IP Library Granted Patent US 11,712,485
Granted Patent B2
US 11,712,485 · App. 17/129,825 · Granted Aug 1, 2023

Triazine based radiopharmaceuticals and radioimaging agents

Inventors: John W. Babich (New York, NY); Craig Zimmerman (Topsfield, MA); John L. Joyal (Melrose, MA); Genliang Lu (Winchester, MA)
Assignee: Molecular Insight Pharmaceuticals, Inc.
A61K51/0497A61B6/481A61B6/50C07D401/14C07D403/14C07D413/14C07F5/003
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Quick Facts
Patent No.
US 11,712,485
App. No.
17/129,825
Granted
Aug 1, 2023
Kind
B2
Abstract

Metal complexes including a radionuclide and a compound of Formula I and Formula II are potent inhibitors of PSMA.

Claims (49)

1. A metal complex comprising copper and a compound represented by Formula I

wherein:

A is (CHR 1 ) m or C(O);

W is —C(O)—(CH 2 ) p —; —C(O)[—CH 2 —CH 2 —O] n —, —[CH 2 —CH 2 —O] n —(CH 2 ) 2 —, —C(O)—[CH(R 3 ) t ] q —, —(CH 2 ) m —O—(CH 2 ) n —, —(CH 2 ) m —S—(CH 2 ) n —, —(CH 2 ) m —S(O)—(CH 2 ) n —, —(CH 2 ) m —S(O) 2 —(CH 2 ) n —, or —(CH 2 ) m —NR a —(CH 2 ) n —,

Y is —NH—, —NR 2 — or;

X is —(C 1 -C 10 )alkylene-(C 3 -C 10 )arylene, —(C 3 -C 10 )arylene, —(C 3 -C 10 )arylene-(C 1 -C 10 )alkylene-, phenylene, —(C 1 -C 10 )alkylene-(C 3 -C 10 )cycloalkylene, —(C 3 -C 10 )cycloalkylene, or —(C 3 -C 10 )cycloalkylene-(C 1 -C 10 )alkylene-;

R 1 and R 2 are each independently H, —(C 1 -C 10 )alkyl, —C(O)—(C 1 -C 10 )alkyl, benzyl, —(C 3 -C 10 )cycloalkyl, or —(C 3 -C 10 )aryl;

R a and R b are each independently H, —OH, —(C 1 -C 10 )alkyl, —[CH 2 —CH 2 —O] n —(CH 2 ) 2 -T, —C(O)—(C 1 -C 10 )alkyl, —(C 1 -C 10 )alkylene-C(O)—, —(C 1 -C 10 )alkylene-C(O)—Z, benzyl, —(C 3 -C 10 )cycloalkyl, —(C 3 -C 10 )aryl-(C 1 -C 10 )alkylene, —(C 3 -C 10 )aryl, halo-(C 1 -C 10 )alkyl, hydroxy-(C 1 -C 10 )alkyl, —NH—(C 1 -C 10 )alkyl, or —(C 1 -C 10 )alkylene-NR d R e —, or R a and R b together with the nitrogen to which they are bonded form a (C 3 -C 6 )-heteroaryl or (C 3 -C 6 )-heterocycloalkyl;

Z is-OH, —O(C 1 -C 10 )alkyl,

R c is —OH, —O(C 1 -C 10 )alkyl, —Obenzyl, —O(C 3 -C 10 )cycloalkyl, —O(C 3 -C 10 )aryl, —O—(C 1 -C 10 )alkylene-(C 3 -C 10 )aryl, or —O—(C 1 -C 10 )alkylene-(C 3 -C 10 )cycloalkyl,

R 3 is H, halogen, —OH, —NH 2 , —(CH 2 ) p —COOH, or —(CH 2 ) p —NH 2 ;

T is —H, —OH, —COOH, or —NR d R e ;

R d and R e are each independently H, bond, —OH, —(C 1 -C 10 )alkyl, or —(C 3 -C 10 )heteroaryl-(C 1 -C 10 )alkylene;

m, n, p, q, t and r are each independently 0, 1, 2, 3, 4, 5, 6, 7, 8 9, or 10; and

