Patent Application
20230121312
Sorbitol-dehydrogenase (SDH) is a member of the medium-chain dehydrogenase/reductase protein family and the second enzyme of the polyol pathway of glucose metabolism. In this pathway, when glucose concentration in the cell becomes too high, Aldose Reductase (AR) reduces glucose to sorbitol using nicotinamide adenine dinucleotide phosphate (NADPH) as a cofactor. Sorbitol is then oxidized to fructose by sorbitol dehydrogenase, which uses nictotinamide adenine dinucleotide (NAD) as a cofactor (Tang et al., (2012), Frontiers in Pharmacology, 3;87). SDH is expressed almost in all mammalian tissues.
Sorbitol-dehydrogenase (SDH) deficiency and other genetic deficiencies of enzymes involved in sorbitol metabolism or genetic conditions that elevate sorbitol levels are characterized by damage to the eyes, central nervous system, and kidneys among other things. SDH deficiency is a genetic condition characterized by the failure to breakdown sorbitol into fructose due to a deficiency of the enzyme. Sorbitol is an alcohol, highly hydrophilic by nature, does not diffuse easily through the cell membrane and therefore accumulates intracellularly.
The clinical effects of SDH deficiency are due to accumulation of sorbitol leading to osmotic swelling, changes in membrane permeability and also oxidative stress, thereby culminating in tissue injury. Id. Indeed, excess formation of sorbitol has been linked to damage to the eyes, central nervous system, and kidney. Id. For example, accumulation of intracellular sorbitol due to increased aldose reductase activity has been implicated in the development of various secondary complications of diabetes, such as cataracts, retinopathy, nephropathy, and neuropathy.
There is currently no cure for complications associated with sorbitol accumulation. Accordingly, there is a recognized but unmet need for methods for the treatment and/or the management of genetic and or metabolic disorders that alter sorbitol metabolism or causesover production of sorbitol.
This disclosure relates to methods for treating genetic and or metabolic disorders that alter sorbitol metabolism or causesover production of sorbitol, such as sorbitol-dehydrogenase (SDH) deficiency, elevated aldose reductase activity, fructokinase deficiency. The method comprises administering a therapeutically effective amount of an Aldose Reducatase (AR) inhibitor to a subject in need thereof. Without wishing to be bound by any particular theory, it is believed that inhibition of AR can reduce the accumulation of sorbitol in tissues such as retina, sciatic nerves, spinal cords, liver and kidney.
The disclosure also relates to methods for decreasing sorbitol accumulation in a subject with sorbitol-dehydrogenase (SDH) deficiency, comprising administering a therapeutically effective amount of an aldose reductase inhibitor to the subject.
In some embodiments, the disclosure relates to methods for decreasing sorbitol accumulation in a subject with a genetic disorder, comprising administering a therapeutically effective amount of an aldose reductase inhibitor to the subject.
The genetic disorder is any disorder that alters metabolism of sorbitol or causes over-production of sorbitol.
This disclosure also relates to a method for treating hereditary neuropathies, such as Charcot-Marie-Tooth disease (CMT) including Charcot-Marie-Tooth neuropathy type 1 (CMT1), a demyelinating peripheral neuropathy, or Charcot-Marie-Tooth neuropathy type 2 (CMT2), an axonal (non-demyelinating) peripheral neuropathy. In some aspects the CMT2 is distal hereditary motor neuropathy (dHMN).
In examples, the methods comprise administering to a subject in need thereof a therapeutically effective amount of zopolrestat. In examples, the methods comprise administering to a subject in need thereof an therapeutically effective amount of a compound of any one of Formulas (I)-(VI). In some aspects, the AR inhibitor administered is not ponalrestat, epalrestat, sorbinil or sorbinol, imirestat, AND-138, CT-112, zopolrestat, zenarestat, BAL-AR18, AD-5467, M-79175, tolrestat, alconil, statil, berberine or SPR-210. In examples, the methods exclude the administration of Epalrestat.
In other embodiments, the disclosure relates to a method of treating sorbitol-dehydrogenase (SDH) deficiency in a subject in need thereof comprising, administering a therapeutically effective amount of a pharmaceutical composition comprising AR inhibitor, such as a compound of any one of Formulas (I)-(VI), and a pharmaceutically acceptable carrier.
In other embodiments, the disclosure relates to a method of treating sorbitol-dehydrogenase (SDH) deficiency in a subject in need thereof comprising, administering an therapeutically effective amount of
(a) a compound of Formulas (I)-(VI) and a pharmaceutically acceptable carrier; and
(b) one or more of alponalrestat, epalrestat, sorbinil or sorbinol, imirestat, AND-138, CT-112, zopolrestat, zenarestat, BAL-AR18, AD-5467, M-79175, tolrestat, alconil, statil, berberine or SPR-210.
In other embodiments, this disclosure relates to the use of an AR inhibitor in the treatment of genetic and/or metabolic disorders that alter sorbitol metabolism or causesover production of sorbitol, such as SDH deficiency.
In other embodiments, this disclosure relates to the use of an AR inhibitor for the manufacture of a medicament for treating genetic and/or metabolic disorders that alter sorbitol metabolism or causes over production of sorbitol, such as SDH deficiency.
The disclosure also relates to the use of an AR inhibitor (e.g., zopolrestat, epalrestat, compound of any one of Formulas (I)-(VI)) for the treatment of genetic and/or metabolic disorders that alter sorbitol metabolism or causesover production of sorbitol, such as SDH deficiency.
The disclosure also relates to an AR inhibitor (e.g., zopolrestat, epalrestat, compound of any one of Formulas (I)-(VI)) for the manufacture of a medicament for the treatment of genetic and/or metabolic disorders that alter sorbitol metabolism or causes over production of sorbitol, such as SDH deficiency.
The disclosure also relates to a pharmaceutical formulation for the treatment of genetic and/or metabolic disorders that alter sorbitol metabolism or causes over production of sorbitol, such as SDH deficiency, that contains an AR inhibitor (e.g., zopolrestat, epalrestat, compound of any one of Formulas (I)-(VI) as an active ingredient.
In yet another aspect, the disclosure relates to treatment of various other disorders, such as diabetes, complications arising from diabetes, where excess formation of sorbitol has been directly linked to the onset and progression of diabetic complications. Such disorders can include, but not limited to “sugar” cataracts, hyperglycemia, diabetic nephropathy, diabetic neuropathy, diabetic retinopathy, and the like. Without wishing to be bound by any particular theory, it is believed that high glucose levels in diabetic subjects triggers the polyol pathway and glucose is converted to sorbitol with AR and then sorbitol is converted to fructose. Since glucose is reduced faster than sorbitol is oxidized, the net effect is the intracellular accumulation of the osmolyte sorbitol.
Various aspects now will be described more fully hereinafter. Such aspects may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein; rather, these embodiments are provided so that this disclosure will be thorough and complete.
This disclosure relates to the use of AR inhibitors for the treatment of genetic and/or metabolic disorders that alter sorbitol metabolism or causes over production of sorbitol, such as SDH deficiency.
Where a range of values is provided in this disclosure, it is intended that each intervening value between the upper and lower limit of that range and any other stated or intervening value in that stated range is encompassed within the disclosure. For example, if a range of 1 μM to 8 μM is stated, it is intended that 2 μM, 3 μM, 4 μM, 5 μM, 6 μM, and 7 μM are also explicitly disclosed, as well as the range of values greater than or equal to 1 μM and the range of values less than or equal to 8 μM.
The singular forms “a,” “an,” and “the” include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to a “compound of Formula (I)” includes a single compound as well as two or more of the same or different compounds; reference to an “excipient” includes a single excipient as well as two or more of the same or different excipients, and the like.
The word “about” means a range of plus or minus 10% of that value, e.g., “about 50” means 45 to 55, “about 25,000” means 22,500 to 27,500, etc., unless the context of the disclosure indicates otherwise, or is inconsistent with such an interpretation. For example in a list of numerical values such as “about 49, about 50, about 55, “about 50” means a range extending to less than half the interval(s) between the preceding and subsequent values, e.g., more than 49.5 to less than 52.5. Furthermore, the phrases “less than about” a value or “greater than about” a value should be understood in view of the definition of the term “about” provided herein.
In order to provide a complete, concise and clear description of the various embodiments, this disclosure includes descriptions of various components, groups of components, ranges and other elements of the broader disclosure. It is intended that such elements can be variously combined to provide additional embodiments of the disclosure. It is also intended that any disclosed features (e.g., substituent, analog, compound, structure, component) including individual members of any disclosed group, including any sub-ranges or combinations of sub-ranges within the group, may be excluded from the disclosure or any embodiments of the disclosure for any reason.
The various embodiments of the present disclosure are further described in detail in the numbered paragraphs below.
