MA43518A - 3-azabicyclo[3.1.0]hexanes substitués servant d'inhibiteurs de cétohexokinase - Google Patents

3-azabicyclo[3.1.0]hexanes substitués servant d'inhibiteurs de cétohexokinase

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Publication number
MA43518A
MA43518A MA043518A MA43518A MA43518A MA 43518 A MA43518 A MA 43518A MA 043518 A MA043518 A MA 043518A MA 43518 A MA43518 A MA 43518A MA 43518 A MA43518 A MA 43518A
Authority
MA
Morocco
Prior art keywords
azabicyclo
serving
hexanes
substituted
ketohexokinase
Prior art date
Application number
MA043518A
Other languages
English (en)
Other versions
MA43518B1 (fr
Inventor
Matthew Dowling
Dilinie Fernando
Kentaro Futatsugi
Kim Huard
Thomas Victor Magee
Brian Raymer
Andre Shavnya
Aaron Smith
Benjamin Thuma
Andy Tsai
Meihua Tu
Original Assignee
Pfizer
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 Pfizer filed Critical Pfizer
Publication of MA43518A publication Critical patent/MA43518A/fr
Publication of MA43518B1 publication Critical patent/MA43518B1/fr

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • 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
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
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    • 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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    • 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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    • 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
    • C07D401/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
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    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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Abstract

L'invention concerne des 3-azabicyclo[3.1.0]hexanes substitués servant d'inhibiteurs de cétohexokinase, des procédés de fabrication de ces composés ainsi que des procédés comprenant l'administration desdits composés à un mammifère en ayant besoin.
MA43518A 2015-12-29 2016-12-16 3-azabicyclo[3.1.0]hexanes substitués servant d'inhibiteurs de cétohexokinase MA43518B1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201562272598P 2015-12-29 2015-12-29
US201662423549P 2016-11-17 2016-11-17
PCT/IB2016/057728 WO2017115205A1 (fr) 2015-12-29 2016-12-16 3-azabicyclo[3.1.0]hexanes substitués servant d'inhibiteurs de cétohexokinase

Publications (2)

Publication Number Publication Date
MA43518A true MA43518A (fr) 2018-11-07
MA43518B1 MA43518B1 (fr) 2021-05-31

Family

ID=57755415

Family Applications (1)

Application Number Title Priority Date Filing Date
MA43518A MA43518B1 (fr) 2015-12-29 2016-12-16 3-azabicyclo[3.1.0]hexanes substitués servant d'inhibiteurs de cétohexokinase

Country Status (39)

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US (6) US9809579B2 (fr)
EP (1) EP3397631B1 (fr)
JP (1) JP6503515B2 (fr)
KR (1) KR102073048B1 (fr)
CN (1) CN108473469B (fr)
AU (1) AU2016380920B2 (fr)
CA (1) CA2952466A1 (fr)
CL (1) CL2018001667A1 (fr)
CO (1) CO2018006714A2 (fr)
CU (1) CU24540B1 (fr)
CY (1) CY1124389T1 (fr)
DK (1) DK3397631T3 (fr)
EC (1) ECSP18048517A (fr)
ES (1) ES2871251T3 (fr)
GE (1) GEP20207147B (fr)
HK (1) HK1259073A1 (fr)
HR (1) HRP20210769T1 (fr)
HU (1) HUE054380T2 (fr)
IL (1) IL260330B (fr)
LT (1) LT3397631T (fr)
MA (1) MA43518B1 (fr)
MD (1) MD3397631T2 (fr)
MX (1) MX2018007755A (fr)
NI (1) NI201800072A (fr)
PE (1) PE20181289A1 (fr)
PH (1) PH12018501375A1 (fr)
PL (1) PL3397631T3 (fr)
PT (1) PT3397631T (fr)
RS (1) RS61896B1 (fr)
RU (1) RU2696269C1 (fr)
SG (1) SG11201804363UA (fr)
SI (1) SI3397631T1 (fr)
SV (1) SV2018005709A (fr)
TN (1) TN2018000198A1 (fr)
TW (1) TWI653232B (fr)
UA (1) UA121271C2 (fr)
UY (1) UY37051A (fr)
WO (1) WO2017115205A1 (fr)
ZA (1) ZA201803449B (fr)

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IL292968A (en) 2016-09-02 2022-07-01 Cyclerion Therapeutics Inc scg motors in converging cycles
CN109316601B (zh) * 2017-07-31 2021-11-09 武汉朗来科技发展有限公司 药物组合物及其用途
TWI707683B (zh) 2018-06-13 2020-10-21 美商輝瑞股份有限公司 Glp-1受體促效劑及其用途
CR20210110A (es) 2018-08-31 2021-05-13 Pfizer Combinaciones para tratamiento de ehna/ehgna y enfermedades relacionadas
TWI714231B (zh) * 2018-09-04 2020-12-21 美商美國禮來大藥廠 2,6-二胺基吡啶化合物
KR102558308B1 (ko) * 2018-09-27 2023-07-24 주식회사 엘지화학 3-아자바이사이클로[3,1,1]헵탄 유도체 및 이를 포함하는 약제학적 조성물
JP7248255B2 (ja) * 2019-01-29 2023-03-29 シャンドン スアンズ ファーマ カンパニー,リミテッド ヘキソングルコキナーゼ阻害剤およびその使用
CA3140972C (fr) 2019-05-20 2024-06-18 Pfizer Inc. Combinaisons comprenant du benzodioxol en tant qu'agonistes de glp-1r destinees a etre utilisees dans le traitement de la nash/nafld et de maladies associees
CN111978296A (zh) * 2019-05-22 2020-11-24 山东轩竹医药科技有限公司 己酮糖激酶抑制剂及其用途
JP2022534425A (ja) 2019-05-31 2022-07-29 イケナ オンコロジー, インコーポレイテッド Tead阻害剤およびその使用
TWI750685B (zh) 2019-06-17 2021-12-21 美商美國禮來大藥廠 二取代吡唑化合物
KR20220112811A (ko) 2019-12-10 2022-08-11 화이자 인코포레이티드 2-((4-((S)-2-(5-클로로피리딘-2-일)-2-메틸벤조[d][1,3]디옥솔-4-일)피페리딘-1-일)메틸)-1-(((S)-옥세탄-2-일)메틸)-1H-벤조[d]이미다졸-6-카르복실산, 1,3-디히드록시-2-(히드록시메틸)프로판-2-아민 염의 고체 형태
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CN114846008B (zh) * 2019-12-25 2024-05-28 杭州中美华东制药有限公司 具有果糖激酶(khk)抑制作用的嘧啶类化合物
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US20230167087A1 (en) * 2020-02-13 2023-06-01 Eli Lilly And Company 2-[2-methylazetidin-1-yl]-4-phenyl-6-(trifluoromethyl)-pyrimidine compounds
JP2022058085A (ja) 2020-02-24 2022-04-11 ファイザー・インク ジアシルグリセロールアシルトランスフェラーゼ2阻害剤とアセチル-CoAカルボキシラーゼ阻害剤との組合せ
JP2021134211A (ja) 2020-02-24 2021-09-13 ファイザー・インク Nafld/nashおよび関連疾患の処置のための組合せ
US20230201185A1 (en) 2020-03-27 2023-06-29 Pfizer Inc. Treatment of type 2 diabetes or obesity or overweight with 2-[(4-{6-[(4-cyano-2-fluorobenzyl)oxy]pyridin-2-yl}piperidin-1-yl)methyl]-1-[(2s)-oxetan-2-ylmethyl]-1h-benzimidazole-6-carboxylic acid or a pharmaceutically salt thereof
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