Zum Hauptinhalt springen

Radiolabeled amine compounds and their use

de Jong, Rudolf B. J. ; Nielsen, Jan
1983
Online Patent

Titel:
Radiolabeled amine compounds and their use
Autor/in / Beteiligte Person: de Jong, Rudolf B. J. ; Nielsen, Jan
Link:
Veröffentlichung: 1983
Medientyp: Patent
Sonstiges:
  • Nachgewiesen in: USPTO Patent Grants
  • Sprachen: English
  • Patent Number: 4,406,875
  • Publication Date: September 27, 1983
  • Appl. No: 06/194,797
  • Application Filed: October 07, 1980
  • Assignees: Byk-Mallinckrodt CIL B.V. (Petten, NLX)
  • Claim: What is claimed is
  • Claim: 1. A radiolabeled amine compound of the general formula: [equation included]
  • Claim: wherein X is selected from the group consisting of oxygen; sulfur; lower alkylene; radioactive selenium; and radioactive tellurium; and when X is a radioactive selenium or tellurium atom, Y is a hydrocarbyl amino group, and when X is an oxygen atom, a sulfur atom or a lower alkylene group, Y is a radioactive iodine-substituted hydrocarbyl amino group; or a pharmaceutically acceptable acid salt of said amine compound.
  • Claim: 2. A radiolabeled amine compound in accordance with claim 1 wherein X is lower alkylene containing 1 to about 6 carbon atoms.
  • Claim: 3. A radiolabeled amine compound in accordance with claim 2 wherein the lower alkylene group is selected from the group consisting of methylene, ethylene and trimethylene.
  • Claim: 4. A radiolabeled amine compound in accordance with claim 1 wherein the hydrocarbyl amino group comprises an aromatic-substituted, aliphatic group.
  • Claim: 5. A radiolabeled amine compound in accordance with claim 4 wherein the hydrocarbyl amino group has the general formula: ##STR4## or the general formula: ##STR5## where Ar comprises an aryl group, R, R.sub.1 and R.sub.2 are straight or branched alkyl and n is an integer from 1 to 2.
  • Claim: 6. A radiolabeled amine compound in accordance with claim 1 wherein the hydrocarbyl amino group comprises an arylsulfonamido group.
  • Claim: 7. A radiolabeled amine compound in accordance with claim 6 wherein the arylsulfonamido group has the general formula: ##STR6## where Ar comprises aryl group selected from phenyl and naphthyl.
  • Claim: 8. A radiolabeled amine compound in accordance with claim 7 wherein Ar is substituted with a dimethylamino group.
  • Claim: 9. A radiolabeled amine compound in accordance with claims 4, 5 or 6 wherein X is lower alkylene containing 1 to about 6 carbon atoms.
  • Claim: 10. A radiolabeled amine compound in accordance with claim 9 wherein the lower alkylene group is selected from the group consisting of methylene, ethylene and trimethylene.
  • Claim: 11. A radiolabeled amine compound of the general formula
  • Claim: wherein X is selected from the group consisting of oxygen, sulfur, lower alkylene, radioactive selenium and radioactive tellurium, and where, if X is radioactive selenium or tellurium, Y is an arylamino group selected from the group consisting of a benzenesulfonamido-, naphthalenesulfonamido-, dibenzylamino-, bis(phenylethyl)amino- and benzyhdrylamino group, or where, if X is oxygen, sulphur, or lower alkylene, Y is a radioactive iodine-substituted arylamino group selected from benzenesulfonamido-, naphthalenesulfonamido-, dibenzylamino-, bis(phenylethyl)amino- and benzhydrylamino-; or a pharmaceutically-acceptable, acid salt of said amine compound.
  • Claim: 12. A radiolabeled amine compound in accordance with claim 11 wherein the arylamino group is substituted by one or more substituent groups selected from the group consisting of halogen, nitro, cyano, hydroxy and carbon containing groups of up to about 6 carbon atoms.
  • Claim: 13. A radiolabeled amine compound in accordance with claim 12 wherein the substituent group is a carbon-containing group selected from the group consisting of alkyl, alkoxy, alkanoyl, aminoalkyl, monoalkylamino, dialkylamino, carboxy and alkoxycarbonyl.
  • Claim: 14. A radiolabeled amine compound in accordance with claim 11 wherein X is selected from oxygen, sulphur, lower alkylene and Y is an arylamino selected from a benzenesulfonamido-, naphthalenesulfonamido-, dibenzylamino, bis(phenylethyl)amino or benzhydrylamino- group which is substituted with radioactive iodine.
  • Claim: 15. A radiolabeled amine compound in accordance with claim 14 wherein X is lower alkylene selected from the group consisting of methylene, ethylene and trimethylene.
  • Claim: 16. A radiolabeled amine compound in accordance with claim 14 wherein Y is selected from the group consisting of a radioactive iodine-substituted benzene-sulfonamido- and a radioactive iodine substituted naphthalenesulfonamido- group.
