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ME02938B - Fluorirani antagonisti integrina - Google Patents

Fluorirani antagonisti integrina

Info

Publication number
ME02938B
ME02938B MEP-2017-281A MEP2017281A ME02938B ME 02938 B ME02938 B ME 02938B ME P2017281 A MEP2017281 A ME P2017281A ME 02938 B ME02938 B ME 02938B
Authority
ME
Montenegro
Prior art keywords
compound according
pharmaceutically acceptable
solvate
acceptable salt
compound
Prior art date
Application number
MEP-2017-281A
Other languages
German (de)
English (en)
French (fr)
Inventor
Ben C Askew
Richard W Heidebrecht
Takeru Furuya
Mark E Duggan
D Scott Edwards
Original Assignee
Scifluor Life Sciences 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
Application filed by Scifluor Life Sciences Inc filed Critical Scifluor Life Sciences Inc
Publication of ME02938B publication Critical patent/ME02938B/me

Links

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    • 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
    • A61K31/4375Heterocyclic 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 six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
    • 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4709Non-condensed quinolines and containing further heterocyclic 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
    • A61K31/495Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/02Inorganic compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/16Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing nitrogen, e.g. nitro-, nitroso-, azo-compounds, nitriles, cyanates
    • A61K47/18Amines; Amides; Ureas; Quaternary ammonium compounds; Amino acids; Oligopeptides having up to five amino acids
    • A61K47/183Amino acids, e.g. glycine, EDTA or aspartame
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/34Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyesters, polyamino acids, polysiloxanes, polyphosphazines, copolymers of polyalkylene glycol or poloxamers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/36Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
    • A61K47/40Cyclodextrins; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0048Eye, e.g. artificial tears
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs 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
    • CCHEMISTRY; METALLURGY
    • 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

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Ophthalmology & Optometry (AREA)
  • Diabetes (AREA)
  • Inorganic Chemistry (AREA)
  • Hematology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Obesity (AREA)
  • Urology & Nephrology (AREA)
  • Endocrinology (AREA)
  • Vascular Medicine (AREA)
  • Cardiology (AREA)
  • Emergency Medicine (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicinal Preparation (AREA)

Claims (11)

1. Jedinjenje formule I: ili njegova farmaceutski prihvatljiva so ili solvat, naznačeno time, da: Z je R i R' su svaki nezavisno H ili F, ili R i R', zajedno sa ugljenikovim atomom na koji su vezani, formiraju 3 ili 4-člani karbociklični ili heterociklični prsten; Q je X je CH ili N; Y je CH ili N; R1 je metoksi supstituisan sa 0, 1, 2, ili 3 atoma fluora; i pod uslovom da jedinjenje formule (I) sadrži najmanje jedan atom fluora.
2. Jedinjenje prema patentnom zahtjevu 1, naznačeno time, da R i R’su svaki H.
3. Jedinjenje prema patentnom zahtjevu 1, naznačeno time, da X je N i Y je CH.
4. Jedinjenje prema patentnom zahtjevu 1, naznačeno time, da X i Y su svaki CH.
5. Jedinjenje prema patentnom zahtjevu 1, naznačeno time, da X i Y su svaki N.
6. Jedinjenje prema patentnom zahtjevu 1, naznačeno time, da R1 je OCHF2.
7. Jedinjenje prema patentnom zahtjevu 1, koje ima formulu II: ili njegova farmaceutski prihvatljiva so ili solvat.
8. Jedinjenje prema patentnom zahtjevu 1, odabrano iz grupe koja se sastoji od: i ili njegova farmaceutski prihvatljiva so ili solvat.
9. Jedinjenje prema patentnom zahtjevu 8, gde je jedinjenje ili njegova farmaceutski prihvatljiva so ili solvat.
10. Farmaceutski preparat, koji sadrži jedinjenje prema bilo kom od prethodnih patentnih zahtjeva ili njegovu farmaceutski prihvatljivu so ili solvat, i farmaceutski prihvatljiv nosač ili ekscipijens, naznačen time, da farmaceutski preparat opciono dalje sadrži aktivni sastojak izabran iz grupe koja se sastoji od a) antagoniste integrina α5β1, b) citotoksičnog / antiproliferativnog agensa, c) inhibitora faktora rasta izvedenog iz epiderma, izvedenog iz fibroblasta, ili izvedenog iz trombocita, d) inhibitora VEGF, e) inhibitora Flk-1/KDR, Flt-1, Tck/Tie-2 ili Tic-1, i f) inhibitora fosfoinozitid 3-kinaze i njihove mešavine.
11. Jedinjenje prema bilo kom od patentnih zahtjeva 1 do 9 ili njegova farmaceutski prihvatljiva so ili solvat, opciono u kombinaciji sa jednom ili više terapija, ili preparat prema patentnom zahtevu 10, za upotrebu u postupku lečenja ili prevencije bolesti ili stanja posredovanog αv integrinom kod subjekta.
<!--[if !supportLists]-->1. <!--[endif]--> Jedinjenje ili preparat za upotrebu prema patentnom zahtjevu 11, naznačen time, da je bolest ili stanje odabrano iz grupe koja se sastoji od makularne degeneracije, dijabetične retinopatije (DR), makularnog edema, dijabetičnog makularnog edema (DME) i makularnog edema nakon okluzije retinalne vene (RVO).
MEP-2017-281A 2013-02-07 2014-02-07 Fluorirani antagonisti integrina ME02938B (me)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201361762087P 2013-02-07 2013-02-07
US201361900706P 2013-11-06 2013-11-06
PCT/US2014/015372 WO2014124302A1 (en) 2013-02-07 2014-02-07 Fluorinated integrin antagonists
EP14749249.0A EP2953948B1 (en) 2013-02-07 2014-02-07 Fluorinated integrin antagonists

