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YU40402A - 4-pirimidinil-n-acil-l-fenilalanini - Google Patents

4-pirimidinil-n-acil-l-fenilalanini

Info

Publication number
YU40402A
YU40402A YU40402A YUP40402A YU40402A YU 40402 A YU40402 A YU 40402A YU 40402 A YU40402 A YU 40402A YU P40402 A YUP40402 A YU P40402A YU 40402 A YU40402 A YU 40402A
Authority
YU
Yugoslavia
Prior art keywords
phenylalanines
pyrimidinyl
acyl
vcam
binding
Prior art date
Application number
YU40402A
Other languages
English (en)
Inventor
Achyutharao Sidduri
Jefferson Wright Tilley
Original Assignee
F.Hoffmann-La Roche Ag.
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 F.Hoffmann-La Roche Ag. filed Critical F.Hoffmann-La Roche Ag.
Publication of YU40402A publication Critical patent/YU40402A/sh
Publication of RS50371B publication Critical patent/RS50371B/sr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/52Two oxygen atoms
    • C07D239/54Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • 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
    • A61P19/00Drugs for skeletal disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/52Two oxygen atoms
    • C07D239/54Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
    • C07D239/545Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals with other hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/553Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals with other hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms with halogen atoms or nitro radicals directly attached to ring carbon atoms, e.g. fluorouracil
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06Dipeptides
    • C07K5/06139Dipeptides with the first amino acid being heterocyclic
    • C07K5/06165Dipeptides with the first amino acid being heterocyclic and Pro-amino acid; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Biomedical Technology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Pulmonology (AREA)
  • Genetics & Genomics (AREA)
  • Rheumatology (AREA)
  • Immunology (AREA)
  • Molecular Biology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Biophysics (AREA)
  • Biochemistry (AREA)
  • Hospice & Palliative Care (AREA)
  • Pain & Pain Management (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Psychiatry (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
  • Medicinal Preparation (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

Otkrivena su jedinjenja formule (I) u kojima su R1 do R6 definisani kao što je dato u specifikaciji i koja su inhibitori vezivanja izmedju VCAM-1 i ćelija koje istiskuju (ekspresuju) VLA-4 i koja su prema tome prikladna za lečenje bolesti čiji su simptomi i/ili povreda u vezi sa vezivanjem VCAM-1 za ćelije koje istiskuju (ekspresuju) VLA-4.[Coumpounds of Formula (I) are disclosed, wherein R1 to R6 are as defined in specification and which are inhibitors of binding between VCAM-1 and cells expressing VLA-4, and accordingly are useful for treating diseases whose symptoms and or damage are related to the binding of VCAM-1 to cells expressing VLA-4.
YUP-404/02A 1999-12-06 2000-11-28 4-pirimidinil-n-acil-l-fenilalanini RS50371B (sr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US16908999P 1999-12-06 1999-12-06

Publications (2)

Publication Number Publication Date
YU40402A true YU40402A (sh) 2005-03-15
RS50371B RS50371B (sr) 2009-11-10

Family

ID=22614222

Country Status (35)

Country Link
EP (1) EP1237878B1 (sh)
JP (1) JP3824935B2 (sh)
KR (1) KR100522344B1 (sh)
CN (1) CN1218943C (sh)
AR (1) AR034401A1 (sh)
AT (1) ATE357433T1 (sh)
AU (1) AU783348B2 (sh)
BR (1) BR0016195A (sh)
CA (1) CA2392570C (sh)
CO (1) CO5080772A1 (sh)
CY (1) CY1106626T1 (sh)
CZ (1) CZ303435B6 (sh)
DE (1) DE60034061T2 (sh)
DK (1) DK1237878T3 (sh)
EG (1) EG24361A (sh)
ES (1) ES2282162T3 (sh)
HK (1) HK1054384B (sh)
HR (1) HRP20020468B1 (sh)
HU (1) HU229105B1 (sh)
IL (2) IL149617A0 (sh)
JO (1) JO2283B1 (sh)
MA (1) MA26850A1 (sh)
MX (1) MXPA02005564A (sh)
MY (1) MY126972A (sh)
NO (1) NO322866B1 (sh)
NZ (1) NZ518828A (sh)
PE (1) PE20010961A1 (sh)
PL (1) PL207160B1 (sh)
PT (1) PT1237878E (sh)
RS (1) RS50371B (sh)
RU (1) RU2266901C2 (sh)
SI (1) SI1237878T1 (sh)
TW (1) TWI256387B (sh)
WO (1) WO2001042225A2 (sh)
ZA (1) ZA200203533B (sh)

