Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
  • A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
  • A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
  • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
  • A61K31/445—Non condensed piperidines, e.g. piperocaine
  • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
  • A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
  • A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
  • C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
  • C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
  • C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
  • C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
  • C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
  • C07D235/18—Benzimidazoles; Hydrogenated benzimidazoles with aryl radicals directly attached in position 2
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
  • C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
  • C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
  • C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
  • C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
  • C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
  • C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
  • C07D235/30—Nitrogen atoms not forming part of a nitro radical
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
  • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
  • C07D401/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
  • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
  • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
  • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
  • C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
  • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
  • C07D409/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
  • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
  • C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings

Definitions

• proteostasis The regulation of protein synthesis, degradation, folding, trafficking and aggregation within a cell are collectively known as proteostasis.
• proteostasis is maintained by a wide array of cellular machinery that work to ensure that proteins are present in the proper location, amounts and form to perform their respective functions.
• proteostasis becomes dysregulated there can be disastrous effects on the cell and even on neighboring ceils.
• neurodegenerative diseases such as Parkinson’s disease (PD), Alzheimer’s disease (AD), Huntington’s disease (HD) and amyotrophic lateral sclerosis (ALS).
• IDPs intrinsically disordered proteins
• aggregation and oligomerization are used interchangeably.
• IDPs IDP ⁇ -synuclein
• oligomers are associated with the pathogenesis of PD.
• IDPs are named far their lack of tertiary structure allowing them to adopt numerous conformations and interact with multiple binding partners. IDPs are generally short-lived signaling proteins or transcription factors that are highly bound to other cellular components keeping free cytosolic levels low.
• IDPs are readily degraded by the 20S proteasome, the default protease responsible for IDP digestion.
• the accumulation of IDPs seen in neurodegenerative diseases can begin as a result of one of several disruptions (e.g. mutations, changes in expression, oxidative stress, aging, proteasome impairment, etc.) to their normal regulation. While a-syn may not be the sole cause of PD, there is strong evidence supporting its key role in the disease, including familial forms of PD resulting from mutations in the SNCA gene. Elevated monomeric a-syn levels are also known to cause apoptosis-inducing aggregation in neurons.
• oligomeric forms of a-syn and other IDPs have recently been snown to directly inhibit the proteasome, further disrupting its ability to regulate IDPs concentrations.
• FIG. 1A is the structure of astemizole, which is referred to herein as “compound 1 ,” and acyl astemizole, which is referred to herein as “compound 2,”
• FIG. 1 B is a plot of percent fold activation over vehicle as a function of log[M] astemizole and acyl astemizole and includes two tables describing each compound’s increase activity by 200% (AC 200 ) and max fold increase.
• FIG. 2A is a representative silver stain illustrating induced degradation of ⁇ -synuclein by the 20S proteasome in the presence of 1 , 3, 5, and 10 ⁇ M astemizole (1 ).
• FIG. 3A is a representative silver stain illustrating induced degradation of a-synuclein by the 20S proteasome in the presence of 1 , 3, 5, and 10 ⁇ M acyl astemizole (2).
• FIG. 4 A is tables and accompanying plots of % luminescence as a function of astemizole concentration.
• FIG. 4B is tables and accompanying plots of % luminescence as a function of acyl astemizole concentration.
• FIG. 4C is tables and accompanying plots of % luminescence as a function of AV-1 -10 concentration.
• FIG. 5 is the chemical structure of the compound AV-1 -10 mentioned in FIG. 4G.
• the disclosure relates to small molecules that enhance proteasome function and restore the activity of impaired proteasomes.
• Small molecule proteasome enhancers prevent the toxic accumulation of aggregation-prone proteins and prevent neuronal ceil death caused by aggregation-prone proteins.
• the disclosure therefore relates to the use of small molecules as therapeutic agents to treat neurodegenerative diseases.
• Neurodegenerative diseases include, but are not limited to Alzheimer’s disease (AD) and other dementias, Parkinson’s disease (PD) and PD-reiated disorders, Prion disease, Motor neuron diseases (MND), Huntington's disease (HD), Spinocerebellar ataxia (SCA), Spinal muscular atrophy (SMA).
• the disclosure relates to a chemotype that has been shown herein to be a biologically active enhancers of mammalian proteasomes.
• the chemotype described herein is based on astemizole and derivatives thereof.
• the disclosure relates to astemizole and derivates thereof, and their use to, among other things, prevent or slow down the progression of neurodegenerative diseases.
• the disclosure therefore relates to compounds of the formula (I): or a pharmaceutically acceptable salt, polymorph, prodrug, solvate or clathrate thereof, wherein: R 1 is aryl (e.g., phenyl) or heteroaryl (e.g., an indolinyl group or a benzimidazolinyl group);
• R 2 is H, alkyl, aryl or heteroaryl
• X 1 is alkyl (e.g., C 1 -C 6 alkyl) or alkenyl;
• X 2 is N or CR 3 , wherein R 3 is absent (e.g., when X 1 is alkenyl), hydrogen, alkyl, heterocyclyi, or aryl;
• R 4 is hydrogen, alkyl, cycloalkyl, heterocyclyi, aryl or heteroaryl
• R 5 is hydrogen, alkyi, cycloalkyl, heterocyciyl, aryi or heteroaryl.
• Another example of a compound of formula (I) is a compound of the or a pharmaceutically acceptable salt, polymorph, prodrug, solvate or clathrate thereof; wherein:
• R 6 is aryl or heteroaryl (e.g., tricyclic heteroaryl, such as a phenothiazinyl group and a carbazolyl group; and bicyclic heteroaryl, such as an indolinyl group or a benzimidazolinyl group).
• tricyclic heteroaryl such as a phenothiazinyl group and a carbazolyl group
• bicyclic heteroaryl such as an indolinyl group or a benzimidazolinyl group
• R 1 is aryl (e.g., phenyl) or heteroaryl (e.g., an indolinyl group or a benzimidazolinyi group);
• R 2 is H, alkyl, aryl or heteroaryl
• X 1 is alkyl or alkenyl
• X 2 is N or CR 3 , wherein R 3 is absent (e.g., when X1 is alkenyl), hydrogen, alkyl, heterocyclyi, or aryl; and R 6 is aryl or heteroaryl (e.g., tricyclic heteroaryl, such as a phenothiazinyl group and a carbazoiyl group; and bicyclic heteroaryl, such as an indolinyl group or a benzimidazolinyi group), such as a compound of the formula: wherein : q is 0, 1 , 2 or 3;
• R 9 is alkyl, cycloalkyl aryl, heteroaryl, acyl, amide or carbamate; and each R 10 is independently H, halo, alkyl, haloalkyl (e.g., CF 3 ), alkoxy (e.g., -OR 11 , wherein R 11 is alkyl, cycloalkyl or aryl, heteroaryi, acyl, amide or carbamate) or heterocyclyi (e.g., heteroaryl); or two R 10 groups on adjacent carbon atoms, together with those carbon atoms, can form a cycloalkenyl, aryl or heterocyclyi (e.g., heteroaryl); or
• R 9 and an R 10 together with the atoms to which they are attached, can form a heterocyiyl group.
• R 1 can be aryl, such as substituted aryl.
• R 1 can be substituted or unsubstituted phenyl.
• R 2 can be H.
• X 1 can be alkyl, such as C 1 -C 6 alkyl, branched or unbranched, substituted or unsubstiuted.
• the aryl and heteroaryl groups of R 1 can be unsubstituted or substituted as described herein.
• halo e.g., Cl, Br, and F
• OR 7 wherein R 7 is hydrogen, alkyl, cycloalkyl, aryl or arylalkyi, S(O) X , wherein x is 0, 1 or 2, acyl, amido or heterocyclyi.
• the alkyl, aryl, and heteroaryl groups of R 2 can be unsubstituted or substituted as described herein.
• the alkyl, aryl or heteroaryl groups of R 2 when they are substituted, they can be substituted with halo (e.g., Cl, Br, and F), amino, OR 7 , wherein R 7 is hydrogen, alkyl, cycloalkyl, aryl or arylalkyi, S(O) X , wherein x is 0, 1 or 2, acyl, amido or heterocyclyi.
• the alkyl, cycloaikyl, heterocyclyi, aryl, and heteroaryl groups of R 4 can be unsubstituted or substituted as described herein.
• alkyl, cycloalkyl, heterocyclyi, aryl or heteroaryl groups of R 4 when they are substituted, they can be substituted with alkyl, cycloaikyl, aryl, heteroaryl, halo (e.g., Cl, Br, and F), amino, OR 7 , wherein R 7 is hydrogen, alkyl, cycloaikyl, aryl or arylalkyi, S(O) X , wherein x is 0, 1 or 2, acyl, amido or heterocyclyi.
• halo e.g., Cl, Br, and F
• the alkyl, cycloaikyl, heterocyclyi, aryl, and heteroaryl groups of R 5 can be unsubstituted or substituted as described herein.
• alkyl, cycloaikyl, heterocyclyi, aryl or heteroaryl groups of R 5 when they are substituted, they can be substituted with alkyl, cycloaikyl, aryl, heteroaryl, halo (e.g., Cl, Br, and F), amino, OR 7 , wherein R 7 is hydrogen, alkyl, cycloaikyl, aryl or arylalkyi, S(O) X , wherein x is 0, 1 or 2, acyl, amido or heterocyclyi.
