PE20141410A1 - 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
PE20141410A1
PE20141410A1 PE2014000186A PE2014000186A PE20141410A1 PE 20141410 A1 PE20141410 A1 PE 20141410A1 PE 2014000186 A PE2014000186 A PE 2014000186A PE 2014000186 A PE2014000186 A PE 2014000186A PE 20141410 A1 PE20141410 A1 PE 20141410A1
Authority
PE
Peru
Prior art keywords
alkyl
naphthyridinones
pirrol
cyclopenta
dihydro
Prior art date
Application number
PE2014000186A
Other languages
English (en)
Spanish (es)
Inventor
Jerome Emile Georges Guillemont
David Francis Alain Lancois
Magali Madeleine Simone Motte
Anil Koul
Wendy Mia Albert Balemans
Eric Pierre Alexandre Arnoult
Original Assignee
Janssen Randd 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=PE20141410(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Janssen Randd Ireland filed Critical Janssen Randd Ireland
Publication of PE20141410A1 publication Critical patent/PE20141410A1/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)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (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)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
PE2014000186A 2011-08-10 2012-08-10 3,4 dihidro 1h[1,8] naftiridinonas antibacterianas sustituidas con ciclopenta [c] pirrol PE20141410A1 (es)

Applications Claiming Priority (1)

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

Publications (1)

Publication Number Publication Date
PE20141410A1 true PE20141410A1 (es) 2014-10-13

Family

ID=46650549

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2014000186A PE20141410A1 (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 (https=)
EP (1) EP2742045B1 (https=)
JP (2) JP5921687B2 (https=)
KR (1) KR101996862B1 (https=)
CN (2) CN103874698B (https=)
AR (1) AR087508A1 (https=)
AU (1) AU2012293621B2 (https=)
BR (1) BR112014003063B1 (https=)
CA (1) CA2842518C (https=)
CL (1) CL2014000289A1 (https=)
DK (1) DK2742045T3 (https=)
EA (1) EA201490438A1 (https=)
ES (1) ES2721658T3 (https=)
HU (1) HUE042978T2 (https=)
IL (1) IL230549A (https=)
JO (1) JO3611B1 (https=)
MX (1) MX348128B (https=)
PE (1) PE20141410A1 (https=)
PH (1) PH12014500317A1 (https=)
TR (1) TR201905537T4 (https=)
TW (1) TWI568731B (https=)
UA (1) UA111210C2 (https=)
UY (1) UY34253A (https=)
WO (1) WO2013021054A1 (https=)