In general, the disclosure relates to a method for the treatment of a genetic and/or metabolic disorders that alter sorbitol metabolism or causes over production of sorbitol, such as SDH deficiency, comprising administering to a subject in need thereof a therapeutically effective amount of a compound that inhibits aldose reductase activity. The compound can be any suitable compound that inhibits AR activity, such as a small molecule compound (e.g., having a size of 5 kDa or less), a biologic agent (e.g., an inhibitory RNA directed against aldose reductase) or a combination thereof. Preferably, the AR inhibitor is a small molecule compound. Suitable small molecule AR inhibitors are known in the art and are disclosed herein. Small molecule AR inhibitors include ponalrestat, sorbinil, sorbinol, imirestat, AND-138, CT-112, zenarestat, BAL-AR18, AD-5467, M-79175, tolrestat, alconil, statil, berberine, SPR-210, zopolrestat, epalrestat, the compounds disclosed in U.S. Pat. Nos. 8,916,563, 9,650,383, 10,150,779 and the compounds disclosed herein. Preferred AR inhibitors for use in the invention include zopolrestat, epalrestat, the compounds disclosed in U.S. Pat. Nos. 8,916,563, 9,650,383, 10,150,779 and the compounds disclosed herein. The AR inhibitors can be administered in any suitable molecular form including pharmaceutically acceptable salts, solvates, prodrugs, and compounds that contain stable isotopic forms of one or more atoms, e.g., deuterium in place of hydrogen.
In one example, the method for the treatment of a genetic and/or metabolic disorder that alters sorbitol metabolism or causes over production of sorbitol, such as SDH deficiency, comprises administering to a subject in need thereof a therapeutically effective amount of zopolrestat.
In one example, the method for the treatment of a genetic and/or metabolic disorder that alters sorbitol metabolism or causes over production of sorbitol, such as SDH deficiency, comprises administering to a subject in need thereof an therapeutically effective amount of epalrestat.
In one example, the method for the treatment of a genetic and/or metabolic disorder that alters sorbitol metabolism or causes over production of sorbitol, such as SDH deficiency, comprises administering to a subject in need thereof an therapeutically effective amount of an aldose reductase, wherein the aldose reductase inhibitor is not ponalrestat, epalrestat, sorbinil or sorbinol, imirestat, AND-138, CT-112, zopolrestat, zenarestat, BAL-AR18, AD-5467, M-79175, tolrestat, alconil, statil, berberine or SPR-210. In particular embodiments, the methods for the treatment ofsorbitol-dehydrogenase (SDH) deficiency disclosed herein do not include administering epalrestat.
In one example, the method for the treatment of a genetic and/or metabolic disorder that alters sorbitol metabolism or causes over production of sorbitol, such as SDH deficiency, comprises administering to a subject in need thereof an therapeutically effective amount of a compound of any one of Formulas (I)-(VI). In certain examples, the compound that is administered is Compound A, or the compound that is administered is Compound B, or a physiologically acceptable salt, hydrate, solvate or prodrug of Compound A or Compund B.
As used herein, the term “treating” refers to curative or palliative (e.g., control or mitigate a disease or disease symptoms) therapy. This can include reversing, reducing, arresting or delaying the symptoms, clinical signs, and underlying pathology of a genetic and/or metabolic disorder that alters sorbitol metabolism or causes over production of sorbitol, such as SDH deficiency, in a manner to improve or stabilize a subject's condition. Thus, the method can be used for treatment of a genetic and/or metabolic disorder that alters sorbitol metabolism or causes over production of sorbitol, such as SDH deficiency, including, for example, treatment of complications (e.g., symptoms and clinical signs) of sorbitol-dehydrogenase (SDH) deficiency, and/or treatment and prevention of complications (e.g., symptoms and clinical signs) of sorbitol-dehydrogenase (SDH) deficiency.
As used herein “a therapeutically effective amount” is an amount of a compound that is sufficient to achieve the desired therapeutic effect under the conditions of administration, such as an amount that reduces or ameliorates the severity of a genetic and/or metabolic disorder that alters sorbitol metabolism or causes over production of sorbitol, such as SDH deficiency, that results in reduced levels of sorbitol, that prevents the advancement of conditions or symptoms related to elevated levels of sorbitol and/or sorbital accumulation in cells, or enhances or otherwise improves therapeutic effect(s) of another therapy for the treatment or management of a genetic and/or metabolic disorder that alters sorbitol metabolism or causes over production of sorbitol, such as SDH deficiency. A therapeutically effective amount can be an amount that decreases sorbitol in the subject being treated. The actual amount administered can be determined by an ordinarily skilled clinician based upon, for example, the subjects age, weight, sex, general heath and tolerance to drugs, severity of disease, dosage form selected, route of administration and other factors. Typically, the amount of an AR inhibitor that is administered is from about 0.5 to about 60 mg/kg body weight per day, such as from about 1.0 to 10 mg/kg.
In some examples of the practice of the methods disclosed herein, the therapeutically effective amount is an amount sufficient to reduce intracellular aldose reductase activity at least by about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, about 90%, about 95%, about 99%, or more, e.g., about 100% (e.g., compared to pre-treatment level). The therapeutically effective amount can be an amount that derease sorbitol levels at least by about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, about 90%, about 95%, about 99%, or more, e.g., about 100% (e.g., compared to pre-treatment level). The therapeutically effective amount can be sufficient to normalize sorbitol levels in a subject with a genetic and/or metabolic disorder that alters sorbitol metabolism or causes over production of sorbitol, such as SDH deficiency.
A “subject” can be any animal with a genetic and/or metabolic disorder that alters sorbitol metabolism or causes over production of sorbitol, such as SDH deficiency, particularly a mammal, and including, but by no means limited to, humans, domestic animals, such as feline or canine subjects, farm animals, such as but not limited to bovine, equine, caprine, ovine, avian and porcine subjects, wild animals (whether in the wild or in a zoological garden), research or laboratory animals, such as mice, rats, rabbits, goats, sheep, pigs, dogs, cats, etc., avian species, such as chickens, turkeys, songbirds, and the like. Typically, a human subject to be treated using the methods disclosed herein is diagnosed with a genetic and/or metabolic disorder that alters sorbitol metabolism or causes over production of sorbitol, such as SDH deficiency, for example as a new born through enzymatic or genetic screening, and/or has accumulation of sorbitol in tissues.
This disclosure also relates to the prophylaxis or treatment of at least one clinical feature or complication of a genetic and/or metabolic disorder that alters sorbitol metabolism or causes over production of sorbitol, such as SDH deficiency, in a subject. Representative clinical features or complications which can be present in children, adolescents or adults, include, e.g., cataracts, neuropathy, retinopathy, cardiomyopathy, nephropathy, microvascular complications, atherosclerosis and other cardiovascular complications, albuminuria, and diabetes.
In a particular aspect, the disclosure relates to a method for the treatment of a clinical feature or complication of a genetic and/or metabolic disorder that alters sorbitol metabolism or causes over production of sorbitol, such as SDH deficiency, and comprises administering to a subject in need thereof a therapeutically effective amount of zopolrestat.
In one example, the disclosure relates to a method for the treatment of a clinical feature or complication of a genetic and/or metabolic disorder that alters sorbitol metabolism or causes over production of sorbitol, such as SDH deficiency, and comprises administering to a subject in need thereof a therapeutically effective amount of epalrestat.
In one example, the disclosure relates to a method for the treatment of a clinical feature or complication of a genetic and/or metabolic disorder that alters sorbitol metabolism or causes over production of sorbitol, such as SDH deficiency, and comprises administering to a subject in need thereof a therapeutically effective amount of a compound of any one of Formulas (I)-(VI).
In some embodiments, the aforementioned methods are carried out by administering a formulation comprising of one or more AR inhibitors. The formulations can be adapted for administration once daily, twice daily, three times daily or four times daily to a subject in need thereof for the desired treatment period. Typically, the formulations are adapted for chronic administration over the course of several weeks, months, years or decades. In still other embodiments, the methods are carried out by administering formulations that are adapted for administration over the course of several weeks. Typically, the methods are carried out by administering formulations that are adapted for administration over the course of several years or decades.
Suitable small molecule AR inhibitors are known in the art and are disclosed herein. Small molecule AR inhibitors include ponalrestat, sorbinil, sorbinol, imirestat, AND-138, CT-112, zenarestat, BAL-AR18, AD-5467, M-79175, tolrestat, alconil, statil, berberine, SPR-210, zopolrestat, epalrestat, the compounds disclosed in U.S. Pat. Nos. 8,916,563, 9,650,383, WO2012/009553 and the compounds disclosed herein. Preferred AR inhibitors for use in the invention zopolrestat, epalrestat, the compounds disclosed in U.S. Pat. Nos. 8,916,563, 9,650,383, WO 2017/038505, U.S. Pat. No. 10,150,779 and the compounds disclosed herein. The disclosures of U.S. Pat. Nos. 8,916,563, 9,650,383, 10,150,779, WO 2012/009553, and WO 2017/038505 are incorporated by reference herein in their entirety, and disclose compounds that are suitable for use in the methods described herein.
