Na channels, disease, and related assays and compositions
Disclosed are molecules and their synthesis, for use in blocking gated ion channels such as voltage-gated sodium channels (VGSCs) and prostate voltage sodium channels (PVSCs). These inhibitors have superior blocking efficacy, for instance in displacing the radioligand [ 3 H]-Batrachotoxin-B ([ 3 H]-BTX-B) that binds to site 2 of a VGSC. The molecules of the invention comprise a moiety which increases the binding affinity of molecules for the protein binding site in prostate cancer cells (PCs), and which is also fluorescent. In one embodiment the invention molecules are an inhibition system that can be used to target over-abundant or hyperactive VGSCs selectively in pain, epilepsy or prostate cancer, inhibiting the proliferation of PCs. The fluorescent moiety also facilitates screening, tracking, and pharmacodynamic studies of the drug in a biological system both in vitro and in vivo.
1. A compound comprising:
a residue that can bind to one or more isoforms of an ion channel to modulate ion flow across said channel, wherein the residue is selected from the group consisting of hermitamide A, hermitamide B, diphenyl hydantoin, an enantiomer of 2-(3-chloro-phenyl)-2-hydroxy-nonanoic acid amide, and a N-(5-(4-(3-chlorophenyl)-2,5-dioxoimidazolidin-4-yl)pentyl)-species,
a lipophilic linker or optionally a covalent bond, wherein the linker is a linear, branched or cyclic C 1 -C 11 hydrocarbon residue, and wherein the backbone atoms of the linker are carbons, and
a fluorophore moiety, wherein the fluorophore moiety is selected from the group consisting of dansyl, 4-(Diethylamino)azobenzene-4′-sulfonyl, fluorescein isothiocyanate (FITC), 5,6-carboxymethyl fluorescein, Texas red, nitrobenz-2-oxa-1,3-diazol-4-yl (NBD), coumarin, dansyl chloride, rhodamine, amino-methyl coumarin (AMCA), Eosin, Erythrosin, BODIPY®, Cascade Blue®, Oregon Green®, pyrene, lissamine, xanthenes, acridines, oxazines, phycoerythrin, macrocyclic chelates of lanthanide ions, quantum Dye™, fluorescent energy transfer dyes, thiazole orange-ethidium heterodimer, the cyanine dyes Cy3, Cy3.5, Cy5, Cy5.5 and Cy7,3-Hydroxypyrene 5,8,10-Tri Sulfonic acid, 5-Hydroxy Tryptamine (5-HT), Acid Fuchsin, Alizarin Complexon, Alizarin Red, Allophycocyanin, Aminocoumarin, Anthroyl Stearate, Astrazon Brilliant Red 4G, Astrazon Orange R, Astrazon Red 6B, Astrazon Yellow 7 GLL, Atabrine, Auramine, Aurophosphine, Aurophosphine G, BAO 9 (Bisaminophenyloxadiazole), BCECF, Berberine Sulphate, Bisbenzamide, Blancophor FFG Solution, Blancophor SV, Bodipy F1, Brilliant Sulphoflavin FF, Calcien Blue, Calcium Green, Calcofluor RW Solution, Calcofluor White, Calcophor White ABT Solution, Calcophor White Standard Solution, Carbostyryl, Cascade Yellow, Catecholamine, Chinacrine, Coriphosphine O, Coumarin-Phalloidin, CY3.18, CY5.18, CY7, Dans (1-Dimethyl Amino Naphaline 5 Sulphonic Acid), Dansa (Diamino Naphtyl Sulphonic Acid), Dansyl NH—CH3, Diamino Phenyl Oxydiazole (DAO), Dimethylamino-5-Sulphonic acid, Dipyrrometheneboron Difluoride, Diphenyl Brilliant Flavine 7GFF, Dopamine, Erythrosin ITC, Euchrysin, FIF (Formaldehyde Induced Fluorescence), Flazo Orange, Fluo 3, Fluorescamine, Fura-2, Genacryl Brilliant Red B, Genacryl Brilliant Yellow 10GF, Genacryl Pink 3G, Genacryl Yellow 5GF, Gloxalic Acid, Granular Blue, Haematoporphyrin, Indo-1, Intrawhite Cf Liquid, Leucophor PAF, Leucophor SF, Leucophor WS, Lissamine Rhodamine B200 (RD200), Lucifer Yellow CH, Lucifer Yellow VS, Magdala Red, Marina Blue, Maxilon Brilliant Flavin 10 GFF, Maxilon Brilliant Flavin 8 GFF, MPS (Methyl Green Pyronine Stilbene), Mithramycin, NBD Amine, Nitrobenzoxadidole, Noradrenaline, Nuclear Fast Red, Nuclear Yellow, Nylosan Brilliant Flavin E8G, Oxadiazole, Pacific Blue, Pararosaniline (Feulgen), Phorwite AR Solution, Phorwite BKL, Phorwite Rev, Phorwite RPA, Phosphine 3R, Phthalocyanine, Phycoerythrin R, Polyazaindacene Pontochrome Blue Black, Porphyrin, Primuline, Procion Yellow, Pyronine, Pyronine B, Pyrozal Brilliant Flavin 7GF, Quinacrine Mustard, Rhodamine 123, Rhodamine 5 GLD, Rhodamine 6G, Rhodamine B, Rhodamine B 200, Rhodamine B Extra, Rhodamine BB, Rhodamine BG, Rhodamine WT, Serotonin, Sevron Brilliant Red 2B, Sevron Brilliant Red 4G, Sevron Brilliant Red B, Sevron Orange, Sevron Yellow L, SITS (Primuline), SITS (Stilbene Isothiosulphonic acid), Stilbene, Snarf 1, sulpho Rhodamine B Can C, Sulpho Rhodamine G Extra, Tetracycline, Thiazine Red R, Thioflavin S, Thioflavin TCN, Thioflavin 5, Thiolyte, Thiozol Orange, Tinopol CBS, True Blue, Ultralite, Uranine B, Uvitex SFC, Xylene Orange, and XRITC,
wherein the linker is covalently bonded to each of the residue and the fluorophore moiety.
