WO2013059587A1 - Substituted bicyclic aza-heterocycles and analogues as sirtuin modulators - Google Patents
Substituted bicyclic aza-heterocycles and analogues as sirtuin modulators Download PDFInfo
- Publication number
- WO2013059587A1 WO2013059587A1 PCT/US2012/061015 US2012061015W WO2013059587A1 WO 2013059587 A1 WO2013059587 A1 WO 2013059587A1 US 2012061015 W US2012061015 W US 2012061015W WO 2013059587 A1 WO2013059587 A1 WO 2013059587A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- alkyl
- substituted
- halo
- phenyl
- sirtuin
- Prior art date
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
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- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A61P5/50—Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
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- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Definitions
- the Silent Information Regulator (SIR) family of genes represents a highly conserved group of genes present in the genomes of organisms ranging from archaebacteria to eukaryotes.
- the encoded SIR proteins are involved in diverse processes from regulation of gene silencing to DNA repair.
- a well-characterized gene in this family is S. cerevisiae SIR2, which is involved in silencing HM loci that contain information specifying yeast mating type, telomere position effects and cell aging.
- the yeast Sir2 protein belongs to a family of histone deacetylases.
- the proteins encoded by members of the SIR gene family show high sequence conservation in a 250 amino acid core domain.
- the Sir2 homolog, CobB, in Salmonella typhimurium functions as an NAD (nicotinamide adenine dinucleotide)-dependent ADP-ribosyl transferase.
- the Sir2 protein is a class III deacetylase which uses NAD as a cosubstrate.
- Sir2 is insensitive to class I and II histone deacetylase inhibitors like trichostatin A (TSA).
- TSA histone deacetylase inhibitors
- acetylation of acetyl-lysine by Sir2 is tightly coupled to NAD hydrolysis, producing nicotinamide and a novel acetyl-ADP ribose compound.
- the NAD-dependent deacetylase activity of Sir2 is essential for its functions, which can connect its biological role with cellular metabolism in yeast.
- Mammalian Sir2 homologs have NAD-dependent histone deacetylase activity.
- SIRT1-SIRT7 are seven Sir2-like genes that share the conserved catalytic domain of Sir2.
- SIRT1 is a nuclear protein with the highest degree of sequence similarity to Sir2.
- SIRT1 regulates multiple cellular targets by deacetylation including the tumor suppressor p53, the cellular signaling factor NF- ⁇ , and the FOXO transcription factor.
- SIRT3 is a homolog of SIRT1 that is conserved in prokaryotes and eukaryotes.
- the SIRT3 protein is targeted to the mitochondrial cristae by a unique domain located at the N-terminus.
- SIRT3 has NAD -dependent protein deacetylase activity and is ubiquitously expressed, particularly in metabolically active tissues. Upon transfer to the mitochondria, SIRT3 is believed to be cleaved into a smaller, active form by a mitochondrial matrix processing peptidase (MPP).
- MPP mitochondrial matrix processing peptidase
- Caloric restriction has been known for over 70 years to improve the health and extend the lifespan of mammals. Yeast life span, like that of metazoans, is also extended by interventions that resemble caloric restriction, such as low glucose. The discovery that both yeast and flies lacking the SIR2 gene do not live longer when calorically restricted provides evidence that SIR2 genes mediate the beneficial health effects of a restricted calorie diet. Moreover, mutations that reduce the activity of the yeast glucose-responsive cAMP (adenosine 3',5'-monophosphate)-dependent (PKA) pathway extend life span in wild type cells but not in mutant sir2 strains, demonstrating that SIR2 is likely to be a key downstream component of the caloric restriction pathway.
- yeast glucose-responsive cAMP adenosine 3',5'-monophosphate
- novel sirtuin-modulating compounds and methods of use thereof.
- the invention provides sirtuin-modulating compounds of Structural
- the invention provides methods for using sirtuin-modulating compounds, or compositions comprising sirtuin-modulating compounds.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be used for a variety of therapeutic applications including, for example, increasing the lifespan of a cell, and treating and/or preventing a wide variety of diseases and disorders including, for example, diseases or disorders related to aging or stress, diabetes, obesity, neurodegenerative diseases, chemotherapeutic-induced neuropathy, neuropathy associated with an ischemic event, ocular diseases and/or disorders, cardiovascular disease, blood clotting disorders, inflammation, and/or flushing, etc.
- Sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may also be used for treating a disease or disorder in a subject that would benefit from increased mitochondrial activity, for enhancing muscle performance, for increasing muscle ATP levels, or for treating or preventing muscle tissue damage associated with hypoxia or ischemia.
- sirtuin-modulating compounds that decrease the level and/or activity of a sirtuin protein may be used for a variety of therapeutic applications including, for example, increasing cellular sensitivity to stress, increasing apoptosis, treatment of cancer, stimulation of appetite, and/or stimulation of weight gain, etc.
- the methods comprise administering to a subject in need thereof a pharmaceutically effective amount of a sirtuin-modulating compound.
- the sirtuin-modulating compounds may be administered alone or in combination with other compounds, including other sirtuin-modulating compounds, or other therapeutic agents.
- agent is used herein to denote a chemical compound, a mixture of chemical compounds, a biological macromolecule (such as a nucleic acid, an antibody, a protein or portion thereof, e.g., a peptide), or an extract made from biological materials such as bacteria, plants, fungi, or animal (particularly mammalian) cells or tissues.
- a biological macromolecule such as a nucleic acid, an antibody, a protein or portion thereof, e.g., a peptide
- an extract made from biological materials such as bacteria, plants, fungi, or animal (particularly mammalian) cells or tissues.
- bioavailable when referring to a compound, is art-recognized and refers to a form of a compound that allows for all or a portion of the amount of compound administered to be absorbed by, incorporated into, or otherwise physiologically available to a subject or patient to whom it is administered.
- Biologically active portion of a sirtuin refers to a portion of a sirtuin protein having a biological activity, such as the ability to deacetylate ("catalytically active").
- Catalytically active portions of a sirtuin may comprise the core domain of sirtuins.
- Catalytically active portions of SIRT1 having GenBank Accession No. NP 036370 that encompass the NAD + binding domain and the substrate binding domain for example, may include without limitation, amino acids 240-664 or 240-505 of GenBank Accession No. NP 036370, which are encoded by the polynucleotide of GenBank Accession No. NM 012238. Therefore, this region is sometimes referred to as the core domain.
- SIRT1 also sometimes referred to as core domains
- Other catalytically active portions of SIRT1 include about amino acids 261 to 447 of GenBank Accession No. NP 036370, which are encoded by nucleotides 834 to 1394 of GenBank Accession No. NM 012238; about amino acids 242 to 493 of GenBank Accession No. NP 036370, which are encoded by nucleotides 777 to 1532 of GenBank Accession No. NM 012238; or about amino acids 254 to 495 of GenBank Accession No. NP 036370, which are encoded by nucleotides 813 to 1538 of GenBank Accession No. NM 012238.
- Another "biologically active" portion of SIRT1 is amino acids 62-293 or 183-225 of GenBank Acession No.
- NP 036370 which comprise a domain N-terminal to the core domain that is important to the compound binding site.
- cat(s) refers to a feline animal including domestic cats and other members of the family Felidae, genus Felis.
- Diabetes refers to high blood sugar or ketoacidosis, as well as chronic, general metabolic abnormalities arising from a prolonged high blood sugar status or a decrease in glucose tolerance. “Diabetes” encompasses both the type I and type II (Non Insulin Dependent Diabetes Mellitus or NIDDM) forms of the disease.
- the risk factors for diabetes include the following factors: waistline of more than 40 inches for men or 35 inches for women, blood pressure of 130/85 mmHg or higher, triglycerides above 150 mg/dl, fasting blood glucose greater than 100 mg/dl or high-density lipoprotein of less than 40 mg/dl in men or 50 mg/dl in women.
- ED 50 refers to the art-recognized measure of effective dose.
- ED 50 means the dose of a drug which produces 50% of its maximum response or effect, or alternatively, the dose which produces a pre-determined response in refers to the art-recognized measure of lethal dose.
- LD 50 means the dose of a drug which is lethal in 50% of test subjects.
- therapeutic index is an art-recognized term which refers to the therapeutic index of a drug, defined as LD 5 o/ED 5 o.
- hyperinsulinemia refers to a state in an individual in which the level of insulin in the blood is higher than normal.
- insulin resistance refers to a state in which a normal amount of insulin produces a subnormal biologic response relative to the biological response in a subject that does not have insulin resistance.
- insulin resistance disorder refers to any disease or condition that is caused by or contributed to by insulin resistance. Examples include: diabetes, obesity, metabolic syndrome, insulin-resistance syndromes, syndrome X, insulin resistance, high blood pressure, hypertension, high blood cholesterol, dyslipidemia, hyperlipidemia, atherosclerotic disease including stroke, coronary artery disease or myocardial infarction, hyperglycemia, hyperinsulinemia and/or hyperproinsulinemia, impaired glucose tolerance, delayed insulin release, diabetic complications, including coronary heart disease, angina pectoris, congestive heart failure, stroke, cognitive functions in dementia, retinopathy, peripheral neuropathy, nephropathy,
- glomerulonephritis glomerulosclerosis
- nephrotic syndrome hypertensive nephrosclerosis
- some types of cancer such as endometrial, breast, prostate, and colon
- complications of pregnancy poor female reproductive health (such as menstrual irregularities, infertility, irregular ovulation, polycystic ovarian syndrome (PCOS)), lipodystrophy, cholesterol- related disorders, such as gallstones, cholecystitis and cholelithiasis, gout, obstructive sleep apnea and respiratory problems, osteoarthritis, and bone loss, e.g., osteoporosis in particular.
- PCOS polycystic ovarian syndrome
- livestock animals refers to domesticated quadrupeds, which includes those being raised for meat and various byproducts, e.g., a bovine animal including cattle and other members of the genus Bos, a porcine animal including domestic swine and other members of the genus Sus, an ovine animal including sheep and other members of the genus Ovis, domestic goats and other members of the genus Capra; domesticated quadrupeds being raised for specialized tasks such as use as a beast of burden, e.g., an equine animal including domestic horses and other members of the family Equidae, genus Equus.
- mammals include humans, primates, livestock animals (including bovines, porcines, etc.), companion animals (e.g., canines, felines, etc.) and rodents (e.g., mice and rats).
- livestock animals including bovines, porcines, etc.
- companion animals e.g., canines, felines, etc.
- rodents e.g., mice and rats.
- Obese individuals or individuals suffering from obesity are generally individuals having a body mass index (BMI) of at least 25 or greater. Obesity may or may not be associated with insulin resistance.
- BMI body mass index
- parenteral administration and “administered parenterally” are art- recognized and refer to modes of administration other than enteral and topical administration, usually by injection, and includes, without limitation, intravenous, intramuscular, intraarterial, intrathecal, intracapsular, intraorbital, intracardiac, intradermal, intraperitoneal, transtracheal, subcutaneous, subcuticular, intra-articular, subcapsular, subarachnoid, intraspinal, and intrasternal injection and infusion.
- a "patient”, “subject”, “individual” or “host” refers to either a human or a non- human animal.
- pharmaceutically acceptable carrier refers to a pharmaceutically-acceptable material, composition or vehicle, such as a liquid or solid filler, diluent, excipient, solvent or encapsulating material, involved in carrying or transporting any subject composition or component thereof.
- a pharmaceutically-acceptable material such as a liquid or solid filler, diluent, excipient, solvent or encapsulating material, involved in carrying or transporting any subject composition or component thereof.
- Each carrier must be “acceptable” in the sense of being compatible with the subject composition and its components and not injurious to the patient.
- materials which may serve as pharmaceutically acceptable carriers include: (1) sugars, such as lactose, glucose and sucrose; (2) starches, such as corn starch and potato starch; (3) cellulose, and its derivatives, such as sodium carboxymethyl cellulose, ethyl cellulose and cellulose acetate; (4) powdered tragacanth; (5) malt; (6) gelatin; (7) talc; (8) excipients, such as cocoa butter and suppository waxes; (9) oils, such as peanut oil, cottonseed oil, safflower oil, sesame oil, olive oil, corn oil and soybean oil; (10) glycols, such as propylene glycol; (11) polyols, such as glycerin, sorbitol, mannitol and polyethylene glycol; (12) esters, such as ethyl oleate and ethyl laurate; (13) agar; (14) buffering agents, such as magnesium hydroxide and aluminum hydroxide;
- preventing is art-recognized, and when used in relation to a condition, such as a local recurrence (e.g., pain), a disease such as cancer, a syndrome complex such as heart failure or any other medical condition, is well understood in the art, and includes administration of a composition which reduces the frequency of, or delays the onset of, symptoms of a medical condition in a subject relative to a subject which does not receive the composition.
- a condition such as a local recurrence (e.g., pain)
- a disease such as cancer
- a syndrome complex such as heart failure or any other medical condition
- prevention of cancer includes, for example, reducing the number of detectable cancerous growths in a population of patients receiving a prophylactic treatment relative to an untreated control population, and/or delaying the appearance of detectable cancerous growths in a treated population versus an untreated control population, e.g., by a statistically and/or clinically significant amount.
- Prevention of an infection includes, for example, reducing the number of diagnoses of the infection in a treated population versus an untreated control population, and/or delaying the onset of symptoms of the infection in a treated population versus an untreated control population.
- Prevention of pain includes, for example, reducing the magnitude of, or alternatively delaying, pain sensations experienced by subjects in a treated population versus an untreated control population.
- prophylactic or therapeutic treatment refers to administration of a drug to a host. 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).
- pyrogen-free refers to a composition that does not contain a pyrogen in an amount that would lead to an adverse effect (e.g., irritation, fever, inflammation, diarrhea, respiratory distress, endotoxic shock, etc.) in a subject to which the composition has been administered.
- an adverse effect e.g., irritation, fever, inflammation, diarrhea, respiratory distress, endotoxic shock, etc.
- the term is meant to encompass compositions that are free of, or substantially free of, an endotoxin such as, for example, a lipopolysaccharide (LPS).
- LPS lipopolysaccharide
- Replicative lifespan of a cell refers to the number of daughter cells produced by an individual "mother cell.”
- Increasing the lifespan of a cell or “extending the lifespan of a cell,” as applied to cells or organisms, refers to increasing the number of daughter cells produced by one cell; increasing the ability of cells or organisms to cope with stresses and combat damage, e.g., to DNA, proteins; and/or increasing the ability of cells or organisms to survive and exist in a living state for longer under a particular condition, e.g., stress (for example, heatshock, osmotic stress, high energy radiation, chemically- induced stress, DNA damage, inadequate salt level, inadequate nitrogen level, or inadequate nutrient level). Lifespan can be increased by at least about 10%, 20%, 30%, 40%, 50%, 60% or between 20% and 70%, 30% and 60%, 40% and 60% or more using methods described herein.
- sirtuin-modulating compound refers to a compound that increases the level of a sirtuin protein and/or increases at least one activity of a sirtuin protein.
- a sirtuin-modulating compound may increase at least one biological activity of a sirtuin protein by at least about 10%, 25%, 50%, 75%, 100%, or more.
- Exemplary biological activities of sirtuin proteins include deacetylation, e.g., of histones and p53; extending lifespan; increasing genomic stability; silencing transcription; and controlling the segregation of oxidized proteins between mother and daughter cells.
- sirtuin protein refers to a member of the sirtuin deacetylase protein family, or preferably to the sir2 family, which include yeast Sir2 (GenBank Accession No. P53685), C. elegans Sir-2.1 (GenBank Accession No. NP 501912), and human SIRTl (GenBank Accession No. NM 012238 and NP 036370 (or AF083106)) and SIRT2 (GenBank Accession No. NM 012237, NM 030593, NP 036369, NP 085096, and AF083107) proteins.
- HST genes additional yeast Sir2-like genes termed "HST genes” (homologues of Sir two) HST1, HST2, HST3 and HST4, and the five other human homologues hSIRT3, hSIRT4, hSIRT5, hSIRT6 and hSIRT7 (Brachmann et al. (1995) Genes Dev. 9:2888 and Frye et al. (1999) BBRC 260:273).
- HST genes homologues of Sir two HST1, HST2, HST3 and HST4
- SIRT1 protein refers to a member of the sir2 family of sirtuin deacetylases.
- a SIRT1 protein includes yeast Sir2 (GenBank Accession No. P53685), C. elegans Sir-2.1 (GenBank Accession No. NP 501912), human SIRT1 (GenBank Accession No.
- a SIRT1 protein includes a polypeptide comprising a sequence consisting of, or consisting essentially of, the amino acid sequence set forth in GenBank Accession Nos. NP 036370, NP 501912, NP 085096, NP 036369, or P53685.
- SIRT1 proteins include polypeptides comprising all or a portion of the amino acid sequence set forth in GenBank Accession Nos. NP 036370, NP 501912, NP 085096, NP 036369, or P53685; the amino acid sequence set forth in GenBank Accession Nos.
- Polypeptides of the invention also include homologs (e.g., orthologs and paralogs), variants, or fragments, of GenBank Accession Nos.
- NP 036370 NP 501912, NP 085096, NP 036369, or P53685.
- SIRT2 protein As used herein "SIRT2 protein”, “SIRT3 protein”, “SIRT4 protein”, SIRT5 protein”, “SIRT6 protein”, and “SIRT7 protein” refer to other mammalian, e.g. human, sirtuin deacetylase proteins that are homologous to SIRT1 protein, particularly in the approximately 275 amino acid conserved catalytic domain.
- SIRT3 protein refers to a member of the sirtuin deacetylase protein family that is homologous to SIRT1 protein.
- a SIRT3 protein includes human SIRT3 (GenBank Accession No.
- a SIRT3 protein includes a polypeptide comprising a sequence consisting of, or consisting essentially of, the amino acid sequence set forth in GenBank Accession Nos. AAH01042, NP 036371, NP 001017524, or NP 071878.
- SIRT3 proteins include polypeptides comprising all or a portion of the amino acid sequence set forth in GenBank Accession AAH01042, NP 036371, NP 001017524, or NP 071878; the amino acid sequence set forth in GenBank Accession Nos.
- a SIRT3 protein includes a fragment of SIRT3 protein that is produced by cleavage with a mitochondrial matrix processing peptidase (MPP) and/or a mitochondrial intermediate peptidase (MIP).
- MIP mitochondrial matrix processing peptidase
- stereoisomer refers to any portion of the compound or the compound in its entirety.
- diastereomers and enantiomers are stereoisomers.
- systemic administration and “administered systemically,” are art- recognized and refer to the administration of a subject composition, therapeutic or other material enterally or parenterally.
- tautomer as used herein is art-recognized and refers to any one of the possible alternative structures that may exist as a result of tautomerism, which refers to a form of constitutional isomerism in which a structure may exist in two or more constitutional arrangements, particularly with respect to the position of hydrogens bonded to oxygen.
- tautomer is readily interconvertible and exists in equilibrium. For example, keto and enol tautomers exist in proportions determined by the equilibrium of conditions:
- therapeutic agent is art-recognized and refers to any biologically, physiologically, or pharmacologically active substance that acts locally or systemically in a subject.
- the term also means any substance intended for use in the diagnosis, cure, mitigation, treatment or prevention of disease or in the enhancement of desirable physical or mental development and/or conditions in an animal or human.
- therapeutic effect is art-recognized and refers to a beneficial local or systemic effect in animals, particularly mammals, and more particularly humans, caused by a pharmacologically active substance.
- therapeuticically-effective amount means that amount of such a substance that produces some desired local or systemic effect at a reasonable benefit/risk ratio applicable to any treatment.
- compositions described herein may be administered in a sufficient amount to produce a desired effect at a reasonable benefit/risk ratio applicable to such treatment.
- Treating refers to curing as well as ameliorating at least one symptom of the condition or disease.
