MD20140103A2 - Inhibitori ai diacilglicerol aciltransferazei 2 - Google Patents

Inhibitori ai diacilglicerol aciltransferazei 2

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Publication number
MD20140103A2
MD20140103A2 MDA20140103A MD20140103A MD20140103A2 MD 20140103 A2 MD20140103 A2 MD 20140103A2 MD A20140103 A MDA20140103 A MD A20140103A MD 20140103 A MD20140103 A MD 20140103A MD 20140103 A2 MD20140103 A2 MD 20140103A2
Authority
MD
Moldova
Prior art keywords
diacylglycerol acyltransferase
inhibitors
dgat2
imidazo
compounds
Prior art date
Application number
MDA20140103A
Other languages
English (en)
Moldavian (mo)
Russian (ru)
Inventor
К Эн
Маркус БОЭМ
Шон КАБРАЛ
Филипп А. КАПРИНО
Кентаро Футацуги
Дэвид Хепуорт
Дэниел В. КУН
Суви ОРР
Цзянь ВАН
Original Assignee
Pfizer Inc.
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=48428540&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MD20140103(A2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Pfizer Inc. filed Critical Pfizer Inc.
Publication of MD20140103A2 publication Critical patent/MD20140103A2/ro

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-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
    • A61K31/435Heterocyclic 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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    • 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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    • 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
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/5381,4-Oxazines, e.g. morpholine ortho- or peri-condensed with carbocyclic ring systems
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Abstract

Invenţia se referă la noi compuşi farmaceutici, inhibitori ai activităţii diacilglicerol aciltransferazei 2 (DGAT2), la compoziţii farmaceutice care conţin aceşti compuşi şi la utilizarea lor în tratamentul bolilor asociate cu DGAT2 la animale.Sunt descrişi derivaţi ai purinei, 3H-imidazo[4,5-b]pirimidinei şi 1H-imidazo[4,5-d]pirazinei cu formula I:de exemplu, compusul 109-B:
MDA20140103A 2012-04-06 2013-03-26 Inhibitori ai diacilglicerol aciltransferazei 2 MD20140103A2 (ro)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201261621144P 2012-04-06 2012-04-06
PCT/IB2013/052404 WO2013150416A1 (en) 2012-04-06 2013-03-26 Diacylglycerol acyltransferase 2 inhibitors

Publications (1)

Publication Number Publication Date
MD20140103A2 true MD20140103A2 (ro) 2015-01-31

Family

ID=48428540

Family Applications (1)

Application Number Title Priority Date Filing Date
MDA20140103A MD20140103A2 (ro) 2012-04-06 2013-03-26 Inhibitori ai diacilglicerol aciltransferazei 2

Country Status (27)

Country Link
US (1) US9296745B2 (ro)
EP (1) EP2834238B1 (ro)
JP (1) JP2015515472A (ro)
KR (1) KR20140137404A (ro)
CN (1) CN104334557A (ro)
AP (1) AP2014007953A0 (ro)
AU (1) AU2013245353A1 (ro)
CA (1) CA2869587A1 (ro)
CL (1) CL2014002541A1 (ro)
CO (1) CO7160030A2 (ro)
CR (1) CR20140468A (ro)
CU (1) CU20140115A7 (ro)
DO (1) DOP2014000225A (ro)
EA (1) EA201400990A1 (ro)
EC (1) ECSP14021251A (ro)
GT (1) GT201400213A (ro)
HK (1) HK1206735A1 (ro)
IL (1) IL234928A0 (ro)
MA (1) MA37385B1 (ro)
MD (1) MD20140103A2 (ro)
MX (1) MX2014011373A (ro)
NI (1) NI201400120A (ro)
PE (1) PE20142164A1 (ro)
PH (1) PH12014502057A1 (ro)
SG (1) SG11201405477XA (ro)
TN (1) TN2014000419A1 (ro)
WO (1) WO2013150416A1 (ro)

