[go: up one dir, main page]

WO2008136324A1 - ヘテロ環およびホスホノアミノ基が置換したピリジン誘導体ならびにそれらを含有する抗真菌剤 - Google Patents

ヘテロ環およびホスホノアミノ基が置換したピリジン誘導体ならびにそれらを含有する抗真菌剤 Download PDF

Info

Publication number
WO2008136324A1
WO2008136324A1 PCT/JP2008/057851 JP2008057851W WO2008136324A1 WO 2008136324 A1 WO2008136324 A1 WO 2008136324A1 JP 2008057851 W JP2008057851 W JP 2008057851W WO 2008136324 A1 WO2008136324 A1 WO 2008136324A1
Authority
WO
WIPO (PCT)
Prior art keywords
alkyl
atom
phosphonoamino
hydrogen atom
alkoxylated
Prior art date
Application number
PCT/JP2008/057851
Other languages
English (en)
French (fr)
Inventor
Keigo Tanaka
Eiichi Yamamoto
Naoaki Watanabe
Original Assignee
Eisai R & D Management Co., Ltd.
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 Eisai R & D Management Co., Ltd. filed Critical Eisai R & D Management Co., Ltd.
Priority to EP08740790A priority Critical patent/EP2141171A4/en
Priority to NZ578930A priority patent/NZ578930A/en
Priority to JP2009512940A priority patent/JPWO2008136324A1/ja
Priority to AU2008246754A priority patent/AU2008246754B2/en
Priority to CA002684503A priority patent/CA2684503A1/en
Priority to BRPI0808833-0A priority patent/BRPI0808833A2/pt
Priority to MX2009011532A priority patent/MX2009011532A/es
Publication of WO2008136324A1 publication Critical patent/WO2008136324A1/ja
Priority to IL201421A priority patent/IL201421A0/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
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6558Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
    • C07F9/65583Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system each of the hetero rings containing nitrogen as ring hetero atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/66Phosphorus compounds
    • A61K31/664Amides of phosphorus acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/10Antimycotics
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Oncology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Communicable Diseases (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

 本発明は、優れた抗真菌作用を有し、物性、特に、水への溶解性、および安全性の面でも優れた抗真菌剤を提供する。本発明によれば、下式(I)で表される化合物またはその塩;  [式中、 R1が、水素原子、ハロゲン原子、アミノ基、R11-NH-(R11が、C1-6アルキル基、ヒドロキシC1-6アルキル基、C1-6アルコキシC1-6アルキル基、またはC1-6アルコキシカルボニルC1-6アルキル基を意味する。)、R12-(CO)-NH-(R12が、C1-6アルキル基またはC1-6アルコキシC1-6アルキル基)、C1-6アルキル基、ヒドロキシC1-6アルキル基、シアノC1-6アルキル基、C1-6アルコキシ基、またはC1-6アルコキシC1-6アルキル基、またはホスホノアミノ基を意味し;R2が、水素原子、C1-6アルキル基、アミノ基、ジC1-6アルキルアミノ基、またはホスホノアミノ基を意味し;XおよびYの一方が、窒素原子を、他方が、窒素原子または酸素原子を意味し;環Aが、ハロゲン原子もしくはC1-6アルキル基を1個もしくは2個有していてもよい、5もしくは6員のへテロアリール環またはベンゼン環を意味し;Zが、単結合、メチレン基、エチレン基、酸素原子、硫黄原子、-CH2O-、-OCH2-、-NH-、-CH2NH-、-NHCH2-、-CH2S-、または-SCH2-を意味し;R3が、水素原子、ハロゲン原子、または、置換基を1個もしくは2個有していてもよい、C1-6アルキル基、C3-8シクロアルキル基、C6-10アリール基、5もしくは6員へテロアリール基、または5もしくは6員の非芳香族系へテロ環式基を意味し;R4が、水素原子またはハロゲン原子を意味する。  ただし、R1およびR2のいずれか一方はホスホノアミノ基を意味する。」を開示する。
PCT/JP2008/057851 2007-04-27 2008-04-23 ヘテロ環およびホスホノアミノ基が置換したピリジン誘導体ならびにそれらを含有する抗真菌剤 WO2008136324A1 (ja)

Priority Applications (8)