- vision impairment refers to diminished vision, which is often only partially reversible or irreversible upon treatment (e.g., surgery). Particularly severe vision impairment is termed “blindness” or “vision loss”, which refers to a complete loss of vision, vision worse than 20/200 that cannot be improved with corrective lenses, or a visual field of less than 20 degrees diameter (10 degrees radius).
- the invention provides novel compounds for treating and/or preventing a wide variety of diseases and disorders including, for example, diseases or disorders related to aging or stress, diabetes, obesity, neurodegenerative diseases, ocular diseases and disorders, cardiovascular disease, blood clotting disorders, inflammation, cancer, and/or flushing, etc.
- Subject compounds such as sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein, may also be used for treating a disease or disorder in a subject that would benefit from increased mitochondrial activity, for enhancing muscle performance, for increasing muscle ATP levels, or for treating or preventing muscle tissue damage associated with hypoxia or ischemia.
- Compounds disclosed herein may be suitable for use in pharmaceutical compositions and/or one or more methods disclosed herein.
- compounds of the invention are represented by Structural Formula (I): wherein one of D and E is N and the other is C; and
- each R is independently selected from hydrogen, halo, OH, C ⁇ N, C1-C4 alkyl, halo-substituted C2-C4 alkyl, C1-C4 alkoxy-substituted C1-C4 alkyl, hydroxy-substituted Ci-Cs alkyl, OR 3 , 0-(Ci-C 4 alkyl)-OR 3 , S-(Ci-C 2 alkyl), S-(halo-substituted C1-C4 alkyl), N(hydroxy-substituted C1-C4 alkyl) 2 , N(methoxy-substituted C1-C4 alkyl) 2 , N(Ci-C 4 alkyl)(hydroxy-substituted C1-C4 alkyl), N(Ci-C 4 alkyl)(methoxy-substituted C1-C4 alkyl), N(hydroxy-substituted C1-C4 al
- each R 3 is independently selected from hydrogen and C1-C4 alkyl optionally substituted with one or more of OH, -0-(Ci-C 4 alkyl), halo, NH 2 , NH(Ci-C 4 alkyl), N(Ci-C 4 alkyl) 2 , NH(methoxy-substituted C C 4 alkyl), NH(hydroxy-substituted C C 4 alkyl), N(methoxy-substituted C]-C 4 alkyl)(hydroxy-substituted C1-C4 alkyl), N(hydroxy- substituted C]-C 4 alkyl)2 and N(methoxy-substituted C1-C4 alkyl)2; or
- ⁇ represents where X is bound to R 1 ;
- each R 4 and R 5 is independently selected from hydrogen, C1-C4 alkyl, CF3 and(Ci-C 3 alkyl)-CF 3 .
- both E and B are N.
- E, B and A are N.
- the compound of Structural Formula (I) is represented by
- E and B are N and A is CR.
- the compound of Structural Formula (I) is represented by Structural Formula (lb):
- both D and B are N and A is CR.
- the compound of Structural Formula (I) is represented by Structural Formula (Ic):
- both D and A are N and B is CR. In such embodiments, the
- Formula (I) is represented by Structural Formula (Id):
- R at each occurrence may be selected from hydrogen, halo, C1-C4 alkyl, O-R 3 and 4- to 8-membered non-aromatic heterocycle, such as selected from hydrogen, C1-C4 alkyl, and 4- to 8-membered non- aromatic heterocycle.
- R 1 may be selected from optionally substituted aromatic heterocycle, such as pyridinyl, thiazolyl, oxazolyl, pyrimidinyl, pyrazole, triazole, imidazole, pyrazine and pyridazine.
- R 1 may be selected from optionally substituted aromatic heterocycle, such as pyridinyl, thiazolyl, oxazolyl, pyrimidinyl, pyrazole, triazole, imidazole, pyrazine and pyridazine.
- R 2 may be selected from optionally substituted carbocycle and optionally substituted non-aromatic heterocycle.
- R 2 may be selected from optionally substituted aromatic carbocycle and optionally substituted non-aromatic heterocycle.
- R 2 may be selected from optionally substituted non-aromatic carbocycle and optionally substituted non-aromatic heterocycle.
- R 2 may be selected from an optionally substituted non-aromatic heterocycle and R 2 may be attached to the remainder of the compound by a nitrogen atom of R 2 .
- R 2 may be selected from optionally substituted aromatic carbocycle, such as phenyl.
- R 2 may be selected from optionally substituted non-aromatic heterocycle, e.g., nitrogen-containing heterocycles, such as pyrrolidine, piperidine and azetidine.
- R 2 may be selected from
- R at each occurrence may be selected from hydrogen, halo, OH, C ⁇ N, C1-C4 alkyl, halo-substituted C2-C4 alkyl, C1-C4 alkoxy- substituted C1-C4 alkyl, hydroxy-substituted Ci-C 8 alkyl, OR 3 , 0-(Ci-C 4 alkyl)-OR 3 , S-(C C2 alkyl), S-(halo-substituted C1-C4 alkyl), N(hydroxy-substituted C C 4 alkyl) 2 , N(methoxy-substituted Ci-C 4 alkyl) 2 , N(Ci-C 4 alkyl)(hydroxy-substituted C1-C4 alkyl), C5-C7 cycloalkyl, and 4- to 8-membered non-aromatic heterocycle, and when one or both of E and A is N, then R
- the compound is any one of Compound Numbers 14, 94,
- the invention includes pharmaceutical compositions of any of the compounds of Structural Formulas (I), (la), (lb), (Ic), or (Id), or as otherwise set forth above.
- the pharmaceutical composition of the compound of Structural Formulas (I), (la), (lb), (Ic), or (Id) may comprise one or more pharmaceutically acceptable carriers or diluents.
- compounds of the invention are represented by Structural
- each R' is independently selected from hydrogen, halo, C ⁇ N, C1-C4 alkyl, halo-substituted C1-C4 alkyl, O-R 3 , 0-(Ci-C 4 alkyl)-OR 3 , S-(Ci-C 4 alkyl),
- each R" is independently selected from hydrogen, halo, C ⁇ N, chloro- or bromo-substituted C C 4 alkyl, 0-(halo-substituted C C 4 alkyl), 0-(C C 4 alkyl)-OR 3 , C C 4 alkoxy-substituted C1-C4 alkyl, hydroxy-substituted Ci-Cg alkyl, S-(Ci-C4 alkyl), S-(halo-substituted C1-C4 alkyl), N(hydroxy-substituted C1-C4 alkyl) 2 , N(methoxy- substituted C1-C4 alkyl) 2 , N(Ci-C 4 alkyl)(hydroxy-substituted C1-C4 alkyl), N(Ci-C 4 alkyl)(methoxy-substituted C1-C4 alkyl), N(hydroxy-substituted C1-C4 alky
- each R 3 is independently selected from hydrogen and Ci-C 4 alkyl optionally substituted with one or more of OH, 0-(C C 4 alkyl), halo, NH 2 , NH(C C 4 alkyl), N(Ci-C 4 alkyl) 2 , NH(methoxy-substituted Ci-C 4 alkyl), NH(hydroxy-substituted Ci-C 4 alkyl), N(methoxy-substituted Ci-C 4 alkyl)(hydroxy-substituted Ci-C 4 alkyl), N(hydroxy- substituted Ci-C 4 alkyl) 2 and N(methoxy-substituted Ci-C 4 alkyl) 2 ; or
- ⁇ represents where X is bound to R 1 ;
- each R 4 and R 5 is independently hydrogen, C1-C4 alkyl, CF3 or (C1-C3 alkyl)-CF3.
- a C1-C4 alkoxy-substituted group may include one or more alkoxy substituents such as one, two or three methoxy groups or a methoxy group and an ethoxy group, for example.
- Exemplary C1-C4 alkoxy substituents include methoxy, ethoxy, isopropoxy, and tert-butoxy.
- a hydroxy-substituted group may include one or more hydroxy substituents, such as two or three hydroxy groups.
- a "halo-substituted"group includes from one halo substituent up to perhalo substitution.
- exemplary halo-substituted C1-C4 alkyl includes CFH 2 , CC1H 2, CBrH 2, CF 2 H, CC1 2 H, CBr 2 H, CF 3 , CC1 3, CBr 3, CH 2 CH 2 F, CH 2 CH 2 C1, CH 2 CH 2 Br, CH 2 CHF 2 , CHFCH3, CHCICH 3 , CHBrCH 3, CF 2 CHF 2 , CF 2 CHC1 2> CF 2 CHBr 2 , CH(CF 3 ) 2, and C(CF 3 ) 3 .
- Perhalo-substituted C C 4 alkyl for example, includes CF 3, CC1 3, CBr 3 , CF 2 CF 3 , CC1 2 CF 3 and CBr 2 CF 3 .
- a "carbocycle” group may refer to a monocyclic carbocycle embodiment and/or a poly cyclic carbocycle embodiment, such as a fused, bridged or bicyclic carbocycle embodiment.
- Carbocycle” groups of the invention may further refer to an aromatic carbocycle embodiment and/or a non-aromatic carbocycle embodiment, or, in the case of polycyclic embodiments, a carbocycle having both one or more aromatic rings and/or one or more non-aromatic rings.
- Polycyclic carbocycle embodiments may be a bicyclic ring, a fused ring or a bridged bicycle.
- Non-limiting exemplary carbocycles include phenyl, cyclohexane, cyclopentane, or cyclohexene, amantadine, cyclopentane, cyclohexane, bicyclo[2.2.1]heptane, 1,5-cyclooctadiene, 1,2,3,4-tetrahydronaphthalene, bicyclo[4.2.0]oct-3-ene, naphthalene, adamantane, decalin, naphthalene, 1,2,3,4-tetrahydronaphthalene, norbornane, decalin, spiropentane, memantine, biperiden, rimantadine, camphor, cholesterol, 4-phenylcyclcohexanol, bicyclo[4.2.0]octane, memantine and 4,5,6,7-tetrahydro-lH-indene and bicyclo[4.1.0]hept- 3-ene.
- a “heterocycle” group may refer to a monocyclic heterocycle embodiment and/or a poly cyclic heterocyclic embodiment, such as a fused, bridged or bicyclic heterocycle embodiment.
- “Heterocycle” groups of the invention may further refer to an aromatic heterocycle embodiment and/or a non-aromatic heterocycle embodiment, or, in the case of polycyclic embodiments, a heterocycle having both one or more aromatic rings and/or one or more non-aromatic rings.
- Polycyclic heterocycle embodiments may be a bicyclic ring, a fused ring or a bridged bicycle.
- Non- limiting exemplary heterocycles include pyridyl, pyrrolidine, piperidine, piperazine, pyrrolidine, morpholine, pyrimidine, benzofuran, indole, quinoline, lactones, lactams, benzodiazepine, indole, quinoline, purine, adenine, guanine, 4,5,6,7- tetrahydrobenzo[d]thiazole, hexamine and methenamine.
- Certain compounds of the present invention may exist in particular geometric or stereoisomeric forms.
- the present invention contemplates all such compounds, including cis- and /rans-isomers, (R)- and (>S)-enantiomers, diastereomers, (D)-isomers, (L)-isomers, the racemic mixtures thereof, and other mixtures thereof, as falling within the scope of the invention.
- Additional asymmetric carbon atoms may be present in a substituent such as an alkyl group. All such isomers, as well as mixtures thereof, are intended to be included in this invention.
- the compounds and salts thereof described herein can also be present as the corresponding hydrates (e.g., hemihydrate, monohydrate, dihydrate, trihydrate, tetrahydrate) or solvates. Suitable solvents for preparation of solvates and hydrates can generally be selected by a skilled artisan.
- the compounds and salts thereof can be present in amorphous or crystalline (including co-crystalline and polymorph) forms.
- Sirtuin-modulating compounds of the invention advantageously modulate the level and/or activity of a sirtuin protein, particularly the deacetylase activity of the sirtuin protein.
- sirtuin-modulating compounds of the invention do not substantially have one or more of the following activities: inhibition of PI3-kinase, inhibition of aldoreductase, inhibition of tyrosine kinase, transactivation of EGFR tyrosine kinase, coronary dilation, or spasmolytic activity, at concentrations of the compound that are effective for modulating the deacetylation activity of a sirtuin protein (e.g., such as a SIRT1 and/or a SIRT3 protein).
- a sirtuin protein e.g., such as a SIRT1 and/or a SIRT3 protein.
- alkyl group or “alkane” is a straight chained or branched non-aromatic hydrocarbon which is completely saturated. Typically, a straight chained or branched alkyl group has from 1 to about 20 carbon atoms, preferably from 1 to about 10 unless otherwise defined. Examples of straight chained and branched alkyl groups include methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, tert-butyl, pentyl, hexyl, pentyl and octyl. A straight chained or branched alkyl group is also referred to as a "lower alkyl" group.
- alkenyl (“alkene”) and “alkynyl” (“alkyne”) refer to unsaturated aliphatic groups analogous in length and possible substitution to the alkyl groups described above, but that contain at least one double or triple bond respectively.
- aromatic carbocycle refers to an aromatic hydrocarbon ring system containing at least one aromatic ring.
- the ring may be fused or otherwise attached to other aromatic carbocyclic rings or non-aromatic carbocyclic rings.
- aromatic carbocyclegroups include carbocyclic aromatic groups such as phenyl, naphthyl, and anthracyl.
- Azabicyclo refers to a bicyclic molecule that contains a nitrogen atom in the ring skeleton.
- the two rings of the bicycle may be fused at two mutually bonded atoms, e.g., indole, across a sequence of atoms, e.g., azabicyclo[2.2.1]heptane, or joined at a single atom, e.g., spirocycle.
- Bicycle or “bicyclic” refers to a two-ring system in which one, two or three or more atoms are shared between the two rings.
- Bicycle includes fused bicycles in which two adjacent atoms are shared by each of the two rings, e.g., decalin, indole.
- Bicycle also includes spiro bicycles in which two rings share a single atom, e.g., spiro[2.2]pentane, 1- oxa-6-azaspiro[3.4]octane.
- Bicycle further includes bridged bicycles in which at least three atoms are shared between two rings, e.g., norbornane.
- Bridged bicycle compounds are bicyclic ring systems in which at least three atoms are shared by both rings of the system, i.e., they include at least one bridge of one or more atoms connecting two bridgehead atoms.
- Bridged azabicyclo refers to a bridged bicyclic molecule that contains a nitrogen atom in at least one of the rings.
- carbocycle refers to a saturated or unsaturated ring in which each atom of the ring is carbon.
- carbocycle includes both aromatic carbocycles and non-aromatic carbocycles.
- Non-aromatic carbocycles include both cycloalkane rings, in which all carbon atoms are saturated, and cycloalkene rings, which contain at least one double bond.
- Carbocycle includes 5-7 membered monocyclic and 8-12 membered bicyclic rings. Each ring of a bicyclic carbocycle may be selected fromnon-aromatic and aromatic rings.
- Carbocycle includes bicyclic molecules in which one, two or three or more atoms are shared between the two rings.
- the term "fused carbocycle” refers to a bicyclic carbocycle in which each of the rings shares two adjacent atoms with the other ring.
- Each ring of a fused carbocycle may be selected fromnon- aromaticaromatic rings.
- an aromatic ring e.g., phenyl
- a non-aromatic or aromatic ring e.g., cyclohexane, cyclopentane, or cyclohexene. Any combination of non-aromtatic and aromatic bicyclic rings, as valence permits, is included in the definition of carbocyclic.
- Exemplary "carbocycles” include cyclopentane, cyclohexane, bicyclo[2.2.1]heptane, 1,5-cyclooctadiene, 1,2,3,4- tetrahydronaphthalene, bicyclo[4.2.0]oct-3-ene, naphthalene and adamantane.
- Exemplary fused carbocycles include decalin, naphthalene, 1,2,3,4-tetrahydronaphthalene, bicyclo[4.2.0]octane, 4,5,6,7-tetrahydro-lH-indene and bicyclo[4.1.0]hept-3-ene.
- Carbocycles may be substituted at any one or more positions capable of bearing a hydrogen atom.
- a “cycloalkyl” group is a cyclic hydrocarbon which is completely saturated (non- aromatic). Typically, a cycloalkyl group has from 3 to about 10 carbon atoms, more typically 3 to 8 carbon atoms unless otherwise defined.
- a “cycloalkenyl” group is a cyclic hydrocarbon containing one or more double bonds.
- a “halogen” designates F, CI, Br or I.
- halogen-substitution or “halo” substitution designates replacement of one or more hydrogens with F, CI, Br or I.
- heteroaryl or "aromatic heterocycle” includes substituted or unsubstituted aromatic single ring structures, preferably 5- to 7-membered rings, more preferably 5- to 6-membered rings, whose ring structures include at least one heteroatom, preferably one to four heteroatoms, more preferably one or two heteroatoms.
- heteroaryl also includes ring systems having one or two rings wherein at least one of the rings is heteroaromatic, e.g., the other cyclic rings can be cycloalkyl, cycloalkenyl, cycloalkynyl, aromatic carbocycle, heteroaryl, and/or heterocyclyl.
- Heteroaryl groups include, for example, pyrrole, furan, thiophene, imidazole, oxazole, thiazole, pyrazole, pyridine, pyrazine, pyridazine, and pyrimidine.
- heterocycle refers to a non- aromatic or aromatic ring comprising one or more heteroatoms selected from, for example, N, O, B and S atoms, preferably N, O, or S.
- heterocycle includes both "aromatic heterocycles” and “non-aromatic heterocycles.”
- Heterocycles include 4-7 membered monocyclic and 8-12 membered bicyclic rings.
- Heterocycle includes bicyclic molecules in which one, two or three or more atoms are shared between the two rings. Each ring of a bicyclic heterocycle may be selected fromnon-aromatic and aromatic rings.
- fused heterocycle refers to a bicyclic heterocycle in which each of the rings shares two adjacent atoms with the other ring.
- Each ring of a fused heterocycle may be selected fromnon-aromatic and aromatic rings.
- an aromatic ring e.g., pyridyl
- a non-aromatic or aromatic ring e.g., cyclohexane, cyclopentane, pyrrolidine, 2,3-dihydrofuran or cyclohexene.
- Heterocycle groups include, for example, piperidine, piperazine, pyrrolidine, morpholine, pyrimidine, benzofuran, indole, quinoline, lactones, and lactams.
- exemplary "fused heterocycles” include benzodiazepine, indole, quinoline, purine, and 4,5,6,7-tetrahydrobenzo[d]thiazole.
- Heterocycles may be substituted at any one or more positions capable of bearing a hydrogen atom.
- “Monocyclic rings” include 5-7 membered aromatic carbocycle or heteroaryl, 3-7 membered cycloalkyl or cycloalkenyl, and 5-7 membered non-aromatic heterocyclyl.
- Exemplary monocyclic groups include substituted or unsubstituted heterocycles or carbocycles such as thiazolyl, oxazolyl, oxazinyl, thiazinyl, dithianyl, dioxanyl, isoxazolyl, isothiazolyl, triazolyl, furanyl, tetrahydrofuranyl, dihydrofuranyl, pyranyl, tetrazolyl, pyrazolyl, pyrazinyl, pyridazinyl, imidazolyl, pyridinyl, pyrrolyl, dihydropyrrolyl, pyrrolidinyl, piperidinyl, piperazinyl, pyrimidinyl,
- substituted means substituting a hydrogen atom in a structure with an atom or molecule other than hydrogen.
- a substitutable atom such as a
- substituted nitrogen is an atom that bears a hydrogen atom in at least one resonance form.
- the hydrogen atom may be substituted for another atom or group such as a Q3 ⁇ 4 or an OH group.
- the nitrogen in a piperidine molecule is substitutable if the nitrogen is bound to a hydrogen atom. If, for example, the nitrogen of a piperidine is bound to an atom other than hydrogen, the nitrogen is not substitutable.
- An atom that is not capable of bearing a hydrogen atom in any resonance form is not substitutable.
- the compounds disclosed herein also include partially and fully deuterated variants.
- deuterated variants may be used for kinetic studies.
- One of skill in the art can select the sites at which such deuterium atoms are present.
