ES2113892T3 - Inmunoreactivos radiactivos dirigidos. - Google Patents
Inmunoreactivos radiactivos dirigidos.Info
- Publication number
- ES2113892T3 ES2113892T3 ES91920573T ES91920573T ES2113892T3 ES 2113892 T3 ES2113892 T3 ES 2113892T3 ES 91920573 T ES91920573 T ES 91920573T ES 91920573 T ES91920573 T ES 91920573T ES 2113892 T3 ES2113892 T3 ES 2113892T3
- Authority
- ES
- Spain
- Prior art keywords
- immunoreactive
- radioactive
- directed
- directed radioactive
- compound
- 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.)
- Expired - Lifetime
Links
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K49/00—Preparations for testing in vivo
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/44—Radicals substituted by doubly-bound oxygen, sulfur, or nitrogen atoms, or by two such atoms singly-bound to the same carbon atom
- C07D213/53—Nitrogen atoms
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- 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
- A61K47/56—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 organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule
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- 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
- A61K47/6835—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 the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site
- A61K47/6887—Antibody-chelate conjugates using chelates for therapeutic purposes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K51/00—Preparations containing radioactive substances for use in therapy or testing in vivo
- A61K51/02—Preparations containing radioactive substances for use in therapy or testing in vivo characterised by the carrier, i.e. characterised by the agent or material covalently linked or complexing the radioactive nucleus
- A61K51/04—Organic compounds
- A61K51/08—Peptides, e.g. proteins, carriers being peptides, polyamino acids, proteins
- A61K51/10—Antibodies or immunoglobulins; Fragments thereof, the carrier being an antibody, an immunoglobulin or a fragment thereof, e.g. a camelised human single domain antibody or the Fc fragment of an antibody
- A61K51/1045—Antibodies or immunoglobulins; Fragments thereof, the carrier being an antibody, an immunoglobulin or a fragment thereof, e.g. a camelised human single domain antibody or the Fc fragment of an antibody against animal or human tumor cells or tumor cell determinants
- A61K51/1054—Antibodies or immunoglobulins; Fragments thereof, the carrier being an antibody, an immunoglobulin or a fragment thereof, e.g. a camelised human single domain antibody or the Fc fragment of an antibody against animal or human tumor cells or tumor cell determinants the tumor cell being from lung
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K51/00—Preparations containing radioactive substances for use in therapy or testing in vivo
- A61K51/02—Preparations containing radioactive substances for use in therapy or testing in vivo characterised by the carrier, i.e. characterised by the agent or material covalently linked or complexing the radioactive nucleus
- A61K51/04—Organic compounds
- A61K51/08—Peptides, e.g. proteins, carriers being peptides, polyamino acids, proteins
- A61K51/10—Antibodies or immunoglobulins; Fragments thereof, the carrier being an antibody, an immunoglobulin or a fragment thereof, e.g. a camelised human single domain antibody or the Fc fragment of an antibody