• halo e.g., Cl, Br, and F
• the aryl or heteroaryl groups of R 6 can be unsubstituted or substituted as described herein.
• the aryl or heteroaryl groups of R 6 when they are substituted, they can be substituted with alkyl, cycloaikyl, aryl, heteroaryi, halo (e.g., Ci, Br, and F), amino, OR 7 , wherein R 7 is hydrogen, alkyl, cycloalkyl, aryl or arylalkyl, S(O) X , wherein x is 0, 1 or 2, acyl, amido or heterocyclyl.
• An example of a compound of the formulae (I) and (la)-(lc) includes, but is not limited to, a compound of the formula: pharmaceutically acceptable salts, polymorphs, prodrugs, solvates or clathrates thereof.
• This disclosure also relates to compounds of the formula (II) and (Ila)- o r a pnarmaceutically acceptable salt, polymorph, prodrug, soivate or clatnrate thereof, wherein: q is 0, 1 , 2 or 3; each X’ is independently alkyl (e.g., -(CH 2 ) n -, wherein n is 0, 1 , or 2) or alkenyl;
• R 8 and R 9 are each independently alkyl, cycloalkyi aryl, heteroaryi, acyl, amide or carbamate;
• W is N or C- R 10 ;
• X is N or C-R 10 ;
• Y is N or C-R 10 ; and
• Z is N or C-R 10 ; wherein each R 10 is independently H, halo, alkyl, haloalkyl (e.g., CF 3 ), alkoxy (e.g., -OR 11 , wherein R 11 is alkyl, cycloalkyl or aryl, heteroaryl, acyl, amide or carbamate) or heterocyclyl (e.g., heteroaryl); or two R 10 groups on adjacent carbon atoms, together with those carbon atoms, can form a cycloalkenyl, aryl or heterocyclyl (e.g., heteroaryi); or
• R 9 and an R 10 together with the atoms to which they are attached, can form a heterocyiyl group.
• R 9 and R 10 together with the atoms to which they are attached, can form a heterocyiyl group such .
• Another variation on compounds of the formula (II) include compounds of the formula:
• This disclosure also relates to compounds of the formula (III): such as
• X 1 is alkyl (e.g., "(CH 2 ) n -) or alkenyl;
• W is N or C-R 10 ;
• X is N or C-R 10 ;
• Y is N or C-R'°; and
• Z is N or C-R 10 ; wherein each R 10 is independently H, halo, alkyl, haloalkyl (e.g., CF 3 ), aikoxy (e.g., -OR 11 , wherein R 11 is alkyl, cycloalkyl or aryl, heteroaryl, acyl, amide or carbamate) or heterocyclyl (e.g., heteroaryl); or two R 10 groups on adjacent carbon atoms, together with those carbon atoms, can form a cycloalkenyl, aryl or heterocyclyl (e.g., heteroaryl); or
• R 9 and an R 10 together with the atoms to which they are attached, can form a heterocylyl group
• R 12 and R 13 are each independently alkyl, cycloalkyl aryl, heteroaryl, acyl, amide or carbamate.
• R 9 and R 10 or R 9 and R 13 together with the atoms to which they are attached, can form a heterocylyl group such as:
• Examples of compounds of the formula (III) include: or a pharmaceutically acceptable salt, polymorph, prodrug, solvate or clathrate thereof.
• This disclosure also relates to compounds of the formula (IV): or a pharmaceutically acceptable salt, polymorph, prodrug, solvate or clathrate thereof, wherein: q is 0, 1 , 2 or 3;
• X 1 is alkyl (e.g., -(CH 2 )n-) or alkenyl;
• W is N or C-R 10 ;
• X is N or C-R 10 ;
• Y is N or C-R 10 ; and
• Z is N or C-R 10 ; wherein each
• R 10 is independently H, halo, alkyl, haloalkyl (e.g., CF 3 ), alkoxy (e.g., -OR 11 , wherein R 11 is alkyl, cycloalkyl or aryl, heteroaryl, acyl, amide or carbamate) or heterocyclyl (e.g., heteroaryl); or two R 10 groups on adjacent carbon atoms, together with those carbon atoms, can form a cycloalkenyl, aryl or heterocyclyl (e.g., heteroaryl); or
• R 9 and an R 10 together with the atoms to which they are attached, can form a heterocylyl group; and R 14 is aryl (e.g., phenyl) or heterocyclyl (e.g., heteroaryl); or
• R 9 and R 14 together with the atoms to which they are attached, can forma an aryl or a hetorcyclyl.
• R 9 and R 10 or R 9 and R 14 together with the atoms to which they are attached, can form a heterocylyl group such as:
• each R 10 is independently H, halo, alkyl, haloalkyl (e.g., CF 3 ), alkoxy (e.g., -OR 11 , wherein R’ 1 is alkyl, cycloalkyi or aryl, heteroaryl, acyl, amide or carbamate) or heterocyclyi (e.g., heteroaryi); and two R 10 groups on adjacent carbon atoms, together with those carbon atoms, can form a cycloalkenyl, aryl or heterocyclyi (e.g., heteroaryl); or
• R 9 and an R 10 together with the atoms to which they are attached, can form a heterocylyl group.
• R 9 and R 10 together with the atoms to which they are attached, can form a heterocylyl group such as:
• An example of a compound of the formula (V) includes: or a pharmaceutically acceptable salt, polymorph, prodrug, solvate or clathrate thereof.
• compositions comprising one or more compounds and one or more pharmaceutically acceptable excipients.
• a “pharmaceutical composition” refers to a chemical or biological composition suitable for administration to a subject (e.g., mammal).
• compositions can be specifically formulated for administration via one or more of a number of routes, including but not limited to buccal, cutaneous, epicutaneous, epidural, infusion, inhalation, intraarterial, intracardial, intracerebroventricular, intradermal, intramuscular, intranasal, intraocular, intraperitoneal, intraspinai, intrathecal, intravenous, oral, parenteral, pulmonary, rectaliy via an enema or suppository, subcutaneous, subdermai, sublingual, transdermal, and transmucosai.
• administration can by means of capsule, drops, foams, gei, gum, injection, liquid, patch, piii, porous pouch, powder, tablet, or other suitable means of administration.
• a “pharmaceutical excipient” or a “pharmaceutically acceptable excipient” is a carrier, sometimes a liquid, in which an active therapeutic agent is formulated.
• the excipient generally does not provide any pharmacological activity to the formulation, though it can provide chemical and/or biological stability, and release characteristics. Examples of suitable formulations can be found, for exampie, in Remington, The Science And Practice of Pharmacy, 20th Edition, (Gennaro, A. R., Chief Editor), Philadelphia College of Pharmacy and Science, 2000, which is incorporated by reference in its entirety.
• pharmaceutically acceptable carrier includes, but is not limited to, any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents that are physiologically compatible.
• the carrier is suitable for parenteral administration.
• the carrier can be suitable for intravenous, intraperitoneal, intramuscular, sublingual, or oral administration.
• Pharmaceutically acceptable carriers include sterile aqueous solutions or dispersions and steriie powders for the extemporaneous preparation of steriie injectable solutions or dispersion. The use of such media and agents for pharmaceutically active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the active compound, use thereof in the pharmaceutical compositions of the invention is contemplated. Supplementary active compounds can also be incorporated into the compositions.
• compositions can be sterile and stable under the conditions of manufacture and storage.
• the composition can be formulated as a solution, microemulsion, liposome, or other ordered structure suitable to high drug concentration.
• the carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (e.g., glycerol, propylene glycol, and liquid polyethylene glycol), and suitable mixtures thereof.
• the proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants.
• isotonic agents for example, sugars, polyaicohols such as mannitol, sorbitol, or sodium chloride in the composition.
• Prolonged absorption of injectable compositions can be brought about by including in the composition an agent which delays absorption, for example, monostearate salts and gelatin.
• the compounds described herein can be formulated in a time release formulation, for example in a composition that includes a slow release polymer.
• the active compounds can be prepared with carriers that will protect the compound against rapid release, such as a controlled release formulation, including implants and microencapsulated delivery systems.
• Biodegradable, biocompatibie polymers can be used, such as ethylene vinyi acetate, polyanhydrides, polyglycolic acid, collagen, polyorthoesters, polylactic acid and polylactic, polyglycolic copolymers (PLG). Many methods for the preparation of such formulations are known to those skilled in the art. [0047] Oral forms of administration are also contemplated herein.
• the pharmaceutical compositions of the present invention can be orally administered as a capsule (hard or soft), tablet (film coated, enteric coated or uncoated), powder or granules (coated or uncoated) or liquid (solution or suspension).
• the formulations can be conveniently prepared by any of the methods well-known in the art.
• compositions of the present invention can include one or more suitable production aids or excipients including fillers, binders, disintegrants, lubricants, diluents, flow agents, buffering agents, moistening agents, preservatives, colorants, sweeteners, flavors, and pharmaceutically compatible carriers.
• suitable production aids or excipients including fillers, binders, disintegrants, lubricants, diluents, flow agents, buffering agents, moistening agents, preservatives, colorants, sweeteners, flavors, and pharmaceutically compatible carriers.
