JP5685581B2 - Ccr2の4−アゼチジニル−1−ヘテロ原子結合シクロヘキサンアンタゴニスト - Google Patents

Ccr2の4−アゼチジニル−1−ヘテロ原子結合シクロヘキサンアンタゴニスト Download PDF

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JP5685581B2
JP5685581B2 JP2012506227A JP2012506227A JP5685581B2 JP 5685581 B2 JP5685581 B2 JP 5685581B2 JP 2012506227 A JP2012506227 A JP 2012506227A JP 2012506227 A JP2012506227 A JP 2012506227A JP 5685581 B2 JP5685581 B2 JP 5685581B2
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alkyl
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substituted
methyl
optionally
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JP2012524110A (ja
JP2012524110A5 (enExample
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ツアン,スーチン
ハフナゲル,ヘザー・ラエ
スイ,ツイーフア
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Janssen Pharmaceutica NV
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    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/08Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing alicyclic rings
    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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    • C07D401/02Heterocyclic 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
    • C07D401/08Heterocyclic 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 alicyclic rings
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    • C07DHETEROCYCLIC COMPOUNDS
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    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/08Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing alicyclic rings
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/08Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing alicyclic rings
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/08Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing alicyclic rings

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  • General Health & Medical Sciences (AREA)
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  • Cardiology (AREA)
  • Hematology (AREA)
  • Urology & Nephrology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Oncology (AREA)
  • Obesity (AREA)
  • Communicable Diseases (AREA)
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  • Dermatology (AREA)
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  • Neurosurgery (AREA)
  • Transplantation (AREA)
  • Child & Adolescent Psychology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Pain & Pain Management (AREA)
  • Hospice & Palliative Care (AREA)
  • Vascular Medicine (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
JP2012506227A 2009-04-17 2010-04-15 Ccr2の4−アゼチジニル−1−ヘテロ原子結合シクロヘキサンアンタゴニスト Expired - Fee Related JP5685581B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US17022509P 2009-04-17 2009-04-17
US61/170,225 2009-04-17
PCT/US2010/031255 WO2010121036A1 (en) 2009-04-17 2010-04-15 4-azetidinyl-1-heteroatom linked-cyclohexane antagonists of ccr2

Publications (3)

Publication Number Publication Date
JP2012524110A JP2012524110A (ja) 2012-10-11
JP2012524110A5 JP2012524110A5 (enExample) 2013-05-09
JP5685581B2 true JP5685581B2 (ja) 2015-03-18

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JP2012506227A Expired - Fee Related JP5685581B2 (ja) 2009-04-17 2010-04-15 Ccr2の4−アゼチジニル−1−ヘテロ原子結合シクロヘキサンアンタゴニスト

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US (1) US8324186B2 (enExample)
EP (1) EP2419418B1 (enExample)
JP (1) JP5685581B2 (enExample)
KR (1) KR20120006051A (enExample)
CN (1) CN102459226B (enExample)
AR (1) AR076329A1 (enExample)
AU (1) AU2010236336B2 (enExample)
BR (1) BRPI1016205A2 (enExample)
CA (1) CA2758929A1 (enExample)
ES (1) ES2541607T3 (enExample)
MX (1) MX2011010963A (enExample)
NZ (1) NZ595433A (enExample)
TW (1) TW201102379A (enExample)
WO (1) WO2010121036A1 (enExample)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2745969C (en) 2008-12-10 2017-04-25 Janssen Pharmaceutica Nv 4-azetidinyl-1-heteroaryl-cyclohexanol antagonists of ccr2
MX2011010919A (es) * 2009-04-16 2011-11-02 Janssen Pharmaceutica Nv Antagonistas del receptor 2 de citocina quimioatrayente de 4-azetidinil-1-heteroaril-ciclohexano.
NZ595432A (en) * 2009-04-17 2013-12-20 Janssen Pharmaceutica Nv 4-azetidinyl-1-phenyl-cyclohexane antagonists of ccr2
KR20120006051A (ko) 2009-04-17 2012-01-17 얀센 파마슈티카 엔.브이. Ccr2의 4-아제티디닐-1-헤테로원자 연결된 사이클로헥산 길항제
TW201211027A (en) * 2010-06-09 2012-03-16 Janssen Pharmaceutica Nv Cyclohexyl-azetidinyl antagonists of CCR2
WO2011159854A1 (en) 2010-06-17 2011-12-22 Janssen Pharmaceutica Nv Cyclohexyl-azetidinyl antagonists of ccr2
EP2771484A1 (en) 2011-10-28 2014-09-03 Galderma Research & Development New leukocyte infiltrate markers for rosacea and uses thereof
JPWO2015056782A1 (ja) 2013-10-17 2017-03-09 塩野義製薬株式会社 新規アルキレン誘導体
WO2021202381A2 (en) * 2020-03-30 2021-10-07 Memorial Sloan Kettering Cancer Center Methods and compositions for modulating lipid storage in adipose tissue

