[go: up one dir, main page]

ATE284382T1 - Hydroxamsäurederivat als inhibitor der produktion von löslichem menschlichem cd23 - Google Patents

Hydroxamsäurederivat als inhibitor der produktion von löslichem menschlichem cd23

Info

Publication number
ATE284382T1
ATE284382T1 AT00975954T AT00975954T ATE284382T1 AT E284382 T1 ATE284382 T1 AT E284382T1 AT 00975954 T AT00975954 T AT 00975954T AT 00975954 T AT00975954 T AT 00975954T AT E284382 T1 ATE284382 T1 AT E284382T1
Authority
AT
Austria
Prior art keywords
inhibitor
production
acid derivative
hydroxamic acid
soluble human
Prior art date
Application number
AT00975954T
Other languages
English (en)
Inventor
Andrew S Faller
John Gerard Ward
Original Assignee
Smithkline Beecham Plc
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 Smithkline Beecham Plc filed Critical Smithkline Beecham Plc
Application granted granted Critical
Publication of ATE284382T1 publication Critical patent/ATE284382T1/de

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C259/00—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups
    • C07C259/04—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids
    • C07C259/06—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids having carbon atoms of hydroxamic groups bound to hydrogen atoms or to acyclic carbon atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/16—Amides, e.g. hydroxamic acids
    • A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/08—Antiallergic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
    • C07C237/22—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Immunology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Pain & Pain Management (AREA)
  • Transplantation (AREA)
  • Rheumatology (AREA)
  • Pulmonology (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Hydrogenated Pyridines (AREA)
AT00975954T 1999-10-27 2000-10-25 Hydroxamsäurederivat als inhibitor der produktion von löslichem menschlichem cd23 ATE284382T1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB9925470.8A GB9925470D0 (en) 1999-10-27 1999-10-27 Novel compounds
PCT/EP2000/010649 WO2001030747A1 (en) 1999-10-27 2000-10-25 Hydroxamic acid derivative as inhibitor of the formation of soluble human cd23

Publications (1)

Publication Number Publication Date
ATE284382T1 true ATE284382T1 (de) 2004-12-15

Family

ID=10863507

Family Applications (1)

Application Number Title Priority Date Filing Date
AT00975954T ATE284382T1 (de) 1999-10-27 2000-10-25 Hydroxamsäurederivat als inhibitor der produktion von löslichem menschlichem cd23

Country Status (32)

Country Link
US (2) US6673965B1 (de)
EP (1) EP1224164B1 (de)
JP (1) JP3922431B2 (de)
KR (1) KR20020044578A (de)
CN (1) CN1182107C (de)
AR (1) AR026244A1 (de)
AT (1) ATE284382T1 (de)
AU (1) AU766072B2 (de)
BR (1) BR0015082A (de)
CA (1) CA2389319A1 (de)
CO (1) CO5261576A1 (de)
CZ (1) CZ20021424A3 (de)
DE (1) DE60016622T2 (de)
DK (1) DK1224164T3 (de)
ES (1) ES2233474T3 (de)
GB (1) GB9925470D0 (de)
GC (1) GC0000142A (de)
HK (1) HK1049146A1 (de)
HU (1) HUP0203270A3 (de)
IL (1) IL149364A0 (de)
MX (1) MXPA02004228A (de)
MY (1) MY133601A (de)
NO (1) NO20021965L (de)
NZ (1) NZ518566A (de)
PE (1) PE20010898A1 (de)
PL (1) PL356524A1 (de)
PT (1) PT1224164E (de)
SI (1) SI1224164T1 (de)
TW (1) TW561141B (de)
UY (1) UY26416A1 (de)
WO (1) WO2001030747A1 (de)
ZA (1) ZA200203255B (de)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5524215B2 (ja) 2008-09-19 2014-06-18 ファイザー・インク 抗菌剤として有用なヒドロキサム酸誘導体
EP2507266B1 (de) 2009-12-01 2015-02-18 Boston Medical Center Corporation Behandlung von ige-vermittelten erkrankungen
PT2512474E (pt) 2009-12-16 2014-12-23 Pfizer Derivados de ácido hidroxâmico n-ligado úteis como agentes antibacterianos
CN104529883A (zh) 2011-03-07 2015-04-22 辉瑞大药厂 可用作抗菌剂的氟吡啶酮衍生物
WO2012137094A1 (en) 2011-04-08 2012-10-11 Pfizer Inc. Isoxazole derivatives useful as antibacterial agents
MX2013011432A (es) 2011-04-08 2013-12-09 Pfizer Derivados de imidazol, pirazol, y triazol utiles como agentes antibacterianos.
EP2525213A1 (de) * 2011-05-16 2012-11-21 Renishaw plc Spektroskopievorrichtung und Verfahren zur Bestimmung der in einer Probe vorkommenden Komponenten

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9513331D0 (en) 1995-06-30 1995-09-06 British Biotech Pharm Matrix metalloproteinase inhibitors
GB9813451D0 (en) * 1998-06-22 1998-08-19 Smithkline Beecham Plc Novel compounds