Application Number Priority Date Filing Date Title
EP08740790A EP2141171A4 (en) 2007-04-27 2008-04-23 HETEROCYCLE-SUBSTITUTED PYRIDINE DERIVATIVE AND PHOSPHONOAMINO AND ANTIFUNGAL AGENT CONTAINING THE SAME
NZ578930A NZ578930A (en) 2007-04-27 2008-04-23 Pyridine derivatives substituted by heterocycle ring and phosphonoamino and antifungal agent containing the same
JP2009512940A JPWO2008136324A1 (ja) 2007-04-27 2008-04-23 ヘテロ環およびホスホノアミノ基が置換したピリジン誘導体ならびにそれらを含有する抗真菌剤
AU2008246754A AU2008246754B2 (en) 2007-04-27 2008-04-23 Pyridine derivatives substituted by heterocyclic ring and phosphonoamino group, and anti-fungal agent containing same
CA002684503A CA2684503A1 (en) 2007-04-27 2008-04-23 Pyridine derivatives substituted by heterocyclic ring and phosphonoamino group, and anti-fungal agent containing same
BRPI0808833-0A BRPI0808833A2 (pt) 2007-04-27 2008-04-23 Derivados de piridina substituídos por anel heterocíclico e grupo fosfonoamino, e agente antifúngico contendo o mesmo
MX2009011532A MX2009011532A (es) 2007-04-27 2008-04-23 Derivados de piridina sustituidos por un anillo heterociclico y grupo fosfonoamino, y agente anti-fungal que contiene los mismos.
IL201421A IL201421A0 (en) 2007-04-27 2009-10-11 Pyridine derivatives substituted by heterocyclic ring and phosphonoamino group, and anti-fungal agent containing same

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US91461507P 2007-04-27 2007-04-27
JP2007118356 2007-04-27
US60/914,615 2007-04-27
JP2007-118356 2007-04-27

Publications (1)

Publication Number Publication Date
WO2008136324A1 true WO2008136324A1 (ja) 2008-11-13

Family

ID=39943436

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2008/057851 WO2008136324A1 (ja) 2007-04-27 2008-04-23 ヘテロ環およびホスホノアミノ基が置換したピリジン誘導体ならびにそれらを含有する抗真菌剤

Country Status (16)

Country Link
US (1) US8507530B2 (ja)
EP (1) EP2141171A4 (ja)
JP (1) JPWO2008136324A1 (ja)
KR (1) KR20100015909A (ja)
CN (1) CN101668767A (ja)
AU (1) AU2008246754B2 (ja)
BR (1) BRPI0808833A2 (ja)
CA (1) CA2684503A1 (ja)
IL (1) IL201421A0 (ja)
MX (1) MX2009011532A (ja)
NZ (1) NZ578930A (ja)
RU (1) RU2009143926A (ja)
SA (1) SA08290258B1 (ja)
TW (1) TW200841879A (ja)
WO (1) WO2008136324A1 (ja)
ZA (1) ZA200905435B (ja)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009084621A1 (ja) * 2007-12-27 2009-07-09 Eisai R & D Management Co., Ltd. ヘテロ環およびホスホノキシメチル基が置換したピリジン誘導体ならびにそれらを含有する抗真菌剤
WO2010032874A1 (ja) * 2008-09-19 2010-03-25 住友化学株式会社 農業用組成物
WO2011051198A2 (de) 2009-10-30 2011-05-05 Bayer Cropscience Ag Pyridin-derivate als pflanzenschutzmittel
US8188119B2 (en) 2008-10-24 2012-05-29 Eisai R&D Management Co., Ltd Pyridine derivatives substituted with heterocyclic ring and γ-glutamylamino group, and antifungal agents containing same
US8507530B2 (en) 2007-04-27 2013-08-13 Eisai R&D Management Co., Ltd. Pyridine derivatives substituted by heterocyclic ring and phosphonoamino group, and anti-fungal agent containing same
JP2014034523A (ja) * 2012-08-07 2014-02-24 Manac Inc モノまたはジハロゲノピリジルアミン類の製造方法
WO2017178549A1 (en) 2016-04-12 2017-10-19 Syngenta Participations Ag Microbiocidal oxadiazole derivatives
WO2020179859A1 (ja) 2019-03-06 2020-09-10 第一三共株式会社 ピロロピラゾール誘導体
JP2021512946A (ja) * 2018-02-05 2021-05-20 ユニヴェルスィテ・ドゥ・ストラスブール 疼痛を治療するための化合物および組成物
JP7574450B2 (ja) 2020-12-15 2024-10-28 シーセン ファーマシューティカル カンパニー リミテッド アミノピリジン系化合物及びその使用

