IL137974A0 - Indole derivatives having antiviral activity - Google Patents

Indole derivatives having antiviral activity

Info

Publication number
IL137974A0
IL137974A0 IL13797499A IL13797499A IL137974A0 IL 137974 A0 IL137974 A0 IL 137974A0 IL 13797499 A IL13797499 A IL 13797499A IL 13797499 A IL13797499 A IL 13797499A IL 137974 A0 IL137974 A0 IL 137974A0
Authority
IL
Israel
Prior art keywords
antiviral activity
indole derivatives
indole
derivatives
antiviral
Prior art date
Application number
IL13797499A
Other languages
English (en)
Original Assignee
Shionogi & Co
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 Shionogi & Co filed Critical Shionogi & Co
Publication of IL137974A0 publication Critical patent/IL137974A0/xx

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/10Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/12Radicals substituted by oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/10Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/18Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/10Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/18Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D209/20Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals substituted additionally by nitrogen atoms, e.g. tryptophane
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/10Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/18Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D209/22Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with an aralkyl radical attached to the ring nitrogen atom

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Virology (AREA)
  • Public Health (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • AIDS & HIV (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Molecular Biology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
IL13797499A 1998-03-26 1999-03-26 Indole derivatives having antiviral activity IL137974A0 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP7820398 1998-03-26
PCT/JP1999/001547 WO1999050245A1 (fr) 1998-03-26 1999-03-26 Derives d'indole exerçant une activite antivirale

Publications (1)

Publication Number Publication Date
IL137974A0 true IL137974A0 (en) 2001-10-31

Family

ID=13655476

Family Applications (1)

Application Number Title Priority Date Filing Date
IL13797499A IL137974A0 (en) 1998-03-26 1999-03-26 Indole derivatives having antiviral activity

Country Status (17)

Country Link
US (3) US6333323B1 (fr)
EP (1) EP1069111A4 (fr)
JP (1) JP3794469B2 (fr)
KR (1) KR20010041705A (fr)
CN (1) CN1142909C (fr)
AU (1) AU752005B2 (fr)
BR (1) BR9909146A (fr)
CA (1) CA2326166A1 (fr)
HU (1) HUP0103460A3 (fr)
ID (1) ID26031A (fr)
IL (1) IL137974A0 (fr)
NO (1) NO317423B1 (fr)
NZ (1) NZ506435A (fr)
PL (1) PL343249A1 (fr)
RU (1) RU2217421C2 (fr)
WO (1) WO1999050245A1 (fr)
ZA (1) ZA200004047B (fr)