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WO1998057641A1 (en) 1997-06-18 1998-12-23 Merck & Co., Inc. ALPHA 1a ADRENERGIC RECEPTOR ANTAGONISTS
US6037354A (en) * 1997-06-18 2000-03-14 Merck & Co., Inc. Alpha 1a adrenergic receptor antagonists
CN1192773C (zh) 1999-08-04 2005-03-16 帝人株式会社 环胺ccr3拮抗剂
CA2390531A1 (en) 1999-11-08 2001-05-17 Wyeth ¬(indol-3-yl)-cycloalkyl|-3-substituted azetidines for the treatment of central nervous system disorders
US6245799B1 (en) * 1999-11-08 2001-06-12 American Home Products Corp [(Indol-3-yl)-cycloalkyl]-3-substituted azetidines for the treatment of central nervous system disorders
US6706712B2 (en) * 2000-12-20 2004-03-16 Bristol-Myers Squibb Pharma Company Cyclic derivatives as modulators of chemokine receptor activity
PL376925A1 (pl) * 2002-11-27 2006-01-09 Incyte Corporation Pochodne 3-aminopirolidyny jako modulatory receptorów chemokiny
UA87449C2 (ru) * 2002-11-27 2009-07-27 Инсайт Корпорейшн Производные 3-аминопиролидина как модуляторы рецепторов хемокина
GB0417801D0 (en) * 2004-08-10 2004-09-15 Novartis Ag Organic compounds
EP1802602A1 (en) * 2004-09-28 2007-07-04 Janssen Pharmaceutica N.V. Substituted dipiperdine ccr2 antagonists
PA8653301A1 (es) * 2004-11-22 2006-11-09 Incyte Corp Incyte Corp Sales de la n-[2-({(3r)-1-[trans-4-hidroxi-4-(6-metoxipiridin-3-il) ciclohexil)pirrolidin
GB0513747D0 (en) 2005-07-06 2005-08-10 Merck Sharp & Dohme Therapeutic compounds
US8067457B2 (en) 2005-11-01 2011-11-29 Millennium Pharmaceuticals, Inc. Compounds useful as antagonists of CCR2
US20070197590A1 (en) 2006-01-31 2007-08-23 Demong Duane E Substituted dipiperidine ccr2 antagonists
KR20100102646A (ko) * 2007-12-11 2010-09-24 가부시키가이샤 사이토파스파인더 카르복스아미드 화합물 및 케모카인 수용체 길항제로서의 이의 용도
CA2745969C (en) 2008-12-10 2017-04-25 Janssen Pharmaceutica Nv 4-azetidinyl-1-heteroaryl-cyclohexanol antagonists of ccr2
MX2011010919A (es) 2009-04-16 2011-11-02 Janssen Pharmaceutica Nv Antagonistas del receptor 2 de citocina quimioatrayente de 4-azetidinil-1-heteroaril-ciclohexano.
NZ595432A (en) 2009-04-17 2013-12-20 Janssen Pharmaceutica Nv 4-azetidinyl-1-phenyl-cyclohexane antagonists of ccr2
KR20120006051A (ko) 2009-04-17 2012-01-17 얀센 파마슈티카 엔.브이. Ccr2의 4-아제티디닐-1-헤테로원자 연결된 사이클로헥산 길항제

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Publication number Publication date
US8324186B2 (en) 2012-12-04
TW201102379A (en) 2011-01-16
EP2419418A1 (en) 2012-02-22
EP2419418B1 (en) 2015-04-15
NZ595433A (en) 2013-12-20
ES2541607T3 (es) 2015-07-22
US20100267668A1 (en) 2010-10-21
AU2010236336A1 (en) 2011-11-03
AU2010236336B2 (en) 2015-01-15
AR076329A1 (es) 2011-06-01
CN102459226A (zh) 2012-05-16
JP2012524110A (ja) 2012-10-11
BRPI1016205A2 (pt) 2016-04-19
CA2758929A1 (en) 2010-10-21
KR20120006051A (ko) 2012-01-17
CN102459226B (zh) 2014-09-17
MX2011010963A (es) 2011-11-02
WO2010121036A1 (en) 2010-10-21

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