CA2232391A1 - Agents de chelation amidosulfoniques sulfures bifonctionnels du type xsns pour isotopes radioactifs - Google Patents
Agents de chelation amidosulfoniques sulfures bifonctionnels du type xsns pour isotopes radioactifs Download PDFInfo
- Publication number
- CA2232391A1 CA2232391A1 CA 2232391 CA2232391A CA2232391A1 CA 2232391 A1 CA2232391 A1 CA 2232391A1 CA 2232391 CA2232391 CA 2232391 CA 2232391 A CA2232391 A CA 2232391A CA 2232391 A1 CA2232391 A1 CA 2232391A1
- Authority
- CA
- Canada
- Prior art keywords
- ile
- leu
- asp
- phe
- val
- 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.)
- Abandoned
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/575—Hormones
- C07K14/57536—Endothelin, vasoactive intestinal contractor [VIC]
-
- 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
- A61K51/0474—Organic compounds complexes or complex-forming compounds, i.e. wherein a radioactive metal (e.g. 111In3+) is complexed or chelated by, e.g. a N2S2, N3S, NS3, N4 chelating group
- A61K51/0478—Organic compounds complexes or complex-forming compounds, i.e. wherein a radioactive metal (e.g. 111In3+) is complexed or chelated by, e.g. a N2S2, N3S, NS3, N4 chelating group complexes from non-cyclic ligands, e.g. EDTA, MAG3
-
- 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
- A61K51/0497—Organic compounds conjugates with a carrier being an organic compounds
-
- 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
- A61K51/088—Peptides, e.g. proteins, carriers being peptides, polyamino acids, proteins conjugates with carriers being peptides, polyamino acids or proteins
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B59/00—Introduction of isotopes of elements into organic compounds ; Labelled organic compounds per se
- C07B59/004—Acyclic, carbocyclic or heterocyclic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur, selenium or tellurium
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/64—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and sulfur atoms, not being part of thio groups, bound to the same carbon skeleton
- C07C323/67—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and sulfur atoms, not being part of thio groups, bound to the same carbon skeleton containing sulfur atoms of sulfonamide groups, bound to the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F13/00—Compounds containing elements of Groups 7 or 17 of the Periodic System
- C07F13/005—Compounds without a metal-carbon linkage
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/05—Isotopically modified compounds, e.g. labelled
Abstract
L'invention concerne de nouveaux composés de la formule générale (I): M - L dans laquelle M est un radioisotope de Tc ou Re, L désigne un ligand de la formule générale (II): B-CO-(CR?1¿R?2¿)¿n=1,2?-S-CHR?3¿-CHR?4¿-SO¿2?-NH-CR?5¿R?6¿-(CR?7¿R?8¿)¿m=1,2?-SR?9¿ dans laquelle R?1¿, R?2¿, R?3¿, R?4¿, R?5¿, R?6¿, R?7¿, R?8¿ et R?9¿ peuvent avoir différentes notations, et B désigne un autre groupe approprié pour la liaison dative d'ions métal et le couplage avec des composés à concentration sélective. Ce couplage peut également s'effectuer en variante sur R?8¿. Ces nouveaux composés servent à la complexation du technétium et du rhénium et ont des applications diagnostiques et thérapeutiques médicales.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE1995136781 DE19536781A1 (de) | 1995-09-21 | 1995-09-21 | Bifunktionelle sulfidhaltige Sulfonamid-Chelatbildner vom Typ XSNS für radioaktive Isotope |
DE19536781.2 | 1995-09-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2232391A1 true CA2232391A1 (fr) | 1997-03-27 |
Family
ID=7773888
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA 2232391 Abandoned CA2232391A1 (fr) | 1995-09-21 | 1996-09-19 | Agents de chelation amidosulfoniques sulfures bifonctionnels du type xsns pour isotopes radioactifs |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0853488A2 (fr) |
AU (1) | AU1435997A (fr) |
CA (1) | CA2232391A1 (fr) |
DE (1) | DE19536781A1 (fr) |
WO (1) | WO1997010852A2 (fr) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19652374A1 (de) * | 1996-12-04 | 1998-06-10 | Schering Ag | Verwendung von Endothelin-Konjugaten in der Therapie, neue Endothelin-Konjugate, diese enthaltende Mittel, sowie Verfahren zu deren Herstellung |
WO1998018497A2 (fr) * | 1996-10-28 | 1998-05-07 | Nycomed Imaging As | Agents de contraste |
US6537520B1 (en) | 1998-03-31 | 2003-03-25 | Bristol-Myers Squibb Pharma Company | Pharmaceuticals for the imaging of angiogenic disorders |