- A61K51/1045—Antibodies or immunoglobulins; Fragments thereof, the carrier being an antibody, an immunoglobulin or a fragment thereof, e.g. a camelised human single domain antibody or the Fc fragment of an antibody against animal or human tumor cells or tumor cell determinants
- A61K51/1063—Antibodies or immunoglobulins; Fragments thereof, the carrier being an antibody, an immunoglobulin or a fragment thereof, e.g. a camelised human single domain antibody or the Fc fragment of an antibody against animal or human tumor cells or tumor cell determinants the tumor cell being from stomach or intestines
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K51/00—Preparations containing radioactive substances for use in therapy or testing in vivo
- A61K51/02—Preparations containing radioactive substances for use in therapy or testing in vivo characterised by the carrier, i.e. characterised by the agent or material covalently linked or complexing the radioactive nucleus
- A61K51/04—Organic compounds
- A61K51/08—Peptides, e.g. proteins, carriers being peptides, polyamino acids, proteins
- A61K51/10—Antibodies or immunoglobulins; Fragments thereof, the carrier being an antibody, an immunoglobulin or a fragment thereof, e.g. a camelised human single domain antibody or the Fc fragment of an antibody
- A61K51/1093—Antibodies or immunoglobulins; Fragments thereof, the carrier being an antibody, an immunoglobulin or a fragment thereof, e.g. a camelised human single domain antibody or the Fc fragment of an antibody conjugates with carriers being antibodies
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/61—Halogen atoms or nitro radicals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/76—Nitrogen atoms to which a second hetero atom is attached
- C07D213/77—Hydrazine radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Epidemiology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Immunology (AREA)
- Oncology (AREA)
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Cell Biology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Biomedical Technology (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyridine Compounds (AREA)
Abstract
UN INMUNOREACTIVO CON FOCO DE EMISION RADIOACTIVO COMPRENDE UN ION METALICO RADIONUCLEOSIDO, UN AGENTE DE COMPLEXION Y UN GRUPO INMUNOREACTIVO LIGADO POR COVALENCIA AL MENCIONADO AGENTE DE COMPLEXION, TENIENDO EL AGENTE DE COMPLEXION UNA ESTRUCTURA (A-I), EN LA QUE R REPRESENTA HIDROGENO, ALQUILO, ALCOXI, ALQUILTIO, ALQUILAMINO, ALQUILFORMAMIDO, ARILO, ARILOXI, HETEROCICLILO O UN GRUPO REACTIVO DE PROTEINAS; R1 REPRESENTA HIDROGENO, ALQUILO, ALCOXI, ALQUILTIO, ALQUILAMINO, ALQUILFORMAMIDO, ARILO, ARILOXI, HETEROCICLILO O UN GRUPO REACTIVO DE PROTEINAS; R2 REPRESENTA HIDROXI, CARBOXI, HIDROXIALQUILO, ACIDO CARBONILIMINOACETICO, ACIDO METILENOIMINODIACETICO, ACIDO METILENOETIOETILENOIMINODIACETICO, ACIDO HIDRACINILILIDENODIACETICO O UNA SAL DE DICHOS ACIDOS, O DOS GRUPOS R2, TOMADOS JUNTOS, REPRESENTAN LOS ATOMOS NECESARIOS PARA COMPLETAR UNA ESTRUCTURA DE ANILLO MACROCICLICO QUE CONTIENE AL MENOS UNA ZONA DE COORDINACION HETEROATOMICA Y AL MENOS UNO, PREFERIBLEMENTE DOS GRUPOS ALQUILENO QUEFORMEN PARTE DE LA ESTRUCTURA DE ANILLO; R3 REPRESENTA HIDROGENO, ALQUIL, ALCOXI, ALQUILTIO, ALQUILAMINO, ALQUILFORMAMIDO, ARILO, ARILOXI, HETEROCICLILO O UN GRUPO REACTIVO DE