Publications (1)

Publication Number Publication Date
ME02938B true ME02938B (me) 2018-04-20

Family

ID=51300167

Family Applications (1)

Application Number Title Priority Date Filing Date
MEP-2017-281A ME02938B (me) 2013-02-07 2014-02-07 Fluorirani antagonisti integrina

Country Status (24)

Country Link
US (6) US9518053B2 (me)
EP (3) EP2953948B1 (me)
JP (2) JP6494528B2 (me)
KR (1) KR102216091B1 (me)
CN (2) CN105246889B (me)
AU (1) AU2014214737B2 (me)
BR (2) BR122019026750B1 (me)
CA (1) CA2899321C (me)
CY (1) CY1120213T1 (me)
DK (1) DK2953948T3 (me)
ES (2) ES2763556T3 (me)
HR (1) HRP20171873T1 (me)
HU (1) HUE035357T2 (me)
IL (2) IL240181A (me)
LT (1) LT2953948T (me)
ME (1) ME02938B (me)
PL (1) PL2953948T3 (me)
PT (1) PT2953948T (me)
RS (1) RS56711B1 (me)
RU (1) RU2698195C2 (me)
SI (1) SI2953948T1 (me)
SM (1) SMT201700611T1 (me)
WO (1) WO2014124302A1 (me)
ZA (1) ZA201505575B (me)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8901144B2 (en) * 2013-02-07 2014-12-02 Scifluor Life Sciences, Llc Fluorinated 3-(2-oxo-3-(3-arylpropyl)imidazolidin-1-yl)-3-arylpropanoic acid derivatives
ME02938B (me) * 2013-02-07 2018-04-20 Scifluor Life Sciences Inc Fluorirani antagonisti integrina
ES2899860T3 (es) 2013-09-24 2022-03-15 Fujifilm Corp Nuevo compuesto que contiene nitrógeno o sal del mismo, o complejo de metal de los mismos
WO2015175954A1 (en) * 2014-05-16 2015-11-19 Scifluor Life Sciences, Inc. Alpha v integrin antagonist compositions
US9790222B2 (en) * 2015-02-19 2017-10-17 Scifluor Life Sciences, Inc. Fluorinated tetrahydronaphthyridinyl nonanoic acid derivatives and uses thereof
MX2017013880A (es) 2015-04-30 2018-08-01 Scifluor Life Sciences Inc Derivados del acido tetrahidronaftiridinil propionico y usos de los mismos.
US10118929B2 (en) 2016-04-27 2018-11-06 Scifluor Life Sciences, Inc. Nonanoic and decanoic acid derivatives and uses thereof
AU2017292754B2 (en) * 2016-07-05 2021-06-17 Icahn School Of Medicine At Mount Sinai Tetrahydronaphthyridinepentanamide integrin antagonists
BR112019009245A2 (pt) * 2016-11-08 2019-07-16 Bristol-Myers Squibb Company azol amidas e aminas como inibidores de alfav integrina
RS61453B1 (sr) * 2016-11-08 2021-03-31 Bristol Myers Squibb Co Amidi pirola kao inhibitori alfa v integrina
WO2018183795A1 (en) * 2017-03-30 2018-10-04 Scifluor Life Sciences, Inc. Method of making tetrahydronaphthyridinyl nonanoic acid compounds
WO2021231581A1 (en) 2020-05-12 2021-11-18 Scifluor Life Sciences, Inc. METHODS OF TREATING OR PREVENTING VIRAL INFECTION WITH FLUORINATED α V INTEGRIN ANTAGONISTS
WO2023230042A1 (en) * 2022-05-23 2023-11-30 Ocuterra Therapeutics, Inc. Treating diabetic retinopathy using an integrin inhibitor
WO2024006248A1 (en) * 2022-06-27 2024-01-04 Ocuterra Therapeutics, Inc. Stable ophthalmic formulations of a fluorinated integrin antagonist
GB202301024D0 (en) * 2023-01-24 2023-03-08 Univ Bradford Compounds
CN116239665B (zh) * 2023-03-10 2024-08-23 山东大学 Ncf4在制备调控炎症小体激活的制剂中的应用和作为炎症性疾病的治疗靶点中的应用