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005033079A1 (ja) * 2003-09-30 2005-04-14 Eisai Co., Ltd. ヘテロ環化合物を含有する新規な抗真菌剤
TWI385169B (zh) * 2005-10-31 2013-02-11 Eisai R&D Man Co Ltd 經雜環取代之吡啶衍生物及含有彼之抗真菌劑
WO2008035726A1 (fr) 2006-09-21 2008-03-27 Eisai R & D Management Co., Ltd. Dérivé de pyridine substitué par un cycle hétéroaryle, et agent antifongique le comprenant
JP2012176900A (ja) * 2009-06-24 2012-09-13 Eisai R & D Management Co Ltd ((ホスホノオキシ)メチル)ピリジニウム環を有するピリジン誘導体およびそれらを含有する抗真菌剤
ITMI20110362A1 (it) * 2011-03-09 2012-09-10 F I S Fabbrica Italiana Sint P A Procedimento per la preparazione di 1-(6-metilpiridin-3-il)-2-[4-(metilsolfonil)fenil]etanone, un intermedio dell'etoricoxib.
WO2014160739A2 (en) * 2013-03-27 2014-10-02 Cellmosaic Inc. Trifluoroborate mass spectrometric tags
EP3816155A1 (en) * 2013-08-23 2021-05-05 Virginia Commonwealth University Ester nitrates derivatives of aromatic aldehydes with multiple pharmalogic properties to treat sickle cell disease
PT3720438T (pt) 2017-12-07 2023-12-07 Amplyx Pharmaceuticals Inc Agentes antifúngicos derivados de piridina substituídos por heterociclo
JP2021530445A (ja) 2018-06-25 2021-11-11 アンプリックス ファーマシューティカルズ,インク. 複素環およびアミノ基によって置換されたピリジン誘導体
AU2019387370A1 (en) 2018-11-30 2021-06-10 Nuvation Bio Inc. Pyrrole and pyrazole compounds and methods of use thereof

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0124154A2 (en) * 1983-04-22 1984-11-07 Shell Internationale Researchmaatschappij B.V. Aniline compositions, their preparation, compositions containing them, and method of combating fungus and/or combating or regulating plant growth
US5691336A (en) 1994-03-04 1997-11-25 Merck & Co., Inc. Morpholine compounds are prodrugs useful as tachykinin receptor antagonists
WO2002004626A1 (fr) 2000-07-07 2002-01-17 Eisai Co., Ltd. Gene de synthese de la paroi des cellules fongiques
WO2002085897A1 (en) 2001-04-05 2002-10-31 Alangudi Sankaranarayanan Heterocyclic compounds for aging-related and diabetic vascular complications
WO2003031435A1 (en) 2001-10-06 2003-04-17 Merck Patent Gmbh Pyrazole derivatives as glycine transporter inhibitors
WO2004089931A1 (de) 2003-04-05 2004-10-21 Merck Patent Gmbh Substituierte pyrazole
WO2005033079A1 (ja) 2003-09-30 2005-04-14 Eisai Co., Ltd. ヘテロ環化合物を含有する新規な抗真菌剤
JP2005526751A (ja) * 2002-03-08 2005-09-08 ビーエーエスエフ アクチェンゲゼルシャフト prothioconazoleをベースにし、殺虫剤を含有する殺菌性混合物
JP2006519247A (ja) * 2003-03-01 2006-08-24 アストラゼネカ アクチボラグ 抗生物質として有用なヒドロキシメチル置換ジヒドロイソオキサゾール誘導体

