Compositions, methods, and systems for the synthesis and use of imaging agents
View Patent ↗The present invention provides compounds with imaging moieties for imaging a subject. The present invention also relates to systems, compositions, and methods for the synthesis and use of imaging agents, or precursors thereof. An imaging agent precursor may be converted to an imaging agent using the methods described herein. In some cases, a composition or plurality of imaging agents is enriched in 18 F. In some cases, an imaging agent may be used to image an area of interest in a subject, including, but not limited to, the heart, cardiovascular system, cardiac vessels, brain, and other organs.
1. A compound comprising the structure:
or a pharmaceutically acceptable salt thereof, wherein:
R 1 is selected from the group consisting of hydrogen, alkyl optionally substituted, heteroalkyl optionally substituted, alkoxy optionally substituted, alkoxyalkyl optionally substituted, aryl optionally substituted, heteroaryl optionally substituted, and an imaging moiety;
R 2 is selected from the group consisting of hydrogen, alkyl optionally substituted, heteroalkyl optionally substituted, alkoxy optionally substituted, alkoxyalkyl optionally substituted, aryl optionally substituted, heteroaryl optionally substituted, halo, haloalkyl, —NO 2 , and an imaging moiety;
R 3 is selected from the group consisting of hydrogen, alkyl optionally substituted, heteroalkyl optionally substituted, alkoxy optionally substituted, alkoxyalkyl optionally substituted, aryl optionally substituted, heteroaryl optionally substituted, —CN, —NO 2 , and an imaging moiety;
J is selected from the group consisting of N(R 7 ), S, O, C(═O), C(═O)O, OC(═O), C(═O)N(R 7 ), N(R 7 )C(═O), CH 2 O, and a bond;
R 4 and R 5 are each independently selected from the group consisting of hydrogen, alkyl optionally substituted, and an imaging moiety, or optionally any two of R 4 and R 5 are joined together to form a ring;
n is 0, 1, 2, or 3;
W is heteroaryl, naphthyl, heterocyclyl, or aryl;
each R 6 is independently selected from the group consisting of hydrogen, alkyl optionally substituted, alkenyl optionally substituted, alkynyl optionally substituted, heteroalkyl optionally substituted, alkoxy optionally substituted, aryloxy optionally substituted, heteroaryloxy optionally substituted, alkoxyalkyl optionally substituted, aryl optionally substituted, heteroaryl optionally substituted, halo, haloalkyl, —N(R 7 ) 2 , —NO 2 , —OH, —C(═O)R 8 , —C(═O)OR 8 , —OC(═O)R 8 , —C(═O)N(R 7 ) 2 , —N(R 7 )C(═O)R 8 , —CN, —Si(R 9 ) 3 , —B(R 9′ ) 3 , —OR 8 , and an imaging moiety;
m is 0, 1, 2, 3, 4, 5, 6, or 7;
each R 7 is independently selected from the group consisting of hydrogen, alkyl optionally substituted, alkenyl optionally substituted, alkynyl optionally substituted, heteroalkyl optionally substituted, alkoxy optionally substituted, alkoxyalkyl optionally substituted, aryl optionally substituted, heteroaryl optionally substituted, halo, haloalkyl, and an imaging moiety, or optionally, any two R 7 may be joined together to form a ring;
each R 8 is independently selected from the group consisting of hydrogen, alkyl optionally substituted, heteroalkyl optionally substituted, alkoxyalkyl optionally substituted, aryl optionally substituted, heteroaryl optionally substituted, haloalkyl, and an imaging moiety;
each R 9 is independently selected from the group consisting of hydrogen, alkyl optionally substituted, aryl optionally substituted, haloalkyl, halogen, and an imaging moiety; and
each R 9 ′ is independently selected from the group consisting of halo, alkyl optionally substituted , aryl optionally substituted, and an imaging moiety,
provided that at least one imaging moiety is present in the compound; and
provided that when W is aryl, a) R 3 is not alkyl, or b) at least one R 6 is selected from the group consisting of alkynyl optionally substituted, alkenyl optionally substituted, alkyl substituted with —CN, alkyl substituted with —C(═O)OR 8 , alkyl substituted with —C(═O)R 8 , alkyl substituted with —N(R 7 ) 2 , —CN, —NO 2 , —N(R 7 ) 2 , —C(═O)OR 8 , —OC(═O)R 8 , —C(═O)R 8 , —C(═O)N(R 7 ) 2 , and —N(R 7 )C(═O)R 8 .
2. A compound, wherein the compound is selected from the group consisting of:
or a pharmaceutically acceptable salt thereof, wherein I m is an imaging moiety.
3. A pharmaceutical composition comprising a compound or a salt thereof of claim 1 , and optionally a pharmaceutically acceptable excipient.
4. A sterile aqueous solution comprising a compound or a salt thereof of claim 1 .
5. A method of imaging a portion of a subject, comprising:
administering to the subject a compound or a salt thereof of claim 1 , and
acquiring at least one image of a portion of the subject.
6. A method of imaging a portion of a subject, comprising:
administering to a radiolabeled subject a compound or a salt thereof of claim 1 ,
detecting radiation emitted by the compound; and
forming an image therefrom.
7. A diagnostic kit comprising one or more vials containing a precursor to a compound or a salt thereof of claim 1 ; and optionally other components.
8. A method of imaging myocardial perfusion, comprising:
administering to a patient a compound or a salt thereof of claim 1 , and
scanning the patient using diagnostic imaging.
9. A method of detecting myocardial perfusion, comprising:
administering to a patient a compound or a salt thereof of claim 1 , and
scanning the patient using diagnostic imaging.
10. A method of monitoring myocardial perfusion, comprising:
administering to a patient a compound or a salt thereof of claim 1 , and
scanning the patient using diagnostic imaging.