AR012293A1 - Derivado de pirimidina y agentes para tratar una enfermedad alergica, asma o dermatitis atopica y para producir inhibicion de no, tnf-alfa, citocinas o5-lipoxigenasa que lo comprenden. - Google Patents

Derivado de pirimidina y agentes para tratar una enfermedad alergica, asma o dermatitis atopica y para producir inhibicion de no, tnf-alfa, citocinas o5-lipoxigenasa que lo comprenden.

Info

Publication number
AR012293A1
AR012293A1 ARP980101135A ARP980101135A AR012293A1 AR 012293 A1 AR012293 A1 AR 012293A1 AR P980101135 A ARP980101135 A AR P980101135A AR P980101135 A ARP980101135 A AR P980101135A AR 012293 A1 AR012293 A1 AR 012293A1
Authority
AR
Argentina
Prior art keywords
alkyl group
group
asthma
lower alkyl
treat
Prior art date
Application number
ARP980101135A
Other languages
English (en)
Original Assignee
Otsuka Pharma 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 Otsuka Pharma Co Ltd filed Critical Otsuka Pharma Co Ltd
Publication of AR012293A1 publication Critical patent/AR012293A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents

Landscapes

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

Abstract

Derivados de piridina representados por la formula (I) y sales farma farmacéuticamente aceptables de los mismos en donde R representa un grupo de laformula: II en donde R1 es un átomo de hidrogeno o un grupo alquilo inferior, R2 es un átomode hidrogeno o un grupo alcoxilo inferior, R3 es un átomo dehidrogeno, un grupo alquilo, un grupo alcanoilo inferior, entre otros, A es un átomo de azufre o átomo de oxigeno además R1 y R2 pueden combinarse el uno conel otro para formar un grupohet erocíclico de 5 0 6 miembros, n es 0 - 2, R4 es un átomo de hidrogeno, un grupo alquilo inferior o un grupo alcoxilo inferior,R8 es un átomo de hidrogeno, un grupo alquilo inferior o un grupo alquilo inferior o un grupo alquilo inferioralcoxil o inferior. Los derivados depirimidina (1) poseen actividad para inhibir la produccion de mediadores tales como citocinas (por ej. IL-4, IL-5 e IL-8 (Interleuquina-4, -5 y -8), TNF-alfa(factor de necrosis de tumor-alfa), LT(leucotrienos),PAF (facto r de activacion de plaquetas), PGs(prostaglandinas), GM-CSF(factor que estimula colonia degranulocito macrofago) y actividad para inhibir 5-lipoxigenasa, así estos derivados son utiles para tratar diversas enfermedades alérgicas,inflamatoriasy cánceres. Además poseen permeabilidad a los vasos sanguíneos de la via aérea, y actividad para inhibir infiltracion celular en el alveolo, particularmenteoptimo para tratar asma bronquial, inhibiendo la respuesta asmática tardía enel asma bronqui al, y enfermedades asmáticas viciosas tales como asma tolerantede droga esteroide, y asma resistente a droga esteroide, y para tratar dermatitis atopica. Los derivados de pirimidina (1) están caracterizados porposeer fuertesactividades para inhibir la formacion de NO, teniendo un tiempo de actividad prolongado, buena propiedad de translocacion en la sangre,
ARP980101135A 1997-03-14 1998-03-13 Derivado de pirimidina y agentes para tratar una enfermedad alergica, asma o dermatitis atopica y para producir inhibicion de no, tnf-alfa, citocinas o5-lipoxigenasa que lo comprenden. AR012293A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6155097 1997-03-14

Publications (1)

Publication Number Publication Date
AR012293A1 true AR012293A1 (es) 2000-10-18

Family

ID=13174349

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP980101135A AR012293A1 (es) 1997-03-14 1998-03-13 Derivado de pirimidina y agentes para tratar una enfermedad alergica, asma o dermatitis atopica y para producir inhibicion de no, tnf-alfa, citocinas o5-lipoxigenasa que lo comprenden.

