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NO20015722D0 - Antibakterielle forbindelser - Google Patents

Antibakterielle forbindelser

Info

Publication number
NO20015722D0
NO20015722D0 NO20015722A NO20015722A NO20015722D0 NO 20015722 D0 NO20015722 D0 NO 20015722D0 NO 20015722 A NO20015722 A NO 20015722A NO 20015722 A NO20015722 A NO 20015722A NO 20015722 D0 NO20015722 D0 NO 20015722D0
Authority
NO
Norway
Prior art keywords
antibacterial compounds
antibacterial
compounds
Prior art date
Application number
NO20015722A
Other languages
English (en)
Other versions
NO20015722L (no
Inventor
William H Miller
Kenneth Allen Newlander
Mark Seefeld
Original Assignee
Smithkline Beecham Corp
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
Application filed by Smithkline Beecham Corp filed Critical Smithkline Beecham Corp
Publication of NO20015722D0 publication Critical patent/NO20015722D0/no
Publication of NO20015722L publication Critical patent/NO20015722L/no

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic 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
    • C07D471/02—Heterocyclic 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
    • C07D471/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

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)
  • Plural Heterocyclic Compounds (AREA)
NO20015722A 1999-06-01 2001-11-23 Antibakterielle forbindelser NO20015722L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US13700499P 1999-06-01 1999-06-01
PCT/US2000/015154 WO2000072846A1 (en) 1999-06-01 2000-06-01 Antibacterial compounds

Publications (2)

Publication Number Publication Date
NO20015722D0 true NO20015722D0 (no) 2001-11-23
NO20015722L NO20015722L (no) 2001-11-23

Family

ID=22475391

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20015722A NO20015722L (no) 1999-06-01 2001-11-23 Antibakterielle forbindelser

Country Status (23)

Country Link
US (2) US6573272B1 (no)
EP (1) EP1180030B1 (no)
JP (1) JP4733836B2 (no)
KR (1) KR20020005767A (no)
CN (1) CN1365280A (no)
AR (1) AR024158A1 (no)
AT (1) ATE283049T1 (no)
AU (1) AU773550B2 (no)
BR (1) BR0011121A (no)
CA (1) CA2375630A1 (no)
CO (1) CO5370679A1 (no)
CZ (1) CZ20014290A3 (no)
DE (1) DE60016198T2 (no)
HK (1) HK1045644A1 (no)
HU (1) HUP0201206A3 (no)
IL (1) IL146514A0 (no)
MX (1) MXPA01012326A (no)
NO (1) NO20015722L (no)
NZ (1) NZ515611A (no)
PL (1) PL351959A1 (no)
TR (1) TR200103485T2 (no)
WO (1) WO2000072846A1 (no)
ZA (1) ZA200109733B (no)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CO5180550A1 (es) 1999-04-19 2002-07-30 Smithkline Beecham Corp Inhibidores de fab i
CO5370679A1 (es) 1999-06-01 2004-02-27 Smithkline Beecham Corp Inhibidores fab 1
US6762201B1 (en) 1999-10-08 2004-07-13 Affinium Pharmaceuticals, Inc. Fab I inhibitors
WO2001026652A1 (en) * 1999-10-08 2001-04-19 Smithkline Beecham Corporation Fab i inhibitors
CZ302015B6 (cs) * 1999-10-08 2010-09-08 Affinium Pharmaceuticals, Inc. Inhibitory Fab I
US6730684B1 (en) * 1999-10-08 2004-05-04 Affinium Pharmaceuticals, Inc. Fab I inhibitors
EP1347759B1 (en) * 2000-12-08 2005-06-29 Smithkline Beecham Corporation Antibacterial compounds
ATE402693T1 (de) * 2000-12-21 2008-08-15 Rima W Mcleod Fab i und hemmung von apicomplexan-parasiten
AU2002246728A1 (en) * 2001-02-12 2002-08-28 Lilly Icos Llc Carboline derivatives
ATE420640T1 (de) * 2001-04-06 2009-01-15 Affinium Pharm Inc Fab-i-inhibitoren
US7790709B2 (en) * 2002-12-06 2010-09-07 Affinium Pharmaceuticals, Inc. Heterocyclic compounds, methods of making them and their use in therapy
JP4880448B2 (ja) * 2003-03-17 2012-02-22 アフィナム ファーマシューティカルズ，インコーポレーテッド 複数の抗生物質を含む組成物、及びそれを用いる方法
CA2524125A1 (en) * 2003-04-29 2004-11-11 Oscient Pharmaceuticals Antibiotic tetrahydro-.beta.-carboline derivatives
EP2848614A3 (en) * 2004-06-04 2015-07-29 Debiopharm International SA Acrylamide derivatives as antibiotic agents
WO2007067416A2 (en) * 2005-12-05 2007-06-14 Affinium Pharmaceuticals, Inc. Heterocyclylacrylamide compounds as fabi inhibitors and antibacterial agents
CA2658506C (en) 2006-07-20 2016-01-26 Affinium Pharmaceuticals, Inc. Acrylamide derivatives as fab 1 inhibitors
US7854963B2 (en) * 2006-10-13 2010-12-21 Solopower, Inc. Method and apparatus for controlling composition profile of copper indium gallium chalcogenide layers
EP3255045A1 (en) 2007-02-16 2017-12-13 Debiopharm International SA Salts, prodrugs and polymorphs of fab i inhibitors
US8124616B2 (en) * 2007-11-30 2012-02-28 Biota Scientific Management Pty Ltd Bicyclic PPAT inhibitors as antibacterial agents
KR101135179B1 (ko) * 2009-02-20 2012-04-16 한국생명공학연구원 ＦａｂＩ 저해 물질 비나산손을 포함하는 항균용 조성물
EP2687531B1 (en) 2011-03-18 2016-07-13 ONO Pharmaceutical Co., Ltd. Tetrahydrocarboline derivative
ME03392B (me) 2012-06-19 2020-01-20 Debiopharm Int Sa Prolek derivati (e)-n-meтil-n-( (з-метi lbenzofuran-2-il)meтil)-3-(7 -okso-5 ,6, 7,8-тетrанidr0-1,8-nafтiridin-3-il)akrilamida
EA037121B1 (ru) 2016-02-26 2021-02-09 Дебиофарм Интернэшнл C.A. Лекарственное средство для лечения инфекций на фоне диабетической стопы
JP2021534246A (ja) * 2018-08-16 2021-12-09 レクレオ ファーマシューティカルス アイエヌシー １，３，４，９−テトラヒドロ−２ｈ−ピリド［３，４−ｂ］インドール誘導体化合物及びその使用