Families Citing this family (66)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6142163A (en) * 1996-03-29 2000-11-07 Lam Research Corporation Method and apparatus for pressure control in vacuum processors
WO1999050245A1 (fr) * 1998-03-26 1999-10-07 Shionogi & Co., Ltd. Derives d'indole exerçant une activite antivirale
CA2333707A1 (fr) * 1998-06-03 1999-12-09 Melissa Egbertson Inhibiteurs de vih integrase
CA2333771A1 (fr) * 1998-06-03 1999-12-09 Mark W. Embrey Inhibiteurs de vih integrase
ID29027A (id) 1998-12-25 2001-07-26 Shionogi & Co Turunan-turunan heteroaromatik yang mempunyai aktivitas penghambatan terhadap integrase hiv
US7294481B1 (en) * 1999-01-05 2007-11-13 Immunex Corporation Method for producing recombinant proteins
CN1367784A (zh) 1999-06-02 2002-09-04 盐野义制药株式会社 新的取代丙烯酮衍生物的制备方法
JP2003503386A (ja) * 1999-06-25 2003-01-28 メルク エンド カムパニー インコーポレーテッド 1−(芳香族またはヘテロ芳香族置換)−3−(ヘテロ芳香族置換)−1,3−プロパンジオン類およびそれの使用
ATE504572T1 (de) * 1999-09-02 2011-04-15 Shionogi & Co Derivate von aromatische heterocyclen enthaltende integraseinhibitoren
BR0111678A (pt) * 2000-06-13 2003-06-03 Shionogi & Co Composições medicinais contendo derivados de propenona
EP1297834A4 (fr) * 2000-06-14 2007-05-09 Shionogi & Co Inhibiteur d'enzymes possedant deux ions metal divalents en tant que centres actifs
DK1341414T3 (da) * 2000-11-16 2013-03-25 Univ California Marint actinomycet-taxon til opdagelse af medikamenter og fermenteringsprodukter
US7507767B2 (en) 2001-02-08 2009-03-24 Schering Corporation Cannabinoid receptor ligands
US7067539B2 (en) 2001-02-08 2006-06-27 Schering Corporation Cannabinoid receptor ligands
KR20030078958A (ko) 2001-03-01 2003-10-08 시오노기세이야쿠가부시키가이샤 Hiv 인테그라제 저해 활성을 갖는 질소 함유의헤테로아릴 화합물
EP2181985B1 (fr) 2001-08-10 2011-10-26 Shionogi & Co., Ltd. Agent antiviral
ITMI20012060A1 (it) * 2001-10-05 2003-04-05 Recordati Chem Pharm Nuovi eterocilcli n-acilati
US7169780B2 (en) * 2001-10-26 2007-01-30 Istitute Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. N-substituted hydroxypyrimidinone carboxamide inhibitors of HIV integrase
PL369952A1 (en) 2001-11-14 2005-05-02 Schering Corporation Cannabinoid receptor ligands
EP1463741A4 (fr) * 2001-12-07 2006-07-05 Us Gov Health & Human Serv Composes destines a traiter l'infection au vih et le sida
US20030236277A1 (en) * 2002-02-14 2003-12-25 Kadow John F. Indole, azaindole and related heterocyclic pyrrolidine derivatives
EP1539693B9 (fr) 2002-06-19 2008-10-08 Schering Corporation Agonistes du recepteur cannabinoide
US7176232B2 (en) * 2002-06-24 2007-02-13 The Regents Of The University Of California Salinosporamides and methods for use thereof
US7919497B2 (en) 2002-08-02 2011-04-05 Nereus Pharmaceuticals, Inc. Analogs of dehydrophenylahistins and their therapeutic use
US7935704B2 (en) * 2003-08-01 2011-05-03 Nereus Pharmaceuticals, Inc. Dehydrophenylahistins and analogs thereof and the synthesis of dehydrophenylahistins and analogs thereof
CA2494049C (fr) * 2002-08-02 2011-10-18 Nereus Pharmaceuticals, Inc. Deshydrophenylahistines et analogues de ceux-ci et synthese de ces deshydrophenylahistines et d'analogues de ceux-ci
JP3908248B2 (ja) 2002-08-13 2007-04-25 塩野義製薬株式会社 Hivインテグラーゼ阻害活性を有するヘテロ環化合物
US7112581B2 (en) * 2002-09-27 2006-09-26 Nereus Pharmaceuticals, Inc. Macrocyclic lactams
TW200505902A (en) 2003-03-20 2005-02-16 Schering Corp Cannabinoid receptor ligands
EP1638552B1 (fr) * 2003-06-20 2011-03-02 Nereus Pharmaceuticals, Inc. Utilisation de composes (3.2.0) heterocycliques et d'analogues correspondants pour le traitement du cancer
US8217072B2 (en) * 2003-06-20 2012-07-10 The Regents Of The University Of California Salinosporamides and methods for use thereof
WO2005070922A2 (fr) * 2004-01-23 2005-08-04 Nereus Pharmaceuticals, Inc. Bis-indole pyrroles utiles en tant qu'agents antimicrobiens
US7776883B2 (en) 2004-03-10 2010-08-17 The United States Of America As Represented By The Department Of Health And Human Services Quinolin-4-ones as inhibitors of retroviral integrase for the treatment of HIV, AIDS and AIDS related complex (ARC)
MXPA06012421A (es) 2004-04-30 2007-01-31 Nereus Pharmaceuticals Inc Compuestos de heterociclicos y metodos para utilizar los mismos.
US7579371B2 (en) 2004-04-30 2009-08-25 Nereus Pharmaceuticals, Inc. Methods of using [3.2.0] heterocyclic compounds and analogs thereof
DK1799696T3 (da) 2004-09-17 2009-03-09 Idenix Pharmaceuticals Inc Phosphoindoler som HIV-inhibitorer
US20060100432A1 (en) 2004-11-09 2006-05-11 Matiskella John D Crystalline materials of 1-(4-benzoyl-piperazin-1-yl)-2-[4-methoxy-7-(3-methyl-[1,2,4]triazol-1-yl)-1H-pyrrolo[2,3-c]pyridin-3-yl]-ethane-1,2-dione
DK1830838T3 (da) 2004-12-03 2013-01-21 Dana Farber Cancer Inst Inc Sammensætninger og fremgangsmåder til behandling af neoplastiske sygdomme
CN1316968C (zh) * 2005-09-30 2007-05-23 青岛大学 吲哚-2,3-二酮在制备抗病毒或免疫增强剂药物中的应用
US7851476B2 (en) 2005-12-14 2010-12-14 Bristol-Myers Squibb Company Crystalline forms of 1-benzoyl-4-[2-[4-methoxy-7-(3-methyl-1H-1,2,4-triazol-1-YL)-1-[(phosphonooxy)methyl]-1H-pyrrolo[2,3-C]pyridin-3-YL]-1,2-dioxoethyl]-piperazine
MX2008011127A (es) 2006-03-02 2008-10-31 Astellas Pharma Inc INHIBIDOR DE 17ß HSD TIPO 5.
JP2009530256A (ja) * 2006-03-17 2009-08-27 シプラ・リミテッド 4−[1−(4−シアノフェニル)−1−(1,2,4−トリアゾール−1−イル)メチル]ベンゾニトリルおよび4−[1−(1h−1,2,4−トリアゾール−1−イル)メチレンベンゾニトリル中間体
BRPI0709474A2 (pt) 2006-04-06 2011-07-12 Nerus Pharmaceuticals Inc sìntese total de salinosporamida a e seus análogos
US7807671B2 (en) 2006-04-25 2010-10-05 Bristol-Myers Squibb Company Diketo-piperazine and piperidine derivatives as antiviral agents
MX2009003410A (es) 2006-09-29 2009-07-17 Idenix Pharmaceuticals Inc Fosfoindoles enantiomericamente puros como inhibidores de vih.
US8129527B2 (en) * 2006-11-03 2012-03-06 Nereus Pharmacuticals, Inc. Analogs of dehydrophenylahistins and their therapeutic use
US7824698B2 (en) * 2007-02-02 2010-11-02 Nereus Pharmaceuticals, Inc. Lyophilized formulations of Salinosporamide A
US8394816B2 (en) * 2007-12-07 2013-03-12 Irene Ghobrial Methods of using [3.2.0] heterocyclic compounds and analogs thereof in treating Waldenstrom's Macroglobulinemia
EP2234608A2 (fr) 2007-12-11 2010-10-06 Viamet Pharmaceuticals, Inc. Inhibiteurs de métalloenzymes utilisant des fractions de liaison à un métal en combinaison avec des fractions de ciblage
AU2009246467A1 (en) * 2008-05-12 2009-11-19 Nereus Pharmaceuticals, Inc. Salinosporamide derivatives as proteasome inhibitors
US8835643B2 (en) 2012-02-23 2014-09-16 Empire Technology Development Llc Molecules, compositions, and methods for light absorption
CN103420894A (zh) * 2012-05-22 2013-12-04 中国科学院上海药物研究所 丁-2-烯-1,4-二酮类化合物及其制备方法和用途
EP4166141A1 (fr) 2014-09-14 2023-04-19 Avanir Pharmaceuticals, Inc. Combinaisons du dextrométhorphane deuterée et de la quinidine destinées au traitement de l'agitation et de l'aggresitivé chez la démence d'alzheimer
CA2978567A1 (fr) 2015-03-06 2016-09-15 Beyondspring Pharmaceuticals, Inc. Methode de traitement du cancer associee a une mutation du ras au moyen de plinabulin
AU2016229295B2 (en) 2015-03-06 2021-11-04 Beyondspring Pharmaceuticals, Inc. Method of treating a brain tumor
KR102686692B1 (ko) * 2015-03-31 2024-07-19 더 로얄 인스티튜션 포 디 어드밴스먼트 오브 러닝/맥길 유니버시티 5-옥소-ete 수용체 길항제로서의 인돌 유사체 및 이의 사용 방법
BR112018000229A2 (pt) 2015-07-13 2018-09-04 Beyondspring Pharmaceuticals Inc composições de plinabulina
MX2018009413A (es) 2016-02-08 2019-05-15 Beyondspring Pharmaceuticals Inc Composiciones que contienen tucaresol o sus analogos.
AU2017278245B2 (en) 2016-06-06 2022-09-15 Beyondspring Pharmaceuticals, Inc. Composition and method for reducing neutropenia
US11633393B2 (en) 2017-01-06 2023-04-25 Beyondspring Pharmaceuticals, Inc. Tubulin binding compounds and therapeutic use thereof
KR20190109479A (ko) 2017-02-01 2019-09-25 비욘드스프링 파마수티컬스, 인코포레이티드. 호중구감소증의 감소 방법
CN106995400B (zh) * 2017-04-10 2019-08-06 湘潭大学 一种化合物及其盐及其合成方法
CN107226810B (zh) * 2017-06-16 2020-04-28 郑州大学 吲哚衍生物及其制备方法和其抗流感病毒作用
SG11202006985TA (en) 2018-01-24 2020-08-28 Beyondspring Pharmaceuticals Inc Composition and method for reducing thrombocytopenia via the administration of plinabulin
CN109810044B (zh) * 2019-02-27 2022-05-03 贵州医科大学 一种具有hiv-1整合酶抑制活性的化合物及其制备和应用
AU2022417301A1 (en) * 2021-12-20 2024-08-01 Fairhaven Pharmaceuticals Inc. Oxer1 antagonists and uses thereof

