UY34253A - 3,4-dihidro-1h-[1,8]naftiridinonas antibacterianas sustituidas con ciclopenta[c]pirrol - Google Patents

3,4-dihidro-1h-[1,8]naftiridinonas antibacterianas sustituidas con ciclopenta[c]pirrol

Info

Publication number
UY34253A
UY34253A UY0001034253A UY34253A UY34253A UY 34253 A UY34253 A UY 34253A UY 0001034253 A UY0001034253 A UY 0001034253A UY 34253 A UY34253 A UY 34253A UY 34253 A UY34253 A UY 34253A
Authority
UY
Uruguay
Prior art keywords
naftiridinones
pirrol
dihidro
cyclopenta
antibacterial
Prior art date
Application number
UY0001034253A
Other languages
English (en)
Spanish (es)
Inventor
Guillemont Jerome Emile Georges
Lancois David Francis Alain
Motte Magali Madeleine Simone
Koul Anil
Balemans Wendy Mia Albert
Arnoult Eric Pierre Alexandre
Original Assignee
Janssen R & D Ireland
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=46650549&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=UY34253(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Janssen R & D Ireland filed Critical Janssen R & D Ireland
Publication of UY34253A publication Critical patent/UY34253A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
UY0001034253A 2011-08-10 2012-08-10 3,4-dihidro-1h-[1,8]naftiridinonas antibacterianas sustituidas con ciclopenta[c]pirrol UY34253A (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP11177119 2011-08-10

Publications (1)

Publication Number Publication Date
UY34253A true UY34253A (es) 2013-02-28

Family

ID=46650549

Family Applications (1)

Application Number Title Priority Date Filing Date
UY0001034253A UY34253A (es) 2011-08-10 2012-08-10 3,4-dihidro-1h-[1,8]naftiridinonas antibacterianas sustituidas con ciclopenta[c]pirrol

Country Status (24)

Country Link
US (7) US8906923B2 (esLanguage)
EP (1) EP2742045B1 (esLanguage)
JP (2) JP5921687B2 (esLanguage)
KR (1) KR101996862B1 (esLanguage)
CN (2) CN103874698B (esLanguage)
AR (1) AR087508A1 (esLanguage)
AU (1) AU2012293621B2 (esLanguage)
BR (1) BR112014003063B1 (esLanguage)
CA (1) CA2842518C (esLanguage)
CL (1) CL2014000289A1 (esLanguage)
DK (1) DK2742045T3 (esLanguage)
EA (1) EA201490438A1 (esLanguage)
ES (1) ES2721658T3 (esLanguage)
HU (1) HUE042978T2 (esLanguage)
IL (1) IL230549A (esLanguage)
JO (1) JO3611B1 (esLanguage)
MX (1) MX348128B (esLanguage)
PE (1) PE20141410A1 (esLanguage)
PH (1) PH12014500317A1 (esLanguage)
TR (1) TR201905537T4 (esLanguage)
TW (1) TWI568731B (esLanguage)
UA (1) UA111210C2 (esLanguage)
UY (1) UY34253A (esLanguage)
WO (1) WO2013021054A1 (esLanguage)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JO3611B1 (ar) 2011-08-10 2020-08-27 Janssen Sciences Ireland Uc سايكلو بنتا (سي (بيرول 4,3 ثاني هيدرو 1 hمستبدله [8,1] نافثيريدينونات مضادة للجراثيم
AU2012293619B2 (en) 2011-08-10 2017-05-04 Janssen Sciences Ireland Uc Antibacterial piperidinyl substituted 3,4-dihydro-1h-[1,8]naphthyridinones
WO2014023814A1 (en) * 2012-08-10 2014-02-13 Janssen R&D Ireland New antibacterial compounds
US9540324B2 (en) 2013-09-26 2017-01-10 Luc Therapeutics, Inc. Selective octahydro-cyclopenta[C] pyrrole negative modulators of NR2B
JO3579B1 (ar) * 2014-09-26 2020-07-05 Luc Therapeutics Inc مُعدِلات تفاغرية سالبة لمستقبل nr2b من المركب n-ألكيل أريل-5-أوكسي أريل-ثامن هيدرو-خماسي الحلقة [c] بيرول
US11014927B2 (en) 2017-03-20 2021-05-25 Forma Therapeutics, Inc. Pyrrolopyrrole compositions as pyruvate kinase (PKR) activators
WO2019177975A1 (en) 2018-03-12 2019-09-19 The Board Of Trustees Of The University Of Illinois Antibiotics effective for gram-negative pathogens
JP7450610B2 (ja) 2018-09-19 2024-03-15 ノヴォ・ノルディスク・ヘルス・ケア・アーゲー ピルビン酸キナーゼrの活性化
MA53668B1 (fr) 2018-09-19 2024-06-28 Novo Nordisk Health Care Ag Traitement de la drépanocytose avec un composé activant la pyruvate kinase r
BR112021009106A2 (pt) 2018-11-12 2021-08-10 Debiopharm International S.A. compostos antibióticos, métodos de fabricação dos mesmos, composições farmacêuticas que os contêm e seus usos
MA57202B1 (fr) 2019-09-19 2025-09-30 Novo Nordisk Health Care Ag Compositions d'activation de la pyruvate kinase r (pkr)
CA3212074A1 (en) * 2021-03-17 2022-09-22 Janssen Sciences Ireland Unlimited Company Antibacterial compounds
US12128035B2 (en) 2021-03-19 2024-10-29 Novo Nordisk Health Care Ag Activating pyruvate kinase R

