ES2103287T3 - Nuevos derivados de tiazolidina. - Google Patents

Nuevos derivados de tiazolidina.

Info

Publication number
ES2103287T3
ES2103287T3 ES91111866T ES91111866T ES2103287T3 ES 2103287 T3 ES2103287 T3 ES 2103287T3 ES 91111866 T ES91111866 T ES 91111866T ES 91111866 T ES91111866 T ES 91111866T ES 2103287 T3 ES2103287 T3 ES 2103287T3
Authority
ES
Spain
Prior art keywords
group
carbon atom
general formula
atom
single bond
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Lifetime
Application number
ES91111866T
Other languages
English (en)
Inventor
Masaaki Toda
Shuichi Shinbayashida Ohuchida
Hiroyuki Ohno
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ono Pharmaceutical Co Ltd
Original Assignee
Ono Pharmaceutical 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 Ono Pharmaceutical Co Ltd filed Critical Ono Pharmaceutical Co Ltd
Application granted granted Critical
Publication of ES2103287T3 publication Critical patent/ES2103287T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/06Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/04Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyrrole Compounds (AREA)

Abstract

UN NUEVO DERIVADO DE TIAZOLIDINA DE LA FORMULA GENERAL: DONDE R REPRESENTA UN GRUPO DE LA FORMULA GENERAL: G-E-D-B-ADONDE A REPRESENTA UN GRUPO ALCALINO DE UNION SIMPLE DE 1 A 6 ATOMO(S) DE CARBONO, UN GRUPO ALKENILENO DE 2 A 6 ATOMOS DE CARBONO, UN GRUPO DE LA FORMULA GENERAL: O DE ANILLO DE HIDROCARBURO SATURADO DE 4 A 7 ATOMOS DE CARBONO O DE UN ANILLO HETEROCICLICO MONOAROMATICO QUE CONTIENE DE 4 A 7 MIEMBROS DE ANILLO QUE INCLUYEN UN ATOMO DE NITROGENO Y/O UN ATOMO DE AZUFRE QUE PUEDEN SER TOTAL O PARCIALMENTE SATURADOS, Y REPRESENTA UN GRUPO ALKILENO DE 1 A 4 ATOMO(S) DE CARBONO O UN GRUPO ALKENILENO DE 2 A 4 ATOMOS DE CARBONO, B REPRESENTA UN GRUPO ALCALINO DE UNION SIMPLE DE 1 A 6 ATOMO(S) DE CARBONO, D REPRESENTA UN ATOMO DE OXIGENO DE UNION SIMPLE, UN GRUPO CARBONILO U OTRO DE LA FORMULA GENERAL: R ELEVADO 1 REPRESENTA UN ATOMO DE HIDROGENO, UN GRUPO ALCALINO DE 1 A 4 ATOMO(S) DE CARBONO, UN GRUPO FENILO O BENCILO, E REPRESENTA UN GRUPO ALCALINO DE UNION SIMPLE DE 1 A 8 ATOMO(S) DE CARBONO O UN GRUPO ALCALINO DE 1 A 8 ATOMO(S) DE CARBONO SUSTITUIDOS POR UN GRUPO FENILO O BENCILO, G REPRESENTA ANILLO(S) CARBONCICLICOS MONO, BI O TRIAROMATICOS QUE CONTIENEN NO MAS DE 15 ATOMOS DE CARBONO QUE PUEDEN SER PARCIAL O COMPLETAMENTE SATURADOS, O G REPRESENTA ANILLO(S) HETEROCICLICOS MONO, BI O TRIAROMATICOS QUE CONTIENEN NO MAS DE 15 MIEMBROS DE ANILLOS QUE INCLUYEN UN ATOMO DE NITROGENO QUE PUEDE SER PARCIAL O COMPLETAMENTE SATURADO DONDE DICHO ANILLO CARBOCICLICO O HETEROCICLICO REPRESENTADO POR G PUEDE SUSTITUIRSE O NO, POR UNO A TRES GRUPOS ALCALINOS DE 1 A 6 ATOMO(S) DE CARBONO, POR UN GRUPO ALKOXI DE 1 A 6 ATOMO(S) DE CARBONO, POR ATOMO HALOGENO, POR UN GRUPO TRIFLUOROMETILO O NITRO, CON LA CONDICION DE QUE A Y B NO REPRESENTEN UNIONES SIMPLES AL MISMO TIEMPO POSEE ACTIVIDAD INHIBITORIA EN LA PROLIL ENDOPEPTIDASA Y, POR LO TANTO, ES UTIL COMO AGENTE PARA EL TRATAMIENTO Y/O PREVENCION DE LA AMNESIA.
ES91111866T 1987-02-23 1988-02-16 Nuevos derivados de tiazolidina. Expired - Lifetime ES2103287T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3784487 1987-02-23