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US9255154B2 (en) 2012-05-08 2016-02-09 Alderbio Holdings, Llc Anti-PCSK9 antibodies and use thereof
AR098394A1 (es) * 2013-11-25 2016-05-26 Lilly Co Eli Inhibidores de dgat2 (diacilglicerol o-aciltransferasa 2)
JP6152229B2 (ja) * 2014-03-17 2017-06-21 ファイザー・インク 代謝性および関連障害の処置において使用するための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
CN107567443B (zh) * 2014-12-24 2023-04-28 株式会社Lg化学 作为gpr120激动剂的联芳基衍生物
US10053429B2 (en) 2015-05-20 2018-08-21 Eli Lilly And Company DGAT2 inhibitors
MX2018000412A (es) * 2015-07-10 2018-03-14 Ionis Pharmaceuticals Inc Moduladores de diaciglicerol aciltransferasa 2 (dgat2).
WO2017143011A1 (en) * 2016-02-16 2017-08-24 Chrysalis, Inc. Histone demethylase inhibitors
AR109179A1 (es) 2016-08-19 2018-11-07 Pfizer Inhibidores de diacilglicerol aciltransferasa 2
TWI841671B (zh) 2019-01-24 2024-05-11 日商第一三共股份有限公司 具有取代基之脲化合物
TWI771766B (zh) 2019-10-04 2022-07-21 美商輝瑞股份有限公司 二醯基甘油醯基轉移酶2 抑制劑
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
CN111214449B (zh) * 2020-03-02 2021-09-07 广东彼迪药业有限公司 一种盐酸西替利嗪片剂及其制备方法
US11478533B2 (en) 2020-04-27 2022-10-25 Novo Nordisk A/S Semaglutide for use in medicine
AR122092A1 (es) 2020-05-18 2022-08-10 Merck Sharp & Dohme Inhibidores de diacilglicerol o-aciltransferasa 2
TWI817191B (zh) * 2020-09-04 2023-10-01 南韓商Lg化學股份有限公司 新穎聯芳基衍生物及其作為針對二醯基甘油醯基轉移酶2之抑制劑之用途
IL301791A (en) 2020-10-08 2023-05-01 Merck Sharp ַ& Dohme Llc Preparation of benzimidazolone derivatives as new inhibitors of diacylglyceride O-acyltransferase-2
WO2023026180A1 (en) 2021-08-26 2023-03-02 Pfizer Inc. Amorphous form of (s)-2-(5-((3-ethoxypyridin-2-yl)oxy)pyridin-3-yl)-n-(tetrahydrofuran-3- yl)pyrimidine-5-carboxamide
WO2023159154A1 (en) * 2022-02-18 2023-08-24 Bristol-Myers Squibb Company Substituted imidazopyridinyl compounds useful as inhibitors of tlr9
US20240254114A1 (en) 2022-12-02 2024-08-01 Merck Sharp & Dohme Llc Preparation of fused azole derivatives as novel diacylglyceride 0-acyltransferase 2 inhibitors

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KR20140137404A (ko) 2014-12-02
DOP2014000225A (es) 2014-11-30
GT201400213A (es) 2015-06-02
AP2014007953A0 (en) 2014-09-30
NI201400120A (es) 2015-11-18
MA201637385A2 (fr) 2016-03-31
EP2834238B1 (en) 2017-02-01
HK1206735A1 (en) 2016-01-15
CO7160030A2 (es) 2015-01-15
ECSP14021251A (es) 2015-09-30
PE20142164A1 (es) 2014-12-27
WO2013150416A1 (en) 2013-10-10
CN104334557A (zh) 2015-02-04
TN2014000419A1 (fr) 2016-03-30
EA201400990A1 (ru) 2015-01-30
SG11201405477XA (en) 2014-11-27
JP2015515472A (ja) 2015-05-28
CA2869587A1 (en) 2013-10-10
CU20140115A7 (es) 2014-11-27
MX2014011373A (es) 2014-10-14
AU2013245353A1 (en) 2014-09-25
EP2834238A1 (en) 2015-02-11
CL2014002541A1 (es) 2015-01-16
IL234928A0 (en) 2014-12-31
MA37385A3 (fr) 2016-12-30
PH12014502057A1 (en) 2014-12-10
CR20140468A (es) 2014-11-17
MA37385B1 (fr) 2019-09-30

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