NO912864L - Stedsspesifikk in vivo-aktivering av terapeutiske forbindelser - Google Patents
Stedsspesifikk in vivo-aktivering av terapeutiske forbindelserInfo
- Publication number
- NO912864L NO912864L NO91912864A NO912864A NO912864L NO 912864 L NO912864 L NO 912864L NO 91912864 A NO91912864 A NO 91912864A NO 912864 A NO912864 A NO 912864A NO 912864 L NO912864 L NO 912864L
- Authority
- NO
- Norway
- Prior art keywords
- prodrug according
- anthracycline
- group
- prodrug
- negatively charged
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/68—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
- A61K47/6891—Pre-targeting systems involving an antibody for targeting specific cells
- A61K47/6899—Antibody-Directed Enzyme Prodrug Therapy [ADEPT]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/08—Vasodilators for multiple indications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Molecular Biology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Immunology (AREA)
- Nanotechnology (AREA)
- Medical Informatics (AREA)
- Cardiology (AREA)
- General Engineering & Computer Science (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Biotechnology (AREA)
- Biophysics (AREA)
- Mycology (AREA)
- Microbiology (AREA)
- Crystallography & Structural Chemistry (AREA)
- Heart & Thoracic Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicinal Preparation (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Peptides Or Proteins (AREA)
- Enzymes And Modification Thereof (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Steroid Compounds (AREA)
Abstract
1. Aktivator-målsøkingsdel-konjugat, karakterisert ved at det omfatter lysozym som aktivator og et humant monoklonalt antistoff eller et fragment av dette som målsøkingsdel. 2. Prodroge, karakterisert ved at den omfatter et anti- kreftmiddel som bærer et spaltbart molekyl som hindrer celle- opptak. 3. Prodroge ifølge krav 2, karakterisert ved at den omfatter et anti- kreftmiddel som er derivatisert med et kitinoligomer-avstands- materiale. 4. Prodroge ifølge krav 3, karakterisert ved at antikreftmidlet er et antracyklin. 5. Prodroge ifølge krav 4, karakterisert ved at kitinoligomer-avstands- materialet er festet via en aminogruppe på et sted valgt fra gruppen som består av C13-karbonylstedet på antracyklinet og sukkerdelen av antracyklinet. 6. Prodroge ifølge krav 5, karakterisert ved at kitinoligomer-derivatet inneholder (GlcNAc)n, hvor n er 1-10, som bærer negativt ladede grupper og en reaktiv gruppe som gir mulighet for kovalent festing til antracyklinet. 7. Prodroge ifølge krav 6, karakterisert ved at de negativt ladede grupper representerer sulfonater, fosfater, karboksylater eller fosfonater. 8. Prodroge ifølge krav 6, karakterisert ved at antallet negativt ladede grupper er fra l til 10. 9. Prodroge ifølge krav 3, karakterisert ved at kitinoligoroer-avstands- materialet er bundet kovalent til drogen via en aktiv gruppe valgt blant disulfid-, tioester-, imid-, halogen-, amin-, karboksyl-, ester-, tiol- og alkoholgrupper. 10. Prodroge ifølge krav 6, karakterisert ved at den reaktive gruppe er valgt blant disulfid-, tioester-, imid-, halogen-, amin-, karboksyl-, ester-, tiol- og alkoholgrupper.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US30099989A | 1989-01-23 | 1989-01-23 | |
| PCT/US1990/000503 WO1990007929A1 (en) | 1989-01-23 | 1990-01-23 | Site specific in-vivo activation of therapeutic drugs |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO912864D0 NO912864D0 (no) | 1991-07-22 |
| NO912864L true NO912864L (no) | 1991-09-19 |
Family
ID=23161497
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO91912864A NO912864L (no) | 1989-01-23 | 1991-07-22 | Stedsspesifikk in vivo-aktivering av terapeutiske forbindelser |
Country Status (12)
| Country | Link |
|---|---|
| EP (1) | EP0454783B1 (no) |
| JP (1) | JP3273608B2 (no) |
