HK1223367A1 - 新型 抑制劑 - Google Patents

新型 抑制劑

Info

Publication number
HK1223367A1
HK1223367A1 HK16111635.0A HK16111635A HK1223367A1 HK 1223367 A1 HK1223367 A1 HK 1223367A1 HK 16111635 A HK16111635 A HK 16111635A HK 1223367 A1 HK1223367 A1 HK 1223367A1
Authority
HK
Hong Kong
Prior art keywords
dgat2
novel
inhibitors
dgat2 inhibitors
novel dgat2
Prior art date
Application number
HK16111635.0A
Other languages
English (en)
Inventor
Nicholas Paul Camp
Manisha Naik
Original Assignee
Lilly Co Eli
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=52016867&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=HK1223367(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Lilly Co Eli filed Critical Lilly Co Eli
Publication of HK1223367A1 publication Critical patent/HK1223367A1/zh

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/32—One oxygen, sulfur or nitrogen atom
    • C07D239/42—One nitrogen atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic 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
    • C07D403/12—Heterocyclic 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 linked by a chain containing hetero atoms as chain links
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/16—Amides, e.g. hydroxamic acids
    • A61K31/18—Sulfonamides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/06—Antihyperlipidemics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Hematology (AREA)
  • Diabetes (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Obesity (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
HK16111635.0A 2013-11-25 2016-10-06 新型 抑制劑 HK1223367A1 (zh)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201361908339P 2013-11-25 2013-11-25
PCT/US2014/066339 WO2015077299A1 (en) 2013-11-25 2014-11-19 Novel dgat2 inhibitors

Publications (1)

Publication Number Publication Date
HK1223367A1 true HK1223367A1 (zh) 2017-07-28

Family

ID=52016867

Family Applications (1)

Application Number Title Priority Date Filing Date
HK16111635.0A HK1223367A1 (zh) 2013-11-25 2016-10-06 新型 抑制劑

Country Status (24)

Country Link
US (1) US9073901B2 (zh)
EP (1) EP3074381B1 (zh)
JP (1) JP6155395B2 (zh)
KR (1) KR20160072252A (zh)
CN (1) CN105764889B (zh)
AP (1) AP2016009230A0 (zh)
AR (1) AR098394A1 (zh)
AU (1) AU2014353109B2 (zh)
CA (1) CA2928468A1 (zh)
CL (1) CL2016001172A1 (zh)
CR (1) CR20160216A (zh)
DO (1) DOP2016000120A (zh)
EA (1) EA201690847A1 (zh)
ES (1) ES2695302T3 (zh)
HK (1) HK1223367A1 (zh)
IL (1) IL245245A0 (zh)
MA (1) MA39048B1 (zh)
MX (1) MX2016006665A (zh)
NZ (1) NZ719444A (zh)
PE (1) PE20161099A1 (zh)
PH (1) PH12016500963A1 (zh)
TN (1) TN2016000146A1 (zh)
TW (1) TW201609668A (zh)
WO (1) WO2015077299A1 (zh)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2982267C (en) * 2015-05-20 2019-11-12 Eli Lilly And Company Novel dgat2 inhibitors
AR109179A1 (es) 2016-08-19 2018-11-07 Pfizer Inhibidores de diacilglicerol aciltransferasa 2
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
EP4153584A1 (en) 2020-05-18 2023-03-29 Merck Sharp & Dohme LLC Novel diacylglyceride o-acyltransferase 2 inhibitors
TW202229243A (zh) 2020-10-08 2022-08-01 美商默沙東藥廠 作為新穎二醯基甘油酯o-醯基轉移酶2抑制劑之苯并咪唑酮衍生物的製備
CA3198344A1 (en) 2020-11-20 2022-05-27 Patrick T. GUNNING Methods and composition for kras modifications
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

