JP2005536522A5 - - Google Patents

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Publication number
JP2005536522A5
JP2005536522A5 JP2004523742A JP2004523742A JP2005536522A5 JP 2005536522 A5 JP2005536522 A5 JP 2005536522A5 JP 2004523742 A JP2004523742 A JP 2004523742A JP 2004523742 A JP2004523742 A JP 2004523742A JP 2005536522 A5 JP2005536522 A5 JP 2005536522A5
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JP
Japan
Prior art keywords
pain
compound according
phenyl
pharmaceutically acceptable
enantiomer
Prior art date
Legal status (The legal status 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 status listed.)
Granted
Application number
JP2004523742A
Other languages
English (en)
Japanese (ja)
Other versions
JP2005536522A (ja
JP4588444B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/DK2003/000510 external-priority patent/WO2004011468A1/en
Publication of JP2005536522A publication Critical patent/JP2005536522A/ja
Publication of JP2005536522A5 publication Critical patent/JP2005536522A5/ja
Application granted granted Critical
Publication of JP4588444B2 publication Critical patent/JP4588444B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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JP2004523742A 2002-07-26 2003-07-24 ジアザビシクロノナン及び−デカン誘導体並びにこれをオピオイドレセプターリガンドとして使用する方法 Expired - Fee Related JP4588444B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DKPA200201143 2002-07-26
PCT/DK2003/000510 WO2004011468A1 (en) 2002-07-26 2003-07-24 Diazabicyclononane and -decane derivatives and their use as opioid receptor ligands

Publications (3)

Publication Number Publication Date
JP2005536522A JP2005536522A (ja) 2005-12-02
JP2005536522A5 true JP2005536522A5 (enExample) 2010-05-20
JP4588444B2 JP4588444B2 (ja) 2010-12-01

Family

ID=30775758

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2004523742A Expired - Fee Related JP4588444B2 (ja) 2002-07-26 2003-07-24 ジアザビシクロノナン及び−デカン誘導体並びにこれをオピオイドレセプターリガンドとして使用する方法

Country Status (11)

Country Link
US (1) US7358243B2 (enExample)
EP (1) EP1527075B1 (enExample)
JP (1) JP4588444B2 (enExample)
CN (1) CN100340561C (enExample)
AT (1) ATE390427T1 (enExample)
AU (1) AU2003280306B2 (enExample)
CA (1) CA2489165A1 (enExample)
DE (1) DE60319989T2 (enExample)
MX (1) MXPA05001002A (enExample)
NZ (1) NZ537182A (enExample)
WO (1) WO2004011468A1 (enExample)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ITMI20040954A1 (it) * 2004-05-12 2004-08-12 Univ Degli Studi Milano Derivati del 3,6-diazabiciclo 3.1.i.eptano ad attivita' analgesica
IT1395452B1 (it) * 2009-02-25 2012-09-21 Neuroscienze Pharmaness S C A Rl Microemulsioni
IT1390848B1 (it) 2008-07-31 2011-10-19 Neuroscienze Pharmaness S C A R L Composti farmaceutici
IT1390850B1 (it) * 2008-07-31 2011-10-19 Neuroscienze Pharmaness S C A R L Microemulsioni
EP2149370A1 (en) * 2008-07-31 2010-02-03 Neuroscienze Pharmaness S.C. A R.L. Diazabicyclic compounds and microemulsions thereof
IT1394400B1 (it) 2009-02-25 2012-06-15 Neuroscienze Pharmaness S C Ar L Composizioni farmaceutiche
IT1396951B1 (it) * 2009-12-18 2012-12-20 Neuroscienze Pharmaness S C A R L Composti farmaceutici
EP2789619A1 (en) 2013-04-12 2014-10-15 Kemotech S.r.l. Pharmaceutical compounds wiht angiogenesis inbhibitory activity

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1274018B (it) 1994-02-23 1997-07-14 Riace Ets Derivati del 3,8-diazabiciclo(3.2.1.)ottano ad attivita' analgesica
NZ513575A (en) 1999-05-04 2003-07-25 Neurosearch As Heteroaryl diazabicycloalkanes useful for treating or preventing a disease or a disorder responsive to the activity of nAChR modulators
IT1317841B1 (it) * 2000-02-18 2003-07-15 Univ Degli Studi Milano Derivati del 3,9-diazabiciclo(3.3.1)nonano ad attivita' analgesica.
WO2001072303A1 (en) 2000-03-29 2001-10-04 Research Triangle Institute Selective ligands for the delta opioid receptor

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