation Prodrugs of nicotinamide n-methyltransferase (nnmt) inhibitors and uses thereof
US20250154171A1 (en) 2023-10-12 2025-05-15 Revolution Medicines, Inc. Ras inhibitors

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JP2016505002A (en) 2012-12-21 2016-02-18 エピザイム,インコーポレイティド PRMT5 inhibitors containing dihydroisoquinoline or tetrahydroisoquinoline and uses thereof
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Also Published As

Publication number Publication date
WO2018065365A1 (en) 2018-04-12

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