Family Cites Families (103)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB919073A (en) 1960-09-15 1963-02-20 Farmaceutici Italia Benzylamine derivatives
JPS542325A (en) 1977-06-07 1979-01-09 Sankyo Co Ltd Agricultural and horticultural pesticide
US4551532A (en) * 1980-05-08 1985-11-05 Takeda Chemical Industries, Ltd. Ethylene glycol derivatives having anti-protozoan, anti-fungal and anti-tumor activity
JPS57179192A (en) 1981-04-27 1982-11-04 Takeda Chem Ind Ltd Ethylene glycol derivative
JPS5973575A (ja) * 1982-10-05 1984-04-25 Shionogi & Co Ltd プロピニルアミノイソオキサゾ−ル誘導体
JPS5984824A (ja) 1982-11-08 1984-05-16 Takeda Chem Ind Ltd 抗腫瘍剤
DE3316187A1 (de) 1983-05-04 1984-11-08 Cassella Ag, 6000 Frankfurt 2-(aminomethyl)-pyrrol-derivate, verfahren zu ihrer herstellung und ihre verwendung
EP0124067B1 (de) * 1983-05-04 1986-12-17 CASSELLA Aktiengesellschaft 2-(Aminoalkyl)-pyrrol-Derivate, Verfahren zu ihrer Herstellung und ihre Verwendung
WO1986003203A1 (fr) 1984-11-22 1986-06-05 Yoshitomi Pharmaceutical Industries, Ltd. Derives de thienylthiazole
JP2556849B2 (ja) * 1986-02-13 1996-11-27 三共株式会社 グリセリン誘導体
US5070082A (en) * 1986-10-23 1991-12-03 American Cyanamid Company Solubilized pro-drugs
US4851423A (en) 1986-12-10 1989-07-25 Schering Corporation Pharmaceutically active compounds
IL89028A0 (en) 1988-01-29 1989-08-15 Lilly Co Eli Quinoline,quinazoline and cinnoline derivatives
US5034393A (en) 1989-07-27 1991-07-23 Dowelanco Fungicidal use of pyridopyrimidine, pteridine, pyrimidopyrimidine, pyrimidopyridazine, and pyrimido-1,2,4-triazine derivatives
US5120704A (en) * 1989-11-08 1992-06-09 The United States Of America As Represented By The Secretary Of The Navy Method of making Tl-Sr-Ca-Cu-oxide superconductors comprising heating at elevated pressures in a sealed container
US5371086A (en) * 1991-03-15 1994-12-06 The Green Cross Corporation Aminopyridine compounds
US5208247A (en) * 1991-08-01 1993-05-04 American Cyanamid Company Pyridinium compounds which are useful as antagonists of platelet activating factor
EP0533130A1 (de) 1991-09-19 1993-03-24 Hoechst Aktiengesellschaft 2-Hydroxymethylpyridine, die entsprechenden Pyridin-N-oxide und ihre Derivate, Verfahren zu ihrer Herstellung sowie deren Verwendung
WO1993007138A1 (en) 1991-10-08 1993-04-15 Nippon Soda Co., Ltd. Pyrazole derivative and agrohorticultural bactericide containing same
US5710181A (en) * 1991-12-16 1998-01-20 Washington University Inhibition of nitric oxide formation in inflammatory bowel disease
SE9103776D0 (sv) 1991-12-19 1991-12-19 Astra Ab New compounds
US5235728A (en) * 1992-07-30 1993-08-17 H.M. Electronics, Inc. Fastening device for portable equipment and method of using same
KR100196356B1 (ko) 1993-09-28 1999-06-15 오스카 아끼히꼬 당뇨병 치료제
JPH09507245A (ja) 1994-01-07 1997-07-22 ダウエランコ N−(4−ピリミジニル)アミド有害生物防除剤
DE4434637A1 (de) * 1994-09-28 1996-04-04 Hoechst Schering Agrevo Gmbh Substituierte Pyridine, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel und Fungizide
DE69618370T2 (de) * 1995-04-11 2002-09-26 Mitsui Chemicals, Inc. Substituierte Thiophenderivate und diese als aktiver Bestandteil enthaltenden Fungizide für Land- und Gartenbauwirtschaft
US5710171A (en) * 1995-05-24 1998-01-20 Merck & Co., Inc. Bisphenyl inhibitors of farnesyl-protein transferase
US6080767A (en) * 1996-01-02 2000-06-27 Aventis Pharmaceuticals Products Inc. Substituted n-[(aminoiminomethyl or aminomethyl)phenyl]propyl amides
AU1608397A (en) 1996-02-02 1997-08-22 Zeneca Limited Heterocyclic compounds useful as pharmaceutical agents
US5945431A (en) * 1996-03-15 1999-08-31 Biochem Therapeutics Incorporated Cytomegalovirus inhibiting compounds
GB9605437D0 (en) 1996-03-15 1996-05-15 Iaf Biochem Int Cytomegalovirus inhibiting compounds
WO1998010732A1 (en) 1996-09-12 1998-03-19 Bio-Enhancement Systems Corporation Human applications of controlled stress
US6174905B1 (en) * 1996-09-30 2001-01-16 Mitsui Chemicals, Inc. Cell differentiation inducer
GB9702194D0 (en) * 1997-02-04 1997-03-26 Lilly Co Eli Sulphonide derivatives
JP2000510481A (ja) * 1997-04-04 2000-08-15 ファイザー・プロダクツ・インク ニコチンアミド誘導体
US20020111495A1 (en) * 1997-04-04 2002-08-15 Pfizer Inc. Nicotinamide acids, amides, and their mimetics active as inhibitors of PDE4 isozymes
ES2179490T3 (es) 1997-05-08 2003-01-16 Merck Sharp & Dohme Derivados de 1,2,4-triazolo(3,4-a)ftalazina sustituidos como ligandos de gaba alfa 5.
DE19727117A1 (de) 1997-06-26 1999-01-07 Boehringer Ingelheim Pharma Phenylalkylderivate, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung
DE19732033A1 (de) * 1997-07-25 1999-01-28 Bayer Ag Triazolinthion-phosphorsäure-Derivate
AU9002598A (en) * 1997-09-16 1999-04-05 Takeda Chemical Industries Ltd. Nitrogenous fused-ring compounds, process for the preparation of the same, and drugs
US6022884A (en) * 1997-11-07 2000-02-08 Amgen Inc. Substituted pyridine compounds and methods of use
BR9815166A (pt) * 1997-12-11 2000-10-10 Iaf Biochem Int "método de inibição da replicação de vìrus, composto, método de inibição da replicação de citomegalovìrus, composto antiviral, utilização de um composto, composição farmacêutica, composição farmacêutica inibidora da replicação de vìrus e de citomegalovìrus e composição farmacêutica antiviral"
CA2317008C (en) * 1997-12-31 2009-01-20 The University Of Kansas Water soluble prodrugs of tertiary amine containing drugs and methods of making thereof
PE20000942A1 (es) 1998-07-31 2000-09-28 Lilly Co Eli Derivados de amida, carbamato y urea
JP2000178243A (ja) 1998-12-14 2000-06-27 Teijin Ltd ビフェニルアミジン誘導体
US6235728B1 (en) * 1999-02-19 2001-05-22 Bristol-Myers Squibb Company Water-soluble prodrugs of azole compounds
AU777040B2 (en) * 1999-02-22 2004-09-30 Shire Biochem Inc. (1,8) naphthyridine derivatives having antiviral activity
US6319944B1 (en) 1999-05-10 2001-11-20 Merck & Co., Inc. Aryl amidines, compositions containing such compounds and methods of use
GB9919588D0 (en) * 1999-08-18 1999-10-20 Hoechst Schering Agrevo Gmbh Fungicidal compounds
TWI262185B (en) 1999-10-01 2006-09-21 Eisai Co Ltd Carboxylic acid derivatives having anti-hyperglycemia and anti-hyperlipemia action, and pharmaceutical composition containing the derivatives