• the compounds can be administered by a variety of dosage forms as known in the art. Any biologically- acceptable dosage form known to persons of ordinary skill in the art, and combinations thereof, are contemplated. Examples of such dosage forms include, without limitation, chewable tablets, quick dissolve tablets, effervescent tablets, reconstitutable powders, elixirs, liquids, solutions, suspensions, emulsions, tablets, multi-layer tablets, bi-layer tablets, capsules, soft gelatin capsules, hard gelatin capsules, caplets, lozenges, chewable lozenges, beads, powders, gum, granules, particles, microparticles, dispersible granules, cachets, douches, suppositories, creams, topicals, inhalants, aerosol inhalants, patches, particle inhalants, implants, depot implants, ingestibies, injectables (including subcutaneous, intramuscular, intravenous, and intradermal), infusions, and
• Other compounds which can be included by admixture are, for example, medically inert ingredients (e.g., solid and liquid diluent), such as lactose, dextrosesaccharose, cellulose, starch or calcium phosphate for tablets or capsules, olive oil or ethyl oleate for soft capsules and water or vegetable oil for suspensions or emulsions; lubricating agents such as silica, taic, stearic acid, magnesium or calcium stearate and/or polyethylene glycols; gelling agents such as colloidal clays; thickening agents such as gum tragacanth or sodium alginate, binding agents such as starches, arabic gums, gelatin, methyicelluiose, carboxymethylcellulose or polyvinylpyrrolidone; disintegrating agents such as starch, alginic acid, alginates or sodium starch glycolate; effervescing mixtures; dyestuff; sweeteners; wetting agents
• Liquid dispersions for oral administration can be syrups, emulsions, solutions, or suspensions.
• the syrups can contain as a carrier, for example, saccharose or saccharose with glycerol and/or mannitol and/or sorbitol.
• the suspensions and the emulsions can contain a carrier, for example a natural gum, agar, sodium alginate, pectin, methylcellulose, carboxymethylcellulose, or polyvinyl alcohol.
• the amount of active compound in a therapeutic composition can vary according to factors such as the disease state, age, gender, weight, patient history, risk factors, predisposition to disease, administration route, pre-existing treatment regime (e.g., possible interactions with other medications), and weight of the subject. Dosage regimens can be adjusted to provide the optimum therapeutic response. For example, a single bolus can be administered, several divided doses can be administered over time, or the dose can be proportionally reduced or increased as indicated by the exigencies of therapeutic situation.
• a “dosage unit form,” as used herein, refers to physically discrete units suited as unitary dosages for the mammalian subjects to be treated; each unit containing a predetermined quantity of active compound calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier.
• the specification for the dosage unit forms of the invention are dictated by and directly dependent on the unique characteristics of the active compound and the particular therapeutic effect to be achieved, and the limitations inherent in the art of compounding such an active compound for the treatment of sensitivity in subjects.
• the compounds of the present invention can be administered in an effective amount.
• the dosages as suitable for this invention can be a composition, a pharmaceutical composition or any other compositions described herein.
• the dosage is typically administered once, twice, or thrice a day, although more frequent dosing intervals are possible.
• the dosage can be administered every day, every 2 days, every 3 days, every 4 days, every 5 days, every 6 days, and/or every 7 days (once a week).
• the dosage can be administered daily for up to and including 30 days, preferably between 7-10 days.
• the dosage can be administered twice a day for 10 days. If the patient requires treatment for a chronic disease or condition, the dosage can be administered for as iong as signs and/or symptoms persist. The patient can require "maintenance treatment" where the patient is receiving dosages every day for months, years, or the remainder of their lives.
• the composition of this invention can be to effect prophylaxis of recurring symptoms.
• the dosage can be administered once or twice a day to prevent the onset of symptoms in patients at risk, especially for asymptomatic patients.
• the absolute weight of a given compound included in a unit dose for administration to a subject can vary widely. For example, about 0.0001 to about 1 g, or about 0.001 to about 0.5 g, of at least one compound of this disclosure, or a plurality of compounds can be administered.
• the unit dosage can vary from about 0.001 g to about 2g, from about 0.005 g to about 0.5 g, from about 0.01 g to about 0.25 g, from about 0.02 g to about 0.2 g, from about 0.03 g to about 0.15 g, from about 0.04 g to about 0.12 g, or from about 0.05 g to about 0.1 g.
• Daily doses of the compounds can vary as well.
• Such daily doses can range, for example, from about 0.01 g/day to about 10 g/day, from about 0.02 g/day to about 5 g/day, from about 0.03 g/day to about 4 g/day, from about 0.04 g/day to about 3 g/day, from about 0.05 g/day to about 2 g/day, and from about 0.05 g/day to about 1 g/day.
• the amount of compound(s) for use in treatment will vary not only with the particular carrier selected but also with the route of administration, the nature of the condition being treated, and the age and condition of the patient. Ultimately the attendant health care provider may determine proper dosage.
• compositions described herein can be administered in any of the following routes: buccal, epicutaneous, epidural, infusion, inhalation, intraarterial, intracardial, intracerebroventricular, intradermal, intramuscular, Intranasal, intraocular, intraperitoneal, intraspinal, intrathecal, intravenous, oral, parenteral, pulmonary, rectally via an enema or suppository, subcutaneous, subdermal, sublingual, transdermal, and transmucosal.
• routes of administration are buccal and oral.
• the administration can be local, where the composition is administered directly, close to, in the locality, near, at, about, or in the vicinity of, the site(s) of disease, e.g., inflammation, or systemic, wherein the composition is given to the patient and passes through the body widely, thereby reaching the site(s) of disease.
• Local administration can be administration to, for example, tissue, organ, and/or organ system, which encompasses and/or is affected by the disease, and/or where the disease signs and/or symptoms are active or are likely to occur.
• Administration can be topical with a local effect, composition is applied directly where its action is desired.
• Administration can be enteral wherein the desired effect is systemic (non-local), composition is given via the digestive tract.
• Administration can be parenteral, where the desired effect is systemic, composition is given by other routes than the digestive tract.
• compositions can include the compounds described herein in a “therapeutically effective amount.”
• a therapeutically effective amount is an amount sufficient to obtain the desired physiological effect, such as a reduction of at least one symptom of cancer or an inflammatory disease or condition.
• compositions contemplated herein can contain other ingredients such as chemotherapeutic agents, anti-inflammatory agents, anti-viral agents, antibacterial agents, antimicrobial agents, immunomodulatory drugs, such as lenalidomide, pomalidomide or thalidomide, histone deacetylase inhibitors, such as panobinostat, preservatives or combinations thereof.
• chemotherapeutic agents anti-inflammatory agents
• anti-viral agents antibacterial agents
• antimicrobial agents antimicrobial agents
• immunomodulatory drugs such as lenalidomide, pomalidomide or thalidomide
• histone deacetylase inhibitors such as panobinostat, preservatives or combinations thereof.
• This disclosure also includes methods for treating neurodegenerative diseases, such as Parkinson's disease, Alzheimer's disease, Huntington's disease, and ALS, comprising administering a therapeutically effective amount of at least one of the compounds described herein (e.g., astemizole or compounds of the formulae (I), (la)-(Ic), (II), (IIa)-(IId), (III)-(V), and (Va)) to a subject in need thereof.
• a therapeutically effective amount of at least one of the compounds described herein e.g., astemizole or compounds of the formulae (I), (la)-(Ic), (II), (IIa)-(IId), (III)-(V), and (Va)
• This disclosure also includes methods for reducing, substantially eliminating or eliminating dysreguiation of proteostasis comprising administering a therapeutically effective amount of at least one of the compounds described herein (e.g., astemizole or compounds of the formulae (I), (la)-(lc), (ll)-(V), and (Va)) to a subject in need thereof.
• a therapeutically effective amount of at least one of the compounds described herein e.g., astemizole or compounds of the formulae (I), (la)-(lc), (ll)-(V), and (Va)
• This disclosure also includes methods for reducing, substantially eliminating or eliminating the accumulation of intrinsically disordered proteins (e.g., a-syn) comprising administering a therapeutically effective amount of at least one of the compounds described herein (e.g., astemizole or compounds of the formulae (I), (la)- (Ic), (H)-(V), and (Va)) to a subject in need thereof.
• the terms “treat” and “treating” are not limited to the case where the subject (e.g. patient) is cured and the disease is eradicated. Rather, treatment that merely reduces symptoms, and/or delays disease progression is also contemplated.
• compositions disclosed herein can have the ability to effectively treat new patient segments where proteasome inhibition and reduced toxicity is desired or warranted.
• the compounds and methods described herein can be used prophylactically or therapeutically.
• the term “prophylactic” or “therapeutic” treatment refers to administration of a drug to a host before or after onset of a disease or condition. If it is administered prior to clinical manifestation of the unwanted condition (e.g., disease or other unwanted state of the host animal) then the treatment is prophylactic, i.e., it protects the host against developing the unwanted condition, whereas if administered after manifestation of the unwanted condition, the treatment is therapeutic (i.e., it is intended to diminish, ameliorate or maintain the existing unwanted condition or side effects therefrom).
• Administering the compounds described herein (including enantiomers and salts thereof) is contemplated in both a prophylactic treatment (e.g. to patients at risk for disease, such as elderly patients who, because of their advancing age, are at risk for arthritis, cancer, and the like) and therapeutic treatment (e.g. to patients with symptoms of disease or to patients diagnosed with disease).