Also Published As

Publication number Publication date
AU1389501A (en) 2001-05-08
UY26416A1 (es) 2001-05-31
US6673965B1 (en) 2004-01-06
TW561141B (en) 2003-11-11
CO5261576A1 (es) 2003-03-31
MXPA02004228A (es) 2002-10-17
GC0000142A (en) 2005-06-29
PT1224164E (pt) 2005-04-29
MY133601A (en) 2007-11-30
ES2233474T3 (es) 2005-06-16
HK1049146A1 (en) 2003-05-02
PL356524A1 (en) 2004-06-28
CA2389319A1 (en) 2001-05-03
US20040077727A1 (en) 2004-04-22
NO20021965L (no) 2002-06-13
HUP0203270A2 (hu) 2003-02-28
DE60016622D1 (de) 2005-01-13
IL149364A0 (en) 2002-11-10
DE60016622T2 (de) 2005-11-03
EP1224164A1 (de) 2002-07-24
WO2001030747A1 (en) 2001-05-03
NZ518566A (en) 2004-02-27
AR026244A1 (es) 2003-02-05
JP3922431B2 (ja) 2007-05-30
BR0015082A (pt) 2003-04-15
DK1224164T3 (da) 2005-03-29
GB9925470D0 (en) 1999-12-29
JP2003512450A (ja) 2003-04-02
CZ20021424A3 (cs) 2002-09-11
ZA200203255B (en) 2003-03-20
HUP0203270A3 (en) 2003-11-28
CN1182107C (zh) 2004-12-29
PE20010898A1 (es) 2001-10-13
AU766072B2 (en) 2003-10-09
CN1411436A (zh) 2003-04-16
EP1224164B1 (de) 2004-12-08
KR20020044578A (ko) 2002-06-15
SI1224164T1 (en) 2005-06-30
NO20021965D0 (no) 2002-04-25

Similar Documents

Publication Publication Date Title
DE60035631D1 (de) Inhibitoren der Interleukin-4 Produktion
DE60103935D1 (de) Imidazol-5-yl-2-anilino-pyrimidine als inhibitoren der zellproliferation
DE69820906D1 (de) Hydroxamsäure-derivate als matrix metalloproteinaseinhibitoren
NO20000877D0 (no) Forbedret syrekorrosjonsinhibitor
DE69906059D1 (de) Anthranilsäurederivate als inhibitoren der c-gmp-phosphodiesterase
IS6039A (is) Tálmi við súlfamatóhýdroxamsýrumálmprótínkljúfi
ATE304997T1 (de) Derivate von beta-aminosäurenitrilen
IS7682A (is) Samsetning og andveiruvirkni skiptitengdra azaindóloxóediksýru píperazín afleiðna
DE69511240D1 (de) Derivate des hydroxamsäure als metalloproteinaseinhibitoren
DE60043730D1 (de) Arylsulfonamid-substituierte hydroxamsäure-derivate
EE03745B1 (et) Asendatud 4-bifenüül-4-hüdroksübutaanhappe derivaadid metalloproteaasimaatriksi inhibiitoritena
DE60307556D1 (de) Verbindungsstruktur von Verbindern
DE60012303D1 (de) Alkinylische hydroxamsäureverbindungen als tace inhibitoren
ATE284382T1 (de) Hydroxamsäurederivat als inhibitor der produktion von löslichem menschlichem cd23
AU6689900A (en) 3-arylsulfonyl-2-(substituted methyl)propanoic acid derivates as matrix metalloproteinase inhibitors
ATE428691T1 (de) 3-phenyl-2-arylalkylthiopropionsäure-derivate als selektive agonisten von ppar-alpha
ATE269296T1 (de) Hydroxamsäure-derivate als inhibitoren der produktion von menschlichen cd23 und der freigabe von tnf
DK1228026T3 (da) 15-Hydroxyicosatetraensyrerelaterede forbindelser og fremgangsmåde til anvendelse
ATE205822T1 (de) Substituierte 4-arylbutyrsäurederivate als matrix metalloprotease inhibitoren
ATE227288T1 (de) Acetylenische ortho-sulfonamido- und phosphinsäure-amido-bicyclische heteroarylhydroxamsäure als tace-inhibitoren
ATE303995T1 (de) Substituierte phenylcyclohexancarbonsäureamide und ihre verwendung als adenosinaufnahme- inhibitoren
DE60336549D1 (de) Hepatoprotektor aktivität von 2'-p-hydroxybenzoylmussaenosidsäure
DE60010725D1 (de) Herstellung von arylcarbonsäureestern
DE60101472T2 (de) Derivate von p-hydroxyphenyl-propionsäure als antiproliferative mittel
DE50012694D1 (de) Verwendung von fettsäurealkanolaminestern

Legal Events

Date Code Title Description
UEP Publication of translation of european patent specification

Ref document number: 1224164

Country of ref document: EP

REN Ceased due to non-payment of the annual fee