WO2011071758A1 - 3,6-diazabicyclo[3.1.1]heptanes comme ligands des récepteurs nicotiniques neuronaux à l'acétycholine - Google Patents

3,6-diazabicyclo[3.1.1]heptanes comme ligands des récepteurs nicotiniques neuronaux à l'acétycholine Download PDF

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WO2011071758A1
WO2011071758A1 PCT/US2010/058836 US2010058836W WO2011071758A1 WO 2011071758 A1 WO2011071758 A1 WO 2011071758A1 US 2010058836 W US2010058836 W US 2010058836W WO 2011071758 A1 WO2011071758 A1 WO 2011071758A1
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Prior art keywords
diazabicyclo
compound
heptane
disease
carbonyl
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PCT/US2010/058836
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English (en)
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Srinivasa Rao Akireddy
Balwinder Singh Bhatti
Ronald Joseph Heemstra
Srinivasa V. Murthy
Jon-Paul Strachan
Yunde Xiao
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Targacept, Inc.
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Priority to CA2782409A priority Critical patent/CA2782409A1/fr
Priority to US13/514,084 priority patent/US8802694B2/en
Priority to JP2012542213A priority patent/JP2013512922A/ja
Priority to RU2012128583/04A priority patent/RU2012128583A/ru
Priority to KR1020127017478A priority patent/KR20120120190A/ko
Priority to BR112012013765A priority patent/BR112012013765A2/pt
Priority to EP10787978A priority patent/EP2509982A1/fr
Priority to CN2010800553917A priority patent/CN102648202A/zh
Priority to SG2012039293A priority patent/SG181109A1/en
Priority to AU2010328419A priority patent/AU2010328419A1/en
Application filed by Targacept, Inc. filed Critical Targacept, Inc.
Priority to MX2012006484A priority patent/MX2012006484A/es
Publication of WO2011071758A1 publication Critical patent/WO2011071758A1/fr
Priority to IL219960A priority patent/IL219960A0/en
Priority to ZA2012/04143A priority patent/ZA201204143B/en
Priority to ECSP12012023 priority patent/ECSP12012023A/es
Priority to US14/321,179 priority patent/US20140315880A1/en

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    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/08—Bridged systems
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    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/4995—Pyrazines or piperazines forming part of bridged ring systems
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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
    • C07D487/08—Bridged systems

Definitions

  • the present invention relates to compounds that bind to and modulate the activity of neuronal nicotinic acetylcholine receptors, to processes for
  • CNS central nervous system
  • NNRs neuronal nicotinic receptors
  • nAChRs nicotinic acetylcholine receptors
  • NNR ligands have been proposed as therapies are cognitive disorders, including Alzheimer's disease, attention deficit disorder, and schizophrenia
  • Parkinson's disease (Bordia et al., J Pharmacol. Exp. Ther. 327. 239 (2008), Jonnala and Buccafusco, J. Neurosci. Res. 66. 565 (2001)); addiction (Dwoskin and Crooks, Biochem. Pharmacol. 63: 89 (2002), Coe et al., Bioorg. Med. Chem. Lett. 15(22): 4889 (2005)); obesity (Li et al., Curr. Top. Med. Chem. 3: 899 (2003)); and Tourette's syndrome (Sacco et al., J. Psychopharmacol. 18(4): 457 (2004), Young et al., Clin. Ther. 23(4): 532 (2001)).
  • nAChR subtypes there exists a heterogeneous distribution of nAChR subtypes in both the central and peripheral nervous systems.
  • the ⁇ 4 ⁇ 2, 6 containing, ⁇ 7, and ⁇ 3 ⁇ 2 subtypes are predominant in vertebrate brain, whereas the ⁇ 3 ⁇ 4 subtype is predominate at the autonomic ganglia, and the ⁇ and ⁇ subtypes are predominant at the neuromuscular junction (see Dwoskin et al., Exp. Opin. Ther. Patents 10: 1561 (2000) and Holliday et al. J. Med. Chem. 40(26), 4169 (1997)).
  • Compounds which selectively target the CNS predominant subtypes have potential utility in treating various CNS disorders.
  • nicotinic compounds lack the selectivity required to preferentially target CNS receptors over receptor located in the muscle and ganglion. Such drugs are often associated with various undesirable side effects. Therefore, there is a need to have compounds, compositions, and methods for preventing or treating various conditions or disorders where the compounds exhibit a high enough degree of nAChR subtype specificity to elicit a beneficial effect, without significantly affecting those receptor subtypes which have the potential to induce undesirable side effects, including, for example, appreciable activity at cardiovascular and skeletal muscle sites.
  • the present invention includes compounds which bind with high affinity to NNRs of either the ⁇ 4 ⁇ 2 subtype, or the a6-containing subtype, or both NNR subtypes.
  • the present invention also relates to pharmaceutically acceptable salts prepared from these compounds.
  • the present invention includes pharmaceutical compositions comprising a compound of the present invention or a pharmaceutically acceptable salt thereof.
  • the pharmaceutical compositions of the present invention can be used for treating or preventing a wide variety of conditions or disorders, particularly those disorders mediated by nicotinic acetylcholine receptors.
  • the present invention includes a method for treating, preventing, delaying the onset of, or slowing the progression of disorders mediated by nicotinic acetylcholine receptors, in mammals in need of such treatment.
  • the methods involve administering to a subject a therapeutically effective amount of a compound of the present invention, including a salt thereof, or a pharmaceutical composition that includes such compounds.
  • Figure 1 illustrates a dose effect curve of Compound A (3- cyclopropylcarbonyl-3,6-diazabicyclo[3.1.1], as the heptane di-p-toluoyl-D- tartrate salt) and nicotine on TH positive neurons after 48h pretreatment, followed by MPP + injury (4 ⁇ , 48h).
  • Compound A 3- cyclopropylcarbonyl-3,6-diazabicyclo[3.1.1], as the heptane di-p-toluoyl-D- tartrate salt
  • Figure 2 illustrates a dose effect curve of Compound A (3- cyclopropylcarbonyl-3,6-diazabicyclo[3.1.1], as the heptane di-p-toluoyl-D- tartrate salt) and nicotine on total TH neurite length after 48h pretreatment, followed by MPP + injury (4 ⁇ , 48h).
  • Compound A 3- cyclopropylcarbonyl-3,6-diazabicyclo[3.1.1], as the heptane di-p-toluoyl-D- tartrate salt
  • Figure 3 illustrates a dose effect curve of Compound B (3- ethylcarbonyl-3,6-diazabicyclo[3.1.1], as the heptane di-p-toluoyl-D-tartrate salt) and nicotine on TH positive neurons after 48h pretreatment, followed by MPP + injury (4 ⁇ , 48h).
  • Figure 4 illustrates a dose effect curve of Compound B (3- ethylcarbonyl-3,6-diazabicyclo[3.1.1], as the heptane di-p-toluoyl-D-tartrate salt) and nicotine on total TH neurite length after 48h pretreatment, followed by MPP + injury (4 ⁇ , 48h).
  • Figure 5 illustrates a dose effect curve of BDNF (50 ng/ml) and nicotine (10nM) on TH positive neurons after 48h pretreatment, followed by MPP + injury (4 ⁇ , 48h).
  • Figure 6 illustrates a dose effect curve of BDNF (50 ng/ml) and nicotine (10nM) on total TH neurite length after 48h pretreatment, followed by MPP + injury (4 ⁇ , 48h).