• therapeutically effective amount refers to that amount of one or more compounds of the various examples of the present invention that elicits a biological or medicinal response in a tissue system, animal or human, that is being sought by a researcher, veterinarian, medical doctor or other clinician, which includes alleviation of the symptoms of the disease or disorder being treated.
• the therapeutically effective amount is that which can treat or alleviate the disease or symptoms of the disease at a reasonable benefit/risk ratio applicable to any medical treatment.
• the total daily usage of the compounds and compositions described herein can be decided by the attending physician within the scope of sound medical judgment.
• the specific therapeutically-effective dose level for any particular patient will depend upon a variety of factors, including the condition being treated and the severity of the condition; activity of the specific compound employed; the specific composition employed; the age, body weight, general health, gender and diet of the patient: the time of administration, route of administration, and rate of excretion of the specific compound employed; the duration of the treatment; drugs used in combination or coincidentally with the specific compound employed; and like factors well known to the researcher, veterinarian, medical doctor or other clinician. It is also appreciated that the therapeutically effective amount can be selected with reference to any toxicity, or other undesirable side effect, that might occur during administration of one or more of the compounds described herein.
• alkyl refers to substituted or unsubstituted straight chain, branched and cyclic, saturated mono- or bi-valent groups having from 1 to 20 carbon atoms, 10 to 20 carbon atoms, 12 to 18 carbon atoms, 6 to about 10 carbon atoms, 1 to 10 carbons atoms, 1 to 8 carbon atoms, 2 to 8 carbon atoms, 3 to 8 carbon atoms, 4 to 8 carbon atoms, 5 to 8 carbon atoms, 1 to 6 carbon atoms, 2 to 6 carbon atoms, 3 to 6 carbon atoms, or 1 to 3 carbon atoms.
• Examples of straight chain mono-valent (C 1 -C 20 )-alkyl groups include those with from 1 to 8 carbon atoms such as methyl (i.e., CH 3 ), ethyl, n-propyi, n-butyl, n-pentyi, n-hexyl, n-heptyl, n-octyl groups.
• Examples of branched mono-valent (C 1 -CsoJ-aikyl groups include isopropyl, iso-butyl, sec-butyl, t-butyi, neopentyl, and isopentyl.
• Examples of straight chain bi- valent (C 1 -C 20 )aikyi groups include those with from 1 to 6 carbon atoms such as -CH 2 - -CH 2 CH 2 -, -CH 2 CH 2 CH 2 -, -CH 2 CH 2 CH 2 CH 2 -, and -CH 2 CH 2 CH 2 CH 2 CH 2 -.
• Examples of branched bi-valent alkyl groups include -CH(CH3)CH 2 - and -CH 2 CH(CH 3 )CH 2 -.
• cyclic alkyl groups include cyclopropyl, cyclobutyl, cyclopently, cyciohexyi, cyclooctyl, bicyclo[1.1 .I]pentyl, bicyclo[2.1 .1 ]hexyi, and bicyclo[2.2.1 ]heptyl.
• Cycioalkyl groups further include polycyclic cycloalkyl groups such as, but not limited to, norbornyl, adamantyl, bornyl, camphenyl, isocamphenyl, and carenyl groups, and fused rings such as, but not limited to, decaiinyl, and the like.
• aikyl includes a combination of substituted and unsubstituted alkyl.
• alkyl, and also (C 1 )alkyl includes methyl and substituted methyl.
• (C 1 )aikyl includes benzyl.
• alkyl can include methyl and substituted (C 2 -C 2 falkyl.
• Alkyl can also include substituted methyl and unsubstituted (C 2 -Csjalkyl.
• alkyl can be methyl and C 2 -Cg linear alkyl.
• alkyl can be methyl and C 2 -C 8 branched alkyl.
• methyl is understood to be -CH 3 , which is not substituted.
• methylene is understood to be -CH 2 -, which is not substituted.
• (C 1 )alkyl is understood to be a substituted or an unsubstituted -CH 3 or a substituted or an unsubstituted -CH 2 -.
• Representative substituted alkyl groups can be substituted one or more times with any of the groups listed herein, for example, cycloalkyl, heterocyclyl, aryl, amino, haloalkyl , hydroxy, cyano, carboxy, nitro, thio, alkoxy, and halogen groups.
• representative substituted alkyl groups can be substituted one or more fluoro, chloro, bromo, iodo, amino, amido, alkyl, alkoxy, alkylamido, alkenyl, alkynyl, aikoxycarbonyl, acyl, formyl, arylcarbonyi, aryloxycarbonyl, aryloxy, carboxy, haloalkyl, hydroxy, cyano, nitroso, nitro, azido, trifluoromethyl, trifiuoromethoxy, thio, alkylthio, arylthioi, alkylsulfonyl, aikyisulfinyl, dialkyiaminosuifonyl, sulfonic acid, carboxylic acid, dialkylamino and dialkyiamido.
• representative substituted alkyl groups can be substituted from a set of groups including amino, hydroxy, cyano, carboxy, nitro, thio and alkoxy, but not including halogen groups.
• alkyl can be substituted with a non-halogen group.
• representative substituted alkyl groups can be substituted with a fluoro group, substituted with a bromo group, substituted with a halogen other than bromo, or substituted with a halogen other than fluoro.
• representative substituted alkyl groups can be substituted with one, two, three or more fluoro groups or they can be substituted with one, two, three or more non-fluoro groups.
• aikyl can be trifluoromethyl, difluoromethyl, or fluoromethyl, or alkyi can be substituted aikyl other than trifluoromethyl, difluoromethyl or fluoromethyl.
• Alkyl can be haloalkyl or alkyl can be substituted alkyl other than haloalkyl.
• alkyl also generally refers to alkyl groups that can comprise one or more heteroatoms in the carbon chain.
• alkyi also encompasses groups such as --[(CH 2 )pO]qH and the like.
• alkenyl refers to substituted or unsubstituted straight chain, branched and cyclic, saturated mono- or bi-valent groups having at least one carbon-carbon double bond and from 2 to 20 carbon atoms, 10 to 20 carbon atoms, 12 to 18 carbon atoms, 6 to about 10 carbon atoms, 2 to 10 carbons atoms, 2 to 8 carbon atoms, 3 to 8 carbon atoms, 4 to 8 carbon atoms, 5 to 8 carbon atoms, 2 to 6 carbon atoms, 3 to 6 carbon atoms, 4 to 6 carbon atoms, 2 to 4 carbon atoms, or 2 to 3 carbon atoms.
• the double bonds can be be trans or cis orientation.
• the double bonds can be terminal or internal.
• the alkenyl group can be attached via the portion of the aikenyl group containing the double bond, e.g., vinyl, propen-1 -yl and buten-1 -yl, or the alkenyl group can be attached via a portion of the alkenyl group that does not contain the double bond, e.g., penten-4-yl.
• Examples of mono-valent (C 2 -C 20 )-alkenyl groups include those with from 1 to 8 carbon atoms such as vinyl, propenyl, propen-1 - yl, propen-2-yl, butenyl, buten-1-yl, buten-2-yl, sec-buten-1 -yl, sec-buten-3-yl, pentenyl, hexenyl, heptenyl and octenyl groups.
• Examples of branched mono-valent (C 2 -C 20 )-alkenyl groups include isopropenyl, iso-butenyi, sec-butenyl, t-butenyl, neopentenyl, and isopentenyl.
• Examples of straight chain bi-valent (C 2 -C 20 )alkenyl groups include those with from 2 to 6 carbon atoms such as -CHCH-, -CHCHCH 2 -, - CHCHCH 2 CH 2 -, and -CHCHCH 2 CH 2 CH 2 -.
• Examples of branched bi-vailing alkyl groups include -C(CH 3 )CH- and
• alkenyl groups include cyclopentenyl, cyclohexenyl and cyclooctenyl. It is envisaged that alkenyl can also include masked alkenyl groups, precursors of aikenyl groups or other related groups. As such, where alkenyl groups are described it, compounds are also envisaged where a carbon- carbon double bond of an alkenyl is replaced by an epoxide or aziridine ring.
• Substituted alkenyl also includes aikenyl groups which are substantially tautomeric with a non-alkenyi group.
• substituted alkenyl can be 2-aminoalkenyl, 2- alkylaminoalkenyl, 2-hydroxyalkenyl, 2-hydroxyvinyl, 2-hydroxypropenyl, but substituted alkenyl is also understood to include the group of substituted alkenyl groups other than alkenyl which are tautomeric with non-alkenyl containing groups.
• alkenyl can be understood to include a combination of substituted and unsubstituted alkenyl.
• alkenyl can be vinyl and substituted vinyl.
• alkenyl can be vinyl and substituted (C 3 -C 8 )alkenyl.
• Alkenyl can also include substituted vinyl and unsubstituted (C3-Cs)alkenyl.
• Representative substituted alkenyl groups can be substituted one or more times with any of the groups listed herein, for example, monoalkylamino, dialkylamino, cyano, acetyl, amido, carboxy, nitro, alkylthio, alkoxy, and halogen groups.
• representative substituted alkenyl groups can be substituted one or more fluoro, chloro, bromo, iodo, amino, amido, alkyl, aikoxy, alkylamido, alkenyl, alkynyi, alkoxycarbonyl, acyl, formyl, arylcarbonyl, aryloxycarbonyl, aryloxy, carboxy, haloalkyl, hydroxy, cyano, nitroso, nitro, azido, trifluoromethyl, trifluoromethoxy, thio, alkylthio, arylthiol, alkylsulfonyl, aikylsulfinyl, dialkylaminosulfonyl, sulfonic acid, carboxylic acid, dialkylamino and dialkylamido.