- salts particularly pharmaceutically acceptable salts, of the compounds described herein.
- the compounds of the present invention that possess a sufficiently acidic, a sufficiently basic, or both functional groups can react with any of a number of inorganic bases, and inorganic and organic acids, to form a salt.
- compounds that are inherently charged, such as those with a quaternary nitrogen can form a salt with an appropriate counterion (e.g., a halide such as bromide, chloride, or fluoride, particularly bromide).
- Acids commonly employed to form acid addition salts are inorganic acids such as hydrochloric acid, hydrobromic acid, hydroiodic acid, sulfuric acid, phosphoric acid, and the like, and organic acids such as p-toluenesulfonic acid, methanesulfonic acid, oxalic acid, p-bromophenyl-sulfonic acid, carbonic acid, succinic acid, citric acid, benzoic acid, acetic acid, and the like.
- inorganic acids such as hydrochloric acid, hydrobromic acid, hydroiodic acid, sulfuric acid, phosphoric acid, and the like
- organic acids such as p-toluenesulfonic acid, methanesulfonic acid, oxalic acid, p-bromophenyl-sulfonic acid, carbonic acid, succinic acid, citric acid, benzoic acid, acetic acid, and the like.
- salts include the sulfate, pyrosulfate, bisulfate, sulfite, bisulfite, phosphate, monohydrogenphosphate, dihydrogenphosphate, metaphosphate, pyrophosphate, chloride, bromide, iodide, acetate, propionate, decanoate, caprylate, acrylate, formate, isobutyrate, caproate, heptanoate, propiolate, oxalate, malonate, succinate, suberate, sebacate, fumarate, maleate, butyne-l,4-dioate, hexyne-1,6- dioate, benzoate, chlorobenzoate, methylbenzoate, dinitrobenzoate, hydroxybenzoate, methoxybenzoate, phthalate, sulfonate, xylenesulfonate, phenylacetate, phenylpropionate, phenylbutyrate
- Base addition salts include those derived from inorganic bases, such as ammonium or alkali or alkaline earth metal hydroxides, carbonates, bicarbonates, and the like.
- bases useful in preparing the salts of this invention thus include sodium hydroxide, potassium hydroxide, ammonium hydroxide, potassium carbonate, and the like.
- the present invention provides methods of producing the above-defined compounds.
- the compounds may be synthesized using conventional techniques.
- these compounds are conveniently synthesized from readily available starting materials.
- Synthetic chemistry transformations and methodologies useful in synthesizing the compounds described herein are known in the art and include, for example, those described in R. Larock, Comprehensive Organic Transformations (1989); T. W. Greene and P. G. M. Wuts, Protective Groups in Organic Synthesis, 2d. Ed. (1991); L. Fieser and M. Fieser, Fieser and Fieser's Reagents for Organic Synthesis (1994); and L.
- a therapeutic compound may traverse the cytoplasmic membrane of a cell.
- a compound may have a cell-permeability of at least about 20%, 50%, 75%, 80%, 90% or 95%.
- the compound may be essentially non-toxic to a cell or subject; the compound may be an organic molecule or a small molecule of 2000 amu or less, 1000 amu or less; a compound may have a half-life under normal atmospheric conditions of at least about 30 days, 60 days, 120 days, 6 months or 1 year; the compound may have a half-life in solution of at least about 30 days, 60 days, 120 days, 6 months or 1 year; a compound may be more stable in solution than resveratrol by at least a factor of about 50%, 2 fold, 5 fold, 10 fold, 30 fold, 50 fold or 100 fold; a compound may promote deacetylation of the DNA repair factor Ku70; a compound may promote deacetylation of RelA/p65; a compound may increase general turnover rates and enhance the sensitivity of cells to TNF-induced apoptosis.
- a sirtuin-modulating compound does not have any substantial ability to inhibit a histone deacetylase (HDAC) class I, and/or an HDAC class II at concentrations (e.g., in vivo) effective for modulating the deacetylase activity of the sirtuin.
- HDAC histone deacetylase
- the sirtuin-modulating compound is a sirtuin-modulating compound and is chosen to have an EC 50 for activating sirtuin deacetylase activity that is at least 5 fold less than the EC 50 for inhibition of an HDAC I and/or HDAC II, and even more preferably at least 10 fold, 100 fold or even 1000 fold less.
- kits to perform such assays may be purchased commercially. See e.g., Bio Vision, Inc. (Mountain View, CA; world wide web at biovision.com) and Thomas Scientific (Swedesboro, NJ; world wide web at tomassci.com).
- a sirtuin-modulating compound does not have any substantial ability to modulate sirtuin homologs.
- an activator of a human sirtuin protein may not have any substantial ability to activate a sirtuin protein from lower eukaryotes, particularly yeast or human pathogens, at concentrations (e.g., in vivo) effective for activating the deacetylase activity of human sirtuin.
- a sirtuin-modulating compound may be chosen to have an EC 50 for activating a human sirtuin, such as SIRTl and/or SIRT3, deacetylase activity that is at least 5 fold less than the EC 50 for activating a yeast sirtuin, such as Sir2 (such as Candida, S. cerevisiae, etc.), and even more preferably at least 10 fold, 100 fold or even 1000 fold less.
- a human sirtuin such as SIRTl and/or SIRT3
- deacetylase activity that is at least 5 fold less than the EC 50 for activating a yeast sirtuin, such as Sir2 (such as Candida, S. cerevisiae, etc.)
- Sir2 such as Candida, S. cerevisiae, etc.
- an inhibitor of a sirtuin protein from lower eukaryotes, particularly yeast or human pathogens does not have any substantial ability to inhibit a sirtuin protein from humans at concentrations (e.g., in vivo) effective for inhibiting the deacetylase activity of a sirtuin protein from a lower eukaryote.
- a sirtuin-inhibiting compound may be chosen to have an IC 50 for inhibiting a human sirtuin, such as SIRTl and/or SIRT3, deacetylase activity that is at least 5 fold less than the IC 50 for inhibiting a yeast sirtuin, such as Sir2 (such as Candida, S. cerevisiae, etc.), and even more preferably at least 10 fold, 100 fold or even 1000 fold less.
- a sirtuin-modulating compound may have the ability to modulate one or more sirtuin protein homologs, such as, for example, one or more of human SIRTl, SIRT2, SIRT3, SIRT4, SIRT5, SIRT6, or SIRT7.
- a sirtuin-modulating compound has the ability to modulate both a SIRTl and a SIRT3 protein.
- a SIRTl modulator does not have any substantial ability to modulate other sirtuin protein homologs, such as, for example, one or more of human SIRT2, SIRT3, SIRT4, SIRT5, SIRT6, or SIRT7, at concentrations (e.g., in vivo) effective for modulating the deacetylase activity of human SIRTl.
- a sirtuin- modulating compound may be chosen to have an ED 50 for modulating human SIRTl deacetylase activity that is at least 5 fold less than the ED 50 for modulating one or more of human SIRT2, SIRT3, SIRT4, SIRT5, SIRT6, or SIRT7, and even more preferably at least 10 fold, 100 fold or even 1000 fold less.
- a SIRTl modulator does not have any substantial ability to modulate a SIRT3 protein.
- a SIRT3 modulator does not have any substantial ability to modulate other sirtuin protein homologs, such as, for example, one or more of human SIRTl, SIRT2, SIRT4, SIRT5, SIRT6, or SIRT7, at concentrations (e.g., in vivo) effective for modulating the deacetylase activity of human SIRT3.
- a sirtuin- modulating compound may be chosen to have an ED 50 for modulating human SIRT3 deacetylase activity that is at least 5 fold less than the ED 50 for modulating one or more of human SIRTl, SIRT2, SIRT4, SIRT5, SIRT6, or SIRT7, and even more preferably at least 10 fold, 100 fold or even 1000 fold less.
- a SIRT3 modulator does not have any substantial ability to modulate a SIRTl protein.
- a sirtuin-modulating compound may have a binding affinity for a sirtuin protein of about 10 "9 M, 10 "10 M, 10 "U M, 10 "12 M or less.
- a sirtuin- modulating compound may reduce (activator) or increase (inhibitor) the apparent Km of a sirtuin protein for its substrate or NAD + (or other cofactor) by a factor of at least about 2, 3, 4, 5, 10, 20, 30, 50 or 100.
- Km values are determined using the mass spectrometry assay described herein.
- Preferred activating compounds reduce the Km of a sirtuin for its substrate or cofactor to a greater extent than caused by resveratrol at a similar concentration or reduce the Km of a sirtuin for its substrate or cofactor similar to that caused by resveratrol at a lower concentration.
- a sirtuin-modulating compound may increase the Vmax of a sirtuin protein by a factor of at least about 2, 3, 4, 5, 10, 20, 30, 50 or 100.
- a sirtuin-modulating compound may have an ED 50 for modulating the deacetylase activity of a SIRT1 and/or SIRT3 protein of less than about 1 nM, less than about 10 nM, less than about 100 nM, less than about 1 ⁇ , less than about 10 ⁇ , less than about 100 ⁇ , or from about 1-10 nM, from about 10-100 nM, from about 0.1-1 ⁇ , from about 1-10 ⁇ or from about 10-100 ⁇ .
- a sirtuin-modulating compound may modulate the deacetylase activity of a SIRT1 and/or SIRT3 protein by a factor of at least about 5, 10, 20, 30, 50, or 100, as measured in a cellular assay or in a cell based assay.
- a sirtuin-modulating compound may cause at least about 10%, 30%, 50%, 80%, 2 fold, 5 fold, 10 fold, 50 fold or 100 fold greater induction of the deacetylase activity of a sirtuin protein relative to the same concentration of resveratrol.
- a sirtuin-modulating compound may have an ED 50 for modulating SIRT5 that is at least about 10 fold, 20 fold, 30 fold, 50 fold greater than that for modulating SIRT1 and/or SIRT3.
- the invention provides methods for modulating the level and/or activity of a sirtuin protein and methods of use thereof.
- the invention provides methods for using sirtuin- modulating compounds wherein the sirtuin-modulating compounds activate a sirtuin protein, e.g., increase the level and/or activity of a sirtuin protein.
- Sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be useful for a variety of therapeutic applications including, for example, increasing the lifespan of a cell, and treating and/or preventing a wide variety of diseases and disorders including, for example, diseases or disorders related to aging or stress, diabetes, obesity,
- the methods comprise administering to a subject in need thereof a pharmaceutically effective amount of a sirtuin-modulating compound, e.g., a sirtuin-modulating compound.
- activators of the instant invention may interact with a sirtuin at the same location within the sirtuin protein (e.g., active site or site affecting the Km or Vmax of the active site). It is believed that this is the reason why certain classes of sirtuin activators and inhibitors can have substantial structural similarity.
- the sirtuin-modulating compounds described herein may be taken alone or in combination with other compounds.
- a mixture of two or more sirtuin-modulating compounds may be administered to a subject in need thereof.
- a sirtuin-modulating compound that increases the level and/or activity of a sirtuin protein may be administered with one or more of the following compounds: resveratrol, butein, fisetin, piceatannol, or quercetin.
- a sirtuin-modulating compound that increases the level and/or activity of a sirtuin protein may be administered in combination with nicotinic acid or nicotinamide riboside.
- a sirtuin-modulating compound that decreases the level and/or activity of a sirtuin protein may be administered with one or more of the following compounds: nicotinamide (NAM), suramin; NF023 (a G-protein antagonist); NF279 (a purinergic receptor antagonist); Trolox (6-hydroxy-
- one or more sirtuin-modulating compounds may be administered with one or more therapeutic agents for the treatment or prevention of various diseases, including, for example, cancer, diabetes, neurodegenerative diseases, cardiovascular disease, blood clotting, inflammation, flushing, obesity, aging, stress, etc.
- combination therapies comprising a sirtuin-modulating compound may refer to (1) pharmaceutical compositions that comprise one or more sirtuin-modulating compounds in combination with one or more therapeutic agents (e.g., one or more therapeutic agents described herein); and (2) coadministration of one or more sirtuin-modulating compounds with one or more therapeutic agents wherein the sirtuin-modulating compound and therapeutic agent have not been formulated in the same compositions (but may be present within the same kit or package, such as a blister pack or other multi-chamber package; connected, separately sealed containers (e.g., foil pouches) that can be separated by the user; or a kit where the compound(s) and other therapeutic agent(s) are in separate vessels).
- the sirtuin-modulating compound may be administered simultaneous with, intermittent with, staggered with, prior to, subsequent to, or combinations thereof, the administration of another therapeutic agent.
- methods for reducing, preventing or treating diseases or disorders using a compound described herein may also comprise increasing the protein level of a sirtuin, such as human SIRT1, SIRT2 and/or SIRT3, or homologs thereof.
- Increasing protein levels can be achieved by introducing into a cell one or more copies of a nucleic acid that encodes a sirtuin.
- the level of a sirtuin can be increased in a mammalian cell by introducing into the mammalian cell a nucleic acid encoding the sirtuin, e.g., increasing the level of SIRT1 by introducing a nucleic acid encoding the amino acid sequence set forth in GenBank Accession No. NP 036370 and/or increasing the level of SIRT3 by introducing a nucleic acid encoding the amino acid sequence set forth in GenBank Accession No. AAH01042.
- a nucleic acid that is introduced into a cell to increase the protein level of a sirtuin may encode a protein that is at least about 80%, 85%, 90%, 95%, 98%, or 99% identical to the sequence of a sirtuin, e.g., SIRT1 and/or SIRT3 protein.
- the nucleic acid encoding the protein may be at least about 80%, 85%, 90%, 95%, 98%, or 99% identical to a nucleic acid encoding a SIRT1 (e.g. GenBank Accession No. NM 012238) and/or
- the nucleic acid may also be a nucleic acid that hybridizes, preferably under stringent hybridization conditions, to a nucleic acid encoding a wild-type sirtuin, e.g., SIRT1 and/or SIRT3 protein.
- Stringent hybridization conditions may include hybridization and a wash in 0.2 x SSC at 65 °C.
- the protein is preferably biologically active, e.g., is capable of deacetylation.
- a protein that differs from wild-type SIRT1 having GenBank Accession No. NP 036370 preferably contains the core structure thereof.
- the core structure sometimes refers to amino acids 62-293 of GenBank Accession No. NP 036370, which are encoded by nucleotides 237 to 932 of GenBank Accession No. NM 012238, which encompasses the NAD binding as well as the substrate binding domains.
- the core domain of SIRT1 may also refer to about amino acids 261 to 447 of GenBank Accession No. NP 036370, which are encoded by nucleotides 834 to 1394 of GenBank Accession No.
- Whether a protein retains a biological function, e.g., deacetylation capabilities, can be determined according to methods known in the art.
- methods for reducing, preventing or treating diseases or disorders using a sirtuin-modulating compound may also comprise decreasing the protein level of a sirtuin, such as human SIRT1, SIRT2 and/or SIRT3, or homologs thereof.
- Decreasing a sirtuin protein level can be achieved according to methods known in the art.
- an siRNA, an antisense nucleic acid, or a ribozyme targeted to the sirtuin can be expressed in the cell.
- a dominant negative sirtuin mutant e.g., a mutant that is not capable of deacetylating, may also be used.
- mutant H363Y of SIRT1 described, e.g., in Luo et al. (2001) Cell 107:137 can be used.
- agents that inhibit transcription can be used.
- Methods for modulating sirtuin protein levels also include methods for modulating the transcription of genes encoding sirtuins, methods for stabilizing/destabilizing the corresponding mRNAs, and other methods known in the art.
- the invention provides a method extending the lifespan of a cell, extending the proliferative capacity of a cell, slowing aging of a cell, promoting the survival of a cell, delaying cellular senescence in a cell, mimicking the effects of calorie restriction, increasing the resistance of a cell to stress, or preventing apoptosis of a cell, by contacting the cell with a sirtuin-modulating compound of the invention that increases the level and/or activity of a sirtuin protein.
- the methods comprise contacting the cell with a sirtuin-modulating compound.
- the methods described herein may be used to increase the amount of time that cells, particularly primary cells (i.e., cells obtained from an organism, e.g., a human), may be kept alive in a cell culture.
- Embryonic stem (ES) cells and pluripotent cells, and cells differentiated therefrom may also be treated with a sirtuin-modulating compound that increases the level and/or activity of a sirtuin protein to keep the cells, or progeny thereof, in culture for longer periods of time.
- ES Embryonic stem
- Such cells can also be used for transplantation into a subject, e.g., after ex vivo modification.
- cells that are intended to be preserved for long periods of time may be treated with a sirtuin-modulating compound that increases the level and/or activity of a sirtuin protein.
- the cells may be in suspension (e.g., blood cells, serum, biological growth media, etc.) or in tissues or organs.
- blood collected from an individual for purposes of transfusion may be treated with a sirtuin-modulating compound that increases the level and/or activity of a sirtuin protein to preserve the blood cells for longer periods of time.
- blood to be used for forensic purposes may also be preserved using a sirtuin-modulating compound that increases the level and/or activity of a sirtuin protein.
- Other cells that may be treated to extend their lifespan or protect against apoptosis include cells for consumption, e.g., cells from non-human mammals (such as meat) or plant cells (such as vegetables).
- Sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may also be applied during developmental and growth phases in mammals, plants, insects or microorganisms, in order to, e.g., alter, retard or accelerate the developmental and/or growth process.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be used to treat cells useful for transplantation or cell therapy, including, for example, solid tissue grafts, organ transplants, cell suspensions, stem cells, bone marrow cells, etc.
- the cells or tissue may be an autograft, an allograft, a syngraft or a xenograft.
- the cells or tissue may be treated with the sirtuin-modulating compound prior to administration/implantation, concurrently with
- the cells or tissue may be treated prior to removal of the cells from the donor individual, ex vivo after removal of the cells or tissue from the donor individual, or post implantation into the recipient.
- the donor or recipient individual may be treated systemically with a sirtuin-modulating compound or may have a subset of cells/tissue treated locally with a sirtuin-modulating compound that increases the level and/or activity of a sirtuin protein.
- the cells or tissue may additionally be treated with another therapeutic agent useful for prolonging graft survival, such as, for example, an immunosuppressive agent, a cytokine, an angiogenic factor, etc.
- cells may be treated with a sirtuin-modulating compound that increases the level and/or activity of a sirtuin protein in vivo, e.g., to increase their lifespan or prevent apoptosis.
- skin can be protected from aging (e.g., developing wrinkles, loss of elasticity, etc.) by treating skin or epithelial cells with a sirtuin-modulating compound that increases the level and/or activity of a sirtuin protein.
- skin is contacted with a pharmaceutical or cosmetic composition comprising a sirtuin-modulating compound that increases the level and/or activity of a sirtuin protein.
- Exemplary skin afflictions or skin conditions that may be treated in accordance with the methods described herein include disorders or diseases associated with or caused by inflammation, sun damage or natural aging.
- the compositions find utility in the prevention or treatment of contact dermatitis (including irritant contact dermatitis and allergic contact dermatitis), atopic dermatitis (also known as allergic eczema), actinic keratosis, keratinization disorders (including eczema), epidermolysis bullosa diseases (including pemphigus), exfoliative dermatitis, seborrheic dermatitis, erythemas (including erythema multiforme and erythema nodosum), damage caused by the sun or other light sources, discoid lupus erythematosus, dermatomyositis, psoriasis, skin cancer and the effects of natural aging.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be used for the treatment of wounds and/or burns to promote healing, including, for example, first-, second- or third-degree burns and/or thermal, chemical or electrical burns.
- the formulations may be administered topically, to the skin or mucosal tissue.
- Topical formulations comprising one or more sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may also be used as preventive, e.g., chemopreventive, compositions.
- preventive e.g., chemopreventive
- susceptible skin is treated prior to any visible condition in a particular individual.
- Sirtuin-modulating compounds may be delivered locally or systemically to a subject.
- a sirtuin-modulating compound is delivered locally to a tissue or organ of a subject by injection, topical formulation, etc.