| KR (1) | KR0185967B1 (no) |
| AT (1) | ATE123414T1 (no) |
| AU (1) | AU648015B2 (no) |
| CA (1) | CA2025899A1 (no) |
| DE (1) | DE69019959T2 (no) |
| DK (1) | DK0454783T3 (no) |
| ES (1) | ES2075893T3 (no) |
| FI (1) | FI97692C (no) |
| NO (1) | NO912864L (no) |
| WO (1) | WO1990007929A1 (no) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5773435A (en) * | 1987-08-04 | 1998-06-30 | Bristol-Myers Squibb Company | Prodrugs for β-lactamase and uses thereof |
| US5851527A (en) * | 1988-04-18 | 1998-12-22 | Immunomedics, Inc. | Method for antibody targeting of therapeutic agents |
| US5474772A (en) * | 1989-08-02 | 1995-12-12 | Cobe Laboratories, Inc. | Method of treatment with medical agents |
| US6610299B1 (en) | 1989-10-19 | 2003-08-26 | Aventis Pharma Deutschland Gmbh | Glycosyl-etoposide prodrugs, a process for preparation thereof and the use thereof in combination with functionalized tumor-specific enzyme conjugates |
| DE4106389A1 (de) * | 1991-02-28 | 1992-09-03 | Behringwerke Ag | Fusionsproteine zur prodrug-aktivierung, ihre herstellung und verwendung |
| US6475486B1 (en) | 1990-10-18 | 2002-11-05 | Aventis Pharma Deutschland Gmbh | Glycosyl-etoposide prodrugs, a process for preparation thereof and the use thereof in combination with functionalized tumor-specific enzyme conjugates |
| US7241595B2 (en) | 1989-10-20 | 2007-07-10 | Sanofi-Aventis Pharma Deutschland Gmbh | Glycosyl-etoposide prodrugs, a process for preparation thereof and the use thereof in combination with functionalized tumor-specific enzyme conjugates |
| WO1991008770A1 (en) * | 1989-12-11 | 1991-06-27 | Immunomedics, Inc. | Method for antibody targeting of diagnostic or therapeutic agents |
| SE9100142L (sv) | 1991-01-17 | 1992-07-18 | Bengt Sandberg | En metod och ett system foer foerbaettrad in vivo reducering av diagnostiska och/eller terapeutiska substanser medelst extrakorporeal borttagning, och anvaendandet av naemnda substanser foer detta aendamaal |
| FR2676058B1 (fr) * | 1991-04-30 | 1994-02-25 | Hoechst Lab | Prodrogues glycosylees, leur procede de preparation et leur utilisation dans le traitement des cancers. |
| WO1994001137A1 (en) * | 1992-07-06 | 1994-01-20 | Hybritech Incorporated | Method for delivery of cytotoxic agents and components thereof |
| GB9323429D0 (en) * | 1993-11-12 | 1994-01-05 | Wellcome Found | Therapy |
| RU2189251C2 (ru) * | 1994-12-23 | 2002-09-20 | Зенека Лимитед | Химические соединения |
| HUP9900062A3 (en) | 1995-08-16 | 1999-11-29 | Zeneca Ltd | Chemical compounds |
| EP0795334B1 (de) * | 1996-03-12 | 2006-02-01 | Sanofi-Aventis Deutschland GmbH | Neuartige Prodrugs für die Therapie von Tumoren und entzündlichen Erkrankungen |
| PL229108B1 (pl) * | 2014-08-22 | 2018-06-29 | Celther Polska Spolka Z Ograniczona Odpowiedzialnoscia | Sposób wydzielania i oczyszczania estrów chityny (mono-, di‑podstawionych) oraz kopoliestrów chityny z mieszanin poreakcyjnych |
| EP3970752A1 (en) * | 2020-09-17 | 2022-03-23 | Merck Patent GmbH | Molecules with solubility tag and related methods |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4067774A (en) * | 1971-05-14 | 1978-01-10 | Syva Company | Compounds for enzyme amplification assay |
| US4631190A (en) | 1981-06-26 | 1986-12-23 | Shen Wei C | Acidity-sensitive spacer molecule to control the release of pharmaceuticals from molecular carriers |
| LU85581A1 (fr) * | 1984-10-10 | 1986-06-11 | Smb Lab | Ensembles d'anticorps monoclonaux diriges contre la lactoferrine humaine et le lysozyme humain |
| JPS62138496A (ja) * | 1985-12-11 | 1987-06-22 | Ihara Chem Ind Co Ltd | キチンオリゴマ−の製造方法 |
| WO1989000050A1 (en) * | 1987-07-02 | 1989-01-12 | Akzo N.V. | Antigen recognized by mca 16-88 |
| NZ225599A (en) * | 1987-08-04 | 1991-09-25 | Bristol Myers Co | Antibody-enzyme conjugates and combinations with prodrugs for the treatment of tumour cells |
