CN1257160C - 氨基喹啉衍生物和它们的作为腺苷a3配体的应用 - Google Patents

氨基喹啉衍生物和它们的作为腺苷a3配体的应用 Download PDF

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CN1257160C
CN1257160C CNB02810840XA CN02810840A CN1257160C CN 1257160 C CN1257160 C CN 1257160C CN B02810840X A CNB02810840X A CN B02810840XA CN 02810840 A CN02810840 A CN 02810840A CN 1257160 C CN1257160 C CN 1257160C
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straight
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cyano
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Chinese (zh)
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CN1512985A (zh
Inventor
P·奥拉尼
L·鲍拉日
M·鲍洛格
I·鲍陶
S·巴托里
L·T·纳吉
G·蒂马里
K·博埃尔
O·菲南斯
Z·考普伊
E·米库什
Z·绍莫什沃尔吉
G·塞莱茨基
K·乌尔班-绍博
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Sanofi Aventis France
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Sanofi Synthelabo SA
Sanofi Aventis France
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Priority claimed from HU0102279A external-priority patent/HUP0102279A3/hu
Priority claimed from HU0200774A external-priority patent/HUP0200774A2/hu
Application filed by Sanofi Synthelabo SA, Sanofi Aventis France filed Critical Sanofi Synthelabo SA
Publication of CN1512985A publication Critical patent/CN1512985A/zh
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    • C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
    • C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
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    • C07D213/04—Heterocyclic 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
    • C07D213/60—Heterocyclic 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
    • C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
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    • C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
    • C07D215/38—Nitrogen atoms
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    • C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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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    • C07D405/12—Heterocyclic 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 chain containing hetero atoms as chain links
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  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Ophthalmology & Optometry (AREA)
  • Cardiology (AREA)
  • Diabetes (AREA)
  • Pain & Pain Management (AREA)
  • Urology & Nephrology (AREA)
  • Immunology (AREA)
  • Psychology (AREA)
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  • Hematology (AREA)
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  • Emergency Medicine (AREA)
  • Rheumatology (AREA)
  • Dermatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Quinoline Compounds (AREA)
CNB02810840XA 2001-05-31 2002-05-29 氨基喹啉衍生物和它们的作为腺苷a3配体的应用 Expired - Fee Related CN1257160C (zh)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
HUP0102279 2001-05-31
HU0102279A HUP0102279A3 (en) 2001-05-31 2001-05-31 A3 antagonist amino-quinoline-derivatives, process for their preparation, pharmaceutical compositions containing them and their use
HU0200774A HUP0200774A2 (hu) 2002-03-01 2002-03-01 Amino-piridin és amino-kinolin származékok, eljárás előállításukra, ezeket tartalmazó gyógyszerkészítmények és intermedierjeik
HUP0200774 2002-03-01

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CN1512985A CN1512985A (zh) 2004-07-14
CN1257160C true CN1257160C (zh) 2006-05-24

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CNB02810840XA Expired - Fee Related CN1257160C (zh) 2001-05-31 2002-05-29 氨基喹啉衍生物和它们的作为腺苷a3配体的应用

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US (1) US6969723B2 (enExample)
EP (1) EP1390349B1 (enExample)
JP (1) JP4409935B2 (enExample)
KR (1) KR100745307B1 (enExample)
CN (1) CN1257160C (enExample)
AR (1) AR036074A1 (enExample)
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Families Citing this family (16)