PROTEINAS; R4 REPRESENTA HIDROGENO O UN GRUPO REACTIVO DE PROTEINAS; N ES DE 0 A 4, O ES DE 0 A 1, M ES 0 O 1; SIEMPRE QUE AL MENOS N O M SEA 0 Y AL MENOS 1 DE ENTRE R, R1, R3 Y R4 SEA UN GRUPO REACTIVO DE PROTEINAS. EN UNA COMPOSICION DE TAL ASPECTO, ESTA INVENCION PROPORCIONA NUEVAS TERPIRIDINAS Y FENANTROLINAS. LAS TERPIRIDINAS PREFERIDAS TIENEN LA ESTRUCTURA (A-I) DE ARRIBA, DONDE N=1, M=0 Y R ES UN FENILO SUSTITUIDO QUE CONTIENE UN SUBSTITUYENTE ALQUILO O ALCOXI Y UN GRUPO REACTIVO DE PROTEINAS. LAS FENANTROLINAS PREFERIDAS TIENEN LA ESTRUCTURA (A-I) DE ARRIBA, DONDE N=0, M=1 Y AL MENOS UN R4 ES UN GRUPO REACTIVO DE PROTEINAS. LOS INMUNOREACTIVOS CON FOCO DE EMISION RADIOACTIVO SON PARTICULARMENTE UTILES EN COMPOSICIONES Y METODOS DE IMAGENES TERAPEUTICAS Y DE DIAGNOSIS.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US61086190A | 1990-11-08 | 1990-11-08 | |
US07/784,333 US5367080A (en) | 1990-11-08 | 1991-10-29 | Complexing agents and targeting radioactive immunoreagents useful in therapeutic and diagnostic imaging compositions and methods |
PCT/US1991/008253 WO1992008494A2 (en) | 1990-11-08 | 1991-11-07 | Targeting radioactive immunoreagents |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2113892T3 true ES2113892T3 (es) | 1998-05-16 |
Family
ID=27086372
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES91920573T Expired - Lifetime ES2113892T3 (es) | 1990-11-08 | 1991-11-07 | Inmunoreactivos radiactivos dirigidos. |
Country Status (21)
Country | Link |
---|---|
US (4) | US5367080A (es) |
EP (1) | EP0624097B1 (es) |
JP (1) | JP3292301B2 (es) |
KR (1) | KR930701974A (es) |
AT (1) | ATE164082T1 (es) |
AU (2) | AU667030B2 (es) |
BR (1) | BR9107074A (es) |
CA (1) | CA2095123A1 (es) |
DE (1) | DE69129127T2 (es) |
DK (1) | DK0624097T3 (es) |
ES (1) | ES2113892T3 (es) |
FI (1) | FI932083A (es) |
GR (1) | GR3026713T3 (es) |
HU (1) | HUT67298A (es) |
IE (1) | IE913907A1 (es) |
MX (1) | MX9101999A (es) |
NO (1) | NO931631L (es) |
NZ (1) | NZ240521A (es) |
PT (1) | PT99460B (es) |
TW (1) | TW201271B (es) |
WO (1) | WO1992008494A2 (es) |
Families Citing this family (88)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5367080A (en) * | 1990-11-08 | 1994-11-22 | Sterling Winthrop Inc. | Complexing agents and targeting radioactive immunoreagents useful in therapeutic and diagnostic imaging compositions and methods |
CA2135059A1 (en) * | 1992-05-07 | 1993-11-11 | John L. Toner | Complexing agents and targeting immunoreagents |
KR950703582A (ko) * | 1992-10-14 | 1995-09-20 | 조이스 이. 마임스 | 킬레이트화 중합체(chelating polymers) |
CA2152777A1 (en) * | 1992-12-28 | 1994-07-07 | Hirofusa Shirai | Pharmaceutical use of terpyridine derivatives |
US5760191A (en) * | 1993-02-05 | 1998-06-02 | Nycomed Imaging As | Macrocyclic complexing agents and targeting immunoreagents useful in therapeutic and diagnostic compositions and methods |
EP0691981A1 (en) * | 1993-03-10 | 1996-01-17 | The Wellcome Foundation Limited | Tumor targeting with l-enantiomeric oligonucleotide conjugates of immunoreagents and of chelated radionuclides |
US5744119A (en) * | 1993-05-11 | 1998-04-28 | Sterling Winthrop | Preparation of a radioconjugate formulation |
US5559214A (en) | 1993-05-28 | 1996-09-24 | Sterling Winthrop Inc. | Unsymmetrical complexing agents and targeting immunoreagents useful in thearpeutic and diagnostic compositions and methods |