  • the present invention includes compounds of Formula I:
  • each m is identical and is 0 or 1 ;
  • each n is identical and is 0 or 1 ;
  • each n is 1 ;
  • each n is 0;
  • q is 1 , 2, 3, 4, 5, or 6;
  • X is -0-, -S-, -NH-, or -NHC(O)-;
  • R 2 is H or alkyl
  • R 3 is alkyl, alkenyl, alkynyl, cycloalkyi, cycloalkenyl, cycloalkynyl, aryl, heteroaryl, or heterocyclic;
  • each R 3 individually may be optionally substituted with one or more alkyl, alkenyl, alkynyl, aryl, aryloxy, amino, amido, heteroaryl, halogen, hydroxyl, alkoxy, cycloalkyi, cycloalkenyl, cycloalkynyl, heterocyclic, or alkylamido substituents;
  • the present invention includes compounds of Formula I:
  • each m is identical and is 0 or 1 ;
  • each n is identical and is 0 or 1 ;
  • each n is 1 ;
  • each n is 0;
  • q is 1 , 2, 3, 4, 5, or 6;
  • X is -0-, -S-, -NH-, or -NHC(O)-;
  • R 2 is H or alkyl
  • R 3A is methyl, propyl, butyl, pentyi, hexyl, alkenyl, alkynyl, cycloalkyi, cycloalkenyl, cycloalkynyl, aryl, heteroaryl, or heterocyclic;
  • R 3A is methyl, ethyl, propyl, butyl, pentyi, hexyl, alkenyl, alkynyl, cycloalkyi, cycloalkenyl, cycloalkynyl, aryl, heteroaryl, or heterocyclic;
  • R 3B is methyl, ethyl, propyl, n-butyl, isobutyl, sec-butyl, pentyi, hexyl, alkenyl, alkynyl, cycloalkyi, cycloalkenyl, cycloalkynyl, aryl, heteroaryl, or heterocyclic; when R 2 is H and each m is 1 and each n is 0, or when R 2 is alkyl, then R 3B is methyl, ethyl, propyl, butyl, pentyi, hexyl, alkenyl, alkynyl, cycloalkyi, cycloalkenyl, cycloalkynyl, aryl, heteroaryl, or heterocyclic; each R 3C individually is alkyl, alkenyl, alkynyl, cycloalkyi, cycloal
  • each R 3 individually may be optionally substituted with one or more alkyl, alkenyl, alkynyl, aryl, aryloxy, amino, amido, heteroaryl, halogen, hydroxyl, alkoxy, cycloalkyi, cycloalkenyl, cycloalkynyl, heterocyclic, or alkylamido substituents;
  • a compound is selected from the group consisting of:
  • the present invention is compound, 3- cyclopropylcarbonyl-3,6-diazabicyclo[3.1.1]heptane, Compound A, or a pharmaceutically acceptable salt thereof.
  • One aspect of the present invention includes a pharmaceutical composition comprising a compound of the present invention and a pharmaceutically acceptable carrier.
  • One aspect of the present invention includes a method for the treatment or prevention of a disease or condition mediated by neuronal nicotinic receptors comprising the administration of a compound of the present invention.
  • the neuronal nicotinic receptors are of the ⁇ 4 ⁇ 2 subtype.
  • the neuronal nicotinic receptors are of the a6-containing subtype.
  • the neuronal nicotinic receptors are a combination of the ⁇ 4 ⁇ 2 and a6-containing subtypes.
  • One aspect of the present invention includes use of a compound of the present invention for the preparation of a medicament for the treatment or prevention of a disease or condition mediated by neuronal nicotinic receptors comprising the administration of a compound of the present invention.
  • the neuronal nicotinic receptors are of the ⁇ 4 ⁇ 2 subtype.
  • the neuronal nicotinic receptors are of the a6-containing subtype.
  • the neuronal nicotinic receptors are a combination of the ⁇ 4 ⁇ 2 and a6-containing subtypes.
  • One aspect of the present invention includes a compound of the present invention for use as an active therapeutic substance.
  • One aspect thus, includes a compound of the present invention for use in the treatment or prevention of a disease or condition mediated by neuronal nicotinic receptors comprising the administration of a compound of the present invention.
  • the neuronal nicotinic receptors are of the ⁇ 4 ⁇ 2 subtype.
  • the neuronal nicotinic receptors are of the a6-containing subtype.
  • the neuronal nicotinic receptors are a combination of the ⁇ 4 ⁇ 2 and ⁇ -containing subtypes.
  • C x . y alkyl refers to an alkyl group, as herein defined, containing the . specified number of carbon atoms. Similar terminology will apply for other preferred terms and ranges as well.
  • C -6 alkyl represents a straight or branched chain hydrocarbon containing one to six carbon atoms.
  • alkyl refers to a straight or branched chain hydrocarbon, which may be optionally substituted, with multiple degrees of substitution being allowed.
  • alkyl as used herein include, but are not limited to, methyl, ethyl, propyl, isopropyl, isobutyl, n-butyl, tert-butyl, isopentyl, and n-pentyl.
  • cycloalkyl refers to a fully saturated optionally substituted monocyclic, bicyclic, or bridged hydrocarbon ring, with multiple degrees of substitution being allowed.
  • exemplary "cycloalkyl” groups as used herein include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and cycloheptyl.
  • heterocycle refers to an optionally substituted mono- or polycyclic ring system, optionally containing one or more degrees of unsaturation, and also containing one or more heteroatoms, which may be optionally substituted, with multiple degrees of substitution being allowed.
  • exemplary heteroatoms include nitrogen, oxygen, or sulfur atoms, including N-oxides, sulfur oxides, and dioxides.
  • the ring is three to twelve-membered, preferably three- to eight-membered and is either fully saturated or has one or more degrees of unsaturation.
  • Such rings may be optionally fused to one or more of another heterocyclic ring(s) or cycloalkyl rtng(s).
  • heterocyclic groups as used herein include, but are not limited to, tetrahydrofuran, pyran, tetrahydropyran, 1 ,4- dioxane, 1 ,3-dioxane, piperidine, pyrrolidine, morpholine, tetrahydrothiopyran, and tetrahydrothiophene.
  • aryl refers to a single benzene ring or fused benzene ring system which may be optionally substituted, with multiple degrees of substitution being allowed.
  • aryl groups as used include, but are not limited to, phenyl, 2-naphthyl, 1-naphthyl, anthracene, and phenanthrene.
  • Preferable aryl rings have five- to ten-members.
  • a fused benzene ring system encompassed within the term "aryl” includes fused polycyclic hydrocarbons, namely where a cyclic hydrocarbon with less than maximum number of noncumulative double bonds, for example where a saturated hydrocarbon ring (cycloalkyl, such as a cyclopentyl ring) is fused with an aromatic ring (aryl, such as a benzene ring) to form, for example, groups such as indanyl and acenaphthalenyl, and also includes such groups as, for non-limiting examples, dihydronaphthalene and tetrahydronaphthalene.
  • aryl fused polycyclic hydrocarbons, namely where a cyclic hydrocarbon with less than maximum number of noncumulative double bonds, for example where a saturated hydrocarbon ring (cycloalkyl, such as a cyclopentyl ring) is fused with an aromatic ring (aryl, such as a benzene ring) to form
  • heteroaryl refers to a monocyclic five to seven membered aromatic ring, or to a fused bicyclic aromatic ring system comprising two of such aromatic rings, which may be optionally substituted, with multiple degrees of substitution being allowed. Preferably, such rings contain five- to ten-members. These heteroaryl rings contain one or more nitrogen, sulfur, and/or oxygen atoms, where N-oxides, sulfur oxides, and dioxides are permissible heteroatom substitutions.
