ES2184786T3 - Nuevos derivados 2,2'-bi-1h-pirrol con actividad inmunosupresora. - Google Patents

Nuevos derivados 2,2'-bi-1h-pirrol con actividad inmunosupresora.

Info

Publication number
ES2184786T3
ES2184786T3 ES95902113T ES95902113T ES2184786T3 ES 2184786 T3 ES2184786 T3 ES 2184786T3 ES 95902113 T ES95902113 T ES 95902113T ES 95902113 T ES95902113 T ES 95902113T ES 2184786 T3 ES2184786 T3 ES 2184786T3
Authority
ES
Spain
Prior art keywords
sub
alkilo
replaced
alcoxi
alquenilo
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
ES95902113T
Other languages
English (en)
Inventor
Gianfederico Doria
Anna Maria Isetta
Marcellino Tibolla
Maria Chiara Fornasiero
Mario Ferrari
Domenico Trizio
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.)
Pfizer Italia SRL
Original Assignee
Pharmacia Italia SpA
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 Pharmacia Italia SpA filed Critical Pharmacia Italia SpA
Application granted granted Critical
Publication of ES2184786T3 publication Critical patent/ES2184786T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/44Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/30Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D207/34Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/36Oxygen or sulfur atoms

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Epidemiology (AREA)
  • Immunology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Transplantation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyrrole Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Cephalosporin Compounds (AREA)
  • Saccharide Compounds (AREA)

Abstract

SE DESCRIBEN NUEVOS Y CONOCIDOS DERIVADOS 5-[[](()2H-PIRROLO-2ILIDENO())METILO[]]-2,2''-BI-1H-PIRROLO, QUE TIENEN ACTIVIDAD INMUNOMODULADORA Y, REPRESENTADOS POR LA FORMULA GENERAL (I), EN DONDE, SUJETO A UNA CONDICION, R{SUB, 1} REPRESENTA HIDROGENO, FENILO, ALKILO C{SUB, 1}-C{SUB, 20} O ALQUENILO C{SUB, 2}-C{SUB, 20}, EN DONDE LOS GRUPOS ALKILO Y ALQUENILO PUEDEN SER NO SUSTITUIDOS O SUSTITUIDOS POR 1 A 3 SUSTITUYENTES SELECCIONADOS INDEPENDIENTEMENTE DE HALOGENO, ALCOXI C{SUB, 1}-C{SUB, 6}, HIDROXI, ARILO Y ARILOXI; R{SUB, 2} REPRESENTA HIDROGENO, ALKILO C{SUB, 1}-C{SUB, 6}, CIANO, CARBOXI O (()ALCOXI C{SUB, 1}-C{SUB, 6}())CARBONILO; R{SUB, 3} REPRESENTA HALOGENO, HIDROXI O ALCOXI C{SUB, 1}-C{SUB, 11} NO SUSTITUIDO O SUSTITUIDO POR FENILO; R{SUB, 4} REPRESENTA HIDROGENO, ALKILO C{SUB, 1}-C{SUB, 6} O FENILO; CADA UNO DE R{SUB, 5} Y R{SUB, 6} REPRESENTA INDEPENDIENTEMENTE HIDROGENO, ALCANOILO C{SUB, 2}-C{SUB, 20}, ALQUENOILO C{SUB, 3}-C{SUB, 20}, FENILO, ALKILO C{SUB, 1}-C{SUB, 20}, O ALQUENILO C{SUB, 2}-C{SUB, 20}, EN DONDE EL ALCANOILO, ALQUENOILO, ALKILO Y LOS GRUPOS ALQUENILOS PUEDEN SER NO SUSTITUIDOS O SUSTITUIDOS POR DE 1 A 3 SUSTITUYENTES SELECCIONADOS INDEPENDIENTEMENTE DE HALOGENO, ALCOXI C{SUB, 1}C{SUB, 6}, HIDROXI, ARILO, ARILOXI, CIANO, CARBOXI, (()ALCOXI C{SUB, 1}-C{SUB, 6}())CARBONILO, (()ALQUENILO C{SUB, 3}-C{SUB, 4}())CARBAMOILO, ARALKILCARBAMOILO, ARILCARBAMOILO Y CONR{SUB,C}R{SUB,D} EN EL CUAL CADA UNO DE R{SUB,C} Y R{SUB, 4} ES INDEPENDIENTEMENTE HIDROGENO O ALKILO C{SUB, 1}-C{SUB, 6} O R{SUB, C} Y R{SUB, D} TOMADOS JUNTOS CON EL ATOMO DE NITROGENO AL QUE ESTAN ENLAZADOS, FORMAN UN ANILLO MORFOLINO O PIPERIDINO; O DOS DE R{SUB, 4}, R{SUB, 5} Y R{SUB, 6} TOMADOS JUNTOS FORMAN UNA CADENA DE POLIMETILENO C{SUB,4}-C{SUB,12}, QUE PUEDE SER NO SUSTITUIDA O SUSTITUIDA POR UN ALKILO C{SUB, 1}-C{SUB, 12}, POR UN ALQUENILO C{SUB, 2}-C{SUB, 12} O POR UN GRUPO DE ALKILIDENO C{SUB, 1}-C{SUB, 12}, EN DONDE LOS GRUPOS ALKILO, ALQUENILO Y ALKILIDENO PUEDE SER A SU VEZ NOSUSTITUIDOS O SUSTITUIDOS POR UN SUSTITUYENTE SELECCIONADO DE HALOGENO; ALCOXI C{SUB, 1}-C{SUB, 6}, HIDROXI, CIANO, CARBOXI, (()ALCOXI C{SUB, 1}-C{SUB, 6}())CARBONILO, ARILOXI Y ARILO; EL RESTO SIENDO HIDROGENO O ALKILO C{SUB, 1}-C{SUB, 12}; Y LAS SALES FARMACEUTICAMENTE ACEPTABLES DEL MISMO.
ES95902113T 1993-12-23 1994-12-02 Nuevos derivados 2,2'-bi-1h-pirrol con actividad inmunosupresora. Expired - Lifetime ES2184786T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB939326284A GB9326284D0 (en) 1993-12-23 1993-12-23 Pyrrolydenemethyl-derivatives and process for their preparation