CO5251397A1 (es) 1999-10-08 2003-02-28 Smithkline Beecham Corp Inhibidores de fab i
WO2001036003A2 (en) 1999-11-15 2001-05-25 Drug Innovation & Design, Inc. Selective cellular targeting: multifunctional delivery vehicles
US6414013B1 (en) * 2000-06-19 2002-07-02 Pharmacia & Upjohn S.P.A. Thiophene compounds, process for preparing the same, and pharmaceutical compositions containing the same background of the invention
CN100467597C (zh) * 2000-07-07 2009-03-11 卫材R&D管理有限公司 真菌细胞壁合成基因
DE10039477A1 (de) * 2000-08-08 2002-02-21 Aventis Cropscience Gmbh Heterocyclylalkylazol-Derivate und ihre Verwendung als Schädlingsbekämpfungsmittel
BR0113931A (pt) 2000-09-15 2004-01-13 Anormed Inc Compostos heterocìclicos ligantes receptores de quimiocinas
JP2004518629A (ja) * 2000-09-18 2004-06-24 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー 殺菌・殺カビ剤として使用するためのピリジニルアミド類およびイミド類
EP1217000A1 (en) 2000-12-23 2002-06-26 Aventis Pharma Deutschland GmbH Inhibitors of factor Xa and factor VIIa
ES2239203T3 (es) 2001-01-31 2005-09-16 Pfizer Products Inc. Derivados nicotinamida y sus mimeticos como inhibidores de isozimas pde4.
JP2002275159A (ja) 2001-03-16 2002-09-25 Japan Tobacco Inc Hcp阻害剤及びhcp阻害活性を有する化合物
GB0109122D0 (en) * 2001-04-11 2001-05-30 Smithkline Beecham Spa Novel compounds
EP1275301A1 (en) 2001-07-10 2003-01-15 Bayer CropScience S.A. Trisubstituted heterocyclic compounds and their use as fungicides
EP1275653A1 (en) 2001-07-10 2003-01-15 Bayer CropScience S.A. Oxazolopyridines and their use as fungicides
JP2005509594A (ja) 2001-07-13 2005-04-14 バーチャル ドラッグ ディヴェロップメント、インコーポレイティッド Nadシンテターゼ阻害剤およびその使用
US20040198773A1 (en) * 2001-09-26 2004-10-07 Barry Hart Substituted 3-pyridyl oxazoles as c17,20 lyase inhibitors
KR100437972B1 (ko) * 2001-10-27 2004-07-02 한국과학기술연구원 피롤리디논 유도체, 이의 제조 방법 및 이를 포함하는제약 조성물
EP1440072A4 (en) 2001-10-30 2005-02-02 Conforma Therapeutic Corp PURINE ANALOGS HAVING HSP90 INHIBITORY ACTIVITY
PL370978A1 (en) 2001-11-27 2005-06-13 F.Hoffmann-La Roche Ag Benzothiazole derivatives
CA2468159A1 (en) 2001-11-27 2003-06-05 Merck & Co., Inc. 4-aminoquinoline compounds
US20030191158A1 (en) 2002-02-11 2003-10-09 Magee Thomas V. Nicotinamide derivatives and a tiotropium salt in combination for the treatment of diseases
ATE485275T1 (de) 2002-02-12 2010-11-15 Glaxosmithkline Llc Nicotinamide und deren verwendung als p38 inhibitoren
GEP20074230B (en) 2002-03-20 2007-11-12 Bristol Myers Squibb Co Phosphate prodrugs of fluorooxindoles
SI1501808T1 (sl) * 2002-04-26 2008-10-31 Lilly Co Eli Antagonisti tahikininskega receptorja
EP1369420A1 (en) 2002-06-06 2003-12-10 Aventis Pharma Deutschland GmbH Inhibitors of the GPib - vWF interaction
TW200812986A (en) 2002-08-09 2008-03-16 Nps Pharma Inc New compounds
PA8578101A1 (es) * 2002-08-13 2004-05-07 Warner Lambert Co Derivados de heterobiarilo como inhibidores de metaloproteinasa de la matriz
GB0222495D0 (en) 2002-09-27 2002-11-06 Glaxo Group Ltd Compounds
AU2003271117A1 (en) 2002-10-09 2004-05-04 Ssp Co., Ltd. Novel pyrazole compounds having antifungal activity
CN101092628B (zh) 2002-11-22 2010-11-03 卫材R&D管理有限公司 筛选在疟原虫中抑制gpi生物合成的化合物的方法
AU2003293376A1 (en) 2002-12-10 2004-06-30 Imclone Systems Incorporated Anti-angiogenic compounds and their use in cancer treatment
SI1569907T1 (sl) * 2002-12-13 2016-06-30 Ym Biosciences Australia Pty Ltd Na nikotinamidu osnovani kinazni inhibitorji
JP4156460B2 (ja) 2003-07-09 2008-09-24 Tdk株式会社 ワークのピックアップ方法及びその装置、実装機
ATE412642T1 (de) * 2003-07-25 2008-11-15 Novartis Ag Inhibitoren von p-38-kinase
JO2525B1 (en) 2004-04-08 2010-03-17 شركة جانسين فارماسوتيكا ان. في Derived 4-alkyl-and-4-canoelperidine derivatives and their use as anti-neroquin
KR101169694B1 (ko) 2004-06-30 2012-07-31 토야마 케미칼 컴퍼니 리미티드 신규의 아릴아미딘유도체 및 그 염과 그들을 함유하는 항진균제
EP1782811A4 (en) 2004-08-09 2010-09-01 Eisai R&D Man Co Ltd INNOVATIVE ANTIPALUDITIC AGENT CONTAINING A HETEROCYCLIC COMPOUND
US20090227799A1 (en) * 2004-08-09 2009-09-10 Kazutaka Nakamoto Novel Antimalarial Agent Containing Heterocyclic Compound
JP4874958B2 (ja) 2005-03-30 2012-02-15 エーザイ・アール・アンド・ディー・マネジメント株式会社 ピリジン誘導体を含有する抗真菌剤
TWI385169B (zh) * 2005-10-31 2013-02-11 Eisai R&D Man Co Ltd 經雜環取代之吡啶衍生物及含有彼之抗真菌劑
AU2006309762B2 (en) 2005-10-31 2010-02-25 Eisai R&D Management Co., Ltd. Heterocyclic substituted pyridine derivatives and antifungal agent containing same
US20070099877A1 (en) 2005-11-02 2007-05-03 Cytovia, Inc. N-aryl-thienopyrimidin-4-amines and analogs as activators of caspases and inducers of apoptosis and the use thereof
US20110201496A1 (en) * 2006-03-27 2011-08-18 Joachim Rheinheimer Substituted 5-Hetaryl-4-Aminopyrimidines
WO2008035726A1 (fr) * 2006-09-21 2008-03-27 Eisai R & D Management Co., Ltd. Dérivé de pyridine substitué par un cycle hétéroaryle, et agent antifongique le comprenant
MX2009003533A (es) 2006-10-06 2009-07-17 Toyama Chemical Co Ltd Composición farmacéutica que comprende derivado de fenilamidina y método para usar la composición farmacéutica en combinación con el aceite antifúngico.
WO2008070149A2 (en) 2006-12-05 2008-06-12 Neurogesx, Inc. Prodrugs and methods of making and using the same
WO2008136279A1 (ja) * 2007-04-27 2008-11-13 Eisai R & D Management Co., Ltd. ヘテロ環置換ピリジン誘導体の塩またはその結晶
TW200841879A (en) 2007-04-27 2008-11-01 Eisai R&D Man Co Ltd Pyridine derivatives substituted by heterocyclic ring and phosphonoamino group, and anti-fungal agent containing same
BRPI0821689A2 (pt) 2007-12-26 2015-06-16 Eisai R&D Man Co Ltd Processo para a produção de derivados de piridina substituídos por heterociclo
US8513287B2 (en) 2007-12-27 2013-08-20 Eisai R&D Management Co., Ltd. Heterocyclic ring and phosphonoxymethyl group substituted pyridine derivatives and antifungal agent containing same
WO2009130462A1 (en) 2008-04-23 2009-10-29 Leafgreen Limited Manual pump type fluid dispenser
GB0809773D0 (en) 2008-05-29 2008-07-09 F2G Ltd Antifungal combination therapy
US8188119B2 (en) * 2008-10-24 2012-05-29 Eisai R&D Management Co., Ltd Pyridine derivatives substituted with heterocyclic ring and γ-glutamylamino group, and antifungal agents containing same
JP2012176900A (ja) * 2009-06-24 2012-09-13 Eisai R & D Management Co Ltd ((ホスホノオキシ)メチル)ピリジニウム環を有するピリジン誘導体およびそれらを含有する抗真菌剤

