NO314545B1 - Kaskadepolymerkomplekser, fremgangsmåter for fremstilling av disse og farmasöytiske midler inneholdende disse - Google Patents
Kaskadepolymerkomplekser, fremgangsmåter for fremstilling av disse og farmasöytiske midler inneholdende disse Download PDFInfo
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- NO314545B1 NO314545B1 NO19982903A NO982903A NO314545B1 NO 314545 B1 NO314545 B1 NO 314545B1 NO 19982903 A NO19982903 A NO 19982903A NO 982903 A NO982903 A NO 982903A NO 314545 B1 NO314545 B1 NO 314545B1
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- JHVLLYQQQYIWKX-UHFFFAOYSA-N benzyl 2-bromoacetate Chemical compound BrCC(=O)OCC1=CC=CC=C1 JHVLLYQQQYIWKX-UHFFFAOYSA-N 0.000 description 1
- JMXXMORECWYVQP-UHFFFAOYSA-N benzyl N-[2-[[4-[4,7-bis[4-[bis[2-(phenylmethoxycarbonylamino)ethyl]amino]-4-oxobutanoyl]-1,4,7,10-tetrazacyclododec-1-yl]-4-oxobutanoyl]-[2-(phenylmethoxycarbonylamino)ethyl]amino]ethyl]carbamate Chemical compound C=1C=CC=CC=1COC(=O)NCCN(C(=O)CCC(=O)N1CCN(CCN(CCNCC1)C(=O)CCC(=O)N(CCNC(=O)OCC=1C=CC=CC=1)CCNC(=O)OCC=1C=CC=CC=1)C(=O)CCC(=O)N(CCNC(=O)OCC=1C=CC=CC=1)CCNC(=O)OCC=1C=CC=CC=1)CCNC(=O)OCC1=CC=CC=C1 JMXXMORECWYVQP-UHFFFAOYSA-N 0.000 description 1
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 1
- 229940073608 benzyl chloride Drugs 0.000 description 1
- HSDAJNMJOMSNEV-UHFFFAOYSA-N benzyl chloroformate Chemical compound ClC(=O)OCC1=CC=CC=C1 HSDAJNMJOMSNEV-UHFFFAOYSA-N 0.000 description 1
- GDZIODIYBLTRRJ-UHFFFAOYSA-N benzyl cyanoformate Chemical compound N#CC(=O)OCC1=CC=CC=C1 GDZIODIYBLTRRJ-UHFFFAOYSA-N 0.000 description 1
- RNKVSVXLSRFYGG-UHFFFAOYSA-N benzyl n-[4-[4,7-bis[5-(phenylmethoxycarbonylamino)-2-[3-(phenylmethoxycarbonylamino)propyl]pentanoyl]-1,4,7,10-tetrazacyclododecane-1-carbonyl]-7-(phenylmethoxycarbonylamino)heptyl]carbamate Chemical compound C=1C=CC=CC=1COC(=O)NCCCC(C(=O)N1CCN(CCN(CCNCC1)C(=O)C(CCCNC(=O)OCC=1C=CC=CC=1)CCCNC(=O)OCC=1C=CC=CC=1)C(=O)C(CCCNC(=O)OCC=1C=CC=CC=1)CCCNC(=O)OCC=1C=CC=CC=1)CCCNC(=O)OCC1=CC=CC=C1 RNKVSVXLSRFYGG-UHFFFAOYSA-N 0.000 description 1
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- 239000007853 buffer solution Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
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- XLJKHNWPARRRJB-UHFFFAOYSA-N cobalt(2+) Chemical compound [Co+2] XLJKHNWPARRRJB-UHFFFAOYSA-N 0.000 description 1
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- IOIFRTZBJMZZFO-UHFFFAOYSA-N dysprosium(3+) Chemical compound [Dy+3] IOIFRTZBJMZZFO-UHFFFAOYSA-N 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- JHFPQYFEJICGKC-UHFFFAOYSA-N erbium(3+) Chemical compound [Er+3] JHFPQYFEJICGKC-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
- 238000007306 functionalization reaction Methods 0.000 description 1
- HZHFFEYYPYZMNU-UHFFFAOYSA-K gadodiamide Chemical compound [Gd+3].CNC(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CCN(CC([O-])=O)CC(=O)NC HZHFFEYYPYZMNU-UHFFFAOYSA-K 0.000 description 1
- RJOJUSXNYCILHH-UHFFFAOYSA-N gadolinium(3+) Chemical compound [Gd+3] RJOJUSXNYCILHH-UHFFFAOYSA-N 0.000 description 1
- 229940083124 ganglion-blocking antiadrenergic secondary and tertiary amines Drugs 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 238000002523 gelfiltration Methods 0.000 description 1