- a sirtuin-modulating compound that increases the level and/or activity of a sirtuin protein may be used for treating or preventing a disease or condition induced or exacerbated by cellular senescence in a subject; methods for decreasing the rate of senescence of a subject, e.g., after onset of senescence; methods for extending the lifespan of a subject; methods for treating or preventing a disease or condition relating to lifespan; methods for treating or preventing a disease or condition relating to the proliferative capacity of cells; and methods for treating or preventing a disease or condition resulting from cell damage or death.
- the method does not act by decreasing the rate of occurrence of diseases that shorten the lifespan of a subject.
- the method does not act by decreasing the rate of
- a sirtuin-modulating compound that increases the level and/or activity of a sirtuin protein may be administered to a subject in order to generally increase the lifespan of its cells and to protect its cells against stress and/or against apoptosis. It is believed that treating a subject with a compound described herein is similar to subjecting the subject to hormesis, i.e., mild stress that is beneficial to organisms and may extend their lifespan.
- Sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be administered to a subject to prevent aging and aging-related consequences or diseases, such as stroke, heart disease, heart failure, arthritis, high blood pressure, and Alzheimer's disease.
- Other conditions that can be treated include ocular disorders, e.g., associated with the aging of the eye, such as cataracts, glaucoma, and macular degeneration.
- Sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein can also be administered to subjects for treatment of diseases, e.g., chronic diseases, associated with cell death, in order to protect the cells from cell death.
- Exemplary diseases include those associated with neural cell death, neuronal dysfunction, or muscular cell death or dysfunction, such as Parkinson's disease, Alzheimer's disease, multiple sclerosis, amyotrophic lateral sclerosis, and muscular dystrophy; AIDS;
- fulminant hepatitis diseases linked to degeneration of the brain, such as Creutzfeld- Jakob disease, retinitis pigmentosa and cerebellar degeneration; myelodysplasia such as aplastic anemia; ischemic diseases such as myocardial infarction and stroke; hepatic diseases such as alcoholic hepatitis, hepatitis B and hepatitis C; joint-diseases such as osteoarthritis; atherosclerosis; alopecia; damage to the skin due to UV light; lichen planus; atrophy of the skin; cataract; and graft rejections.
- Cell death can also be caused by surgery, drug therapy, chemical exposure or radiation exposure.
- Sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein can also be administered to a subject suffering from an acute disease, e.g., damage to an organ or tissue, e.g., a subject suffering from stroke or myocardial infarction or a subject suffering from a spinal cord injury.
- Sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may also be used to repair an alcoholic's liver. Cardiovascular Disease
- the invention provides a method for treating and/or preventing a cardiovascular disease by administering to a subject in need thereof a sirtuin- modulating compound that increases the level and/or activity of a sirtuin protein.
- Cardiovascular diseases that can be treated or prevented using the sirtuin- modulating compounds that increase the level and/or activity of a sirtuin protein include cardiomyopathy or myocarditis; such as idiopathic cardiomyopathy, metabolic cardiomyopathy, alcoholic cardiomyopathy, drug-induced cardiomyopathy, ischemic cardiomyopathy, and hypertensive cardiomyopathy.
- cardiomyopathy or myocarditis such as idiopathic cardiomyopathy, metabolic cardiomyopathy, alcoholic cardiomyopathy, drug-induced cardiomyopathy, ischemic cardiomyopathy, and hypertensive cardiomyopathy.
- atheromatous disorders of the major blood vessels such as the aorta, the coronary arteries, the carotid arteries, the cerebrovascular arteries, the renal arteries, the iliac arteries, the femoral arteries, and the popliteal arteries.
- vascular diseases that can be treated or prevented include those related to platelet aggregation, the retinal arterioles, the glomerular arterioles, the vasa nervorum, cardiac arterioles, and associated capillary beds of the eye, the kidney, the heart, and the central and peripheral nervous systems.
- the sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may also be used for increasing HDL levels in plasma of an individual.
- a sirtuin-modulating compound that increases the level and/or activity of a sirtuin protein may be administered as part of a combination therapy with another cardiovascular agent.
- a sirtuin-modulating compound that increases the level and/or activity of a sirtuin protein may be administered as part of a combination therapy with an anti-arrhythmia agent.
- a sirtuin-modulating compound that increases the level and/or activity of a sirtuin protein may be administered as part of a combination therapy with another cardiovascular agent.
- Sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be administered to subjects who have recently received or are likely to receive a dose of radiation or toxin.
- the dose of radiation or toxin is received as part of a work-related or medical procedure, e.g., administered as a prophylactic measure.
- the radiation or toxin exposure is received unintentionally.
- the compound is preferably administered as soon as possible after the exposure to inhibit apoptosis and the subsequent development of acute radiation syndrome.
- Sirtuin-modulating compounds may also be used for treating and/or preventing cancer.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be used for treating and/or preventing cancer.
- Calorie restriction has been linked to a reduction in the incidence of age-related disorders including cancer.
- an increase in the level and/or activity of a sirtuin protein may be useful for treating and/or preventing the incidence of age-related disorders, such as, for example, cancer.
- Exemplary cancers that may be treated using a sirtuin- modulating compound are those of the brain and kidney; hormone-dependent cancers including breast, prostate, testicular, and ovarian cancers; lymphomas, and leukemias.
- a modulating compound may be administered directly into the tumor.
- Cancer of blood cells e.g., leukemia
- Benign cell growth e.g., warts
- Other diseases that can be treated include autoimmune diseases, e.g., systemic lupus erythematosus, scleroderma, and arthritis, in which autoimmune cells should be removed.
- Viral infections such as herpes, HIV, adenovirus, and HTLV-1 associated malignant and benign disorders can also be treated by administration of sirtuin-modulating compound.
- cells can be obtained from a subject, treated ex vivo to remove certain undesirable cells, e.g., cancer cells, and administered back to the same or a different subject.
- Chemotherapeutic agents may be co-administered with modulating compounds described herein as having anti-cancer activity, e.g., compounds that induce apoptosis, compounds that reduce lifespan or compounds that render cells sensitive to stress.
- Chemotherapeutic agents may be used by themselves with a sirtuin-modulating compound described herein as inducing cell death or reducing lifespan or increasing sensitivity to stress and/or in combination with other chemotherapeutics agents.
- the sirtuin-modulating compounds described herein may also be used with antisense RNA, RNAi or other polynucleotides to inhibit the expression of the cellular components that contribute to unwanted cellular proliferation.
- Combination therapies comprising sirtuin-modulating compounds and a conventional chemotherapeutic agent may be advantageous over combination therapies known in the art because the combination allows the conventional chemotherapeutic agent to exert greater effect at lower dosage.
- the effective dose (ED 50 ) for a chemotherapeutic agent, or combination of conventional chemotherapeutic agents, when used in combination with a sirtuin-modulating compound is at least 2 fold less than the ED 50 for the chemotherapeutic agent alone, and even more preferably at 5 fold, 10 fold or even 25 fold less.
- the therapeutic index (TI) for such chemotherapeutic agent or combination of such chemotherapeutic agent when used in combination with a sirtuin-modulating compound described herein can be at least 2 fold greater than the TI for conventional chemotherapeutic regimen alone, and even more preferably at 5 fold, 10 fold or even 25 fold greater.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein can be used to treat patients suffering from neurodegenerative diseases, and traumatic or mechanical injury to the central nervous system (CNS), spinal cord or peripheral nervous system (PNS).
- Neurodegenerative disease typically involves reductions in the mass and volume of the human brain, which may be due to the atrophy and/or death of brain cells, which are far more profound than those in a healthy person that are attributable to aging.
- Neurodegenerative diseases can evolve gradually, after a long period of normal brain function, due to progressive degeneration (e.g., nerve cell dysfunction and death) of specific brain regions.
- neurodegenerative diseases can have a quick onset, such as those associated with trauma or toxins.
- neurodegenerative diseases include, but are not limited to, Alzheimer's disease (AD), Parkinson's disease (PD), Huntington's disease (HD), amyotrophic lateral sclerosis (ALS; Lou Gehrig's disease), diffuse Lewy body disease, chorea-acanthocytosis, primary lateral sclerosis, ocular diseases (ocular neuritis), chemotherapy-induced neuropathies (e.g., from vincristine, paclitaxel, bortezomib), diabetes-induced neuropathies and Friedreich's ataxia.
- Sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein can be used to treat these disorders and others as described below.
- AD is a CNS disorder that results in memory loss, unusual behavior, personality changes, and a decline in thinking abilities. These losses are related to the death of specific types of brain cells and the breakdown of connections and their supporting network (e.g. glial cells) between them. The earliest symptoms include loss of recent memory, faulty judgment, and changes in personality.
- PD is a CNS disorder that results in uncontrolled body movements, rigidity, tremor, and dyskinesia, and is associated with the death of brain cells in an area of the brain that produces dopamine.
- ALS motor neuron disease
- ALS motor neuron disease
- HD is another neurodegenerative disease that causes uncontrolled movements, loss of intellectual faculties, and emotional disturbance.
- Tay-Sachs disease and Sandhoff disease are glycolipid storage diseases where GM2 ganglioside and related glycolipids substrates for ⁇ -hexosaminidase accumulate in the nervous system and trigger acute neurodegeneration.
- HIV-1 also induces neurological disease, which can be treated with sirtuin-modulating compounds of the invention.
- Neuronal loss is also a salient feature of prion diseases, such as Creutzfeldt- Jakob disease in human, BSE in cattle (mad cow disease), Scrapie Disease in sheep and goats, and feline spongiform encephalopathy (FSE) in cats.
- Sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be useful for treating or preventing neuronal loss due to these prior diseases.
- a sirtuin-modulating compound that increases the level and/or activity of a sirtuin protein may be used to treat or prevent any disease or disorder involving axonopathy.
- Distal axonopathy is a type of peripheral neuropathy that results from some metabolic or toxic derangement of peripheral nervous system (PNS) neurons. It is the most common response of nerves to metabolic or toxic disturbances, and as such may be caused by metabolic diseases such as diabetes, renal failure, deficiency syndromes such as malnutrition and alcoholism, or the effects of toxins or drugs.
- PNS peripheral nervous system
- Those with distal axonopathies usually present with symmetrical glove-stocking sensori-motor disturbances. Deep tendon reflexes and autonomic nervous system (ANS) functions are also lost or diminished in affected areas.
- ANS autonomic nervous system
- Diabetic neuropathies are neuropathic disorders that are associated with diabetes mellitus. Relatively common conditions which may be associated with diabetic neuropathy include third nerve palsy; mononeuropathy; mononeuritis multiplex; diabetic amyotrophy; a painful polyneuropathy; autonomic neuropathy; and thoracoabdominal neuropathy.
- Peripheral neuropathy is the medical term for damage to nerves of the peripheral nervous system, which may be caused either by diseases of the nerve or from the side- effects of systemic illness.
- Major causes of peripheral neuropathy include seizures, nutritional deficiencies, and HIV, though diabetes is the most likely cause.
- a sirtuin-modulating compound that increases the level and/or activity of a sirtuin protein may be used to treat or prevent multiple sclerosis (MS), including relapsing MS and monosymptomatic MS, and other demyelinating conditions, such as, for example, chronic inflammatory demyelinating polyneuropathy (CIDP), or symptoms associated therewith.
- MS multiple sclerosis
- CIDP chronic inflammatory demyelinating polyneuropathy
- a sirtuin-modulating compound that increases the level and/or activity of a sirtuin protein may be used to treat trauma to the nerves, including, trauma due to disease, injury (including surgical intervention), or environmental trauma (e.g., neurotoxins, alcoholism, etc.).
- Sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may also be useful to prevent, treat, and alleviate symptoms of various PNS disorders.
- peripheral neuropathy encompasses a wide range of disorders in which the nerves outside of the brain and spinal cord— peripheral nerves— have been damaged. Peripheral neuropathy may also be referred to as peripheral neuritis, or if many nerves are involved, the terms polyneuropathy or polyneuritis may be used.
- PNS diseases treatable with sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein include: diabetes, leprosy, Charcot-Marie-Tooth disease, Guillain-Barre syndrome and Brachial Plexus Neuropathies (diseases of the cervical and first thoracic roots, nerve trunks, cords, and peripheral nerve components of the brachial plexus.
- a sirtuin-modulating compound may be used to treat or prevent a polyglutamine disease.
- exemplary polyglutamine diseases include Spinobulbar muscular atrophy (Kennedy disease), Huntington's Disease (HD), Dentatorubral- pallidoluysian atrophy (Haw River syndrome), Spinocerebellar ataxia type 1 ,
- Spinocerebellar ataxia type 2 Spinocerebellar ataxia type 3 (Machado- Joseph disease), Spinocerebellar ataxia type 6, Spinocerebellar ataxia type 7, and Spinocerebellar ataxia type 17.
- the invention provides a method to treat a central nervous system cell to prevent damage in response to a decrease in blood flow to the cell.
- the severity of damage that may be prevented will depend in large part on the degree of reduction in blood flow to the cell and the duration of the reduction.
- apoptotic or necrotic cell death may be prevented.
- ischemic-mediated damage such as cytotoxic edema or central nervous system tissue anoxemia, may be prevented.
- the central nervous system cell may be a spinal cell or a brain cell.
- the ischemic condition is a stroke that results in any type of ischemic central nervous system damage, such as apoptotic or necrotic cell death, cytotoxic edema or central nervous system tissue anoxia.
- the stroke may impact any area of the brain or be caused by any etiology commonly known to result in the occurrence of a stroke.
- the stroke is a brain stem stroke.
- the stroke is a cerebellar stroke.
- the stroke is an embolic stroke.
- the stroke may be a hemorrhagic stroke.
- the stroke is a thrombotic stroke.
- a sirtuin-modulating compound may be administered to reduce infarct size of the ischemic core following a central nervous system ischemic condition. Moreover, a sirtuin-modulating compound may also be beneficially administered to reduce the size of the ischemic penumbra or transitional zone following a central nervous system ischemic condition.
- a combination drug regimen may include drugs or compounds for the treatment or prevention of neurodegenerative disorders or secondary conditions associated with these conditions.
- a combination drug regimen may include one or more sirtuin activators and one or more anti-neurodegeneration agents.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein can be used to treat or prevent blood coagulation disorders (or hemostatic disorders).
- blood coagulation disorders or hemostatic disorders
- the terms “hemostasis”, “blood coagulation,” and “blood clotting” refer to the control of bleeding, including the physiological properties of vasoconstriction and coagulation. Blood coagulation assists in maintaining the integrity of mammalian circulation after injury, inflammation, disease, congenital defect, dysfunction or other disruption. Further, the formation of blood clots does not only limit bleeding in case of an injury (hemostasis), but may lead to serious organ damage and death in the context of atherosclerotic diseases by occlusion of an important artery or vein. Thrombosis is thus blood clot formation at the wrong time and place.
- the present invention provides anticoagulation and antithrombotic treatments aiming at inhibiting the formation of blood clots in order to prevent or treat blood coagulation disorders, such as myocardial infarction, stroke, loss of a limb by peripheral artery disease or pulmonary embolism.
- blood coagulation disorders such as myocardial infarction, stroke, loss of a limb by peripheral artery disease or pulmonary embolism.
- modulating or modulation of hemostasis and “regulating or regulation of hemostasis” includes the induction (e.g., stimulation or increase) of hemostasis, as well as the inhibition (e.g., reduction or decrease) of hemostasis.
- the invention provides a method for reducing or inhibiting hemostasis in a subject by administering a sirtuin-modulating compound that increases the level and/or activity of a sirtuin protein.
- the compositions and methods disclosed herein are useful for the treatment or prevention of thrombotic disorders.
- thrombotic disorder includes any disorder or condition characterized by excessive or unwanted coagulation or hemostatic activity, or a hypercoagulable state.
- Thrombotic disorders include diseases or disorders involving platelet adhesion and thrombus formation, and may manifest as an increased propensity to form thromboses, e.g., an increased number of thromboses, thrombosis at an early age, a familial tendency towards thrombosis, and thrombosis at unusual sites.
- a combination drug regimen may include drugs or compounds for the treatment or prevention of blood coagulation disorders or secondary conditions associated with these conditions.
- a combination drug regimen may include one or more sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein and one or more anti-coagulation or anti-thrombosis agents.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be used for treating or preventing weight gain or obesity in a subject.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be used, for example, to treat or prevent hereditary obesity, dietary obesity, hormone related obesity, obesity related to the administration of medication, to reduce the weight of a subject, or to reduce or prevent weight gain in a subject.
- a subject in need of such a treatment may be a subject who is obese, likely to become obese, overweight, or likely to become overweight.
- Subjects who are likely to become obese or overweight can be identified, for example, based on family history, genetics, diet, activity level, medication intake, or various combinations thereof.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be administered to subjects suffering from a variety of other diseases and conditions that may be treated or prevented by promoting weight loss in the subject.
- diseases include, for example, high blood pressure, hypertension, high blood cholesterol, dyslipidemia, type 2 diabetes, insulin resistance, glucose intolerance, hyperinsulinemia, coronary heart disease, angina pectoris, congestive heart failure, stroke, gallstones, cholecystitis and cholelithiasis, gout, osteoarthritis, obstructive sleep apnea and respiratory problems, some types of cancer (such as endometrial, breast, prostate, and colon), complications of pregnancy, poor female reproductive health (such as menstrual irregularities, infertility, irregular ovulation), bladder control problems (such as stress incontinence); uric acid nephrolithiasis; psychological disorders (such as depression, eating disorders, distorted body image,
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be used for inhibiting adipogenesis or fat cell differentiation, whether in vitro or in vivo. Such methods may be used for treating or preventing obesity.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be used for reducing appetite and/or increasing satiety, thereby causing weight loss or avoidance of weight gain.
- a subject in need of such a treatment may be a subject who is overweight, obese or a subject likely to become overweight or obese.
- the method may comprise administering daily or, every other day, or once a week, a dose, e.g., in the form of a pill, to a subject.
- the dose may be an "appetite reducing dose.”
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be administered as a combination therapy for treating or preventing weight gain or obesity.
- one or more sirtuin- modulating compounds that increase the level and/or activity of a sirtuin protein may be administered in combination with one or more anti-obesity agents.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be administered to reduce drug-induced weight gain.
- a sirtuin-modulating compound that increases the level and/or activity of a sirtuin protein may be administered as a combination therapy with medications that may stimulate appetite or cause weight gain, in particular, weight gain due to factors other than water retention.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be used for treating or preventing a metabolic disorder, such as insulin-resistance, a pre-diabetic state, type II diabetes, and/or complications thereof.
- Administration of a sirtuin-modulating compound that increases the level and/or activity of a sirtuin protein may increase insulin sensitivity and/or decrease insulin levels in a subject.
- a subject in need of such a treatment may be a subject who has insulin resistance or other precursor symptom of type II diabetes, who has type II diabetes, or who is likely to develop any of these conditions.
- the subject may be a subject having insulin resistance, e.g., having high circulating levels of insulin and/or associated conditions, such as hyperlipidemia, dyslipogenesis, hypercholesterolemia, impaired glucose tolerance, high blood glucose sugar level, other manifestations of syndrome X, hypertension, atherosclerosis and lipodystrophy.
- insulin resistance e.g., having high circulating levels of insulin and/or associated conditions, such as hyperlipidemia, dyslipogenesis, hypercholesterolemia, impaired glucose tolerance, high blood glucose sugar level, other manifestations of syndrome X, hypertension, atherosclerosis and lipodystrophy.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be administered as a combination therapy for treating or preventing a metabolic disorder.
- one or more sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be administered in combination with one or more anti-diabetic agents.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein can be used to treat or prevent a disease or disorder associated with inflammation.
- Sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be administered prior to the onset of, at, or after the initiation of inflammation.
- the compounds are preferably provided in advance of any inflammatory response or symptom. Administration of the compounds may prevent or attenuate inflammatory responses or symptoms.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be used to treat or prevent allergies and respiratory conditions, including asthma, bronchitis, pulmonary fibrosis, allergic rhinitis, oxygen toxicity, emphysema, chronic bronchitis, acute respiratory distress syndrome, and any chronic obstructive pulmonary disease (COPD).