  • heteroaryl groups as used herein include, but are not limited to, furan, thiophene, pyrrole, imidazole, pyrazole, triazole, tetrazole, thiazole, oxazole, isoxazole, oxadiazole, thiadiazole, isothiazole, pyridine, pyridazine, pyrazine, pyrimidine, quinoline, isoquinoline, quinoxaline, benzofuran, benzoxazole,
  • Cy may be pyridinyl which may be substituted first by a halogen, such as F, and second by an alkoxy, such as -OCH 3 .
  • halogen refers to fluorine, chlorine, bromine, or iodine.
  • haloalkyl refers to an alkyl group, as defined herein, which is substituted with at least one halogen.
  • branched or straight chained “haloalkyl” groups as used herein include, but are not limited to, methyl, ethyl, propyl, isopropyl, n-butyl, and t-butyl substituted independently with one or more halogens, for example, fluoro, chloro, bromo, and iodo.
  • haloalkyl should be interpreted to include such substituents as perfluoroalkyl groups such as -CF 3 .
  • alkoxy refers to a group -OR a , where R a is alkyl as herein defined.
  • alkylthio refers to a group -SR a , where R a is alkyl as herein defined.
  • aryloxy refers to a group -OR a , where R a is aryl as herein defined.
  • arylthio refers to a group -SR a , where R a is aryl as herein defined.
  • amino refers to a group -NR a R b , where each of R a and R b is hydrogen. Additionally, “substituted amino” refers to a group -NR a R wherein each of R a and R b individually is alkyl, alkenyl, alkynyl, cycloalkyi, aryl, heterocylcyl, or heteroaryl. As used herein, when either R a or R b is other than hydrogen, such a group may be referred to as a “substituted amino" or, for example if R a is H and R b is alkyl, as an "alkylamino.”
  • the term "pharmaceutically acceptable” refers to carrier(s), diluent(s), excipient(s) or salt forms of the compounds of the present invention that are compatible with the other ingredients of the formulation and not deleterious to the recipient of the pharmaceutical composition.
  • composition refers to a compound of the present invention optionally admixed with one or more pharmaceutically acceptable carriers, diluents, or exipients.
  • Pharmaceutical compositions preferably exhibit a degree of stability to environmental conditions so as to make them suitable for manufacturing and
  • the terms "effective amount”, “therapeutic amount”, and “effective dose” refer to an amount of the compound of the present invention sufficient to elicit the desired pharmacological or therapeutic effects, thus resulting in an effective treatment of a disorder.
  • Treatment of a disorder may be manifested by delaying or preventing the onset or progression of the disorder, as well as the onset or progression of symptoms associated with the disorder.
  • Treatment of a disorder may also be manifested by a decrease or elimination of symptoms, reversal of the progression of the disorder, as well as any other contribution to the well being of the patient.
  • the effective dose can vary, depending upon factors such as the condition of the patient, the severity of the symptoms of the disorder, and the manner in which the pharmaceutical composition is administered.
  • compounds may be administered in an amount of less than 5 mg/kg of patient weight.
  • the compounds may be administered in an amount from less than about 1 mg/kg patient weight to less than about 100 ⁇ g/kg of patient weight, and further between about 1 pg/kg to less than 100 pg/kg of patient weight.
  • the foregoing effective doses typically represent that amount that may be administered as a single dose, or as one or more doses that may be administered over a 24 hours period.
  • the compounds of this invention may be made by a variety of methods, including well-established synthetic methods. Illustrative general synthetic methods are set out below and then specific compounds of the invention are prepared in the working Examples.
  • protecting groups for sensitive or reactive groups are employed where necessary in accordance with general principles of synthetic chemistry.
  • Protecting groups are manipulated according to standard methods of organic synthesis (T. W. Green and P. G. M. Wuts (1999) Protecting Groups in Organic Synthesis, 3 rd Edition, John Wiley & Sons, herein incorporated by reference with regard to protecting groups). These groups are removed at a convenient stage of the compound synthesis using methods that are readily apparent to those skilled in the art. The selection of processes as well as the reaction conditions and order of their execution shall be consistent with the preparation of compounds of the present invention.
  • the present invention also provides a method for the synthesis of compounds useful as intermediates in the preparation of compounds of the present invention along with methods for their preparation.
  • the compounds can be prepared according to the methods described below using readily available starting materials and reagents. In these reactions, variants may be employed which are themselves known to those of ordinary skill in this art but are not described in detail here.
  • structures depicted herein are also meant to include compounds which differ only in the presence of one or more isotopically enriched atoms.
  • Compounds having the present structure except for the replacement of a hydrogen atom by a deuterium or tritium, or the replacement of a carbon atom by a 3 C- or 14 C-enriched carbon are within the scope of the invention.
  • deuterium has been widely used to examine the pharmacokinetics and metabolism of biologically active compounds. Although deuterium behaves similarly to hydrogen from a chemical perspective, there are significant differences in bond energies and bond lengths between a deuterium-carbon bond and a hydrogen-carbon bond.
  • the compounds of the present invention may crystallize in more than one form, a characteristic known as polymorphism, and such polymorphic forms (“polymorphs”) are within the scope of the present invention.
  • Polymorphism generally can occur as a response to changes in temperature, pressure, or both. Polymorphism can also result from variations in the crystallization process. Polymorphs can be distinguished by various physical characteristics known in the art such as x-ray diffraction patterns, solubility, and melting point.
  • Certain of the compounds described herein contain one or more chiral centers, or may otherwise be capable of existing as multiple stereoisomers.
  • the scope of the present invention includes mixtures of stereoisomers as well as purified enantiomers or enantiomerically/diastereomerically enriched mixtures. Also included within the scope of the invention are the individual isomers of the compounds represented by the formulae of the present invention, as well as any wholly or partially equilibrated mixtures thereof.
  • the present invention also includes the individual isomers of the compounds represented by the formulas above as mixtures with isomers thereof in which one or more chiral centers are inverted.
  • a compound When a compound is desired as a single enantiomer, such may be obtained by stereospecific synthesis, by resolution of the final product or any convenient intermediate, or by chiral chromatographic methods as are known in the art. Resolution of the final product, an intermediate, or a starting material may be effected by any suitable method known in the art. See, for example, Stereochemistry of Organic Compounds (Wiley-lnterscience, 1994).
  • the present invention includes a salt or solvate of the compounds herein described, including combinations thereof such as a solvate of a salt.
  • the compounds of the present invention may exist in solvated, for example hydrated, as well as unsolvated forms, and the present invention
  • the salts of the present invention are pharmaceutically acceptable salts. Salts encompassed within the term
  • “pharmaceutically acceptable salts” refer to non-toxic salts of the compounds of this invention.
  • suitable pharmaceutically acceptable salts include inorganic acid addition salts such as chloride, bromide, sulfate, phosphate, and nitrate; organic acid addition salts such as acetate, galactarate, propionate, succinate, lactate, glycolate, malate, tartrate, citrate, maleate, fumarate, methanesulfonate, p-toluenesulfonate, and ascorbate; salts with acidic amino acid such as aspartate and glutamate; alkali metal salts such as sodium salt and potassium salt; alkaline earth metal salts such as magnesium salt and calcium salt; ammonium salt; organic basic salts such as trimethylamine salt, triethylamine salt, pyridine salt, picoline salt, dicyclohexylamine salt, and ⁇ , ⁇ '-dibenzylethylenediamine salt; and salts with basic amino acid such
  • the compounds of the present invention can be prepared via the coupling of a mono-protected [3.1.1]heptyl-diazabicycle, namely one in which one of the two amine functional groups is rendered un-reactive by suitable derivatization, with a suitably activated carboxylic acid, chloroformate, or isothionate derivative (Scheme 1).