• representative substituted alkenyl groups can be substituted from a set of groups including monoalkylamino, dialkylamino, cyano, acetyl, amido, carboxy, nitro, alkylthio and alkoxy, but not including halogen groups.
• alkenyl can be substituted with a non-halogen group.
• representative substituted alkenyl groups can be substituted with a fluoro group, substituted with a bromo group, substituted with a halogen other than bromo, or substituted with a halogen other than fluoro.
• alkenyl can be 1- fluorovinyl, 2-fluorovinyl, 1 ,2-difiuorovinyi, 1 ,2,2-trifluorovinyl, 2,2-difiuorovinyl, trifluoropropen-2-yl, 3,3,3-trifiuoropropenyl, 1 -fluoropropenyl, 1 -chlorovinyl, 2- chlorovinyl, 1 ,2-dichlorovinyl, 1 ,2,2-trichlorovinyl or 2,2-dichlorovinyl.
• representative substituted alkenyl groups can be substituted with one, two, three or more fluoro groups or they can be substituted with one, two, three or more non-fluoro groups.
• alkynyi refers to substituted or unsubstituted straight and branched chain aikyi groups, except that at least one triple bond exists between two carbon atoms.
• alkynyi groups have from 2 to 50 carbon atoms, 2 to 20 carbon atoms, 10 to 20 carbon atoms, 12 to 18 carbon atoms, 6 to about 10 carbon atoms, 2 to 10 carbons atoms, 2 to 8 carbon atoms, 3 to 8 carbon atoms, 4 to 8 carbon atoms, 5 to 8 carbon atoms, 2 to 6 carbon atoms, 3 to 6 carbon atoms, 4 to 6 carbon atoms, 2 to 4 carbon atoms, or 2 to 3 carbon atoms.
• Examples include, but are not limited to ethynyl, propynyl, propyn-1 -yi, propyn-2-yl, butynyl, butyn-1 -yl, butyn- 2-yl, butyn-3-yl, butyn-4-yl, pentynyl, pentyn-1 -yl, hexynyl, Examples include, but are not limited to -C ⁇ CH, -C ⁇ C(CH 3 ). -C ⁇ C(CH 2 CH 3 ), -CH 2 G ⁇ CH, -CH 2 C ⁇ C(CH 3 ), and -CH 2 C ⁇ C(CH S CH 3 ) among others.
• aryl refers to substituted or unsubstituted univalent groups that are derived by removing a hydrogen atom from an arene, which is a cyclic aromatic hydrocarbon, having from 6 to 20 carbon atoms, 10 to 20 carbon atoms, 12 to 20 carbon atoms, 6 to about 10 carbon atoms or 6 to 8 carbon atoms.
• Examples of (C 6 -C2o)aryl groups include phenyl, napthaienyl, azulenyl, biphenylyl, indacenyl, fluorenyi, phenanthrenyl, triphenylenyl, pyrenyl, naphthacenyl, chrysenyl, anthracenyl groups.
• Examples include substituted phenyl, substituted napthaienyl, substituted azulenyl, substituted biphenylyl, substituted indacenyl, substituted fluorenyl, substituted phenanthrenyl, substituted triphenylenyl, substituted pyrenyl, substituted naphthacenyl, substituted chrysenyl, and substituted anthracenyl groups.
• Examples also include unsubstituted phenyl, unsubstituted napthaienyl, unsubstituted azulenyl, unsubstituted biphenyiyl, unsubstituted indacenyl, unsubstituted fluorenyi, unsubstituted phenanthrenyl, unsubstituted tnphenylenyl, unsubstituted pyrenyl, unsubstituted naphthacenyl, unsubstituted chrysenyl, and unsubstituted anthracenyi groups.
• Aryl includes phenyl groups and also non-phenyl aryl groups.
• (C 6 -C 20 )aryl encompasses mono- and polycyclic (C 6 - C 20 )aryl groups, including fused and non-fused polycyclic (C 6 -C 20 )aryl groups.
• heterocyclyl refers to substituted aromatic, unsubstituted aromatic, substituted non-aromatic, and unsubstituted non-aromatic rings containing 3 or more atoms in the ring, of which, one or more is a heteroatom such as, but not limited to, N, O, and S.
• a heterocyclyl can be a cyclo hetero a Iky I, or a heteroaryl, or if polycyclic, any combination thereof.
• heterocyclyl groups include 3 to about 20 ring members, whereas other such groups have 3 to about 15 ring members.
• heterocyclyl groups include heterocyclyl groups that include 3 to 8 carbon atoms (C 3 -C 8 ), 3 to 6 carbon atoms (C3- C 6 ) or 6 to 8 carbon atoms (C 6 -C 8 ).
• a heterocyclyl group designated as a C 2 - heterocyclyl can be a 5-membered ring with two carbon atoms and three heteroatoms, a 6-membered ring with two carbon atoms and four heteroatoms and so forth.
• a C4-heterocyclyl can be a 5-membered ring with one heteroatom, a 6-membered ring with two heteroatoms, and so forth.
• heterocyclyl group includes fused ring species including those that include fused aromatic and non-aromatic groups.
• heterocyclyl groups include, but are not limited to piperidynyl, piperazinyl, morpholinyl, furanyl, pyrrolidinyl, pyridinyl, pyrazinyl, pyrimidinyl, triazinyl, thiophenyl, tetrahydrofuranyl, pyrrolyl, oxazolyl, imidazolyl, triazyolyl , tetrazolyl, benzoxazolinyl, and benzimidazolinyl groups.
• heterocyclyl groups include, without limitation:
• a nitrogen- containing heterocyclyl group is a heterocyciyi group containing a nitrogen atom as an atom in toe ring.
• the heterocyciyi is other than thiophene or substituted thiophene.
• the heterocyciyi is other than furan or substituted furan.
• alkoxy refers to an oxygen atom connected to an alkyl group, including a cycloalkyl group, as are defined herein.
• linear alkoxy groups include but are not limited to methoxy, ethoxy, propoxy, butoxy, pentyloxy, hexyloxy, and the like.
• branched alkoxy include but are not limited to isopropoxy, sec-butoxy, tert-butoxy, isopentyloxy, isohexyloxy, and the like.
• cyclic alkoxy examples include but are not limited to cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, cyclohexyloxy, and the like.
• An alkoxy group can include one to about 12-20 or about 12-40 carbon atoms bonded to the oxygen atom, and can further include double or triple bonds, and can also include heteroatoms.
• alkyoxy also includes an oxygen atom connected to an aikyenyl group and oxygen atom connected to an alkynyl group.
• an ailyloxy group is an alkoxy group within the meaning herein.
• a methoxyethoxy group is also an alkoxy group within the meaning herein, as is a methylenedioxy group in a context where two adjacent atoms of a structure are substituted therewith.
• aryloxy refers to an oxygen atom connected to an aryl group as are defined herein.
• aralkyl and “arylalkyl” as used herein refers to alkyl groups as defined herein in which a hydrogen or carbon bond of an alkyl group is replaced with a bond to an aryl group as defined herein.
• Representative aralkyl groups include benzyl, biphenylmethyl and phenylethyl groups and fused (cycloalkylaryl)alkyl groups such as 4-ethyl-indanyl.
• Aralkenyl groups are alkenyl groups as defined herein in which a hydrogen or carbon bond of an alkyl group is replaced with a bond to an aryl group as defined herein.
• halo means, unless otherwise stated, a fluorine, chlorine, bromine, or iodine atom.
• amine and “amino” as used herein refers to a substituent of the form -NH 2 , -NHR, -NR 2 , -NR 3 + , wherein each R is independently selected, and protonated forms of each, except for -NR 3 + , which cannot be protonated. Accordingly, any compound substituted with an amino group can be viewed as an amine.
• An “amino group” within the meaning herein can be a primary, secondary, tertiary, or quaternary amino group.
• An “alkylamino” group includes a monoalkylamino, dialkylamino, and trialkylamino group.
• acyl refers io a group containing a carbonyl moiety wherein the group is bonded via the carbonyl carbon atom.
• the carbonyl carbon atom is also bonded to another carbon atom, which can be part of a substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, cycloalkyl, heterocyclyl, group or the like.
• formyl refers to a group containing a carbonyl moiety wherein the group is bonded via the carbonyl carbon atom.
• the carbonyl carbon atom is also bonded to a hydrogen atom.
• alkoxycarbonyl refers to a group containing a carbonyi moiety wherein the group is bonded via the carbonyl carbon atom.
• the carbonyl carbon atom is also bonded to an oxygen atom which is further bonded to an alkyl group.
• Alkoxycarbonyl also includes the group where a carbonyl carbon atom is also bonded to an oxygen atom which is further bonded to an alkyenyl group.
• Alkoxycarbonyl also includes the group where a carbonyl carbon atom is also bonded to an oxygen atom which is further bonded to an alkynyl group.
• alkoxycarbonyl as the term is defined herein, and is also included in the term “aryloxycarbonyl,” the carbonyl carbon atom is bonded to an oxygen atom which is bonded to an aryl group instead of an alkyl group.
• arylcarbonyl refers to a group containing a carbonyl moiety wherein the group is bonded via the carbonyl carbon atom.