- the compounds may be used to treat chronic hepatitis infection, including hepatitis B and hepatitis C.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be used to treat autoimmune diseases, and/or inflammation associated with autoimmune diseases, such as arthritis, including rheumatoid arthritis, psoriatic arthritis, and ankylosing spondylitis, as well as organ-tissue autoimmune diseases (e.g., Raynaud's syndrome), ulcerative colitis, Crohn's disease, oral mucositis, scleroderma, myasthenia gravis, transplant rejection, endotoxin shock, sepsis, psoriasis, eczema, dermatitis, multiple sclerosis, autoimmune thyroiditis, uveitis, systemic lupus erythematosis, Addison's disease, autoimmune polyglandular disease (also known as autoimmune polyglandular syndrome), and Grave's disease.
- autoimmune diseases such as arthritis, including rheumatoid arthritis,
- one or more sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be taken alone or in combination with other compounds useful for treating or preventing inflammation.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be used for reducing the incidence or severity of flushing and/or hot flashes which are symptoms of a disorder.
- the subject method includes the use of sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein, alone or in combination with other agents, for reducing incidence or severity of flushing and/or hot flashes in cancer patients.
- the method provides for the use of sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein to reduce the incidence or severity of flushing and/or hot flashes in menopausal and post-menopausal woman.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be used as a therapy for reducing the incidence or severity of flushing and/or hot flashes which are side-effects of another drug therapy, e.g., drug- induced flushing.
- a method for treating and/or preventing drug- induced flushing comprises administering to a patient in need thereof a formulation comprising at least one flushing inducing compound and at least one sirtuin-modulating compound that increases the level and/or activity of a sirtuin protein.
- a method for treating drug induced flushing comprises separately administering one or more compounds that induce flushing and one or more sirtuin- modulating compounds, e.g., wherein the sirtuin-modulating compound and flushing inducing agent have not been formulated in the same compositions.
- the sirtuin-modulating compound may be administered (1) at the same as administration of the flushing inducing agent, (2) intermittently with the flushing inducing agent, (3) staggered relative to administration of the flushing inducing agent, (4) prior to administration of the flushing inducing agent, (5) subsequent to administration of the flushing inducing agent, and (6) various combination thereof.
- Exemplary flushing inducing agents include, for example, niacin, raloxifene, antidepressants, anti-psychotics, chemotherapeutics, calcium channel blockers, and antibiotics.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be used to reduce flushing side effects of a vasodilator or an antilipemic agent (including anticholesteremic agents and lipotropic agents).
- a sirtuin-modulating compound that increases the level and/or activity of a sirtuin protein may be used to reduce flushing associated with the administration of niacin.
- the invention provides a method for treating and/or preventing hyperlipidemia with reduced flushing side effects.
- the method involves the use of sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein to reduce flushing side effects of raloxifene.
- the method involves the use of sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein to reduce flushing side effects of antidepressants or anti-psychotic agent.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein can be used in conjunction (administered separately or together) with a serotonin reuptake inhibitor, or a 5HT2 receptor antagonist.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be used as part of a treatment with a serotonin reuptake inhibitor (SRI) to reduce flushing.
- SRI serotonin reuptake inhibitor
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be used to reduce flushing side effects of chemotherapeutic agents, such as cyclophosphamide and tamoxifen.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be used to reduce flushing side effects of calcium channel blockers, such as amlodipine.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be used to reduce flushing side effects of antibiotics.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein can be used in combination with levofloxacin.
- One aspect of the present invention is a method for inhibiting, reducing or otherwise treating vision impairment by administering to a patient a therapeutic dosage of sirtuin modulator selected from a compound disclosed herein, or a pharmaceutically acceptable salt, prodrug or a metabolic derivative thereof.
- the vision impairment is caused by damage to the optic nerve or central nervous system.
- optic nerve damage is caused by high intraocular pressure, such as that created by glaucoma.
- optic nerve damage is caused by swelling of the nerve, which is often associated with an infection or an immune (e.g., autoimmune) response such as in optic neuritis.
- the vision impairment is caused by retinal damage.
- retinal damage is caused by disturbances in blood flow to the eye (e.g., arteriosclerosis, vasculitis).
- retinal damage is caused by disruption of the macula (e.g., exudative or non-exudative macular degeneration).
- Exemplary retinal diseases include Exudative Age Related Macular Degeneration, Nonexudative Age Related Macular Degeneration, Retinal Electronic Prosthesis and RPE Transplantation Age Related Macular Degeneration, Acute Multifocal Placoid Pigment Epitheliopathy, Acute Retinal Necrosis, Best Disease, Branch Retinal Artery Occlusion, Branch Retinal Vein Occlusion, Cancer Associated and Related Autoimmune
- Retinopathies Central Retinal Artery Occlusion, Central Retinal Vein Occlusion, Central Serous Chorioretinopathy, Eales Disease, Epimacular Membrane, Lattice Degeneration, Macroaneurysm, Diabetic Macular Edema, Irvine-Gass Macular Edema, Macular Hole, Subretinal Neovascular Membranes, Diffuse Unilateral Subacute Neuroretinitis, Nonpseudophakic Cystoid Macular Edema, Presumed Ocular Histoplasmosis Syndrome, Exudative Retinal Detachment, Postoperative Retinal Detachment, Proliferative Retinal Detachment, Rhegmatogenous Retinal Detachment, Tractional Retinal Detachment, Retinitis Pigmentosa, CMV Retinitis, Retinoblastoma, Retinopathy of Prematurity, Birdshot Retinopathy, Background Diabetic Re
- exemplary diseases include ocular bacterial infections (e.g. conjunctivitis, keratitis, tuberculosis, syphilis, gonorrhea), viral infections (e.g., Ocular Herpes Simplex Virus, Varicella Zoster Virus, Cytomegalovirus retinitis, Human Immunodeficiency Virus (HIV)) as well as progressive outer retinal necrosis secondary to HIV or other HIV- associated and other immunodeficiency-associated ocular diseases.
- ocular bacterial infections e.g. conjunctivitis, keratitis, tuberculosis, syphilis, gonorrhea
- viral infections e.g., Ocular Herpes Simplex Virus, Varicella Zoster Virus, Cytomegalovirus retinitis, Human Immunodeficiency Virus (HIV)
- HIV Human Immunodeficiency Virus
- ocular diseases include fungal infections (e.g., Candida choroiditis, histoplasmosis), protozoal infections (e.g., toxoplasmosis) and others such as ocular toxocariasis and sarcoidosis.
- fungal infections e.g., Candida choroiditis, histoplasmosis
- protozoal infections e.g., toxoplasmosis
- others such as ocular toxocariasis and sarcoidosis.
- One aspect of the invention is a method for inhibiting, reducing or treating vision impairment in a subject undergoing treatment with a chemotherapeutic drug (e.g., a neurotoxic drug, or a drug that raises intraocular pressure, such as a steroid), by administering to the subject in need of such treatment a therapeutic dosage of a sirtuin modulator disclosed herein.
- a chemotherapeutic drug e.g., a neurotoxic drug, or a drug that raises intraocular pressure, such as a steroid
- Another aspect of the invention is a method for inhibiting, reducing or treating vision impairment in a subject undergoing surgery, including ocular or other surgeries performed in the prone position such as spinal cord surgery, by administering to the subject in need of such treatment a therapeutic dosage of a sirtuin modulator disclosed herein.
- Ocular surgeries include cataract, iridotomy and lens replacements.
- Another aspect of the invention is the treatment, including inhibition and prophylactic treatment, of age related ocular diseases include cataracts, dry eye, age- related macular degeneration (AMD), retinal damage and the like, by administering to the subject in need of such treatment a therapeutic dosage of a sirtuin modulator disclosed herein.
- age related ocular diseases include cataracts, dry eye, age- related macular degeneration (AMD), retinal damage and the like.
- Another aspect of the invention is the prevention or treatment of damage to the eye caused by stress, chemical insult or radiation, by administering to the subject in need of such treatment a therapeutic dosage of a sirtuin modulator disclosed herein.
- Radiation or electromagnetic damage to the eye can include that caused by CRT's or exposure to sunlight or UV.
- a combination drug regimen may include drugs or compounds for the treatment or prevention of ocular disorders or secondary conditions associated with these conditions.
- a combination drug regimen may include one or more sirtuin activators and one or more therapeutic agents for the treatment of an ocular disorder.
- a sirtuin modulator can be administered in conjunction with a therapy for reducing intraocular pressure. In another embodiment, a sirtuin modulator can be administered in conjunction with a therapy for treating and/or preventing glaucoma. In yet another embodiment, a sirtuin modulator can be administered in conjunction with a therapy for treating and/or preventing optic neuritis. In certain embodiments, a sirtuin modulator can be administered in conjunction with a therapy for treating and/or preventing CMV Retinopathy. In another embodiment, a sirtuin modulator can be administered in conjunction with a therapy for treating and/or preventing multiple sclerosis.
- the invention provides methods for treating diseases or disorders that would benefit from increased mitochondrial activity.
- the methods involve administering to a subject in need thereof a therapeutically effective amount of a sirtuin- modulating compound.
- Increased mitochondrial activity refers to increasing activity of the mitochondria while maintaining the overall numbers of mitochondria (e.g., mitochondrial mass), increasing the numbers of mitochondria thereby increasing mitochondrial activity (e.g., by stimulating mitochondrial biogenesis), or combinations thereof.
- diseases and disorders that would benefit from increased mitochondrial activity include diseases or disorders associated with mitochondrial dysfunction.
- methods for treating diseases or disorders that would benefit from increased mitochondrial activity may comprise identifying a subject suffering from a mitochondrial dysfunction.
- Methods for diagnosing a mitochondrial dysfunction may involve molecular genetics, pathologic and/or biochemical analyses.
- Diseases and disorders associated with mitochondrial dysfunction include diseases and disorders in which deficits in mitochondrial respiratory chain activity contribute to the development of pathophysiology of such diseases or disorders in a mammal.
- Diseases or disorders that would benefit from increased mitochondrial activity generally include for example, diseases in which free radical mediated oxidative injury leads to tissue degeneration, diseases in which cells inappropriately undergo apoptosis, and diseases in which cells fail to undergo apoptosis.
- the invention provides methods for treating a disease or disorder that would benefit from increased mitochondrial activity that involves administering to a subject in need thereof one or more sirtuin-modulating compounds in combination with another therapeutic agent such as, for example, an agent useful for treating mitochondrial dysfunction or an agent useful for reducing a symptom associated with a disease or disorder involving mitochondrial dysfunction.
- the invention provides methods for treating diseases or disorders that would benefit from increased mitochondrial activity by administering to a subject a therapeutically effective amount of a sirtuin-modulating compound.
- diseases or disorders include, for example, neuromuscular disorders (e.g., Friedreich's Ataxia, muscular dystrophy, multiple sclerosis, etc.), disorders of neuronal instability (e.g., seizure disorders, migraine, etc.), developmental delay, neurodegenerative disorders (e.g., Alzheimer's Disease, Parkinson's Disease, amyotrophic lateral sclerosis, etc.), ischemia, renal tubular acidosis, age-related neurodegeneration and cognitive decline, chemotherapy fatigue, age-related or chemotherapy-induced menopause or irregularities of menstrual cycling or ovulation, mitochondrial myopathies, mitochondrial damage (e.g., calcium accumulation, excitotoxicity, nitric oxide exposure, hypoxia, etc.), and mitochondrial deregulation.
- mitochondrial myopathies e.g., calcium accumulation, excitotoxicity
- Muscular dystrophy refers to a family of diseases involving deterioration of neuromuscular structure and function, often resulting in atrophy of skeletal muscle and myocardial dysfunction, such as Duchenne muscular dystrophy.
- sirtuin-modulating compounds may be used for reducing the rate of decline in muscular functional capacities and for improving muscular functional status in patients with muscular dystrophy.
- sirtuin-modulating compounds may be useful for treatment mitochondrial myopathies.
- Mitochondrial myopathies range from mild, slowly progressive weakness of the extraocular muscles to severe, fatal infantile myopathies and multisystem encephalomyopathies. Some syndromes have been defined, with some overlap between them.
- Established syndromes affecting muscle include progressive external ophthalmoplegia, the Kearns-Sayre syndrome (with ophthalmoplegia, pigmentary retinopathy, cardiac conduction defects, cerebellar ataxia, and sensorineural deafness), the MELAS syndrome (mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes), the MERFF syndrome (myoclonic epilepsy and ragged red fibers), limb-girdle distribution weakness, and infantile myopathy (benign or severe and fatal).
- sirtuin-modulating compounds may be useful for treating patients suffering from toxic damage to mitochondria, such as, toxic damage due to calcium accumulation, excitotoxicity, nitric oxide exposure, drug induced toxic damage, or hypoxia.
- sirtuin-modulating compounds may be useful for treating diseases or disorders associated with mitochondrial deregulation.
- the invention provides methods for enhancing muscle performance by administering a therapeutically effective amount of a sirtuin-modulating compound.
- sirtuin-modulating compounds may be useful for improving physical endurance (e.g., ability to perform a physical task such as exercise, physical labor, sports activities, etc.), inhibiting or retarding physical fatigues, enhancing blood oxygen levels, enhancing energy in healthy individuals, enhance working capacity and endurance, reducing muscle fatigue, reducing stress, enhancing cardiac and cardiovascular function, improving sexual ability, increasing muscle ATP levels, and/or reducing lactic acid in blood.
- the methods involve administering an amount of a sirtuin- modulating compound that increase mitochondrial activity, increase mitochondrial biogenesis, and/or increase mitochondrial mass.
- Sports performance refers to the ability of the athlete's muscles to perform when participating in sports activities. Enhanced sports performance, strength, speed and endurance are measured by an increase in muscular contraction strength, increase in amplitude of muscle contraction, shortening of muscle reaction time between stimulation and contraction. Athlete refers to an individual who participates in sports at any level and who seeks to achieve an improved level of strength, speed and endurance in their performance, such as, for example, body builders, bicyclists, long distance runners, short distance runners, etc. Enhanced sports performance in manifested by the ability to overcome muscle fatigue, ability to maintain activity for longer periods of time, and have a more effective workout.
- the methods of the present invention will also be effective in the treatment of muscle related pathological conditions, including acute sarcopenia, for example, muscle atrophy and/or cachexia associated with burns, bed rest, limb immobilization, or major thoracic, abdominal, and/or orthopedic surgery.
- acute sarcopenia for example, muscle atrophy and/or cachexia associated with burns, bed rest, limb immobilization, or major thoracic, abdominal, and/or orthopedic surgery.
- the invention provides novel dietary compositions comprising sirtuin modulators, a method for their preparation, and a method of using the compositions for improvement of sports performance. Accordingly, provided are therapeutic compositions, foods and beverages that have actions of improving physical endurance and/or inhibiting physical fatigues for those people involved in broadly-defined exercises including sports requiring endurance and labors requiring repeated muscle exertions. Such dietary compositions may additional comprise electrolytes, caffeine, vitamins, carbohydrates, etc.
- Sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be used for treating or preventing viral infections (such as infections by influenza, herpes or papilloma virus) or as antifungal agents.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be administered as part of a combination drug therapy with another therapeutic agent for the treatment of viral diseases.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be administered as part of a combination drug therapy with another anti-fungal agent.
- Subjects that may be treated as described herein include eukaryotes, such as mammals, e.g., humans, ovines, bovines, equines, porcines, canines, felines, non-human primate, mice, and rats.
- Cells that may be treated include eukaryotic cells, e.g., from a subject described above, or plant cells, yeast cells and prokaryotic cells, e.g., bacterial cells.
- modulating compounds may be administered to farm animals to improve their ability to withstand farming conditions longer.
- Sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may also be used to increase lifespan, stress resistance, and resistance to apoptosis in plants.
- a compound is applied to plants, e.g., on a periodic basis, or to fungi.
- plants are genetically modified to produce a compound.
- plants and fruits are treated with a compound prior to picking and shipping to increase resistance to damage during shipping. Plant seeds may also be contacted with compounds described herein, e.g., to preserve them.
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may be used for modulating lifespan in yeast cells.
- Situations in which it may be desirable to extend the lifespan of yeast cells include any process in which yeast is used, e.g., the making of beer, yogurt, and bakery items, e.g., bread.
- Use of yeast having an extended lifespan can result in using less yeast or in having the yeast be active for longer periods of time.
- Yeast or other mammalian cells used for recombinantly producing proteins may also be treated as described herein.
- Sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may also be used to increase lifespan, stress resistance and resistance to apoptosis in insects.
- compounds would be applied to useful insects, e.g., bees and other insects that are involved in pollination of plants.
- a compound would be applied to bees involved in the production of honey.
- the methods described herein may be applied to any organism, e.g., eukaryote, which may have commercial importance. For example, they can be applied to fish (aquaculture) and birds (e.g., chicken and fowl).
- sirtuin-modulating compounds that increase the level and/or activity of a sirtuin protein may also be used as a pesticide by interfering with the regulation of silenced genes and the regulation of apoptosis during development.
- a compound may be applied to plants using a method known in the art that ensures the compound is bio-available to insect larvae, and not to plants.
- sirtuin- modulating compounds that increase the level and/or activity of a sirtuin protein can be applied to affect the reproduction of organisms such as insects, animals and microorganisms.
- an agent may be a nucleic acid, such as an aptamer.
- Assays may be conducted in a cell based or cell free format.
- an assay may comprise incubating (or contacting) a sirtuin with a test agent under conditions in which a sirtuin can be modulated by an agent known to modulate the sirtuin, and monitoring or determining the level of modulation of the sirtuin in the presence of the test agent relative to the absence of the test agent.
- the level of modulation of a sirtuin can be determined by determining its ability to deacetylate a substrate.
- Exemplary substrates are acetylated peptides which can be obtained from BIOMOL (Plymouth Meeting, PA).
- Preferred substrates include peptides of p53, such as those comprising an acetylated K382.
- a particularly preferred substrate is the Fluor de Lys-SIRTl (BIOMOL), i.e., the acetylated peptide Arg-His-Lys-Lys.
- Other substrates are peptides from human histones H3 and H4 or an acetylated amino acid.
- Substrates may be fluorogenic.
- the sirtuin may be SIRT1, Sir2, SIRT3, or a portion thereof.
- recombinant SIRT1 can be obtained from BIOMOL.
- the reaction may be conducted for about 30 minutes and stopped, e.g., with nicotinamide.
- the HDAC fluorescent activity assay/drug discovery kit (AK-500, BIOMOL Research Laboratories) may be used to determine the level of acetylation. Similar assays are described in Bitterman et al. (2002) J. Biol. Chem. 277:45099.
- the level of modulation of the sirtuin in an assay may be compared to the level of modulation of the sirtuin in the presence of one or more (separately or simultaneously) compounds described herein, which may serve as positive or negative controls.
- Sirtuins for use in the assays may be full length sirtuin proteins or portions thereof.
- proteins for use in the assays include N-terminal portions of sirtuins, e.g., about amino acids 1-176 or 1-255 of SIRT1; about amino acids 1-174 or 1- 252 of Sir2.
- a screening assay comprises (i) contacting a sirtuin with a test agent and an acetylated substrate under conditions appropriate for the sirtuin to deacetylate the substrate in the absence of the test agent; and (ii) determining the level of acetylation of the substrate, wherein a lower level of acetylation of the substrate in the presence of the test agent relative to the absence of the test agent indicates that the test agent stimulates deacetylation by the sirtuin, whereas a higher level of acetylation of the substrate in the presence of the test agent relative to the absence of the test agent indicates that the test agent inhibits deacetylation by the sirtuin.
- the screening assay may detect the formation of a 273'-0- acetyl-ADP-ribose product of sirtuin-mediated NAD-dependent deacetylation.
- This O- acetyl-ADP-ribose product is formed in equimolar quantities with the deacetylated peptide product of the sirtuin deacetylation reaction.
