Substrates and inhibitors of antiplasmin cleaving enzyme and fibroblast activation protein and methods of use
The presently disclosed and claimed inventive concepts include inhibitors of antiplasmin cleaving enzyme (APCE) and fibroblast activation protein alpha (FAP) which can be used in various therapies related to disorders of fibrin and α 2 -antiplasmin and abnormal cell proliferation. The presently disclosed and claimed inventive concepts also include substrates of APCE and FAP, which may be used, for example, in screening methods for identifying such inhibitors. The presently disclosed and claimed inventive concepts further include, but are not limited to, methods of treating or inhibiting atherosclerosis and thrombus disorders by altering the ratios of types of plasma α 2 -antiplasmin and to methods of treating conditions involving abnormal cell proliferation such as cancers.
1. A compound having formula (Ib):
B-Xaa 1 -Sp-Xaa 2 (Ib)
wherein:
B is a protecting group;
Xaa 1 is a positively-charged amino-acid;
Sp is a spacer molecule having a length in a range of from 0.3 nm to 2.5 nm;
Xaa 2 is glycine, D-alanine, D-serine, or D-threonine; and
wherein the compound is able to bind to the active site of Antiplasmin Cleaving Enzyme (APCE) and to the active site of Fibroblast Activation Protein-alpha (FAP).
2. The compound of claim 1 , wherein Xaa 1 comprises α,β-diaminopropionic acid; α,Υ-diaminobutyric acid; ornithine; β-homoornithine; arginine; β-homoarginine; homoarginine; lysine; homolysine; β-homolysine; or histidine.
3. The compound of claim 2 , wherein Xaa 1 comprises a methylene group in substitution for the carbonyl group adjacent Sp.
4. The compound of claim 1 , wherein Sp comprises at least one of Υ-aminobutyric acid; ε-aminocaproic acid; 8-amino-3,6-dioxaoctanoic acid; 11-amino-3,6,9-trioxaundecanoic acid; 14-amino-3,6,9,12-tetraoxatetradecanoic acid; α-aminobutyric acid; 5-aminopentanoic acid; 6-aminohexanoic acid; 7-aminoheptanoic acid; 8-aminooctanoic acid; 3-(aminooxy)acetic acid; β-alanine; glycine; alanine; threonine; tryptophan; tyrosine; methionine; leucine; isoleucine; valine; serine; proline; ethylene glycol; PEG n ; propylene glycol; PPG n ; amino-PEG n -carboxy; amino-PPG n -carboxy; or any combination thereof, and wherein n=1-6.
5. The compound of claim 1 , wherein B comprises at least one of aminobenzoyl (Abz), acetyl (Ac), benzoyl (Bz), benzyloxycarbonyl (Z), τ-Butyloxycarbonyl (Boc), Furylacryloyl (Fa), Methoxysuccinyl (MeOSuc), Pyroglutamate (Pyr), Phenylalanine, a 1-3 mer peptide, and Succinyl (Suc).
6. The compound of claim 1 , wherein Sp is ethylene glycol, PEG n , propylene glycol, PPG n , amino-PEG n -carboxy group, or an amino-PPG n -carboxy group, wherein n=1-6, or any combination thereof.
7. The compound of claim 1 , comprising an isostere bond between Xaa 1 and Sp.
8. The compound of claim 1 , wherein Xaa 2 is a glycine, D-alanine, or D-serine.
9. The compound of claim 1 , wherein Sp has a length in a range of 0.6 nm to 1.75 nm.
10. A compound having formula Ib:
B-Xaa 1 -Sp-Xaa 2 (Ib)
wherein:
B is at least one of acetyl, pyroglutamate, and succinyl;
Xaa 1 is a positively-charged amino-acid;
Sp is a spacer molecule having a length in a range of from 0.3 nm to 2.5 nm;
Xaa 2 is glycine, D-alanine, D-threonine, or D-serine; and
wherein the compound binds to the active site of Antiplasmin Cleaving Enzyme (APCE) and to the active site of Fibroblast Activation Protein-alpha (FAP).