• the carbonyl carbon atom is also bonded to an aryl group.
• alkylamido refers to a group containing a carbonyl moiety wherein the group is bonded via the carbonyl carbon atom.
• the carbonyl carbon atom is also bonded to a nitrogen group which is bonded to one or more alkyl groups.
• the carbonyl carbon atom is bonded to a nitrogen atom which is bonded to one or more aryl group instead of, or in addition to, the one or more alkyl group.
• the carbonyl carbon atom is bonded to an nitrogen atom which is bonded to one or more alkenyl group instead of, or in addition to, the one or more alkyl and or/aryl group.
• the carbonyl carbon atom is bonded to a nitrogen atom which is bonded to one or more alkynyl group instead of, or in addition to, the one or more alkyl, alkenyl and/or aryl group.
• carboxy refers to a group containing a carbonyl moiety wherein the group is bonded via the carbonyl carbon atom.
• the carbonyl carbon atom is also bonded to a hydroxy group or oxygen anion so as to result in a carboxylic acid or carboxylate.
• Carboxy also includes both the protonated form of the carboxylic acid and the salt form.
• carboxy can be understood as COOH or CO 2 H.
• amido refers to a group having the formula C(O)NRR, wherein R is defined herein and can each independently be, e.g., hydrogen, alkyl, aryl or each R, together with the nitrogen atom to which they are attached, form a heterocyciyl group.
• alkylthio refers to a sulfur atom connected to an alkyl, alkenyl, or alkynyl group as defined herein.
• arylthio refers to a sulfur atom connected to an aryl group as defined herein.
• alkylsulfonyl refers to a sulfonyl group connected to an alkyl, alkenyl, or alkynyl group as defined herein.
• alkylsulfinyl refers to a sulfinyl group connected to an alkyl, alkenyl, or alkynyl group as defined herein.
• diaikylaminosuifonyl refers to a sulfonyl group connected to a nitrogen further connected to two alkyl groups, as defined herein, and which can optionally be linked together to form a ring with the nitrogen. This term also includes the group where the nitrogen is further connected to one or two alkenyl groups in place of the alkyl groups.
• dialkylamino refers to an amino group connected to two alkyl groups, as defined herein, and which can optionally be linked together to form a ring with the nitrogen. This term also includes the group where the nitrogen is further connected to one or two alkenyl groups in place of the alkyl groups.
• dialkylamido refers to an amido group connected to two alkyl groups, as defined herein, and which can optionally be linked together to form a ring with the nitrogen. This term also includes the group where the nitrogen is further connected to one or two alkenyl groups in place of the alkyl groups.
• substituted refers to a group that is substituted with one or more groups including, but not limited to, the following groups: halogen (e.g., F, Ci, Br, and I), R, OR, ROH (e.g., CH 2 OH), OC(O)N(R) 2 , CN, NO, NO 2 , ONO2, azido, CF 3 , OCF3, methylenedioxy, ethylenedioxy, (C3-C2o)heteroaryl, N(R) 2 , Si(R) 3 , SR, SOR, SOsR, SO 2 N(R) 2 , SO 3 R, P(O)(OR) 2 , OP(O)(OR) 2 , C(O)R, C(O)C(O)R, C(O)CH 2 C(O)R, C(S)R, C(O)OR, OC(O)R, C(O)N(R) 2
• halogen e.g., F, Ci,
• f and g are each independently an integer from 1 to 5Q (e.g., 1 to 10, 1 to 5, 1 to 3 or 2 to 5).
• Substituted also includes a group that is substituted with one or more groups including, but not limited to, the following groups: fluoro, chloro, bromo, iodo, amino, amido, alkyl, hydroxy, alkoxy, alkylamido, alkenyl, alkynyl, alkoxycarbonyl, acyl, formyl, arylcarbonyl, aryloxycarbonyl, aryloxy, carboxy, haloalkyl, hydroxy, cyano, nitroso, nitro, azido, trifluoromethyl, trifluoromethoxy, thio, aikylthio, arylthiol, alkylsulfonyl, alkylsulfinyi, dialkyiaminosulfonyi, sulfonic acid, carboxylic acid, dialkyiamino and dialkylamido.
• groups including, but not limited to, the following groups: fluoro, chloro, bro
• the substituents can be linked to form a carbocyclic or heterocyclic ring.
• Such adjacent groups can have a vicinal or germinal relationship, or they can be adjacent on a ring in, e.g., an ortho- arrangement.
• Each instance of substituted is understood to be independent.
• a substituted aryl can be substituted with bromo and a substituted heterocycle on the same compound can be substituted with aikyl.
• a substituted group can be substituted with one or more non-fluoro groups.
• a substituted group can be substituted with one or more non-cyano groups.
• a substituted group can be substituted with one or more groups other than haloalkyl.
• a substituted group can be substituted with one or more groups other than tert-butyl.
• a substituted group can be substituted with one or more groups other than trifluoromethyi.
• a substituted group can be substituted with one or more groups other than nitro, other than methyl, other than methoxymethyl, other than dialkyiaminosulfonyi, other than bromo, other than chloro, other than amido, other than halo, other than benzodioxepinyl, other than polycyclic heterocyclyl, other than polycyclic substituted aryl, other than meth oxy carbonyl, other than alkoxycarbonyl, other than thiophenyl, or other than nitrophenyl, or groups meeting a combination of such descriptions.
• substituted is also understood to include fluoro, cyano, haloalkyl, tert-butyl, trifluoromethyi, nitro, methyl, methoxymethyl, dialkyiaminosulfonyi, bromo, chloro, amido, haio, benzodioxepinyl, polycyclic heterocyclyl, polycyclic substituted aryl, methoxycarbonyl, alkoxycarbonyl, thiophenyl, and nitrophenyl groups.
• the compounds described herein can contain chiral centers. All diastereomers of the compounds described herein are contemplated herein, as well as racemates.
• salts and “pharmaceutically acceptable salts” refer to derivatives of the disclosed compounds wherein the parent compound is modified by making acid or base salts thereof.
• pharmaceutically acceptable salts include, but are not limited to, mineral or organic acid salts of basic groups such as amines; and alkali or organic salts of acidic groups such as carboxylic acids.
• Pharmaceutically acceptable salts include the conventional non-toxic salts or the quaternary ammonium salts of the parent compound formed, for example, from non-toxic inorganic or organic acids.
• such conventional non-toxic salts include those derived from inorganic acids such as hydrochloric, hydrobromic, sulfuric, sulfamic, phosphoric, and nitric; and the salts prepared from organic acids such as acetic, propionic, succinic, glycolic, stearic, lactic, malic, tartaric, citric, ascorbic, pamoic, maleic, hydroxymaieic, phenyiacetic, glutamic, benzoic, salicylic, sulfanilic, 2- acetoxybenzoic, fumaric, toluenesulfonic, methanesulfonic, ethane disulfonic, oxalic, and isethionic, and the like.
• inorganic acids such as hydrochloric, hydrobromic, sulfuric, sulfamic, phosphoric, and nitric
• organic acids such as acetic, propionic, succinic, glycolic, stearic, lactic,
• salts can be synthesized from the parent compound which contains a basic or acidic moiety by conventional chemical methods.
• such salts can be prepared by reacting the free acid or base forms of these compounds with a stoichiometric (or larger) amount of the appropriate base or acid in water or in an organic solvent, or in a mixture of the two; generally, nonaqueous media like ether, ethyl acetate, ethanol, isopropanol, or acetonitrile are preferred.
• Lists of suitable salts are found in Remington’s Pharmaceutical Sciences, 17th ed., Mack Publishing Company, Easton, Pa., 1985, the disclosure of which is hereby incorporated by reference.
• solvate means a compound, or a salt thereof, that further includes a stoichiometric or non-stoichlometric amount of solvent bound by non- covalent intermolecular forces. Where the solvent is water, the solvate is a hydrate.
• prodrug means a derivative of a compound that can hydrolyze, oxidize, or otherwise react under biological conditions (in vitro or in vivo) to provide an active compound, particularly a compound of the invention.
• prodrugs include, but are not limited to, derivatives and metabolites of a compound of the invention that include biohydrolyzabie moieties such as biohydrolyzable amides, biohydrolyzabie esters, biohydrolyzable carbamates, biohydrolyzabie carbonates, biohydrolyzabie ureides, and biohydrolyzabie phosphate analogues.
• Specific prodrugs of compounds with carboxyl functional groups are the lower alkyl esters of the carboxylic acid.
• the carboxylate esters are conveniently formed by esterifying any of the carboxylic acid moieties present on the molecule.
• Prodrugs can typically be prepared using well-known methods, such as those described by Burger’s Medicinal Chemistry and Drug Discovery 6th ed. (Donald J. Abraham ed., 2001 , Wiley) and Design and Application of Prodrugs (H. Bundgaard ed., 1985, Harwood Academic Publishers GmbH).
• the term “subject” or “patient” refers to any organism to which a composition described herein can be administered, e.g., for experimental, diagnostic, prophylactic and/or therapeutic purposes.
• Subject refers to a mammal receiving the compositions disclosed herein or subject to disclosed methods. It is understood and herein contemplated that “mammal” includes but is not limited to humans, non-human primates, cows, horses, dogs, cats, mice, rats, rabbits, and guinea pigs.