Family Cites Families (46)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1318254C (en) 1988-01-06 1993-05-25 Munehiro Tomikawa Inhibitory agent of hepatic fibrosis containing pantethine
DK0581904T3 (da) 1991-04-01 1997-12-29 Univ Duke Fremgangsmåde til inhibering af fibrose
US5501969A (en) 1994-03-08 1996-03-26 Human Genome Sciences, Inc. Human osteoclast-derived cathepsin
JP3818322B2 (ja) 1994-04-28 2006-09-06 敏一 中村 コラーゲン分解促進剤
US5736357A (en) 1994-10-27 1998-04-07 Arris Pharmaceutical Cathespin O protease
US6544767B1 (en) 1994-10-27 2003-04-08 Axys Pharmaceuticals, Inc. Cathespin O2 protease
US5645839A (en) 1995-06-07 1997-07-08 Trustees Of Boston University Combined use of angiotensin inhibitors and nitric oxide stimulators to treat fibrosis
US6664227B1 (en) 1996-03-01 2003-12-16 Genetics Institute, Llc Treatment of fibrosis by antagonism of IL-13 and IL-13 receptor chains
US6211184B1 (en) 1996-08-29 2001-04-03 Merck & Co., Inc. Integrin antagonists
AU3215597A (en) 1996-08-30 1998-03-19 Biomeasure Incorporated Method of inhibiting fibrosis with a somatostatin agonist
US6017926A (en) 1997-12-17 2000-01-25 Merck & Co., Inc. Integrin receptor antagonists
JP2002508323A (ja) * 1997-12-17 2002-03-19 メルク エンド カムパニー インコーポレーテッド インテグリン受容体拮抗薬
US6048861A (en) * 1997-12-17 2000-04-11 Merck & Co., Inc. Integrin receptor antagonists
US6066648A (en) 1997-12-17 2000-05-23 Merck & Co., Inc. Integrin receptor antagonists
WO1999031061A1 (en) * 1997-12-17 1999-06-24 Merck & Co., Inc. Integrin receptor antagonists
ATE298338T1 (de) * 1997-12-17 2005-07-15 Merck & Co Inc Integrin-rezeptor-antagonisten
CN1284955A (zh) * 1997-12-17 2001-02-21 麦克公司 整联蛋白受体拮抗剂
US6117445A (en) 1998-01-28 2000-09-12 Link Technology Inc. Methods for the prevention and treatment of fibrosis and sclerosis
US6677360B2 (en) * 1998-12-16 2004-01-13 Bayer Aktiengesellschaft Biphenyl and biphenyl-analogous compounds as integrin antagonists
DE69927050T2 (de) * 1998-12-16 2006-06-29 Bayer Healthcare Ag Biphenylverbindungen und biphenyl-analoge als intergrin-antagonisten
US6291503B1 (en) 1999-01-15 2001-09-18 Bayer Aktiengesellschaft β-phenylalanine derivatives as integrin antagonists
ATE368462T1 (de) * 1999-06-02 2007-08-15 Merck & Co Inc Alpha v integrin-rezeptor antagonisten
US6407241B1 (en) 1999-11-08 2002-06-18 Merck & Co., Inc. Process and intermediates for the preparation of imidazolidinone αv integrin antagonists
US6455539B2 (en) 1999-12-23 2002-09-24 Celltech R&D Limited Squaric acid derivates
EP1252162B1 (en) 2000-01-20 2012-07-25 Merck Sharp & Dohme Corp. Alpha v integrin receptor antagonists
CA2397665A1 (en) 2000-01-24 2001-07-26 Merck & Co., Inc. Alpha v integrin receptor antagonists
EP1192949A4 (en) 2000-02-22 2005-11-09 Daiichi Suntory Pharma Co Ltd PREVENTIVE OR THERAPEUTIC DRUGS FOR TREATING FIBROSIS AND CONTAINING CHYMASE INHIBITORS AS ACTIVE INGREDIENTS
GB0011817D0 (en) 2000-05-16 2000-07-05 Pharmacia & Upjohn Spa Antagonists of integrin receptors
AU2001277935B2 (en) * 2000-07-26 2005-08-04 Merck & Co., Inc. Alpha v integrin receptor antagonists
WO2002022616A2 (en) 2000-09-14 2002-03-21 Merck & Co., Inc. Alpha v integrin receptor antagonists
JP2004509123A (ja) 2000-09-14 2004-03-25 メルク エンド カムパニー インコーポレーテッド アルファνインテグリン受容体アンタゴニスト
WO2002022124A1 (en) 2000-09-18 2002-03-21 Merck & Co., Inc. Treatment of inflammation with a combination of a cyclooxygenase-2 inhibitor and an integrin alpha-v antagonist
EP1444231A4 (en) 2001-11-06 2005-11-09 Merck & Co Inc AMINO SALT OF AN INTEGRIN RECEPTOR ANTAGONIST
US20040053968A1 (en) * 2001-12-28 2004-03-18 Hartman George D. Methods and compositions for treating peridontal disease
AU2003267216A1 (en) * 2002-09-20 2004-04-08 Merck & Co., Inc. Mannitol formulation for integrin receptor antagonist
CA2507699A1 (en) * 2002-12-20 2004-07-15 Pharmacia Corporation Heteroarylalkanoic acids as integrin receptor antagonists
CA2540730C (en) 2003-10-01 2012-08-21 Merck Patent Gmbh Alfavbeta3 and alfavbeta6 integrin antagonists as antifibrotic agents
WO2011060395A1 (en) 2009-11-16 2011-05-19 Schering Corporation Cyclic ureas useful as hiv inhibitors
MX351368B (es) 2010-05-26 2017-10-12 Sunovion Pharmaceuticals Inc Compuestos heteroarilo y metodos para utilizarlos.
KR102165421B1 (ko) 2011-05-09 2020-10-14 알레그로 파마슈티칼스, 인코포레이티드. 인테그린 수용체 길항물질 및 이의 사용 방법
EP2726057A1 (en) 2011-06-28 2014-05-07 Bayer HealthCare LLC Topical ophthalmological pharmaceutical composition containing sorafenib
ME02938B (me) * 2013-02-07 2018-04-20 Scifluor Life Sciences Inc Fluorirani antagonisti integrina
US8901144B2 (en) 2013-02-07 2014-12-02 Scifluor Life Sciences, Llc Fluorinated 3-(2-oxo-3-(3-arylpropyl)imidazolidin-1-yl)-3-arylpropanoic acid derivatives
US9790222B2 (en) 2015-02-19 2017-10-17 Scifluor Life Sciences, Inc. Fluorinated tetrahydronaphthyridinyl nonanoic acid derivatives and uses thereof
MX2017013880A (es) 2015-04-30 2018-08-01 Scifluor Life Sciences Inc Derivados del acido tetrahidronaftiridinil propionico y usos de los mismos.
WO2018183795A1 (en) 2017-03-30 2018-10-04 Scifluor Life Sciences, Inc. Method of making tetrahydronaphthyridinyl nonanoic acid compounds

