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AR021427A1 - Compuestos de benzimidazol que son antagonistas de receptor de vitronectina - Google Patents

Compuestos de benzimidazol que son antagonistas de receptor de vitronectina

Info

Publication number
AR021427A1
AR021427A1 ARP990106061A ARP990106061A AR021427A1 AR 021427 A1 AR021427 A1 AR 021427A1 AR P990106061 A ARP990106061 A AR P990106061A AR P990106061 A ARP990106061 A AR P990106061A AR 021427 A1 AR021427 A1 AR 021427A1
Authority
AR
Argentina
Prior art keywords
alkyl
arylcycloalkyl
heterocycloalkylalkyl
heteroaralkyl
cycloalkylalkyl
Prior art date
Application number
ARP990106061A
Other languages
English (en)
Original Assignee
Schering Corp
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 Schering Corp filed Critical Schering Corp
Publication of AR021427A1 publication Critical patent/AR021427A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D235/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/06Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
    • C07D235/14Radicals substituted by nitrogen atoms

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Rheumatology (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Ophthalmology & Optometry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

La presente invencion proporciona compuestos que tienen la formula (1), en donde n, p, q y r son cada uno independientemente seleccionados entre0 o 1; a, b, c y d representan cada uno independientemente un átomo de carbono o nitrogeno, con la condicion que no más de dos a, b, c y d sean átomosde nitrogeno; Y e Y1 representan cada uno independientemente 1-4 sustituyentes opcionales seleccionados entre alquilo, alcoxi, halo, -CF3 y -C(O)OH; R1 es Halquilo, arilo, aralquilo, arilcicloalquilo, heteroarilo, cicloalquilo, heterocicloalquilo, heteroaralquilo, cicloalquilalquilo, heterocicloalquilalquilo,NHRA, -NHC(O)RA, -NHSO2RA, NHC(O)NHRA, o -NHC(O)ORA; R1 es opcionalmente sustituido con 1-3 grupos seleccionados entre halo, alquilo, -CF3, -CN, -ORB, -SRB,SRB, -CO2RB, -C(O)RB, -OC(O)RB, -OC(O)ORB y -SO2RB, y RA y RB son independientemente seleccionados entre H, alquilo, arilo, aralquilo, arilcicloalquilo,heteroarilo, cicloalquilo, heterocicloalquilo, heteroaralquilo, cicloalquilalquilo o heterocicloalquilalquilo, con la condicion que cuando R1 es alquilo,R1 no es sustituido con halo, la condicion que cuando R1 es -NHSO2RA o -NHC(O)ORA, RA no es H, y la condicion que para -SO2RB o -OC(O)ORB, RB no esH; R2 es H, alquilo, arilo, aralquilo,arilcicloalquilo, heteroarilo, cicloalquilo, heterocicloalquilo, heteroaralquilo, cicloalquilalquilo,o heterocicloalquilalquilo; R2 es opcionalmente sustituido con 1-3 grupos seleccionados entre halo, alquilo, -CF3, -CN, -ORC, -SRC, -CO2RC, -C(O)RC,-OC(O)RC,-OC(O)ORC y -SO2RC, en donde RC se selecciona entre H, alquilo, arilo, aralquilo, arilcicloalquilo, heteroarilo, cicloalquilo, heterocicloalquilo,heteroaralquilo, cicloalquilalquilo o heterocicloalquilalquilo, con la condicion que cuando R2es alquilo, R2 no es sustituido con halo, y la condicion quepara -SO2RC o -OC(O)ORC, RC no es H; R3 es H, alquilo, aralquilo, arilcicloalquilo, cicloalquilalquilo, heterocicloalquilalquilo, heteroaralquilo, arilo,heteroarilo, cicloalquilo, heterocicloalquilo, -C(O)RD, -C(O)ORD, -SO2RE, -C(O)NRFRG, -C(O)NRFSO2RE, o -C(=S)NRFRG, en donde RD, RE, RF y RG son
ARP990106061A 1998-11-30 1999-11-29 Compuestos de benzimidazol que son antagonistas de receptor de vitronectina AR021427A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US20161198A 1998-11-30 1998-11-30

Publications (1)

Publication Number Publication Date
AR021427A1 true AR021427A1 (es) 2002-07-17

Family

ID=22746536

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP990106061A AR021427A1 (es) 1998-11-30 1999-11-29 Compuestos de benzimidazol que son antagonistas de receptor de vitronectina