- the screening assay may include (i) contacting a sirtuin with a test agent and an acetylated substrate under conditions appropriate for the sirtuin to deacetylate the substrate in the absence of the test agent ; and (ii) determining the amount of O-acetyl-ADP-ribose formation, wherein an increase in O-acetyl-ADP- ribose formation in the presence of the test agent relative to the absence of the test agent indicates that the test agent stimulates deacetylation by the sirtuin, while a decrease in O-acetyl-ADP- ribose formation in the presence of the test agent relative to the absence of the test agent indicates that the test agent inhibits deacetylation by the sirtuin.
- Methods for identifying an agent that modulates, e.g., stimulates, sirtuins in vivo may comprise (i) contacting a cell with a test agent and a substrate that is capable of entering a cell in the presence of an inhibitor of class I and class II HDACs under conditions appropriate for the sirtuin to deacetylate the substrate in the absence of the test agent; and (ii) determining the level of acetylation of the substrate, wherein a lower level of acetylation of the substrate in the presence of the test agent relative to the absence of the test agent indicates that the test agent stimulates deacetylation by the sirtuin, whereas a higher level of acetylation of the substrate in the presence of the test agent relative to the absence of the test agent indicates that the test agent inhibits deacetylation by the sirtuin.
- a preferred substrate is an acetylated peptide, which is also preferably fluorogenic, as further described herein.
- the method may further comprise lysing the cells to determine the level of acetylation of the substrate.
- Substrates may be added to cells at a concentration ranging from about luM to about lOmM, preferably from about ⁇ to lmM, even more preferably from about ⁇ to lmM, such as about 200 ⁇ .
- a preferred substrate is an acetylated lysine, e.g., ⁇ -acetyl lysine (Fluor de Lys, FdL) or Fluor de Lys-SIRTl.
- a preferred inhibitor of class I and class II HDACs is trichostatin A (TSA), which may be used at concentrations ranging from about 0.01 to ⁇ , preferably from about 0.1 to ⁇ , such as ⁇ .
- TSA trichostatin A
- Incubation of cells with the test compound and the substrate may be conducted for about 10 minutes to 5 hours, preferably for about 1-3 hours. Since TSA inhibits all class I and class II HDACs, and that certain substrates, e.g., Fluor de Lys, is a poor substrate for SIRT2 and even less a substrate for SIRT3-7, such an assay may be used to identify modulators of SIRT1 in vivo.
- the compounds described herein may be formulated in a conventional manner using one or more physiologically or pharmaceutically acceptable carriers or excipients.
- compounds and their pharmaceutically acceptable salts and solvates may be formulated for administration by, for example, injection (e.g. SubQ, IM, IP), inhalation or insufflation (either through the mouth or the nose) or oral, buccal, sublingual, transdermal, nasal, parenteral or rectal administration.
- a compound may be administered locally, at the site where the target cells are present, i.e., in a specific tissue, organ, or fluid (e.g., blood, cerebrospinal fluid, etc.).
- the compounds can be formulated for a variety of modes of administration, including systemic and topical or localized administration. Techniques and formulations generally may be found in Remington's Pharmaceutical Sciences, Meade Publishing Co., Easton, PA.
- parenteral administration injection is preferred, including intramuscular, intravenous, intraperitoneal, and subcutaneous.
- the compounds can be formulated in liquid solutions, preferably in physiologically compatible buffers such as Hank's solution or Ringer's solution.
- the compounds may be formulated in solid form and redissolved or suspended immediately prior to use. Lyophilized forms are also included.
- the pharmaceutical compositions may take the form of, for example, tablets, lozenges, or capsules prepared by conventional means with pharmaceutically acceptable excipients such as binding agents (e.g., pregelatinized maize starch, polyvinylpyrrolidone or hydroxypropyl methylcellulose); fillers (e.g., lactose, microcrystalline cellulose or calcium hydrogen phosphate); lubricants (e.g., magnesium stearate, talc or silica); disintegrants (e.g., potato starch or sodium starch glycolate); or wetting agents (e.g., sodium lauryl sulphate).
- binding agents e.g., pregelatinized maize starch, polyvinylpyrrolidone or hydroxypropyl methylcellulose
- fillers e.g., lactose, microcrystalline cellulose or calcium hydrogen phosphate
- lubricants e.g., magnesium stearate, talc or silica
- disintegrants e.g
- Liquid preparations for oral administration may take the form o for example, solutions, syrups or suspensions, or they may be presented as a dry product for constitution with water or other suitable vehicle before use.
- Such liquid preparations may be prepared by conventional means with pharmaceutically acceptable additives such as suspending agents (e.g., sorbitol syrup, cellulose derivatives or hydrogenated edible fats); emulsifying agents (e.g., lecithin or acacia); non-aqueous vehicles (e.g., almond oil, oily esters, ethyl alcohol or fractionated vegetable oils); and preservatives (e.g., methyl or propyl-p-hydroxybenzoates or sorbic acid).
- the preparations may also contain buffer salts, flavoring, coloring and sweetening agents as appropriate.
- Preparations for oral administration may be suitably formulated to give controlled release of the active compound.
- the compounds may be conveniently delivered in the form of an aerosol spray presentation from pressurized packs or a nebulizer, with the use of a suitable propellant, e.g., dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas.
- a suitable propellant e.g., dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas.
- a suitable propellant e.g., dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas.
- a suitable propellant e.g., dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas.
- the compounds may be formulated for parenteral administration by injection, e.g., by bolus injection or continuous infusion.
- Formulations for injection may be presented in unit dosage form, e.g., in ampoules or in multi-dose containers, with an added preservative.
- the compositions may take such forms as suspensions, solutions or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilizing and/or dispersing agents.
- the active ingredient may be in powder form for constitution with a suitable vehicle, e.g., sterile pyrogen-free water, before use.
- the compounds may also be formulated in rectal compositions such as suppositories or retention enemas, e.g., containing conventional suppository bases such as cocoa butter or other glycerides.
- compounds may also be formulated as a depot preparation. Such long acting formulations may be administered by implantation (for example subcutaneously or intramuscularly) or by intramuscular injection.
- compounds may be formulated with suitable polymeric or hydrophobic materials (for example as an emulsion in an acceptable oil) or ion exchange resins, or as sparingly soluble derivatives, for example, as a sparingly soluble salt.
- Controlled release formula also includes patches.
- the compounds described herein can be formulated for delivery to the central nervous system (CNS) (reviewed in Begley, Pharmacology & Therapeutics 104: 29-45 (2004)).
- CNS central nervous system
- Conventional approaches for drug delivery to the CNS include: neurosurgical strategies (e.g., intracerebral injection or intracerebroventricular infusion); molecular manipulation of the agent (e.g., production of a chimeric fusion protein that comprises a transport peptide that has an affinity for an endothelial cell surface molecule in combination with an agent that is itself incapable of crossing the BBB) in an attempt to exploit one of the endogenous transport pathways of the BBB; pharmacological strategies designed to increase the lipid solubility of an agent (e.g., conjugation of water- soluble agents to lipid or cholesterol carriers); and the transitory disruption of the integrity of the BBB by hyperosmotic disruption (resulting from the infusion of a mannitol solution into the carotid artery or the use of a biological
- Liposomes are a further drug delivery system which is easily injectable.
- the active compounds can also be administered in the form of a liposome delivery system.
- Liposomes are well known by those skilled in the art. Liposomes can be formed from a variety of phospholipids, such as cholesterol, stearylamine of phosphatidylcholines. Liposomes usable for the method of invention encompass all types of liposomes including, but not limited to, small unilamellar vesicles, large unilamellar vesicles and multilamellar vesicles.
- cyclodextrin is meant ⁇ -, ⁇ -, or ⁇ - cyclodextrin.
- Cyclodextrins are described in detail in Pitha et al., U.S. Pat. No. 4,727,064, which is incorporated herein by reference. Cyclodextrins are cyclic oligomers of glucose; these compounds form inclusion complexes with any drug whose molecule can fit into the lipophile-seeking cavities of the cyclodextrin molecule.
- Rapidly disintegrating or dissolving dosage forms are useful for the rapid absorption, particularly buccal and sublingual absorption, of pharmaceutically active agents.
- Fast melt dosage forms are beneficial to patients, such as aged and pediatric patients, who have difficulty in swallowing typical solid dosage forms, such as caplets and tablets. Additionally, fast melt dosage forms circumvent drawbacks associated with, for example, chewable dosage forms, wherein the length of time an active agent remains in a patient's mouth plays an important role in determining the amount of taste masking and the extent to which a patient may object to throat grittiness of the active agent.
- compositions may comprise from about 0.00001 to 100% such as from 0.001 to 10% or from 0.1% to 5% by weight of one or more compounds described herein.
- the pharmaceutical composition comprises: (i) 0.05 to 1000 mg of the compounds of the invention, or a pharmaceutically acceptable salt thereof, and (ii) 0.1 to 2 grams of one or more pharmaceutically acceptable excipients.
- a compound described herein is incorporated into a topical formulation containing a topical carrier that is generally suited to topical drug administration and comprising any such material known in the art.
- the topical carrier may be selected so as to provide the composition in the desired form, e.g., as an ointment, lotion, cream, microemulsion, gel, oil, solution, or the like, and may be comprised of a material of either naturally occurring or synthetic origin. It is preferable that the selected carrier not adversely affect the active agent or other components of the topical formulation.
- suitable topical carriers for use herein include water, alcohols and other nontoxic organic solvents, glycerin, mineral oil, silicone, petroleum jelly, lanolin, fatty acids, vegetable oils, parabens, waxes, and the like.
- Formulations may be colorless, odorless ointments, lotions, creams, microemulsions and gels.
- the compounds may be incorporated into ointments, which generally are semisolid preparations which are typically based on petrolatum or other petroleum derivatives.
- ointments which generally are semisolid preparations which are typically based on petrolatum or other petroleum derivatives.
- the specific ointment base to be used is one that will provide for optimum drug delivery, and, preferably, will provide for other desired characteristics as well, e.g., emolliency or the like.
- an ointment base should be inert, stable, nonirritating and nonsensitizing.
- the compounds may be incorporated into lotions, which generally are preparations to be applied to the skin surface without friction, and are typically liquid or semiliquid preparations in which solid particles, including the active agent, are present in a water or alcohol base.
- Lotions are usually suspensions of solids, and may comprise a liquid oily emulsion of the oil-in-water type.
- the compounds may be incorporated into creams, which generally are viscous liquid or semisolid emulsions, either oil-in-water or water-in-oil.
- Cream bases are water- washable, and contain an oil phase, an emulsifier and an aqueous phase.
- the oil phase is generally comprised of petrolatum and a fatty alcohol such as cetyl or stearyl alcohol; the aqueous phase usually, although not necessarily, exceeds the oil phase in volume, and generally contains a humectant.
- the emulsifier in a cream formulation as explained in Remington's, supra, is generally a nonionic, anionic, cationic or amphoteric surfactant.
- microemulsions which generally are thermodynamically stable, isotropically clear dispersions of two immiscible liquids, such as oil and water, stabilized by an interfacial film of surfactant molecules (Encyclopedia of Pharmaceutical Technology (New York: Marcel Dekker, 1992), volume 9).
- the compounds may be incorporated into gel formulations, which generally are semisolid systems consisting of either suspensions made up of small inorganic particles (two-phase systems) or large organic molecules distributed substantially uniformly throughout a carrier liquid (single phase gels). Although gels commonly employ aqueous carrier liquid, alcohols and oils can be used as the carrier liquid as well.
- sunscreen formulations e.g., other anti- inflammatory agents, analgesics, antimicrobial agents, antifungal agents, antibiotics, vitamins, antioxidants, and sunblock agents commonly found in sunscreen formulations including, but not limited to, anthranilates, benzophenones (particularly benzophenone-3), camphor derivatives, cinnamates (e.g., octyl methoxycinnamate), dibenzoyl methanes (e.g., butyl methoxydibenzoyl methane), p-aminobenzoic acid (PABA) and derivatives thereof, and salicylates (e.g., octyl salicylate).
- sunscreen formulations including, but not limited to, anthranilates, benzophenones (particularly benzophenone-3), camphor derivatives, cinnamates (e.g., octyl methoxycinnamate), dibenzoyl methanes (e.g.
- the active agent is present in an amount in the range of approximately 0.25 wt. % to 75 wt. % of the formulation, preferably in the range of approximately 0.25 wt. % to 30 wt. % of the formulation, more preferably in the range of approximately 0.5 wt. % to 15 wt. % of the formulation, and most preferably in the range of approximately 1.0 wt. % to 10 wt. % of the formulation.
- Conditions of the eye can be treated or prevented by, e.g., systemic, topical, intraocular injection of a compound, or by insertion of a sustained release device that releases a compound.
- a compound may be delivered in a pharmaceutically acceptable ophthalmic vehicle, such that the compound is maintained in contact with the ocular surface for a sufficient time period to allow the compound to penetrate the corneal and internal regions of the eye, as for example the anterior chamber, posterior chamber, vitreous body, aqueous humor, vitreous humor, cornea, iris/ciliary, lens, choroid/retina and sclera.
- the pharmaceutically acceptable ophthalmic vehicle may, for example, be an ointment, vegetable oil or an encapsulating material.
- the compounds of the invention may be injected directly into the vitreous and aqueous humour.
- the compounds may be administered systemically, such as by intravenous infusion or injection, for treatment of the eye.
- compositions described herein may be stored in oxygen free environment.
- a composition can be prepared in an airtight capsule for oral administration, such as Capsugel from Pfizer, Inc.
- Cells e.g., treated ex vivo with a compound as described herein, can be administered according to methods for administering a graft to a subject, which may be accompanied, e.g., by administration of an immunosuppressant drug, e.g., cyclosporin A.
- an immunosuppressant drug e.g., cyclosporin A.
- the reader is referred to Cell Therapy: Stem Cell Transplantation, Gene Therapy, and Cellular Immunotherapy, by G. Morstyn & W. Sheridan eds, Cambridge University Press, 1996; and Hematopoietic Stem Cell Therapy, E. D. Ball, J. Lister & P. Law, Churchill Livingstone, 2000.
- Toxicity and therapeutic efficacy of compounds can be determined by standard pharmaceutical procedures in cell cultures or experimental animals.
- the LD 50 is the dose lethal to 50% of the population.
- the ED 50 is the dose therapeutically effective in 50% of the population.
- the dose ratio between toxic and therapeutic effects (LD 50 / ED 50 ) is the therapeutic index.
- Compounds that exhibit large therapeutic indexes are preferred. While compounds that exhibit toxic side effects may be used, care should be taken to design a delivery system that targets such compounds to the site of affected tissue in order to minimize potential damage to uninfected cells and, thereby, reduce side effects.
- the data obtained from the cell culture assays and animal studies can be used in formulating a range of dosage for use in humans.
- the dosage of such compounds may lie within a range of circulating concentrations that include the ED50 with little or no toxicity.
- the dosage may vary within this range depending upon the dosage form employed and the route of administration utilized.
- the therapeutically effective dose can be estimated initially from cell culture assays.
- a dose may be formulated in animal models to achieve a circulating plasma concentration range that includes the IC50 (i.e., the concentration of the test compound that achieves a half-maximal inhibition of symptoms) as determined in cell culture.
- IC50 i.e., the concentration of the test compound that achieves a half-maximal inhibition of symptoms
- levels in plasma may be measured, for example, by high performance liquid chromatography.
- kits e.g., kits for therapeutic purposes or kits for modulating the lifespan of cells or modulating apoptosis.
- a kit may comprise one or more compounds as described herein, e.g., in premeasured doses.
- a kit may optionally comprise devices for contacting cells with the compounds and instructions for use. Devices include syringes, stents and other devices for introducing a compound into a subject (e.g., the blood vessel of a subject) or applying it to the skin of a subject.
- the invention provides a composition of matter comprising a compound of this invention and another therapeutic agent (the same ones used in combination therapies and combination compositions) in separate dosage forms, but associated with one another.
- the term "associated with one another" as used herein means that the separate dosage forms are packaged together or otherwise attached to one another such that it is readily apparent that the separate dosage forms are intended to be sold and administered as part of the same regimen.
- the compound and the other agent are preferably packaged together in a blister pack or other multi-chamber package, or as connected, separately sealed containers (such as foil pouches or the like) that can be separated by the user (e.g., by tearing on score lines between the two containers).
- the invention provides a kit comprising in separate vessels, a) a compound of this invention; and b) another therapeutic agent such as those described elsewhere in the specification.
- HATU 1,3,3- tetramethyluronium hexafluorophosphate
- DIEA AyV-
- 6-(mo holinomethyl)pyridin-2-amine (24.4 mg, 0.24 mmol)
- 6-(2-(trifluoromethyl)phenyl)imidazo[l,2-b]pyridazine-3-carboxylic acid 50.0 mg, 0.16 mmol
- HATU 119.0 mg, 0.32 mmol
- DIEA 41.0 mg, 0.32 mmol
- This general coupling procedure could be used to prepare a variety of 6-(2- trifluoromethyl)phenyl), 6-(2-trifluoromethoxyphenyl), 6-(3-trifluoromethylphenyl), 6- (3-chlorophenyl), 6-(3-fluorophenyl), 6-(2,5-difluorophenyl), 6-(2,4-difluorophenyl), 6- (3,4-difluorophenyl), 6-(3,5-difluorophenyl), 6-(2,3-difluorophenyl), 6-(2-chloro-3- fluorophenyl), 6-(2-(methylsulfonyl)phenyl and 6-(2-cyanophenyl)imidazo[l,2- b]pyridazine-3-carboxamides by substituting the appropriate amine moiety for 6- (mo holinomethyl)pyridin-2-amine.
- N-(2-(3-hydroxy-2-(hydroxymethyl)-2-methylpropoxy)pyrimidin-4-yl)-6-(2- (trifluoromethyl)phenyl)imidazo[l,2-b]pyridazine-3-carboxamide was prepared using the general coupling method above.
- the ring opening of the oxetane in the final product N- (2-(3-hydroxy-2-(hydroxymethyl)-2-methylpropoxy)pyrimidin-4-yl)-6-(2- 10 (trifluoromethyl)phenyl)imidazo[l,2-b]pyridazine-3-carboxamide) occurred during preparative HPLC purification.
- This general coupling procedure could be used to prepare 6-((2,2-dimethyl-l,3-dioxolan-4- yl)methoxy)pyrazin-2-amine, 2-((2,2-dimethyl-l,3-dioxolan-4-yl)methoxy)pyrimidin-4- amine, 4-((2,2-dimethyl-l,3-dioxolan-4-yl)methoxy)pyrimidin-2-amine, 6-((2,2-dimethyl- l,3-dioxolan-4-yl)methoxy)pyridin-3-amine, 5-((2,2-dimethyl-l,3-dioxolan-4- yl)methoxy)pyrazin-2-amine, 2-((2,2-dimethyl-l,3-dioxolan-4-yl)methoxy)pyridin-4- amine, 4-((2,2-dimethyl-l,3-dioxolan-4-yl)methoxy)-6
- 6-((2,2-dimethyl-l,3-dioxolan-4-yl)methoxy)pyridin-2-amine 110.0 mg, 0.49 mmol was taken up in DMF (1 mL) along with 6-(2-(trifluoromethyl)phenyl)imidazo[l,2- b]pyridazine-3-carboxylic acid (100.0 mg, 0.33 mmol), HATU (247.0 mg, 0.65 mmol) and DIEA (84.0 mg, 0.65 mmol). The resulting reaction mixture was stirred at 65 °C for 24 h.
- Ethyl 6-chloroimidazo[l,2-b]pyridazine-3-carboxylate (903.0 mg, 4 mmol) was taken up in 5 mL of dioxane/water (4:1) along with 2-formylphenylboronic acid (720.0 mg, 4.8 mmol), Pd(PPh 3 ) 4 (231.0 mg, 0.2 mmol) and Na 2 C0 3 ( 1.02 g, 9.6 mmol).