  • One means of making amides of the present invention is to couple a suitable mono N-protected-3,6-diazabicyclo[3.1.1]heptane with a suitably functionalized carboxylic acid, followed by removal of any protecting groups.
  • carboxylic acids are commercially available.
  • the condensation of an amine and a carboxylic acid, to produce an amide typically requires the use of a suitable activating agent, such as ⁇ , ⁇ '- dicyclohexylcarbodiimide (DCC), (benzotriazol-1- yloxy)tris(dimethylamino)phosphonium hexafluorophosphate (BOP),
  • amides of the present invention can be prepared by coupling a mono-protected diazabicycle with a suitably functionalized acid chloride, which may be available commercially or may be prepared by conversion of the suitably functionalized carboxylic acid.
  • the acid chloride may be prepared by treatment of the appropriate carboxylic acid with, among other reagents, thionyl chloride or oxalyl chloride.
  • carbamates of the present invention can be prepared by coupling a suitable functionalized alkyl- , aryl-, or heteroaryl-chloroformate with a suitable mono N-protected-3,6- diazabicyclo[3.1.1]heptane, followed by removal of any protecting groups.
  • a suitable mono N-protected-3,6-diazabicyclo[3.1.1]heptane can be coupled with a suitable functionalized alkyl-, aryl-, or heteroaryl-isocyanate, followed by removal of any protecting groups, to prepare ureas of the present invention.
  • the present invention includes pharmaceutical compositions comprising one or more compounds of Formula I and/or pharmaceutically acceptable salts thereof and one or more pharmaceutically acceptable carriers, diluents, or excipients.
  • Another aspect of the invention provides a process for the preparation of a pharmaceutical composition including admixing one or more compounds of Formula I and/or pharmaceutically acceptable salts thereof with one or more pharmaceutically acceptable carriers, diluents or excipients.
  • the manner in which the compound of the present invention is administered can vary.
  • the compound of the present invention is preferably administered orally.
  • Preferred pharmaceutical compositions for oral administration include tablets, capsules, caplets, syrups, solutions, and suspensions.
  • the pharmaceutical compositions of the present invention may be provided in modified release dosage forms such as time-release tablet and capsule formulations.
  • compositions can also be administered via injection, namely, intravenously, intramuscularly, subcutaneously, intraperitoneally, intraarterially, intrathecally, and intracerebroventricularly.
  • Intravenous administration is a preferred method of injection.
  • Suitable carriers for injection are well known to those of skill in the art and include 5% dextrose solutions, saline, and phosphate buffered saline.
  • the formulations may also be administered using other means, for example, rectal administration.
  • Formulations useful for rectal administration such as suppositories, are well known to those of skill in the art.
  • the compounds can also be administered by inhalation, for example, in the form of an aerosol; topically, such as, in lotion form; transdermally, such as, using a transdermal patch (for example, by using technology that is commercially available from Novartis and Alza Corporation); by powder injection; or by buccal, sublingual, or intranasal absorption.
  • intranasal delivery or “nasal delivery” as used herein means a method for drug absorption through and within the nose.
  • bonal delivery as used herein means a method for presenting the drug for absorption through the buccal, including inner cheek, tissue.
  • sublingual delivery means delivery of the active agent under the tongue.
  • Drugs can be absorbed through mucosal surfaces, such as those in the nasal passage and in the oral cavity. Drug delivery via mucosal surfaces can be efficient because they lack the stratum corneum of the epidermis, a major barrier to absorption across the skin. Mucosal surfaces are also typically rich in blood supply, which can rapidly transport drugs systemically while avoiding significant degradation by first-pass hepatic metabolism.
  • oral transmucosal absorption is generally rapid because of the rich vascular supply to the mucosa and the lack of a stratum corneum in the epidermis.
  • Such drug transport typically provides a rapid rise in blood concentrations, and similarly avoids the enterohepatic circulation and immediate destruction by gastric acid or partial first-pass effects of gut wall and hepatic metabolism.
  • Drugs typically need to have prolonged exposure to an oral mucosal surface for significant drug absorption to occur. Factors affecting drug delivery include taste, which can affect contact time, and drug ionization.
  • Drug absorption is generally greater from the buccal or oral mucosa than from the tongue and gingiva.
  • One limitation associated with buccal drug delivery is low flux, which often results in low drug bioavailability. Low flux may be somewhat offset by using buccal penetration enhancers, as are known in the art, to increase the flux of drugs through the mucosa.
  • the intranasal, buccal, and sublingual routes can be preferred for use in treating patients who have difficulty in swallowing tablets, capsules, or other oral solids, or those who have disease-compromised intestinal absorption.
  • compositions may be formulated in unit dose form, or in multiple or subunit doses.
  • the administration of the pharmaceutical compositions described herein can be intermittent, or at a gradual, continuous, constant or controlled rate.
  • the pharmaceutical compositions may be administered to a warmblooded animal, for example, a mammal such as a mouse, rat, cat, rabbit, dog, pig, cow, or monkey; but advantageously is administered to a human being.
  • a warmblooded animal for example, a mammal such as a mouse, rat, cat, rabbit, dog, pig, cow, or monkey; but advantageously is administered to a human being.
  • the time of day and the number of times per day that the pharmaceutical composition is administered can vary.
  • the compounds of the present invention may be used in the treatment of a variety of disorders and conditions and, as such, may be used in combination with a variety of other suitable therapeutic agents useful in the treatment or prophylaxis of those disorders or conditions.
  • one embodiment of the present invention includes the administration of the compound of the present invention in combination with other therapeutic compounds.
  • the compound of the present invention can be used in combination with other NNR ligands (such as varenicline), allosteric modulators of NNRs, antioxidants (such as free radical scavenging agents), antibacterial agents (such as penicillin antibiotics), antiviral agents (such as nucleoside analogs, like zidovudine and acyclovir), anticoagulants (such as warfarin), anti-inflammatory agents (such as NSAIDs), anti-pyretics, analgesics, anesthetics (such as used in surgery), acetylcholinesterase inhibitors (such as donepezil and galantamine), antipsychotics (such as haloperidol, clozapine, olanzapine, and quetiapine), immuno-suppressants (such as cyclosporin and methotrexate), neuroprotective agents, steroids (such as steroid hormones), corticosteroids (such as dexamethasone, predisone, and hydrocor
  • Such a combination of pharmaceutically active agents may be administered together or separately and, when administered separately, administration may occur simultaneously or sequentially, in any order.
  • the amounts of the compounds or agents and the relative timings of administration will be selected in order to achieve the desired therapeutic effect.
  • the administration in combination of a compound of the present invention with other treatment agents may be in combination by
  • administration concomitantly in: (1) a unitary pharmaceutical composition including both compounds; or (2) separate pharmaceutical compositions each including one of the compounds.
  • the combination may be administered separately in a sequential manner wherein one treatment agent is administered first and the other second. Such sequential administration may be close in time or remote in time.
  • Another aspect of the present invention includes combination therapy comprising administering to the subject a therapeutically or prophylactically effective amount of the compound of the present invention and one or more other therapy including chemotherapy, radiation therapy, gene therapy, or immunotherapy.
  • the compounds of the present invention can be used for the prevention or treatment of various conditions or disorders for which other types of nicotinic compounds have been proposed or are shown to be useful as therapeutics, such as CNS disorders, inflammation, inflammatory response associated with bacterial and/or viral infection, pain, diabetes, metabolic syndrome, autoimmune disorders, dermatological conditions, addictions, obesity or other disorders described in further detail herein.
