JP2005503432A5 - - Google Patents

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Publication number
JP2005503432A5
JP2005503432A5 JP2003530649A JP2003530649A JP2005503432A5 JP 2005503432 A5 JP2005503432 A5 JP 2005503432A5 JP 2003530649 A JP2003530649 A JP 2003530649A JP 2003530649 A JP2003530649 A JP 2003530649A JP 2005503432 A5 JP2005503432 A5 JP 2005503432A5
Authority
JP
Japan
Prior art keywords
group
disease
formula
compound
pharmaceutical composition
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.)
Pending
Application number
JP2003530649A
Other languages
English (en)
Japanese (ja)
Other versions
JP2005503432A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/IL2001/000909 external-priority patent/WO2003027058A1/en
Publication of JP2005503432A publication Critical patent/JP2005503432A/ja
Publication of JP2005503432A5 publication Critical patent/JP2005503432A5/ja
Pending legal-status Critical Current

Links

JP2003530649A 2001-09-26 2001-09-26 スフィンゴリピド Pending JP2005503432A (ja)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/IL2001/000909 WO2003027058A1 (en) 2001-09-26 2001-09-26 Sphingolipids

Publications (2)

Publication Number Publication Date
JP2005503432A JP2005503432A (ja) 2005-02-03
JP2005503432A5 true JP2005503432A5 (enExample) 2008-11-20

Family

ID=11043096

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2003530649A Pending JP2005503432A (ja) 2001-09-26 2001-09-26 スフィンゴリピド

Country Status (8)

Country Link
EP (1) EP1430019B1 (enExample)
JP (1) JP2005503432A (enExample)
AT (1) ATE453614T1 (enExample)
CA (1) CA2461801A1 (enExample)
DE (1) DE60140964D1 (enExample)
ES (1) ES2337654T3 (enExample)
IL (1) IL160850A0 (enExample)
WO (1) WO2003027058A1 (enExample)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005032462A2 (en) 2003-02-27 2005-04-14 Enzo Therapeutics, Inc. Glucocerebroside treatment of disease
US9717754B2 (en) 2003-02-27 2017-08-01 Enzo Therapeutics, Inc. Glucocerebroside treatment of disease
JP2007533632A (ja) 2003-09-30 2007-11-22 エンゾー セラピューティクス, インコーポレイテッド 疾患のグルコセレブロシド処理
CN101214249A (zh) 2003-11-25 2008-07-09 纽约大学西奈山医学院 尼曼-皮克病的基于陪伴分子的治疗
WO2007136635A1 (en) * 2006-05-16 2007-11-29 Musc Foundation For Research Development Enhancement of radiation therapy and/or chemotherapy with acid ceramidase modulators
IL187247A0 (en) * 2007-11-08 2008-12-29 Hadasit Med Res Service Novel synthetic analogs of sphingolipids
IL187245A0 (en) * 2007-11-08 2008-12-29 Hadasit Med Res Service Synthetic sphingolipid analogs
JP5757022B2 (ja) * 2011-09-26 2015-07-29 国立大学法人名古屋大学 光学活性アルキルアミノスルホンアミド誘導体の製造方法及び光学活性β−アミノアルコール誘導体

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5041441A (en) * 1988-04-04 1991-08-20 The Regents Of The University Of Michigan Method of chemotherapy using 1-phenyl-2-decanoylamino-3-morpholino-1-propanol
DD275670A1 (de) * 1988-09-20 1990-01-31 Akad Wissenschaften Ddr Verfahren zur herstellung von d,l-threo-2-amino-1(p-aminophenyl)-propan-1,3-diolen
DE3916072A1 (de) * 1989-05-17 1990-11-22 Thera Ges Fuer Patente Ceramidderivate und ihre verwendung als inhibitoren der sphingolipidsynthese
JP3800434B2 (ja) * 1994-05-31 2006-07-26 生化学工業株式会社 擬似糖脂質
US5763438A (en) * 1994-06-10 1998-06-09 Seikagaku Corporation 2-acylaminopropanol compound and medical composition
EP0821068A3 (en) * 1996-03-29 1999-06-02 Rohm And Haas Company Novel sphingolipids and a process thereto
US5830432A (en) * 1997-03-31 1998-11-03 Amur Pharmacuticals, Inc. Phospholipid drug derivatives
JP2001213858A (ja) * 1999-11-24 2001-08-07 Sagami Chem Res Center スフィンゴシン誘導体
AU2001252506A1 (en) * 2000-04-19 2001-10-30 Yissum Research Development Company Of The Hebrew University Of Jerusalem Sphingolipids
FR2810037B1 (fr) * 2000-06-09 2004-04-23 Aventis Pharma Sa Utilisation de derives de 2-aminothiazoline comme inhibiteurs de no-synthase inductible

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