BRPI0519337A2 - composto de pirazol heteroarilas éteis no tratamento de doenÇas mediadas pela tnf-alfa e il-1 - Google Patents

composto de pirazol heteroarilas éteis no tratamento de doenÇas mediadas pela tnf-alfa e il-1

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Publication number
BRPI0519337A2
BRPI0519337A2 BRPI0519337-0A BRPI0519337A BRPI0519337A2 BR PI0519337 A2 BRPI0519337 A2 BR PI0519337A2 BR PI0519337 A BRPI0519337 A BR PI0519337A BR PI0519337 A2 BRPI0519337 A2 BR PI0519337A2
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BR
Brazil
Prior art keywords
tnf
alpha
compound
treatment
pyrazole
Prior art date
Application number
BRPI0519337-0A
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English (en)
Inventor
Laszlo Revesz
Original Assignee
Novartis 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 Novartis Ag filed Critical Novartis Ag
Publication of BRPI0519337A2 publication Critical patent/BRPI0519337A2/pt

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    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4151,2-Diazoles
    • A61K31/41621,2-Diazoles condensed with heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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    • 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

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  • Organic Chemistry (AREA)
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  • Hospice & Palliative Care (AREA)
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  • Child & Adolescent Psychology (AREA)
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  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

COMPOSTOS DE PIRAZOL HETEROARILAS éTEIS NO TRATAMENTO DE DOENÇAS MEDIADAS PELA TNF-ALFA E IL-1. A presente invenção refere-se a um composto da fórmula I em que os groupos de RI a R4, X e Y, são tal como definido na especificação, útil para tratar as doenças mediadas pela TNF-c e a IL-1.
BRPI0519337-0A 2004-12-16 2005-12-14 composto de pirazol heteroarilas éteis no tratamento de doenÇas mediadas pela tnf-alfa e il-1 BRPI0519337A2 (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB0427604.4A GB0427604D0 (en) 2004-12-16 2004-12-16 Organic compounds
PCT/EP2005/013453 WO2006063820A1 (en) 2004-12-16 2005-12-14 Pyrazolo-heteroaryl compounds useful to treat tnf-alpha and il-1 mediated diseases

Publications (1)

Publication Number Publication Date
BRPI0519337A2 true BRPI0519337A2 (pt) 2009-01-20

Family

ID=34090176

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI0519337-0A BRPI0519337A2 (pt) 2004-12-16 2005-12-14 composto de pirazol heteroarilas éteis no tratamento de doenÇas mediadas pela tnf-alfa e il-1

Country Status (17)

Country Link
US (1) US20090258874A1 (pt)
EP (1) EP1833477B1 (pt)
JP (1) JP2008524141A (pt)
KR (1) KR20070087607A (pt)
CN (1) CN101076333A (pt)
AT (1) ATE469646T1 (pt)
AU (1) AU2005315849B2 (pt)
BR (1) BRPI0519337A2 (pt)
CA (1) CA2586543A1 (pt)
DE (1) DE602005021697D1 (pt)
ES (1) ES2345207T3 (pt)
GB (1) GB0427604D0 (pt)
MX (1) MX2007007218A (pt)
PL (1) PL1833477T3 (pt)
PT (1) PT1833477E (pt)
RU (1) RU2007126968A (pt)
WO (1) WO2006063820A1 (pt)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101011956B1 (ko) * 2005-08-25 2011-01-31 에프. 호프만-라 로슈 아게 P38 mαp 키나아제 저해제 및 이의 사용 방법
KR101011958B1 (ko) 2005-08-25 2011-01-31 에프. 호프만-라 로슈 아게 p38 MAP 키나아제 저해제로서의 융합형 피라졸
CN102666537A (zh) * 2009-10-20 2012-09-12 艾格尔生物制药股份有限公司 治疗黄病毒科病毒感染的氮杂吲唑
US8362023B2 (en) 2011-01-19 2013-01-29 Hoffmann-La Roche Inc. Pyrazolo pyrimidines
US11466017B2 (en) 2011-03-10 2022-10-11 Board Of Regents, The University Of Texas System Heterocyclic inhibitors of PTPN11
WO2013017479A1 (en) 2011-07-29 2013-02-07 Cellzome Limited Pyrazolo[4,3-c]pyridine derivatives as jak inhibitors
WO2013017480A1 (en) 2011-07-29 2013-02-07 Cellzome Limited Pyrazolo[4,3-c]pyridine derivatives as jak inhibitors
CN103874699A (zh) 2011-09-20 2014-06-18 赛尔佐姆有限公司 吡唑并[4,3-c]吡啶衍生物作为激酶抑制剂
WO2014113942A1 (en) * 2013-01-23 2014-07-31 Merck Sharp & Dohme Corp. Btk inhibitors
WO2017210134A1 (en) 2016-05-31 2017-12-07 Board Of Regents, University Of Texas System Heterocyclic inhibitors of ptpn11
US12583852B2 (en) 2018-05-02 2026-03-24 Jw Pharmaceutical Corporation Heterocycle derivative
MX2020011528A (es) 2018-05-02 2021-02-09 Navire Pharma Inc Inhibidores heterociclicos sustituidos de ptpn11.
CN112601750B (zh) 2018-08-10 2023-10-31 纳维尔制药有限公司 Ptpn11(shp2)抑制剂
JP2023550643A (ja) * 2020-11-25 2023-12-04 レネオ ファーマシューティカルズ,インク. Pparデルタアゴニストの製造方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003029209A2 (en) * 2001-10-02 2003-04-10 Smithkline Beecham Corporation Chemical compounds
ES2314224T3 (es) * 2002-03-07 2009-03-16 F. Hoffmann-La Roche Ag Inhibidores pirimidina y piridina biciclicos de p38 quinasa.
TW200400034A (en) * 2002-05-20 2004-01-01 Bristol Myers Squibb Co Pyrazolo-pyrimidine aniline compounds useful as kinase inhibitors
US7468376B2 (en) * 2003-02-27 2008-12-23 Palau Pharma, S.A. Pyrazolopyridine derivates
WO2005085249A1 (en) * 2004-02-27 2005-09-15 F. Hoffmann-La Roche Ag Fused derivatives of pyrazole
CN1934111A (zh) * 2004-02-27 2007-03-21 霍夫曼-拉罗奇有限公司 杂芳基稠合的吡唑并衍生物

Also Published As

Publication number Publication date
ATE469646T1 (de) 2010-06-15
CN101076333A (zh) 2007-11-21
AU2005315849A1 (en) 2006-06-22
EP1833477B1 (en) 2010-06-02
WO2006063820A1 (en) 2006-06-22
JP2008524141A (ja) 2008-07-10
EP1833477A1 (en) 2007-09-19
PT1833477E (pt) 2010-08-20
MX2007007218A (es) 2007-08-14
DE602005021697D1 (de) 2010-07-15
GB0427604D0 (en) 2005-01-19
KR20070087607A (ko) 2007-08-28
AU2005315849B2 (en) 2009-05-28
PL1833477T3 (pl) 2010-11-30
RU2007126968A (ru) 2009-01-27
US20090258874A1 (en) 2009-10-15
ES2345207T3 (es) 2010-09-17
CA2586543A1 (en) 2006-06-22

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

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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 PUBLICADO NA RPI 2160 DE 29/05/2012.