- 150000003278 haem Chemical class 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 230000009931 harmful effect Effects 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 239000012477 high molecular weight ligand Substances 0.000 description 1
- SCKNFLZJSOHWIV-UHFFFAOYSA-N holmium(3+) Chemical compound [Ho+3] SCKNFLZJSOHWIV-UHFFFAOYSA-N 0.000 description 1
- 238000007327 hydrogenolysis reaction Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 238000002354 inductively-coupled plasma atomic emission spectroscopy Methods 0.000 description 1
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- 230000003993 interaction Effects 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 238000010253 intravenous injection Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 150000004694 iodide salts Chemical class 0.000 description 1
- 230000005865 ionizing radiation Effects 0.000 description 1
- DGAIEPBNLOQYER-UHFFFAOYSA-N iopromide Chemical compound COCC(=O)NC1=C(I)C(C(=O)NCC(O)CO)=C(I)C(C(=O)N(C)CC(O)CO)=C1I DGAIEPBNLOQYER-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000000302 ischemic effect Effects 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000002372 labelling Methods 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 229910052747 lanthanoid Inorganic materials 0.000 description 1
- 150000002602 lanthanoids Chemical class 0.000 description 1
- CZMAIROVPAYCMU-UHFFFAOYSA-N lanthanum(3+) Chemical compound [La+3] CZMAIROVPAYCMU-UHFFFAOYSA-N 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 210000005228 liver tissue Anatomy 0.000 description 1
- 230000004807 localization Effects 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
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- 230000005291 magnetic effect Effects 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- MIKKOBKEXMRYFQ-WZTVWXICSA-N meglumine amidotrizoate Chemical compound C[NH2+]C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.CC(=O)NC1=C(I)C(NC(C)=O)=C(I)C(C([O-])=O)=C1I MIKKOBKEXMRYFQ-WZTVWXICSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- 230000002107 myocardial effect Effects 0.000 description 1
- 210000004165 myocardium Anatomy 0.000 description 1
- QEFYFXOXNSNQGX-UHFFFAOYSA-N neodymium atom Chemical compound [Nd] QEFYFXOXNSNQGX-UHFFFAOYSA-N 0.000 description 1
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 1
- 238000013421 nuclear magnetic resonance imaging Methods 0.000 description 1
- 238000003199 nucleic acid amplification method Methods 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 150000002892 organic cations Chemical class 0.000 description 1
- 230000003204 osmotic effect Effects 0.000 description 1
- 230000005414 paramagnetic center Effects 0.000 description 1
- 229960003330 pentetic acid Drugs 0.000 description 1
- 230000010412 perfusion Effects 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 239000008055 phosphate buffer solution Substances 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- WCWKKSOQLQEJTE-UHFFFAOYSA-N praseodymium(3+) Chemical compound [Pr+3] WCWKKSOQLQEJTE-UHFFFAOYSA-N 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 230000000637 radiosensitizating effect Effects 0.000 description 1
