SI2124565T1 - N-substituirani glicinski derivati: inhibitorji hidroksilaze - Google Patents

N-substituirani glicinski derivati: inhibitorji hidroksilaze

Info

Publication number
SI2124565T1
SI2124565T1 SI200831409T SI200831409T SI2124565T1 SI 2124565 T1 SI2124565 T1 SI 2124565T1 SI 200831409 T SI200831409 T SI 200831409T SI 200831409 T SI200831409 T SI 200831409T SI 2124565 T1 SI2124565 T1 SI 2124565T1
Authority
SI
Slovenia
Prior art keywords
hydroxylase inhibitors
substituted glycine
glycine derivatives
derivatives
hydroxylase
Prior art date
Application number
SI200831409T
Other languages
English (en)
Slovenian (sl)
Inventor
Antony N. Shaw
Kevin J. Duffy
William Henry Miller
Andrea K. Myers
Michael N. Zimmerman
Original Assignee
Glaxosmithkline Llc
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=39636631&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SI2124565(T1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Glaxosmithkline Llc filed Critical Glaxosmithkline Llc
Publication of SI2124565T1 publication Critical patent/SI2124565T1/sl

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
    • C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D237/24—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • 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
    • A61K31/50—Pyridazines; Hydrogenated pyridazines
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/06—Antianaemics
    • 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

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Hematology (AREA)
  • Diabetes (AREA)
  • Cardiology (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Enzymes And Modification Thereof (AREA)
SI200831409T 2007-01-12 2008-01-11 N-substituirani glicinski derivati: inhibitorji hidroksilaze SI2124565T1 (sl)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US88471007P 2007-01-12 2007-01-12
EP08727581.4A EP2124565B1 (en) 2007-01-12 2008-01-11 N-substituted glycine derivatives: hydroxylase inhibitors
PCT/US2008/050833 WO2008089052A2 (en) 2007-01-12 2008-01-11 N-substituted glycine derivatives: hydroxylase inhibitors

Publications (1)

Publication Number Publication Date
SI2124565T1 true SI2124565T1 (sl) 2015-04-30

Family

ID=39636631

Family Applications (1)

Application Number Title Priority Date Filing Date
SI200831409T SI2124565T1 (sl) 2007-01-12 2008-01-11 N-substituirani glicinski derivati: inhibitorji hidroksilaze

Country Status (20)

Country Link
US (2) US7608621B2 (enExample)
EP (2) EP2889289B1 (enExample)
JP (1) JP5313925B2 (enExample)
KR (1) KR101458655B1 (enExample)
CN (1) CN101626685B (enExample)
AR (1) AR064878A1 (enExample)
AU (1) AU2008206441B2 (enExample)
BR (1) BRPI0806566A2 (enExample)
CA (1) CA2675252C (enExample)
CL (1) CL2008000066A1 (enExample)
DK (1) DK2124565T3 (enExample)
EA (1) EA017112B1 (enExample)
ES (2) ES2614355T3 (enExample)
HR (1) HRP20150119T1 (enExample)
MX (1) MX2009007548A (enExample)
PL (1) PL2124565T3 (enExample)
PT (1) PT2124565E (enExample)
SI (1) SI2124565T1 (enExample)
TW (1) TW200845991A (enExample)
WO (1) WO2008089052A2 (enExample)