• substantially refers to a majority of, or mostly, as in at least about 50%, 60%, 70%, 80%, 90%, 95%, 96%, 97%, 98%, 99%, 99.5%, 99.9%, 99.99%, or at least about 99.999% or more.
• the human proteasome is part of the cellular machinery that regulates protein degradation. Most proteins are degraded by the 26S proteasome via a ubiquitin-dependent mechanism, however intrinsically disordered proteins (unstructured) proteins can also be degraded the 20S isoform of the proteasome via a ubiquitin-independent mechanism. Intrinsically disordered proteins (IDPs) are named for their lack of tertiary structure allowing them to adopt numerous conformations and interact with multiple binding partners. When the synthesis of IDPs outpaces their rate of degradation, they accumulate and induce toxic signaling events that drive many human diseases.
• IDPs Intrinsically disordered proteins
• c-MYC pro-oncogenic transcription factor
• Overexpression of c-MYC is the driving force in an astonishing 60-70% of all human cancers including multiple myeloma, histiocytic sarcoma, myeloid leukemia, glioblastoma, melanoma, breast cancer, colon cancer, cervical cancer, small-cell lung carcinoma, and osteosarcoma.
• Small molecule 20S proteasome activators can reduce c-MYC protein levels and therefore prevent the initiation progression and relapse in c-MYC driven cancers.
• the disclosure relates to small molecule 20S proteasome activators of the formulae (I), (I a)-(lc), (Il)-(V), and (Va) as therapeutic agents to treat amyioidogenic diseases including neurodegenerative diseases and type II diabetes.
• Neurodegenerative diseases include: Alzheimer's disease (AD) and other dementias, Parkinson’s disease (PD) and PD-related disorders, Prion disease, Motor neuron diseases (MND), Huntington’s disease (HD), Spinocerebellar ataxia (SCA) and Spinal muscular atrophy (SMA).
• AD Alzheimer's disease
• PD Parkinson’s disease
• PD-related disorders Prion disease
• Motor neuron diseases MND
• HD Huntington’s disease
• SCA Spinocerebellar ataxia
• SMA Spinal muscular atrophy
• IDPs intrinsically disordered proteins
• DPR dipeptide repeat
• the antihistamine drug astemizole (FIG. 1 A, 1 ) as a promising new scaffold for the development of 20S activators due to its strong enhancement of 20S proteolysis.
• Astemizole Astemizole’s 20S proteasome activity, a series of assays were performed using each of three fluorogenic peptide substrates. These substrates were a chymotryptic-like (CT-L), a trypsin-like (T-L) and a caspase-like (Casp-L) substrate, one for each of the catalytic sites of the proteasome. It has been shown that the proteasome’s active sites aliosterically regulate each other in the presence of their individual substrates.
• C-L chymotryptic-like
• T-L trypsin-like
• Casp-L caspase-like
• Astemizole is a potent antihistamine as an H1 receptor antagonist. As such, it has good drug-like properties and penetrates the blood brain barrier (BBB) effectively, which makes it a promising scaffold for the development of novel 20S activators. On the other hand, due to its activity and side-effects (QTc interval prolongation and related arrhythmias due to hERG channel blockade) it cannot be repurposed therapeutically without modification. Therefore, structural modifications known to reduce its H1 - receptor activity and possible side effects were prepared. N- acyiated astemizole (2), was designed to eliminate fluspirilene’s H1 receptor activity. In this scaffold, the basicity of the piperidine’s amine has been reduced through its conversion to an amide.
• N-acyl astemizole (2) was prepared as described in Scheme 1).
• Benzylation of compound 3 was accomplished using KOH and 4- fluorobenzyl bromide.
• Various substituents can be incorporated into the C-2 position using different nucleophiles.
• compound 4 was prepared by heating 3 with ethyl 4-aminopiperidinecarboxylate. Deprotection of the ethyl carbamate using HBr provided compound 7. Acylation of the piperidine with 4-methoxyphenylacetyl chloride rendered N-acyl astemizoles (2).
• HCT-116 cells stable transfected Myc-Luc reported cells were seeded in a white, clear bottom, 96-well micropiate at 25,000 cells/well, in McCoy's 5A media supplemented with 10% FBS and 1 % Penicillin/Streptomycin. The plate was incubated at 37°C with 5% CO2 overnight.
• NF-KB reporter assay HCT-116 stable transfected NF-kappaB-luc reporter cells were seeded into in a white, clear bottom, 96-well micropiate at 5,000 cells/well, in McCoy’s 5A media supplemented with 10% FBS and 1% Penicillin/Streptomycin. The plate was incubated at 37°C with 5% C02 overnight.
• Ffoorogenlc peptide degradation 20S proteasome activity assay were carried out in a 100 pL reaction volume. Different concentrations (1-80 pM) of test compounds were added to a black flat/clear bottom 96-well plate containing 1 nM of human constitutive 20S proteasome, in 50 mM Tris- HCI at pH 7,8, 100 mM NaCI and allowed to incubate for 15 min at 37°C, Fluorogenic substrates were then added and the enzymatic activity measured at 37°G on a SpectraMax M5e spectrometer by measuring the change in fluorescence unit per minute for 1 hour at 380-460 nm.
• the fluorescence units for the vehicle control were set at a 100%, and the ratio of drug-treated sample set to that of vehicle control was used to calculate the fold change in enzymatic activity.
• the fluorogenic substrates used were one of the following: Suc-LLVY-AMC (CT-L activity, 20 pM), Z-LLE-AMC (Gasp- L activity, 20 pM), Boc-LRR-AMC (T-L activity, 40 pM) or a combination of the three substrates each at 6.67 pM.
• Digestion of a-synuclein was carried out in a 50 ⁇ L reaction volume made of 50 mM Tris, 100 mM NaCI at pH 7.8; 0.5 ⁇ M purified a-synuclein and 15 nM purified human 20S proteasome. Briefly, 20S proteasome was diluted to 17 nM in the reaction buffer. Test compounds or vehicle (1 pL of 50x stock or DMSO) were added to 44 pL of 7.58 nM 20S and incubated at 37°C for 15 min. 5 ⁇ L of 5 pM a-synuclein substrate was then added to the reaction mixture and incubated at 37°C for 2 hours.
• Myo reporter (Luc) HCT-116 cells were seeded in a white, clear bottom, 96-well microplate at 25,000 ceils/well, in McCoy’s 5A media supplemented with 10% FBS and 1% Penicillin/Streptomycin. The plate was incubated at 37°C with 5% CO 2 overnight. The next day, cells were treated with O.O ⁇ M, 0.1 pM, 1 ,0pM, 2.5 ⁇ M, 5.0pM, 10pM, or 20pM TCH-165, in Opti-MEM supplemented with 0.5% FBS, 1% Non- essential amino acids, 1 mM Sodium Pyruvate and 1% Penicillin/Streptomycin. The plate was incubated at 37 ° C with 5% CO 2 for 16 hours. Firefly luminescence was measured using the One-Step Luciferase Assay System from BPS Biosciences.
• Embodiment 1 relates to a compound of the formula (I): or a pharmaceutically acceptable salt, polymorph, prodrug, solvate or clathrate thereof, wherein:
• R 1 is aryl or heteroaryl
• R 2 is H, alkyl, aryl or heteroaryl
• X 1 is alkyl or alkenyl
• X 2 is N or CR 3 , wherein R 3 is absent, hydrogen, alkyl, heterocyclyi, or aryl;
• R 4 is hydrogen, alkyl, cycloalkyl, heterocyclyi, aryl or heteroaryl
• R 5 is hydrogen, alkyl, cycloalkyl, heterocyclyi, aryl or heteroaryl.
• Embodiment 2 relates to the compound of Embodiment 1 , wherein R' is aryl.
• Embodiment 3 relates to the compound of Embodiments 1 -2, wherein
• R' is substituted aryl
• Embodiment 4 relates to the compound of Embodiments 1 -3, wherein R ! is substituted phenyl.
• Embodiment 5 relates to the compound of Embodiment 1 , wherein R ! is heteroaryl.
• Embodiment 6 relates to the compound of Embodiment 1 , wherein R 1 is benzimidazolinyi.
• Embodiment 7 relates to the compound of Embodiments 1 -6, wherein R 2 is H.
• Embodiment 8 relates to the compound of Embodiments 1 -7, wherein
• Embodiment 9 relates to the compound of Embodiments 1 -8, wherein X 1 is C 1 -C 6 alkyl.
• Embodiment 10 relates to the compound of Embodiments 1 -9, wherein the compound of formula (I) is a compound of the formula (la): or a pharmaceutically acceptable salt, polymorph, prodrug, solvate or clathrate thereof; wherein:
• Embodiment 11 relates to the compound of Embodiments 1 -10, wherein the compound of formula (I) is a compound of the formula (lb) or (Ic):
• Embodiment 12 relates to the compound of Embodiments 1 -11 , wherein the compound of formula (I) is a compound of the formula:
• Embodiment 13 relates to a compound of the formula: or a pharmaceutically acceptable salt, polymorph, prodrug, solvate or clathrate thereof, wherein:
• R 1 is aryl or heteroaryl
• R 2 is H, alkyl, aryl or heteroaryl
• X 1 is alkyl or alkenyl
• X 2 is N or CR 3 , wherein R 3 is absent, hydrogen, alkyl, heterocyclyi, or aryl;
• R 6 is aryl or heteroaryl.