- 230000003439 radiotherapeutic effect Effects 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- DOSGOCSVHPUUIA-UHFFFAOYSA-N samarium(3+) Chemical compound [Sm+3] DOSGOCSVHPUUIA-UHFFFAOYSA-N 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 239000003579 shift reagent Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- HKCRVXUAKWXBLE-UHFFFAOYSA-N terbium(3+) Chemical compound [Tb+3] HKCRVXUAKWXBLE-UHFFFAOYSA-N 0.000 description 1
- BNWCETAHAJSBFG-UHFFFAOYSA-N tert-butyl 2-bromoacetate Chemical compound CC(C)(C)OC(=O)CBr BNWCETAHAJSBFG-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 125000005490 tosylate group Chemical group 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 238000000844 transformation Methods 0.000 description 1
- 125000004665 trialkylsilyl group Chemical group 0.000 description 1
- 125000004044 trifluoroacetyl group Chemical group FC(C(=O)*)(F)F 0.000 description 1
- 125000000025 triisopropylsilyl group Chemical group C(C)(C)[Si](C(C)C)(C(C)C)* 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 229960000281 trometamol Drugs 0.000 description 1
- 210000004881 tumor cell Anatomy 0.000 description 1
- 229940005605 valeric acid Drugs 0.000 description 1
- 230000000304 vasodilatating effect Effects 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K49/00—Preparations for testing in vivo
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K49/00—Preparations for testing in vivo
- A61K49/06—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations
- A61K49/08—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by the carrier
- A61K49/085—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by the carrier conjugated systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K49/00—Preparations for testing in vivo
- A61K49/04—X-ray contrast preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K49/00—Preparations for testing in vivo
- A61K49/06—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations
- A61K49/08—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by the carrier
- A61K49/10—Organic compounds
- A61K49/12—Macromolecular compounds
- A61K49/124—Macromolecular compounds dendrimers, dendrons, hyperbranched compounds
Landscapes
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Radiology & Medical Imaging (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Plural Heterocyclic Compounds (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19549286A DE19549286A1 (de) | 1995-12-22 | 1995-12-22 | Kaskaden-Polymer-Komplexe, Verfahren zu ihrer Herstellung und diese enthaltende pharmazeutische Mittel |
| PCT/EP1996/005315 WO1997023245A1 (de) | 1995-12-22 | 1996-11-29 | Kaskaden-polymer-komplexe, verfahren zu ihrer herstellung und diese enthaltende pharmazeutische mittel |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO982903L NO982903L (no) | 1998-06-22 |
| NO982903D0 NO982903D0 (no) | 1998-06-22 |
| NO314545B1 true NO314545B1 (no) | 2003-04-07 |
Family
ID=7781739
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO19982903A NO314545B1 (no) | 1995-12-22 | 1998-06-22 | Kaskadepolymerkomplekser, fremgangsmåter for fremstilling av disse og farmasöytiske midler inneholdende disse |
Country Status (23)
| Country | Link |
|---|---|
| US (1) | US6057419A (ja) |
| EP (1) | EP0868202B1 (ja) |
| JP (1) | JP4031041B2 (ja) |
| KR (1) | KR100461476B1 (ja) |
| AT (1) | ATE222776T1 (ja) |
| BG (1) | BG63105B1 (ja) |
| CA (1) | CA2241187A1 (ja) |
| CZ (1) | CZ294238B6 (ja) |
| DE (2) | DE19549286A1 (ja) |
| DK (1) | DK0868202T3 (ja) |
