IL230549A - 3, 4-Dihydro-h1 - [8,1] Naphthyridinones are preserved in cyclopenta [c] pyrolytic with antibacterial activity - Google Patents

3, 4-Dihydro-h1 - [8,1] Naphthyridinones are preserved in cyclopenta [c] pyrolytic with antibacterial activity

Info

Publication number
IL230549A
IL230549A IL230549A IL23054914A IL230549A IL 230549 A IL230549 A IL 230549A IL 230549 A IL230549 A IL 230549A IL 23054914 A IL23054914 A IL 23054914A IL 230549 A IL230549 A IL 230549A
Authority
IL
Israel
Prior art keywords
naphthyridinones
dihydro
pyrrole substituted
cyclopenta
antibacterial
Prior art date
Application number
IL230549A
Other languages
English (en)
Hebrew (he)
Other versions
IL230549A0 (en
Original Assignee
Janssen Sciences Ireland Uc
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=IL230549(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Janssen Sciences Ireland Uc, Janssen R& D Ireland filed Critical Janssen Sciences Ireland Uc
Publication of IL230549A0 publication Critical patent/IL230549A0/en
Publication of IL230549A publication Critical patent/IL230549A/en

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)
IL230549A 2011-08-10 2014-01-20 3, 4-Dihydro-h1 - [8,1] Naphthyridinones are preserved in cyclopenta [c] pyrolytic with antibacterial activity IL230549A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP11177119 2011-08-10
PCT/EP2012/065733 WO2013021054A1 (en) 2011-08-10 2012-08-10 Antibacterial cyclopenta[c]pyrrole substituted 3,4-dihydro-1h-[1,8]naphthyridinones

Publications (2)

Publication Number Publication Date
IL230549A0 IL230549A0 (en) 2014-03-31
IL230549A true IL230549A (en) 2017-07-31

Family

ID=46650549

Family Applications (1)

Application Number Title Priority Date Filing Date
IL230549A IL230549A (en) 2011-08-10 2014-01-20 3, 4-Dihydro-h1 - [8,1] Naphthyridinones are preserved in cyclopenta [c] pyrolytic with antibacterial activity

Country Status (24)

Country Link
US (7) US8906923B2 (enExample)
EP (1) EP2742045B1 (enExample)
JP (2) JP5921687B2 (enExample)
KR (1) KR101996862B1 (enExample)
CN (2) CN105461684B (enExample)
AR (1) AR087508A1 (enExample)
AU (1) AU2012293621B2 (enExample)
BR (1) BR112014003063B1 (enExample)
CA (1) CA2842518C (enExample)
CL (1) CL2014000289A1 (enExample)
DK (1) DK2742045T3 (enExample)
EA (1) EA201490438A1 (enExample)
ES (1) ES2721658T3 (enExample)
HU (1) HUE042978T2 (enExample)
IL (1) IL230549A (enExample)
JO (1) JO3611B1 (enExample)
MX (1) MX348128B (enExample)
PE (1) PE20141410A1 (enExample)
PH (1) PH12014500317A1 (enExample)
TR (1) TR201905537T4 (enExample)
TW (1) TWI568731B (enExample)
UA (1) UA111210C2 (enExample)
UY (1) UY34253A (enExample)
WO (1) WO2013021054A1 (enExample)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2742047B1 (en) 2011-08-10 2021-05-12 Janssen Sciences Ireland Unlimited Company Antibacterial piperidinyl 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
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
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
KR102007135B1 (ko) 2017-03-20 2019-08-02 포르마 세라퓨틱스 인크. 피루베이트 키나제 (pkr) 활성화제로서의 피롤로피롤 조성물
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
US20200129485A1 (en) 2018-09-19 2020-04-30 Forma Therapeutics, Inc. Treating sickle cell disease with a pyruvate kinase r activating compound
PL3880675T3 (pl) * 2018-11-12 2025-02-10 Debiopharm International Sa Związki antybiotykowe, sposoby ich wytwarzania, kompozycje farmaceutyczne zawierające te związki oraz ich zastosowanie
US20220378756A1 (en) 2019-09-19 2022-12-01 Forma Therapeutics, Inc. Activating pyruvate kinase r
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
DE60029235T2 (de) 1999-10-08 2007-06-14 Affinium Pharmaceuticals, Inc., Toronto Fab-i-hemmer
DE60017180T2 (de) 1999-10-08 2005-12-08 Affinium Pharmaceuticals, Inc., Toronto Fab i inhibitoren
WO2001026654A1 (en) 1999-10-08 2001-04-19 Smithkline Beecham Corporation Fab i inhibitors
CA2444597A1 (en) 2001-04-06 2002-10-06 Affinium Pharmaceuticals, Inc. Fab i inhibitors
US8450307B2 (en) * 2004-06-04 2013-05-28 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
WO2008009122A1 (en) * 2006-07-20 2008-01-24 Affinium Pharmaceuticals, Inc. Acrylamide derivatives as fab i inhibitors
EP2125802A4 (en) 2007-02-16 2014-08-20 Debiopharm Int Sa SALTS, PRODRUGS AND POLYMORPHES OF FAB I INHIBITORS
JP5816629B2 (ja) 2009-11-18 2015-11-18 ファブ ファーマ エスエーエス 新規の複素環式アクリルアミド及び医薬としてのその使用
WO2013019710A1 (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
HK1200445A1 (en) 2011-08-10 2015-08-07 Janssen Sciences Ireland Uc Antibacterial homopiperidinyl substituted 3,4 dihydro 1h [1,8]naphthyridinones
EP2742047B1 (en) 2011-08-10 2021-05-12 Janssen Sciences Ireland Unlimited Company Antibacterial piperidinyl 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
US9617262B2 (en) 2017-04-11
BR112014003063B1 (pt) 2020-11-17
UY34253A (es) 2013-02-28
US20170174683A1 (en) 2017-06-22
TR201905537T4 (tr) 2019-05-21
US20140171451A1 (en) 2014-06-19
WO2013021054A1 (en) 2013-02-14
AR087508A1 (es) 2014-03-26
HK1223352A1 (zh) 2017-07-28
PH12014500317A1 (en) 2014-04-14
JP2016190843A (ja) 2016-11-10
US10155759B2 (en) 2018-12-18
CA2842518C (en) 2019-07-23
CL2014000289A1 (es) 2014-07-11
DK2742045T3 (en) 2019-04-23
AU2012293621A1 (en) 2014-02-13
US8906923B2 (en) 2014-12-09
US9884864B2 (en) 2018-02-06
UA111210C2 (uk) 2016-04-11
CN103874698B (zh) 2016-03-23
US10526331B2 (en) 2020-01-07
ES2721658T3 (es) 2019-08-02
JO3611B1 (ar) 2020-08-27
US9290493B2 (en) 2016-03-22
TWI568731B (zh) 2017-02-01
US20160194324A1 (en) 2016-07-07
EA201490438A1 (ru) 2014-06-30
PE20141410A1 (es) 2014-10-13
HK1199243A1 (zh) 2015-06-26
CN105461684A (zh) 2016-04-06
MX2014001600A (es) 2014-04-25
US20190084982A1 (en) 2019-03-21
MX348128B (es) 2017-05-26
HUE042978T2 (hu) 2019-07-29
CN103874698A (zh) 2014-06-18
NZ620212A (en) 2015-10-30
BR112014003063A2 (pt) 2017-02-21
TW201313714A (zh) 2013-04-01
KR20140072034A (ko) 2014-06-12
US20180105525A1 (en) 2018-04-19
IL230549A0 (en) 2014-03-31
JP2014531404A (ja) 2014-11-27
CA2842518A1 (en) 2013-02-14
JP5921687B2 (ja) 2016-05-24
AU2012293621B2 (en) 2016-07-21
CN105461684B (zh) 2018-09-25
US10501463B2 (en) 2019-12-10
US20150080413A1 (en) 2015-03-19
EP2742045A1 (en) 2014-06-18
US20190194194A1 (en) 2019-06-27
EP2742045B1 (en) 2019-01-23
KR101996862B1 (ko) 2019-07-05