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HUP0203976A3 (en) * 2002-11-15 2004-08-30 Sanofi Aventis Adenozine a3 receptors, process for their preparation and pharmaceutical compositions containing them
US8729107B2 (en) * 2002-12-06 2014-05-20 Purdue Research Foundation Pyridines for treating injured mammalian nerve tissue
CA2508165C (en) 2002-12-06 2014-05-06 Purdue Research Foundation Pyridines for treating injured mammalian nerve tissue
JP2007500689A (ja) * 2003-07-31 2007-01-18 サノフイ−アベンテイス アミノキノリン誘導体およびアデノシンa3リガンドとしてのそれらの使用
RU2317290C2 (ru) * 2003-07-31 2008-02-20 Санофи-Авентис Производные аминохинолина и их применение в качестве лигандов аденозина а3
HUP0400812A2 (en) * 2004-04-19 2006-02-28 Sanofi Aventis Crystalline forms of 2-amino-3-cyano-quinoline derivatives, process for their preparation and pharmaceutical compositions containing them
WO2006040645A1 (en) * 2004-10-11 2006-04-20 Ranbaxy Laboratories Limited N-(3,5-dichloropyridin-4-yl)-2,4,5-alkoxy and 2,3,4-alkoxy benzamide derivatives as pde-iv (phophodiesterase type-iv) inhibitors for the treatment of inflammatory diseases such as asthma
HUP0402371A2 (en) * 2004-11-15 2006-09-28 Sanofi Aventis Novel 125-i-labeled amino-quinoline derivatives
KR100788161B1 (ko) * 2006-01-06 2007-12-21 (주)아모레퍼시픽 벤즈이미다졸 아민 유도체 또는 아미노퀴놀린 유도체를 함유하는 피부 미백용 조성물
HUP0700395A2 (en) * 2007-06-07 2009-03-02 Sanofi Aventis Substituted [1,2,4] triazolo [1,5-a] quinolines, process for their preparation, pharmaceutical compositions thereof, and intermediates
KR101106050B1 (ko) * 2009-03-25 2012-01-18 한국과학기술연구원 아미노퀴놀린 화합물, 이의 제조 방법 및 이를 함유하는 의약 조성물
WO2012030918A1 (en) * 2010-09-01 2012-03-08 Ambit Biosciences Corporation Adenosine a3 receptor modulating compounds and methods of use thereof
WO2012166654A1 (en) * 2011-05-27 2012-12-06 The Regents Of The University Of California Cyanoquinoline compounds having activity in correcting mutant-cftr processing and increasing ion transport and uses thereof
CA2754237A1 (en) 2011-05-27 2012-11-27 The Regents Of The University Of California Cyanoquinoline compounds having activity in correcting mutant-cftr processing and increasing ion transport and uses thereof
ES2578363B1 (es) 2015-01-22 2017-01-31 Palobiofarma, S.L. Moduladores de los receptores A3 de adenosina
CN108137547B (zh) 2015-08-03 2021-11-12 百时美施贵宝公司 可用作TNFα调节剂的杂环化合物

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DE265143C (enExample)
FR2582514B1 (fr) * 1985-05-30 1988-02-19 Rhone Poulenc Sante Medicaments a base d'amides, nouveaux amides et leur preparation
JPH01180518A (ja) * 1988-01-12 1989-07-18 Nissan Chem Ind Ltd 配向処理剤
IL111266A (en) * 1993-10-22 2002-03-10 Zeneca Ltd 2-HETEROARYL OR 2-ARYLPYRIDAZINO [4,5-b] QUINOLINE - 1, 10 - DIONES, THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
IL146105A (en) * 1999-04-23 2005-09-25 Tadeda Pharmaceutical Company 5-pyridyl-1, 3-azole compounds, process for producing the same and use therefor

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US20040186133A1 (en) 2004-09-23
EE05304B1 (et) 2010-06-15
NZ529966A (en) 2004-11-26
AU2002304358B2 (en) 2007-08-23
KR20040030648A (ko) 2004-04-09
WO2002096879A1 (en) 2002-12-05
TNSN03117A1 (en) 2005-12-23
JP4409935B2 (ja) 2010-02-03
CO5550457A2 (es) 2005-08-31
HRP20031091B1 (en) 2012-05-31
EP1390349A1 (en) 2004-02-25
CZ20033510A3 (cs) 2005-01-12
JP2004536074A (ja) 2004-12-02
WO2002096879A9 (en) 2003-11-20
IL158854A0 (en) 2004-05-12
MXPA03010870A (es) 2004-02-27
BR0209719A (pt) 2004-07-27
MA26236A1 (fr) 2004-08-01
BG108477A (bg) 2005-01-31
RU2003137836A (ru) 2005-05-27
HRP20031091A2 (en) 2005-10-31
CN1512985A (zh) 2004-07-14
SK14142003A3 (sk) 2005-03-04
EA006854B1 (ru) 2006-04-28
NO327710B1 (no) 2009-09-14
AR036074A1 (es) 2004-08-11
EA200301317A1 (ru) 2004-06-24
RU2278112C2 (ru) 2006-06-20
EE200300574A (et) 2004-02-16
IS2773B (is) 2012-01-15
US6969723B2 (en) 2005-11-29
CA2448561A1 (en) 2002-12-05
EP1390349B1 (en) 2012-07-25
RS95003A (sr) 2007-02-05
KR100745307B1 (ko) 2007-08-01
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