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4377698A (en) * 1976-01-22 1983-03-22 Sterling Drug Inc. 2,4 Bis(2-indolyl-3)-4-oxobutanoic acids
WO1993005020A1 (fr) * 1991-09-06 1993-03-18 Merck & Co., Inc. Indoles utilises comme inhibiteurs de la transcriptase inverse du vih
US5475109A (en) 1994-10-17 1995-12-12 Merck & Co., Inc. Dioxobutanoic acid derivatives as inhibitors of influenza endonuclease
DE69622031T2 (de) * 1995-04-10 2002-12-12 Fujisawa Pharmaceutical Co., Ltd. INDOLDERIVATE ALS cGMP-PDE INHIBITOREN
US5858738A (en) * 1996-11-07 1999-01-12 Merck & Co., Inc. Ermophilane sesquiterpenoids as HIV intergrase inhibitors
WO1999050245A1 (fr) * 1998-03-26 1999-10-07 Shionogi & Co., Ltd. Derives d'indole exerçant une activite antivirale
CA2333771A1 (fr) 1998-06-03 1999-12-09 Mark W. Embrey Inhibiteurs de vih integrase
CA2329134A1 (fr) 1998-06-03 1999-12-09 David L. Clark Inhibiteurs de vih integrase
CA2333707A1 (fr) 1998-06-03 1999-12-09 Melissa Egbertson Inhibiteurs de vih integrase
JP2003503386A (ja) 1999-06-25 2003-01-28 メルク エンド カムパニー インコーポレーテッド 1−(芳香族またはヘテロ芳香族置換)−3−(ヘテロ芳香族置換)−1,3−プロパンジオン類およびそれの使用

