IP Library Patent Application 11517676
Patent Application
App. No. 11/517,676

Boat tropanes

Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US None
App. No.
11/517,676
Abstract

Radiopharmaceutical compounds are disclosed. A tropane compound is linked through the N atom at the 8-position to a chelating ligand capable of complexing technetium or rhenium to produce a neutral labeled complex that selectively binds to the dopamine transporter over the serotonin transporter with a ratio of 10 or more. These compounds can be prepared as separate diastereoisomers as well as a mixture of diastereoisomers. Also disclosed are radiopharmaceutical kits for preparing the labeled radiopharmaceutical compounds.

Claims (29)

1 . A radiopharmaceutical compound which is capable of complexing with 99m Tc, said compound having the following structural formula:

wherein

R 1 is α or β and is selected from COOR a , COR a , and CON(CH 3 )OR a ;

R 2 is α or β and is selected from the group consisting of C 6 H 4 X, C 6 H 3 XY, C 10 H 7 X, and C 10 H 6 XY;

R a is C 1 -C 5 alkyl;

X and Y are independently selected from the group consisting of R a , H, Br, Cl, I, F, OH, and OCH 3 ;

L is —(CH 2 ) n where n is an integer from 1 to 6, or —(CH 2 ) n —(aryl, arylalkyl, ethenyl or ethynyl)-(CH 2 ) m -where m and n are integers and the sum of n plus m is an integer from 1 to 6; and

Ch is a tridentate or tetradentate chelating ligand that forms a neutral complex with technetium or rhenium.

2 . A compound according to claim 1 labeled with a radionuclide that is complexed with the chelating ligand.

3 . A compound according to claim 2 , wherein the radionuclide is 99m Tc.

4 . A compound according to claim 2 , wherein the radionuclide is rhenium.

5 . A compound according to claim 1 , wherein the tropane analog has a 3α-group.

6 . A compound according to claim 1 , wherein the tropane analog has a 3β-group.

7 . A compound according to claim 1 , wherein the chelating ligand comprises a bisamido-bisthiol group, a monoamide, monoamino-bisthiol group or a bisamino-bisthiol group covalently attached to linker L.

8 . (canceled)

9 . A compound according to claim 1 , wherein the chelating ligand is N-(2-((2-((triphenylmethyl)thio)-ethyl)amino)acetyl)-S-(triphenylmethyl)-2-aminoethanethiol.

10 .- 17 . (canceled)

18 . A method for detecting the density of tropane recognition sites in a mammal as an indication of neurodegenerative or neuropsychiatric disorders characterized by changes in the density of dopamine transporters or dopamine neurons, said method comprising providing in a suitable pharmacological carrier a radiopharmaceutical compound according to claim 1 labeled with 99m Tc, injecting the compound into the mammal and scanning the mammal using a radiodiagnostic imaging apparatus.

19 . A method for monitoring in a mammal neurodegenerative or neuropsychiatric disorders characterized by changes in the density of dopamine transporters or dopamine neurons, said method comprising providing in a suitable pharmacological carrier a radiopharmaceutical compound according to claim 1 labeled with 99m Tc, injecting the compound into the mammal and scanning the mammal using a radiodiagnostic imaging apparatus.

20 . A radiopharmaceutical kit for preparing a radiopharmaceutical preparation, said kit comprising a sealed, sterile, apyrogenic vial containing a radiopharmaceutical compound of claim 1 and a reducing agent for labeling said compound with a radionuclide.

21 . (canceled)

22 . A compound having the following structural formula:

wherein

R 1 is α or β and is selected from COOR a , COR a , and CON(CH 3 )OR a ;

R 2 is α and is selected from C 6 H 4 X, C 6 H 3 )(Y, C 10 H 7 X, and C 10 H 6 XY;

R a is a C 1 -C 5 alkyl;

X and Y are independently selected from R a , H, Br, Cl, I, F, OH, and OCH 3 ;

wherein the compound is in the 1R or 1S configuration;

and wherein N 8 is substituted with either H or CH 3 .

Assignments (1)
CONFIRMATORY LICENSE Recorded Nov 8, 2021
From: HARVARD UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 058045/0120 →