HRP20200894T1 - Novi antibakterijski spojevi - Google Patents

Novi antibakterijski spojevi Download PDF

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HRP20200894T1
HRP20200894T1 HRP20200894TT HRP20200894T HRP20200894T1 HR P20200894 T1 HRP20200894 T1 HR P20200894T1 HR P20200894T T HRP20200894T T HR P20200894TT HR P20200894 T HRP20200894 T HR P20200894T HR P20200894 T1 HRP20200894 T1 HR P20200894T1
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alkylenyl
image
infection
bond
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HRP20200894TT
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Rosella Ombrato
Gabriele Magaro'
Barbara Garofalo
Guido Furlotti
Giorgina Mangano
Alessandra CAPEZZONE DE JOANNON
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Aziende Chimiche Riunite Angelini Francesco A.C.R.A.F. S.P.A.
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Publication of HRP20200894T1 publication Critical patent/HRP20200894T1/hr

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    • 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
    • C07D401/14Heterocyclic 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 three or more hetero rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/436Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having oxygen as a ring hetero atom, e.g. rapamycin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/4985Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring 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
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    • 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
    • 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
    • C07D471/12Heterocyclic 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 three hetero rings
    • C07D471/16Peri-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
    • C07D491/044Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • C07D491/052Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being six-membered
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D493/00Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C07D493/04Ortho-condensed systems
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04Ortho-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

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
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  • 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)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Cephalosporin Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Claims (15)