| ZA893284B (en) * | 1988-05-04 | 1990-03-28 | Igen Inc | Peptide analogs and their use as haptens to elicit catalytic antibodies |
-
1990
- 1990-01-23 JP JP50311690A patent/JP3273608B2/ja not_active Expired - Fee Related
- 1990-01-23 AT AT90902934T patent/ATE123414T1/de not_active IP Right Cessation
- 1990-01-23 KR KR1019900702129A patent/KR0185967B1/ko not_active Expired - Fee Related
- 1990-01-23 CA CA002025899A patent/CA2025899A1/en not_active Abandoned
- 1990-01-23 WO PCT/US1990/000503 patent/WO1990007929A1/en not_active Ceased
- 1990-01-23 AU AU50397/90A patent/AU648015B2/en not_active Ceased
- 1990-01-23 DE DE69019959T patent/DE69019959T2/de not_active Expired - Fee Related
- 1990-01-23 DK DK90902934.0T patent/DK0454783T3/da active
- 1990-01-23 EP EP90902934A patent/EP0454783B1/en not_active Revoked
- 1990-01-23 ES ES90902934T patent/ES2075893T3/es not_active Expired - Lifetime
-
1991
- 1991-07-22 FI FI913511A patent/FI97692C/fi active
- 1991-07-22 NO NO91912864A patent/NO912864L/no unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE69019959D1 (de) | 1995-07-13 |
| NO912864D0 (no) | 1991-07-22 |
| EP0454783A1 (en) | 1991-11-06 |
| WO1990007929A1 (en) | 1990-07-26 |
| ATE123414T1 (de) | 1995-06-15 |
| EP0454783B1 (en) | 1995-06-07 |
| KR910700072A (ko) | 1991-03-13 |
| AU648015B2 (en) | 1994-04-14 |
| EP0454783A4 (en) | 1992-01-15 |
| ES2075893T3 (es) | 1995-10-16 |
| DK0454783T3 (da) | 1995-10-16 |
| AU5039790A (en) | 1990-08-13 |
| FI913511A0 (fi) | 1991-07-22 |
| JP3273608B2 (ja) | 2002-04-08 |
| KR0185967B1 (ko) | 1999-05-01 |
| FI97692B (fi) | 1996-10-31 |
| FI97692C (fi) | 1997-02-10 |
| CA2025899A1 (en) | 1990-07-24 |
| JPH04503068A (ja) | 1992-06-04 |
| DE69019959T2 (de) | 1995-10-05 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO912864L (no) | Stedsspesifikk in vivo-aktivering av terapeutiske forbindelser | |
| AU671247B2 (en) | Paclitaxel derivatives | |
| Mellado et al. | Preparation and biological activity of taxol acetates | |
| AU669218B2 (en) | Prodrugs, their preparation and use as pharmaceuticals | |
| DE69637383T2 (de) | Cytotoxinkonjugate umfassend dipeptide | |
| JP5392956B2 (ja) | 担体−薬物複合体 | |
| US5760072A (en) | Paclitaxel prodrugs, method for preparation as well as their use in selective chemotherapy | |
| EA003790B1 (ru) | Соединение сдлс и способ его измерения | |
| de Bont et al. | Synthesis and biological activity of β-glucuronyl carbamate-based prodrugs of paclitaxel as potential candidates for ADEPT | |
| EP2911696A1 (en) | Drug-protein conjugates | |
| Hesek et al. | Synthesis of a fragment of bacterial cell wall | |
| Suzawa et al. | Synthesis of a novel duocarmycin derivative DU-257 and its application to immunoconjugate using poly (ethylene glycol)-dipeptidyl linker capable of tumor specific activation | |
| Yang et al. | Convergent synthesis of hydrophilic monomethyl dolastatin 10 based drug linkers for antibody–drug conjugation | |
| Wei et al. | A photoactivated prodrug | |
| EP3166644B1 (en) | Method of synthesising adcs using photocleavable linkers on solid support | |
| JPH0654681A (ja) | レシチン化スーパーオキシドディスムターゼ及びそれを有効成分とする医薬 | |
| Suzawa et al. | Synthesis and HPLC analysis of enzymatically cleavable linker consisting of poly (ethylene glycol) and dipeptide for the development of immunoconjugate | |
| JPH07316205A (ja) | シクロデキストリン誘導体 | |
| White Jr | [48] Thiolation | |
| ES2292750T3 (es) | Procedimiento para preparar lipido ii. | |
| KR20030011306A (ko) | 지질 ⅱ의 제조 방법 | |
| CA2114629C (en) | Receptor conjugates for targeting antibiotics to bacteria | |
| JP2594803B2 (ja) | レクチン複合体及びそれを製造する方法及びプローブ | |
| SAWADA et al. | Studies on the β-lysine peptide. IV. Preparation of semi-synthetic racemomycins and their antimicrobial activities | |
| LaTour | Understanding transglycosylase inhibition: Chlorobiphenyl vancomycin and moenomycin A as targets for synthesis and modification |