JP4065567B2 - 置換２―（２，６―ジオキソピペリジン―３―イル）フタルイミド類及び―１―オキソイソインドリン類ならびにＴＮＦαレベルの減少方法 - Google Patents

置換２―（２，６―ジオキソピペリジン―３―イル）フタルイミド類及び―１―オキソイソインドリン類ならびにＴＮＦαレベルの減少方法 Download PDF

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JP4065567B2
JP4065567B2 JP50725998A JP50725998A JP4065567B2 JP 4065567 B2 JP4065567 B2 JP 4065567B2 JP 50725998 A JP50725998 A JP 50725998A JP 50725998 A JP50725998 A JP 50725998A JP 4065567 B2 JP4065567 B2 JP 4065567B2
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Prior art keywords
dioxopiperidin
oxo
dione
mixture
mmol
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Expired - Lifetime
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JP50725998A
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JP2001503384A (ja
JP2001503384A5 (enExample
Inventor
ミュラー，ジョージ，ダブリュー
スターリング，デビッド，アイ
チェン，ロジャー，シェン―チュー
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Celgene Corp
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Celgene Corp
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Priority claimed from US08690258 external-priority patent/US5635517B1/en
Priority claimed from US08/701,494 external-priority patent/US5798368A/en
Application filed by Celgene Corp filed Critical Celgene Corp
Publication of JP2001503384A publication Critical patent/JP2001503384A/ja
Publication of JP2001503384A5 publication Critical patent/JP2001503384A5/ja
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/04—Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
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    • A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
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    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
    • A61K9/0056—Mouth soluble or dispersible forms; Suckable, eatable, chewable coherent forms; Forms rapidly disintegrating in the mouth; Lozenges; Lollipops; Bite capsules; Baked products; Baits or other oral forms for animals
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    • A61K9/2018—Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
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    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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  • Public Health (AREA)
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  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Zoology (AREA)
  • Nutrition Science (AREA)
  • Physiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
JP50725998A 1996-07-24 1997-07-24 置換２―（２，６―ジオキソピペリジン―３―イル）フタルイミド類及び―１―オキソイソインドリン類ならびにＴＮＦαレベルの減少方法 Expired - Lifetime JP4065567B2 (ja)

Applications Claiming Priority (7)

Application Number Priority Date Filing Date Title
US08/690,258 1996-07-24
US08690258 US5635517B1 (en) 1996-07-24 1996-07-24 Method of reducing TNFalpha levels with amino substituted 2-(2,6-dioxopiperidin-3-YL)-1-oxo-and 1,3-dioxoisoindolines
US08/701,494 US5798368A (en) 1996-08-22 1996-08-22 Tetrasubstituted 2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolines and method of reducing TNFα levels
US08/701,494 1996-08-22
US4827897P 1997-05-30 1997-05-30
US60/048,278 1997-05-30
PCT/US1997/013375 WO1998003502A1 (en) 1996-07-24 1997-07-24 Substituted 2(2,6-dioxopiperidin-3-yl)phthalimides and -1-oxoisoindolines and method of reducing tnf-alpha levels

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2007289533A Division JP2008050368A (ja) 1996-07-24 2007-11-07 置換２−（２，６−ジオキソピペリジン−３−イル）フタルイミド類及び−１−オキソイソインドリン類ならびにＴＮＦαレベルの減少方法

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Publication Number Publication Date
JP2001503384A JP2001503384A (ja) 2001-03-13
JP2001503384A5 JP2001503384A5 (enExample) 2005-09-08
JP4065567B2 true JP4065567B2 (ja) 2008-03-26

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JP50725998A Expired - Lifetime JP4065567B2 (ja) 1996-07-24 1997-07-24 置換２―（２，６―ジオキソピペリジン―３―イル）フタルイミド類及び―１―オキソイソインドリン類ならびにＴＮＦαレベルの減少方法

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EP (4) EP0925294B3 (enExample)
JP (1) JP4065567B2 (enExample)
KR (2) KR100534498B1 (enExample)
CN (1) CN1117089C (enExample)
AT (4) ATE500240T1 (enExample)
CA (3) CA2560523C (enExample)
CZ (3) CZ295762B6 (enExample)
DE (4) DE69739802D1 (enExample)
DK (2) DK0925294T6 (enExample)
ES (4) ES2339425T3 (enExample)
FI (1) FI120687B (enExample)
FR (1) FR07C0056I2 (enExample)
HU (1) HUS1300056I1 (enExample)
LU (1) LU91359I2 (enExample)
NL (1) NL300291I2 (enExample)
NZ (1) NZ333903A (enExample)
PL (2) PL195916B1 (enExample)
PT (4) PT2177517E (enExample)
SK (1) SK9199A3 (enExample)
UA (1) UA60308C2 (enExample)
WO (1) WO1998003502A1 (enExample)

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USRE48890E1 (en) 2002-05-17 2022-01-11 Celgene Corporation Methods for treating multiple myeloma with 3-(4-amino-1-oxo-1,3-dihydroisoindol-2-yl)-piperidine-2,6-dione after stem cell transplantation
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