Multifunctional chelators, complexes, and compositions thereof, and methods of using same
Multifunctional chelators, metal complexes thereof, compositions thereof, and methods of making and use in diagnostic imaging and treatment of cellular disorders.
1. A compound of formula (I):
where k is 0 or 1; m is 0 or 1; and each of Y 1 -Y 4 independently is one of a structure of formula (a-1), (a-2), or (a-3):
where p is 1 or 2; Z is hydrogen, formula (a-2), formula (a-3), Ar, a pyridylalkyl, a protecting group, an aryl containing group, an alkynyl containing group, an amine containing group, an azide containing group, or an amide containing group; Ar is or includes an aromatic ring or a heteroaromatic ring; and each R′ independently is OH, NH 2 , OR″, NR 2 ″ wherein each R″ is one of alkyl, tert-butyl, allyl, benzyl, benzyloxy, or a protecting group; and
wherein each of R 1-18 independently is or includes hydrogen, carboxyalkyl, alkylamido, alkyl, allyl, benzyl, benzyloxyalkyl, cycloalkyl, alkoxy, hydroxyalkyl, aryl, aryloxy, hydroxyaryl, heteroaryl, phenyl, vinyl, alkynyl, alkenyl, furannylalkyl, alkylthioalkyl, arylhydroxyalkyl, indanyl, inolylalkyl, naphthylalkyl, imidazolylalkyl, pyridiylalkyl, benzothiophenylalkyl, thiophenylalkyl, thioalkyl, thioaryl, thiobenzyl, hydroxy, an alkynyl containing group, substituted carbonyl, hydroxyalkyl, triazolylalkyl, aminoalkyl, benzothiophenylalkyl, carboxyl, carboxyalkyloxy, amine, a protected amine, carboxylic acid, holoalkylamido, aldehyde, ester, amido, tosyl, phthalimidyl, maleimidyl, trityl, tert-butyloxycarbonyl, carbobenzyloxy, o-nosyl, acetyl, fluoroacetyl, dimethoxybenzyl, p-methoxybenzyl, an amide containing group, a thioamide containing group, an amino acid-containing group, an ester containing group, a protecting group, an amine protecting group or:
where W is NH, oxygen, or sulfur, n is 1-5, and each of X 1 -X 5 independently is or includes hydrogen, halo, cyano, alkyl, hydroxy, nitro, amino, alkylamino, thiocyano, isothiocyano, alkoxy, aryloxy, carboxyl, carboxyalkyl, carboxyalkyloxy, ester, amido, aldehydo, alkylamido, holoalkylamido, an ester containing group, an carbonyl containing group, an amide containing group, an amine containing group, a thioamide containing group, an alkynyl containing group, or an amino acid-containing group;
wherein more than one of Y 1 -Y 4 is formula (a-1); and
wherein at least one of Y 1 -Y 4 comprises:
where X 1 is described above or comprises NH 2 , NHBoc, NCS or NPhth.
2. The compound of claim 1 , wherein at least one Z of Y 1 -Y 4 is hydrogen.
3. The compound of claim 1 , wherein Ar is selected from:
where W is NH, oxygen, or sulfur, n is 0-5, and each of X 1 -X 5 independently is or includes hydrogen, halo, cyano, alkyl, hydroxy, nitro, amino, alkylamino, thiocyano, isothiocyano, alkoxy, aryloxy, carboxyl, carboxyalkyl, carboxyalkyloxy, ester, amido, aldehydo, alkylamido, holoalkylamido, an ester containing group, an carbonyl containing group, an amide containing group, an amine containing group, a thioamide containing group, an alkynyl containing group, or an amino acid-containing group.
4. The compound of claim 1 , wherein one of R 13 -R 18 comprises:
where n is 1-5.
5. The compound of claim 1 , wherein X 5 comprises NO 2 .
6. The compound of claim 1 , wherein at least three of Y 1 -Y 4 is formula (a-1).
7. The compound of claim 1 , wherein an other of Y 1 -Y 4 is formula (a-3) with one of R 17-18 comprising:
and n is 1-5.
8. The compound of claim 1 , wherein Z is selected from:
where W is NH, oxygen, or sulfur and n is 1-5.
9. The compound of claim 8 , wherein an other of Y 1 -Y 4 is formula (a-3) with one of R 17-18 comprising:
and n is 1-5.
