NO20063921L - Nye piperidiner som kjemokinmodulatorer (CCR) - Google Patents

Nye piperidiner som kjemokinmodulatorer (CCR)

Info

Publication number
NO20063921L
NO20063921L NO20063921A NO20063921A NO20063921L NO 20063921 L NO20063921 L NO 20063921L NO 20063921 A NO20063921 A NO 20063921A NO 20063921 A NO20063921 A NO 20063921A NO 20063921 L NO20063921 L NO 20063921L
Authority
NO
Norway
Prior art keywords
ccr
chemokine modulators
piperidines
new piperidines
new
Prior art date
Application number
NO20063921A
Other languages
English (en)
Inventor
Mark Furber
Lilian Alcaraz
Aaron Rigby
Christopher Luckhurst
Peter Cage
Elizabeth Kinchin
Original Assignee
Astrazeneca Ab
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 Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of NO20063921L publication Critical patent/NO20063921L/no

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    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/40Oxygen atoms
    • C07D211/44Oxygen atoms attached in position 4
    • C07D211/46Oxygen atoms attached in position 4 having a hydrogen atom as the second substituent in position 4
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    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/40Oxygen atoms
    • C07D211/44Oxygen atoms attached in position 4
    • C07D211/52Oxygen atoms attached in position 4 having an aryl radical as the second substituent in position 4
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    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
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  • Health & Medical Sciences (AREA)
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  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
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  • Psychiatry (AREA)
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Abstract

Forbindelser med formel (I):. er modulatorer for kjemokin (for eksempel CCR3) aktivitet (for anvendelse i for eksempel å behandle astma).
NO20063921A 2004-02-02 2006-09-01 Nye piperidiner som kjemokinmodulatorer (CCR) NO20063921L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE0400208A SE0400208D0 (sv) 2004-02-02 2004-02-02 Chemical compounds
PCT/SE2005/000110 WO2005073192A1 (en) 2004-02-02 2005-01-31 Novel piperidines as chemokine modulators (ccr)

Publications (1)

Publication Number Publication Date
NO20063921L true NO20063921L (no) 2006-11-02

Family

ID=31713276

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20063921A NO20063921L (no) 2004-02-02 2006-09-01 Nye piperidiner som kjemokinmodulatorer (CCR)

Country Status (19)

Country Link
US (1) US7956070B2 (no)
EP (1) EP1713772A1 (no)
JP (2) JP4814109B2 (no)
KR (1) KR20060128992A (no)
CN (1) CN1938274A (no)
AR (1) AR049770A1 (no)
AU (2) AU2005207817B2 (no)
BR (1) BRPI0507366A (no)
CA (1) CA2553089A1 (no)
CO (1) CO5700747A2 (no)
IL (1) IL176992A0 (no)
NO (1) NO20063921L (no)
NZ (1) NZ548781A (no)
RU (2) RU2348616C2 (no)
SE (1) SE0400208D0 (no)
TW (1) TW200529843A (no)
UY (1) UY28731A1 (no)
WO (1) WO2005073192A1 (no)
ZA (1) ZA200606199B (no)

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SE0400208D0 (sv) 2004-02-02 2004-02-02 Astrazeneca Ab Chemical compounds
TW200812582A (en) * 2006-04-06 2008-03-16 Astrazeneca Ab Medicaments
US7897621B2 (en) 2008-03-31 2011-03-01 Hoffmann-La Roche Inc. 2-trifluoromethylnicotinamide derivatives as HDL-cholesterol raising agents
TWI433838B (zh) * 2008-06-25 2014-04-11 必治妥美雅史谷比公司 作為趨化因子受體活性調節劑之六氫吡啶衍生物
US8410107B2 (en) 2010-10-15 2013-04-02 Hoffmann-La Roche Inc. N-pyridin-3-yl or N-pyrazin-2-yl carboxamides
US8669254B2 (en) 2010-12-15 2014-03-11 Hoffman-La Roche Inc. Pyridine, pyridazine, pyrimidine or pyrazine carboxamides as HDL-cholesterol raising agents
TW201418242A (zh) 2012-10-26 2014-05-16 Du Pont 作為除草劑之經取代的三唑
HUE049600T2 (hu) 2014-07-03 2020-10-28 Univ Texas GLS1 inhibitorok betegségek kezelésére
US20160002204A1 (en) * 2014-07-03 2016-01-07 Board Of Regents, The University Of Texas System Gls1 inhibitors for treating disease
EP3316887B1 (en) 2015-06-30 2020-04-08 Board of Regents, The University of Texas System Gls1 inhibitors for treating disease
RU2018124266A (ru) 2015-12-22 2020-01-23 Боард Оф Реджентс, Де Юниверсити Оф Техас Систем Солевые формы и полиморфы (R)-1-(4-(6-(2-(4-(3,3-дифторциклобутокси)-6-метилпиридин-2-ил)ацетамидо)пиридазин-3-ил)-2- фторбутил) -N-метил-1Н-1,2,3-триазол-4-карбоксамид
RU2020112558A (ru) 2017-10-18 2021-11-18 Боард Оф Регентс, Зе Юниверсити Оф Тексас Систем Терапия на основе ингибитора глутаминазы
WO2020025574A1 (en) 2018-08-03 2020-02-06 Bayer Aktiengesellschaft Process for the preparation of 6-(haloalkyl)-2-halo-5-acylpyridines and intermediates for this process
CN113121417A (zh) * 2019-12-30 2021-07-16 苏州盛迪亚生物医药有限公司 一种新型哌啶衍生物及其药物用途

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SE0400208D0 (sv) 2004-02-02
NZ548781A (en) 2008-11-28
RU2348616C2 (ru) 2009-03-10
KR20060128992A (ko) 2006-12-14
JP2007519717A (ja) 2007-07-19
CO5700747A2 (es) 2006-11-30
RU2008140910A (ru) 2010-04-27
US7956070B2 (en) 2011-06-07
AR049770A1 (es) 2006-09-06
TW200529843A (en) 2005-09-16
IL176992A0 (en) 2006-12-10
AU2005207817A1 (en) 2005-08-11
RU2006130686A (ru) 2008-03-10
CN1938274A (zh) 2007-03-28
AU2005207817B2 (en) 2008-07-24
JP4814109B2 (ja) 2011-11-16
ZA200606199B (en) 2008-04-30
JP2009019055A (ja) 2009-01-29
BRPI0507366A (pt) 2007-07-03
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AU2008229856A1 (en) 2008-11-06
US20070054924A1 (en) 2007-03-08

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