MA42678B1 - Nouveaux analogues nucléosidiques substitués à cycle aromatique bicyclique 6-6 pour une utilisation en tant qu'inhibiteurs de prmt5 - Google Patents

Nouveaux analogues nucléosidiques substitués à cycle aromatique bicyclique 6-6 pour une utilisation en tant qu'inhibiteurs de prmt5

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Publication number
MA42678B1
MA42678B1 MA42678A MA42678A MA42678B1 MA 42678 B1 MA42678 B1 MA 42678B1 MA 42678 A MA42678 A MA 42678A MA 42678 A MA42678 A MA 42678A MA 42678 B1 MA42678 B1 MA 42678B1
Authority
MA
Morocco
Prior art keywords
bicyclic aromatic
nucleoside analogs
substituted nucleoside
prmt5 inhibitors
new substituted
Prior art date
Application number
MA42678A
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English (en)
Other versions
MA42678A (fr
Inventor
Lieven Meerpoel
Gaston Diels
Marcel Viellevoye
Tongfei Wu
Dirk Brehmer
Lijs Beke
An Boeckx
Ronaldus Gilissen
Edward Lawson
Vineet Pande
Marcus Parade
Wim Schepens
Johannes Thuring
Weimei Sun
Original Assignee
Janssen Pharmaceutica Nv
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Publication date
Application filed by Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Publication of MA42678A publication Critical patent/MA42678A/fr
Publication of MA42678B1 publication Critical patent/MA42678B1/fr

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    • A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
    • A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
    • A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
    • A61K31/7076—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines containing purines, e.g. adenosine, adenylic acid
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic 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
    • A61K31/50—Pyridazines; Hydrogenated pyridazines
    • A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
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    • A61K31/495—Heterocyclic 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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    • A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
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    • C07D471/02—Heterocyclic 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
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    • C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/23—Heterocyclic radicals containing two or more heterocyclic rings condensed among themselves or condensed with a common carbocyclic ring system, not provided for in groups C07H19/14 - C07H19/22
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Abstract

La présente invention concerne des analogues nucléosidiques substitués par un cycle aromatique bicyclique 6-6 de formule (i) dans laquelle les variables sont telles que définies dans les revendications. Les composés selon la présente invention sont utiles comme inhibiteurs de prmt5. L'invention concerne en outre des compositions pharmaceutiques comprenant lesdits composés comme principe actif ainsi que l'utilisation desdits composés comme médicament.
MA42678A 2015-08-26 2016-08-25 Nouveaux analogues nucléosidiques substitués à cycle aromatique bicyclique 6-6 pour une utilisation en tant qu'inhibiteurs de prmt5 MA42678B1 (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201562209941P 2015-08-26 2015-08-26
EP15184011 2015-09-07
US201662306233P 2016-03-10 2016-03-10
PCT/EP2016/070097 WO2017032840A1 (fr) 2015-08-26 2016-08-25 Nouveaux analogues nucléosidiques substitués par un cycle aromatique bicyclique 6-6 utiles comme inhibiteurs de prmt5

Publications (2)

Publication Number Publication Date
MA42678A MA42678A (fr) 2021-05-19
MA42678B1 true MA42678B1 (fr) 2021-11-30

Family

ID=54065259

Family Applications (1)

Application Number Title Priority Date Filing Date
MA42678A MA42678B1 (fr) 2015-08-26 2016-08-25 Nouveaux analogues nucléosidiques substitués à cycle aromatique bicyclique 6-6 pour une utilisation en tant qu'inhibiteurs de prmt5

Country Status (34)

Country Link
US (4) US10653711B2 (fr)
EP (3) EP3341368B1 (fr)
JP (3) JP6917978B2 (fr)
KR (1) KR20180041222A (fr)
CN (2) CN107922413B (fr)
AR (1) AR105820A1 (fr)
AU (4) AU2016311295B2 (fr)
BR (2) BR112018003595B1 (fr)
CA (1) CA2992688A1 (fr)
CL (1) CL2018000510A1 (fr)
CO (1) CO2018002063A2 (fr)
CY (1) CY1125359T1 (fr)
DK (1) DK3341368T3 (fr)
EA (1) EA201890573A1 (fr)
ES (1) ES2901972T3 (fr)
HK (2) HK1253898A1 (fr)
HR (1) HRP20211997T1 (fr)
HU (1) HUE057312T2 (fr)
IL (3) IL311843A (fr)
LT (1) LT3341368T (fr)
MA (1) MA42678B1 (fr)
MD (1) MD3341368T2 (fr)
MX (2) MX2018002326A (fr)
MY (1) MY198472A (fr)
PE (2) PE20221629A1 (fr)
PH (1) PH12018500425A1 (fr)
PL (1) PL3341368T3 (fr)
PT (1) PT3341368T (fr)
RS (1) RS62698B1 (fr)
SG (1) SG10202003775VA (fr)
SI (1) SI3341368T1 (fr)
TN (1) TN2018000043A1 (fr)
TW (3) TWI730980B (fr)
WO (1) WO2017032840A1 (fr)

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UA123637C2 (uk) * 2016-03-10 2021-05-05 Янссен Фармацевтика Нв Заміщені аналоги нуклеозидів для застосування як інгібіторів prmt5
CA2969295A1 (fr) 2016-06-06 2017-12-06 Pfizer Inc. Derives de carbonucleosides substitues et leur utilisation comme inhibiteur de prmt5
EP3512858B1 (fr) 2016-09-14 2023-11-08 Janssen Pharmaceutica NV Inhibiteur bicyclique fusionné d'interaction menin-mll
KR102493644B1 (ko) 2016-09-14 2023-01-30 얀센 파마슈티카 엔.브이. 메닌-mll 상호작용의 스피로 바이사이클릭 억제제
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KR102513564B1 (ko) 2016-12-15 2023-03-22 얀센 파마슈티카 엔.브이. 메닌-mll 상호작용의 아제판 억제제
GB201700526D0 (en) * 2017-01-12 2017-03-01 Univ Of Hull Therapeutic use
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DK3724190T3 (da) * 2017-12-13 2022-10-10 Lupin Ltd Substituerede bicykliske heterocykliske forbindelser som PRMT5 inhibitorer
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CN109369507A (zh) * 2018-12-26 2019-02-22 重庆市碚圣医药科技股份有限公司 一种n-(2,2-二乙氧基乙基)邻苯二甲酰亚胺的提纯方法
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CN114072407A (zh) 2019-04-02 2022-02-18 阿里戈斯治疗公司 靶向prmt5的化合物
WO2020206289A1 (fr) * 2019-04-05 2020-10-08 Prelude Therapeutics, Incorporated Inhibiteurs sélectifs de la protéine arginine méthyltransférase 5
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CN114126614A (zh) * 2019-05-30 2022-03-01 安杰斯制药公司 作为prmt5抑制剂的杂环化合物
TW202112375A (zh) 2019-06-06 2021-04-01 比利時商健生藥品公司 使用ｐｒｍｔ５抑制劑治療癌症之方法
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CA3154566A1 (fr) * 2019-09-18 2021-03-25 Prelude Therapeutics Incorporated Inhibiteurs selectifs de la proteine arginine methyltransferase 5 (prmt5)
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GB201915447D0 (en) * 2019-10-24 2019-12-11 Johnson Matthey Plc Polymorphs of avapritinib and methods of preparing the polymorphs
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CN111233869B (zh) * 2020-03-12 2022-09-16 杭州新博思生物医药有限公司 用于制备瑞德西韦关键中间体的新化合物及其制备方法
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