Publications (1)

Publication Number Publication Date
ES2103287T3 true ES2103287T3 (es) 1997-09-16

Family

ID=12508841

Family Applications (2)

Application Number Title Priority Date Filing Date
ES91111866T Expired - Lifetime ES2103287T3 (es) 1987-02-23 1988-02-16 Nuevos derivados de tiazolidina.
ES88102243T Expired - Lifetime ES2052619T3 (es) 1987-02-23 1988-02-16 Un procedimiento para la preparacion de los nuevos derivados de tiazolidina.

Family Applications After (1)

Application Number Title Priority Date Filing Date
ES88102243T Expired - Lifetime ES2052619T3 (es) 1987-02-23 1988-02-16 Un procedimiento para la preparacion de los nuevos derivados de tiazolidina.

Country Status (7)

Country Link
US (1) US4857537A (es)
EP (2) EP0461677B1 (es)
KR (1) KR960001205B1 (es)
AT (1) ATE151760T1 (es)
DE (2) DE3875361T2 (es)
ES (2) ES2103287T3 (es)
GR (1) GR3006406T3 (es)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01250370A (ja) * 1987-12-23 1989-10-05 Zeria Pharmaceut Co Ltd 新規アミノ酸イミド誘導体、製法ならびに用途
JP2515568B2 (ja) * 1987-12-25 1996-07-10 株式会社ヤクルト本社 新規なチアゾリジン誘導体
US5212191A (en) * 1988-04-08 1993-05-18 Ono Pharmaceutical Co., Ltd. Heterocyclic compounds
US5053414A (en) * 1988-04-08 1991-10-01 Ono Pharmaceutical Co., Ltd. Heterocyclic compounds
CA2004028C (en) * 1988-12-08 1998-09-22 Motoki Torizuka Condensed benzene derivative
WO1990012005A1 (fr) * 1989-04-13 1990-10-18 Japan Tobacco Inc. Nouveaux derives aminoacides possedant une activite d'inhibiteur de la prolylendopeptidase
US4999349A (en) * 1990-03-22 1991-03-12 Bristol-Myers Squibb Co. BU-4164E - A and B, prolyl endopeptidase inhibitors
US5073549A (en) * 1990-03-22 1991-12-17 Bristol-Myers Squibb Company BU-4164E - A and B, prolyl endopeptidase inhibitors and their methods of use
FI925500A7 (fi) * 1990-06-04 1992-12-03 Pfizer Aromaattisia pyrrolidiini- ja tiatsolidiiniamideja
US5506256A (en) * 1990-07-27 1996-04-09 Yoshitomi Pharmaceutical Industries, Ltd. Proline derivatives possessing prolyl endopeptidase-inhibitory activity
IT1283782B1 (it) * 1996-08-09 1998-04-30 Ct Lab Farm Srl Uso di ammidi dell'acido gamma-idrossibutirrico nel trattamento di tossicodipendenze,ed in particolare sell'alcolismo
US6419857B1 (en) * 1999-12-06 2002-07-16 Baker Hughes Incorporated Thiazolidines and use thereof for corrosion inhibition
ATE462432T1 (de) 2003-05-05 2010-04-15 Probiodrug Ag Glutaminylcyclase-hemmer