D is

wherein any alkyl, alkylene, aryl, arylene, heteroaryl, heteroarylene, cycloalkyl, cycloalkylene, heterocycloalkyl, or heterocycloalkylene is optionally substituted with 1, 2, or 3 substituent groups selected from the group consisting of —(C 1 -C 10 )alkyl, —(C 1 -C 10 )haloalkyl, —(C 1 -C 10 ) aminoalkyl, —(C 1 -C 10 )alkylene-COOH, —(C 1 -C 10 )hydroxyalkyl, —OH, halogen, —NH 2 , —COOH, —C(O)—(C 1 -C 10 )alkyl, —(C 1 -C 10 )alkylene-C(O)—, —(C 1 -C 10 )alkylene-C(O)—X, —NH—(C 1 -C 10 )alkyl, and —(C 1 -C 10 )alkylene-NR d R e —, and —NR d R e .

2. The metal complex of claim 1 , wherein X is phenylene, r is 1 and D is

3. The metal complex of claim 2 , wherein the compound is represented by Formula (II)

wherein:

A is (CHR 1 ) m or C(O);

W is selected from the group consisting of —C(O)—(CH 2 ) p —; —C(O)[—CH 2 —CH 2 —O] n —, —[CH 2 —CH 2 —O] n —(CH 2 ) 2 —, —C(O)—[CH(R 3 ) t ] q —, —(CH 2 ) m —O—(CH 2 ) n —, —(CH 2 ) m —S—(CH 2 ) n —, —(CH 2 ) m —S(O)—(CH 2 ) n —, —(CH 2 ) m —S(O) 2 —(CH 2 ) n —, and —(CH 2 ) m —NR a —(CH 2 ) n —,

Y is selected from —NH—, —NR 2 — or

R 1 and R 2 are each independently selected from H, —(C 1 -C 10 )alkyl, —C(O)—(C 1 -C 10 )alkyl, benzyl, —(C 3 -C 10 )cycloalkyl, or —(C 3 -C 10 )aryl;

R a and R b are each independently selected from the group consisting of H, —OH, —(C 1 -C 10 )alkyl, —[CH 2 —CH 2 —O] n —(CH 2 ) 2 -T, —C(O)—(C 1 -C 10 )alkyl, —(C 1 -C 10 )alkylene-C(O)—, —(C 1 -C 10 )alkylene-C(O)—Z, benzyl, —(C 3 -C 10 )cycloalkyl, —(C 3 -C 10 )aryl-(C 1 -C 10 )alkylene, —(C 3 -C 10 )aryl, halo-(C 1 -C 10 )alkyl, hydroxy-(C 1 -C 10 )alkyl, —NH—(C 1 -C 10 )alkyl, and —(C 1 -C 10 )alkylene-NR d R e —, or R a and R b together with the nitrogen to which they are bonded form a (C 3 -C 6 )-heteroaryl or (C 3 -C 6 )-heterocycloalkyl;

Z is selected from —OH, —O(C 1 -C 10 )alkyl,

R c is selected from —OH, —O(C 1 -C 10 )alkyl, —Obenzyl, —O(C 3 -C 10 )cycloalkyl, —O(C 3 -C 10 )aryl, —O—(C 1 -C 10 )alkylene-(C 3 -C 10 )aryl, or —O—(C 1 -C 10 )alkylene-(C 3 -C 10 )cycloalkyl,

R 3 is selected from H, halogen, —OH, —NH 2 , —(CH 2 ) p —COOH, or —(CH 2 ) p —NH 2 ;

T is selected from —H, —OH, —COOH, or —NR d R e ;