In one example, the AR inhibitor is a compound of Formula (I) or pharmaceutically acceptable salts, prodrugs and solvates thereof,
wherein,
R1 is H, (C1-C6)-alkyl, (C1-C6)-hydroxyalkyl, or (C1-C6)-aminoalkyl;
X1 is N or CR3;
X2 is N or CR4;
X3 is N or CR5;
X4 is N or CR6; with the proviso that two or three of X1, X2, X3, or X4 are N;
Y is a bond, C═O, C═S, C═NH, or C═N(C1-C4)-alkyl;
Z is
A1 is NR11, O, S or CH2;
A2 is N or CH;
A3 is NR11, O, or S;
R3 through R10 are independently hydrogen, halogen, cyano, acyl, haloalkyl, haloalkoxy, haloalkylthio, trifluoroacetyl, (C1-C4)-alkyl, (C1-C4)-alkoxy, (C1-C4)-alkylthio, (C1-C4)-alkylsulfinyl, or (C1-C4)-alkylsulfonyl; or two of R3 through R6 or two of R7 through R10 taken together are (C1-C4)-alkylenedioxy; and
R11 is hydrogen, C1-C4 alkyl, or C(O)O-(C1-C4)-alkyl.
It will be recognized by those of skill in the art that the designation of Z is
indicates that when Z is
the compounds of formula (I) encompass
and when Z is
the compounds of formula (I) encompass
In certain embodiments, R1 is hydrogen or (C1-C6)-alkyl. In certain embodiments, R1 is hydrogen. In certain embodiments, R1 is (C1-C6)-alkyl. In certain embodiments, R1 is tert-butyl.
In certain embodiments, R3 through R10 are independently hydrogen, halogen or haloalkyl. In certain embodiments, R3 through R10 are independently hydrogen, halogen or trihaloalkyl.
In certain embodiments, R3 through R6 are hydrogen.
In certain embodiments, R7 through R10 are independently hydrogen, halogen or haloalkyl. In certain embodiments, R7 through R10 are independently hydrogen, halogen or trihaloalkyl.
In certain embodiments, R7 and R10 are hydrogen.
In certain embodiments, R8 is hydrogen, halogen or haloalkyl. In certain embodiments, R8 is hydrogen. In certain embodiments, R8 is halogen. In certain embodiments, R8 is haloalkyl.
In certain embodiments, R9 is hydrogen, halogen or haloalkyl. In certain embodiments, R9 is hydrogen. In certain embodiments, R9 is halogen. In certain embodiments, R9 is haloalkyl.
In certain embodiments, Y is C═O, C═S, C═NH, or C═N(C1-C4)-alkyl. In certain embodiments, Y is C═O or C═S. In certain embodiments, Y is C═O. In certain embodiments, Y is C═S. In certain embodiments, Y is C═NH, or C═N(C1-C4)-alkyl.
In certain embodiments, A1 is NR11, S or CH2. In certain embodiments, A1 is NR11 or O. In certain embodiments, A1 is NR11 or S. In certain embodiments, A1 is NR11. In certain embodiments, A1 is O. In certain embodiments, A1 is S.
In certain embodiments, A2 is N or CH. In certain embodiments, A1 is N. In certain embodiments, A1 is CH.
In certain embodiments, A3 is O or S. In certain embodiments, A3 is O. In certain embodiments, A3 is S.
In certain embodiments, X1 and X4 are nitrogen.
In certain embodiments, X1 and X2 are nitrogen.
In certain embodiments, X1 and X3 are nitrogen.
In certain embodiments, X2 and X3 are nitrogen.
In certain embodiments, X2 and X4 are nitrogen.
In certain embodiments, X3 and X4 are nitrogen.
In certain embodiments, Z is
In certain embodiments, Z is
In certain embodiments, R1 is hydrogen or (C1-C6)-alkyl;
X1 and X4 are N;
X2 is CR4;
X3 is CR5;
Y is C═O;
Z is
A1 is NR11, O, or S;
A2 is N;
A3 is O, or S;
R4 and R5 are hydrogen;
R7 through R10 are independently hydrogen, halogen, cyano, acyl, haloalkyl, haloalkoxy, haloalkylthio, (C1-C4)-alkoxy, (C1-C4)-alkylthio, (C1-C4)-alkylsulfinyl, or (C1-C4)-alkylsulfonyl; and
R11 is hydrogen, C1-C4 alkyl, or C(O)O-(C1-C4)-alkyl.
In certain embodiments, R1 is hydrogen or tert-butyl;
X1 and X4 are N;
X2 is CR4;
X3 is CR5;
Y is C═O;
Z is
A1 is NR11, O or S;
A2 is N;
A3 is O or S;
R4 and R5 are hydrogen;
R7 through R10 are independently hydrogen, halogen, or haloalkyl; and
R11 is hydrogen, (C1-C4)-alkyl, or C(O)O-tert-butyl.
In certain embodiments, R1 is hydrogen or tert-butyl;
X1 and X4 are N;
X2 is CH;
X3 is CH;
Y is C═O;
Z is
A1 is NR11, Oor S;
A2 is N;
A3 is O or S;
R7, R8 and R10 are independently hydrogen, halogen, or haloalkyl;
R9 is halogen, or haloalkyl; and
R11 is hydrogen or methyl.
In certain embodiments, R1 is hydrogen or tert-butyl;
X1 and X4 are N;
X2 is CH;
X3 is CH;
Y is C═O;
Z is
A1 is NR11, O or S;
A2 is N;
A3 is O or S;
R7, R8 and R10 are independently hydrogen, halogen, or haloalkyl;
R9 is chlorine, or trifluoromethyl; and
R11 is hydrogen or methyl.
In certain embodiments, the AR inhibitor is a compound of Formula (II) or pharmaceutically acceptable salt or solvate thereof:
Wherein R1, R7-R9 and Y are as described in Formula (I), and preferable wherein R1 is hydrogen or (C1-C6)-alkyl and Y is C═O. Exemplary compounds of Formula (II) include the following and salts thereof:
The AR inhibitors can be a compound of Formula (III) or pharmaceutically acceptable salts, pro-drugs and solvates thereof,
wherein,
R1 is CO2R2 or CO2−X+;
R2 is H, (C1-C6)-alkyl, (C1-C6)-hydroxyalkyl, or (C1-C6)-aminoalkyl;
X1 is H or halogen;
X2 is H or halogen;
Y is a bond, C═O, C═S, C═NH, or C═N(C1-C4)-alkyl;
Z is
A1 is NR7, O, S or CH2;
A2 is N or CH;
A3 is NR7, O, or S;
R3 through R6 are independently hydrogen, halogen, cyano, acyl, haloalkyl, haloalkoxy, haloalkylthio, trifluoroacetyl, (C1-C4)-alkyl, (C1-C4)-alkoxy, (C1-C4)-alkylthio, (C1-C4)-alkylsulfinyl, or (C1-C4)-alkylsulfonyl;
R7 is hydrogen, C1-C4 alkyl, or C(O)O-(C1-C4)-alkyl; and
X+ is a counter ion.
It will be recognized by those of skill in the art that the designation of
Z is
indicates that when Z is
the compounds of Formula (III) are understood to encompass
and when Z is
the compounds of Formula (I) are understood to encompass
In certain embodiments, R1 is CO2R2 or CO2−X+. In certain embodiments, R1 is CO2R2. In certain embodiments, R1 is CO2−X+.
In certain embodiments, R2 is hydrogen or (C1-C6)-alkyl. In certain embodiments, R2 is hydrogen or (C1-C4)-alkyl. In certain embodiments, R2 is hydrogen or (C1-C3)-alkyl. In certain embodiments, R2 is hydrogen, methyl, or ethyl. In certain embodiments, R2 is hydrogen or methyl. In certain embodiments, R2 is methyl or ethyl. In certain embodiments, R2 is methyl. In certain embodiments, R2 is hydrogen. In certain embodiments, R2 is (C1-C6)-alkyl. In certain embodiments, R2 is (C1-C6)-n-alkyl. In certain embodiments, R2 is (C1-C2)-alkyl. In certain embodiments, R2 is (C1-C3)-alkyl. In certain embodiments, R2 is (C1-C4)-alkyl. In certain embodiments, R2 is tert-butyl.
In certain embodiments, R3 through R6 are independently hydrogen, halogen, cyano, acyl, haloalkyl, haloalkoxy, haloalkylthio, trifluoroacetyl, (C1-C4)-alkyl, (C1-C4)-alkoxy, (C1-C4)-alkylthio, (C1-C4)-alkylsulfinyl, or (C1-C4)-alkylsulfonyl.
In certain embodiments, R3 through R6 are independently hydrogen, halogen or haloalkyl. In certain embodiments, R3 through R6 are independently hydrogen, halogen or trihaloalkyl.
In certain embodiments, R3 and R6 are hydrogen. In certain embodiments, R3, R5, and R6 are hydrogen.
In certain embodiments, R4 is hydrogen, halogen or haloalkyl. In certain embodiments, R4 is hydrogen. In certain embodiments, R4 is halogen. In certain embodiments, R4 is haloalkyl. I n certain embodiments, R4 is CF3.