1. Spoj, naznačen time, da je predstavljen sljedećom formulom (1): A-L1-Y-L2-R-B (1) u kojoj A je ciklička skupina koja ima sljedeću formulu (II): [image] gdje G3 je CH ili N, kada crtkana linija predstavlja dvostruku vezu, ili je CH2, NH ili O, kada crtkana linija predstavlja jednostruku vezu; C1 predstavlja atome koji su potrebni za tvorbu alifatskog ili aromatskog šesteročlanog prstena koji izborno sadrži jedan ili više heteroatoma odabranih od atoma dušika i atoma kisika, dok je navedeni prsten izborno supstituiran s jednim ili više supstituenata koji su odabrani iz skupine koja se sastoji od atoma halogena, (C1-3)alkil-skupine, cijano-skupine, okso-skupine (=O) i (C1-3)alkoksi-skupine; L1 je δ-veza ili (C1-3)alkilenil-skupina izborno supstituirana s hidroksi-skupinom; Y je prsten odabran iz skupine koja se sastoji od sljedećih prstena: piperidinila, piperazinila, pirolidinila, 1,3-ciklobutila, 1,3-ciklopentila, 1,2-ciklopropila, azetidinila, azabiciklo-oktila, morfolinila i cikloheksila, pri čemu je navedeni prsten izborno supstituiran s jednim ili više supstituenata koji su odabrani iz skupine koja se sastoji od hidroksi-skupine, (C1-3)alkilenil-OH-skupine, (C1-3)alkilenil-O-(C1-3)alkil-skupine, (C1-3)alkilenil-CONR'R''-skupine i CONR'R''-skupine, gdje su R' i R'' atom vodika ili (C1-3)alkil; L2 je δ-veza, -(C1-3)alkilenil-skupina, NR'''-skupina, NR'''-(C1-3)alkilenil-skupina, (C1-3)alkilenil-NR'''-skupina, NR'''-(C1-3)alkilenil-NR'''-skupina ili (C1-3)alkilenil-NR'''-(C1-3)alkilenil-skupina, gdje je navedena skupina izborno supstituirana s hidroksi-skupinom, dok R''' je vodik, (C1-3)alkil, (C1-3)alkilenil-OH, (C1-3)alkilenil-O-(C1-3)alkil ili (C1-3)alkilenil-CONR'R'', pri čemu su R' i R'' atom vodika ili (C1-3)alkil; R je δ-veza ili heterociklički, alifatski ili aromatski prsten koji ima pet članova s jednim ili više atoma dušika, koji je izborno supstituiran sa CH2OH, CH2CN, CN ili CONR'R'', pri čemu R' i R'' predstavljaju atom vodika ili (C1-3)alkil; te B je ciklička skupina koja ima sljedeću formulu (VI): [image] u kojoj G6 je CH ili N; R2 je atom vodika ili atom halogena; i adicijske soli s farmaceutski prihvatljivim organskim ili anorganskim kiselinama ili lužinama, enantiomeri, N-oksidi i kvaternarne amonijeve soli navedenog spoja formule (1).
2. Spoj prema patentnom zahtjevu 1, naznačen time, da je R2 odabran iz skupine koju čine atom vodika, atom fluora, atom klora i atom broma.
3. Spoj prema patentnom zahtjevu 1, naznačen time, da je R2 odabran iz skupine koju čine atom vodika i atom fluora.
4. Spoj prema patentnom zahtjevu 1, naznačen time, da L1 je δ-veza ili metilen-skupina (-CH2-).
5. Spoj prema patentnom zahtjevu 1, naznačen time, da L2 je δ-veza, (C1-3)alkilenil-skupina, NR'''-skupina, NR'''-(C1-3)alkilenil-skupina, (C1-3)alkilenil-NR'''-skupina, NR'''-(C1-3)alkilenil-NR'''-skupina ili (C1-3)alkilenil-NR'''-(C1-3)alkilenil-skupina, gdje je navedena skupina izborno supstituirana s jednom ili više hidroksi-skupina.
6. Spoj prema patentnom zahtjevu 5, naznačen time, da L2 je δ-veza, (C1-2)alkilenil-skupina, NR'''-skupina, NR'''-(C1-2)alkilenil-skupina, (C1-2)alkilenil-NR'''-skupina, NR'''-(C1-2)alkilenil-NR'''-skupina ili (C1-2)alkilenil-NR'''-(C1-2)alkilenil-skupina, gdje je navedena skupina izborno supstituirana s jednom hidroksi-skupinom.
7. Spoj prema patentnom zahtjevu 1, naznačen time, da R je δ-veza ili aromatski heterociklički prsten koji ima pet članova s jednim ili više atoma dušika, koji je izborno supstituiran sa CH2CN ili CN.
8. Spoj prema patentnom zahtjevu 7, naznačen time, da R je δ-veza, 1H-imidazol-4-il-skupina ili 1H-pirol-2-il-skupina, koja je izborno supstituirana sa CH2CN ili CN.
9. Spoj prema patentnom zahtjevu 1, naznačen time, da A je ciklička skupina koja ima jednu od sljedećih formula: [image] [image] [image] [image] [image] .
10. Spoj prema patentnom zahtjevu 1, naznačen time, da Y je prsten koji ima jednu od sljedećih formula: [image] [image] [image] [image] [image] [image] .
11. Spoj prema patentnom zahtjevu 1, naznačen time, da B je ciklička skupina koja ima jednu od sljedećih formula: [image] .
12. Farmaceutski pripravak, naznačen time, da obuhvaća najmanje jedan spoj formule (1) u skladu s bilo kojim od prethodnih patentnih zahtjeva 1 do 11, njegovu sol s farmaceutski prihvatljivom organskom ili anorganskom kiselinom ili s farmaceutski prihvatljivom organskom ili anorganskom lužinom, njegov enantiomer, njegovu kvaternarnu amonijevu sol ili njegov N-oksid, te najmanje jedno inertno farmaceutski prihvatljivo pomoćno sredstvo.
13. Spoj formule (1) prema bilo kojem od prethodnih patentnih zahtjeva 1 do 11, naznačen time, da se upotrebljava u medicini.
14. Spoj formule (1) prema bilo kojem od prethodnih patentnih zahtjeva 1 do 11, naznačen time, da se upotrebljava u liječenju bakterijskih infekcija.
15. Spoj formule (1) prema bilo kojem od prethodnih patentnih zahtjeva 1 do 11, za uporabu prema patentnom zahtjevu 14, naznačen time, da se navedena bakterijska infekcija odabire iz skupine koju čine kožna infekcija, mukozna infekcija, ginekološka infekcija, infekcija respiratornog trakta (RTI), infekcija centralnog nervnog sustava (CNS), gastro-intestinalna infekcija, infekcija kostiju, kardiovaskularna infekcija, infekcija prenesena seksualnim putem ili infekcija urinarnog trakta.
HRP20200894TT 2016-06-08 2020-06-04 Novi antibakterijski spojevi HRP20200894T1 (hr)