- the resulting reaction mixture was stirred at 120 °C for 20 min in a microwave reactor. Upon cooling to room temp, the mixture was diluted with methylene chloride (DCM) (20 mL) and filtered. The filtrate was dried (Na 2 S0 4 ) and concentrated under reduced pressure.
- DCM methylene chloride
- This general coupling procedure could be used to prepare 6-(3,5-dimethylisoxazol-4-yl), 6-(l-methyl-lH-pyrazol-4-yl), 6-(2-methylpyridin-3-yl), 6-(5-(difluoromethyl)pyridin- 3-yl), 6-(2,4-dimethylthiazole), 6-(2,3,4-trifluromethyl phenyl), 6-(2-flourophenyl), 6-(2- chlorophenyl), 6-(2-fluoro-3-chlorophenyl) and 6-(2-chloro-6-fluorophenyl)imidazo[l,2- b]pyridazine-3-carboxamides by substituting the appropriate amine moiety for 2- (pyrrolidin- 1 -yl)pyridin-4-amine.
- Example 11 Preparation of 6-(thiazol-2-yl)imidazo[l,2-b]pyridazine-3-carboxylic acid: To a solution of ethyl 6-chloroimidazo[l,2-b]pyridazine-3-carboxylate (250.0 mg, 1.1 mmol) and 2-(tributylstannyl)thiazole (619.0 mg, 1.65 mmol) in dioxane (5 mL), Pd(PPh 3 )4 (150.0 mg, 0.17 mmol) was added and the reaction was heated to 80 °C for 17 h.
- MS (ESI) calcd for C 28 H 3 oN 6 0 5 : 530.2.
- This general procedure could be used to prepare a variety of 6-(2-(2,3- dihydroxypropoxy)phenyl)-N-(substituted), 6-(3-(2,3-dihydroxypropoxy)phenyl)-N- (substituted) and 6-(2-(2,3-dihydroxypropoxy)phenyl)-N-(substituted) imidazo[l,2- b]pyridazine-3-carboxamides.
- This general coupling procedure could be used to prepare a variety of 6-(3- fluoropyrrolidin- 1 -yl), 6-(3 ,3-difluoropyrrolidin- 1 -yl), 6-(3 -dimethylpyrrolidin-3 - amine), 6-(pyrrolidin-l-yl), 6-(3,3-difluoroazetidin-l-yl), 6-(4,4-difluoropiperidin-l-yl), 6-(3 -methylpyrrolidm- 1 -yl), 6-(3 -hydroxypyrrolidm- 1 -yl), 6-(3 -methoxypyrrolidm- 1 - yl), 6-(3-fluoropiperidin-l-yl), 6-(morpolin-l-yl), 6-(3,5- 6-(N-methylpiperazin-l-yl) and 6-(3-fluoropiperidin-l-yl) imidazo[l,2-b]pyrid
- a pressure tube was charged with a solution of CDI (75.5 mg, 0.47 mmol) in dioxane (2 mL).
- a solution of 2-methyl-6-(2-(trifluoromethyl)phenyl)imidazo[l,2-b]pyridazine-3- carboxylic acid (100.0 mg, 0.31 mmol) in dioxane: DMA (1:1, 2 mL) was added and the mixture was heated to 100 °C for 15 h.
- 6-methoxypyrimidin-4-amine 117.0 mg, 0.93 mmol was then added and the heating was continued for 3 d.
- H 2 O was added and suspension was extracted with CH 2 CI 2 .
- This general procedure could be used to prepare 6-(3-((2,2-dimethyl-l,3-dioxolan-4- yl)methoxy)phenyl)-2-methylimidazo[l,2-b]pyridazine-3-carboxylic acid by substituting 3-hydroxyphenylboronic acid for 2-hydroxyphenylboronic acid.
- This general procedure could be used to prepare (5)-4-nitrophenyl 6-(3-((2,2-dimethyl-l,3- dioxolan-4-yl)methoxy)phenyl)-2-methylimidazo[l,2-b]pyridazine-3-carboxylate by starting from 6-(3-((2,2-dimethyl-l,3-dioxolan-4-yl)methoxy)phenyl)-2- methylimidazo[l,2-b]pyridazine-3-carboxylic acid.
- Step 3 Synthesis of ethyl 8-methyl-6-(2-(trifluoromethyl)phenyl)imidazo[l,2- b pyridazine-3-carboxylate :
- Example 22 Preparation of 7-methyl-N-(pyridin-4-yl)-6-(2- (trifluoromethyl)phenyl)imidazo[l,2-b]pyridazine-3-carboxamide (Compound 223): Step 1. Synthesis of ethyl 7-methyl-6-(2-(trifluoromethyl)phenyl)imidazo[l,2-
- Ethyl 6-chloro-7,8-dimethylimidazo[l,2-b]pyridazine-3-carboxylate 750.0 mg, 2.96 mmol
- 2-(trifluoromethyl)phenylboronic acid 562.0 mg, 2.96 mmol
- Dicyclohexyl(2',6'-dimethoxybiphenyl-2-yl)phosphine 97.0 mg, 0.236 mmol
- K 3 PO 4 (1.88 g, 8.87 mmol
- Step 1 Synthesis of ethyl 6-chloro-2,8-dimethylimidazo[l,2-b]pyridazine-3- carboxylate (and ethyl 6-chloro-2,7-dimethylimidazo[l,2-b]pyridazine-3- carboxylate):
- Ethyl 6-chloro-2,8-dimethylimidazo[l,2-b]pyridazine-3-carboxylate (7.4 g, 29 mmol), 2- (trifluoromethyl)phenylboronic acid (6.6 g, 35 mmol), cesium carbonate (19.0 g, 58 mmol), Pd(PPli 3 )4 (3.3 g, 3 mmol) were dissolved in a mixture of dioxane: water (4:1) plus 10 drops of EtOH. The mixture was heated to 75 °C for 5 h, then concentrated. Water (200 mL) was added and this was extracted with CH 2 CI 2 (300 mL).
- Ethyl 2,8-dimethyl-6-(2-(trifluoromethyl)phenyl)imidazo[l,2-b]pyridazine-3-carboxylate (8.0 g, 22 mmol) was dissolved in dioxane (100 mL). NaOH (1.76 g, 44 mmol) in water (100 mL) was added. The mixture was heated to 60 °C for 2 h, then concentrated. Water (100 mL) was added and the mixture was filtered. The pH was adjusted to 5 with aqueous HCl.
- This general coupling procedure could be used to prepare a variety of 2,8-dimethyl-6-(2- trifluromethyl)phenyl) and 2,8-dimethyl-6-(2-trifluromethoxy)phenyl) imidazo[l,2- b]pyridazine-3-carboxamides by substituting the appropriate amine moiety for 3- aminopyridazine.
- 6-chloropyridazin-3 -amine (10.0 g, 77.2 mmol) and 2-(trifluoromethyl)phenylboronic acid (29.3 g, 154.4 mmol) were added to a 250 mL flask.
- Cs 2 C0 3 (50.3 g, 154.4 mol), Pd2(dba)3 (3.5 g, 3.82 mmol), and XPhos (1.8 g, 3.82 mmol) were added, followed by dioxane (100 mL) and water (20 mL).
- the reaction was heated to 100 °C for 3 h, followed by cooling to room temp.
- the mixture was concentrated in vacuo, and the residue was resuspended in DCM (500 mL).
- 6-(2-(trifluoromethyl)phenyl)pyridazin-3-amine (3.0 g, 12.55 mmol) and NaHCC>3 (2.1 g, 25.1 mmol) were suspended in MeOH (30 mL). Br 2 was added (3.0 g, 0.96 mL, 18.8 mmol) dropwise at room temp. The reaction was allowed to stir for 1 h at room temp, then poured into bicarb (300 mL) after which a precipitate formed. The solid was collected by filtration, washed with water, and dried in vacuo to give 4-bromo-6-(2- (trifluoromethyl)phenyl)pyridazin-3-amine (3.8 g, 95%). MS (ESI) calcd for
- Ethyl 8-bromo-2-methyl-6-(2-(trifluoromethyl)phenyl)imidazo[l,2-b]pyridazine-3- carboxylate (246.0 mg, 0.573 mmol) was dissolved in THF (11.0 mL). Water was added (13.0 mL), followed by lithium hydroxide (55.0 mg, 2.29 mmol). The reaction was allowed to stir at room temp for 3.5 h. Aqueous HCl (1.0 N, 2.4 mL) was added, and the mixture was extracted with EtOAc (3x20 mL).
- Step 7 Synthesis of (i?)-8-(2,3-dihydroxypropoxy)-2-methyl-N-(pyridazin-3-yl)-6- :
- Ethyl 2-methyl-8-mo holino-6-(2-(trifluoromethyl)phenyl)imidazo[l,2-b]pyridazine-3- carboxylate (26.0 mg, 0.060 mmol) was suspended in THF (1.2 mL) water (2.4 mL) and MeOH (1 mL). Lithium hydroxide was added (7.0 mg, 0.300 mmol) and the mixture was heated to reflux for 3 h, followed by cooling to room temp. HC1 was added (1.0 N, 0.35 mL), and the mixture was extracted with EtOAc (3x10 mL).
- Pd/C 10 wt% 200 mg was added to a degassed solution of benzyl 6-(2- (trifluoromethyl)phenyl)imidazo[l,2-b]pyridazin-3-ylcarbamate (1.07 g, 2.59 mmol) in THF MeOH (40 mL, 1:1). The mixture was hydrogenated under balloon pressure at 25 °C for 16 h. The catalyst was removed by filtration and the mixture concentrated.
- HATU 109 mg, 0.0.29 mmol
- 6-(2- (trifluoromethyl)phenyl)imidazo[l,2-b]pyridazin-3-amine 50.0 mg, 0.18 mmol
- 5- methylpyrazine-2-carboxylic acid 37.0 mg, 0.27 mmol
- DIEA 78 ⁇ , 0.44 mmol
- the mixture was stirred at 60 °C for 3 h.
- 3 ⁇ 40 45 mL was added and the resulting ppt was collected by filtration, rinsed with 3 ⁇ 40, and dried under vacuum.
- the crude residue was purified by MPLC eluting with CH 2 Cl 2 MeOH (0-5%).
- This general coupling procedure could be used to prepare a variety of 6-(2- trifluromethyl)phenyl) imidazo[l,2-b]pyridazin-3-yl)pyrazine-2-carboxamides by substituting the appropriate carboxylic acid moiety for 5-methylpyrazine-2-carboxylic acid.
- HATU (203.0 mg, 0.53 mmol) was added to a solution of 6-(2- (trifluoromethyl)phenyl)imidazo[l,2-b]pyridazin-3-amine (93.0 mg, 0.33 mmol), 6- hydroxypyrimidine-4-carboxylic acid (70.0 mg, 0.50 mmol), and pyridine (81 ⁇ , 1.00 mmol) in CH 3 CN (15 mL). The reaction mixture was heated at reflux for 72 h. 3 ⁇ 40 was added and the resulting ppt was collected by filtration rinsed with 3 ⁇ 40 and dried under vacuum.
- 3N HC1 (100 mL, 0.30 mmol) was added to a suspension of f ⁇ -6-((2,2-dimethyl-l,3- dioxolan-4-yl)methoxy)-N-(6-(2-(trifluoromethyl)phenyl)imidazo[l,2-b]pyridazin-3- yl)pyrazine-2-carboxamide (113.0 mg, 0.22 mmol) in EtOH (10 mL). The mixture was heated at 60 °C until the mixture became homogenous then stirred at room temp for 16 h.
- diphenylphosphorylamide (0.537 mL, 2.49 mmol) over 15 min.
- the mixture was warmed to 55 °C for 2 h, then heated to reflux for 19 h, followed by cooling and concentration, resuspension in EtOAc and saturated aqueous NaHCCh.
- the layers were separated and the aqueous layer was washed with EtOAc (3x50 mL).
- the combined organics were washed with brine, dried with anhydrous Na2SC>4, filtered and concentrated.
- 6-methoxypicolinic acid (40.0 mg, 0.26 mmol) was dissolved in dimethylformamide (1.0 mL).
- HATU 147.0 mg, 0.39 mmol
- diisopropylethylamine (0.18 mL, 1.03 mmol).
- 2,8-dimethyl-6-(2-(trifluoromethyl)phenyl)imidazo[l,2-b]pyridazin-3- amine (79.0 mg, 0.26 mmol) was dissolved in 2.1 mL dimethylformamide and added to the reaction mixture, which was then warmed to 50 °C for 4 h. The mixture was cooled to room temp and saturated aqueous NaHCC (4 mL) and water (4 mL) were added.
- CS2CO3 64.20 g, 197.20 mmol was added to a solution of ethyl 5-amino-lH-pyrazole- 4-carboxylate (20.40 g, 131.40 mmol) and ethyl-3-ethoxyacrylate (28.6 mL, 197.20 mmol) in DMF (250 mL).
- the reaction mixture was stirred at 110 °C for 16 h.
- the mixture was cooled to room temp and the pH was adjusted to 4 by the addition of AcOH (80 mL).
- the mixture was concentrated in vacuo and the residue partitioned between CH 2 CI 2 H 2 O (1000 mL, 1:1).
- 4-aminopyridine (122 mg, 1.30 mmol) was added to a solution of 5-(2- (trifluoromethyl)phenyl)pyrazolo[l,5-a]pyrimidine-3-carboxylic acid (100.0 mg, 0.33 mmol), pyridine (105 ⁇ , 1.30 mmol) and HATU (149.0 mg, 0.39 mmol) in CH 3 CN (15 mL), and the reaction was heated at reflux for 72 h. 3 ⁇ 40 was added and the resulting precipitate was collected by filtration, rinsed with 3 ⁇ 40, and dried under vacuum.
- This general coupling procedure could be used to prepare N-(pyrazin-2-yl)-5-(2- (trifluoromethyl)phenyl)pyrazolo[l,5-a]pyrimidine-3-carboxamide, N-(pyridazin-3 5-(2-(trifluoromethyl)phenyl)pyrazolo[l,5-a]pyrimidine-3-carboxamide and N-(2- methylpyridin-4-yl)-5-(2-(trifluoromethoxy)phenyl)pyrazolo[l,5-a]pyrimidine-3- carboxamide.
- This general coupling procedure could be used to prepare a variety of N-(substituted)-5- (2-(trifluoromethyl)phenyl) and N-(substituted)-5-(2-(trifluoromethoxy)phenyl) pyrazolo[l,5-a]pyrimidine-3-carboxamides by starting with the appropriate carboxylic acid and substituting the appropriate amine for 2-aminopyridine.
- Diphenylphosphoryl azide (674.0 mg, 2.45 mmol) was added to a solution of 5-(2- (trifluoromethyl)phenyl)pyrazolo[l,5-a]pyrimidine-3-carboxylic acid (500.0 mg, 1.63 mmol) and triethylamine (329.0 mg, 3.26 mmol) in toluene (10 mL). The mixture was stirred for 1 h at 25 °C then heated at reflux for 2 h. tert-Butyl alcohol (1.22 g, 16.30 mmol) was added and the mixture was heated at reflux for 3 h. After cooling to room temp, the reaction mixture was poured into 3 ⁇ 40.
- Example 45 Preparation of N-(2-methoxypyrimidin-4-yl)-2-methyl-5-(2- (trifluoromethyl)phenyl)pyrazolo[l,5-a]pyrimidine-3-carboxainide (Compound 793): Step 1. Synthesis of 4-nitrophenyl 2-methyl-5-(2- (trifluoromethyl)phenyl)pyrazolo[l,5-a]pyrimidine-3-carb
- N-(6-(azetidin-l-yl)pyridin-2-yl)-2-oxo-2-(2-(6-(2-(trifluoromethyl)phenyl)pyridazin-3- yl)hydrazinyl)acetamide (100.0 mg, 0.22 mmol) was dissolved in xylene (15 mL), and the reaction was heated in a microwave at 150 °C for 6 h. Upon cooling to room temp, the reaction was poured into 3 ⁇ 40, and extracted with DCM.
- 6-((2,2-dimethyl-l,3-dioxolan-4-yl)methoxy)pyrazine-2-carbaldehyde was prepared using the same method described above as for the preparation of 6-((2,2-dimethyl-l,3- dioxolan-4-yl)methoxy)picolinaldehyde.
- 6-(2,2,2-trifluoroethoxy)pyridin-2-amine was prepared similarly to 2-(2,2,2- trifluoroethoxy)pyridin-4-amine above, using 6-chloropyridin-2-amine.
- MS (ESI) calcd for C 7 H 7 F 3 N 2 O: 192.05.