11. The compound of claim 10 , wherein Xaa 1 comprises α,β-diaminopropionic acid; α,Υ-diaminobutyric acid; ornithine; β-homoornithine; arginine; β-homoarginine; homoarginine; lysine; homolysine; β-homolysine; or histidine.
12. The compound of claim 10 , wherein Sp comprises at least one of Υ-aminobutyric acid; ε-aminocaproic acid; 8-amino-3,6-dioxaoctanoic acid; 11-amino-3,6,9-trioxaundecanoic acid; 8,11,14-amino-3,6,9,12-tetraoxatetradecanoic acid; α-aminobutyric acid; 5-aminopentanoic acid; 6-aminohexanoic acid; 7-aminoheptanoic acid; 8-aminooctanoic acid; 3-(aminooxy)acetic acid; β-alanine; alanine; threonine; tryptophan; tyrosine; methionine; leucine; isoleucine; valine; serine; proline; ethylene glycol; PEG n ; propylene glycol; PPG n ; amino-PEG n -carboxy; amino-PPG n -carboxy; or any combination thereof, and wherein n=1-6.
13. The compound of claim 10 , wherein Sp comprises PEG n or PPG n or a heteropolymer of ethylene glycol and propylene glycol units, wherein n=1-6.
14. The compound of claim 10 , wherein Xaa 1 comprises a methylene group in substitution for the carbonyl group adjacent Sp.
15. A compound having formula I:
B-Xaa 1 -Sp-Xaa 2 -Cyc (Formula I)
wherein:
B is a protecting group;
Xaa 1 is a positively-charged amino-acid;
Sp is a spacer molecule having a length in the range of 0.3 nm to 2.5 nm;
Xaa 2 is glycine, D-alanine, D-serine, or D-threonine; and
Cyc is boronyl proline or cyanopyrrolidine; and
wherein the compound binds to the active site of Antiplasmin Cleaving Enzyme (APCE) and to the active site of Fibroblast Activation Protein-alpha (FAP).
16. The compound of claim 15 , wherein Xaa 1 is selected from the group consisting of α,β-diaminopropionic acid, α,Υ-diaminobutyric acid, ornithine, β-homoornithine, arginine, β-homoarginine, homoarginine, lysine, homolysine, β-homolysine, and histidine.
17. The compound of claim 16 , wherein Xaa 1 comprises a methylene group in substitution for the carbonyl group adjacent Sp.
18. The compound of claim 15 , wherein Sp comprises at least one of Υ-aminobutyric acid; ε-aminocaproic acid; 8-amino-3,6-dioxaoctanoic acid; 11-amino-3,6,9-trioxaundecanoic acid; 14-amino-3,6,9,12-tetraoxatetradecanoic acid; α-aminobutyric acid; 5-aminopentanoic acid; 6-aminohexanoic acid; 7-aminoheptanoic acid; 8-aminooctanoic acid; 3-(aminooxy)acetic acid, β-alanine, glycine; alanine; threonine; tryptophan; tyrosine; methionine; leucine; isoleucine; valine; serine; proline; ethylene glycol; PEG n ; propylene glycol; PPG n ; amino-PEG n -carboxy; amino-PPG n -carboxy; or any combination thereof, and wherein n=1-6.
19. The compound of claim 15 , wherein B is selected from the group consisting of:
aminobenzoyl (Abz), acetyl (Ac), benzoyl (Bz), benzyloxycarbonyl (Z), τ-Butyloxycarbonyl (Boc), Furylacryloyl (Fa), Methoxysuccinyl (MeOSuc), Pyroglutamate (Pyr), Phenylalanine, a 1-3 mer peptide, and Succinyl (Suc).
20. The compound of claim 15 , which binds to the active site of APCE or FAP at a Ki <20 nM and which binds to Dipeptidylpeptidase IV (DPPIV) at a Ki>200 nM.
21. The compound of claim 15 , which has a Ki (DPPIV):Ki (APCE/FAP) ratio >500.