Also Published As

Publication number Publication date
CN1142909C (zh) 2004-03-24
HUP0103460A3 (en) 2002-11-28
US6333323B1 (en) 2001-12-25
ZA200004047B (en) 2001-04-25
CN1294580A (zh) 2001-05-09
EP1069111A4 (fr) 2001-06-06
PL343249A1 (en) 2001-07-30
CA2326166A1 (fr) 1999-10-07
US20020019434A1 (en) 2002-02-14
NO20004787L (no) 2000-11-27
ID26031A (id) 2000-11-16
US20030181499A1 (en) 2003-09-25
AU752005B2 (en) 2002-09-05
KR20010041705A (ko) 2001-05-25
RU2217421C2 (ru) 2003-11-27
WO1999050245A1 (fr) 1999-10-07
NZ506435A (en) 2002-08-28
JP3794469B2 (ja) 2006-07-05
BR9909146A (pt) 2000-12-05
EP1069111A1 (fr) 2001-01-17
NO317423B1 (no) 2004-10-25
NO20004787D0 (no) 2000-09-25
US6716605B2 (en) 2004-04-06
AU2958199A (en) 1999-10-18
HUP0103460A2 (hu) 2002-01-28
US6506787B2 (en) 2003-01-14

Similar Documents

Publication Publication Date Title
IL137974A0 (en) Indole derivatives having antiviral activity
EG24081A (en) 4-Substituted-9-deoxo-9a-aza-9a-homerythromycin derivatives
GB9718913D0 (en) Substituted oxindole derivatives
IL141226A0 (en) 1h-imidazopyridine derivatives
HK1040400A1 (zh) 具有抗腫瘤活性的嘧啶衍生物
HUP0003642A3 (en) N-alkanoylphenylalanine derivatives
GB9702194D0 (en) Sulphonide derivatives
PL345540A1 (en) Thiobenzimidazole derivatives
SG71898A1 (en) Benzosulfone derivatives
PL345089A1 (en) Adenosine derivatives
GB9809664D0 (en) a-Ketoamide derivatives
HU9801168D0 (en) Triazinylaminostilbene derivatives
PL349354A1 (en) Substituted phenethylamine derivatives
GB9825988D0 (en) Indole derivatives
EG23802A (en) 2-Phenylpyran-4-one derivatives
GB9715821D0 (en) Amidino-camptothecin derivatives
GB9801711D0 (en) 5-Aroylnaphthalene derivatives
GB9827729D0 (en) Thieno-indole derivatives
GB9725541D0 (en) Amino-benzothiazole derivatives
EP1061912A4 (fr) Derives de phenanthrofuran
IL139276A0 (en) Cyclohexenondioxthio chromanoyl derivatives
HK1042478A1 (zh) 2-氧代-2h-喹啉衍生物
GB9706753D0 (en) Aralkoxy-morphinan derivatives
GB9703060D0 (en) Antiviral benzimidazole derivatives
GB9816279D0 (en) Arylthiazolidinedione derivatives