In certain embodiments, R3 through R6 are hydrogen. In certain embodiments, R3, R5, R6 are hydrogen and R4 is halogen or haloalkyl. In certain embodiments, R3, R5, R6 are hydrogen and R4 is haloalkyl. In certain embodiments, R3, R5, R6 are hydrogen and R4 is CF3. In certain embodiments, R3, R5, R6 are hydrogen and R4 is halogen. In certain embodiments, R3, R5, R6 are hydrogen and R4 is F. In certain embodiments, R3, R5, R6 are hydrogen and R4 is Cl.
In certain embodiments, Y is C═O, C═S, C═NH, or C═N(C1-C4)-alkyl. In certain embodiments, Y is C═O or C═S. In certain embodiments, Y is C═O. In certain embodiments, Y is C═S. In certain embodiments, Y is C═NH, or C═N(C1-C4)-alkyl.
In certain embodiments, A1 is NR7, O, S or CH2. In certain embodiments, A1 is NR7, O, or S. In certain embodiments, A1 is NR7, S or CH2. In certain embodiments, A1 is NR7 or O. In certain embodiments, A1 is NR7 or S. In certain embodiments, A1 is NR7. In certain embodiments, A1 is O. In certain embodiments, A1 is S.
In certain embodiments, A2 is N or CH. In certain embodiments, A2 is N. In certain embodiments, A2 is CH.
In certain embodiments, A3 is NR7, O, or S. In certain embodiments, A3 is O. In certain embodiments, A3 is S. In certain embodiments, A3 is NR7.
In certain embodiments, X1 and X2 are hydrogen.
In certain embodiments, X1 and X2 are halogen. In certain embodiments, X1 and X2 are Cl.
In certain embodiments, X1 and X2 are independently hydrogen or halogen. In certain embodiments, X1 is hydrogen and X2 is Cl. In certain embodiments, X1 is Cl and X2 is hydrogen.
In certain embodiments, Z is
In certain embodiments, Z is
In certain embodiments, R7 is hydrogen, C1-C4 alkyl, or C(O)O-(C1-C4)-alkyl. In certain embodiments, R7 is hydrogen. In certain embodiments, R7 is C1-C4 alkyl. In certain embodiments, R7 is C1-C3 alkyl. In certain embodiments, R7 is C1-C2 alkyl. In certain embodiments, R7 is C1-C4 n-alkyl. In certain embodiments, R7 is C1-C3 n-alkyl. In certain embodiments, R7 is C(O)O-(C1-C4)-alkyl. In certain embodiments, R7 is C(O)O-(C1-C3)-alkyl. In certain embodiments, R7 is C(O)O-(C1-C2)-alkyl. In certain embodiments, R7 is C(O)O-(C1-C4)-n-alkyl. In certain embodiments, R7 is C(O)O-(C1-C3)-n-alkyl.
In certain embodiments, R1 is CO2R2;
R2 is H or (C1-C6)-alkyl;
X1 is H;
X2 is H;
Y is C═O;
Z is
A1 is NR7, O, or S;
A2 is N;
A3 is O or S;
R3 through R6 are independently hydrogen, halogen, cyano, acyl, haloalkyl, haloalkoxy, haloalkylthio, trifluoroacetyl, (C1-C4)-alkyl, (C1-C4)-alkoxy, (C1-C4)-alkylthio, (C1-C4)-alkylsulfinyl, or (C1-C4)-alkylsulfonyl; and
R7 is hydrogen, C1-C4 alkyl, or C(O)O-(C1-C4)-alkyl.
In certain embodiments, R1 is CO2R2;
R2 is H or tert-butyl;
X1 is H;
X2 is H;
Y is C═O;
Z is
A1 is NR7, O, or S;
A2 is N;
A3 is O or S;
R6 through R6 are independently hydrogen, halogen, haloalkyl; and
R7 is hydrogen, C1-C4 alkyl, or C(O)O-(C1-C4)-alkyl.
In certain embodiments, R1 is CO2R2;
R2 is H or tert-butyl;
X1 is H;
X2 is H;
Y is C═O;
Z is
A1 is NR7, O, or S;
A2 is N;
A3 is O or S;
R3, R5, and R6 are hydrogen;
R4 is hydrogen, halogen, or haloalkyl; and
R7 is hydrogen, C1-C4 alkyl, or C(O)O-(C1-C4)-alkyl.
In certain embodiments, R1 is CO2R2;
R2 is H or (C1-C6)-alkyl;
X1 is halogen;
X2 is halogen;
Y is C═O;
Z is
A1 is NR7, O, or S;
A2 is N;
A3 is O or S;
R3 through R6 are independently hydrogen, halogen, cyano, acyl, haloalkyl, haloalkoxy, haloalkylthio, trifluoroacetyl, (C1-C4)-alkyl, (C1-C4)-alkoxy, (C1-C4)-alkylthio, (C1-C4)-alkylsulfinyl, or (C1-C4)-alkylsulfonyl; and
R7 is hydrogen, C1-C4 alkyl, or C(O)O-(C1-C4)-alkyl.
In certain embodiments, R1 is CO2R2;
R2 is H or tert-butyl;
X1 is halogen;
X2 is halogen;
Y is C═O;
Z is
A1 is NR7, O, or S;
A2 is N;
A3 is O or S;
R3 through R6 are independently hydrogen, halogen, haloalkyl; and
R7 is hydrogen, C1-C4 alkyl, or C(O)O-(C1-C4)-alkyl.
In certain embodiments, R1 is CO2R2;
R2 is H or tert-butyl;
X1 is Cl;
X2 is Cl;
Y is C═O;
Z is
A1 is NR7, O, or S;
A2 is N;
A3 is O or S;
R3 through R6 are independently hydrogen, halogen, haloalkyl; and
R7 is hydrogen, C1-C4 alkyl, or C(O)O-(C1-C4)-alkyl.
In certain embodiments, R1 is CO2R2;
R2 is H or tert-butyl;
X1 is Cl;
X2 is Cl;
Y is C═O;
Z is
A1 is NR7, O, or S;
A2 is N;
A3 is O or S;
R3, R5, and R6 are hydrogen;
R4 is hydrogen, halogen, or haloalkyl; and
R7 is hydrogen, C1-C4 alkyl, or C(O)O-(C1-C4)-alkyl.
In certain embodiments, the compound of Formula (III) is selected from the group consisting of:
In certain embodiments, the compound of Formula (III) is
or a pharmaceutically acceptable salt thereof.
In certain embodiments, the compound of Formula (III) is
or a pharmaceutically acceptable salt thereof.
The AR inhibitors can be a compound of Formula (IV) or pharmaceutically acceptable salts, and solvates thereof,
wherein,
X1 is H or halogen;
X2 is H or halogen;
Y is a bond, C═O, C═S, C═NH, or C═N(C1-C4)-alkyl;
Z1 and Z2 are independently selected from the group consisting of hydroxy, alkoxy, aryloxy, or Z1 and Z2 taken together with the boron atom to which they are bonded form
wherein,
X is a substituted or unsubstituted C2-C5 alkylene;
Z is
A1 is NR7, O, S or CH2;
A2 is N or CH;
A3 is NR7, O, or S;
R3 through R6 are independently hydrogen, halogen, cyano, acyl, haloalkyl, haloalkoxy, haloalkylthio, trifluoroacetyl, (C1-C4)-alkyl, (C1-C4)-alkoxy, (C1-C4)-alkylthio, (C1-C4)-alkylsulfinyl, or (C1-C4)-alkylsulfonyl; and
R7 is hydrogen, C1-C4 alkyl, or C(O)O-(C1-C4)-alkyl.
Suitable substituents on the C2-C5 alkylene include one or more alkyl, alkoxy, aryl, aryloxy, halo, haloalkyl, haloalkoxy, haloalkylthio. A preferred substituted C2-C5 alkylene is substituted ethylene. A more preferred substituted C2-C5 alkylene is —C(CH3)2C(CH3)2—.
It will be recognized by those of skill in the art that the designation of
Z is
indicates that when Z is
the compounds of Formula (IV) are understood to encompass
and
when Z is
the compounds of Formula (IV) are understood to encompass
wherein,
Z1 and Z2 are independently selected from the group consisting of hydroxy, alkoxy, aryloxy, or Z1 and Z2 taken together with the boron atom to which they are bonded form
wherein,
X is a substituted or unsubstituted C2-C5 alkylene.
In certain embodiments, R3 through R6 of Formula (IV) are independently hydrogen, halogen, cyano, acyl, haloalkyl, haloalkoxy, haloalkylthio, trifluoroacetyl, (C1-C4)-alkyl, (C1-C4)-alkoxy, (C1-C4)-alkylthio, (C1-C4)-alkylsulfinyl, or (C1-C4)-alkylsulfonyl.
In certain embodiments, R3 through R6 of Formula (IV) are independently hydrogen, halogen or haloalkyl. In certain embodiments, R3 through R6 are independently hydrogen, halogen or trihaloalkyl.
In certain embodiments, R3 and R6 of Formula (IV) are hydrogen. In certain embodiments, R3, R5, and R6 are hydrogen.
In certain embodiments, R4 of Formula (IV) is hydrogen, halogen or haloalkyl. In certain embodiments, R4 is hydrogen. In certain embodiments, R4 is halogen. In certain embodiments, R4 is haloalkyl. In certain embodiments, R4 is CF3.