Publications (1)

Publication Number Publication Date
ES2184786T3 true ES2184786T3 (es) 2003-04-16

Family

ID=10747089

Family Applications (1)

Application Number Title Priority Date Filing Date
ES95902113T Expired - Lifetime ES2184786T3 (es) 1993-12-23 1994-12-02 Nuevos derivados 2,2'-bi-1h-pirrol con actividad inmunosupresora.

Country Status (25)

Country Link
US (1) US5691334A (es)
EP (2) EP0686147B1 (es)
JP (1) JP3594311B2 (es)
KR (1) KR100365057B1 (es)
CN (1) CN1120153C (es)
AT (1) ATE224874T1 (es)
AU (1) AU689169B2 (es)
CA (1) CA2155096A1 (es)
DE (1) DE69431429T2 (es)
DK (1) DK0686147T3 (es)
ES (1) ES2184786T3 (es)
FI (1) FI109688B (es)
GB (1) GB9326284D0 (es)
HU (1) HUT73663A (es)
IL (1) IL112022A (es)
MY (1) MY113304A (es)
NO (1) NO305796B1 (es)
NZ (1) NZ276716A (es)
PL (1) PL183112B1 (es)
PT (1) PT686147E (es)
RU (1) RU2145957C1 (es)
TW (1) TW285670B (es)
UA (1) UA57697C2 (es)
WO (1) WO1995017381A1 (es)
ZA (1) ZA9410203B (es)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2736550B1 (fr) 1995-07-14 1998-07-24 Sandoz Sa Composition pharmaceutique sous la forme d'une dispersion solide comprenant un macrolide et un vehicule
GB9603212D0 (en) * 1996-02-15 1996-04-17 Pharmacia Spa Process for the preparation of 2,2'-bipyrrolyl-pyrromethane derivatives
GB9619706D0 (en) * 1996-09-20 1996-11-06 Pharmacia Spa Synergistic immunosuppressant composition containing a 2,2'-bi-1H-pyrrole comp und
GB9705035D0 (en) * 1997-03-11 1997-04-30 Pharmacia & Upjohn Spa Indolyl-pyrrolydenemethylpyrrole derivatives and process for their preparation
US5989591A (en) * 1997-03-14 1999-11-23 American Home Products Corporation Rapamycin formulations for oral administration
KR100252197B1 (ko) * 1997-09-20 2000-04-15 박호군 세라시아 마르세센스 균주의 배양액으로 부터 분리한 면역억제제용 프로디지오신
GB9802745D0 (en) * 1998-02-09 1998-04-08 Pharmacia & Upjohn Spa Benzyloxy prodigiosine compounds
US6407244B1 (en) 2000-01-26 2002-06-18 Gemin X Biotechnologies Inc. Pyrrole-type compounds, compositions, and methods for treating cancer or viral diseases
US20040014987A1 (en) * 2000-01-26 2004-01-22 Gemin X Biotechnologies Inc. Pyrrole-Type compounds, compositions, and methods for treating cancer or viral diseases
KR20010081515A (ko) * 2000-02-15 2001-08-29 복성해 프로디지오신의 당뇨병 예방 및 치료용 조성물
KR100392225B1 (ko) * 2001-04-19 2003-07-22 한국생명공학연구원 류머티스 관절염 치료용 프로디지오신 조성물
ES2304135T3 (es) 2001-07-18 2008-09-16 Gemin X Biotechnologies Inc. Compuestos tipo pirrol, composiciones y metodos para tratar el cancer, tratar enfermedades virales y causar inmunosupresion.
ES2382377T3 (es) 2003-05-30 2012-06-07 Gemin X Pharmaceuticals Canada Inc. Compuestos triheterocíclicos, composiciones, y métodos para tratar cáncer
WO2006115509A2 (en) 2004-06-24 2006-11-02 Novartis Vaccines And Diagnostics Inc. Small molecule immunopotentiators and assays for their detection
WO2006089397A1 (en) * 2005-02-22 2006-08-31 Gemin X Biotechnologies Inc. Methods for treating arthritis using triheterocyclic compounds
KR100674222B1 (ko) * 2005-07-11 2007-01-24 한국생명공학연구원 세라시아 마르세센스 b-1231 kctc 0386bp로부터분리한 프로디지오신을 유효성분으로 포함한 급성이식편대숙주병의 예방 및 치료용 조성물
NZ569608A (en) 2006-01-06 2011-09-30 Sepracor Inc Tetralone-based monoamine reuptake inhibitors
BRPI0706365A2 (pt) 2006-01-06 2011-03-22 Sepracor Inc Cicloalquilaminas como inibidores da recaptação de monoamina
DK2816024T3 (en) 2006-03-31 2017-10-30 Sunovion Pharmaceuticals Inc CHIRALE AMINER
US7884124B2 (en) 2006-06-30 2011-02-08 Sepracor Inc. Fluoro-substituted inhibitors of D-amino acid oxidase
US20080051400A1 (en) * 2006-07-06 2008-02-28 Gemin X Biotechnologies Inc. Methods for treating or preventing anemia or thrombocytopenia using a triheterocyclic compound
US7902252B2 (en) 2007-01-18 2011-03-08 Sepracor, Inc. Inhibitors of D-amino acid oxidase
AU2008259841B2 (en) 2007-05-31 2015-02-05 Sunovion Pharmaceuticals Inc. Phenyl substituted cycloalkylamines as monoamine reuptake inhibitors
CN103387529B (zh) * 2013-07-30 2016-03-30 中国农业科学院烟草研究所 抗tmv的三吡咯环类化合物及其制备方法和用途
ES2615077B1 (es) * 2015-12-02 2018-03-14 Universidad De Burgos Una nueva familia de compuestos, procedimiento de obtención de los mismos y sus usos en el tratamiento y/o profilaxis de enfermedades