Family Cites Families (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3828068A (en) 1971-05-10 1974-08-06 Tenneco Chem ((substituted indazolyl)-n1-methyl)carbamates
US4154943A (en) 1977-12-29 1979-05-15 University Of Vermont Preparation of vincadifformine
US4267330A (en) * 1978-08-24 1981-05-12 Omnium Chimique Societe Anonyme Process for the synthesis of vincadifformine and related derivatives
FR2619111B1 (fr) 1987-08-07 1991-01-11 Synthelabo Derives de (piperidinyl-4)methyl-2 tetrahydro-1,2,3,4 9h-pyrido (3,4-b) indole, leur preparation et leur application en therapeutique
FR2692575B1 (fr) 1992-06-23 1995-06-30 Sanofi Elf Nouveaux derives du pyrazole, procede pour leur preparation et compositions pharmaceutiques les contenant.
US5416193A (en) * 1993-04-30 1995-05-16 Pfizer Inc. Coupling reagent and method
MA23420A1 (fr) 1994-01-07 1995-10-01 Smithkline Beecham Corp Antagonistes bicycliques de fibrinogene.
US5614551A (en) 1994-01-24 1997-03-25 The Johns Hopkins University Inhibitors of fatty acid synthesis as antimicrobial agents
HUT76344A (en) 1994-06-29 1997-08-28 Smithkline Beecham Corp Vitronectin receptor antagonists
DE19624659A1 (de) 1996-06-20 1998-01-08 Klinge Co Chem Pharm Fab Neue Pyridylalken- und Pyridylalkinsäureamide
US6451816B1 (en) 1997-06-20 2002-09-17 Klinge Pharma Gmbh Use of pyridyl alkane, pyridyl alkene and/or pyridyl alkine acid amides in the treatment of tumors or for immunosuppression
JPH10310582A (ja) * 1997-03-13 1998-11-24 Sankyo Co Ltd ピペリジン環縮合カルバペネム化合物
EP0973767A1 (en) 1997-03-31 2000-01-26 Dupont Pharmaceuticals Company Indazoles of cyclic ureas useful as hiv protease inhibitors
US6207679B1 (en) 1997-06-19 2001-03-27 Sepracor, Inc. Antimicrobial agents uses and compositions related thereto
US5932743A (en) 1997-08-21 1999-08-03 American Home Products Corporation Methods for the solid phase synthesis of substituted indole compounds
TR200001954T2 (tr) * 1997-12-24 2000-12-21 Hoechst Marion Roussel Deutschland Gmbh Faktör XA'nın önleyicileri olarak indol türevleri.
OA11599A (en) * 1998-08-20 2004-08-23 Agouron Pharma Non-peptide GnRH agents, methods and intermediatesfor their preparation.
GT199900167A (es) * 1998-10-01 2001-03-21 Nuevos bis-benzimidazoles.
CO5180550A1 (es) 1999-04-19 2002-07-30 Smithkline Beecham Corp Inhibidores de fab i
AR024077A1 (es) 1999-05-25 2002-09-04 Smithkline Beecham Corp Compuestos antibacterianos
CO5370679A1 (es) 1999-06-01 2004-02-27 Smithkline Beecham Corp Inhibidores fab 1
CO5180605A1 (es) 1999-06-23 2002-07-30 Smithkline Beecham Corp Compuestos de indol
US6346391B1 (en) 1999-07-22 2002-02-12 Trustees Of Tufts College Methods of reducing microbial resistance to drugs
WO2001026652A1 (en) 1999-10-08 2001-04-19 Smithkline Beecham Corporation Fab i inhibitors
CZ302015B6 (cs) 1999-10-08 2010-09-08 Affinium Pharmaceuticals, Inc. Inhibitory Fab I
JP4961084B2 (ja) 1999-10-08 2012-06-27 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
CA2323008C (en) 1999-10-11 2005-07-12 Pfizer Inc. Pharmaceutically active compounds
US6656703B1 (en) 1999-12-29 2003-12-02 Millennium Pharamaceuticals, Inc. High throughput screen for inhibitors of fatty acid biosynthesis in bacteria
US6372752B1 (en) 2000-02-07 2002-04-16 Genzyme Corporation Inha inhibitors and methods of use thereof
JP2004514669A (ja) 2000-11-07 2004-05-20 ブリストル−マイヤーズ　スクイブ　カンパニー セリンプロテアーゼ阻害剤として有用な酸誘導体
US20020107266A1 (en) 2000-12-12 2002-08-08 Marguerita Lim-Wilby Compounds, compositions and methods for treatment of parasitic infections

