IP Library › Granted Patent US 9,226,981
Granted Patent B2
US 9,226,981 · App. 14/211,683 · Granted Jan 5, 2016

PSMA-binding agents and uses thereof

Inventors: Martin G. Pomper (Baltimore, MD); Ronnie Charles Mease (Fairfax, VA); Ying Chen (Timmonium, MD)
Assignee: THE JOHNS HOPKINS UNIVERSITY
A61K51/0402A61K9/127A61K51/0455C07C275/16C07C275/18C07D213/61C07D213/74C07D213/82C07F7/2212C07B2200/05
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Quick Facts
Patent No.
US 9,226,981
App. No.
14/211,683
Granted
Jan 5, 2016
Kind
B2
Abstract

Prostate-specific membrane antigen (PSMA) binding compounds having radioisotope substituents are described, as well as chemical precursors thereof. Compounds include pyridine containing compounds, compounds having phenylhydrazine structures, and acylated lysine compounds. The compounds allow ready incorporation of radionuclides for single photon emission computed tomography (SPECT) and positron emission tomography (PET) for imaging, for example, prostate cancer cells and angiogenesis.

Claims (41)

1. A compound having the structure

wherein

Z is tetrazole or CO 2 Q;

each Q is independently selected from hydrogen or a protecting group;

and wherein

(A) m is 0, 1, 2, 3, 4, 5, or 6;

Y is O, S, N(R′), C(O), NR′C(O), C(O)N(R′), OC(O), C(O)O, NR′C(O)NR′, NR′C(S)NR′, NR′S(O) 2 , S(CH 2 ) p , NR′(CH 2 ) p , O(CH 2 ) p , OC(O)CHR 8 NHC(O), NHC(O)CHR 8 NHC(O), or a covalent bond; wherein p is 1, 2, or 3, R′ is H or C 1 -C 6 alkyl, and R 8 is hydrogen alkyl, aryl or heteroaryl, each of which may be substituted;

R is

wherein

X′ is selected from the group consisting of NHNH 2 , —NHN═CHR 3 , and —NHNH—CH 2 R 3 ; wherein R 3 is alkyl, alkenyl, alkynyl, aryl, or heteroaryl each of which is substituted by fluorine, iodine, a radioisotope of fluorine, a radioisotope of iodine, bromine, a radioisotope of bromine, or a radioisotope of astatine; NO 2 , NH 2 , N + (R 2 ) 3 , Sn(R 2 ) 3 , Si(R 2 ) 3 , Hg(R 2 ), or B(OH) 2 ;

R 2 is C 1 -C 6 alkyl;

n is 1, 2, 3, 4, or 5; or

(B) m is 4,

Y is NR′, and

R is

wherein G is O, NR′ or a covalent bond;

R 7 is selected from the group consisting of NH 2 , N═CHR 3 , NH—CH 2 R 3 , wherein R 3 is alkyl, alkenyl, alkynyl, aryl, or heteroaryl each of which is substituted by fluorine, iodine, a radioisotope of fluorine, a radioisotope of iodine, chlorine, bromine, a radioisotope of bromine, or a radioisotope of astatine, NO 2 , NH 2 , N + (R 2 ) 3 , Sn(R 2 ) 3 , Si(R 2 ) 3 , Hg(R 2 ), B(OH) 2 ; and R 2 is C 1 -C 6 alkyl, and R is H or C 1 -C 6 alkyl; p is 1, 2, 3, or 4.

2. A compound according to claim 1 , wherein Z is CO 2 Q.

3. A compound according to claim 1 , wherein Q is hydrogen.

4. A compound according to claim 1 , where m is 1, 2, 3, or 4.

5. A compound according to claim 1 , wherein

m is 0, 1, 2, 3, 4, 5, or 6;

Y is O, S, N(R′), C(O), NR′C(O), C(O)N(R′), OC(O), C(O)O, NR′C(O)NR′, NR′C(S)NR′, NR′S(O) 2 , S(CH 2 ) p , NR′(CH 2 ) p , O(CH 2 ) p , OC(O)CHR 8 NHC(O), NHC(O)CHR 8 NHC(O), or a covalent bond; wherein p is 1, 2, or 3, R is H or C 1 -C 6 alkyl, and R 8 is hydrogen, alkyl, aryl or heteroaryl, each of which may be substituted;

R is

wherein

X′ is selected from the group consisting of NHNH 2 , —NHN═CHR 3 , —NHNH—CH 2 R 3 ; wherein R 3 is alkyl, alkenyl, alkynyl, aryl, or heteroaryl, each of which is substituted by fluorine, iodine, a radioisotope of fluorine, a radioisotope of iodine, bromine, a radioisotope of bromine, or a radioisotope of astatine; NO 2 , NH 2 , N + (R 2 ) 3 , Sn(R 2 ) 3 , Si(R 2 ) 3 , Hg(R 2 ), and B(OH) 2 , where R 2 is C 1 -C 6 alkyl;

n is 1, 2, 3, 4, or 5.

6. A compound according to claim 1 , wherein n is 1.

7. A compound according to claim 1 , wherein m is 4, Y is NR′, and R is

wherein G is O, NR′ or a covalent bond,

p is 1, 2, 3, or 4, and

R 7 is selected from the group consisting of NH 2 , N═CHR 3 , NH—CH 2 R 3 , wherein R 3 is alkyl, alkenyl, alkynyl, aryl, heteroaryl each of which is substituted by fluorine, iodine, a radioisotope of fluorine, a radioisotope of iodine, chlorine bromine, a radioisotope of bromine, or a radioisotope of astatine NO 2 , NH 2 , N + (R 2 ) 3 , Sn(R 2 ) 3 , Si(R 2 ) 3 , Hg(R 2 ), and B(OH) 2 , wherein R 2 is C 1 -C 6 alkyl.

8. A compound according to claim 7 , wherein G is O or NR′.

9. A compound according to claim 1 , wherein R comprises a radioisotope.

10. A compound according to claim 9 , wherein the radioisotope is selected from the group consisting of 18 F, 123 I, 124 I, 125 I, 126 I, 131 I, 75 Br, 76 Br, 77 Br, 80 Br, 80 BR, 80m Br, 82 Br, 83 Br and 211 At.

11. A method of imaging one or more cells, organs or tissues comprising exposing the cell to or administering to an organism an effective amount of a compound according to claim 9 .

12. The method according to claim 11 , wherein the one or more organs or tissues includes prostate tissue, kidney tissue, brain tissue vascular tissue or tumor tissue.

13. A compound according to claim 1 , having the structure

14. A compound according to claim 1 , having the structure

15. A method of treating a tumor comprising administering a therapeutically effective amount of a compound according to claim 1 comprising a therapeutically effective radioisotope.

16. A kit comprising a compound according to claim 1 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 25, 2014
From: POMPER, MARTIN G.; MEASE, RONNIE CHARLES; CHEN, YING
To: JOHNS HOPKINS UNIVERSITY
Reel/Frame 033172/0658 →
Continuity (4)
Division 13057044
Provisional Application 61085462 · Aug 1, 2008
Provisional Application 61111791 · Nov 6, 2008
Related Publication 20140369931A1 · Dec 18, 2014