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4215123A (en) * 1979-05-07 1980-07-29 American Home Products Corporation Antisecretory 4-oxy-3-carboxy or cyano-1,2-dihydro-2-oxo-1,8-naphthyridine derivatives
EP1225895B1 (en) 1999-10-08 2005-05-04 Affinium Pharmaceuticals, Inc. Fab i inhibitors
CO5251397A1 (es) 1999-10-08 2003-02-28 Smithkline Beecham Corp Inhibidores de fab i
HK1049656A1 (zh) 1999-10-08 2003-05-23 Smithkline Beecham Corporation Fab i抑制剂
US7049310B2 (en) 2001-04-06 2006-05-23 Affinium Pharmaceuticals, Inc. Fab I inhibitors
CA2568914C (en) * 2004-06-04 2013-09-24 Affinium Pharmaceuticals, Inc. Therapeutic agents, and methods of making and using the same
US7732612B2 (en) 2004-09-09 2010-06-08 Janssen Pharmaceutica, N.V. 7-amino alkylidenyl-heterocyclic quinolones and naphthyridones
US7973060B2 (en) 2005-10-13 2011-07-05 Crystalgenomics, Inc. Fab I inhibitor and process for preparing same
EP2687533B1 (en) * 2006-07-20 2017-07-19 Debiopharm International SA Acrylamide derivatives as FAB I inhibitors
WO2008098374A1 (en) * 2007-02-16 2008-08-21 Affinium Pharmaceuticals, Inc. Salts, prodrugs and polymorphs of fab i inhibitors
NZ599444A (en) 2009-11-18 2014-02-28 Fab Pharma Sas Novel heterocyclic acrylamides and their use as pharmaceuticals
JP2014524409A (ja) 2011-07-29 2014-09-22 ザ・チルドレンズ・ホスピタル・オブ・フィラデルフィア Hivの治療のための組成物および方法
US8766017B2 (en) 2011-07-29 2014-07-01 Eastman Chemical Company Integrated process for the preparation of 1,4-cyclohexanedimethanol from terephthalic acid
AU2012293619B2 (en) 2011-08-10 2017-05-04 Janssen Sciences Ireland Uc Antibacterial piperidinyl substituted 3,4-dihydro-1h-[1,8]naphthyridinones
AU2012293618B2 (en) 2011-08-10 2017-04-20 Janssen Sciences Ireland Uc Antibacterial homopiperidinyl substituted 3,4 dihydro 1H (1,8)naphthyridinones
JO3611B1 (ar) * 2011-08-10 2020-08-27 Janssen Sciences Ireland Uc سايكلو بنتا (سي (بيرول 4,3 ثاني هيدرو 1 hمستبدله [8,1] نافثيريدينونات مضادة للجراثيم

Also Published As

Publication number Publication date
MX348128B (es) 2017-05-26
PE20141410A1 (es) 2014-10-13
HK1223352A1 (zh) 2017-07-28
AR087508A1 (es) 2014-03-26
KR101996862B1 (ko) 2019-07-05
TW201313714A (zh) 2013-04-01
AU2012293621B2 (en) 2016-07-21
US9617262B2 (en) 2017-04-11
US9290493B2 (en) 2016-03-22
JP2016190843A (ja) 2016-11-10
US10155759B2 (en) 2018-12-18
US8906923B2 (en) 2014-12-09
KR20140072034A (ko) 2014-06-12
US20170174683A1 (en) 2017-06-22
HK1199243A1 (zh) 2015-06-26
AU2012293621A1 (en) 2014-02-13
UA111210C2 (uk) 2016-04-11
JP5921687B2 (ja) 2016-05-24
CA2842518C (en) 2019-07-23
CN105461684B (zh) 2018-09-25
CN103874698A (zh) 2014-06-18
TR201905537T4 (tr) 2019-05-21
US10526331B2 (en) 2020-01-07
CA2842518A1 (en) 2013-02-14
TWI568731B (zh) 2017-02-01
EP2742045B1 (en) 2019-01-23
MX2014001600A (es) 2014-04-25
IL230549A0 (en) 2014-03-31
BR112014003063B1 (pt) 2020-11-17
JO3611B1 (ar) 2020-08-27
DK2742045T3 (en) 2019-04-23
US9884864B2 (en) 2018-02-06
HUE042978T2 (hu) 2019-07-29
US10501463B2 (en) 2019-12-10
NZ620212A (en) 2015-10-30
CL2014000289A1 (es) 2014-07-11
US20140171451A1 (en) 2014-06-19
PH12014500317A1 (en) 2014-04-14
EP2742045A1 (en) 2014-06-18
WO2013021054A1 (en) 2013-02-14
JP2014531404A (ja) 2014-11-27
ES2721658T3 (es) 2019-08-02
BR112014003063A2 (pt) 2017-02-21
IL230549A (en) 2017-07-31
CN105461684A (zh) 2016-04-06
CN103874698B (zh) 2016-03-23
US20150080413A1 (en) 2015-03-19
US20190194194A1 (en) 2019-06-27
US20190084982A1 (en) 2019-03-21
EA201490438A1 (ru) 2014-06-30
US20160194324A1 (en) 2016-07-07
US20180105525A1 (en) 2018-04-19

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