Also Published As

Publication number Publication date
EP1180030A1 (en) 2002-02-20
HUP0201206A2 (en) 2002-08-28
HUP0201206A3 (en) 2003-07-28
PL351959A1 (en) 2003-07-14
EP1180030A4 (en) 2002-09-25
CZ20014290A3 (cs) 2002-05-15
MXPA01012326A (es) 2002-07-30
AR024158A1 (es) 2002-09-04
AU5177400A (en) 2000-12-18
NO20015722L (no) 2001-11-23
HK1045644A1 (zh) 2002-12-06
TR200103485T2 (tr) 2002-04-22
ATE283049T1 (de) 2004-12-15
KR20020005767A (ko) 2002-01-17
DE60016198D1 (de) 2004-12-30
AU773550B2 (en) 2004-05-27
NZ515611A (en) 2004-05-28
CO5370679A1 (es) 2004-02-27
IL146514A0 (en) 2002-07-25
WO2000072846A1 (en) 2000-12-07
US6573272B1 (en) 2003-06-03
CA2375630A1 (en) 2000-12-07
DE60016198T2 (de) 2005-12-01
US6964970B2 (en) 2005-11-15
EP1180030B1 (en) 2004-11-24
BR0011121A (pt) 2002-02-26
CN1365280A (zh) 2002-08-21
US20030232850A1 (en) 2003-12-18
JP4733836B2 (ja) 2011-07-27
JP2003500448A (ja) 2003-01-07
ZA200109733B (en) 2002-09-11

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Legal Events

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FC2A Withdrawal, rejection or dismissal of laid open patent application