UY37051A - 3-azabiciclo[3.1.0]hexanos sustituidos como inhibidores de cetohexoquinasa - Google Patents

3-azabiciclo[3.1.0]hexanos sustituidos como inhibidores de cetohexoquinasa

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Publication number
UY37051A
UY37051A UY0001037051A UY37051A UY37051A UY 37051 A UY37051 A UY 37051A UY 0001037051 A UY0001037051 A UY 0001037051A UY 37051 A UY37051 A UY 37051A UY 37051 A UY37051 A UY 37051A
Authority
UY
Uruguay
Prior art keywords
inhibitors
cetohexoquinase
hexanos
azabiciclo
replaced
Prior art date
Application number
UY0001037051A
Other languages
English (en)
Inventor
Kentaro Futatsugi
Kim Huard
Benjamin Thuma
Brian Raymer
Matthew Dowling
Dilinie Fernando
Thomas Victor Magee
Andre Shavnya
Aaron Smith
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 UY37051A publication Critical patent/UY37051A/es

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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
    • C07D403/14Heterocyclic 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
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    • C07D401/14Heterocyclic 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 three or more hetero rings
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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
    • A61K31/40Heterocyclic 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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    • 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
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    • 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
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Abstract

En la presente se proporcionan 3-azabiciclo[3.1.0]hexanos sustituidos como inhibidores de cetohexoquinasa, procesos para la elaboración de estos compuestos, y métodos que comprenden administrar estos compuestos a un mamífero que lo necesita.
UY0001037051A 2015-12-29 2016-12-27 3-azabiciclo[3.1.0]hexanos sustituidos como inhibidores de cetohexoquinasa UY37051A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201562272598P 2015-12-29 2015-12-29
US201662423549P 2016-11-17 2016-11-17

Publications (1)

Publication Number Publication Date
UY37051A true UY37051A (es) 2017-07-31

Family

ID=57755415

Family Applications (1)

Application Number Title Priority Date Filing Date
UY0001037051A UY37051A (es) 2015-12-29 2016-12-27 3-azabiciclo[3.1.0]hexanos sustituidos como inhibidores de cetohexoquinasa

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

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KR20230124760A (ko) 2016-09-02 2023-08-25 사이클리온 테라퓨틱스, 인크. 융합된 비시클릭 sGC 자극제
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
US10934279B2 (en) 2018-06-13 2021-03-02 Pfizer Inc. GLP-1 receptor agonists and uses thereof
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
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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
BR112022010599A2 (pt) 2019-12-10 2022-08-16 Pfizer Formas sólidas de ácido 2-((4-((s)-2-(5-cloropiridin-2-il)-2-metilbenzo[d][1,3]dioxol-4-il)piperidin-1-il)metil)-1-(((s)-oxetan-2-il)metil)-1h-benzo[d]imidazol-6-carboxílico, sal de 1,3-dihidróxi-2-(hidroximetil)propan-2-amina
EP4083034A4 (en) * 2019-12-24 2023-12-06 Hangzhou Zhongmeihuadong Pharmaceutical Co., Ltd. ASSOCIATION WITH CHAD-INHIBITING EFFECT
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
GB202001856D0 (en) * 2020-02-11 2020-03-25 Inorbit Therapeutics Ab Compounds useful in inhibiting ketohexokinase and methods of making and using the same
US20230167087A1 (en) * 2020-02-13 2023-06-01 Eli Lilly And Company 2-[2-methylazetidin-1-yl]-4-phenyl-6-(trifluoromethyl)-pyrimidine compounds
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
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
JP2021155415A (ja) 2020-03-27 2021-10-07 ファイザー・インク 2−[(4−{6−[(4−シアノ−2−フルオロベンジル)オキシ]ピリジン−2−イル}ピペリジン−1−イル)メチル]−1−[(2s)−オキセタン−2−イルメチル]−1h−ベンゾイミダゾール−6−カルボン酸またはその薬学的な塩を用いた2型糖尿病、または肥満、または過体重の治療
WO2021215765A1 (ko) 2020-04-20 2021-10-28 주식회사 엘지화학 3-아자바이사이클로알킬 유도체 및 이를 포함하는 약제학적 조성물
CN111423420A (zh) * 2020-04-30 2020-07-17 广州博济医药生物技术股份有限公司 作为己酮糖激酶抑制剂的并环化合物
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