ATE553084T1 - Polycyclische säureverbindungen als crth2- antagonisten und antiallergika - Google Patents

Polycyclische säureverbindungen als crth2- antagonisten und antiallergika

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Publication number
ATE553084T1
ATE553084T1 AT07859872T AT07859872T ATE553084T1 AT E553084 T1 ATE553084 T1 AT E553084T1 AT 07859872 T AT07859872 T AT 07859872T AT 07859872 T AT07859872 T AT 07859872T AT E553084 T1 ATE553084 T1 AT E553084T1
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AT
Austria
Prior art keywords
antiallergenics
acid compounds
crth2 antagonists
polycyclic acid
polycyclic
Prior art date
Application number
AT07859872T
Other languages
German (de)
English (en)
Inventor
Tadashi Terasaka
Tatsuya Zenkoh
Hisashi Hayashida
Hiroshi Matsuda
Junji Sato
Yoshimasa Imamura
Hiroshi Nagata
Norio Seki
Yoshiyuki Tenda
Mamoru Tasaki
Masahiro Takeda
Seiichiro Tabuchi
Minoru Yasuda
Kazunori Tsubaki
Original Assignee
Astellas Pharma Inc
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Publication of ATE553084T1 publication Critical patent/ATE553084T1/de

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    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
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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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    • C07C271/50Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by doubly-bound oxygen atoms
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    • C07D401/06Heterocyclic 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 carbon chain containing only aliphatic carbon atoms
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AT07859872T 2006-12-14 2007-12-13 Polycyclische säureverbindungen als crth2- antagonisten und antiallergika ATE553084T1 (de)

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US8304413B2 (en) 2008-06-03 2012-11-06 Intermune, Inc. Compounds and methods for treating inflammatory and fibrotic disorders
WO2010132163A1 (en) 2009-05-13 2010-11-18 Enanta Pharmaceuticals, Inc. Macrocyclic compounds as hepatitis c virus inhibitors
EP2590944B1 (en) 2010-07-05 2015-09-30 Actelion Pharmaceuticals Ltd. 1-phenyl-substituted heterocyclyl derivatives and their use as prostaglandin d2 receptor modulators
ES2624379T3 (es) 2011-12-21 2017-07-14 Idorsia Pharmaceuticals Ltd Derivados de heterociclilo y su uso como moduladores del receptor de prostaglandina D2
WO2013185284A1 (en) 2012-06-12 2013-12-19 Abbott Laboratories Pyridinone and pyridazinone derivatives
US9169270B2 (en) 2012-07-05 2015-10-27 Actelion Pharmaceuticals Ltd. 1-phenyl-substituted heterocyclyl derivatives and their use as prostaglandin D2 receptor modulators
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AR092742A1 (es) 2012-10-02 2015-04-29 Intermune Inc Piridinonas antifibroticas
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US10005728B2 (en) 2013-08-28 2018-06-26 Vanderbilt University Substituted indole Mcl-1 inhibitors
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RU2692485C2 (ru) 2014-04-02 2019-06-25 Интермьюн, Инк. Противофиброзные пиридиноны
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US10292968B2 (en) 2014-12-11 2019-05-21 Zenith Epigenetics Ltd. Substituted heterocycles as bromodomain inhibitors
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CN105353095B (zh) * 2015-11-16 2017-10-20 华南农业大学 一种西地那非及其结构类似物的免疫检测方法
WO2017104728A1 (ja) * 2015-12-16 2017-06-22 国立大学法人東京大学 食物アレルギー治療薬
WO2017126635A1 (ja) * 2016-01-22 2017-07-27 武田薬品工業株式会社 複素環化合物およびその用途
CN109153643B (zh) 2016-03-04 2022-06-21 范德比尔特大学 取代的吲哚mcl-1抑制剂
US11608320B2 (en) 2020-02-02 2023-03-21 Kuwait University Oxazolidinone hydroxamic acid derivatives

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TW200848036A (en) 2008-12-16
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CA2672601A1 (en) 2008-06-19
WO2008072784A1 (en) 2008-06-19
EP2094662A1 (en) 2009-09-02
US20100009991A1 (en) 2010-01-14
AR064346A1 (es) 2009-04-01
PL2094662T3 (pl) 2012-09-28
MX2009006312A (es) 2009-08-07
PT2094662E (pt) 2012-07-02
EP2094662B1 (en) 2012-04-11
JP5278318B2 (ja) 2013-09-04
JP2010513224A (ja) 2010-04-30
CN102442941A (zh) 2012-05-09
US8273745B2 (en) 2012-09-25
ES2383239T3 (es) 2012-06-19

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