- 3-mo holinopyridin-2-amine was prepared from 3-bromo-2-nitropyridine using the same two-step procedure described above. -amine:
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US10065974B2 (en) | 2015-10-30 | 2018-09-04 | Calithera Biosciences, Inc. | Compositions and methods for inhibiting arginase activity |
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US10758518B2 (en) | 2017-10-31 | 2020-09-01 | Curis, Inc. | Compounds and compositions for treating hematological disorders |
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US11793797B2 (en) | 2016-09-07 | 2023-10-24 | Pharmakea, Inc. | Uses of a lysyl oxidase-like 2 inhibitor |
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4683195A (en) | 1986-01-30 | 1987-07-28 | Cetus Corporation | Process for amplifying, detecting, and/or-cloning nucleic acid sequences |
US4727064A (en) | 1984-04-25 | 1988-02-23 | The United States Of America As Represented By The Department Of Health And Human Services | Pharmaceutical preparations containing cyclodextrin derivatives |
US20070037809A1 (en) * | 2005-08-04 | 2007-02-15 | Sirtris Pharmaceuticals, Inc. | Sirtuin modulating compounds |
US20070037865A1 (en) * | 2005-08-04 | 2007-02-15 | Sirtris Pharmaceuticals, Inc. | Sirtuin modulating compounds |
US20100130488A1 (en) * | 2005-10-21 | 2010-05-27 | Exelixis, Inc. | Pyrazolo-Pyrimidines as Casein Kinase II (CK2) Modulators |
Family Cites Families (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995035298A1 (en) | 1994-06-21 | 1995-12-28 | Otsuka Pharmaceutical Factory, Inc. | PYRAZOLO[1,5-a]PYRIMIDINE DERIVATIVE |
US7067520B2 (en) | 2000-11-17 | 2006-06-27 | Ishihara Sangyo Kaisha, Ltd. | Preventive or therapeutic medicines for diabetes containing fused-heterocyclic compounds or their salts |
US7662826B2 (en) | 2002-04-23 | 2010-02-16 | Shionogi & Co., Ltd. | Pyrazolo [1,5-a] pyrimidine derivative and nad (p) h oxidase inhibitor containing the same |
US7741318B2 (en) | 2004-12-21 | 2010-06-22 | Schering Corporation | Pyrazolo [1,5-A]pyrimidine adenosine A2a receptor antagonists |
AU2006212457B2 (en) * | 2005-02-11 | 2011-04-14 | F. Hoffmann-La Roche Ag | Pyrazolo-pyrimidine derivatives as mGLuR2 antagonists |
EP1853590A1 (en) | 2005-03-03 | 2007-11-14 | Sirtris Pharmaceuticals, Inc. | Fused heterocyclic compounds and their use as sirtuin modulators |
US20100216798A1 (en) | 2005-07-29 | 2010-08-26 | Astellas Pharma Inc | Fused heterocycles as lck inhibitors |
US7750000B2 (en) | 2005-09-02 | 2010-07-06 | Bayer Schering Pharma Ag | Substituted imidazo[1,2b]pyridazines as kinase inhibitors, their preparation and use as medicaments |
EP1873157A1 (en) | 2006-06-21 | 2008-01-02 | Bayer Schering Pharma Aktiengesellschaft | Pyrazolopyrimidines and salts thereof, pharmaceutical compositions comprising same, methods of preparing same and uses of same |
EP1900739A1 (en) | 2006-08-30 | 2008-03-19 | Cellzome Ag | Diazolodiazine derivatives as kinase inhibitors |
AR064420A1 (en) | 2006-12-21 | 2009-04-01 | Alcon Mfg Ltd | OPHTHALMIC PHARMACEUTICAL COMPOSITIONS THAT INCLUDE AN EFFECTIVE AMOUNT OF ANALOGS OF 6-AMINOIMIDAZO [1,2B] PIRIDAZINAS, USEFUL FOR THE TREATMENT OF GLAUCOMA AND / OR CONTROL THE NORMAL OR ELEVATED INTRAOCULAR PRESSURE (IOP). |
EP2014281A1 (en) | 2007-06-19 | 2009-01-14 | Institut National De La Sante Et De La Recherche Medicale (Inserm) | Use of inhibitors of sirtuins and/or ampk for the preparation of a medicament for the treatment of polyalanine diseases. |
WO2009060197A1 (en) * | 2007-11-08 | 2009-05-14 | Centro Nacional De Investigaciones Oncologicas (Cnio) | Imidazopyridazines for use as protein kinase inhibitors |
WO2009086303A2 (en) * | 2007-12-21 | 2009-07-09 | University Of Rochester | Method for altering the lifespan of eukaryotic organisms |
WO2009100375A1 (en) * | 2008-02-06 | 2009-08-13 | Bristol-Myers Squibb Company | Substituted imidazopyridazines useful as kinase inhibitors |
US20100029657A1 (en) | 2008-02-29 | 2010-02-04 | Wyeth | Bridged, Bicyclic Heterocyclic or Spiro Bicyclic Heterocyclic Derivatives of Pyrazolo[1, 5-A]Pyrimidines, Methods for Preparation and Uses Thereof |
WO2009146358A1 (en) * | 2008-05-29 | 2009-12-03 | Sirtris Pharmaceuticals, Inc. | Imidazopyridine and related analogs as sirtuin modulators |
PL2328414T3 (en) | 2008-08-29 | 2014-05-30 | Concert Pharmaceuticals Inc | Substituted triazolo-pyridazine derivatives |
PA8854101A1 (en) | 2008-12-18 | 2010-07-27 | Ortho Mcneil Janssen Pharm | IMIDAZOL BICYCLIC DERIVATIVES REPLACED AS MODULATORS OF GAMMA SECRETASA |
WO2010086040A1 (en) | 2009-01-29 | 2010-08-05 | Biomarin Iga, Ltd. | Pyrazolo-pyrimidines for treatment of duchenne muscular dystrophy |
NZ593951A (en) | 2009-02-06 | 2013-01-25 | Ortho Mcneil Janssen Pharm | Novel substituted bicyclic heterocyclic compounds as gamma secretase modulators |
JP2012519211A (en) | 2009-03-02 | 2012-08-23 | サートリス ファーマシューティカルズ, インコーポレイテッド | 8-Substituted quinolines and related analogs as sirtuin-modulating compounds |
EP2264035A1 (en) | 2009-06-04 | 2010-12-22 | Merz Pharma GmbH & Co. KGaA | Glycine B antagonists |
US8410117B2 (en) | 2010-03-26 | 2013-04-02 | Hoffmann-La Roche Inc. | Imidazopyrimidine derivatives |
RU2603637C2 (en) * | 2010-12-08 | 2016-11-27 | Дзе Юнайтед Стейтс Оф Америка, Эз Репрезентед Бай Дзе Секретэри, Департмент Оф Хелс Энд Хьюмэн Сервисис | Substituted pyrazolopyrimidines as glucocerebrosidase activators |
KR20140077964A (en) | 2011-10-20 | 2014-06-24 | 글락소스미스클라인 엘엘씨 | Substituted bicyclic aza-heterocycles and analogues as sirtuin modulators |
AU2012325916A1 (en) | 2011-10-20 | 2014-05-01 | Glaxosmithkline Llc | Substituted bicyclic aza-heterocycles and analogues as sirtuin modulators |
-
2012
- 2012-10-19 CN CN201280063471.6A patent/CN104394869A/en active Pending
- 2012-10-19 US US14/353,096 patent/US9957271B2/en not_active Expired - Fee Related
- 2012-10-19 EP EP12842273.0A patent/EP2768509B1/en active Active
- 2012-10-19 JP JP2014537283A patent/JP6073343B2/en not_active Expired - Fee Related
- 2012-10-19 AU AU2012325909A patent/AU2012325909B2/en not_active Ceased
- 2012-10-19 CA CA2852936A patent/CA2852936A1/en not_active Abandoned
- 2012-10-19 RU RU2014120166/04A patent/RU2014120166A/en not_active Application Discontinuation
- 2012-10-19 WO PCT/US2012/061015 patent/WO2013059587A1/en active Application Filing
- 2012-10-19 ES ES12842273.0T patent/ES2627347T3/en active Active
- 2012-10-19 KR KR1020147013095A patent/KR20140077963A/en not_active Application Discontinuation
- 2012-10-19 BR BR112014009531A patent/BR112014009531A8/en not_active Application Discontinuation
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4727064A (en) | 1984-04-25 | 1988-02-23 | The United States Of America As Represented By The Department Of Health And Human Services | Pharmaceutical preparations containing cyclodextrin derivatives |
US4683195A (en) | 1986-01-30 | 1987-07-28 | Cetus Corporation | Process for amplifying, detecting, and/or-cloning nucleic acid sequences |
US4683195B1 (en) | 1986-01-30 | 1990-11-27 | Cetus Corp | |
US20070037809A1 (en) * | 2005-08-04 | 2007-02-15 | Sirtris Pharmaceuticals, Inc. | Sirtuin modulating compounds |
US20070037865A1 (en) * | 2005-08-04 | 2007-02-15 | Sirtris Pharmaceuticals, Inc. | Sirtuin modulating compounds |
US20100130488A1 (en) * | 2005-10-21 | 2010-05-27 | Exelixis, Inc. | Pyrazolo-Pyrimidines as Casein Kinase II (CK2) Modulators |
Non-Patent Citations (31)
Title |
---|
"Cell Therapy: Stem Cell Transplantation, Gene Therapy, and Cellular Immunotherapy", 1996, CAMBRIDGE UNIVERSITY PRESS |
"DNA Cloning", vol. I, II, 1985 |
"Encyclopedia of Pharmaceutical Technology", vol. 9, 1992, NEW YORK: MARCEL DEKKER |
"Encyclopedia of Reagents for Organic Synthesis", 1995 |
"Gene Transfer Vectors For Mammalian Cells", 1987, COLD SPRING HARBOR LABORATORY |
"Handbook Of Experimental Immunology", vol. I-IV, 1986 |
"Immobilized Cells And Enzymes", 1986, IRL PRESS |
"Immunochemical Methods In Cell And Molecular Biology", 1987, ACADEMIC PRESS |
"Manipulating the Mouse Embryo", 1986, COLD SPRING HARBOR LABORATORY PRESS |
"Methods In Enzymology", ACADEMIC PRESS, INC. |
"Methods In Enzymology", vol. 154, 155 |
"Molecular Cloning A Laboratory Manual", 1989, COLD SPRING HARBOR LABORATORY PRESS |
"Nucleic Acid Hybridization", 1984 |
"Oligonucleotide Synthesis", 1984 |
"Remington's Pharmaceutical Sciences", MEADE PUBLISHING CO. |
"Transcription And Translation", 1984 |
B. PERBAL, A PRACTICAL GUIDE TO MOLECULAR CLONING, 1984 |
BEGLEY, PHARMACOLOGY & THERAPEUTICS, vol. 104, 2004, pages 29 - 45 |
BITTERMAN ET AL., J. BIOL. CHEM., vol. 277, 2002, pages 45099 |
BRACHMANN ET AL., GENES DEV., vol. 9, 1995, pages 2888 |
E. D. BALL; J. LISTER; P. LAW: "Hematopoietic Stem Cell Therapy", 2000, CHURCHILL LIVINGSTONE |
FRYE ET AL., BBRC, vol. 260, 1999, pages 273 |
J. HETEROCYCLIC. CHEM., vol. 28, 1991, pages 1143 |
J. MED. CHEM., vol. 33, no. 1, 1990, pages 327 - 36 |
KIM ET AL.: "Structure based design and syntheses of amino-1 H-pyrazole amide derivatives as selective Raf kinase inhibitors in melanoma cells", BIOORGANIC & MEDICINAL CHEMISTRY, vol. 19, no. ISS. 6, 15 March 2011 (2011-03-15), pages 1915 - 1923, XP028176794 * |
L. FIESER; M. FIESER, FIESER AND FIESER'S REAGENTSFOR ORGANIC SYNTHESIS, 1994 |
LUO ET AL., CELL, vol. 107, 2001, pages 137 |
R. I. FRESHNEY: "Culture Of Animal Cells", 1987, ALAN R. LISS, INC. |
R. LAROCK: "Comprehensive Organic Transformations", 1989 |
See also references of EP2768509A4 * |
T. W. GREENE; P. G. M. WUTS: "Protective Groups in Organic Synthesis", 1991 |
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WO2015186068A1 (en) | 2014-06-02 | 2015-12-10 | Glaxosmithkline Intellectual Property (No.2) Limited | Preparation and use of crystalline beta-d-nicotinamide riboside |
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US10143699B2 (en) | 2015-06-23 | 2018-12-04 | Calithera Biosciences, Inc. | Compositions and methods for inhibiting arginase activity |
US10398714B2 (en) | 2015-06-23 | 2019-09-03 | Calithera Biosciences, Inc. | Compositions and methods for inhibiting arginase activity |
US10905701B2 (en) | 2015-06-23 | 2021-02-02 | Calithera Biosciences, Inc. | Compositions and methods for inhibiting arginase activity |
US11464774B2 (en) | 2015-09-30 | 2022-10-11 | Vertex Pharmaceuticals Incorporated | Method for treating cancer using a combination of DNA damaging agents and ATR inhibitors |
US10065974B2 (en) | 2015-10-30 | 2018-09-04 | Calithera Biosciences, Inc. | Compositions and methods for inhibiting arginase activity |
US10851118B2 (en) | 2015-10-30 | 2020-12-01 | Calithera Biosciences, Inc. | Compositions and methods for inhibiting arginase activity |
US10844080B2 (en) | 2015-10-30 | 2020-11-24 | Calithera Biosciences, Inc. | Compositions and methods for inhibiting arginase activity |
US10479793B2 (en) | 2015-11-18 | 2019-11-19 | Bristol-Myers Squibb Company | Imidazopyridazine compounds useful as modulators of IL-12, IL-23 and/or IFN alpha responses |
WO2017087590A1 (en) * | 2015-11-18 | 2017-05-26 | Bristol-Myers Squibb Company | Imidazopyridazine compounds useful as modulators of il-12, il-23 and/or ifn alpha responses |
US10988461B2 (en) | 2016-03-03 | 2021-04-27 | Cornell University | Small molecule IRE1-α inhibitors |
WO2017152117A1 (en) * | 2016-03-03 | 2017-09-08 | Cornell University | Small molecule ire1-alpha inhibitors |
US10125123B2 (en) | 2016-03-03 | 2018-11-13 | Cornell University | Small molecule IRE1-α inhibitors |
US11453675B2 (en) | 2016-04-06 | 2022-09-27 | Bial—R&D Investments, S.A. | Imidazo[1,5-a]pyrimidinyl carboxamide compounds and their use in the treatment of medical disorders |
US10934298B2 (en) | 2016-04-06 | 2021-03-02 | BIAL—BioTech Investments, Inc. | Substituted pyrazolo[1,5-a]pyrimidines for the treatment of medical disorders |
WO2017176961A1 (en) * | 2016-04-06 | 2017-10-12 | Lysosomal Therapeutics Inc. | Imidazo [1,5-a]pyrimidinyl carboxamide compounds and their use in the treatment of medical disorders |
US9840510B1 (en) | 2016-04-06 | 2017-12-12 | Lysosomal Therapeutics Inc. | Pyrazolo[1,5-a]pyrimidinyl carboxamide compounds and their use in the treatment of medical disorders |
US9920061B2 (en) | 2016-04-06 | 2018-03-20 | Lysosomal Therapeutics Inc. | Imidazo[1,5-A]pyrimidinyl carboxamide compounds and their use in the treatment of medical disorders |
US11124516B2 (en) | 2016-04-06 | 2021-09-21 | BIAL-BioTech Investments, Inc. | Pyrrolo[1,2-A]pyrimidinyl carboxamide compounds and their use in the treatment of medical disorders |
EP3440083A4 (en) * | 2016-04-06 | 2019-09-18 | Lysosomal Therapeutics Inc. | Imidazo [1,5-a]pyrimidinyl carboxamide compounds and their use in the treatment of medical disorders |
US10787454B2 (en) | 2016-04-06 | 2020-09-29 | BIAL—BioTech Investments, Inc. | Imidazo[1,5-a]pyrimidinyl carboxamide compounds and their use in the treatment of medical disorders |
US11192892B2 (en) | 2016-04-06 | 2021-12-07 | Bial—R&D Investments, S.A. | Substituted pyrazolo[1,5-a]pyrimidines for the treatment of medical disorders |
US11345698B2 (en) | 2016-05-05 | 2022-05-31 | Bial—R&D Investments, S.A. | Substituted imidazo[1,2-a]pyridines, substituted imidazo[1,2-a]pyrazines, related compounds, and their use in the treatment of medical disorders |
CN109311902B (en) * | 2016-05-05 | 2022-07-15 | Bial研发投资股份有限公司 | Substituted imidazo [1,2-b ] pyridazines, imidazo [1,5-b ] pyridazines, related compounds, and uses thereof |
AU2017261291B2 (en) * | 2016-05-05 | 2021-11-18 | Bial - R&D Investments, S.A. | Substituted imidazo[1,2-b]pyridazines, substituted imidazo[1,5-b]pyridazines, related compounds, and their use in the treatment of medical disorders |
US20190389866A1 (en) * | 2016-05-05 | 2019-12-26 | Lysosomal Therapeutics Inc. | SUBSTITUTED IMIDAZO[1,2-b]PYRIDAZINES, SUBSTITUTED IMIDAZO[1,5-b]PYRIDAZINES, RELATED COMPOUNDS, AND THEIR USE IN THE TREATMENT OF MEDICAL DISORDERS |
US11878979B2 (en) | 2016-05-05 | 2024-01-23 | Bial—R&D Investments, S.A. | Substituted imidazo[1,2-b]pyridazines, substituted imidazo[1,5-b]pyridazines, related compounds, and their use in the treatment of medical disorders |
AU2017261291C1 (en) * | 2016-05-05 | 2022-05-26 | Bial - R&D Investments, S.A. | Substituted imidazo[1,2-b]pyridazines, substituted imidazo[1,5-b]pyridazines, related compounds, and their use in the treatment of medical disorders |
RU2773333C2 (en) * | 2016-05-05 | 2022-06-02 | Биал - Ар Энд Ди Инвестментс, С.А. | SUBSTITUTED IMIDAZO[1,2-b]PYRIDAZINES, SUBSTITUTED IMIDAZO[1,5-b]PYRIDAZINES, RELATED COMPOUNDS AND THEIR USE FOR TREATMENT OF PATHOLOGICAL CONDITIONS |
WO2017192930A1 (en) * | 2016-05-05 | 2017-11-09 | Lysosomal Therapeutics Inc. | SUBSTITUTED IMIDAZO[1,2-b]PYRIDAZINES, SUBSTITUTED IMIDAZO[1,5-b]PYRIDAZINES, RELATED COMPOUNDS, AND THEIR USE IN THE TREATMENT OF MEDICAL DISORDERS |
US11168087B2 (en) | 2016-05-05 | 2021-11-09 | Bial—R&D Investments, S.A. | Substituted imidazo[1,2-b]pyridazines, substituted imidazo[1,5-b]pyridazines, related compounds, and their use in the treatment of medical disorders |
US9868742B2 (en) | 2016-05-05 | 2018-01-16 | Lysosomal Therapeutics Inc. | Substituted imidazo[1,2-b]pyridazines, substituted imidazo[1,5-b] pyridazines, related compounds, and their use in the treatment of medical disorders |
US11793797B2 (en) | 2016-09-07 | 2023-10-24 | Pharmakea, Inc. | Uses of a lysyl oxidase-like 2 inhibitor |
US11459309B2 (en) | 2016-09-07 | 2022-10-04 | Pharmakea, Inc. | Crystalline forms of a lysyl oxidase-like 2 inhibitor and methods of making |
US11291674B2 (en) | 2016-11-08 | 2022-04-05 | Calithera Biosciences, Inc. | Arginase inhibitor combination therapies |
KR20190119579A (en) * | 2016-12-22 | 2019-10-22 | 칼리테라 바이오사이언시즈, 인코포레이티드 | Compositions and Methods for Inhibiting Arginase Activity |
TWI818902B (en) * | 2016-12-22 | 2023-10-21 | 美商卡利泰拉生物科技公司 | Compositions and methods for inhibiting arginase activity |
US10287303B2 (en) | 2016-12-22 | 2019-05-14 | Calithera Biosciences, Inc. | Compositions and methods for inhibiting arginase activity |
CN110382508B (en) * | 2016-12-22 | 2022-08-02 | 卡里塞拉生物科学股份公司 | Compositions and methods for inhibiting arginase activity |
US10597411B2 (en) * | 2016-12-22 | 2020-03-24 | Calithera Biosciences, Inc. | Compositions and methods for inhibiting arginase activity |
WO2018119440A1 (en) * | 2016-12-22 | 2018-06-28 | Calithera Biosciences, Inc. | Compositions and methods for inhibiting arginase activity |
CN110382508A (en) * | 2016-12-22 | 2019-10-25 | 卡里塞拉生物科学股份公司 | For inhibiting the composition and method of arginase activities |
EP3842442A1 (en) * | 2016-12-22 | 2021-06-30 | Calithera Biosciences, Inc. | Compositions and methods for inhibiting arginase activity |
US12054501B2 (en) | 2016-12-22 | 2024-08-06 | Precision Pharmaceuticals, Inc. | Compositions and methods for inhibiting arginase activity |
US11021495B2 (en) | 2016-12-22 | 2021-06-01 | Calithera Biosciences, Inc. | Compositions and methods for inhibiting arginase activity |
KR102579849B1 (en) | 2016-12-22 | 2023-09-18 | 칼리테라 바이오사이언시즈, 인코포레이티드 | Compositions and methods for inhibiting arginase activity |
EA038517B1 (en) * | 2016-12-28 | 2021-09-09 | Калитера Байосайнсиз, Инк. | Compositions and methods for inhibiting arginase activity |
US11419875B2 (en) | 2017-03-31 | 2022-08-23 | Aurigene Discovery Technologies Limited | Compounds and compositions for treating hematological disorders |
US10494339B2 (en) | 2017-05-12 | 2019-12-03 | Calithera Biosciences, Inc. | Method of preparing (3R,4S)-3-acetamido-4-allyl-N-(tert-butyl)pyrrolidine-3-carboxamide |
US10906872B2 (en) | 2017-05-12 | 2021-02-02 | Calithera Biosciences, Inc. | Method of preparing (3R,4S)-3-acetamido-4-allyl-n-(tert-butyl)pyrrolidine-3-carboxamide |
US11370754B2 (en) | 2017-05-12 | 2022-06-28 | Calithera Biosciences, Inc. | Method of preparing (3R,4S)-3-acetamido-4-allyl-n-(tert-butyl)pyrrolidine-3-carboxamide |
US10758518B2 (en) | 2017-10-31 | 2020-09-01 | Curis, Inc. | Compounds and compositions for treating hematological disorders |
CN115572282B (en) * | 2021-07-05 | 2024-07-09 | 华东理工大学 | Pyrazole amide compound containing aromatic heterocyclic structure, and preparation method and application thereof |
CN115572282A (en) * | 2021-07-05 | 2023-01-06 | 华东理工大学 | Pyrazole amide compound containing aromatic heterocyclic structure, and preparation method and application thereof |
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