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ES2540561T3 (es) 2005-12-20 2015-07-10 Incyte Corporation N-hidroxiamidinoheterociclos como moduladores de indolamina 2,3-dioxigenasa
US7588924B2 (en) 2006-03-07 2009-09-15 Procter & Gamble Company Crystal of hypoxia inducible factor 1 alpha prolyl hydroxylase
AU2007265460B2 (en) 2006-06-26 2011-03-03 Akebia Therapeutics Inc. Prolyl hydroxylase inhibitors and methods of use
CA2663057C (en) * 2006-09-19 2015-12-08 Incyte Corporation N-hydroxyamidinoheterocycles as modulators of indoleamine 2,3-dioxygenase
CL2007002650A1 (es) 2006-09-19 2008-02-08 Incyte Corp Compuestos derivados de heterociclo n-hidroxiamino; composicion farmaceutica, util para tratar cancer, infecciones virales y desordenes neurodegenerativos entre otras.
US8952160B2 (en) 2008-01-11 2015-02-10 Fibrogen, Inc. Isothiazole-pyridine derivatives as modulators of HIF (hypoxia inducible factor) activity
WO2009100250A1 (en) 2008-02-05 2009-08-13 Fibrogen, Inc. Chromene derivatives and use thereof as hif hydroxylase activity inhibitors
PT2294066E (pt) 2008-04-28 2014-11-21 Janssen Pharmaceutica Nv Benzoimidazoles como inibidores da prolil-hidroxilase
CN104042611B (zh) 2008-07-08 2019-05-14 因塞特控股公司 作为吲哚胺2，3-双加氧酶的抑制剂的1，2，5-噁二唑
EP2334682B1 (en) 2008-08-20 2017-10-04 Fibrogen, Inc. Pyrrolo [ 1, 2 -b] pyridazine derivatives and their use as hif modulators
EP2326179A4 (en) * 2008-08-25 2011-08-17 Smithkline Beecham Corp PROLYLHYDROXYLASEHEMMER
JP5631741B2 (ja) * 2008-11-13 2014-11-26 日本農薬株式会社 ピラジン誘導体類の製造方法及びその中間体類
CN105037323A (zh) 2008-11-14 2015-11-11 菲布罗根有限公司 作为hif羟化酶抑制剂的苯并噻喃衍生物
DE102009004061A1 (de) * 2009-01-08 2010-07-15 Merck Patent Gmbh Pyridazinonderivate
AR077417A1 (es) * 2009-07-17 2011-08-24 Japan Tobacco Inc Compuesto triazolopiridina y su accion como inhibidor de prolil hidroxilasa o agente inductor de la produccion de eritropoyetina
WO2011048611A1 (en) * 2009-10-07 2011-04-28 Torrent Pharmaceuticals Limited Novel fused pyridazine derivatives
RS54323B1 (sr) * 2009-10-21 2016-02-29 Daiichi Sankyo Company, Limited Derivat 5-hidroksipirimidin-4-karboksamida
PH12012500788A1 (en) 2009-11-06 2016-07-27 Aerpio Therapeutics Inc Compositions and methods for treating colitis
WO2011115687A2 (en) * 2010-03-19 2011-09-22 Northwestern University Alkylated sp-b peptoid compounds and related lung surfactant compositions
CN103608346B (zh) 2011-02-02 2016-06-15 菲布罗根有限公司 作为缺氧诱导因子(hif)羟化酶抑制剂的萘啶衍生物
GB201102659D0 (en) 2011-02-15 2011-03-30 Isis Innovation Assay
US8865748B2 (en) 2011-06-06 2014-10-21 Akebia Therapeutics Inc. Compounds and compositions for stabilizing hypoxia inducible factor-2 alpha as a method for treating cancer
NO2686520T3 (enExample) 2011-06-06 2018-03-17
GB201113101D0 (en) 2011-07-28 2011-09-14 Isis Innovation Assay
BR112014009910B1 (pt) 2011-10-25 2020-06-30 Janssen Pharmaceutica N.V. sal di-hidrato de meglumina de ácido 1-(5,6-dicloro-1h-benzo[d]imidazol-2-il)-1h-pirazol-4-carboxílico, composição farmacêuticae pomada tópica
IN2015DN01035A (enExample) 2012-07-30 2015-06-26 Taisho Pharmaceutical Co Ltd
MY204336A (en) 2013-06-13 2024-08-23 Akebia Therapeutics Inc Compositions and methods for treating anemia
MY174254A (en) 2013-11-08 2020-04-01 Incyte Holdings Corp Process for the synthesis of an indoleamine 2,3-dioxygenase inhibitor
CN114890943A (zh) 2013-11-15 2022-08-12 阿克比治疗有限公司 {[5-(3-氯苯基)-3-羟基吡啶-2-羰基]氨基}乙酸固体形式，组合物和用途
EP3190104B1 (en) 2014-09-02 2021-10-27 Sunshine Lake Pharma Co., Ltd. Quinolinone compound and use thereof
AU2016209126A1 (en) 2015-01-23 2017-08-10 Akebia Therapeutics, Inc. Solid forms of 2-(5-(3-fluorophenyl)-3-hydroxypicolinamido)acetic acid, compositions, and uses thereof
UA123308C2 (uk) 2015-04-01 2021-03-17 Екебіа Терапьютікс, Інк. Композиції і способи для лікування анемії
CN105130888A (zh) * 2015-10-09 2015-12-09 中国药科大学 炔基吡啶类脯氨酰羟化酶抑制剂、其制备方法和医药用途
CA3001065A1 (en) 2015-10-14 2017-04-20 Xiaoxi WEI Compositions and methods for reducing ice crystal formation
MX2020011845A (es) 2018-05-09 2021-01-15 Akebia Therapeutics Inc Proceso para preparar acido 2-[[5-(3-clorofenil)-3-hidroxipiridina -2-carbonil]amino]acetico.
US11524939B2 (en) 2019-11-13 2022-12-13 Akebia Therapeutics, Inc. Solid forms of {[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl]amino} acetic acid
WO2021127273A1 (en) * 2019-12-20 2021-06-24 Gb004, Inc. 1 -((6-oxo-1,6-dihydropyridazin-4-yl)methyl)piperazine and 1 -((6-oxo-1,6-dihydropyrimidin-4-yl)methyl)piperazine derivatives as prolyl hydroxylase, hif-1 alpha and pgk modulators for use in treating inflammatory diseases, cancer or infections
WO2022179967A1 (en) 2021-02-23 2022-09-01 Glaxosmithkline Intellectual Property (No.2) Limited Vadadustat for treating covid-19 in a hospitalized subject