Families Citing this family (32)

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US6960597B2 (en) 2000-06-30 2005-11-01 Orth-Mcneil Pharmaceutical, Inc. Aza-bridged-bicyclic amino acid derivatives as α4 integrin antagonists
AU7874001A (en) * 2000-08-18 2002-03-04 Ajinomoto Kk Novel phenylalanine derivatives
AR033765A1 (es) * 2001-05-22 2004-01-07 Syngenta Participations Ag Procedimiento para la preparacion de derivados 3-alquil-3h-isobenzofuran-1-ona 7-sustituidos.
EP1454898A4 (en) * 2001-12-13 2006-12-13 Ajinomoto Kk NEW PHENYL ALANIDE DERIVATIVES
EP1700850B1 (en) 2003-12-22 2015-07-15 Ajinomoto Co., Inc. Phenylalanine derivative
US7618981B2 (en) * 2004-05-06 2009-11-17 Cytokinetics, Inc. Imidazopyridinyl-benzamide anti-cancer agents
CA2576647C (en) * 2004-08-16 2011-12-13 Merck & Co., Inc. Vla-4 antagonists
JP4784224B2 (ja) 2004-09-24 2011-10-05 味の素株式会社 糖鎖転移方法および糖鎖転移酵素
US20090137601A1 (en) * 2005-11-23 2009-05-28 Astrazeneca Ab L-Phenylalanine Derivatives
AR059224A1 (es) * 2006-01-31 2008-03-19 Jerini Ag Compuestos para la inhibicion de integrinas y uso de estas
WO2007091046A1 (en) * 2006-02-09 2007-08-16 Astrazeneca Ab Chemical compounds
US7879837B2 (en) 2006-06-19 2011-02-01 Toray Industries, Inc. Therapeutic or prophylactic agent for multiple sclerosis
EP2222646B1 (en) 2007-09-17 2014-01-22 AbbVie Bahamas Ltd. Uracil or thymine derivative for treating hepatitis c
DK2203431T3 (da) 2007-09-17 2011-11-21 Abbott Lab Antiinfektiøse pyrimidiner og anvendelser heraf
CA2699989C (en) 2007-09-17 2014-03-25 Abbott Laboratories N-phenyl-dioxo-hydro pyrimidines useful as hepatitis c virus (hcv) inhibitor
US8299149B2 (en) * 2008-12-22 2012-10-30 Icl-Ip America Inc. Water miscible solvent based process for purifying a bisphosphate
US9216952B2 (en) 2010-03-23 2015-12-22 Abbvie Inc. Process for preparing antiviral compound
US8975443B2 (en) 2010-07-16 2015-03-10 Abbvie Inc. Phosphine ligands for catalytic reactions
US9255074B2 (en) 2010-07-16 2016-02-09 Abbvie Inc. Process for preparing antiviral compounds
UA113498C2 (xx) 2010-07-16 2017-02-10 Фосфінові ліганди для каталітичних реакцій
SG10201505540SA (en) 2010-07-16 2015-08-28 Abbott Lab Process for preparing antiviral compounds
US8877815B2 (en) 2010-11-16 2014-11-04 Novartis Ag Substituted carbamoylcycloalkyl acetic acid derivatives as NEP
KR20140127234A (ko) * 2012-01-27 2014-11-03 에프. 호프만-라 로슈 아게 Vla-4 발현 세포로의 표적화된 전달을 위한 인테그린 안타고니스트 접합체
US9447035B2 (en) * 2012-01-27 2016-09-20 Hoffmann-La Roche Inc. Integrin antagonist conjugates for targeted delivery to cells expressing VLA-4
WO2015048819A1 (en) 2013-09-30 2015-04-02 The Regents Of The University Of California Anti-alphavbeta1 integrin compounds and methods
MX373389B (es) * 2013-10-29 2020-05-12 Ea Pharma Co Ltd Derivado de sulfonamida y uso farmaceutico del mismo.
WO2016145258A1 (en) 2015-03-10 2016-09-15 The Regents Of The University Of California Anti-alphavbeta1 integrin inhibitors and methods of use
CN112996786B (zh) 2018-10-30 2024-08-20 吉利德科学公司 用于抑制α4β7整合素的化合物
US11179383B2 (en) 2018-10-30 2021-11-23 Gilead Sciences, Inc. Compounds for inhibition of α4β7 integrin
ES3013256T3 (en) 2018-10-30 2025-04-11 Gilead Sciences Inc Imidazo[1,2-a]pyridine derivatives as alpha4beta7 integrin inhibitors for the treatment of inflammatory diseases
WO2020092375A1 (en) 2018-10-30 2020-05-07 Gilead Sciences, Inc. Quinoline derivatives as alpha4beta7 integrin inhibitors
US11578069B2 (en) 2019-08-14 2023-02-14 Gilead Sciences, Inc. Compounds for inhibition of α4 β7 integrin