WO1994029333A1 (en) * | 1993-06-07 | 1994-12-22 | The Wellcome Foundation Limited | Immunoreactive reagents employing monoamine oxidase |
DE19505960A1 (de) * | 1995-02-21 | 1996-08-22 | Deutsches Krebsforsch | Konjugat zur individuellen Dosierung von Arzneimitteln |
US5562626A (en) * | 1995-09-11 | 1996-10-08 | Sanpietro; Joseph A. | Safety syringe |
AUPO066096A0 (en) * | 1996-06-26 | 1996-07-18 | Peptide Delivery Systems Pty Ltd | Oral delivery of peptides |
WO1998009650A1 (fr) | 1996-09-06 | 1998-03-12 | Mitsubishi Chemical Corporation | Preparations vaccinales |
AU9452198A (en) * | 1997-10-15 | 1999-05-17 | Nycomed Imaging As | Complexing agents and targeting immunoreagents |
WO1999039748A1 (en) * | 1998-02-06 | 1999-08-12 | Nycomed Imaging As | Targeting immunoreagents useful in therapeutic and diagnostic compositions and methods |
DE19911329A1 (de) * | 1998-03-27 | 2000-09-21 | Benes Ivan Friedrich | Humantherapeutisch anwendbares Radioimmunkonjugat und Verfahren zu seiner Herstellung |
AU3375599A (en) * | 1998-03-31 | 1999-10-18 | Trustees Of Boston University | Methods for designing molecular conjugates and compositions thereof |
US6314314B1 (en) | 1999-01-14 | 2001-11-06 | Seth J. Karp | Method for locating an internal bleeding site in a human body |
TWI290146B (en) * | 1999-07-29 | 2007-11-21 | Dyax Corp | Binding moieties for fibrin |
DE60111733T2 (de) * | 2000-04-12 | 2006-05-18 | Amersham Health As | Integrinbindende peptidderivate |
NO20004795D0 (no) * | 2000-09-26 | 2000-09-26 | Nycomed Imaging As | Peptidbaserte forbindelser |
WO2002031865A1 (en) * | 2000-10-13 | 2002-04-18 | Emcore Corporation | Method of making an electrode |
US7009040B2 (en) * | 2003-01-21 | 2006-03-07 | Arius Research, Inc. | Cancerous disease modifying antibodies |
US6984373B2 (en) * | 2000-12-23 | 2006-01-10 | Dyax Corp. | Fibrin binding moieties useful as imaging agents |
HU230901B1 (hu) * | 2001-07-10 | 2019-01-28 | Ge Healthcare Limited | Peptidalapú vegyületek és ezeket tartalmazó gyógyszerkészítmények |
ES2500918T3 (es) | 2001-12-21 | 2014-10-01 | Human Genome Sciences, Inc. | Proteínas de fusión de albúmina e interferón beta |
ES2506142T3 (es) | 2002-03-01 | 2014-10-13 | Dyax Corp. | Péptidos de unión a KDR y a VEGF/KDR y su uso en diagnóstico |
EP1587944A4 (en) | 2002-03-01 | 2007-03-21 | Dyax Corp | KDR AND VEGF / KDR BINDING PEPTIDES AND THEIR USE FOR DIAGNOSTIC AND THERAPEUTIC PURPOSES |
US8623822B2 (en) | 2002-03-01 | 2014-01-07 | Bracco Suisse Sa | KDR and VEGF/KDR binding peptides and their use in diagnosis and therapy |
US7261876B2 (en) | 2002-03-01 | 2007-08-28 | Bracco International Bv | Multivalent constructs for therapeutic and diagnostic applications |
US7794693B2 (en) | 2002-03-01 | 2010-09-14 | Bracco International B.V. | Targeting vector-phospholipid conjugates |
US7211240B2 (en) | 2002-03-01 | 2007-05-01 | Bracco International B.V. | Multivalent constructs for therapeutic and diagnostic applications |
CA2488682C (en) * | 2002-06-10 | 2014-04-01 | Vaccinex, Inc. | Gene differentially expressed in breast and bladder cancer and encoded polypeptides |
US7226577B2 (en) | 2003-01-13 | 2007-06-05 | Bracco Imaging, S. P. A. | Gastrin releasing peptide compounds |
US7468254B2 (en) * | 2003-01-21 | 2008-12-23 | Arius Research Inc. | Cytotoxicity mediation of cells evidencing surface expression of MCSP |