10. A compound of formula (I):
where k is 0 or 1; m is 0 or 1; and each of Y 1 -Y 4 independently is one of a structure of formula (a-1), (a-2), or (a-3):
where p is 1 or 2; Z is hydrogen, formula (a-2), formula (a-3), Ar, a pyridylalkyl, a protecting group, an aryl containing group, an alkynyl containing group, an amine containing group, an azide containing group, or an amide containing group; Ar is or includes an aromatic ring or a heteroaromatic ring; and each R′ independently is OH, NH 2 , OR″, NR 2 ″ wherein each R″ is one of alkyl, tert-butyl, allyl, benzyl, benzyloxy, or a protecting group;
wherein each of R 1-18 independently is or includes hydrogen, carboxyalkyl, alkylamido, alkyl, allyl, benzyl, benzyloxyalkyl, cycloalkyl, alkoxy, hydroxyalkyl, aryl, aryloxy, hydroxyaryl, heteroaryl, phenyl, vinyl, alkynyl, alkenyl, furannylalkyl, alkylthioalkyl, arylhydroxyalkyl, indanyl, inolylalkyl, naphthylalkyl, imidazolylalkyl, pyridiylalkyl, benzothiophenylalkyl, thiophenylalkyl, thioalkyl, thioaryl, thiobenzyl, hydroxy, an alkynyl containing group, substituted carbonyl, hydroxyalkyl, triazolylalkyl, aminoalkyl, benzothiophenylalkyl, carboxyl, carboxyalkyloxy, amine, a protected amine, carboxylic acid, holoalkylamido, aldehyde, ester, amido, tosyl, phthalimidyl, maleimidyl, trityl, tert-butyloxycarbonyl, carbobenzyloxy, o-nosyl, acetyl, fluoroacetyl, dimethoxybenzyl, p-methoxybenzyl, an amide containing group, a thioamide containing group, an amino acid-containing group, an ester containing group, a protecting group, an amine protecting group or:
where W is NH, oxygen, or sulfur, n is 1-5, and each of X 1 -X 5 independently is or includes hydrogen, halo, cyano, alkyl, hydroxy, nitro, amino, alkylamino, thiocyano, isothiocyano, alkoxy, aryloxy, carboxyl, carboxyalkyl, carboxyalkyloxy, ester, amido, aldehydo, alkylamido, holoalkylamido, an ester containing group, an carbonyl containing group, an amide containing group, an amine containing group, a thioamide containing group, an alkynyl containing group, or an amino acid-containing group;
wherein more than one of Y 1 -Y 4 is formula (a-1); and
wherein at least one Z comprises:
where X 1 is described above or comprises NH 2 , NHBoc, NCS or NPhth.
11. The compound of claim 1 , wherein k is 1.
12. A complex comprising the compound of claim 1 and a metal ion, a radioactive isotope of the metal ion, or a radioactive isotope of carbon, nitrogen, iodine, fluorine, oxygen, or helium.
13. The complex of claim 12 , wherein the metal ion is selected from the group consisting of Ac, Al, Bi, Pb, Y, Mn, Cr, Fe, Co, Zn, Ni, Tc, Gd, In, Ga, Cu, Re, Sm, Pm, Ho, Zr, Am, Ce, U, a lanthanide, and an actinide.
14. A conjugate comprising the compound of claim 1 and a targeting moiety, a fluorescence moiety, or a nanoparticle.
15. The conjugate according to claim 14 , wherein the targeting moiety comprises a biomolecule selected from a hormone, a bile acid, an amino acid, a peptide, a peptidomimetic, a protein, a deoxyribonucleic acid (DNA), a ribonucleic acid (RNA), a lipid, an albumin, a receptor molecule, a receptor binding molecule, a hapten, a monoclonal antibody, a polyclonal antibody, a peptide, an aptamer, a folic acid, an estrogen, or a transferrin.
16. A pharmaceutical composition comprising the compound of claim 1 and a pharmaceutically acceptable carrier.
17. A method of generating a diagnostic image or measurement, the method comprising:
administering to an animal a composition comprising the compound of claim 1 ; and
imaging or measuring an amount of the composition in a tissue or organ of the animal using magnetic resonance imaging (MRI), fluorescence imaging (FI), x-ray contrast imaging, transmission electron microscopy imaging, a positron emission tomography (PET) imaging, or single photon emission computed spectroscopy (SPECT).
18. The method of claim 17 , wherein the composition includes complex comprising 90 Y, 86 Y, 111 In, 213 Bi, 212 Bi, 212 Pb, 225 Ac, 177 Lu, 68 Ga, 166 Ho, 153 Sm, 149 Pm, 64 Cu, 89 Zr, 18 F or 67 Cu.
19. A method of preparing the compound of claim 1 , comprising:
reacting a compound of formula (Ib-1):
wherein: m is 0 or 1; each of R 1-12 and Y 1-3 is as defined above, with a compound of formula (Ib-2) or (Ib-3):
where m is 0 or 1; p is 0 or 1; each of R 21-22 independently is as defined for R 1-20 ; and Q is a counter anion or a leaving group comprising halide, perchlorate, tetrafluoroborate, hexafluoroantimonate, me sylate, triflate, tosylate, carbonate, nitrate, phthalimide, or succinimide.
20. The method of claim 19 , further comprising providing a compound of formula (f-1):
21. The method of claim 20 , further comprising: converting (b-2) to (b-3) in the presence of halosequestering agent comprising AgClO 4 , AgOTf, Ag 2 CO 3 , AgOTs, AgNO 3 , AgSbF 6 , or AgBF 4 ; and reacting (b-3) in situ with (1b-1) to obtain (f-1).
22. The compound of claim 10 , wherein one of R 15 -R 16 comprises:
where n is 1-5.
23. The compound of claim 10 , wherein k is 1.
24. A complex comprising the compound of claim 10 and a metal ion, a radioactive isotope of the metal ion, or a radioactive isotope of carbon, nitrogen, iodine, fluorine, oxygen, or helium.
25. A conjugate comprising the compound of claim 10 and a targeting moiety, a fluorescence moiety, or a nanoparticle.