US6548663B1 (en) | 1998-03-31 | 2003-04-15 | Bristol-Myers Squibb Pharma Company | Benzodiazepine vitronectin receptor antagonist pharmaceuticals |
EA200001007A1 (ru) | 1998-03-31 | 2001-04-23 | Дюпон Фармасьютикалз Компани | Фармацевтические препараты для визуализации ангиогенных расстройств |
US6524553B2 (en) | 1998-03-31 | 2003-02-25 | Bristol-Myers Squibb Pharma Company | Quinolone vitronectin receptor antagonist pharmaceuticals |
US6511649B1 (en) | 1998-12-18 | 2003-01-28 | Thomas D. Harris | Vitronectin receptor antagonist pharmaceuticals |
US6569402B1 (en) | 1998-12-18 | 2003-05-27 | Bristol-Myers Squibb Pharma Company | Vitronectin receptor antagonist pharmaceuticals |
CN1356913A (zh) | 1998-12-18 | 2002-07-03 | 杜邦药品公司 | 玻连蛋白受体拮抗剂药物 |
US6794518B1 (en) | 1998-12-18 | 2004-09-21 | Bristol-Myers Squibb Pharma Company | Vitronectin receptor antagonist pharmaceuticals |
AU2371400A (en) | 1998-12-18 | 2000-07-03 | Du Pont Pharmaceuticals Company | Vitronectin receptor antagonist pharmaceuticals |
GB0105224D0 (en) * | 2001-03-02 | 2001-04-18 | Nycomed Amersham Plc | Improved peptide-chelate conjugates |
JP2007510643A (ja) * | 2003-11-06 | 2007-04-26 | ジーイー・ヘルスケア・アクスイェ・セルスカプ | 医薬化合物 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4310999C2 (de) * | 1993-03-31 | 1996-07-18 | Diagnostikforschung Inst | Bifunktionelle chalkogenatom-unterbrochene Chelatbildner vom Typ XN¶1¶S¶1¶X' für radioaktive Isotope und deren Metallkomplexe, Verfahren zu ihrer Herstellung sowie diese enthaltende pharmazeutische Mittel |
EP0710228B1 (fr) * | 1993-07-19 | 1998-01-21 | Resolution Pharmaceuticals Inc. | Chelateurs de radionucleides de type hydrazino presentant une configuration n 3?s |
EP0724601A4 (fr) * | 1993-08-17 | 1999-02-03 | Neorx Corp | Composes chelatants de s 3n servant au radiomarquage de ligands, d'antiligands ou d'autres proteines |
-
1995
- 1995-09-21 DE DE1995136781 patent/DE19536781A1/de not_active Withdrawn
-
1996
- 1996-09-19 WO PCT/DE1996/001821 patent/WO1997010852A2/fr not_active Application Discontinuation
- 1996-09-19 AU AU14359/97A patent/AU1435997A/en not_active Abandoned
- 1996-09-19 CA CA 2232391 patent/CA2232391A1/fr not_active Abandoned
- 1996-09-19 EP EP96945139A patent/EP0853488A2/fr not_active Withdrawn
Also Published As
Publication number | Publication date |
---|---|
DE19536781A1 (de) | 1997-03-27 |
WO1997010852A2 (fr) | 1997-03-27 |
AU1435997A (en) | 1997-04-09 |
WO1997010852A3 (fr) | 1997-08-28 |
EP0853488A2 (fr) | 1998-07-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2921482B1 (fr) | Inhibiteurs marqués de l'antigène membranaire spécifique de la prostate (psma), évaluation biologique, et utilisation en tant qu'agents d'imagerie | |
CA2232391A1 (fr) | Agents de chelation amidosulfoniques sulfures bifonctionnels du type xsns pour isotopes radioactifs | |
AU691806B2 (en) | Chelating agents of the type XN1S1O1 for radioactive isotopes, metal complexes thereof, and their use in diagnosis and therapy | |
CA2232340A1 (fr) | Agents de formation de chelates de nicotinamide bifonctionnels du type n2s2 pour isotopes radioactifs | |
CA2232315A1 (fr) | Agents de chelation amidosulfoniques sulfures bifonctionnels du type s2ny pour isotopes radioactifs | |
AU6501594A (en) | Bifunctional chelators and their use in radiopharmaceuticals | |
US6488909B1 (en) | Chelating agents as well as their tricarbonyl complexes with technetium and rhenium | |
AU2015203742A1 (en) | Labeled inhibitors of prostate specific membrane antigen (psma), biological evaluation, and use as imaging agents | |
AU692154B2 (en) | Chelators of type XN1S1X' for radioactive isotopes, their metal complexes and their diagnostic and therapeutical uses | |
US6143275A (en) | Type S3 N2 chelators for radioactive isotopes, their metal complexes and their diagnostic and therapeutical use | |
CA2232620A1 (fr) | Agents chelateurs bifonctionnels au sulfonamide de type xsny contenant des sulfures pour isotopes radioactifs | |
DE4425781A1 (de) | Technetium-Sulfonamid-Komplexe, deren Verwendung, diese enthaltende pharmazeutische Mittel, sowie Verfahren zur Herstellung der Komplexe und Mittel | |
HUT74881A (en) | N-alkyl peptide chelate formers, their metal comlexes with radionuclides, processes for producing them and radio-pharmaceutical compositions containing these compounds | |
WO1996007629A1 (fr) | Chelates au technetium utilises pour evaluer la fonction renale |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FZDE | Dead |