Technetium- and rhenium-bis(heteroaryl) complexes, and methods of use thereof
View Patent ↗One aspect of the invention relates to complexes of a radionuclide with various heteroaryl ligands, e.g., imidazolyl and pyridyl ligands, and their use in radiopharmaceuticals for a variety of clinical diagnostic and therapeutic applications. Another aspect of the invention relates to imidazolyl and pyridyl ligands that form a portion of the aforementioned complexes. Methods for the preparation of the radionuclide complexes are also described. Another aspect of the invention relates to imidazolyl and pyridyl ligands based on derivatized lysine, alanine and bis-amino acids for conjugation to small peptides by solid phase synthetic methods. Additionally, the invention relates to methods for imaging regions of a mammal using the complexes of the invention.
1. A compound represented by A:
wherein, independently for each occurrence,
R 1 is H, alkyl, hydroxyalkyl, alkoxyalkyl, aminoalkyl, thioalkyl, alkenyl, alkynyl, aryl, heteroaryl, aralkyl, heteroaralkyl, acyl, aminoacyl, hydroxyacyl, thioacyl, (amino)alkoxycarbonyl, (hydroxy)alkoxycarbonyl, (amino)alkylaminocarbonyl, (hydroxy)alkylaminocarbonyl, —CO 2 H, —(CH 2 ) d —R 80 , or an amino acid radical;
R 80 is carboxaldehyde, carboxylate, carboxamido, alkoxycarbonyl, aryloxycarbonyl, ammonium, aryl, heteroaryl, cycloalkyl, cycloalkenyl, heterocyclyl, polycyclyl, amino acid, peptide, saccharide, ribonucleic acid, or a (deoxy)ribonucleic acid;
d is an integer in the range 0 to 12 inclusive;
m is an integer in the range 0 to 6 inclusive;
n is an integer in the range 0 to 6 inclusive;
L is
X is —N(R 2 )—, —O—, or —S—;
R is selected from the group consisting of hydrogen, halogen, alkyl, alkenyl, alkynyl, hydroxyl, alkoxyl, acyl, acyloxy, acylamino, silyloxy, amino, nitro, sulfhydryl, alkylthio, imino, amido, phosphoryl, phosphonate, phosphine, carbonyl, carboxyl, carboxamide, anhydride, silyl, thioalkyl, alkylsulfonyl, arylsulfonyl, selenoalkyl, ketone, aldehyde, ester, heteroalkyl, cyano, guanidine, amidine, acetal, ketal, amine oxide, aryl, heteroaryl, aralkyl, heteroaralkyl, azido, aziridine, carbamoyl, epoxide, hydroxamic acid, imide, oxime, sulfonamide, thioamide, thiocarbamate, urea, thiourea, and —(CH 2 ) d —R 80 ;
R 2 is hydrogen or a lipophilic group; and
wherein the compound is complexed with a radionuclide.
2. The compound of claim 1 , wherein said radionuclide is technetium or rhenium.
3. A compound represented by B:
wherein, independently for each occurrence,
R 1 is H, alkyl, hydroxyalkyl, alkoxyalkyl, aminoalkyl, thioalkyl, alkenyl, alkynyl, aryl, heteroaryl, aralkyl, heteroaralkyl, acyl, aminoacyl, hydroxyacyl, thioacyl, (amino)alkoxycarbonyl, (hydroxy)alkoxycarbonyl, (amino)alkylaminocarbonyl, (hydroxy)alkylaminocarbonyl, —CO 2 H, —(CH 2 ) d —R 80 , or an amino acid radical;
R 80 is carboxaldehyde, carboxylate, carboxamido, alkoxycarbonyl, aryloxycarbonyl, ammonium, aryl, heteroaryl, cycloalkyl, cycloalkenyl, heterocyclyl, polycyclyl, amino acid, peptide, saccharide, ribonucleic acid, or a (deoxy)ribonucleic acid;
d is an integer in the range 0 to 12 inclusive;
m is an integer in the range 0 to 6 inclusive;
n is an integer in the range 0 to 6 inclusive;
R is selected from the group consisting of hydrogen, halogen, alkyl, alkenyl, alkynyl, hydroxyl, alkoxyl, acyl, acyloxy, acylamino, silyloxy, amino, nitro, sulfhydryl, alkylthio, imino, amido, phosphoryl, phosphonate, phosphine, carbonyl, carboxyl, carboxamide, anhydride, silyl, thioalkyl, alkylsulfonyl, arylsulfonyl, selenoalkyl, ketone, aldehyde, ester, heteroalkyl, cyano, guanidine, amidine, acetal, ketal, amine oxide, aryl, heteroaryl, aralkyl, heteroaralkyl, azido, aziridine, carbamoyl, epoxide, hydroxamic acid, imide, oxime, sulfonamide, thioamide, thiocarbamate, urea, thiourea, and —(CH 2 ) d —R 80 ; and
R 2 is hydrogen or a lipophilic group.