US7393531B2 (en) * | 2003-01-21 | 2008-07-01 | Arius Research Inc. | Cytotoxicity mediation of cells evidencing surface expression of MCSP |
DK2284180T3 (en) | 2003-03-03 | 2015-12-21 | Dyax Corp | Uses of peptides that specifically bind to the HGF receptor (cMET) |
CA2783275A1 (en) * | 2003-07-24 | 2005-02-03 | Bracco Imaging S.P.A. | Stable radiopharmaceutical compositions and methods for their preparation |
JP4912153B2 (ja) * | 2003-12-01 | 2012-04-11 | イミューノメディクス、インコーポレイテッド | タンパク質とキレート剤とのコンジュゲートを調製するための改良された方法 |
NZ547591A (en) * | 2003-12-04 | 2009-11-27 | Vaccinex Inc | Methods of killing tumor cells by targeting internal antigens exposed on apoptotic tumor cells |
WO2005100340A2 (en) * | 2004-04-13 | 2005-10-27 | Icagen, Inc. | Polycyclic pyridines as potassium ion channel modulators |
US20060024229A1 (en) * | 2004-07-29 | 2006-02-02 | Seth Karp | Method and product for locating an internal bleeding site |
US20100034748A1 (en) * | 2008-08-07 | 2010-02-11 | Guizhi Li | Molecular imaging probes based on loaded reactive nano-scale latex |
CA2619832A1 (en) * | 2005-08-16 | 2007-02-22 | University Of North Carolina At Wilmington | Ligands for metal ions and methods for making and using the same |
US20090098057A1 (en) * | 2007-10-16 | 2009-04-16 | Shiying Zheng | Silica-cored carrier particle |
EP1991577A2 (en) | 2006-01-31 | 2008-11-19 | Parkinson, John F. | Modulation of mdl-1 activity for treatment of inflammatory disease |
US20080167544A1 (en) * | 2006-12-01 | 2008-07-10 | Cold Spring Diagnostics, Inc. | Compositions And Methods For Locating An Internal Bleeding Site |
JP5345945B2 (ja) | 2006-12-11 | 2013-11-20 | ブラッコ・イメージング・ソシエタ・ペル・アチオニ | フィブリン結合ペプチドおよびそのコンジュゲート |
US8906354B2 (en) | 2007-02-28 | 2014-12-09 | Bruker Biospin Corporation | Loaded latex optical molecular imaging probes containing lipophilic large stokes shift dyes |
EP2005970A1 (de) | 2007-06-22 | 2008-12-24 | Berlin Science Partners GmbH i.V. | Bildgebende Diagnostik durch Kombination von Kontrastmitteln |
CN101932333A (zh) * | 2007-12-26 | 2010-12-29 | 瓦西尼斯公司 | 抗c35抗体联合疗法和方法 |
EP2100900A1 (en) | 2008-03-07 | 2009-09-16 | Universitätsspital Basel | Bombesin analog peptide antagonist conjugates |
EP2147684A1 (en) | 2008-07-22 | 2010-01-27 | Bracco Imaging S.p.A | Diagnostic Agents Selective Against Metalloproteases |
US20120045393A1 (en) | 2009-03-17 | 2012-02-23 | Linder Karen E | Lhrh-ii peptide analogs |
AR075900A1 (es) | 2009-03-19 | 2011-05-04 | Wyeth Llc | Metodos para la preparacion de acidos (2-(8,9-dioxo-2,6-diazabiciclico (5.2.0) non-1(7)-en-2-il)etil) fosfonico y sus precursores. |
WO2010121133A2 (en) | 2009-04-17 | 2010-10-21 | The General Hospital Corporation | Multimodal imaging of fibrin |
US8648194B2 (en) * | 2009-09-14 | 2014-02-11 | B.R.A.H.M.S Gmbh | Compounds having phenanthroline structure |
FR2969999B1 (fr) * | 2011-01-03 | 2013-02-08 | Commissariat Energie Atomique | Conjugue, son procede de preparation et ses utilisations |
JP2014509585A (ja) * | 2011-03-11 | 2014-04-21 | ベー・エル・アー・ハー・エム・エス・ゲーエムベーハー | フェナントロリン化合物を配位子とする希土類金属錯体 |
WO2013048832A1 (en) | 2011-09-29 | 2013-04-04 | Ge Healthcare Limited | 18 f - labelled 6 - ( 2 - fluoroethoxy) - 2 - naphthaldehyde for detecting cancer stem cells |
EP2740726A1 (en) | 2012-12-07 | 2014-06-11 | 3B Pharmaceuticals GmbH | Neurotensin receptor ligands |
US10017551B2 (en) | 2013-03-15 | 2018-07-10 | The Regents Of The University Of California | Peptides having reduced toxicity that stimulate cholesterol efflux |