| ES (1) | ES2181924T3 (ja) |
| IL (1) | IL124677A (ja) |
| MX (1) | MX9804860A (ja) |
| NO (1) | NO314545B1 (ja) |
| NZ (1) | NZ323397A (ja) |
| PL (1) | PL187835B1 (ja) |
| PT (1) | PT868202E (ja) |
| RU (1) | RU2197495C2 (ja) |
| SK (1) | SK283334B6 (ja) |
| TW (1) | TW520377B (ja) |
| UA (1) | UA50753C2 (ja) |
| WO (1) | WO1997023245A1 (ja) |
| ZA (1) | ZA9610822B (ja) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19652387A1 (de) * | 1996-12-04 | 1998-06-10 | Schering Ag | Macrocyclische Metallkomplexcarbonsäuren, ihre Verwendung sowie Verfahren zu ihrer Herstellung |
| DE19728954C1 (de) * | 1997-06-30 | 1999-04-22 | Schering Ag | Saccharid-Konjugate, diese enthaltende pharmazeutische Mittel, Verfahren zu ihrer Herstellung und ihre Verwendung |
| DE19744003B4 (de) * | 1997-09-26 | 2004-07-08 | Schering Ag | Kontrastmittel für das Infarkt- und Nekroseimaging |
| DE19758105A1 (de) * | 1997-12-18 | 1999-06-24 | Schering Ag | Dendritische Polymer-Saccharid-Konjugate, diese enthaltende pharmazeutische Mittel, Verfahren zu ihrer Herstellung und ihre Verwendung |
| US7405320B2 (en) * | 1998-06-22 | 2008-07-29 | Immunomedics, Inc. | Therapeutic and diagnostic conjugates for use with multispecific antibodies |
| FR2841258A1 (fr) * | 2002-06-20 | 2003-12-26 | Pf Medicament | Procede et preparation de mononegavirus recombinants et leurs applications |
| JP5518465B2 (ja) * | 2006-03-14 | 2014-06-11 | マリンクロッド エルエルシー | テトラアザ大員環誘導体の金属錯体 |
| DE102007002726A1 (de) * | 2007-01-18 | 2008-07-31 | Bayer Schering Pharma Aktiengesellschaft | Neue Kaskaden-Polymer-Komplexe, Verfahren zu ihrer Herstellung und diese enthaltende pharmazeutische Mittel |
| WO2014197763A1 (en) * | 2013-06-07 | 2014-12-11 | The Board Of Regents Of The University Of Teas System | Molecular design toward dual-modality probes for radioisotope-based imaging (pet or spect) and mri |
| EP3101012A1 (en) | 2015-06-04 | 2016-12-07 | Bayer Pharma Aktiengesellschaft | New gadolinium chelate compounds for use in magnetic resonance imaging |
| JP7034160B2 (ja) | 2016-11-28 | 2022-03-11 | バイエル・ファルマ・アクティエンゲゼルシャフト | 磁気共鳴画像法に使用するための高緩和度ガドリニウムキレート化合物 |
| PE20211471A1 (es) | 2018-11-23 | 2021-08-05 | Bayer Ag | Formulacion de medios de contraste y proceso para prepararlos |
| RU2706705C1 (ru) * | 2019-03-28 | 2019-11-20 | Федеральное государственное бюджетное учреждение науки Иркутский институт химии им.А.Е.Фаворского Сибирского отделения Российской академии наук | Водорастворимые магнитоактивные нанобиокомпозиты флавоноидных комплексов гадолиния на основе природного конъюгата арабиногалактана с биофлавоноидами и способ получения этих нанобиокомпозитов |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5527524A (en) * | 1986-08-18 | 1996-06-18 | The Dow Chemical Company | Dense star polymer conjugates |
| DE3938992A1 (de) * | 1989-11-21 | 1991-05-23 | Schering Ag | Kaskadenpolymer-gebundene komplexbildner, deren komplexe und konjugate, verfahren zu ihrer herstellung und diese enthaltende pharmazeutische mittel |
| DE4344460A1 (de) * | 1993-12-22 | 1995-06-29 | Schering Ag | Metallkomplexe von dendrimeren Makromolekülen, diese enthaltende diagnostische Mittel sowie Verfahren zur Herstellung der Komplexe und Mittel |
| GB9404208D0 (en) * | 1994-03-04 | 1994-04-20 | Nycomed Salutar Inc | Chelants |
| GB9407812D0 (en) * | 1994-04-20 | 1994-06-15 | Nycomed Salutar Inc | Compounds |