4. The compound of claim 3 , wherein said compound is complexed with a radionuclide.
5. The compound of claim 3 , wherein said compound is complexed with a radionuclide, wherein said radionuclide is technetium or rhenium.
6. The compound of claim 3 , wherein m is 1.
7. The compound of claim 3 , wherein n is 1.
8. The compound of claim 3 , wherein m is 1; and n is 1.
9. The compound of claim 3 , wherein R is hydrogen.
10. The compound of claim 3 , wherein R 2 is a lipophilic group.
11. The compound of claim 3 , wherein R 2 is an ether, aralkyl or alkylaryl.
12. The compound of claim 3 , wherein R is hydrogen; and R 2 is an ether, aralkyl or alkylaryl.
13. The compound of claim 3 , wherein m is 1; n is 1; R is hydrogen; and R 2 is an ether, aralkyl or alkylaryl.
14. The compound of claim 3 , wherein R 1 is —(CH 2 ) d —R 80 .
15. The compound of claim 3 , wherein m is 1; n is 1; R is hydrogen; R 2 is an ether, aralkyl or alkylaryl; and R 1 is —(CH 2 ) d —R 80 .
16. The compound of claim 3 , wherein m is 1; n is 1; R is hydrogen; R 2 is an ether, aralkyl or alkylaryl; and R 1 is —(CH 2 ) d —R 80 ; wherein said compound is complexed with a radionuclide.
17. The compound of claim 3 , wherein m is 1; n is 1; R is hydrogen; R 2 is an ether, aralkyl or alkylaryl; and R 1 is —(CH 2 ) d —R 80 ; wherein said compound is complexed with a radionuclide, wherein said radionuclide is technetium or rhenium.
18. The compound of claim 3 , wherein R 1 is an amino acid radical.
19. The compound of claim 3 , wherein R 1 is an amino acid radical; m is 1; and n is 1.
20. The compound of claim 3 , wherein R 1 is an amino acid radical; m is 1; n is 1; and R 2 is an ether, aralkyl or alkylaryl.
21. The compound of claim 3 , wherein R 1 is an amino acid radical; m is 1; n is 1; R is hydrogen; and R 2 is an ether, aralkyl or alkylaryl; wherein said compound is complexed with a radionuclide.
22. The compound of claim 3 , wherein R 1 is an amino acid radical; m is 1; n is 1; R is hydrogen; and R 2 is an ether, aralkyl or alkylaryl; wherein said compound is complexed with a radionuclide, wherein said radionuclide is technetium or rhenium.
23. The compound of claim 3 , wherein the amino acid radical is —CH 2 CH 2 CH 2 CH 2 CH(NH 2 )CO 2 H.
24. The compound of claim 3 , wherein the amino acid radical is —CH(CO 2 H)CH 2 CH 2 CH 2 CH 2 NH 2 .
25. The compound of claim 3 , wherein the amino acid radical is —CH 2 CH 2 CO 2 H.
26. The compound of claim 3 , wherein the amino acid radical is —CH(CO 2 H)(CH 2 ) x CH(NH 2 )CO 2 H, wherein x is an integer from 3 to 9 inclusively.
27. A formulation, comprising a compound according to any one of claims 1 and 3 ; and a pharmaceutically acceptable excipient.
28. A method of imaging a region in a patient, comprising the steps of: administering to a patient a diagnostically effective amount of a compound as in any one of claim 2 , 4 , 5 , 16 , 17 , 21 or 22 ; and obtaining an image of said region of said patient.
29. The method of claim 28 , wherein said region of said patient is the head or thorax.
30. A method of preparing a peptide conjugate incorporating a compound according to claims 1 or 3 comprising the step of synthesizing a peptide conjugate using solid-phase peptide-synthesis techniques.