Applications Claiming Priority (3)

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EP16173550 2016-06-08
EP17732775.6A EP3468975B1 (en) 2016-06-08 2017-06-05 New antibacterial compounds
PCT/EP2017/063600 WO2017211759A1 (en) 2016-06-08 2017-06-05 New antibacterial compounds

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US (2) US10640488B2 (hr)
EP (2) EP3468975B1 (hr)
JP (2) JP2019517545A (hr)
KR (2) KR20190019084A (hr)
CN (2) CN109415373A (hr)
AR (2) AR108777A1 (hr)
AU (2) AU2017276627A1 (hr)
BR (2) BR112018075334A2 (hr)
CA (2) CA3025624A1 (hr)
CY (1) CY1123194T1 (hr)
DK (1) DK3468975T3 (hr)
EA (2) EA201892822A1 (hr)
ES (1) ES2802233T3 (hr)
HR (1) HRP20200894T1 (hr)
HU (1) HUE049547T2 (hr)
IL (2) IL263283A (hr)
LT (1) LT3468975T (hr)
MA (1) MA45221A (hr)
MD (1) MD3468975T2 (hr)
ME (1) ME03738B (hr)
MX (2) MX2018015125A (hr)
PL (1) PL3468975T3 (hr)
PT (1) PT3468975T (hr)
RS (1) RS60511B1 (hr)
SG (2) SG11201810389XA (hr)
SI (1) SI3468975T1 (hr)
WO (2) WO2017211760A1 (hr)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2019517545A (ja) * 2016-06-08 2019-06-24 アジェンデ・キミケ・リウニテ・アンジェリニ・フランチェスコ・ア・チ・エレ・ア・エフェ・ソシエタ・ペル・アチオニAziende Chimiche Riunite Angelini Francesco A.C.R.A.F.Societa Per Azioni 新しい抗菌性化合物
KR20230124583A (ko) 2020-11-23 2023-08-25 이난타 파마슈티칼스, 인코포레이티드 신규한 스피로피롤리딘 유래 항바이러스제
WO2022235605A1 (en) 2021-05-04 2022-11-10 Enanta Pharmaceuticals, Inc. Novel macrocyclic antiviral agents
CN113698412A (zh) * 2021-09-01 2021-11-26 临沂大学 一种香豆素并[4,3-b]吡咯类衍生物及其合成方法和应用
US11919910B2 (en) 2021-11-12 2024-03-05 Enanta Pharmaceuticals, Inc. Spiropyrrolidine derived antiviral agents
WO2023086352A1 (en) 2021-11-12 2023-05-19 Enanta Pharmaceuticals, Inc. Novel spiropyrrolidine derived antiviral agents
WO2023086350A1 (en) 2021-11-12 2023-05-19 Enanta Pharmaceuticals, Inc. Alkyne-containing antiviral agents
WO2023107419A1 (en) 2021-12-08 2023-06-15 Enanta Pharmaceuticals, Inc. Saturated spirocyclics as antiviral agents
WO2023137007A1 (en) * 2022-01-11 2023-07-20 Enanta Pharmaceuticals, Inc. Processes for the preparation of 4,6,7-trifluoro-1h-indole-2-carboxylic acid