JP2007509898A (ja) 2003-11-03 2007-04-19 プロビオドルグ エージー 神経障害治療に有用な組合せ
KR101099206B1 (ko) 2004-02-05 2011-12-27 프로비오드룩 아게 신규한 글루타미닐 시클라제 저해제
EP1760076A1 (en) 2005-09-02 2007-03-07 Ferring B.V. FAP Inhibitors
JP5379692B2 (ja) 2006-11-09 2013-12-25 プロビオドルグ エージー 潰瘍、癌及び他の疾患の治療のためのグルタミニルシクラーゼの阻害薬としての3−ヒドロキシ−1,5−ジヒドロ−ピロール−2−オン誘導体
EP2091948B1 (en) 2006-11-30 2012-04-18 Probiodrug AG Novel inhibitors of glutaminyl cyclase
CA2679446C (en) 2007-03-01 2016-05-17 Probiodrug Ag New use of glutaminyl cyclase inhibitors
US9656991B2 (en) 2007-04-18 2017-05-23 Probiodrug Ag Inhibitors of glutaminyl cyclase
BR112012008346B1 (pt) 2009-09-11 2021-12-21 Vivoryon Therapeutics N.V. Derivados heterocíclicos, seu processo de preparação, e composição farmacêutica
WO2011107530A2 (en) 2010-03-03 2011-09-09 Probiodrug Ag Novel inhibitors
DK2545047T3 (da) 2010-03-10 2014-07-28 Probiodrug Ag Heterocycliske inhibitorer af glutaminylcyclase (QC, EC 2.3.2.5)
EP2560953B1 (en) 2010-04-21 2016-01-06 Probiodrug AG Inhibitors of glutaminyl cyclase
WO2012123563A1 (en) 2011-03-16 2012-09-20 Probiodrug Ag Benz imidazole derivatives as inhibitors of glutaminyl cyclase
PL3461819T3 (pl) 2017-09-29 2020-11-30 Probiodrug Ag Inhibitory cyklazy glutaminylowej

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60188317A (ja) * 1984-03-09 1985-09-25 Yakult Honsha Co Ltd 抗健忘症剤
JPS6137764A (ja) * 1984-07-31 1986-02-22 Suntory Ltd 抗プロリルエンドペプチダ−ゼ活性を有する新規生理活性化合物
JPH0623190B2 (ja) * 1985-04-16 1994-03-30 サントリー株式会社 インヒビタ−活性を有するn−アシルピロリジン誘導体及びその製法並びに用途
EP0201743B1 (en) * 1985-04-16 1992-04-01 Suntory Limited Dipeptide derivatives of fatty acids, process for preparing them, pharmaceutical composition and use
DE3680578D1 (de) * 1985-04-16 1991-09-05 Suntory Ltd Dipeptid-derivate, verfahren zur herstellung, pharmazeutische zusammensetzungen und ihre anwendung.

Also Published As

Publication number Publication date
GR3006406T3 (es) 1993-06-21
ATE151760T1 (de) 1997-05-15
EP0280956A1 (en) 1988-09-07
KR880009949A (ko) 1988-10-06
DE3875361D1 (de) 1992-11-26
KR960001205B1 (ko) 1996-01-24
DE3855875D1 (de) 1997-05-22
EP0461677A1 (en) 1991-12-18
US4857537A (en) 1989-08-15
ES2052619T3 (es) 1994-07-16
DE3875361T2 (de) 1993-03-25
EP0280956B1 (en) 1992-10-21
EP0461677B1 (en) 1997-04-16
DE3855875T2 (de) 1997-08-28

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