WO2015171543A1 (en) | 2014-05-05 | 2015-11-12 | California Institute Of Technology | Mutant akt-specific capture agents, compositions, and methods of using and making |
EP2954933A1 (en) | 2014-06-10 | 2015-12-16 | 3B Pharmaceuticals GmbH | Conjugate comprising a neurotensin receptor ligand |
EP3154638A1 (en) | 2014-06-10 | 2017-04-19 | 3B Pharmaceuticals GmbH | Conjugate comprising a neurotensin receptor ligand and use thereof |
EP2954934A1 (en) | 2014-06-11 | 2015-12-16 | 3B Pharmaceuticals GmbH | Conjugate comprising a neurotensin receptor ligand and use thereof |
WO2017011769A2 (en) | 2015-07-15 | 2017-01-19 | California Institute Of Technology | Il-17f-specific capture agents, compositions, and methods of using and making |
BR112018015143A2 (pt) | 2016-02-09 | 2018-12-18 | Bracco Suisse Sa | proteína quimérica recombinante para direcionamento de selectinas |
EP3440101B1 (en) | 2016-04-04 | 2021-10-06 | Indi Molecular, Inc. | Cd8-specific capture agents, compositions, and methods of using and making |
EP3279197A1 (en) | 2016-08-03 | 2018-02-07 | Friedrich-Alexander-Universität Erlangen-Nürnberg | Diagnosis, treatment and prevention of neurotensin receptor-related conditions |
WO2018064597A1 (en) | 2016-09-29 | 2018-04-05 | Indi Molecular, Inc. | Compositions for detection, inhibition and imaging of indoleamine 2,3-dioxygenase 1 (ido1) and methods of making and using same |
WO2018085375A1 (en) | 2016-11-01 | 2018-05-11 | Ohio State Innovation Foundation | Methods for the iodination of biomolecules |
EP3638687A1 (en) | 2017-06-15 | 2020-04-22 | Indi Molecular, Inc. | Il-17f and il-17a-specific capture agents, compositions, and methods of using and making |
US11638764B2 (en) | 2018-11-08 | 2023-05-02 | Indi Molecular, Inc. | Theranostic capture agents, compositions, and methods of using and making |
US20200291391A1 (en) | 2019-03-12 | 2020-09-17 | Indi Molecular, Inc. | Cross-linked epitopes and methods of use thereof |
WO2020236969A1 (en) | 2019-05-20 | 2020-11-26 | Indi Molecular, Inc. | Compositions and methods relating to detection, inhibition, and imaging of indoleamine 2,3-dioxygenase 1 (ido1) |
US20220218834A1 (en) | 2019-05-20 | 2022-07-14 | Ohio State Innovation Foundation | Apohemoglobin-haptoglobin complexes and methods of using thereof |
CN114341158B (zh) | 2019-07-08 | 2024-08-06 | 3B制药有限公司 | 包含成纤维细胞活化蛋白配体的化合物及其用途 |
EP3763726A1 (en) | 2019-07-08 | 2021-01-13 | 3B Pharmaceuticals GmbH | Compounds comprising a fibroblast activation protein ligand and use thereof |
US11414460B2 (en) | 2019-07-19 | 2022-08-16 | Institute For Systems Biology | KRAS-specific capture agents, compositions, and methods of making and using |
WO2022098743A1 (en) | 2020-11-03 | 2022-05-12 | Indi Molecular, Inc. | Compositions, imaging, and therapeutic methods targeting folate receptor 1 (folr1) |
WO2022098745A1 (en) | 2020-11-03 | 2022-05-12 | Indi Molecular, Inc. | Compositions, delivery systems, and methods useful in tumor therapy |
WO2022123462A1 (en) | 2020-12-09 | 2022-06-16 | 3B Pharmaceuticals Gmbh | Radiolabelled prostate specific membrane antigen (psma) inhibitors and use thereof |
EP4050018A1 (en) | 2021-01-07 | 2022-08-31 | 3B Pharmaceuticals GmbH | Compounds comprising a fibroblast activation protein ligand and use thereof |