• Embodiment 14 relates to the compound of Embodiment 13, wherein the compound is a compound of the formula:
• R 9 is alkyl , cycloalkyl aryl, heteroaryl, acyl, amide or carbamate; and each R 10 is independently H, halo, alkyl, haloalkyl, alkoxy or heterocyciyl; or two R 10 groups on adjacent carbon atoms, together with those carbon atoms, can form a cycloalkenyi, aryl or heterocyciyl; or
• R 9 and an R 10 together with the atoms to which they are attached, can form a heterocylyl group.
• Embodiment 15 relates to a compound of the formula (II) and (lla)-(lld):
• q is 0, 1 , 2 or 3; each X' is independently alkyl or alkenyl;
• R 8 and R 9 are each independently alkyl, cycloalkyl aryl, heteroaryl, acyl, amide or carbamate;
• W is N or C-R 10 ;
• X is N or C-R 10 ;
• Y is N or C-R 10 ; and
• Z is N or C-R 10 ; wherein each R 10 is independently H, halo, alkyl, haloalkyl, alkoxy or heterocyclyl; or two R 10 groups on adjacent carbon atoms, together with those carbon atoms, can form a cycloalkenyl, aryl or heterocyclyl; or
• R 9 and an R 10 together with the atoms to which they are attached, can form a heterocyiyl group.
• Embodiment 16 relates to the compound of Embodiment 15, wherein X 1 is -(CH 2 )n-, wherein n is 0, 1 , or 2.
• Embodiment 17 relates to the compound of Embodiments 15-16, wherein R 10 is alkoxy of the formula -OR 11 , wherein R 11 is alkyl, cycloalkyl or aryi, heteroaryi, acyl, amide or carbamate.
• Embodiment 18 relates to the compound of Embodiments 15-17, wherein the compound is a compound of the formula:
• Embodiment 19 relates to the compound of Embodiments 15-18, wherein the compound is a compound wherein R 9 and R 10 , together with the atoms to which they are atached, can form a heterocylyl group: or a pharmaceutically acceptable salt, polymorph, prodrug, solvate or clathrate thereof.
• Embodiment 20 relates to the compound of Embodiments 15-18, wherein the compound is a compound of the formula: or a pharmaceutically acceptable salt, polymorph, prodrug, solvate or clathrate thereof.
• Embodiment 21 relates to the compound of Embodimen 15, wherein the compound is a compound of the formula: or a pharmaceutically acceptable salt, polymorph, prodrug, solvate or clathrate thereof.
• Embodiment 22 relates to a compound of the formula (III): or a pharmaceutically acceptable salt, polymorph, prodrug, solvate or clathrate thereof, wherein: q is 0, 1 , 2 or 3; X 1 is alkyl or alkenyl;
• W is N or C-R 10 ;
• X is N or C-R 10 ;
• Y is N or C-R 10 ; and
• Z is N or C-R 10 ; wherein each R 10 is independently H, halo, alkyl, haloalkyl, alkoxy or heterocyclyl; or two R 10 groups on adjacent carbon atoms, together with those carbon atoms, can form a cycloalkenyl, aryl or heterocyclyl; or
• R s and an R 10 together with the atoms to which they are attached, can form a heterocylyl group
• R 12 and R 13 are each independently alkyl, cycloalkyl aryl, heteroaryl, acyl, amide or carbamate.
• Embodiment 23 relates to the compound of Embodiment 22, wherein X 1 is -(CH 2 )n-, wherein n is 0, 1 , or 2.
• Embodiment 24 relates to the compound of Embodiments 22-23, wherein R 10 is alkoxy of the formula -OR 11 , wherein R 11 is alkyl, cycloalkyl or aryl, heteroaryl, acyl, amide or carbamate.
• Embodiment 25 relates to the compound of Embodiments 22-24, wherein the compound is a compound of the formula: or a pharmaceutically acceptable salt, polymorph, prodrug, solvate or clathrate thereof.
• Embodiment 26 relates to the compound of Embodiments 22-25, wherein the compound is a compound wherein R 9 and R 10 or R 9 and R 13 , together with the atoms to which they are attached, form a heterocylyl group: or a pharmaceutically acceptable salt, polymorph, prodrug, solvate or clathrate thereof.
• Embodiment 27 relates to the compound of Embodiments 22-26, wherein the compound is a compound of the formula: or a pharmaceutically acceptable salt, polymorph, prodrug, solvate or clathrate thereof.
• Embodiment 28 relates to a compound of the formula (IV): or a pharmaceutically acceptable salt, polymorph, prodrug, solvate or clathrate thereof, wherein: q is 0, 1 , 2 or 3; X 1 is alkyl or alkenyl;
• W is N or C-R 10 ;
• X is N or C-R 10 ;
• Y is N or C-R 10 ; and
• Z is N or C-R 10 ; wherein each
• R 10 is independently H, halo, alkyl, haloalkyl, alkoxy or heterocyclyl; or two R 10 groups on adjacent carbon atoms, together with those carbon atoms, can form a cycloalkenyl, aryl or heterocyclyl; or R 9 and an R 10 , together with the atoms to which they are attached, can form a heterocyiyl group; and
• R 14 is aryl or heterocyclyi
• R 9 and R 14 together with the atoms to which they are attached, can forma an aryl or a hetorcyclyi.
• Embodiment 29 relates to the compound of Embodiment 28, wherein X 1 is -(CH 2 ) n -, wherein n is 0, 1 , or 2.
• Embodiment 30 relates to the compound of Embodiments 28-29, wherein R 10 is alkoxy of the formula -OR 11 , wherein R 11i is alkyl, cycioaikyl or aryl, heteroaryi, acyl, amide or carbamate.
• Embodiment 31 relates to the compound of Embodiments 28-30, wherein the compound is a compound of the formula: or a pharmaceutically acceptable salt, polymorph, prodrug, solvate or clathrate thereof.
• Embodiment 32 relates to the compound of Embodiments 28-31 , wherein the compound is a compound wherein R 9 and R 10 or R 9 and R 14 , together with the atoms to which they are attached, form a heterocyiyl group: or a pharmaceutically acceptable salt, polymorph, prodrug, solvate or clathrate thereof.
• Embodiment 33 relates to a compound of the formula (V): or a pharmaceutically acceptable salt, polymorph, prodrug, solvate or clathrate thereof, wherein: q is 0, 1 , 2 or 3;
• X 1 is alkyl or alkenyl
• Z 1 is absent, N or C-R 10 ; each W is N or C-R 10 ; each X is N or C-R 10 ; each Y is N or C-R 10 ; and each Z is N or C-R 10 ; wherein each R 10 is independently H, halo, alkyl, haloalkyl, alkoxy or heterocyclyl; and two R 10 groups on adjacent carbon atoms, together with those carbon atoms, can form a cycloalkenyl, aryl or heterocyclyl; or
• R 9 and an R 10 together with the atoms to which they are attached, can form a heterocylyl group
• Embodiment 34 relates to the compound of Embodiment 33, wherein X 1 is -(CH 2 )n-, wherein n is 0, 1 , or 2.
• Embodiment 35 relates to the compound of Embodiments 33-34, wherein R 10 is alkoxy of the formula -OR’ 1 , wherein R 11 is alkyl, cycloalkyl or aryl, heteroaryl, acyl, amide or carbamate.
• Embodiment 36 relates to the compound of Embodiments 33-35, wherein the compound is a compound of the formula or a pharmaceutically acceptable salt, polymorph, prodrug, solvate or clathrate thereof.
• Embodiment 37 relates to the compound of Embodiments 33-36, wherein the compound is a compound wherein R 9 and R 10 form a heterocylyl group: or a pharmaceutically acceptable salt, polymorph, prodrug, solvate or clathrate thereof.
• Embodiment 38 relates to the compound of Embodiment 33, wherein the compound is a compound of the formula: or a pharmaceutically acceptable salt, polymorph, prodrug, solvate or clathrate thereof.
• Embodiment 39 relates to the compound of Embodiment 33, wherein the compound is a compound of the formula: acceptable salt, polymorph, prodrug, solvate or clathrate thereof.
• Embodiment 40 relates to a pharmaceutical composition comprising one or more compounds of Embodiments 1 -39 and one or more pharmaceutically acceptable excipients.
• Embodiment 41 relates to a method for treating a neurodegenerative disease comprising administering a therapeutically effective amount of astemizole, at least one compound of Embodiments 1 -39 or a pharmaceutical composition of Embodiment 40 to a subject in need thereof.
• Embodiment 42 relates to the method of Embodiment 40, wherein the neurodegenerative disease is at least one of Parkinson’s disease, Alzheimer’s disease, Huntington's disease, and ALS.
• Embodiment 43 relates to a method for reducing, substantially eliminating or eliminating dysregulation of proteostasis comprising administering a therapeutically effective amount of astemizole, at least one compound of Embodiments 1 -39 or a pharmaceutical composition of Embodiment 40 to a subject in need thereof.
• Embodiment 44 relates to a method for reducing, substantially eliminating or eliminating the accumulation of intrinsically disordered proteins comprising administering a therapeutically effective amount of astemizole, at least one compound of Embodiments 1 -39 or a pharmaceutical composition of Embodiment 40 to a subject in need thereof.
• Embodiment 45 relates to the method of Embodiment 44, wherein the intrinsically disordered proteins comprise ⁇ -syn.

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