IP Library Granted Patent US 9,776,977
Granted Patent B2
US 9,776,977 · App. 14/243,535 · Granted Oct 3, 2017

PSMA-targeting compounds and uses thereof

Inventors: Martin G. Pomper (Baltimore, MD); Ronnie C. Mease (Fairfax, VA); Sangeeta Ray (Ellicott City, MD)
Assignee: THE JOHNS HOPKINS UNIVERSITY
C07D257/02A61K49/0052A61K51/044A61K51/0421A61K51/0446A61K51/0453A61K51/0472C07D209/12C07D209/14C07D213/04C07D249/04C07D255/02C07D311/14C07D311/20C07D311/82C07F5/027C07F13/005G01N33/5091
View Patent ↗
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 9,776,977
App. No.
14/243,535
Granted
Oct 3, 2017
Kind
B2
Abstract

Prostate-specific membrane antigen (PSMA) targeting compounds are described. Uses of the compounds for imaging, therapy, cell sorting, and tumor mapping are also described.

Claims (19)

1. A compound having the following chemical structure:

wherein Z is tetrazole or CO 2 Q; wherein each Q is independently selected from hydrogen or a protecting group, wherein the protecting group is selected from the group consisting of benzyl, p-methoxybenzyl, tertiary butyl, methoxymethyl, methoxyethoxymethyl, methylthiomethyl, tetrahydropyranyl, tetrahydrofuranyl, benzyloxymethyl, trimethylsilyl, triethylsilyl, t-butyldimethylsilyl, and triphenylmethyl;

a is 1, 2, 3, or 4;

R is each independently H or C 1 -C 4 alkyl;

Y is —C(O)—;

V is —C(O)— or —NRC(S)—;

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

n is 1, 2, 3, 4, 5 or 6;

p is 0, 1, 2, or 3, and when p is 2 or 3, each R 1 may be the same or different;

R 1 is H, C 1 -C 6 alkyl, C 2 -C 12 aryl, or C 4 -C 16 alkylaryl

R 2 and R 3 are independently H, CO 2 H, or CO 2 R 4 , where R 4 is a C 1 -C 6 alkyl, C 2 -C 12 aryl, or C 4 -C 16 alkylaryl, wherein when one of R 2 and R 3 is CO 2 H or CO 2 R 4 , the other is H, and when p is 0, one of R 2 and R 3 is CO 2 R 4 , and the other is H; and

Ch is a chelating moiety, optionally including a chelated metal, wherein the chelating moiety is selected from the group consisting of:

 and wherein + is the bond connecting the chelating moiety to the rest of the molecule.

2. A compound according to claim 1 , having a chelated metal, wherein the chelated metal is Tc, In, Ga, Y, Lu, Re, Cu, Ac, Bi, Pb, Sm, Sc, Co, Ho, Gd, Eu, Tb, or Dy.

3. A compound according to claim 1 selected from the group consisting of

4. A method of imaging one or more cells, organs or tissues by exposing the cell to or administering to an organism an effective amount of a compound according to claim 1 , where the compound includes a metal isotope suitable for imaging, and imaging the one or more cells, organs, or tissues.

5. A method of treating a tumor comprising administering a therapeutically effective amount of a compound according to claim 1 , where the compound includes a therapeutically effective radioisotope.

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

7. The compound of claim 1 , comprising a chelated metal selected from the group consisting of Tc-94m, Tc-99m, In-111, Ga-67, Ga-68, Y-86, Y-90, Lu-177, Re-186, Re-188, Cu-64, Cu-67, Co-55, Co-57, Sc-47, Ac-225, Bi-213, Bi-212, Pb-212, Sm-153, Ho-166, and Dy-166.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 30, 2014
From: POMPER, MARTIN G.; MEASE, RONNIE C.; CHEN, YING; RAY, SANGEETA
To: THE JOHNS HOPKINS UNIVERSITY
Reel/Frame 034603/0140 →
Continuity (6)
Division 13257499
Provisional Application 61161485 · Mar 19, 2009
Provisional Application 61161484 · Mar 19, 2009
Provisional Application 61248067 · Oct 2, 2009
Provisional Application 61248934 · Oct 6, 2009
Related Publication 20150104387A1 · Apr 16, 2015