JP6590924B2 - 微生物感染を治療するための相乗的組成物 - Google Patents

微生物感染を治療するための相乗的組成物 Download PDF

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JP6590924B2
JP6590924B2 JP2017523903A JP2017523903A JP6590924B2 JP 6590924 B2 JP6590924 B2 JP 6590924B2 JP 2017523903 A JP2017523903 A JP 2017523903A JP 2017523903 A JP2017523903 A JP 2017523903A JP 6590924 B2 JP6590924 B2 JP 6590924B2
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composition
infection
cell
mupirocin
trna synthetase
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JP2017538675A (ja
JP2017538675A5 (https=
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ポール エム. ダンマン
ポール エム. ダンマン
ウェイン チルダース
ウェイン チルダース
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Temple Univ School of Medicine
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/34Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • A61K31/341Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide not condensed with another ring, e.g. ranitidine, furosemide, bufetolol, muscarine
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    • A61K31/16Amides, e.g. hydroxamic acids
    • A61K31/17Amides, e.g. hydroxamic acids having the group >N—C(O)—N< or >N—C(S)—N<, e.g. urea, thiourea, carmustine
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    • A61K31/34Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • A61K31/343Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
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    • A61K31/35Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
    • A61K31/351Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom not condensed with another ring
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    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404Indoles, e.g. pindolol
    • A61K31/4045Indole-alkylamines; Amides thereof, e.g. serotonin, melatonin
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    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4151,2-Diazoles
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    • A61K31/41641,3-Diazoles
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
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    • 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/443Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with oxygen as a ring hetero atom
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    • 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
    • A61K31/47Quinolines; Isoquinolines
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    • 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
    • A61K31/4965Non-condensed pyrazines
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  • Communicable Diseases (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Otolaryngology (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Apparatus For Disinfection Or Sterilisation (AREA)
  • Medicinal Preparation (AREA)
JP2017523903A 2014-10-31 2015-10-30 微生物感染を治療するための相乗的組成物 Active JP6590924B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201462073100P 2014-10-31 2014-10-31
US62/073,100 2014-10-31
PCT/US2015/058278 WO2016070021A1 (en) 2014-10-31 2015-10-30 Synergistic compositions for treating microbial infections

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JP2017538675A JP2017538675A (ja) 2017-12-28
JP2017538675A5 JP2017538675A5 (https=) 2018-07-19
JP6590924B2 true JP6590924B2 (ja) 2019-10-16

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JP2017523903A Active JP6590924B2 (ja) 2014-10-31 2015-10-30 微生物感染を治療するための相乗的組成物

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US (1) US10028931B2 (https=)
EP (1) EP3212183B1 (https=)
JP (1) JP6590924B2 (https=)
CN (1) CN107106533B (https=)
AU (1) AU2015339039B2 (https=)
CA (1) CA2965839C (https=)
WO (1) WO2016070021A1 (https=)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108456157B (zh) * 2017-02-22 2021-07-20 中国医学科学院药物研究所 1-取代苯甲酰基-4-脂酰基氨基脲类衍生物、制备方法及作为抗菌药物的用途
CN110272364A (zh) * 2018-03-13 2019-09-24 中国医学科学院药物研究所 1-取代苯甲酰基-4-脂酰基氨基脲类衍生物、制备方法及作为抗菌药物的用途
CN116102478B (zh) * 2021-11-09 2025-04-15 中国医学科学院药物研究所 1,4-二羰基氨基硫脲类化合物的制备方法和抗感染的用途

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2002336746A1 (en) * 2001-09-21 2003-04-01 Message Pharmaceuticals, Inc. Inhibitors of rnase p proteins as antibacterial compounds
DK1879877T3 (da) 2005-05-03 2013-04-15 Ranbaxy Lab Ltd Antimikrobielle midler
JP2009533315A (ja) * 2006-04-10 2009-09-17 ランバクシー ラボラトリーズ リミテッド 抗菌剤
US20110207726A1 (en) 2008-04-17 2011-08-25 The Trustees Of The University Of Pennsylvania Inhibitors of Human Cathepsin L, Cathepsin B, and Cathepsin S
WO2010009368A2 (en) * 2008-07-18 2010-01-21 Oragenics, Inc. Compositions for the detection and treatment of colorectal cancer
US9187524B2 (en) 2010-09-15 2015-11-17 The Scripps Research Institute Broad spectrum antibiotic arylomycin analogs
WO2012054738A1 (en) 2010-10-22 2012-04-26 Brown University Combination of an aminoacyl - trna synthetase inhibitor with a further antibacterial agent for attenuating multiple drug resistance
AU2012211253B2 (en) * 2011-01-26 2016-11-10 Board Of Regents Of The University Of Nebraska Small molecule RNase inhibitors and methods of use

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Publication number Publication date
EP3212183B1 (en) 2019-10-02
AU2015339039B2 (en) 2019-11-28
EP3212183A4 (en) 2018-05-16
AU2015339039A1 (en) 2017-05-04
JP2017538675A (ja) 2017-12-28
US20170246139A1 (en) 2017-08-31
EP3212183A1 (en) 2017-09-06
CA2965839A1 (en) 2016-05-06
WO2016070021A1 (en) 2016-05-06
CN107106533B (zh) 2020-11-06
US10028931B2 (en) 2018-07-24
CA2965839C (en) 2023-04-04
CN107106533A (zh) 2017-08-29

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