Selective CXCR4 binding peptide conjugate and methods for making and using the same
View Patent ↗The present invention provides a selective CXCR4 binding peptide conjugate (“PC”), and a method for using and producing the same. In particular, the selective CXCR4 binding peptide conjugate of the invention comprises a peptide portion that selectively binds to CXCR4 and a medically useful compound, such as an imaging agent, a diagnostic agent, or a therapeutically or pharmaceutically active compound. In one particular embodiment, the selective CXCR4 binding peptide conjugate (“PC”) is of the formula: or a pharmaceutically acceptable salt thereof, wherein a, b, AA 1 , AA 2 , Ar 1 , X 1 , and AA 3 are those defined herein. The peptide conjugate of the invention can be used in a variety of medical applications including, but not limited to, a targeted drug delivery or imaging a patient or diagnosing a patient for a disease or a clinical condition associated with overexpression and/or upregulation of CXCR4, such as cancers, HIV infection, and immune disorders. Compositions, kits and methods are also disclosed herein for such uses.
1. A selective CXCR4 binding peptide conjugate (“PC”) of the formula:
or a pharmaceutically acceptable salt thereof,
wherein:
a is 0 or 1;
b is 1;
AA 1 along with the sulfur atom that is attached thereto is 3-mercaptopropionic acid, optionally substituted cysteine, optionally substituted homocysteine, or optionally substituted penicillamine;
AA 2 along with the sulfur atom that is attached thereto is cysteine or homocysteine;
Ar 1 is phenylene;
X 1 is Arg, Dap, Dab, Orn, Lys, Dap(iPr), Dab(iPr), Orn(iPr), or Lys(iPr);
AA 3 is Lys(iPr);
AA 4 is an amino acid or a derivative thereof;
Y 1 is a side-chain function group of amino acid AA 4 ;
L 1a is a polyethylene glycol of about 2 to about 20 monomers;
L 2 is a non-polymeric linker;
Z a medically useful compound; and
Y 2 is a functional group of said medically useful compound or a functional group of L 2 ;
and wherein one or more of AA 1 , AA 2 , X 1 , AA 3 , and AA 4 are optionally isotopically labelled.
2. The selective CXCR4 binding peptide conjugate according to claim 1 , wherein L 1a is a polyethylene glycol of about 2 to about 10 monomers.
3. The selective CXCR4 binding peptide conjugate according to claim 1 , wherein Z is an anticancer agent.
4. The selective CXCR4 binding peptide conjugate according to claim 3 , wherein said anticancer agent is selected from the group consisting of paclitaxel, Altretamine, Asparaginase, Bleomycin, Busulfan, Carboplatin, Carmustine, Chlorambucil, Cisplatin, Cladribine, Cyclophosphamide, Cytarabine, Dacarbazine, Diethylstilbestrol, Eribulin, Ethinyl, estradiol, Etoposide, Mitomycin, Mitotane, Mitoxantrone, Pentastatin, Pipobroman, Plicamycin, Prednisone, Procarbazine, Streptozocin, Tamoxifen, Teniposide, Vinblastine, and Vincristine.
5. The selective CXCR4 binding peptide conjugate according to claim 1 , wherein AA 1 along with the sulfur atom that is attached thereto is optionally substituted cysteine.
6. The selective CXCR4 binding peptide conjugate according to claim 5 , wherein α-amino group of AA 1 is substituted with an acetyl group.
7. The selective CXCR4 binding peptide conjugate according to claim 1 , wherein AA 2 along with the sulfur atom that is attached thereto is optionally substituted cysteine.
8. The selective CXCR4 binding peptide conjugate according to claim 1 , wherein X 1 is Lys(iPr) or Lys(deuterated-iPr).
9. The selective CXCR4 binding peptide conjugate according to claim 1 , wherein Ar 1 is phenyl.
10. A method for treating a subject suffering from a cancer, said method comprising administering to the subject a therapeutically effective amount of a selective CXCR4 binding peptide conjugate of claim 1 , wherein said medically useful compound is an anticancer agent.
11. The method of claim 10 , wherein said cancer is selected from the group consisting of breast cancer, lung cancer, pancreatic cancer, kidney cancer, brain cancer, blood cancer, leukemia, prostate cancer, ovarian cancer, and bladder cancer.