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0124154A2 (en) * 1983-04-22 1984-11-07 Shell Internationale Researchmaatschappij B.V. Aniline compositions, their preparation, compositions containing them, and method of combating fungus and/or combating or regulating plant growth
US5691336A (en) 1994-03-04 1997-11-25 Merck & Co., Inc. Morpholine compounds are prodrugs useful as tachykinin receptor antagonists
WO2002004626A1 (fr) 2000-07-07 2002-01-17 Eisai Co., Ltd. Gene de synthese de la paroi des cellules fongiques
WO2002085897A1 (en) 2001-04-05 2002-10-31 Alangudi Sankaranarayanan Heterocyclic compounds for aging-related and diabetic vascular complications
WO2003031435A1 (en) 2001-10-06 2003-04-17 Merck Patent Gmbh Pyrazole derivatives as glycine transporter inhibitors
JP2005526751A (ja) * 2002-03-08 2005-09-08 ビーエーエスエフ アクチェンゲゼルシャフト prothioconazoleをベースにし、殺虫剤を含有する殺菌性混合物
JP2006519247A (ja) * 2003-03-01 2006-08-24 アストラゼネカ アクチボラグ 抗生物質として有用なヒドロキシメチル置換ジヒドロイソオキサゾール誘導体
WO2004089931A1 (de) 2003-04-05 2004-10-21 Merck Patent Gmbh Substituierte pyrazole
WO2005033079A1 (ja) 2003-09-30 2005-04-14 Eisai Co., Ltd. ヘテロ環化合物を含有する新規な抗真菌剤