Country Status (12)

Country Link
EP (1) EP1135374B9 (es)
JP (1) JP4480117B2 (es)
CN (1) CN1161340C (es)
AR (1) AR021427A1 (es)
AT (1) ATE338751T1 (es)
AU (1) AU1908400A (es)
CA (1) CA2353063C (es)
CO (1) CO5140112A1 (es)
DE (1) DE69933135T2 (es)
ES (1) ES2273517T3 (es)
PE (1) PE20001427A1 (es)
WO (1) WO2000032578A1 (es)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1148349C (zh) * 1999-04-07 2004-05-05 参天制药株式会社 N-取代-N′-取代脲衍生物及其用作TNF-α生成抑制剂的用途
WO2000069810A1 (en) * 1999-05-17 2000-11-23 Novo Nordisk A/S Glucagon antagonists/inverse agonists
FR2809396B1 (fr) * 2000-05-24 2005-10-14 Centre Nat Rech Scient Nouvelles molecules possedant une activite calcimimetique et leur mode de preparation
US6562807B2 (en) 2000-06-23 2003-05-13 Novo Nordisk A/S Glucagon antagonists/inverse agonists
EP2527430B1 (en) 2007-06-07 2014-12-31 Novozymes A/S Method of preparing a dough-based product
EP2595488B1 (en) 2010-07-21 2019-12-04 Novozymes A/S Process for preparing a baked product with anti-staling amylase and peptidase
CA2939021C (en) 2014-02-11 2022-07-12 Bayer Pharma Aktiengesellschaft Benzimidazol-2-amines as midh1 inhibitors
EP3105209B1 (en) 2014-02-11 2019-08-21 Bayer Pharma Aktiengesellschaft Benzimidazol-2-amines as midh1 inhibitors
CN104694290A (zh) * 2014-05-07 2015-06-10 宁波职业技术学院 一种洗脚皂
ES2814151T3 (es) 2014-10-23 2021-03-26 Deutsches Krebsforschungszentrum Stiftung Des Oeffentlichen Rechts 1-Ciclohexilo-2-fenilaminobenzimidazoles como inhibidores de MIDH1 para el tratamiento de tumores
JP6783756B2 (ja) 2014-10-23 2020-11-11 ドイチェス クレープスフォルシュングスツェントルム シュティフトゥング デス エッフェントリッヒェン レヒツ mIDH1阻害剤としてのベンゾイミダゾール−2−アミン
JP6830909B2 (ja) 2015-06-08 2021-02-17 ドイチェス クレープスフォルシュングスツェントルム シュティフトゥング デス エッフェントリッヒェン レヒツ mIDH1阻害剤としてのN−メンチルベンズイミダゾール
EP3322694B1 (en) 2015-07-16 2020-02-19 Bayer Pharma Aktiengesellschaft 5-hydroxyalkylbenzimidazoles as midh1 inhibitors
TW202146416A (zh) 2019-12-11 2021-12-16 德商拜耳廠股份有限公司 吡唑并三𠯤
CA3174507A1 (en) 2020-03-06 2021-09-10 Bayer Aktiengesellschaft Imidazotriazines acting on cancer via inhibition of cdk12

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995032710A1 (en) * 1994-05-27 1995-12-07 Merck & Co., Inc. Compounds for inhibiting osteoclast-mediated bone resorption
CA2193966A1 (en) * 1994-06-29 1996-01-11 Fadia El-Fehail Ali Vitronectin receptor antagonists

Also Published As

Publication number Publication date
AU1908400A (en) 2000-06-19
CO5140112A1 (es) 2002-03-22
PE20001427A1 (es) 2000-12-18
WO2000032578A8 (en) 2002-02-07
JP2002531441A (ja) 2002-09-24
CA2353063C (en) 2009-06-16
ES2273517T3 (es) 2007-05-01
JP4480117B2 (ja) 2010-06-16
CN1333755A (zh) 2002-01-30
DE69933135T2 (de) 2007-08-09
DE69933135D1 (de) 2006-10-19
CA2353063A1 (en) 2000-06-08
EP1135374B9 (en) 2007-02-21
ATE338751T1 (de) 2006-09-15
CN1161340C (zh) 2004-08-11
EP1135374A1 (en) 2001-09-26
EP1135374B1 (en) 2006-09-06
WO2000032578A1 (en) 2000-06-08

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