MX2023007869A (es) | 2021-01-07 | 2023-09-22 | 3B Pharmaceuticals Gmbh | Compuestos que comprenden un ligando de proteina de activacion de fibroblasto y uso del mismo. |
EP4122499A1 (en) | 2021-07-23 | 2023-01-25 | 3B Pharmaceuticals GmbH | Fibroblast activation protein inhibitors and use thereof |
KR20240133798A (ko) | 2021-12-17 | 2024-09-04 | 쓰리비 파마슈티컬스 게엠베하 | 탄산 무수화효소 ix 리간드 |
WO2024052431A1 (en) | 2022-09-07 | 2024-03-14 | 3B Pharmaceuticals Gmbh | Prostate specific membrane antigen (psma) ligands and use thereof |
Family Cites Families (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4801722A (en) * | 1981-07-01 | 1989-01-31 | Eastman Kodak Company | Coumarin chelates |
US4637988A (en) * | 1981-07-01 | 1987-01-20 | Eastman Kodak Company | Fluorescent labels for immunoassay |
US4794191A (en) * | 1981-07-01 | 1988-12-27 | Eastman Kodak Company | Fluorescent chelates |
US4837169A (en) * | 1981-07-01 | 1989-06-06 | Eastman Kodak Company | Polypyridine Fluorescent labels for immunoassay |
US4670572A (en) * | 1981-07-01 | 1987-06-02 | Eastman Kodak Company | Phenolic fluorescent labels |
US4859777A (en) * | 1981-07-01 | 1989-08-22 | Eastman Kodak Company | Terpyridine chelating agents |
US4767611A (en) * | 1984-07-03 | 1988-08-30 | Gordon Robert T | Method for affecting intracellular and extracellular electric and magnetic dipoles |
DE3580420D1 (de) * | 1984-08-13 | 1990-12-13 | Hsc Res Dev Corp | 1,10-phenanthrolin-2,9-dicarbonsaeure-derivate und deren verwendung fuer fluoreszens-immunoassay. |
DK365785A (da) * | 1984-09-17 | 1986-03-18 | Hoffmann La Roche | Metalcomplexer |
US5075447A (en) * | 1984-09-17 | 1991-12-24 | Hoffmann-La Roche Inc. | Ruthenium complexes useful as carriers for immunologically active materials |
US4761481A (en) * | 1985-03-18 | 1988-08-02 | Baxter Travenol Laboratories, Inc. | Substituted pyridine derivatives |
SE8502573D0 (sv) * | 1985-05-23 | 1985-05-23 | Jouko Kanakre | Fluorescent lanthanide chelates useful as labels of physiologically active materials |
WO1987007955A1 (en) * | 1986-06-17 | 1987-12-30 | Baxter Travenol Laboratories, Inc. | Homogeneous fluoroassay methods employing fluorescent background rejection and water-soluble rare earth metal chelate fluorophores |
WO1988002635A1 (en) * | 1986-10-17 | 1988-04-21 | Cytogen Corporation | Method for preparation of protein-chelator-metal ion compositions suitable for injection |
SE8702824L (sv) * | 1987-07-10 | 1989-01-11 | Wallac Oy | Metall-kelaterande 2,6-disubstituerade pyridinfoereningar och deras anvaendning |
US5032677A (en) * | 1987-11-06 | 1991-07-16 | Baxter International Inc. | Fluorescent poly(arylpyridine) rare earth chelates |
JPH082878B2 (ja) * | 1988-02-12 | 1996-01-17 | 富士写真フイルム株式会社 | 4’−アルコキシ−2,2’:6’,2〃−デルピリジン誘導体及びその金属錯体 |
SE8800613D0 (sv) * | 1988-02-23 | 1988-02-23 | Wallac Oy | A novel spectrofluorometric method and compounds that are of value for the method |
US5202423A (en) * | 1988-07-08 | 1993-04-13 | Wallac Oy | Terpyridine derivatives |
SE8802575D0 (sv) * | 1988-07-08 | 1988-07-08 | Wallac Oy | Terpyridine derivatives |
FR2644785B1 (fr) * | 1989-03-24 | 1991-07-05 | Guerbet Sa | Nouveaux ligands macrocycliques azotes, procede de preparation, complexes metalliques formes par ces ligands et composition de diagnostic les contenant |
GB8927503D0 (en) * | 1989-12-04 | 1990-02-07 | Kronem Systems Inc | Enzyme-amplified lanthanide chelate luminescence |