  • This compound can also be used as a diagnostic agent in receptor binding studies (in vitro and in vivo).
  • Such therapeutic and other teachings are described, for example, in references previously listed herein, including Williams et al., Drug News Perspec. 7(4): 205 (1994), Arneric et al., CNS Drug Rev.
  • the compounds and their pharmaceutical compositions are useful in the treatment or prevention of a variety of CNS disorders, including neurodegenerative disorders, neuropsychiatric disorders, neurologic disorders, and addictions.
  • the compounds and their pharmaceutical compositions can be used to treat or prevent cognitive deficits and dysfunctions, age-related and otherwise; attentional disorders and dementias, including those due to infectious agents or metabolic disturbances; to provide neuroprotection; to treat convulsions and multiple cerebral infarcts; to treat mood disorders, compulsions and addictive behaviors; to provide analgesia; to control inflammation, such as mediated by cytokines and nuclear factor kappa B; to treat inflammatory disorders; to provide pain relief; and to treat infections, as anti-infectious agents for treating bacterial, fungal, and viral infections.
  • AAMI age-associated memory impairment
  • MCI mild cognitive impairment
  • ARCD age-related cognitive decline
  • pre-senile dementia early onset Alzheimer's disease
  • senile dementia dementia of the Alzheimer's type
  • Alzheimer's disease cognitive impairment no dementia
  • CIND Lewy body dementia
  • HIV-dementia HIV-dementia
  • AIDS dementia complex vascular dementia
  • Down syndrome head trauma
  • TBI traumatic brain injury
  • dementia pugilistica Creutzfeld-Jacob Disease and prion diseases
  • stroke central ischemia, peripheral ischemia, attention deficit disorder, attention deficit hyperactivity disorder, dyslexia, schizophrenia,
  • schizophreniform disorder schizoaffective disorder, cognitive dysfunction in schizophrenia, cognitive deficits in schizophrenia, Parkinsonism including Parkinson's disease, postencephalitic parkinsonism, parkinsonism-dementia of Gaum, frontotemporal dementia Parkinson's Type (FTDP), Pick's disease, Niemann-Pick's Disease, Huntington's Disease, Huntington's chorea, dyskinesias, L-dopa induced dyskinesia, tardive dyskinesia, spastic dystonia, hyperkinesia, progressive supranuclear palsy, progressive supranuclear paresis, restless leg syndrome, Creutzfeld-Jakob disease, multiple sclerosis, amyotrophic lateral sclerosis (ALS), motor neuron diseases (MND), multiple system atrophy (MSA), corticobasal degeneration, Guillain-Barre Syndrome (GBS), and chronic inflammatory demyelinating polyneuropathy (CIDP), epilepsy, autosomal
  • Cognitive impairments or dysfunctions may be associated with psychiatric disorders or conditions, such as schizophrenia and other psychotic disorders, including but not limited to psychotic disorder, schizophreniform disorder, schizoaffective disorder, delusional disorder, brief psychotic disorder, shared psychotic disorder, and psychotic disorders due to a general medical conditions, dementias and other cognitive disorders, including but not limited to mild cognitive impairment, pre-senile dementia, Alzheimer's disease, senile dementia, dementia of the Alzheimer's type, age-related memory impairment, Lewy body dementia, vascular dementia, AIDS dementia complex, dyslexia, Parkinsonism including Parkinson's disease, cognitive impairment and dementia of Parkinson's Disease, cognitive impairment of multiple sclerosis, cognitive impairment caused by traumatic brain injury, dementias due to other general medical conditions, anxiety disorders, including but not limited to panic disorder without agoraphobia, panic disorder with agoraphobia, agoraphobia without history of panic disorder, specific phobia, social phobia, obsessive-compulsive disorder, posttraumatic stress disorder, acute stress
  • Cognitive performance may be assessed with a validated cognitive scale, such as, for example, the cognitive subscale of the Alzheimer's Disease Assessment Scale (ADAS-cog).
  • ADAS-cog Alzheimer's Disease Assessment Scale
  • One measure of the effectiveness of the compounds of the present invention in improving cognition may include measuring a patient's degree of change according to such a scale.
  • the compounds of the present invention may be used as a therapy for nicotine addiction and for other brain-reward disorders, such as substance abuse including alcohol addiction, illicit and prescription drug addiction, eating disorders, including obesity, and behavioral addictions, such as gambling, or other similar behavioral manifestations of addiction.
  • substance abuse including alcohol addiction, illicit and prescription drug addiction
  • eating disorders including obesity
  • behavioral addictions such as gambling, or other similar behavioral manifestations of addiction.
  • the treatment or prevention of diseases, disorders and conditions occurs without appreciable adverse side effects, including, for example, significant increases in blood pressure and heart rate, significant negative effects upon the gastro-intestinal tract, and significant effects upon skeletal muscle.
  • the compounds of the present invention when employed in effective amounts, are believed to modulate the activity of the ⁇ 4 ⁇ 2 and/or a6- containing NNRs without appreciable interaction with the nicotinic subtypes that characterize the human ganglia, as demonstrated by a lack of the ability to elicit nicotinic function in adrenal chromaffin tissue, or skeletal muscle, further demonstrated by a lack of the ability to elicit nicotinic function in cell preparations expressing muscle-type nicotinic receptors.
  • these compounds are believed capable of treating or preventing diseases, disorders and conditions without eliciting significant side effects associated activity at ganglionic and neuromuscular sites.
  • administering is believed to provide a therapeutic window in which treatment of certain diseases, disorders and conditions is provided, and certain side effects are avoided. That is, an effective dose of the compound is believed sufficient to provide the desired effects upon the disease, disorder or condition, but is believed insufficient, namely is not at a high enough level, to provide undesirable side effects.
  • the present invention provides the use of a compound of the present invention, or a pharmaceutically acceptable salt thereof, for use in therapy, such as a therapy described above.
  • the present invention provides the use of a compound of the present invention, or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for use in the treatment of a CNS disorder, such as a disorder, disease or condition described
  • the nervous system primarily through the vagus nerve, is known to regulate the magnitude of the innate immune response by inhibiting the release of macrophage tumor necrosis factor (TNF).
  • TNF macrophage tumor necrosis factor
  • This physiological mechanism is known as the "cholinergic anti-inflammatory pathway" (see, for example, Tracey, "The Inflammatory Reflex,” Nature 420: 853-9 (2002)).
  • Excessive inflammation and tumor necrosis factor synthesis cause morbidity and even mortality in a variety of diseases. These diseases include, but are not limited to, endotoxemia, rheumatoid arthritis, osteoarthritis, psoriasis, asthma, atherosclerosis, idiopathic pulmonary fibrosis, and inflammatory bowel disease.
  • Inflammatory conditions that can be treated or prevented by administering the compounds described herein include, but are not limited to, chronic and acute inflammation, psoriasis, endotoxemia, gout, acute pseudogout, acute gouty arthritis, arthritis, rheumatoid arthritis, osteoarthritis, allograft rejection, chronic transplant rejection, asthma, atherosclerosis, mononuclear-phagocyte dependent lung injury, idiopathic pulmonary fibrosis, atopic dermatitis, chronic obstructive pulmonary disease, adult respiratory distress syndrome, acute chest syndrome in sickle cell disease, inflammatory bowel disease, irritable bowel syndrome, Crohn's disease, ulcers, ulcerative colitis, acute cholangitis, aphthous stomatitis, cachexia, pouchitis, glomerulonephritis, lupus nephritis, thrombosis, and graft vs. host reaction. Inflammatory Response Associated with Bacterial
  • bacterial and/or viral infections are associated with side effects brought on by the formation of toxins, and the body's natural response to the bacteria or virus and/or the toxins.