Non-Patent Citations (8)

* Cited by examiner, † Cited by third party
Title
"Jikkenkagakukoza", vol. 18, article "This step can be carried out according to the general methods", pages: 20 - 23
BIOORGANIC & MEDICINAL CHEMISTRY, vol. 11, 2003, pages 2427 - 2437
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, vol. 12, no. 6, pages 531 - 536
JOURNAL OF HETEROCYCLIC CHEMISTRY, vol. 41, no. 6, pages 931 - 939
JOURNAL OF MEDICINAL CHEMISTRY, vol. 46, no. 5, pages 702 - 705
JOURNAL OF ORGANIC CHEMISTRY, vol. 49, no. 26, pages 5237 - 5243
TETRAHEDRON LETTERS, vol. 24, no. 31, pages 3165 - 3168
TETRAHEDRON LETTERS, vol. 40, no. 49, pages 8575 - 8578

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8507530B2 (en) 2007-04-27 2013-08-13 Eisai R&D Management Co., Ltd. Pyridine derivatives substituted by heterocyclic ring and phosphonoamino group, and anti-fungal agent containing same
WO2009084621A1 (ja) * 2007-12-27 2009-07-09 Eisai R & D Management Co., Ltd. ヘテロ環およびホスホノキシメチル基が置換したピリジン誘導体ならびにそれらを含有する抗真菌剤
US8513287B2 (en) 2007-12-27 2013-08-20 Eisai R&D Management Co., Ltd. Heterocyclic ring and phosphonoxymethyl group substituted pyridine derivatives and antifungal agent containing same
WO2010032874A1 (ja) * 2008-09-19 2010-03-25 住友化学株式会社 農業用組成物
US8188119B2 (en) 2008-10-24 2012-05-29 Eisai R&D Management Co., Ltd Pyridine derivatives substituted with heterocyclic ring and γ-glutamylamino group, and antifungal agents containing same
WO2011051198A2 (de) 2009-10-30 2011-05-05 Bayer Cropscience Ag Pyridin-derivate als pflanzenschutzmittel
JP2014034523A (ja) * 2012-08-07 2014-02-24 Manac Inc モノまたはジハロゲノピリジルアミン類の製造方法
WO2017178549A1 (en) 2016-04-12 2017-10-19 Syngenta Participations Ag Microbiocidal oxadiazole derivatives
JP2021512946A (ja) * 2018-02-05 2021-05-20 ユニヴェルスィテ・ドゥ・ストラスブール 疼痛を治療するための化合物および組成物
JP7506379B2 (ja) 2018-02-05 2024-06-26 ユニヴェルスィテ・ドゥ・ストラスブール 疼痛を治療するための化合物および組成物
WO2020179859A1 (ja) 2019-03-06 2020-09-10 第一三共株式会社 ピロロピラゾール誘導体
JP7574450B2 (ja) 2020-12-15 2024-10-28 シーセン ファーマシューティカル カンパニー リミテッド アミノピリジン系化合物及びその使用