R d and R e are each independently selected from H, bond, —OH, —(C 1 -C 10 )alkyl, or —(C 3 -C 10 )heteroaryl-(C 1 -C 10 )alkylene;

m, n, p, q, t and x are each independently 0, 1, 2, 3, 4, 5, 6, 7, 8 9, or 10;

wherein any alkyl, alkylene, aryl, arylene, heteroaryl, heteroarylene, cycloalkyl, cycloalkylene, heterocycloalkyl, or heterocycloalkylene is optionally substituted with 1, 2, or 3 substituent groups selected from the group consisting of —(C 1 -C 10 )alkyl, —(C 1 -C 10 )haloalkyl, —(C 1 -C 10 ) aminoalkyl, —(C 1 -C 10 )alkylene-COOH, —(C 1 -C 10 )hydroxyalkyl, —NH 2 , —COOH, —C(O)—(C 1 -C 10 )alkyl, —(C 1 -C 10 )alkylene-C(O)—, —(C 1 -C 10 )alkylene-C(O)—X, —NH—(C 1 -C 10 )alkyl, and —(C 1 -C 10 )alkylene-NR d R e —, and —NR d R e .

4. The metal complex of claim 3 , wherein A is (CHR 1 ) m and W is —C(O)—(CH 2 ) p —.

5. The metal complex of claim 4 , wherein W is —C(O)—(CH 2 ) 7 — or —C(O)—(CH 2 ) 10 —.

6. The metal complex of claim 4 , wherein R 1 is hydrogen and m is 2.

7. The metal complex of claim 3 , wherein Y is —NH— or

8. The metal complex of claim 7 , wherein Y is

9. The metal complex of claim 3 , wherein R a and R b are each independently hydrogen or methyl and R c is —OH.

10. The metal complex of claim 3 , wherein R a and R b together with the nitrogen to which they are bonded form a (C 3 -C 6 )-heterocycloalkyl.

11. The metal complex of claim 10 , wherein the (C 3 -C 6 )-heterocycloalkyl is selected from piperidine, piperazine, morpholine, thiomorpholine, isothiazolidine, isoxazolidine, pyrrolidine, immidazolidine, thiazolidine or oxazolidine.

12. The metal complex of claim 11 , wherein the (C 3 -C 6 )-heterocycloalkyl is piperidine or 4-(piperidin-4-yl)butanoic acid.

13. The metal complex of claim 3 , wherein R a is —H and R b is

14. The metal complex of claim 3 , wherein R d and R e are each independently —(C 3 -C 10 )heteroaryl-(C 1 -C 10 )alkylene.

15. The metal complex of claim 3 , wherein R d and R e are each independently

16. The metal complex of claim 1 , wherein the copper is 64 Cu or 67 Cu.

17. A pharmaceutical composition comprising the metal complex of claim 1 , or a pharmaceutically acceptable salt, solvate, or ester thereof, and a pharmaceutically acceptable carrier.

18. The metal complex of claim 1 , which is:

or a pharmaceutically acceptable salt or solvate thereof.

19. The metal complex of claim 18 , wherein the Cu is 64 Cu or 67 Cu.

20. A pharmaceutical composition comprising the metal complex of claim 18 , or a pharmaceutically acceptable salt, solvate, or ester thereof, and a pharmaceutically acceptable carrier.

Assignments (2)
SECURITY INTEREST Recorded Dec 17, 2025
From: LANTHEUS MEDICAL IMAGING, INC.; PROGENICS PHARMACEUTICALS, INC.; MOLECULAR INSIGHT PHARMACEUTICALS, INC.
To: CITIZENS BANK, N.A., AS COLLATERAL AGENT, NATIONAL BANKING ASSOCIATION
Reel/Frame 073250/0201 →
SECURITY INTEREST Recorded Dec 2, 2022
From: LANTHEUS MEDICAL IMAGING, INC.; MOLECULAR INSIGHT PHARMACEUTICALS, INC.; PSMA DEVELOPMENT COMPANY, LLC; PROGENICS PHARMACEUTICALS, INC.
To: CITIZENS BANK, N.A.
Reel/Frame 062047/0960 →
Continuity (6)
Continuation 16231153 · Dec 21, 2018
Continuation 15233096 · Aug 10, 2016
Division 14152864 · Jan 10, 2014
Provisional Application 61785788 · Mar 14, 2013
Provisional Application 61752350 · Jan 14, 2013
Related Publication 20210338850A1 · Nov 4, 2021