  • the body's response to infection often involves generating a significant amount of TNF and/or other cytokines.
  • the over-expression of these cytokines can result in significant injury, such as septic shock (when the bacteria is sepsis), endotoxic shock, urosepsis, viral pneumonitis and toxic shock syndrome.
  • Cytokine expression is mediated by NNRs, and can be inhibited by administering agonists or partial agonists of these receptors.
  • Those compounds described herein that are agonists or partial agonists of these receptors can therefore be used to minimize the inflammatory response associated with bacterial infection, as well as viral and fungal infections.
  • bacterial infections examples include anthrax, botulism, and sepsis. Some of these compounds may also have antimicrobial properties.
  • Antitoxins can also be used to bind to toxins produced by the infectious agents and allow the bound toxins to pass through the body without generating an inflammatory response. Examples of antitoxins are disclosed, for example, in U.S. Patent No. 6,310,043 to Bundle et al. Other agents effective against bacterial and other toxins can be effective and their therapeutic effect can be
  • the compounds can be administered to treat and/or prevent pain, including acute, neurologic, inflammatory, neuropathic and chronic pain.
  • the compounds can be used in conjunction with opiates to minimize the likelihood of opiate addiction (e.g., morphine sparing therapy).
  • opiate addiction e.g., morphine sparing therapy.
  • the analgesic activity of compounds described herein can be demonstrated in models of persistent inflammatory pain and of neuropathic pain, performed as described in U.S. Published Patent Application No. 20010056084 A1 (Allgeier et al.) (e.g., mechanical hyperalgesia in the complete Freund's adjuvant rat model of inflammatory pain and mechanical hyperalgesia in the mouse partial sciatic nerve ligation model of neuropathic pain).
  • the analgesic effect is suitable for treating pain of various genesis or etiology, in particular in treating inflammatory pain and associated hyperalgesia, neuropathic pain and associated hyperalgesia, chronic pain (e.g., severe chronic pain, post-operative pain and pain associated with various conditions including cancer, angina, renal or biliary colic,
  • Inflammatory pain may be of diverse genesis, including arthritis and rheumatoid disease, teno-synovitis and vasculitis.
  • Neuropathic pain includes trigeminal or herpetic neuralgia, neuropathies such as diabetic neuropathy pain, causalgia, low back pain and deafferentation syndromes such as brachial plexus avulsion.
  • the compounds of the present invention can be also used to prevent or treat certain other conditions, diseases, and disorders in which NNRs play a role.
  • autoimmune disorders such as lupus, disorders associated with cytokine release, cachexia secondary to infection (e.g., as occurs in AIDS, AIDS related complex and neoplasia), obesity, pemphitis, urinary incontinence, overactive bladder, diarrhea, constipation, retinal diseases, infectious diseases, myasthenia, Eaton- Lambert syndrome, hypertension, preeclampsia, osteoporosis,
  • the compounds of this invention can also be administered to treat convulsions such as those that are symptomatic of epilepsy, and to treat conditions such as syphillis and Creutzfeld-Jakob disease.
  • the compounds of this invention may be used to treat a variety of dermatological disorders, including but not limited to psoriasis, dermatitis, acne, pustulosis, vitilago, and the like. Diagnostic Uses
  • the compounds can be used in diagnostic compositions, such as probes, particularly when they are modified to include appropriate labels.
  • the probes can be used, for example, to determine the relative number and/or function of specific receptors, particularly the ⁇ 4 ⁇ 2 and/or a6-containing receptor subtypes.
  • the compounds of the present invention most preferably are labeled with a radioactive isotopic moiety such as 11 C, 18 F, 76 Br, 123 l or 25 l.
  • the administered compounds can be detected using known detection methods appropriate for the label used. Examples of detection methods include position emission topography (PET) and single-photon emission computed tomography (SPECT).
  • PET position emission topography
  • SPECT single-photon emission computed tomography
  • the radiolabels described above are useful in PET (e.g., 11 C, 18 F or 76 Br) and SPECT (e.g., 123 l) imaging, with half-lives of about 20.4 minutes for 11 C, about 109 minutes for 18 F, about 13 hours for 123 l, and about 16 hours for 76 Br.
  • a high specific activity is desired to visualize the selected receptor subtypes at non-saturating concentrations.
  • the administered doses typically are below the toxic range and provide high contrast images.
  • the compounds are expected to be capable of
  • the compounds can be administered using known techniques. See, for example, U.S. Patent No. 5,969,144 to London et al., as noted.
  • the compounds can be administered in formulation compositions that incorporate other ingredients, such as those types of ingredients that are useful in formulating a diagnostic composition.
  • Compounds useful in accordance with carrying out the present invention most preferably are employed in forms of high purity. See, U.S. Patent No. 5,853,696 to Elmalch et al.
  • the compounds are administered to a subject (e.g., a human subject), the presence of that compound within the subject can be imaged and quantified by appropriate techniques in order to indicate the presence, quantity, and functionality of selected NNR subtypes.
  • a subject e.g., a human subject
  • the compounds can also be administered to animals, such as mice, rats, dogs, and monkeys.
  • SPECT and PET imaging can be carried out using any appropriate technique and apparatus. See Villemagne et al., In: Arneric et al. (Eds.) Neuronal Nicotinic Receptors: Pharmacology and Therapeutic
  • the radiolabeled compounds bind with high affinity to selective NNR subtypes (e.g., ⁇ 4 ⁇ 2 and/or ⁇ -containing) and preferably exhibit negligible non-specific binding to other nicotinic cholinergic receptor subtypes (e.g., those receptor subtypes associated with muscle and ganglia).
  • the compounds can be used as agents for noninvasive imaging of nicotinic cholinergic receptor subtypes within the body of a subject, particularly within the brain for diagnosis associated with a variety of CNS diseases and disorders.
  • the diagnostic compositions can be used in a method to diagnose disease in a subject, such as a human patient.
  • the method involves administering to that patient a detectably labeled compound as described herein, and detecting the binding of that compound to selected NNR subtypes (e.g., ⁇ 4 ⁇ 2 and/or a6-containing receptor subtypes).
  • selected NNR subtypes e.g., ⁇ 4 ⁇ 2 and/or a6-containing receptor subtypes.
  • Those skilled in the art of using diagnostic tools, such as PET and SPECT can use the radiolabeled compounds described herein to diagnose a wide variety of conditions and disorders, including conditions and disorders associated with dysfunction of the central and autonomic nervous systems.
  • Such disorders include a wide variety of CNS diseases and disorders, including Alzheimer's disease, Parkinson's disease, and schizophrenia.
  • These and other representative diseases and disorders that can be evaluated include those that are set forth in U.S. Patent No. 5,952,339 to Bencherif et al.
  • the diagnostic compositions can be used in a method to monitor selective nicotinic receptor subtypes of a subject, such as a human patient.
  • the method involves administering a detectably labeled compound as described herein to that patient and detecting the binding of that compound to selected nicotinic receptor subtypes namely, the ⁇ 4 ⁇ 2 and/or ot6-containing receptor subtypes.
  • the compounds of this invention can be used as reference ligands in binding assays for compounds which bind to NNR subtypes, particularly the and/or a6-containing receptor subtypes.