In certain embodiments, R3 through R6 of Formula (IV) are hydrogen. In certain embodiments, R3, R5, R6 are hydrogen and R4 is halogen or haloalkyl. In certain embodiments, R3, R5, R6 are hydrogen and R4 is haloalkyl. In certain embodiments, R3, R5, R6 are hydrogen and R4 is CF3. In certain embodiments, R3, R5, R6 are hydrogen and R4 is halogen. In certain embodiments, R3, R5, R6 are hydrogen and R4 is F. In certain embodiments, R3, R5, R6 are hydrogen and R4 is Cl.
In certain embodiments, Y of Formula (IV) is C═O, C═S, C═NH, or C═N(C1-C4)-alkyl. In certain embodiments, Y is C═O or C═S. In certain embodiments, Y is C═O. In certain embodiments, Y is C═S. In certain embodiments, Y is C═NH, or C═N(C1-C4)-alkyl.
In certain embodiments, A1 of Formula (IV) is NR7, O, S or CH2. In certain embodiments, A1 is NR7, O, or S. In certain embodiments, A1 is NR7, S or CH2. In certain embodiments, A1 is NR7 or O. In certain embodiments, A1 is NR7 or S. In certain embodiments, A1 is NR7. In certain embodiments, A1 is O. In certain embodiments, A1 is S.
In certain embodiments, A2 of Formula (IV) is N or CH. In certain embodiments, A2 is N. In certain embodiments, A2 is CH.
In certain embodiments, A3 of Formula (IV) is NR7, O, or S. In certain embodiments, A3 is O. In certain embodiments, A3 of Formula (IV) is S. In certain embodiments, A3 is NR7.
In certain embodiments, X1 and X2 of Formula (IV) are hydrogen.
In certain embodiments, X1 and X2 of Formula (IV) are halogen. In certain embodiments, X1 and X2 are Cl.
In certain embodiments, X1 and X2 of Formula (IV) are independently hydrogen or halogen. In certain embodiments, X1 is hydrogen and X2 is Cl. In certain embodiments, X1 is Cl and X2 is hydrogen.
In certain embodiments, Z of Formula (IV) is
In certain embodiments, Z of Formula (IV) is
In certain embodiments, R7 of Formula (IV) is hydrogen, C1-C4 alkyl, or C(O)O-(C1-C4)-alkyl. In certain embodiments, R7 is hydrogen. In certain embodiments, R7 is C1-C4 alkyl. In certain embodiments, R7 is C1-C3 alkyl. In certain embodiments, R7 is C1-C2 alkyl. In certain embodiments, R7 is C1-C4 n-alkyl. In certain embodiments, R7 is C1-C3 n-alkyl. In certain embodiments, R7 is C(O)O-(C1-C4)-alkyl. In certain embodiments, R7 is C(O)O-(C1-C3)-alkyl. In certain embodiments, R7 is C(O)O-(C1-C2)-alkyl. In certain embodiments, R7 is C(O)O-(C1-C4)-n-alkyl. In certain embodiments, R7 is C(O)O-(C1-C3)-n-alkyl.
In certain embodiments, the compounds of Formula (IV) is
or pharmaceutically acceptable salts, pro-drugs or solvates thereof;
wherein,
Z1 and Z2 are independently selected from the group consisting of hydroxy, alkoxy, aryloxy, or Z1 and Z2 taken together with the boron atom to which they are bonded form
wherein,
X is a substituted or unsubstituted C2-C5 alkylene.
In certain embodiments, the compounds of Formula (IV) is
or pharmaceutically acceptable salts, pro-drugs or solvates thereof;
wherein,
Z1 and Z2 are independently selected from the group consisting of hydroxy, alkoxy, aryloxy, or Z1 and Z2 taken together with the boron atom to which they are bonded form
wherein,
X is a substituted or unsubstituted C2-C5 alkylene.
In certain embodiments, the compounds of Formula (IV) is
or pharmaceutically acceptable salts, pro-drugs or solvates thereof;
wherein,
Z1 and Z2 are independently selected from the group consisting of hydroxy, alkoxy, aryloxy, or Z1 and Z2 taken together with the boron atom to which they are bonded form
wherein,
X is a substituted or unsubstituted C2-C5 alkylene.
In certain embodiments, the compounds of Formula (IV) is
or pharmaceutically acceptable salts, pro-drugs or solvates thereof;
wherein,
Z1 and Z2 are independently selected from the group consisting of hydroxy, alkoxy, aryloxy, or Z1 and Z2 taken together with the boron atom to which they are bonded form
wherein,
X is a substituted or unsubstituted C2-C5 alkylene.
In another aspect, the aldose reductase inhibitor is a compound of Formula (V)
or pharmaceutically acceptable salts, pro-drugs or solvates thereof;
wherein,
X3 is N or CR8;
X4 is N or CR9;
X5 is N or CR10;
X6 is N or CR11; with the proviso that two or three of X3, X4, X5, or X6 are N;
Z1 and Z2 are independently selected from the group consisting of hydroxy, alkoxy, aryloxy, or Z1 and Z2 taken together with the boron atom to which they are bonded form
wherein,
X is a substituted or unsubstituted C2-C5 alkylene;
Z3 is
A4 is NR16, O, S or CH2;
A5 is N or CH;
A6 is NR16, O, or S;
R8 through R15 are independently hydrogen, halogen, cyano, acyl, haloalkyl, haloalkoxy, haloalkylthio, trifluoroacetyl, (C1-C4)-alkyl, (C1-C4)-alkoxy, (C1-C4)-alkylthio, (C1-C4)-alkylsulfinyl, or (C1-C4)-alkylsulfonyl; or two of R8 through R11 or two of R12 through R15 taken together are (C1-C4)-alkylenedioxy; and
R16 is hydrogen, C1-C4 alkyl, or C(O)O-(C1-C4)-alkyl.
Suitable substituents on the C2-C5 alkylene include one or more alkyl, alkoxy, aryl, aryloxy, halo, haloalkyl, haloalkoxy, haloalkylthio. A preferred substituted C2-C5 alkylene is substituted ethylene. A more preferred substituted C2-C5 alkylene is —C(CH3)2C(CH3)2—.
It will be recognized by those of skill in the art that the designation of
Z is
indicates that when Z is
the compounds of Formula (V) are understood to encompass
and when Z is
the compounds of Formula (V) are understood to encompass
In some compounds of Formula (V), R8 through R15 are independently hydrogen, halogen or haloalkyl, for example, R8 through R15 are independently hydrogen, halogen or trihaloalkyl (e.g., —CF3).
In other compounds of Formula (V), R8 through R11 are hydrogen.
In certain embodiments of compounds of Formula (V), R12 through R15 are independently hydrogen, halogen or haloalkyl, for example, R12 through R15 are independently hydrogen, halogen or trihaloalkyl (e.g., —CF3).
In certain embodiments, R12 and R15 of Formula (V) are hydrogen.
In certain embodiments, R13 of Formula (V) is hydrogen, halogen or haloalkyl. In certain embodiments, R13 is hydrogen. In certain embodiments, R13 is halogen. In certain embodiments, R13 is haloalkyl.
In certain embodiments, R14 of Formula (V) is hydrogen, halogen or haloalkyl. In certain embodiments, R14 is hydrogen. In certain embodiments, R14 is halogen. In certain embodiments, R14 is haloalkyl.
In certain embodiments, Y of Formula (V) is C═O, C═S, C═NH, or C═N(C1-C4)-alkyl. In certain embodiments, Y is C═O or C═S. In certain embodiments, Y is C═O. In certain embodiments, Y is C═S. In certain embodiments, Y is C═NH, or C═N(C1-C4)-alkyl.
In certain embodiments, A4 of Formula (V) is NR16, S or CH2. In certain embodiments, A4 is NR16 or O. In certain embodiments, A4 is NR16 or S. In certain embodiments, A4 is NR16. In certain embodiments, A4 is O. In certain embodiments, A4 is S.
In certain embodiments, A5 of Formula (V) is N or CH. In certain embodiments, A4 is N. In certain embodiments, A4 is CH.
In certain embodiments, A6 of Formula (V) is O or S. In certain embodiments, A6 is O. In certain embodiments, A6 is S.
In certain embodiments, X3 and X6 of Formula (V) are nitrogen.
In certain embodiments, X3 and X4 of Formula (V) are nitrogen.
In certain embodiments, X3 and X5 of Formula (V) are nitrogen.
In certain embodiments, X4 and X5 of Formula (V) are nitrogen.
In certain embodiments, X4 and X6 of Formula (V) are nitrogen.
In certain embodiments, X5 and X6 of Formula (V) are nitrogen.
In certain embodiments, Z3 of Formula (V) is
In certain embodiments, Z3 of Formula (V) is
In some embodiments, the compounds of Formula (V) is
or pharmaceutically acceptable salts, pro-drugs or solvates thereof;
wherein,
R14 is hydrogen, halogen or trihaloalkyl (e.g., —CF3); and
Z1 and Z2 are independently selected from the group consisting of hydroxy, alkoxy, aryloxy, or Z1 and Z2 taken together with the boron atom to which they are bonded form
wherein,
X is a substituted or unsubstituted C2-C5 alkylene.