Country Status (12)

Country Link
US (1) US6197774B1 (es)
EP (1) EP1019501A1 (es)
KR (1) KR100382964B1 (es)
CN (1) CN1092659C (es)
AR (1) AR012293A1 (es)
AU (1) AU731838B2 (es)
BR (1) BR9808845A (es)
CA (1) CA2283896A1 (es)
HK (1) HK1025955A1 (es)
ID (1) ID23177A (es)
TW (1) TW495509B (es)
WO (1) WO1998041526A1 (es)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PE20020394A1 (es) 2000-08-18 2002-06-21 Agouron Pharma Compuestos de pirazol y composiciones farmaceuticas que los contienen, que modulan y/o inhiben la actividad de erab/hadh2
US7196093B2 (en) * 2003-04-09 2007-03-27 General Atomics Reversible inhibitors of SAH hydrolase and uses thereof
US7868011B2 (en) * 2003-04-09 2011-01-11 General Atomics Use of reversible inhibitors of S-adenosyl-L-homocysteine hydrolase for treating lupus
US7517887B2 (en) * 2003-04-09 2009-04-14 General Atomics Reversible inhibitors of S-adenosyl-L-homocysteine hydrolase and uses thereof
FR2861992B1 (fr) * 2003-11-10 2007-07-20 Sanofi Synthelabo Composition pharmaceutique destinee a l'administration orale d'un derive de pyrazole-3-carboxamide.
JP4883996B2 (ja) * 2005-05-24 2012-02-22 四国化成工業株式会社 水溶性プレフラックス及びその利用
US10953012B2 (en) 2011-04-26 2021-03-23 Bioenergenix Llc Heterocyclic compounds for the inhibition of pask
US10392389B2 (en) 2012-10-25 2019-08-27 Bioenergenix Llc Heterocyclic compounds for the inhibition of PASK
WO2014066743A1 (en) 2012-10-25 2014-05-01 Bioenergenix Heterocyclic compounds for the inhibition of pask
CN108658991B (zh) * 2017-04-01 2023-12-15 辽宁利锋科技开发有限公司 3,5-二取代甲基吡唑并[1,5-a]嘧啶-7-酚盐类似物和衍生物制备方法和用途
PE20210340A1 (es) 2017-09-15 2021-02-22 Aduro Biotech Inc Compuestos que contienen pirazolopirimidinona y sus usos

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4261997A (en) * 1980-01-11 1981-04-14 Warner-Lambert Company 4-Alkyl-pyrazolo[5,1-b]-quinazolin-9(4H)-ones and anti-allergic compositions containing them
DE3065963D1 (en) 1979-01-24 1984-02-02 Warner Lambert Co Pyrazolo (5,1-b) quinazolin-9(4h)-one derivatives, process for their preparation and pharmaceutical compositions containing them
CN1030768C (zh) * 1990-10-09 1996-01-24 大塚制药株式会社 嘧啶衍生物或其药用盐的制备方法
AU667575B2 (en) * 1992-10-20 1996-03-28 Otsuka Pharmaceutical Co., Ltd. Condensed pyrazole derivatives, method of manufacturing the same, and androgen inhibitor
KR100315837B1 (ko) * 1994-06-21 2002-02-28 고리 히데아끼 피라졸로[1,5-a]피리미딘유도체
EP0795555A4 (en) 1995-09-28 1998-01-07 Otsuka Pharma Co Ltd ANALGETICS

Also Published As

Publication number Publication date
TW495509B (en) 2002-07-21
BR9808845A (pt) 2000-08-01
US6197774B1 (en) 2001-03-06
KR100382964B1 (ko) 2003-05-09
ID23177A (id) 2000-03-23
CA2283896A1 (en) 1998-09-24
HK1025955A1 (en) 2000-12-01
KR20000076168A (ko) 2000-12-26
EP1019501A1 (en) 2000-07-19
CN1250450A (zh) 2000-04-12
AU6310298A (en) 1998-10-12
AU731838B2 (en) 2001-04-05
CN1092659C (zh) 2002-10-16
WO1998041526A1 (en) 1998-09-24

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