  • the compounds of this invention are preferably labeled with a radioactive isotopic moiety such as 3 H, or 14 C. Examples of such binding assays are described in detail below. V. Synthetic Examples
  • 6-(tert-butoxycarbonyl)-3,6-diazabicyclo[3.1.1]heptane (2) was prepared according to the procedure of WO 2005/108402 to Pinna, et al Example 3: 3-benzyl-6-(trifluoromethylcarbonyl)-3,6- diazabicyclo[3.1.1]heptane (3)
  • Example 6 3-(cyclopropylcarbonyl)-3,6-diazabicyclo[3.1.1]heptane (6)
  • the crude mixture was dissolved in 20 mL of methylene chloride.
  • Trifluoroacetic acid (5 mL) was added and the reaction was stirred for 16 h.
  • the solvent was removed in vacuo and the residue was dissolved in 1 mL of 1 :1 methylene chloride:methanol and passed through a SCX-2 column (Biotage) (eluting with 3 mL 1 :1 methylene chloride:methanol, then 7N methanolic ammonia).
  • the crude product was purified on a silica gel column eluting with a chloroform to 90:9:1 Chloroform:methanol:ammonium hydroxide gradient over 12 column volumes. Appropriate fractions were collected and solvent was removed in vacuo to yield 3-(cyclopropylcarbonyl)-3,6- diazabicyclo[3.1.1]heptane (6) (750 mg; 36% yield) as a yellow oil.
  • Trifluoroacetic acid (3 mL) was added and the reaction was stirred for 2 h.
  • the solvent was removed in vacuo at 40 ° C and the residue was dissolved in 1 :1 methylene chloride:methanol and passed through a SCX-2 column (Biotage) (eluting with 2 mL 1 :1 methylene chloride:methanol, then 7N methanolic ammonia).
  • the crude product was purified on a silica gel column eluting with a chloroform to 90:9:1 Chloroform:methanol:ammonium hydroxide gradient. Appropriate fractions were collected and solvent was removed in vacuo to yield 3-(propoxycarbonyl)-3,6-diazabicyclo[3.1.1]heptane (7) (12 mg, 26%) as a clear oil.
  • Methoxyethyl chloroformate (32 ⁇ , 27.5 mmol) was added and the solution was stirred for 1 h. The solvent was removed in vacuo and the residue was washed with 50 mM sodium acetate in methylene chloride solution. The solution was stirred 10 min and passed through a phase separator. The solvent was removed in vacuo to give crude 3-(methoxyethoxycarbonyl)-6- (tert-butoxycarbonyl)-3,6-diazabicyclo[3.1.1 ]heptane.
  • the crude mixture was dissolved in 3 mL of methylene chloride.
  • Trifluoroacetic acid (3 mL) was added and the reaction was stirred for 2 h.
  • the solvent was removed in vacuo at 40 ° C and the residue was dissolved in 1 :1 methylene chloride:methanol and passed through a SCX-2 column (Biotage) (eluting with 2 mL 1 :1 methylene chloride:methanol, then 7N methanolic ammonia).
  • the crude product was purified on a silica gel column eluting with a chloroform to 90:9:1 Chloroform:methanol:ammonium hydroxide gradient. Appropriate fractions were collected and solvent was removed in vacuo to yield 3-(methoxyethoxycarbonyl)-3,6-diazabicyclo[3.1.1]heptane (8) (15 mg, 27%) as a clear oil.
  • SH-EP1/human ⁇ 4 ⁇ 2 (Eaton et al., 2003), SH-EP1/human ⁇ 4 ⁇ 4 (Gentry et al., 2003), SH-EP1/a6p3p4a5 (Grinevich et alirri 2005), TE671/RD and SH- SY5Y cell lines (obtained from Dr. Ron Lukas, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, Arizona) were maintained in proliferative growth phase in Dulbecco's modified Eagle's medium
  • ⁇ 4 ⁇ 2 and ⁇ 4 ⁇ 4 cell media were supplemented with 0.25 mg/mL zeocin and 0.13 mg/mL hygromycin B.
  • HEK/human a7/RIC3 cells obtained from J. Lindstrom, U.
  • Rat cortices were obtained from Analytical Biological Services, Incorporated (ABS, Wilmington, Delaware). Tissues were dissected from female Sprague-Dawley rats, frozen and shipped on dry ice. Tissues were stored at -20 °C until needed for membrane preparation.
  • Cortices from 10 rats were pooled and homogenized by Polytron (Kinematica GmbH, Switzerland) in 10 volumes (weightvolume) of ice-cold preparative buffer (KCI, 11 mM; KH 2 P0 4 , 6mM; NaC1 137 mM; Na 2 HP0 4 8 mM; HEPES (free acid), 20 mM; iodoacetamide, 5 mM; EDTA, 1.5 mM; 0.1 mM PMSF pH 7.4).
  • the resulting homogenate was centrifuged at 40,000 g for 20 minutes at 4 °C and the resulting pellet was resuspended in 20 volumes of ice-cold water.
  • Protein concentrations were determined using the Pierce BCA Protein Assay kit (Pierce Biotechnology, Rockford, IL), with bovine serum albumin as the standard.
  • [ 3 H]- epibatidine (52 Ci/mmol, Perkin-Elmer Life Sciences) was used for binding studies at the other receptor subtypes. Incubation was terminated by rapid filtration on a multimanifold tissue harvester (Brandel, Gaithersburg, MD) using GF/B filters presoaked in 0.33% polyethyleneimine (w/v) to reduce nonspecific binding. Filters were washed 3 times and the radioactivity retained was determined by liquid scintillation counting.
  • Binding data analysis Binding data were expressed as percent total control binding. Replicates for each point were averaged and plotted against the log of drug concentration. The IC 50 (concentration of the compound that produces 50% inhibition of binding) was determined by least squares non-linear regression using GraphPad Prism software (GraphPAD, San Diego, CA). K, was calculated using the Cheng-Prusoff equation (Cheng and Prusoff, 1973).
  • Example 10 Tabular Spectral and Receptor Binding Data
  • Ki values inhibition constants at the human ⁇ 4 ⁇ 2 subtype in the ranges of 2 nM to 11,000 nM, with a number of compound exhibiting Ki ⁇ 100 nM, indicating high affinity for the ⁇ 4 ⁇ 2 subtype.
  • Ki values at the ⁇ 6 ⁇ 3 ⁇ 4 ⁇ 5 subtype vary within the range of 38 nM to 100,000 nM, indicating variable affinity for the ⁇ 6 ⁇ 3 ⁇ 4 ⁇ 5 subtype.
  • Example 11 Neuroprotective effect of 48h pre-treatment of
  • Rat dopaminergic neurons were cultured as described by Schinelli et al., 1988. Briefly pregnant female rats of 15 days gestation were killed by cervical dislocation (Rats Wistar; Janvier) and the fetuses removed from the uterus. The embryonic midbrains were removed and placed in ice-cold medium of Leibovitz (L15; Invitrogen) containing 1% of Penicillin- Streptomycin (PS; Invitrogen) and 1% of bovine serum albumin (BSA;
  • the cells were seeded at a density of 35000 cells/well in 96 well-plates (wells were pre-coated with poly-L-lysine (greiner)) and were cultured at 37 °C in a humidified air (95%)/C02 (5%) atmosphere. Half of the medium was changed every 2 days with fresh medium. In these conditions, after 5 days of culture, astrocytes were present in the culture and release growth factor allowing neurons differentiation. Five to six percents of the neuronal cell population were dopaminergic neurons.
  • Test compounds (compound A and compound B, as the heptane di-p- toluoyl-D-tartrate salts) were assayed at seven concentrations (0.001 ; 0.01 ; 0.1 ; 1 ; 10; 100 and 1000 nM).
  • Nicotine (10 nM) and BDNF (50 ng/ml) were used as reference test compounds.