2. A composition comprising any of the compounds of claim 1 .
3. A method of treating prostate cancer comprising administering to a mammal in need thereof a composition according to claim 2 .
4. A method of assessing the presence of prostate cancer in a mammalian patient, wherein the method comprises a step in which an ion channel containing tissue culture from the patient is treated with a composition containing a compound according to claim 1 .
5. A method for investigating cell proliferation, electrical depolarization of a tissue, or another phenomenon mediated by ion migration across an ion channel, comprising treating a cell culture, tissue culture, or other sample containing an ion channel, with a composition comprising a compound according to claim 1 , and assessing the location and intensity of fluorescence in the sample.
6. The compound of claim 1 , wherein the linker has between 2 and 7 backbone atoms between the residue and the fluorophore moiety.
7. A pharmaceutical composition comprising a compound of claim 6 .
8. A method of treating prostate cancer comprising administering to a mammal in need thereof a pharmaceutical composition according to claim 7 .
9. A method of assessing the presence of prostate cancer in a mammalian patient, wherein the method comprises a step in which an ion channel containing tissue culture from the patient is treated with a composition containing a compound according to claim 6 .
10. The compound of claim 1 , wherein the ion channel is a voltage-gated sodium channel (Na v ).
11. The compound of claim 1 , wherein the fluorophore moiety comprises an electron donating group in captodative communication with an electron withdrawing group.
12. The compound of claim 1 , wherein the residue comprises hermitamide A.
13. The compound of claim 1 , wherein the residue comprises hermitamide B.
14. The compound of claim 1 , wherein the residue comprises an enantiomer of 2-(3-chloro-phenyl)-2-hydroxy-nonanoic acid amide.
15. The compound of claim 1 , wherein the residue is a N-(5-(4-(3-chlorophenyl)-2,5-dioxoimidazolidin-4-yl)pentyl)-species.
16. The compound of claim 1 , wherein the lipophilic side chain is further substituted with a moiety selected from the group consisting of halogen, C 1 -C 4 organic group, C 1 -C 4 ether, C 1 -C 4 ester, C 1 -C 4 sulfester, C 1 -C 4 phosphoester, mono- or di-C 1 -C 4 alkylamine, C 1 -C 4 amide, C 1 -C 4 sulfamide, C 1 -C 4 phosphoamide, and imidazolidine-2,4-dilactone.
17. The compound of claim 1 , wherein the residue is diphenyl hydantoin.
18. The compound of claim 1 , wherein fluorophore moiety is 5-(dimethylamino)naphthalene sulfamide (dansyl).
19. The compound of claim 1 , wherein the linker is alkyl, alkenyl, alkynyl, polyether, polyethylene glycol, polyethylene alkyl ether, polypropylene glycol, polypropylene glycol alkyl ether, polyalkylamine, and wherein the backbone is optionally substituted with an ester, sulfoester, phosphoester, amide, sulfamide, or phosphoamide moiety.
20. The compound of claim 1 , wherein the linker has between 7 backbone atoms between the residue and the fluorophore moiety.
21. A compound comprising a residue that can bind to one or more isoforms of an ion channel to modulate ion flow across said channel, a lipophilic linker or optionally a covalent bond, and a fluorophore moiety, wherein the linker is covalently bonded to each of the residue and the fluorophore moiety,
wherein the residue is selected from the group consisting of hermitamide A, hermitamide B, an enantiomer of 2-(3-chloro-phenyl)-2-hydroxy-nonanoic acid amide, and a N-(5-(4-(3-chlorophenyl)-2,5-dioxoimidazolidin-4-yl)pentyl)-species,
wherein the linker is a linear, branched or cyclic C 1 -C 11 hydrocarbon residue, and wherein the backbone atoms of the linker are carbons, and
wherein the fluorophore moiety comprises an electron donating group in captodative communication with an electron withdrawing group.