  • Claim: 17. A radiolabeled amine compound in accordance with claim 16 wherein X is lower alkylene selected from the group consisting of methylene, ethylene and trimethylene.
  • Claim: 18. A radiolabeled amine compound in accordance with claim 16 wherein X is methylene and Y is a radioactive iodine-substituted naphthalenesulfonamido group.
  • Claim: 19. N-(5-aminopentyl)-5-iodonaphthalene-1-sulfonamide-I- 131 or a pharmaceutically-acceptable, acid salt thereof.
  • Claim: 20. N-(5-aminopentyl)-5-iodonaphthalene-1-sulfonamide-I- 123 or a pharmaceutically-acceptable, acid salt thereof.
  • Claim: 21. A radiodiagnostic composition adapted for use in tracing and/or locating thrombi in a warm-blooded animal wherein said composition comprises the radiolabeled amine compound in accordance with claims 1, 3, 5, 8, 11, 14, 16, 17, 18, 19 or 20 and a pharmaceutically-acceptable carrier material.
  • Claim: 22. A method for conducting a radiodiagnostic examination for tracing and/or locating thrombi in the body of an animal wherein said method comprises administering to the animal a radiodiagnostic composition containing the radiolabeled amine compound in accordance with 1, 3, 5, 8, 11, 14, 16, 17, 18, 19, or 20 and a pharmaceutically acceptable carrier material, the quantity of radiodiagnostic composition administered having a radioactivity of about 10 uCi to about 25 mCi.
  • Claim: 23. A method for preparing a radiolabeled amine compound useful in radiodiagnostic examinations wherein said method comprises reacting an alkali metal radioactive iodide with a compound of the general formula
  • Claim: Y--(CH.sub.2).su b.2 --X--(CH.sub.2).sub.2 --NH.sub.2
  • Claim: characterized in that X is selected from the group consisting of oxygen, sulfur, and lower alkylene, Y is a arylamino group selected from the group consisting of benzene sulfonamido-, naphthalenesulfonamido-, dibenzylamino-, bis(phenylethyl)amino- and benzhydrylamino-.
  • Claim: 24. A process in accordance with claim 23 wherein the arylamino group is substituted by a substituent group selected from the group consisting of halogen, nitro, cyano, hydroxy and carbon containing groups of up to about 6 carbon atoms.
  • Claim: 25. A process in accordance with claim 24 wherein the substituent groups include iodine.
  • Claim: 26. A process in accordance with claim 23 where the iodide is reacted with the compound in an inert organic solvent.
  • Claim: 27. A radiolabeled amine compound in accordance with claim 12 wherein X is selected from oxygen, sulphur, lower alkylene and Y is an arylamino selected from a benzenesulfonalmido-, naphthalenesulfonamido-, dibenzylamino, bis(phenylethyl)amino or benzhydrylamino- group which is substituted with radioactive iodine.
  • Claim: 28. A radiolabeled amine compound in accordance with claim 13 wherein X is selected from oxygen, sulphur, lower alkylene and Y is an arylamino selected from a benzenesulfonamido-, naphthalenesulfonamido-, dibenzylamino, bis(phenylethyl)amino or benzhydrylamino- group which is substituted with radioactive iodine.
  • Current U.S. Class: 424/1; 564/84; 564/85; 424/9
  • Current International Class: A61K 4900; A61K 4300
  • Patent References Cited: 3933996 January 1976 Charlton et al. ; 4024234 May 1977 Monks et al. ; 4036945 July 1977 Haber ; 4041145 August 1977 van der Veek ; 4069254 January 1978 Hidaka et al. ; 4083947 April 1978 Monks et al. ; 4088747 May 1978 Hunt et al. ; 4091088 May 1978 Hunt et al. ; 4171351 October 1979 van der Veek ; 4250161 February 1981 de Schrijver ; 4268495 May 1981 Muxfeldt et al. ; 4292297 September 1981 Neilsen et al. ; 8812245 May 1974 Dugan
  • Other References: Hoffman et al., J. Med. Chem., vol. 18, No. 3, Mar. 1975, pp. 278-284. ; Dassin et al., Biochem. Biophys. Res. Comm., vol. 91, 1979, pp. 332-337. ; Dassin et al., Biochem. Biophys. Res. Comm., vol. 81, 1978, pp. 329-335.
  • Primary Examiner: Nucker, Christine M.
  • Attorney, Agent or Firm: Bernard, Rothwell & Brown

Klicken Sie ein Format an und speichern Sie dann die Daten oder geben Sie eine Empfänger-Adresse ein und lassen Sie sich per Email zusenden.

oder
oder

Wählen Sie das für Sie passende Zitationsformat und kopieren Sie es dann in die Zwischenablage, lassen es sich per Mail zusenden oder speichern es als PDF-Datei.

oder
oder

Bitte prüfen Sie, ob die Zitation formal korrekt ist, bevor Sie sie in einer Arbeit verwenden. Benutzen Sie gegebenenfalls den "Exportieren"-Dialog, wenn Sie ein Literaturverwaltungsprogramm verwenden und die Zitat-Angaben selbst formatieren wollen.

xs 0 - 576
sm 576 - 768
md 768 - 992
lg 992 - 1200
xl 1200 - 1366
xxl 1366 -