Also Published As

Publication number Publication date
IL201421A0 (en) 2010-05-31
AU2008246754B2 (en) 2012-07-12
TW200841879A (en) 2008-11-01
US8507530B2 (en) 2013-08-13
EP2141171A4 (en) 2012-05-02
ZA200905435B (en) 2010-09-29
EP2141171A1 (en) 2010-01-06
NZ578930A (en) 2011-05-27
AU2008246754A1 (en) 2008-11-13
RU2009143926A (ru) 2011-06-10
SA08290258B1 (ar) 2011-10-08
CA2684503A1 (en) 2008-11-13
BRPI0808833A2 (pt) 2014-08-26
KR20100015909A (ko) 2010-02-12
MX2009011532A (es) 2009-11-10
JPWO2008136324A1 (ja) 2010-07-29
CN101668767A (zh) 2010-03-10
US20090082403A1 (en) 2009-03-26

Similar Documents

Publication Publication Date Title
WO2008136324A1 (ja) ヘテロ環およびホスホノアミノ基が置換したピリジン誘導体ならびにそれらを含有する抗真菌剤
BRPI0817973A2 (pt) derivados de nicotinamida, o respectivo preparo e a respectiva aplicação em terapêutica
UA99637C2 (ru) Производные пиридина, замещенные гетероциклическим кольцом и фосфоноксиметильной группой, и содержащее их противогрибковое средство
CY1121051T1 (el) Περιεχουσα αζωτο ετεροκυκλικη ενωση και γεωργικο/κηπουρικο σποριοκτονο
MX2009004920A (es) Nuevos derivados de aminopirimidina como inhibidores de plk1.
WO2005037783A3 (fr) Composes tricycliques comme inhibiteurs de transport de glycine
WO2009028543A1 (ja) 置換ピラゾール誘導体
MX2009013728A (es) Derivados de bicicloanilina.
WO2009054332A1 (ja) ピリドン置換ジヒドロピラゾロピリミジノン誘導体
WO2013129692A3 (en) Nitrogen-containing heterocyclic derivative having 2-imino group and pest control agent including the same
EP1719763A4 (en) NEW PYRIDINE DERIVATIVE AND PYRIMIDINE DERIVATIVE (2)
MY145746A (en) Heterocyclic substituted pyridine derivatives and antifungal agent containing same
EP1724262A4 (en) 1- (2H) -ISOCHINOLONDERIVAT
TW200605883A (en) Condensed heterocycle derivative having HCV inhibitory activity
WO2008126890A1 (ja) ヒドラジド化合物およびそれを含有する有害節足動物防除剤
NO931433D0 (no) 4,1-benzoksazepinderivater og deres anvendelse
WO2008155668A3 (en) Heteroarylamide pyrimidone compounds
TW200745104A (en) Multikinase inhibitor
WO2008155670A3 (en) Arylamide pyrimidone compounds
MX2010010471A (es) Derivado de tetrahidroisoquinolina novedoso.
BR0308759A (pt) Derivados de fenil amidas siliconadas utilizáveis como microbiocida
MX2025003324A (es) Inhibidores de sik heterociclicos
EP1741714A4 (en) HETEROCYLIC COMPOUND AND ANTI-MALIGNANT TUMOR AGENT CONTAINING THE SAME AS ACTIVE INGREDIENT
WO2009054742A3 (en) Novel precursors
WO2007144769A8 (en) Aryl- and heteroaryl-ethyl-acylguanidine derivatives, their preparation and their application in therapeutics

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 200880013858.4

Country of ref document: CN

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 08740790

Country of ref document: EP

Kind code of ref document: A1

WWE Wipo information: entry into national phase

Ref document number: 2008246754

Country of ref document: AU

ENP Entry into the national phase

Ref document number: 2009512940

Country of ref document: JP

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 12009501476

Country of ref document: PH

WWE Wipo information: entry into national phase

Ref document number: 5064/DELNP/2009

Country of ref document: IN

WWE Wipo information: entry into national phase

Ref document number: 578930

Country of ref document: NZ

ENP Entry into the national phase

Ref document number: 2008246754

Country of ref document: AU

Date of ref document: 20080423

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 2008740790

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 201421

Country of ref document: IL

WWE Wipo information: entry into national phase

Ref document number: 2684503

Country of ref document: CA

WWE Wipo information: entry into national phase

Ref document number: MX/A/2009/011532

Country of ref document: MX

WWE Wipo information: entry into national phase

Ref document number: 2009101584

Country of ref document: EG

ENP Entry into the national phase

Ref document number: 20097022334

Country of ref document: KR

Kind code of ref document: A

NENP Non-entry into the national phase

Ref country code: DE

WWE Wipo information: entry into national phase

Ref document number: 2009143926

Country of ref document: RU

ENP Entry into the national phase

Ref document number: PI0808833

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20090915