CA2857521C - Leukotriene b4 antagonist compound - Google Patents

Leukotriene b4 antagonist compound Download PDF

Info

Publication number
CA2857521C
CA2857521C CA2857521A CA2857521A CA2857521C CA 2857521 C CA2857521 C CA 2857521C CA 2857521 A CA2857521 A CA 2857521A CA 2857521 A CA2857521 A CA 2857521A CA 2857521 C CA2857521 C CA 2857521C
Authority
CA
Canada
Prior art keywords
compound
pharmaceutically acceptable
propyl
ltb4
atherosclerosis
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Fee Related
Application number
CA2857521A
Other languages
English (en)
French (fr)
Other versions
CA2857521A1 (en
Inventor
Douglas Richard Stack
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Eli Lilly and Co
Original Assignee
Eli Lilly and Co
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 Eli Lilly and Co filed Critical Eli Lilly and Co
Publication of CA2857521A1 publication Critical patent/CA2857521A1/en
Application granted granted Critical
Publication of CA2857521C publication Critical patent/CA2857521C/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00—Carboxylic acid amides
    • C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/16—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
    • C07C233/24—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring
    • C07C233/25—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • 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)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Vascular Medicine (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Urology & Nephrology (AREA)
  • Immunology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Rheumatology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
CA2857521A 2012-01-10 2013-01-04 Leukotriene b4 antagonist compound Expired - Fee Related CA2857521C (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201261584975P 2012-01-10 2012-01-10
US61/584,975 2012-01-10
US201261585799P 2012-01-12 2012-01-12
US61/585,799 2012-01-12
PCT/US2013/020195 WO2013106238A1 (en) 2012-01-10 2013-01-04 Leukotriene b4 antagonist compound

Publications (2)

Publication Number Publication Date
CA2857521A1 CA2857521A1 (en) 2013-07-18
CA2857521C true CA2857521C (en) 2016-03-01

Family

ID=47604162

Family Applications (1)

Application Number Title Priority Date Filing Date
CA2857521A Expired - Fee Related CA2857521C (en) 2012-01-10 2013-01-04 Leukotriene b4 antagonist compound

Country Status (14)

Country Link
US (1) US9187411B2 (enExample)
EP (1) EP2802557B1 (enExample)
JP (1) JP2015509917A (enExample)
KR (1) KR20140099546A (enExample)
CN (1) CN104011012B (enExample)
AU (1) AU2013208260A1 (enExample)
BR (1) BR112014016450A2 (enExample)
CA (1) CA2857521C (enExample)
EA (1) EA023067B1 (enExample)
ES (1) ES2571452T3 (enExample)
IN (1) IN2014MN01014A (enExample)
MX (1) MX2014008452A (enExample)
WO (1) WO2013106238A1 (enExample)
ZA (1) ZA201404732B (enExample)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10370368B2 (en) 2015-11-30 2019-08-06 Merck Sharp & Dohme Corp. Aryl acylsulfonamides as BLT1 antagonists
WO2017095725A1 (en) 2015-11-30 2017-06-08 Merck Sharp & Dohme Corp. Aryl sulfonamides as blt1 antagonists
US10336733B2 (en) 2015-11-30 2019-07-02 Merk Sharp & Dohme Corp. Aryl acylsulfonamides as BLT1 antagonists
WO2017095724A1 (en) 2015-11-30 2017-06-08 Merck Sharp & Dohme Corp. Aryl sulfonamides as blt1 antagonists

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5105017A (en) * 1983-07-18 1992-04-14 Eli Lilly And Company Leukotriene antagonist intermediates
GB9027023D0 (en) 1990-12-12 1991-01-30 Wellcome Found Anti-atherosclerotic aryl compounds
PH30449A (en) 1991-11-25 1997-05-28 Lilly Co Eli Substituted phenyl phenol leukotriene antagonists
CN1035001C (zh) * 1993-01-02 1997-05-28 伊莱利利公司 取代的苯基苯酚基白三烯拮抗物
WO1996036347A1 (en) 1995-05-17 1996-11-21 Eli Lilly And Company Use of leukotriene antagonists for alzheimer's disease
WO1998042346A1 (en) 1997-03-21 1998-10-01 Eli Lilly And Company Leukotriene antagonists useful for treating ischemia reperfusion injury
EP1231939A2 (en) 1999-11-11 2002-08-21 Eli Lilly And Company Oncolytic combinations for the treatment of cancer
WO2001034198A2 (en) 1999-11-11 2001-05-17 Eli Lilly And Company Oncolytic combinations for the treatment of cancer
CN1237968C (zh) 2000-05-09 2006-01-25 克赖顿大学 抑制癌细胞的增殖和诱导其凋亡的方法
EP1286982A2 (en) * 2000-06-02 2003-03-05 Eli Lilly & Company Process for the preparation of benzoyl substituted bicylic compounds and chiral bnezopyran derivatives
CN1751037A (zh) 2003-02-14 2006-03-22 伊莱利利公司 作为ppar调节剂的磺酰胺衍生物