In embodiments, the compounds of Formula (V) is
or pharmaceutically acceptable salts, pro-drugs or solvates thereof.
In one aspect, the aldose reductase inhibitor is a compound of Formula (VI)
or pharmaceutically acceptable salts, pro-drugs or solvates thereof;
wherein,
Z1 and Z2 are independently selected from the group consisting of hydroxy, alkoxy, aryloxy, or Z1 and Z2 taken together with the boron atom to which they are bonded form
wherein,
X is a substituted or unsubstituted C2-C5 alkylene.
In an embodiment, the aldose reductase inhibitor of Formula (VI) is
or pharmaceutically acceptable salts, pro-drugs or solvates thereof.
In an embodiment, the AH inhibitor of Formula (VI) is
or pharmaceutically acceptable salts, pro-drugs or solvates thereof.
The term “alkyl”, as used herein, unless otherwise indicated, refers to a monovalent aliphatic hydrocarbon radical having a straight chain, branched chain, monocyclic moiety, or polycyclic moiety or combinations thereof, wherein the radical is optionally substituted at one or more carbons of the straight chain, branched chain, monocyclic moiety, or polycyclic moiety or combinations thereof with one or more substituents at each carbon, where the one or more substituents are independently C1-C10 alkyl. Examples of “alkyl” groups include methyl, ethyl, propyl, isopropyl, butyl, iso-butyl, sec-butyl, tert-butyl, pentyl, hexyl, heptyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, norbornyl, and the like.
The term “halogen” or “halo-”, as used herein, means chlorine (Cl), fluorine (F), iodine (I) or bromine (Br).
As used herein, the term “acyl” is used in a broad sense to designate radicals of the type RCO—, in which R represents an organic radical which may be an alkyl, aralkyl, aryl, alicyclic or heterocyclic radical, substituted or unsubstituted, saturated or unsaturated; or, differently defined, the term “acyl” is used to designate broadly the monovalent radicals left when the OH group of the carboxylic radical is removed from the molecule of a carboxylic acid.
The term “alkoxy” is employed to designate a group of the formula: —O—R wherein R is an alkyl group, which optionally contains substituents, such as halogen. Preferably, the term “alkoxy” is employed to designate an alkoxy with an alkyl group of 1 to 6 carbon atoms. Most preferably, the term “alkoxy” is employed to designate an alkoxy with an alkyl group of 1 to 3 carbon atoms, such as methoxy or ethoxy.
The term “cycloalkyl group” is used herein to identify cycloalkyl groups having 3-6 carbon atoms preferably cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl.
The term “solvate” as used herein means a compound, or a pharmaceutically acceptable salt thereof, wherein molecules of a suitable solvent are incorporated in the crystal lattice. A suitable solvent is physiologically tolerable at the dosage administered. Examples of suitable solvents are ethanol, water and the like. When water is the solvent, the molecule is referred to as a “hydrate.”
A “prodrug” refers to an agent, which is converted into the parent drug in vivo. Prodrugs are often useful because, in some situations, they are easier to administer than the parent drug. They are bioavailable, for instance, by oral administration whereas the parent drug is either less bioavailable or not bioavailable. The prodrug also has improved solubility in pharmaceutical compositions over the parent drug. For example, the compound carries protective groups which are split off by hydrolysis in body fluids, e.g., in the bloodstream, thus releasing active compound or is oxidized or reduced in body fluids to release the compound. The term “prodrug” may apply to such functionalities as, for example; the acid functionalities of the compounds of Formula (I). Prodrugs may be comprised of structures wherein an acid group is masked, for example, as an ester or amide. Further examples of prodrugs are discussed herein. See also Alexander et al. (J. Med. Chem. 1988, 31, 318), which is incorporated by reference. Examples of prodrugs include, but are not limited to, derivatives and metabolites of a compound that include biohydrolyzable moieties such as biohydrolyzable amides, biohydrolyzable esters, biohydrolyzable carbamates, biohydrolyzable carbonates, and biohydrolyzable phosphate analogues. Prodrugs are also described in, for example, The Practice of Medicinal Chemistry (Camille Wermuth, ed., 1999, Academic Press; hereby incorporated by reference in its entirety). In certain embodiments, 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 Gmfh; each of which hereby incorporated by reference in its entirety). Biohydrolyzable moieties of a compound of Formula I (a) do not interfere with the biological activity of the compound but can confer upon that compound advantageous properties in vivo, such as uptake, duration of action, or onset of action; or (b) may be biologically inactive but are converted in vivo to the biologically active compound. Examples of biohydrolyzable esters include, but are not limited to, lower alkyl esters, alkoxyacyloxy esters, alkyl acylamino alkyl esters, and choline esters. Examples of biohydrolyzable amides include, but are not limited to, lower alkyl amides, a-amino acid amides, alkoxyacyl amides, and alkylaminoalkylcarbonyl amides. Examples of biohydrolyzable carbamates include, but are not limited to, lower alkylamines, substituted ethylenediamines, amino acids, hydroxyalkylamines, heterocyclic and heteroaromatic amines, and polyether amines.
The term “salt” includes salts derived from any suitable of organic and inorganic counter ions well known in the art and include, by way of example, hydrochloric acid salt or a hydrobromic acid salt or an alkaline or an acidic salt of the aforementioned amino acids. The term is intended to include salts derived from inorganic or organic acids including, for example hydrochloric, hydrobromic, sulfuric, nitric, perchloric, phosphoric, formic, acetic, lactic, maleic, fumaric, succinic, tartaric, glycolic, salicylic, citric, methanesulfonic, benzenesulfonic, benzoic, malonic, trifluoroacetic, trichloroacetic, naphthalene-2 sulfonic and other acids; and salts derived from inorganic or organic bases including, for example sodium, potassium, calcium, ammonium or tetrafluoroborate. Exemplary pharmaceutically acceptable salts are found, for example, in Berge, et al, (J. Pharm. Sci. 1977, 66(1), 1; and U.S. Pat. Nos. 6,570,013 and 4,939,140; each hereby incorporated by reference in its entirety). Pharmaceutically acceptable salts are also intended to encompass hemi-salts, wherein the ratio of compound: acid is respectively 2:1. Exemplary hemi-salts are those salts derived from acids comprising two carboxylic acid groups, such as malic acid, fumaric acid, maleic acid, succinic acid, tartaric acid, glutaric acid, oxalic acid, adipic acid and citric acid. Other exemplary hemi-salts are those salts derived from diprotic mineral acids such as sulfuric acid. Exemplary preferred hemi-salts include, but are not limited to, hemimaleate, hemifumarate, and hemisuccinate.
The term “acid” contemplates all pharmaceutically acceptable inorganic or organic acids. Inorganic acids include mineral acids such as hydrohalic acids, such as hydrobromic and hydrochloric acids, sulfuric acids, phosphoric acids and nitric acids. Organic acids include all pharmaceutically acceptable aliphatic, alicyclic and aromatic carboxylic acids, dicarboxylic acids, tricarboxylic acids, and fatty acids. Preferred acids are straight chain or branched, saturated or unsaturated C1-C20 aliphatic carboxylic acids, which are optionally substituted by halogen or by hydroxyl groups, or C6-C12 aromatic carboxylic acids. Examples of such acids are carbonic acid, formic acid, fumaric acid, acetic acid, propionic acid, isopropionic acid, valeric acid, alpha-hydroxy acids, such as glycolic acid and lactic acid, chloroacetic acid, benzoic acid, methane sulfonic acid, and salicylic acid. Examples of dicarboxylic acids include oxalic acid, malic acid, succinic acid, tartaric acid and maleic acid. An example of a tricarboxylic acid is citric acid. Fatty acids include all pharmaceutically acceptable saturated or unsaturated aliphatic or aromatic carboxylic acids having 4 to 24 carbon atoms. Examples include butyric acid, isobutyric acid, sec-butyric acid, lauric acid, palmitic acid, stearic acid, oleic acid, linoleic acid, linolenic acid, and phenylsteric acid. Other acids include gluconic acid, glycoheptonic acid and lactobionic acid.
The compounds can be administered in the form a suitable composition, such as a pharmaceutical composition. Pharmaceutical compositions are physiologically acceptable and typically include the active compound and a carrier. The term “carrier” refers to a diluent, adjuvant, excipient, or vehicle with which a compound is administered. Non-limiting examples of such pharmaceutical carriers include liquids, such as water and oils, including those of petroleum, animal, vegetable or synthetic origin, such as peanut oil, soybean oil, mineral oil, sesame oil and the like. The pharmaceutical carriers may also be saline, gum acacia, gelatin, starch paste, talc, keratin, colloidal silica, urea, and the like. In addition, auxiliary, stabilizing, thickening, lubricating and coloring agents may be used. Other examples of suitable pharmaceutical carriers are described in Remington's Pharmaceutical Sciences (Alfonso Gennaro ed., Krieger Publishing Company (1997); Remington's: The Science and Practice of Pharmacy, 21st Ed. (Lippincot, Williams & Wilkins (2005); Modern Pharmaceutics, vol. 121 (Gilbert Banker and Christopher Rhodes, CRC Press (2002); each of which hereby incorporated by reference in its entirety).
