BR0015082A - Derivado de ácido hidroxâmico como inibidor da formação de cd 23 humano solúvel - Google Patents

Derivado de ácido hidroxâmico como inibidor da formação de cd 23 humano solúvel

Info

Publication number
BR0015082A
BR0015082A BR0015082-7A BR0015082A BR0015082A BR 0015082 A BR0015082 A BR 0015082A BR 0015082 A BR0015082 A BR 0015082A BR 0015082 A BR0015082 A BR 0015082A
Authority
BR
Brazil
Prior art keywords
inhibitor
formation
acid derivative
hydroxamic acid
soluble human
Prior art date
Application number
BR0015082-7A
Other languages
English (en)
Inventor
Andrew 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
Publication of BR0015082A publication Critical patent/BR0015082A/pt

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C259/00Compounds 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
    • C07C259/04Compounds 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
    • C07C259/06Compounds 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/16Amides, e.g. hydroxamic acids
    • A61K31/165Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • 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]
    • 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
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/02Carboxylic 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
    • C07C237/22Carboxylic 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)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (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)
  • Epidemiology (AREA)
  • Pulmonology (AREA)
  • Transplantation (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (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)

Abstract

"DERIVADO DE áCIDO HIDROXâMICO COMO INIBIDOR DA FORMAçãO DE CD 23 HUMANO SOLúVEL". A presente invenção refere-se a um composto de fórmula (I), em que: R é isopropila, n é 0, R^ 1^ é naftil metila, R^ 2^ é t-butila, e R^ 3^ é metila, sendo útil no tratamento de distúrbios mediados por s-CD23.
BR0015082-7A 1999-10-27 2000-10-25 Derivado de ácido hidroxâmico como inibidor da formação de cd 23 humano solúvel BR0015082A (pt)

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
BR0015082A true BR0015082A (pt) 2003-04-15

Family

ID=10863507

Family Applications (1)

Application Number Title Priority Date Filing Date
BR0015082-7A BR0015082A (pt) 1999-10-27 2000-10-25 Derivado de ácido hidroxâmico como inibidor da formação de cd 23 humano solúvel

Country Status (32)

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

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2735929C (en) * 2008-09-19 2013-12-17 Pfizer Inc. Hydroxamic acid derivatives useful as antibacterial agents
JP5836968B2 (ja) 2009-12-01 2015-12-24 ボストン メディカル センター コーポレーション IgE媒介性疾患の処置方法
EP2512474B1 (en) 2009-12-16 2014-11-05 Pfizer Inc N-linked hydroxamic acid derivatives useful as antibacterial agents
ES2626457T3 (es) 2011-03-07 2017-07-25 Pfizer Inc. Derivados de fluoro-piridinona útiles como agentes antibacterianos
KR20130140868A (ko) 2011-04-08 2013-12-24 화이자 인코포레이티드 항세균제로서 유용한 이속사졸 유도체
SG193458A1 (en) 2011-04-08 2013-10-30 Pfizer Imidazole, pyrazole, and triazole derivatives useful as antibacterial agents
EP2525213A1 (en) * 2011-05-16 2012-11-21 Renishaw plc Spectroscopic apparatus and methods for determining components present in a sample

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
KR20020044578A (ko) 2002-06-15
EP1224164A1 (en) 2002-07-24
HK1049146A1 (en) 2003-05-02
TW561141B (en) 2003-11-11
IL149364A0 (en) 2002-11-10
US20040077727A1 (en) 2004-04-22
NZ518566A (en) 2004-02-27
MY133601A (en) 2007-11-30
CN1182107C (zh) 2004-12-29
CN1411436A (zh) 2003-04-16
UY26416A1 (es) 2001-05-31
AU1389501A (en) 2001-05-08
MXPA02004228A (es) 2002-10-17
HUP0203270A3 (en) 2003-11-28
AR026244A1 (es) 2003-02-05
HUP0203270A2 (hu) 2003-02-28
AU766072B2 (en) 2003-10-09
PE20010898A1 (es) 2001-10-13
PT1224164E (pt) 2005-04-29
PL356524A1 (en) 2004-06-28
JP2003512450A (ja) 2003-04-02
CA2389319A1 (en) 2001-05-03
DK1224164T3 (da) 2005-03-29
GB9925470D0 (en) 1999-12-29
JP3922431B2 (ja) 2007-05-30
WO2001030747A1 (en) 2001-05-03
DE60016622T2 (de) 2005-11-03
ZA200203255B (en) 2003-03-20
ES2233474T3 (es) 2005-06-16
EP1224164B1 (en) 2004-12-08
GC0000142A (en) 2005-06-29
SI1224164T1 (en) 2005-06-30
NO20021965L (no) 2002-06-13
CZ20021424A3 (cs) 2002-09-11
DE60016622D1 (de) 2005-01-13
US6673965B1 (en) 2004-01-06
CO5261576A1 (es) 2003-03-31
NO20021965D0 (no) 2002-04-25
ATE284382T1 (de) 2004-12-15

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Legal Events

Date Code Title Description
B08F Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette]

Free format text: REFERENTE A 7A E 8A ANUIDADES.

B08K Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette]

Free format text: REFERENTE AO DESPACHO 8.6 DA RPI 2008 DE 30/06/2009.