Also Published As

Publication number Publication date
JP2016507571A (ja) 2016-03-10
LT2953948T (lt) 2018-01-10
CN105246889B (zh) 2018-07-31
EP3674301A1 (en) 2020-07-01
RS56711B1 (sr) 2018-03-30
US11685737B2 (en) 2023-06-27
RU2698195C2 (ru) 2019-08-23
EP3266782B1 (en) 2019-10-30
PL2953948T3 (pl) 2018-03-30
US9518053B2 (en) 2016-12-13
IL245471A0 (en) 2016-06-30
US20160075698A1 (en) 2016-03-17
EP2953948A4 (en) 2016-06-22
KR102216091B1 (ko) 2021-02-16
BR112015019039A8 (pt) 2019-11-12
ZA201505575B (en) 2022-03-30
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US12497399B2 (en) 2025-12-16
CN108690022B (zh) 2021-08-17
EP2953948B1 (en) 2017-09-27
CA2899321A1 (en) 2014-08-14
BR112015019039B1 (pt) 2022-03-03
US9717729B2 (en) 2017-08-01
KR20150115812A (ko) 2015-10-14
RU2015137785A (ru) 2017-03-14
US20190263810A1 (en) 2019-08-29
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US20170071939A1 (en) 2017-03-16
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IL240181A0 (en) 2015-09-24
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BR112015019039A2 (pt) 2017-07-18
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US20210163473A1 (en) 2021-06-03
CN105246889A (zh) 2016-01-13
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