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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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    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • 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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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • 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
    • C07D211/52Oxygen 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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    • A61K31/435Heterocyclic 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
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    • C07D295/04Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/08Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
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    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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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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TW201418242A (zh) 2012-10-26 2014-05-16 Du Pont 作為除草劑之經取代的三唑
WO2016004417A1 (en) * 2014-07-03 2016-01-07 Board Of Regents, University Of Texas System Gls1 inhibitors for treating disease
JP6619758B2 (ja) 2014-07-03 2019-12-11 ボード・オブ・リージエンツ,ザ・ユニバーシテイ・オブ・テキサス・システム 疾患を処置するためのgls1阻害薬
EP3316887B1 (en) 2015-06-30 2020-04-08 Board of Regents, The University of Texas System Gls1 inhibitors for treating disease
AU2016378746B2 (en) 2015-12-22 2021-05-20 Board Of Regents, The University Of Texas System Salt forms and polymorphs of (R)-1-(4-(6-(2-(4-(3,3-difluorocyclobutoxy)-6-methylpyridin-2-yl) acetamido) pyridazin-3-yl)-2-fluorobutyl)-N-methyl-1H-1,2,3-triazole-4-carboxamide
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
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WO2025118148A1 (en) * 2023-12-05 2025-06-12 Biofront Ltd Antioxidant drug-conjugate modulators of fpr1, compositions comprising the modulator, and methods of using the same

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AR049770A1 (es) 2006-09-06
CN1938274A (zh) 2007-03-28
AU2005207817B2 (en) 2008-07-24
BRPI0507366A (pt) 2007-07-03
US7956070B2 (en) 2011-06-07
IL176992A0 (en) 2006-12-10
RU2008140910A (ru) 2010-04-27
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RU2348616C2 (ru) 2009-03-10
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