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

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
EP2742047B1 (en) 2011-08-10 2021-05-12 Janssen Sciences Ireland Unlimited Company Antibacterial piperidinyl substituted 3,4-dihydro-1h-[1,8]naphthyridinones
CA2879623C (en) * 2012-08-10 2021-11-02 Janssen Sciences Ireland Uc Fused bicyclic azole heterocycle as inhibitors of the enzyme fabi
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
SMT201900517T1 (it) 2017-03-20 2019-11-13 Forma Therapeutics Inc Composizioni di pirrolopirrolo come attivatori di piruvato chinasi (pkr)
WO2019177975A1 (en) 2018-03-12 2019-09-19 The Board Of Trustees Of The University Of Illinois Antibiotics effective for gram-negative pathogens
US11001588B2 (en) 2018-09-19 2021-05-11 Forma Therapeutics, Inc. Activating pyruvate kinase R and mutants thereof
CN113166060B (zh) 2018-09-19 2024-01-09 诺沃挪第克健康护理股份公司 用丙酮酸激酶激活化合物治疗镰状细胞病
US20230035837A1 (en) * 2018-11-12 2023-02-02 Debiopharm International S.A. Antibiotic compounds, methods of manufacturing the same, pharmaceutical compositions containing the same and uses thereof
CA3151612A1 (en) 2019-09-19 2021-03-25 George P. Luke Pyruvate kinase r (pkr) activating compositions
EP4308579A1 (en) * 2021-03-17 2024-01-24 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
AU1192501A (en) 1999-10-08 2001-04-23 Smithkline Beecham Corporation Fab i inhibitors
ECSP003699A (es) 1999-10-08 2002-04-23 Smithkline Beecham Corp Inhibidores de fab i
CO5251397A1 (es) 1999-10-08 2003-02-28 Smithkline Beecham Corp Inhibidores de fab i
JP4387804B2 (ja) 2001-04-06 2009-12-24 アフィニアム・ファーマシューティカルズ・インコーポレイテッド FabI阻害剤
PT1828167E (pt) * 2004-06-04 2014-10-08 Debiopharm Int Sa Derivados de acrilamida como agentes antibióticos
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
EP2054422B1 (en) * 2006-07-20 2017-06-14 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
MX2012005759A (es) * 2009-11-18 2012-10-03 Fab Pharma S A S Acrilamidas heterociclicas novedosas y su uso como farmacos.
US8766017B2 (en) 2011-07-29 2014-07-01 Eastman Chemical Company Integrated process for the preparation of 1,4-cyclohexanedimethanol from terephthalic acid
WO2013019710A1 (en) 2011-07-29 2013-02-07 The Children's Hospital Of Philadelphia Compositions and methods for the treatment of hiv
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
CN108003155A (zh) 2011-08-10 2018-05-08 爱尔兰詹森科学公司 抗菌的高哌啶基取代的3,4二氢-1h[1,8]萘啶酮类
EP2742047B1 (en) 2011-08-10 2021-05-12 Janssen Sciences Ireland Unlimited Company Antibacterial piperidinyl substituted 3,4-dihydro-1h-[1,8]naphthyridinones

Also Published As

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

Similar Documents

Publication Publication Date Title
PE20141410A1 (es) 3,4 dihidro 1h[1,8] naftiridinonas antibacterianas sustituidas con ciclopenta [c] pirrol
MA35749B1 (fr) Dérivés nucléosidiques 4'-azido, 3'-fluoro substitués en tant qu'inhibiteurs de la réplication de l'arn du vhc
TN2015000084A1 (fr) Pyridinones bicycliques nouvelles
UY33694A (es) ?inhibidores de n1/n2-lactama acetil-coa carboxilasa?.
GEP20156370B (en) Fluoro-pyridinone derivatives useful as antibacterial agents
WO2010035219A3 (en) Pyrazolo pyridine derivatives as nadph oxidase inhibitors
DOP2011000102A (es) Compuestos heteroaromaticos espirociclicos fusionados para el tratamiento de infecciones bacterianas
MA37712B1 (fr) Inhibiteurs macrocycliques de virus flaviviridae
PE20130010A1 (es) Derivado de 1,3,4,8-tetrahidro-2h-pirido[1,2-a]pirazina como inhibidor de la integrasa del vih
MY183312A (en) Pharmaceutical formulation
MX2010009645A (es) Derivados novedosos de aminometil benceno.
EA200900924A1 (ru) Циклизованные производные как ингибиторы eg-5
MX2012003982A (es) Pirrolidinas n-substituidas.
GEP20166481B (en) (crystalline forms of hydrochloride salt of (4a-r, 9a-s)-1-(1h-benzoimidazole-5-carbonyl)-2, 3, 4, 4a, 9, 9a-hexa- hydro-1h-indeno [2, 1-b] pyridine-6-carbonitrile and their use as hsd 1 inhibitors
NZ598165A (en) Nitroimidazooxazine and nitroimidazooxazole analogues and their uses
GEP20156242B (en) 2-arylimidazole derivatives as pde10a enzyme inhibitors
WO2011143772A9 (en) Inhibitors of hiv replication
MX2013000295A (es) Procedimiento de preparacion de un inhibidor especifico de la trombina.
MX2014002936A (es) Nuevos derivados de acido betulinico con actividad antiviral.
BRPI0511433A (pt) derivados de quinolina substituìda como inibidores de cinesina mitótica
MX2014001598A (es) 3,4-dihidro-1h-[1,8]naftiridinosas sustituidas con homopiperidinilo antibacterianas.
UA103329C2 (ru) Соли соединений-ингибиторов вич
MA32375B1 (fr) Derives de 5-hydroxymethyl-oxazolidine-2-one pour le traitement de maladies intestinales bacteriennes
TW200800951A (en) Substituted imidazole compounds as KSP inhibitors
MY164880A (en) Process for the preparation of isoxazolyl-methoxy-nicotinic acids

Legal Events

Date Code Title Description
FG Grant, registration