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Also Published As

Publication number Publication date
EP2124565B1 (en) 2015-01-07
KR20090101376A (ko) 2009-09-25
JP5313925B2 (ja) 2013-10-09
MX2009007548A (es) 2009-07-22
US20080214549A1 (en) 2008-09-04
USRE44613E1 (en) 2013-11-26
KR101458655B1 (ko) 2014-11-05
CN101626685A (zh) 2010-01-13
BRPI0806566A2 (pt) 2014-05-06
CL2008000066A1 (es) 2008-08-01
WO2008089052A3 (en) 2008-09-18
AU2008206441B2 (en) 2014-06-19
EP2124565A2 (en) 2009-12-02
EP2124565A4 (en) 2011-06-29
EA200970680A1 (ru) 2010-02-26
EA017112B1 (ru) 2012-09-28
CA2675252A1 (en) 2008-07-24
EP2889289A1 (en) 2015-07-01
AR064878A1 (es) 2009-04-29
CN101626685B (zh) 2013-03-13
PL2124565T3 (pl) 2015-05-29
JP2010515756A (ja) 2010-05-13
CA2675252C (en) 2015-05-26
EP2889289B1 (en) 2016-12-21
US7608621B2 (en) 2009-10-27
ES2614355T3 (es) 2017-05-30
PT2124565E (pt) 2015-03-26
DK2124565T3 (en) 2015-02-09
TW200845991A (en) 2008-12-01
WO2008089052A2 (en) 2008-07-24
HRP20150119T1 (hr) 2015-05-08
ES2528745T3 (es) 2015-02-12
AU2008206441A1 (en) 2008-07-24

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