Also Published As

Publication number Publication date
US9187411B2 (en) 2015-11-17
EP2802557B1 (en) 2016-04-06
JP2015509917A (ja) 2015-04-02
CA2857521A1 (en) 2013-07-18
KR20140099546A (ko) 2014-08-12
EA201491099A1 (ru) 2014-11-28
AU2013208260A1 (en) 2014-06-05
CN104011012A (zh) 2014-08-27
EP2802557A1 (en) 2014-11-19
IN2014MN01014A (enExample) 2015-07-03
CN104011012B (zh) 2016-01-20
MX2014008452A (es) 2014-08-27
WO2013106238A1 (en) 2013-07-18
US20140343151A1 (en) 2014-11-20
ES2571452T3 (es) 2016-05-25
BR112014016450A2 (pt) 2019-09-24
EA023067B1 (ru) 2016-04-29
ZA201404732B (en) 2015-11-25

Similar Documents

Publication Publication Date Title
US6562846B2 (en) Bisarylimidazolyl fatty acid amide hydrolase inhibitors
JP6800922B2 (ja) 皮膚の疾患、障害、および異常の治療のための肝臓x受容体(lxr)調節因子
JP3731827B2 (ja) アミノメチルインダン、‐ベンゾフラン及び‐ベンゾチオフエン
EP1536799A1 (en) Novel 2-amino-4-oxoquinazolones as lxr nuclear receptor binding compounds with partial agonistic properties
JPH09507069A (ja) アルツハイマー病の処置のためのpla▲下2▼阻害剤の使用
US9187411B2 (en) Leukotriene B4 antagonist compound
JP2006514614A (ja) 11β−ヒドロキシステロイドデヒドロゲナーゼ1型および2型のインヒビター
EP2567698B1 (en) GPR 17 agonists and screening assay
Sridhar et al. New bivalent PKC ligands linked by a carbon spacer: enhancement in binding affinity
Kamata et al. Melanin-Concentrating Hormone Receptor 1 Antagonists. Synthesis and Structure–Activity Relationships of Novel 3-(Aminomethyl) quinolines
JP2007502263A (ja) アントラニル酸誘導体およびhm74a受容体のアクチベーターとしてのその使用
US20130210883A1 (en) Lipase inhibitors
HUE033574T2 (hu) Fenoxietil-dihidro-1H-izokinolin-vegyületek
JP2003504644A (ja) Scapアンタゴニストである治療剤のスクリーニング
CZ290968B6 (cs) Léčivo pro léčení zánětlivých chorob
Christ et al. Development and characterization of new inhibitors of the human and mouse hematopoietic prostaglandin D2 synthases
CA2338122A1 (en) Macrophage scavenger receptor antagonists
EP2948433B1 (en) Atglistatin as lipase inhibitor
KR100931777B1 (ko) 비타민 d 수용체 조절제
CA2849309C (fr) Nouveaux composes modulateurs de la voie de signalisation des proteines hedgehog, leurs formes marquees, et applications
Cai et al. Design, synthesis and activity evaluation of Hedgehog inhibitor Itraconazole derivatives in A549 cells
US6420563B1 (en) Small molecule modulators of G protein-coupled receptor six
EP4106871B1 (en) Biphenyl compounds as soce modulators, compositions and uses thereof
BRPI0616759A2 (pt) compostos, processo para a sua manufatura, método para o tratamento e/ou prevenção de enfermidades que são moduladas por agonistas de hm74a, e utilização dos compostos
HK40084079A (en) Biphenyl compounds as soce modulators, compositions and uses thereof

Legal Events

Date Code Title Description
EEER Examination request

Effective date: 20140529

MKLA Lapsed

Effective date: 20180104