The composition can be in a desired form, such as a table, capsule, solution, emulsion, suspension, gel, sol, or colloid that is physiologically and/or pharmaceutically acceptable. If desired, the carrier can include a buffer, for example with alkaline buffers, e.g., ammonium buffer, acidic buffers, e.g., ethanoates, citrates, lactates, acetates, etc., or zwitterionic buffers, such as, glycine, alanine, valine, leucine, isoleucine and phenylalanine, Kreb's-Ringer buffer, TRIS, MES, ADA, ACES, PIPES, MOPSO, cholamine chloride, MOPS, BES, TES, HEPES, DIPSO, MOBS, TAPSO, acetamidoglycine, TEA, POPSO, HEPPSO, EPS, HEPPS, Tricine, TRIZMA, Glycinamide, Glycyl-glycine, HEPBS, Bicine, TAPS, AMPB, CHES, AMP, AMPSO, CAPSO, CAPS, and CABS.
In embodiments where the composition is in a liquid form, a carrier can be a solvent or dispersion medium comprising but not limited to, water, ethanol, polyol (e.g., glycerol, propylene glycol, liquid polyethylene glycol, etc.), lipids (e.g., triglycerides, vegetable oils, liposomes) and combinations 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 by dispersion in carriers such as, for example liquid polyol or lipids; by the use of surfactants such as, for example hydroxypropylcellulose; or combinations thereof such methods. If desired tonicity adjusting agents can be included, such as, for example, sugars, sodium chloride or combinations thereof. In some embodiments, the composition is isotonic.
The compositions may also include additional ingredients, such as acceptable surfactants, co-solvents, emollients, agents to adjust the pH and osmolarity and/or antioxidants to retard oxidation of one or more component.
The compositions can be prepared for administration by any suitable route such as ocular (including periocular and intravitreal administration), oral, parenteral, intranasal, anal, vaginal, topical, subcutaneous, intravenous, intra-arterial, intrathecal and intraperitoneal administration. Accordingly, while intrathecal administration is an option and may be selected by a clinician (e.g., when the aldose reductase inhibitor is not central nervous system penetrant), it is generally preferred that the aldose reductase inhibitor is not administered intrathecally. Oral compositions may be incorporated directly with the food of the diet. Preferred carriers for oral administration comprise inert diluents, edible carriers or combinations thereof. Examples of pharmaceutically acceptable carriers may include, for example, water or saline solution, polymers such as polyethylene glycol, carbohydrates and derivatives thereof, oils, fatty acids, or alcohols. Surfactants such as, for example, detergents, are also suitable for use in the formulations. Specific examples of surfactants include polyvinylpyrrolidone, polyvinyl alcohols, copolymers of vinyl acetate and of vinylpyrrolidone, polyethylene glycols, benzyl alcohol, mannitol, glycerol, sorbitol or polyoxyethylenated esters of sorbitan; lecithin or sodium carboxymethylcellulose; or acrylic derivatives, such as methacrylates and others, anionic surfactants, such as alkaline stearates, in particular sodium, potassium or ammonium stearate; calcium stearate or triethanolamine stearate; alkyl sulfates, in particular sodium lauryl sulfate and sodium cetyl sulfate; sodium dodecylbenzenesulphonate or sodium dioctyl sulphosuccinate; or fatty acids, in particular those derived from coconut oil, cationic surfactants, such as water-soluble quaternary ammonium salts of formula N R′R″R′″R″″Y″, in which the R radicals are identical or different optionally hydroxylated hydrocarbon radicals and Y″ is an anion of a strong acid, such as halide, sulfate and sulfonate anions; cetyltrimethylammonium bromide is one of the cationic surfactants which can be used, amine salts of formula NR′R′R″, in which the R radicals are identical or different optionally hydroxylated hydrocarbon radicals; octadecylamine hydrochloride is one of the cationic surfactants which can be used, non-ionic surfactants, such as optionally polyoxyethylenated esters of sorbitan, in particular Polysorbate 80, or polyoxyethylenated alkyl ethers; polyethylene glycol stearate, polyoxyethylenated derivatives of castor oil, polyglycerol esters, polyoxyethylenated fatty alcohols, polyoxyethylenated fatty acids or copolymers of ethylene oxide and of propylene oxide, amphoteric surfactants, such as substituted lauryl compounds of betaine.
If desired, an oral composition may comprise one or more binders, excipients, disintegration agents, lubricants, flavoring agents, and combinations thereof. In certain embodiments, a composition may comprise one or more of the following: a binder, such as, for example, gum tragacanth, acacia, cornstarch, gelatin or combinations thereof; an excipient, such as, for example, dicalcium phosphate, mannitol, lactose, starch, magnesium stearate, sodium saccharine, cellulose, magnesium carbonate or combinations thereof; a disintegrating agent, such as, for example, corn starch, potato starch, alginic acid or combinations thereof; a lubricant, such as, for example, magnesium stearate; a sweetening agent, such as, for example, sucrose, lactose, saccharin or combinations thereof; a flavoring agent, such as, for example peppermint, oil of wintergreen, cherry flavoring, orange flavoring, etc., or combinations thereof containing two or more of the foregoing.
Additional formulations which are suitable for other modes of administration include suppositories. Moreover, sterile injectable solutions may be prepared using an appropriate solvent. Generally, dispersions are prepared by incorporating the various sterilized amino acid components into a sterile vehicle, which contains the basic dispersion medium and/or the other ingredients. Suitable formulation methods for any desired mode of administration are well known in the art (see, generally, Remington's Pharmaceutical Sciences, 18th Ed. Mack Printing Company, 1990).
Typical pharmaceutically acceptable compositions can contain a an AR inhibitor and/or a pharmaceutically acceptable salt thereof at a concentration ranging from about 0.01 to about 2 wt %, such as 0.01 to about 1 wt % or about 0.05 to about 0.5 wt %. The composition can be formulated as a solution, suspension, ointment, or a capsule, and the like. The pharmaceutical composition can be prepared as an aqueous solution and can contain additional components, such as preservatives, buffers, tonicity agents, antioxidants, stabilizers, viscosity-modifying ingredients and the like. Other equivalent modes of administration can be found in U.S. Pat. No. 4,939,140.
When administered to a subject, the AR inhibitor and pharmaceutically acceptable carriers can be sterile. Suitable pharmaceutical carriers may also include excipients such as starch, glucose, lactose, sucrose, gelatin, malt, rice, flour, chalk, silica gel, sodium stearate, glycerol monostearate, talc, sodium chloride, dried skim milk, glycerol, propylene, glycol, polyethylene glycol 300, water, ethanol, polysorbate 20, and the like. The present compositions, if desired, may also contain minor amounts of wetting or emulsifying agents, or pH buffering agents.
The pharmaceutical formulations of the present disclosure are prepared by methods well-known in pharmaceutics. Optionally, one or more accessory ingredients (e.g., buffers, flavoring agents, surface active agents, and the like) also are added. The choice of carrier is determined by the solubility and chemical nature of the compounds, chosen route of administration and standard pharmaceutical practice.
In some embodiments, the composition is in unit dose form such as a tablet, capsule or single-dose vial. Suitable unit doses, i.e., therapeutically effective amounts, may be determined during clinical trials designed appropriately for each of the conditions for which administration of a chosen compound is indicated and will, of course, vary depending on the desired clinical endpoint.
Any of the compounds and/or compositions of the disclosure may be provided in a kit comprising the compounds and/or compositions. Thus, in one embodiment, the compound and/or composition of the disclosure is provided in a kit comprising in the same package or separate package, a carrier and optionally instructions for using the kit for therapeutic or prophylactic end usage.
The methods described herein include the administration of an AR inhibitor and one more additional therapeutic agents. The additional therapeutic agents may be administered before, concurrently with or after the AR inhibitor, but in a manner that provides for overlap of the pharmacological activity of the AR inhibitor and the additional therapeutic agent. The additional therapeutic agent can be, for example, second aldose reductase inhibitor, an antioxidant, or both.
For example, the 2nd aldose reductase can be a compound described in, for example, in U.S. Pat. Nos. 5,677,342; 5,155,259; 4,939,140; US US2006/0293265; and Roy et al., (Diabetes Research and Clinical Practice, 10, Issue 1, 91-97, 1990; and references cited therein; each of which hereby incorporated by reference in its entirety. Aldose reductase inhibitors include, for example, zopolrestat, epalrestat, ranirestat, berberine and sorbinil, as described in, e.g., U.S. Pat. Nos. 4,939,140; 6,159,976; and 6,570,013. Preferably, the 2nd aldose reductase inhibitor is selected from ponalrestat, epalrestat, sorbinil or sorbinol, imirestat, AND-138, CT-112, zopolrestat, zenarestat, BAL-AR18, AD-5467, M-79175, tolrestat, alconil, statil, berberine or SPR-210.