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
CN105503869A (zh) 2011-08-10 2016-04-20 爱尔兰詹森科学公司 抗细菌的哌啶基取代的3,4-二氢-1h-[1,8]萘啶酮
JP6250667B2 (ja) * 2012-08-10 2017-12-20 ヤンセン・サイエンシズ・アイルランド・ユーシー 新しい抗菌化合物
AR097794A1 (es) 2013-09-26 2016-04-13 Mnemosyne Pharmaceuticals Inc Moduladores octahidro-ciclopenta[c]pirrol negativos de 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
LT3483164T (lt) 2017-03-20 2020-05-11 Forma Therapeutics, Inc. Pirolpirolo kompozicijos kaip piruvato kinazės (pkr) aktyvatoriai
US11691967B2 (en) 2018-03-12 2023-07-04 The Board Of Trustees Of The University Of Illinois Antibiotics effective for gram-negative pathogens
EP3852791B1 (en) 2018-09-19 2024-07-03 Novo Nordisk Health Care AG Activating pyruvate kinase r
EP3853206B1 (en) 2018-09-19 2024-04-10 Novo Nordisk Health Care AG Treating sickle cell disease with a pyruvate kinase r activating compound
SMT202400519T1 (it) * 2018-11-12 2025-01-14 Debiopharm Int Sa Composti antibiotici. metodi di produzione degli stessi, composizioni farmaceutiche contenenti gli stessi e loro usi
HRP20251148T1 (hr) 2019-09-19 2025-11-21 Novo Nordisk Health Care Ag Pripravci koji aktiviraju piruvat-kinazu r (pkr)
CN117440958A (zh) * 2021-03-17 2024-01-23 爱尔兰詹森科学公司 抗菌化合物
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
WO2001026652A1 (en) 1999-10-08 2001-04-19 Smithkline Beecham Corporation Fab i inhibitors
ATE294578T1 (de) 1999-10-08 2005-05-15 Affinium Pharm Inc Fab i hemmer
HU230030B1 (hu) 1999-10-08 2015-05-28 Debiopharm International Sa Fab I inhibitorok
EP1560584B1 (en) 2001-04-06 2009-01-14 Affinium Pharmaceuticals, Inc. Fab i inhibitors
DK1828167T3 (da) 2004-06-04 2014-10-20 Debiopharm Int Sa Acrylamidderivater som antibiotiske midler
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
JP5468899B2 (ja) * 2006-07-20 2014-04-09 アフィニウム ファーマシューティカルズ, インク. Fabiインヒビターとしてのアクリルアミド誘導体
EP2125802A4 (en) * 2007-02-16 2014-08-20 Debiopharm Int Sa SALTS, PRODRUGS AND POLYMORPHES OF FAB I INHIBITORS
WO2011061214A1 (en) * 2009-11-18 2011-05-26 Fab Pharma Sas Novel heterocyclic acrylamides and their use as pharmaceuticals
CA2843643A1 (en) 2011-07-29 2013-02-07 The Children's Hospital Of Philadelphia Compositions and methods for the treatment of hiv
US8766017B2 (en) 2011-07-29 2014-07-01 Eastman Chemical Company Integrated process for the preparation of 1,4-cyclohexanedimethanol from terephthalic acid
CN105503869A (zh) 2011-08-10 2016-04-20 爱尔兰詹森科学公司 抗细菌的哌啶基取代的3,4-二氢-1h-[1,8]萘啶酮
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
US9394295B2 (en) 2011-08-10 2016-07-19 Janssen Sciences Ireland Uc Antibacterial homopiperidinyl substituted 3,4-dihydro-1H-[1,8]naphthyridinones

Also Published As

Publication number Publication date
CN103874698B (zh) 2016-03-23
US20180105525A1 (en) 2018-04-19
US20160194324A1 (en) 2016-07-07
MX2014001600A (es) 2014-04-25
TW201313714A (zh) 2013-04-01
HK1223352A1 (zh) 2017-07-28
TR201905537T4 (tr) 2019-05-21
DK2742045T3 (en) 2019-04-23
US20190194194A1 (en) 2019-06-27
NZ620212A (en) 2015-10-30
US10155759B2 (en) 2018-12-18
US9290493B2 (en) 2016-03-22
JP2014531404A (ja) 2014-11-27
KR101996862B1 (ko) 2019-07-05
JO3611B1 (ar) 2020-08-27
EP2742045B1 (en) 2019-01-23
US9617262B2 (en) 2017-04-11
US20170174683A1 (en) 2017-06-22
UY34253A (es) 2013-02-28
CA2842518A1 (en) 2013-02-14
US10526331B2 (en) 2020-01-07
HUE042978T2 (hu) 2019-07-29
US20190084982A1 (en) 2019-03-21
US10501463B2 (en) 2019-12-10
AR087508A1 (es) 2014-03-26
EA201490438A1 (ru) 2014-06-30
AU2012293621A1 (en) 2014-02-13
IL230549A0 (en) 2014-03-31
UA111210C2 (uk) 2016-04-11
CL2014000289A1 (es) 2014-07-11
TWI568731B (zh) 2017-02-01
JP5921687B2 (ja) 2016-05-24
US9884864B2 (en) 2018-02-06
CA2842518C (en) 2019-07-23
US20140171451A1 (en) 2014-06-19
WO2013021054A1 (en) 2013-02-14
ES2721658T3 (es) 2019-08-02
IL230549A (en) 2017-07-31
CN103874698A (zh) 2014-06-18
MX348128B (es) 2017-05-26
JP2016190843A (ja) 2016-11-10
AU2012293621B2 (en) 2016-07-21
HK1199243A1 (zh) 2015-06-26
CN105461684B (zh) 2018-09-25
PH12014500317A1 (en) 2014-04-14
CN105461684A (zh) 2016-04-06
BR112014003063B1 (pt) 2020-11-17
US8906923B2 (en) 2014-12-09
EP2742045A1 (en) 2014-06-18
KR20140072034A (ko) 2014-06-12
BR112014003063A2 (pt) 2017-02-21
US20150080413A1 (en) 2015-03-19

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