Similar Documents

Publication Publication Date Title
IL230549A0 (en) 3, 4-dihydro-1h-[8,1] naphthyridinones modified with antibacterial cyclopenta[c]pyrrole
IL234485A (en) Compounds based on imidazo [2,1 – b] pyridazine
SG11201401342VA (en) 5,7-substituted-imidazo[1,2-c]pyrimidines
ZA201205788B (en) 1,2,4-triazine-4-amine derivatives
ZA201206630B (en) Hetaryl-[1,8]naphthyridine derivatives
EP2699091A4 (en) 2 ', 6'-dioxo-3'-deutero-PIPERIDIN-3-YL-isoindoline COMPOUNDS
PL2531505T3 (pl) Sposób wytwarzania kompleksów 3,7-diaza-bicyklo[3.3.1]nonanu z metalami
ZA201208616B (en) Substituted 2,3-dihydroimidazo[1,2-c]quinazoline-containing combinations
IL229993A (en) 8 - Alkoxy [1,2,4] triazolo [5,1 – c] pyrimidine– 2
ZA201306229B (en) Substituted 4-aryl-n-phenyl-1,3,5-triazin-2- amines
IL232717A0 (en) 3-cyanoaryl-h1-pyrrolo[b-3,2]pyridine derivatives
ZA201503682B (en) 3,3'-dinitro-5,5'-bistriazole-1,1'-diol
MY165626A (en) 1,2,4,-triazolone derivative
ZA201304074B (en) Pyrazino[2,3-d]isoxazole derivative
ZA201304255B (en) Halogenated biphenols as antibacterial agents
GB2477431B (en) Improved audiotactile vision system
PL2531504T3 (pl) Sposób wytwarzania roztworów kompleksów metali z 3,7-diazabicyklo[3.3.1]nonanem
HK1196363A (en) 5,7-substituted-imidazo[1,2-c]pyrimidines
AU2012904837A0 (en) The macwell 100 group
AU2012900472A0 (en) Carpobrotus 'CAR 10'
AU4366P (en) PFS100 Scaevola humilis
AU2012903933A0 (en) Chaz's Knotchamacallit
AU2012902688A0 (en) Type 20 Vehicle Improvements.
AU2011900526A0 (en) Solar system 1
AU2011900849A0 (en) Eradication System

Legal Events

Date Code Title Description
FF Patent granted
KB Patent renewed
KB Patent renewed