Other therapeutic agents that can be administered include, for example corticosteroids, e.g., prednisone, methylprednisolone, dexamethasone, or triamcinalone acetinide, or noncorticosteroid anti-inflammatory compounds, such as ibuprofen or flubiproben,. Similarly, vitamins and minerals, e.g., zinc, and micronutrients can be co-administered. In addition, inhibitors of the protein tyrosine kinase pathway, which include natural protein tyrosine kinase inhibitors like quercetin, lavendustin A, erbstatin and herbimycin A, and synthetic protein tyrosine kinase inhibitors like tyrphostins (e.g., AG490, AG17, AG213 (RG50864), AG18, AG82, AG494, AG825, AG879, AG1112, AG1296, AG1478, AG126, RG13022, RG14620 and AG555), dihydroxy-and dimethoxybenzylidene malononitrile, analogs of lavendustin A (e.g., AG814 and AG957), quinazolines (e.g., AG1478), 4,5-dianilinophthalimides, and thiazolidinediones, can be co-administered with genistein or an analog, prodrug or pharmaceutically acceptable salt thereof (see Levitzki et al., Science 267: 1782-1788 (1995); and Cunningham et al., Anti-Cancer Drug Design 7: 365-384 (1992)). In this regard, potentially useful derivatives of genistein include those set forth in Mazurek et al., U.S. Pat. No. 5,637,703. Selenoindoles (2-thioindoles) and related disulfide selenides, such as those described in Dobrusin et al., U.S. Pat. No. 5,464,961, are useful protein tyrosine kinase inhibitors. Neutralizing proteins to growth factors, such as a monoclonal antibody that is specific for a given growth factor, e.g., VEGF (for an example, see Aiello et al., PNAS USA 92: 10457-10461 (1995)), or phosphotyrosine (Dhar et al., Mol. Pharmacol. 37: 519-525 (1990)), can be co-administered. Other various compounds that can be co-administered include inhibitors of protein kinase C (see, e.g., U.S. Pat. Nos. 5,719,175 and 5,710,145), cytokine modulators, an endothelial cell-specific inhibitor of proliferation, e.g., thrombospondins, an endothelial cell-specific inhibitory growth factor, e.g., TNFα, an anti-proliferative peptide, e.g., SPARC and prolferin-like peptides, a glutamate receptor antagonist, aminoguanidine, an angiotensin-converting enzyme inhibitor, e.g., angiotensin II, calcium channel blockers, y-tectorigenin, ST638, somatostatin analogues, e.g., SMS 201-995, monosialoganglioside GM1, ticlopidine, neurotrophic growth factors, methyl-2,5-dihydroxycinnamate, an angiogenesis inhibitor, e.g., recombinant EPO, a sulphonylurea oral hypoglycemic agent, e.g., gliclazide (non-insulin-dependent diabetes), ST638 (Asahi et al., FEBS Letter 309: 10-14 (1992)), thalidomide, nicardipine hydrochloride, aspirin, piceatannol, staurosporine, adriamycin, epiderstatin, (+)-aeroplysinin-1, phenazocine, halomethyl ketones, anti-lipidemic agents, e.g., etofibrate, chlorpromazine, spinghosines and retinoic acid and analogs thereof (Burke et al., Drugs of the Future 17 (2): 119-131 (1992); and Tomlinson et al., Pharmac. Ther. 54: 151-194 (1992)).
The present disclosure further provides for the use of the compounds of Formula (I)-(VI), or a pharmaceutically acceptable salt, hydrate, solvate, or prodrug thereof, in a method of treating a disease state, and/or condition caused by or related to sorbitol-dehydrogenase (SDH) deficiency. In another embodiment, the disclosure relates to use of the compounds of Formula (I)-(VI), or a pharmaceutically acceptable salt, hydrate, solvate, or prodrug thereof, in a method of treating a disease state, and/or condition caused by or related to sorbitol-dehydrogenase (SDH) deficiency, comprising the steps of: (a) identifying a subject in need of such treatment; (b) providing a compound of Formula (I)-(VI), or a pharmaceutically acceptable salt, hydrate, solvate, prodrug thereof; and (c) administering said compound of Formula (I)-(VI) in a therapeutically effective amount to treat, suppress and/or prevent the disease state or condition in a subject in need of such treatment.
In another embodiment, the disclosure relates to use of the compounds of Formula (I)-(VI), or a pharmaceutically acceptable salt, hydrate, solvate, or prodrug thereof, in a method of treating a disease state, and/or condition caused by or related to sorbitol-dehydrogenase (SDH) deficiency, comprising the steps of: (a) identifying a subject in need of such treatment; (ii) providing a composition comprising a compound of Formula (I)-(VI), or a pharmaceutically acceptable salt, hydrate, solvate, prodrug or tautomer thereof; and (iii) administering said composition in a therapeutically effective amount to treat, suppress and/or prevent the disease state or condition in a subject in need of such treatment.
In the aforementioned embodiments, the compound or composition is preferably used orally.
Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this disclosure belongs.
Fibroblasts were obtained from skin biopsy of normal human volunteers or patients with confirmed sorbitol dehydrogenase deficiency (biallelic c.757delG). Fibroblasts were cultured in triplicate in Dulbecco's modified Eagle's medium (ThermoFisher) supplemented with 10% fetal bovine serum, penicillin and streptomycin (Gibco). Cells were grown in 5% CO2 at 37° C. in a humidified incubator. Asynchronous cell cultures were grown to approximately 80% confluency, and then treated with vehicle, Compound A (100 uM) or Compound B (10 uM) for 72 hours. Th media containing vehicle, Compound A or Compound B, was changed every 24 hours.
Sorbitol and protein were determinated from lysates of human fibroblasts. For protein measurements, fibroblasts were collected and lysed in RIPA buffer (ThermoFisher) containing protease inhibitors (Roche) and sonicated for 5 minutes using a Bioruptor sonication device (Diagenode). Protein quantification was conducted using a Coomassie assay. For sorbitol determination, a UPLC-tandem mass spectrometry (MS/MS) (Waters Acquity UPLC & TQD mass spectrometer) was used, fibroblasts were collected and lysed in RIPA buffer (ThermoFisher) and sonicated for 5 minutes using a Bioruptor sonication device (Diagenode). Cell lysates were centrifuged 13,000 g for 10 minutes at 4° C., and the supernatants were collected for protein quantification and sorbitol measurement. For Sorbitol measurements, the lysate underwent protein precipitation with acetonitrile (1:5), tenfold dilution with acetonitrile/water (50:50) and cleanup on Oasis HLB cartridges (10 mg/ml), before injection (3 ul) into the UPLC system. The UPLC conditions were as follows: column: BHE amid 1.7 um (2.1×100 mm) at 88° C.; eluent A: acetonitrile 90%/water 5%/isopropanol 5%; eluent B: acetonitrile 80%/water 20%; gradient elution, 0 minutes 100% A to 3.6 minutes 100% B; flow rate of 0.45 ml/minute. The retention time of sorbitol was 2.7 minutes. The linearity of the method was assessed between 0.25 and 50 mgl−1. The MS/MS conditions were as follows: interface, electrospray interface in negative ion mode; multiple reaction monitory acquisition, m/z 180.0→88.9 (CV 24, CE 15). The detection limit (signal-to-noise ration=3) was 0.03 mgl−1. Sorbitol levels were normalized to protein concentration.
The study results demonstrated that human fibroblasts from patients with SDH deficiency have dramatically elevated levels of sorbitol. These elevated levels of sorbitol in fibroblasts and other cell types leads to osmotic swelling, changes in membrane permeability and oxidative stress, culminating in cell and tissue injury, including in hereditary neuropathies associated with SDH deficiency, such as Charcot-Marie-Tooth disease (CMT1 and particularly CMT2) and distal hereditary motor neuropathy (dHMN) a form of CMT2 that predominantly effects motor nerves. The study results demonstrate that treating fibroblasts from patients with SDH deficiency with inhibitors of aldose reductase activity reduces the level of sorbitol in the cells. See,
Although methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present disclosure, suitable methods and materials are described in the foregoing paragraphs. In addition, the materials and methods are illustrative only and not intended to be limiting. All United States patents and published or unpublished United States patent applications cited herein are incorporated by reference. All published foreign patents and patent applications cited herein are hereby incorporated by reference. All published references, documents, manuscripts, scientific literature cited herein are hereby incorporated by reference. All identifier and accession numbers pertaining to scientific databases referenced herein (e.g., PUBMED, NCBI, GENBANK, EBI) are hereby incorporated by reference.
This application filed under 35 U.S.C. 111(a) is a continuation of International Application No. PCT/US2021/029286, filed on Apr. 27, 2021, which claims the benefit of U.S. Patent Application No. 63/019,186, filed May 1, 2020 and of U.S. Patent Application No. 63/019,738, filed May 4, 2020, the entire contents of each of which are incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| 63019186 | May 2020 | US | |
| 63019738 | May 2020 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/US2021/029286 | Apr 2021 | US |
| Child | 18050627 | US |