  • TH tyrosine hydroxylase antibody
  • Figure 1 shows a dose effect curve of Compound A (3- cyclopropylcarbonyl-3,6-diazabicyclo[3.1.1], as the heptane di-p-toluoyl-D- tartrate salt) and nicotine on TH positive neurons after 48h pretreatment, followed by MPP + injury (4 ⁇ , 48h).
  • Compound A 3- cyclopropylcarbonyl-3,6-diazabicyclo[3.1.1], as the heptane di-p-toluoyl-D- tartrate salt
  • Figure 2 shows a dose effect curve of Compound A (3- cyclopropylcarbonyl-3,6-diazabicyclo[3.1.1], as the heptane di-p-toluoyl-D- tartrate salt) and nicotine on total TH neurite length after 48h pretreatment, followed by MPP + injury (4 ⁇ , 48h).
  • Compound A 3- cyclopropylcarbonyl-3,6-diazabicyclo[3.1.1], as the heptane di-p-toluoyl-D- tartrate salt
  • Figure 3 shows a dose effect curve of Compound B (3-ethylcarbonyl- 3,6-diazabicyclo[3.1.1], as the heptane di-p-toluoyl-D-tartrate salt) and nicotine on TH positive neurons after 48h pretreatment, followed by MPP + injury (4 ⁇ , 48h).
  • Figure 4 shows a dose effect curve of Compound B (3-ethylcarbonyl- 3,6-diazabicyclo[3.1.1], as the heptane di-p-toluoyl-D-tartrate salt) and nicotine on total TH neurite length after 48h pretreatment, followed by MPP + injury (4 ⁇ , 48h).
  • Figure 5 shows a dose effect curve of BDNF (50 ng/ml) and nicotine (10nM) on TH positive neurons after 48h pretreatment, followed by MPP + injury (4 ⁇ , 48h).
  • Figure 6 shows a dose effect curve of BDNF (50 ng/ml) and nicotine (10nM) on total TH neurite length after 48h pretreatment, followed by MPP + injury (4 ⁇ , 48h).

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Abstract

La présente invention concerne des composés qui se lient aux récepteurs nicotiniques neuronaux (RNN) à l'acétylcholine et qui en modulent l'activité, des procédés permettant de préparer ces composés, des compositions pharmaceutiques contenant ces composés, et des procédés permettant d'utiliser ces composés pour traiter une grande variété de pathologies et troubles, notamment ceux associés au dysfonctionnement du système nerveux central (SNC). La présente invention concerne des composés qui se lient avec une grande affinité aux RNN de sous-type α4β2, ou de sous-type contenant α6-containing, ou des deux sous-types. Formule 1, où chaque m est identique et vaut 0 ou 1; chaque n est identique et vaut 0 ou 1; lorsque chaque m vaut 0, alors chaque n vaut 1; lorsque chaque m vaut 1, alors chaque n vaut 0; R1 est un groupe -C(O)-R3, -C(O)O-R3, -C(O)NH-R3, -C(O)-(CH2)q-X-R3, -C(O)O-(CH2)q-X-R3, ou -C(O)NH-(CH2)q-X-R3 ; q vaut 1, 2, 3, 4, 5, ou 6; X est un groupe -0-, -S-, -NH-, ou -NHC(O)-; R2 est H ou un groupe alkyle; R3 est un groupe alkyle, alcényle, alcynyle, cycloalkyle, cycloalcényle, cycloalcynyle, aryle, hétéroaryle, ou hétérocyclique;
PCT/US2010/058836 2009-12-07 2010-12-03 3,6-diazabicyclo[3.1.1]heptanes comme ligands des récepteurs nicotiniques neuronaux à l'acétycholine WO2011071758A1 (fr)

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MX2012006484A MX2012006484A (es) 2009-12-07 2010-12-03 3,6-diazabiciclo [3.1.1] heptanos como ligandos de receptores nicotinicos neuronales de acetilcolina.
AU2010328419A AU2010328419A1 (en) 2009-12-07 2010-12-03 3,6-diazabicyclo[3.1.1]heptanes as neuronal nicotinic acetylcholine receptor ligands
SG2012039293A SG181109A1 (en) 2009-12-07 2010-12-03 3,6-diazabicyclo[3.1.1]heptanes as neuronal nicotinic acetylcholine receptor ligands
RU2012128583/04A RU2012128583A (ru) 2009-12-07 2010-12-03 3,6-диазабицикло[3.1.1]гептаны в качестве лигандов нейрональных никотиновых ацетилхолиновых рецепторов
US13/514,084 US8802694B2 (en) 2009-12-07 2010-12-03 3,6-diazabicyclo[3.1.1]heptanes as neuronal nicotinic acetycholine receptor ligands
BR112012013765A BR112012013765A2 (pt) 2009-12-07 2010-12-03 3,6-diazabiciclo[3.1.1] heptanos como ligantes de receptor nicotínico neuronal de acetilcolina
EP10787978A EP2509982A1 (fr) 2009-12-07 2010-12-03 3,6-diazabicyclo[3.1.1]heptanes comme ligands des récepteurs nicotiniques neuronaux à l'acétycholine
CA2782409A CA2782409A1 (fr) 2009-12-07 2010-12-03 3,6-diazabicyclo[3.1.1]heptanes comme ligands des recepteurs nicotiniques neuronaux a l'acetycholine
JP2012542213A JP2013512922A (ja) 2009-12-07 2010-12-03 神経型ニコチン性アセチルコリン受容体リガンドとしての３，６−ジアザビシクロ［３．１．１］ヘプタン
KR1020127017478A KR20120120190A (ko) 2009-12-07 2010-12-03 신경원성 니코틴 아세틸콜린 수용체 리간드인 ３，６?디아자비시클로［３．１．１］헵탄
CN2010800553917A CN102648202A (zh) 2009-12-07 2010-12-03 作为神经元烟碱乙酰胆碱受体配体的3,6-二氮杂双环[3.1.1]庚烷
IL219960A IL219960A0 (en) 2009-12-07 2012-05-23 3,6-diazabicyclo[3.1.1]heptanes as neuronal nicotinic acetylcholine receptor ligands
ZA2012/04143A ZA201204143B (en) 2009-12-07 2012-06-06 3,6-diazabicyclo[3.1.1]heptanes as neuronal nicotinic acetylcholine receptor ligands
ECSP12012023 ECSP12012023A (es) 2009-12-07 2012-07-04 3,6-diazabiciclo [3.1.1] heptanos como ligandos de receptores nicotínicos neuronales de acetilcolina
US14/321,179 US20140315880A1 (en) 2009-12-07 2014-07-01 3,6-diazabicyclo[3.1.1]heptaines as neuronal nicotinic acetycholine receptor ligands

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MX2012006484A (es) 2012-08-01
EP2509982A1 (fr) 2012-10-17
AU2010328419A1 (en) 2012-06-21
US20120309737A1 (en) 2012-12-06
JP2013512922A (ja) 2013-04-18
BR112012013765A2 (pt) 2016-04-26
US20140315880A1 (en) 2014-10-23
CN102648202A (zh) 2012-08-22
SG181109A1 (en) 2012-07-30
ECSP12012023A (es) 2012-08-31
PE20121556A1 (es) 2012-12-05
KR20120120190A (ko) 2012-11-01
RU2012128583A (ru) 2014-01-20
CO6541649A2 (es) 2012-10-16
US8802694B2 (en) 2014-08-12
IL219960A0 (en) 2012-07-31
TW201138776A (en) 2011-11-16
ZA201204143B (en) 2013-02-27
CL2012001483A1 (es) 2013-01-18
CA2782409A1 (fr) 2011-06-16

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