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CH516578A (de) * 1967-11-02 1971-12-15 Bayer Ag Verfahren zur Herstellung von heterocyclische Acylaminogruppen enthaltenden Arylsulfonylharnstoffen mit blutdrucksenkender Wirkung
EP1001764A4 (en) * 1997-05-29 2005-08-24 Merck & Co Inc HETEROCYCLIC AMIDE COMPOUNDS AS INHIBITORS OF CELL ADHESION
AU726585B2 (en) * 1997-05-29 2000-11-09 Merck & Co., Inc. Biarylalkanoic acids as cell adhesion inhibitors
JP3727536B2 (ja) * 1997-08-22 2005-12-14 エフ.ホフマン−ラ ロシュ アーゲー N−アルカノイルフェニルアラニン誘導体
DK1005445T3 (da) * 1997-08-22 2004-10-04 Hoffmann La Roche N-alkanoylphenylaninderivater
CN1231212C (zh) * 1999-01-22 2005-12-14 依兰制药公司 抑制vla-4介导的白细胞粘着的多环化合物

Also Published As

Publication number Publication date
RU2266901C2 (ru) 2005-12-27
EP1237878B1 (en) 2007-03-21
CZ303435B6 (cs) 2012-09-12
CO5080772A1 (es) 2001-09-25
CY1106626T1 (el) 2012-01-25
NO20022633L (no) 2002-06-04
ZA200203533B (en) 2003-08-04
AU783348B2 (en) 2005-10-20
NO322866B1 (no) 2006-12-18
HUP0204081A2 (en) 2003-05-28
HRP20020468A2 (en) 2004-04-30
NO20022633D0 (no) 2002-06-04
HK1054384B (zh) 2005-12-09
IL149617A (en) 2007-10-31
PE20010961A1 (es) 2001-09-26
CN1407972A (zh) 2003-04-02
WO2001042225A2 (en) 2001-06-14
CA2392570C (en) 2010-05-11
JP2003516396A (ja) 2003-05-13
RU2002117422A (ru) 2004-03-10
ES2282162T3 (es) 2007-10-16
HU229105B1 (en) 2013-07-29
CZ20022351A3 (cs) 2003-04-16
EP1237878A2 (en) 2002-09-11
CA2392570A1 (en) 2001-06-14
AR034401A1 (es) 2004-02-25
HUP0204081A3 (en) 2003-07-28
KR100522344B1 (ko) 2005-10-20
AU2669601A (en) 2001-06-18
WO2001042225A8 (en) 2002-06-06
PL207160B1 (pl) 2010-11-30
DK1237878T3 (da) 2007-07-30
WO2001042225A3 (en) 2002-02-21
MY126972A (en) 2006-11-30
JO2283B1 (en) 2005-09-12
DE60034061D1 (de) 2007-05-03
IL149617A0 (en) 2002-11-10
MXPA02005564A (es) 2002-09-02
JP3824935B2 (ja) 2006-09-20
EG24361A (en) 2009-03-04
HRP20020468B1 (en) 2009-02-28
BR0016195A (pt) 2002-08-13
MA26850A1 (fr) 2004-12-20
RS50371B (sr) 2009-11-10
PT1237878E (pt) 2007-06-18
HK1054384A1 (en) 2003-11-28
SI1237878T1 (sl) 2007-08-31
TWI256387B (en) 2006-06-11
KR20020063906A (ko) 2002-08-05
DE60034061T2 (de) 2007-12-13
ATE357433T1 (de) 2007-04-15
PL357601A1 (en) 2004-07-26
CN1218943C (zh) 2005-09-14
NZ518828A (en) 2004-03-26

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