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61280429A (ja) * 1985-06-06 1986-12-11 Chugai Pharmaceut Co Ltd 免疫抑制剤
SU1409276A1 (ru) * 1985-11-10 1988-07-15 Донецкий медицинский институт им.М.Горького Способ лечени острых кишечных инфекций
JPH02250828A (ja) * 1989-03-23 1990-10-08 Nippon Kayaku Co Ltd 新規免疫抑制剤

Also Published As

Publication number Publication date
UA57697C2 (uk) 2003-07-15
EP0686147B1 (en) 2002-09-25
PT686147E (pt) 2003-02-28
CN1120153C (zh) 2003-09-03
IL112022A (en) 1998-12-27
PL310387A1 (en) 1995-12-11
FI953919A0 (fi) 1995-08-21
ATE224874T1 (de) 2002-10-15
HUT73663A (en) 1996-09-30
NO953280D0 (no) 1995-08-21
NO953280L (no) 1995-08-21
DE69431429T2 (de) 2003-05-15
AU1109095A (en) 1995-07-10
HU9502782D0 (en) 1995-11-28
NZ276716A (en) 1996-12-20
NO305796B1 (no) 1999-07-26
GB9326284D0 (en) 1994-02-23
FI109688B (fi) 2002-09-30
IL112022A0 (en) 1995-03-15
DK0686147T3 (da) 2003-02-03
KR100365057B1 (ko) 2003-06-09
CA2155096A1 (en) 1995-06-29
CN1118164A (zh) 1996-03-06
TW285670B (es) 1996-09-11
DE69431429D1 (de) 2002-10-31
MY113304A (en) 2002-01-31
JP3594311B2 (ja) 2004-11-24
ZA9410203B (en) 1995-10-20
US5691334A (en) 1997-11-25
JPH08507090A (ja) 1996-07-30
EP1241162A1 (en) 2002-09-18
AU689169B2 (en) 1998-03-26
FI953919A7 (fi) 1995-08-21
KR960701009A (ko) 1996-02-24
PL183112B1 (pl) 2002-05-31
WO1995017381A1 (en) 1995-06-29
EP0686147A1 (en) 1995-12-13
RU2145957C1 (ru) 2000-02-27

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