| DE4425857A1 (de) * | 1994-07-07 | 1996-01-11 | Schering Ag | Kaskaden-Polymer-Komplexe, Verfahren zur ihrer Herstellung und diese enthaltende pharmazeutische Mittel |
| US5919433A (en) * | 1996-12-04 | 1999-07-06 | Schering Aktiengesellschaft | Macrocyclic metal complex carboxylic acids, their use as well as process for their production |
-
1995
- 1995-12-22 DE DE19549286A patent/DE19549286A1/de not_active Withdrawn
-
1996
- 1996-11-29 CA CA002241187A patent/CA2241187A1/en not_active Abandoned
- 1996-11-29 SK SK854-98A patent/SK283334B6/sk unknown
- 1996-11-29 ES ES96941055T patent/ES2181924T3/es not_active Expired - Lifetime
- 1996-11-29 EP EP96941055A patent/EP0868202B1/de not_active Expired - Lifetime
- 1996-11-29 US US09/077,773 patent/US6057419A/en not_active Expired - Fee Related
- 1996-11-29 DE DE59609603T patent/DE59609603D1/de not_active Expired - Fee Related
- 1996-11-29 NZ NZ323397A patent/NZ323397A/xx unknown
- 1996-11-29 RU RU98113782/04A patent/RU2197495C2/ru not_active IP Right Cessation
- 1996-11-29 WO PCT/EP1996/005315 patent/WO1997023245A1/de active IP Right Grant
- 1996-11-29 AT AT96941055T patent/ATE222776T1/de not_active IP Right Cessation
- 1996-11-29 KR KR10-1998-0704746A patent/KR100461476B1/ko not_active IP Right Cessation
- 1996-11-29 PT PT96941055T patent/PT868202E/pt unknown
- 1996-11-29 JP JP52325197A patent/JP4031041B2/ja not_active Expired - Fee Related
- 1996-11-29 IL IL12467796A patent/IL124677A/xx not_active IP Right Cessation
- 1996-11-29 DK DK96941055T patent/DK0868202T3/da active
- 1996-11-29 PL PL32797796A patent/PL187835B1/pl not_active IP Right Cessation
- 1996-11-29 UA UA98073923A patent/UA50753C2/uk unknown
- 1996-11-29 CZ CZ19981981A patent/CZ294238B6/cs not_active IP Right Cessation
- 1996-12-20 ZA ZA9610822A patent/ZA9610822B/xx unknown
- 1996-12-20 TW TW085115801A patent/TW520377B/zh not_active IP Right Cessation
-
1998
- 1998-06-17 MX MX9804860A patent/MX9804860A/es unknown
- 1998-06-19 BG BG102565A patent/BG63105B1/bg unknown
- 1998-06-22 NO NO19982903A patent/NO314545B1/no not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| JP4031041B2 (ja) | 2008-01-09 |
| IL124677A (en) | 2005-03-20 |
| TW520377B (en) | 2003-02-11 |
| IL124677A0 (en) | 1998-12-06 |
| UA50753C2 (uk) | 2002-11-15 |
| DE59609603D1 (de) | 2002-10-02 |
| PT868202E (pt) | 2003-01-31 |
| PL187835B1 (pl) | 2004-10-29 |
| KR100461476B1 (ko) | 2005-04-06 |
| ATE222776T1 (de) | 2002-09-15 |
| BG102565A (en) | 1999-06-30 |
| EP0868202A1 (de) | 1998-10-07 |
| US6057419A (en) | 2000-05-02 |
| ZA9610822B (en) | 1997-06-27 |
| MX9804860A (es) | 1998-10-31 |
| KR19990076638A (ko) | 1999-10-15 |
| SK283334B6 (sk) | 2003-06-03 |
| NO982903L (no) | 1998-06-22 |
| EP0868202B1 (de) | 2002-08-28 |
| CZ198198A3 (cs) | 1998-09-16 |
| RU2197495C2 (ru) | 2003-01-27 |
| ES2181924T3 (es) | 2003-03-01 |
| CZ294238B6 (cs) | 2004-11-10 |
| CA2241187A1 (en) | 1997-07-03 |
| PL327977A1 (en) | 1999-01-04 |
| WO1997023245A1 (de) | 1997-07-03 |
| DK0868202T3 (da) | 2002-12-09 |
| DE19549286A1 (de) | 1997-06-26 |
| JP2000510880A (ja) | 2000-08-22 |
| NZ323397A (en) | 1999-11-29 |
| NO982903D0 (no) | 1998-06-22 |
| BG63105B1 (bg) | 2001-04-30 |
| SK85498A3 (en) | 1998-11-04 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM1K | Lapsed by not paying the annual fees |