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030170691A1 (en) 2001-12-19 2003-09-11 Millennium Pharmaceuticals, Inc. Human diacylglycerol acyltransferase 2 (DGAT2) family members and uses therefor
AU2003253925A1 (en) 2002-07-18 2004-02-09 Banyu Pharmaceutical Co., Ltd. Combination therapy for the treatment of obesity
US7825235B2 (en) 2003-08-18 2010-11-02 Isis Pharmaceuticals, Inc. Modulation of diacylglycerol acyltransferase 2 expression
CN1997640A (zh) * 2004-06-04 2007-07-11 艾尼纳制药公司 作为代谢调节剂的经取代芳基和杂芳基衍生物及其相关病症的预防和治疗
EP1807102A2 (en) 2004-10-29 2007-07-18 Merck & Co., Inc. Compositions and methods for the treatment of obesity and sexual dysfunction
WO2008129080A1 (en) 2007-04-24 2008-10-30 Ingenium Pharmaceuticals Gmbh 4, 6-disubstituted aminopyrimidine derivatives as inhibitors of protein kinases
WO2011078102A1 (ja) * 2009-12-22 2011-06-30 第一三共株式会社 新規フェノキシピリミジン誘導体
WO2011087857A2 (en) 2009-12-22 2011-07-21 The Administrators Of The Tulane Educational Fund Compositions and methods for treating obesity and diabetes
JP5921525B2 (ja) * 2010-03-22 2016-05-24 リード ディスカバリー センター ゲゼルシャフト ミット ベシュレンクテル ハフツング 医薬的に活性のある二置換のトリアジン誘導体
WO2012118563A2 (en) * 2011-03-03 2012-09-07 Vanderbilt University 6-alkyl-n-(pyridin-2-yl)-4-aryloxypicolinamide analogs as mglur5 negative allosteric modulators and methods of making and using the same
EP2561867A1 (en) 2011-08-22 2013-02-27 Lead Discovery Center GmbH CDK9 inhibitors in the treatment of midline carcinoma
EP2562265A1 (en) 2011-08-22 2013-02-27 Lead Discovery Center GmbH Susceptibility to selective CDK9 inhibitors
EP2834238B1 (en) * 2012-04-06 2017-02-01 Pfizer Inc. Diacylglycerol acyltransferase 2 inhibitors

Also Published As

Publication number Publication date
JP2016539115A (ja) 2016-12-15
AR098394A1 (es) 2016-05-26
WO2015077299A1 (en) 2015-05-28
CN105764889A (zh) 2016-07-13
IL245245A0 (en) 2016-06-30
DOP2016000120A (es) 2016-06-15
PH12016500963A1 (en) 2016-06-20
ES2695302T3 (es) 2019-01-03
CL2016001172A1 (es) 2016-12-09
AP2016009230A0 (en) 2016-05-31
MA39048A1 (fr) 2017-05-31
NZ719444A (en) 2017-12-22
CA2928468A1 (en) 2015-05-28
AU2014353109A1 (en) 2016-05-12
TW201609668A (zh) 2016-03-16
CR20160216A (es) 2016-06-27
EP3074381A1 (en) 2016-10-05
PE20161099A1 (es) 2016-10-22
US9073901B2 (en) 2015-07-07
MX2016006665A (es) 2016-07-26
KR20160072252A (ko) 2016-06-22
MA39048B1 (fr) 2018-04-30
US20150148358A1 (en) 2015-05-28
JP6155395B2 (ja) 2017-06-28
TN2016000146A1 (en) 2017-10-06
EP3074381B1 (en) 2018-07-04
EA201690847A1 (ru) 2016-09-30
CN105764889B (zh) 2018-01-02
AU2014353109B2 (en) 2017-02-02

Similar Documents

Publication Publication Date Title
HRP20190373T1 (hr) Inhibitori dnk-pk
HK1220459A1 (zh) 激酶抑制劑
HK1212696A1 (zh) 抑制劑
RS57306B1 (sr) Inhibitori dnk-pk
IL265496A (en) bace1 inhibitors
HK1211578A1 (zh) 作為 激酶抑制劑的酰氨基咪唑並噠嗪
HK1216531A1 (zh) 新的抑制劑
HK1219104A1 (zh) 激酶抑制劑
HK1223367A1 (zh) 新型 抑制劑
HK1222339A1 (zh) 金屬-β-內酰胺酶的抑制劑
IL240763A0 (en) The halopyrazoles as thrombin inhibitors
HK1217950A1 (zh) 新型 抑制劑
GB201305503D0 (en) Inhibitor
GB201307155D0 (en) Kinase inhibitors