GB9001245D0 (en) * | 1990-01-19 | 1990-03-21 | Salutar Inc | Compounds |
US5367080A (en) * | 1990-11-08 | 1994-11-22 | Sterling Winthrop Inc. | Complexing agents and targeting radioactive immunoreagents useful in therapeutic and diagnostic imaging compositions and methods |
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1991
- 1991-10-29 US US07/784,333 patent/US5367080A/en not_active Expired - Lifetime
- 1991-11-07 CA CA002095123A patent/CA2095123A1/en not_active Abandoned
- 1991-11-07 AU AU90291/91A patent/AU667030B2/en not_active Expired
- 1991-11-07 KR KR1019930701386A patent/KR930701974A/ko not_active IP Right Cessation
- 1991-11-07 BR BR919107074A patent/BR9107074A/pt not_active Application Discontinuation
- 1991-11-07 ES ES91920573T patent/ES2113892T3/es not_active Expired - Lifetime
- 1991-11-07 DK DK91920573T patent/DK0624097T3/da active
- 1991-11-07 AT AT91920573T patent/ATE164082T1/de active
- 1991-11-07 WO PCT/US1991/008253 patent/WO1992008494A2/en active IP Right Grant
- 1991-11-07 HU HU9301328A patent/HUT67298A/hu unknown
- 1991-11-07 EP EP91920573A patent/EP0624097B1/en not_active Expired - Lifetime
- 1991-11-07 DE DE69129127T patent/DE69129127T2/de not_active Expired - Lifetime
- 1991-11-07 JP JP50016592A patent/JP3292301B2/ja not_active Expired - Lifetime
- 1991-11-08 NZ NZ240521A patent/NZ240521A/en unknown
- 1991-11-08 PT PT99460A patent/PT99460B/pt not_active IP Right Cessation
- 1991-11-08 MX MX9101999A patent/MX9101999A/es unknown
- 1991-11-08 IE IE390791A patent/IE913907A1/en unknown
-
1992
- 1992-01-07 TW TW081100086A patent/TW201271B/zh active
-
1993
- 1993-05-05 NO NO93931631A patent/NO931631L/no unknown
- 1993-05-07 FI FI932083A patent/FI932083A/fi not_active Application Discontinuation
-
1994
- 1994-08-08 US US08/287,381 patent/US5523402A/en not_active Expired - Lifetime
-
1995
- 1995-01-19 US US08/375,276 patent/US5707603A/en not_active Expired - Lifetime
- 1995-12-15 US US08/573,377 patent/US5677445A/en not_active Expired - Lifetime
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1996
- 1996-06-07 AU AU55835/96A patent/AU5583596A/en not_active Abandoned
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1998
- 1998-04-23 GR GR980400901T patent/GR3026713T3/el unknown
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NO931631L (no) | 1993-06-23 |
US5677445A (en) | 1997-10-14 |
GR3026713T3 (en) | 1998-07-31 |
WO1992008494A3 (en) | 1993-07-08 |
FI932083A0 (fi) | 1993-05-07 |
KR930701974A (ko) | 1993-09-08 |
EP0624097A1 (en) | 1994-11-17 |
DK0624097T3 (da) | 1998-10-19 |
AU9029191A (en) | 1992-06-11 |
EP0624097B1 (en) | 1998-03-18 |
AU667030B2 (en) | 1996-03-07 |
NZ240521A (en) | 1995-01-27 |
MX9101999A (es) | 1992-06-01 |
IE913907A1 (en) | 1992-05-20 |
DE69129127D1 (de) | 1998-04-23 |
JP3292301B2 (ja) | 2002-06-17 |
US5523402A (en) | 1996-06-04 |
CA2095123A1 (en) | 1992-05-09 |
AU5583596A (en) | 1996-08-01 |
ATE164082T1 (de) | 1998-04-15 |
PT99460B (pt) | 1999-02-26 |
US5707603A (en) | 1998-01-13 |
HU9301328D0 (en) | 1993-10-28 |
TW201271B (es) | 1993-03-01 |
WO1992008494A2 (en) | 1992-05-29 |
BR9107074A (pt) | 1993-09-21 |
US5367080A (en) | 1994-11-22 |
FI932083A (fi) | 1993-07-02 |
JPH06501703A (ja) | 1994-02-24 |
PT99460A (pt) | 1992-09-30 |
HUT67298A (en) | 1995-03-28 |
DE69129127T2 (de) | 1998-10-08 |
NO931631D0 (no) | 1993-05-05 |
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