Family Cites Families (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2886570B2 (ja) 1989-09-29 1999-04-26 エーザイ株式会社 縮合ヘテロ環を有する化合物
MX9201991A (es) * 1991-05-02 1992-11-01 Jonh Wyeth & Brother Limited Derivados de piperazina y procedimiento para su preparacion.
US5607936A (en) 1994-09-30 1997-03-04 Merck & Co., Inc. Substituted aryl piperazines as neurokinin antagonists
FR2822154B1 (fr) 2001-03-13 2005-10-21 Aventis Pharma Sa Derives de la quinolyl propyl piperidine, leur preparation et les compositions qui les contiennent
US6921821B2 (en) * 2002-06-12 2005-07-26 Abbott Laboratories Antagonists of melanin concentrating hormone receptor
DE102004041163A1 (de) 2004-08-25 2006-03-02 Morphochem Aktiengesellschaft für kombinatorische Chemie Neue Verbindungen mit antibakterieller Aktivität
WO2006046552A1 (ja) * 2004-10-27 2006-05-04 Toyama Chemical Co., Ltd. 新規な含窒素複素環化合物およびその塩
CA2603322C (en) 2005-03-31 2014-12-16 Janssen Pharmaceutica N.V. Bicyclic pyrazole compounds as antibacterial agents
US20090131444A1 (en) * 2005-05-24 2009-05-21 Astrazeneca Ab Aminopiperidine Quinolines and Their Azaisosteric Analogues with Antibacterial Activity
MY150958A (en) * 2005-06-16 2014-03-31 Astrazeneca Ab Compounds for the treatment of multi-drug resistant bacterial infections
WO2006137485A1 (ja) * 2005-06-24 2006-12-28 Toyama Chemical Co., Ltd. 新規な含窒素複素環化合物およびその塩
CN101346379A (zh) * 2005-10-21 2009-01-14 葛兰素集团有限公司 用作抗菌剂的周环并合的三环化合物
EP2481735A1 (en) * 2007-05-09 2012-08-01 Pfizer Inc. Substituted heterocyclic derivatives and compositions and their pharmaceutical use as antibacterials
JP5620636B2 (ja) * 2007-11-26 2014-11-05 富山化学工業株式会社 新規な複素環化合物またはその塩を含有する抗菌剤
EP2300477A1 (en) * 2008-05-23 2011-03-30 Glaxo Group Limited Tricyclic nitrogen containing compounds and their use as antibacterials
EA018817B1 (ru) 2008-05-23 2013-10-30 Глэксо Груп Лимитед Трициклические азотсодержащие соединения и их применение в качестве бактерицидных средств
TW201022279A (en) * 2008-11-14 2010-06-16 Astrazeneca Ab Chemical compounds
ES2561631T3 (es) 2009-01-15 2016-02-29 Glaxo Group Limited Compuestos de naftiridin-2(1H)-ona útiles como agentes antibacterianos
JP5662346B2 (ja) 2009-01-21 2015-01-28 バジリア ファルマスーチカ アーゲーBasilea Pharmaceutica AG 新規二環式抗生物質
US9156822B2 (en) 2010-07-02 2015-10-13 The University Of North Carolina At Chapel Hill Functionally selective ligands of dopamine D2 receptors
WO2012117421A1 (en) * 2011-03-02 2012-09-07 Orchid Research Laboratories Ltd Histone deacetylase inhibitors
CA2840060A1 (en) * 2011-06-27 2013-01-03 Kyorin Pharmaceutical Co., Ltd. Bridged bicyclic compounds for the treatment of bacterial infections
KR20140096337A (ko) 2011-11-08 2014-08-05 액테리온 파마슈티칼 리미티드 2-옥소-옥사졸리딘-3,5-디일 항생제 유도체
TW201326180A (zh) 2011-11-30 2013-07-01 Actelion Pharmaceuticals Ltd 3,7-二取代八氫-2H-吡啶并[4,3-e][1,3]□嗪-2-酮抗生素
CN105218501A (zh) * 2014-07-03 2016-01-06 南京大学 含哌嗪环的香豆素类衍生物及其制备与在抗菌药物中的应用
EA031589B1 (ru) * 2014-08-22 2019-01-31 Глэксосмитклайн Интеллекчуал Проперти Дивелопмент Лимитед Трициклические азотсодержащие соединения для лечения инфекции, вызываемой neisseria gonorrhoeae
MA41168A (fr) * 2014-12-17 2017-10-24 Acraf Nouveaux composés antibactériens
MA41169A (fr) * 2014-12-17 2017-10-24 Acraf Composés antibactériens à large spectre d'activité
JP2019517545A (ja) * 2016-06-08 2019-06-24 アジェンデ・キミケ・リウニテ・アンジェリニ・フランチェスコ・ア・チ・エレ・ア・エフェ・ソシエタ・ペル・アチオニAziende Chimiche Riunite Angelini Francesco A.C.R.A.F.Societa Per Azioni 新しい抗菌性化合物

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