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Definitions

• This invention relates to novel sulfone compounds, pharmaceutical compositions, processes for their preparation, and use thereof in treating IL-8, GRO ⁇ , GRO ⁇ , GRO ⁇ , NAP-2, and ENA-78 mediated diseases.
• Interleukin-8 Interleukin-8
• NAP-1 neutrophil attractant/activation protein-1
• MDNCF monocyte derived neutrophil chemotactic factor
• NAF neutrophil activating factor
• T-cell lymphocyte chemotactic factor T-cell lymphocyte chemotactic factor.
• Interleukin-8 is a chemoattractant for neutrophils, basophils, and a subset of T-cells. It is produced by a majority of nucleated cells including macrophages, fibroblasts, endothelial and epithelial cells exposed to TNF, IL-1 ⁇ , IL-1 ⁇ or LPS, and by neutrophils themselves when exposed to LPS or chemotactic factors such as FMLP.
• GRO ⁇ , GRO ⁇ , GRO ⁇ and NAP-2 also belong to the chemokine ⁇ family. Like IL-8, these chemokines have also been referred to by different names. For instance GRO ⁇ , ⁇ , ⁇ have been referred to as MGSA ⁇ , ⁇ and ⁇ respectively (Melanoma Growth Stimulating Activity), see Richmond et al., J. Cell Physiology 129, 375 (1986) and Chang et al., J. Immunol. 148, 451 (1992). All of the chemokines of the ⁇ -family which possess the ELR motif directly preceding the CXC motif bind to the IL-8 B receptor (CXCR2).
• CXCR2 IL-8 B receptor
• IL-8, GRO ⁇ , GRO ⁇ , GRO ⁇ , NAP-2, and ENA-78 stimulate a number of functions in vitro. They have all been shown to have chemoattractant properties for neutrophils, while IL-8 and GRO ⁇ have demonstrated T-lymphocyte and basophilic chemotactic activity. In addition, IL-8 can induce histamine release from basophils from both normal and atopic individuals. GRO- ⁇ and IL-8 can, in addition, induce lysozomal enzyme release and respiratory burst from neutrophils. IL-8 has also been shown to increase the surface expression of Mac-1 (CD 11b/CD18) on neutrophils without de novo protein synthesis.
• ELR chemokines (those containing the amino acids ELR motif just prior to the CXC motif) have also been implicated in angiostasis, Strieter et al., Science 258, 1798 (1992).
• IL-8, GRO ⁇ , GRO ⁇ , GRO ⁇ and NAP-2 induce neutrophil shape change, chemotaxis, granule release, and respiratory burst, by binding to and activating receptors of the seven-transmembrane, G-protein-linked family, in particular by binding to IL-8 receptors, most notably the IL-8 ⁇ receptor (CXCR2).
• CXCR2 IL-8 ⁇ receptor
• CXCR2 IL-8 ⁇ receptor
• CXCR1 which binds only IL-8 with high affinity
• CXCR2 which has high affinity for IL-8 as well as for GRO ⁇ , GRO ⁇ , GRO ⁇ and NAP-2.
• CXCR1 which binds only IL-8 with high affinity
• CXCR2 which has high affinity for IL-8 as well as for GRO ⁇ , GRO ⁇ , GRO ⁇ and NAP-2.
• the present invention comprises novel IL-8 receptor antagonists represented by Formula (I), and compositions comprising the present compounds and a pharmaceutically acceptable carrier or diluent.
• the present invention also comprises novel IL-8 receptor antagonists represented by Formula (I) and combinations comprising the present compounds and one or more additional therapeutic ingredients.
• the present invention further comprises a method of treating a chemokine mediated disease wherein the chemokine is one which binds to an IL-8 ⁇ or ⁇ receptor, and which method comprises administering an effective amount of a compound of Formula (I) or a pharmaceutically acceptable salt thereof.
• the present invention also relates to a method of inhibiting the binding of IL-8 to its receptors in a mammal, particularly in a human, in need thereof which comprises administering an effective amount of a compound of Formula (I).
• X is selected from the group consisting of halogen, C 1-3 alkyl, C 1-3 alkoxy, cyano, CF 3 , and OCF 3 ;
• R2 is selected from the group consisting of C 3-6 cycloalkyl, phenyl and heteroaryl, wherein the phenyl or heteroaryl moieties are optionally substituted, once or twice, independently, by a substituent selected from the group consisting of C 1-3 alkyl, halogen, CF 3 , OCF 3 , phenyloxy and benzyloxy; or R2 is phenyl substituted by methylenedioxy or by (di-halo-substituted)-methylenedioxy;
• R1 represents C 4-8 heterocyclyl(CH 2 ) n wherein the heterocyclyl moiety is optionally substituted, independently, once or twice, by a substituent selected from the group consisting of C 1-3 alkyl, C(O)OR4 and C(O)R5;
• R4 and R5 are independently C 1-3 alkyl
• n 0 or 1
• R1 is selected from the following ring systems (a-k):
• R3 is H or C 1-3 alkyl; or a pharmaceutically acceptable salt thereof.
• C 1-3 alkyl refers to a linear or branched saturated hydrocarbon group containing 1 to 3 carbon atoms. Examples of such groups include methyl, ethyl, n-propyl, or isopropyl.
• cycloalkyl refers to a saturated monocyclic hydrocarbon ring of 3 to 6 carbon atoms. Examples of such groups include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and the like.
• heterocyclyl refers to a 4-8 membered saturated or non aromatic, unsaturated monocyclic ring containing 1 to 3 heteroatoms selected from oxygen, nitrogen or sulphur. Examples of such rings include pyrrolidinyl, azetidinyl, pyrazolidinyl, piperidinyl, piperazinyl, and the like.
• heteroaryl refers to a 5-6 membered monocyclic aromatic ring containing 1 to 3 heteroatoms selected from oxygen, nitrogen and sulphur.
• monocyclic aromatic rings include pyridyl, pyrrolyl, pyranyl, pyrazolyl, pyrimidyl, pyridazinyl, pyrazinyl, and the like.
• halogen or “halo” refers to F, Cl, Br or I.
• C 1-3 alkoxy refers to a straight or branched alkoxy moiety containing 1 to 3 carbon atoms. Examples of alkoxy included herein are methoxy, ethoxy, propoxy and prop-2-oxy and the like.
• optionally substituted means substituted, independently, at each occurrence, one to three times, by such groups as halogen, C 1-3 alkyl, C 1-3 alkoxy, heterocyclyl, aryl, and heteroaryl, such that the optional substituents may be further substituted, except for halogen, one to three times, independently, by halogen or C 1-2 alkyl.
• the compounds of the present invention may contain one or more asymmetric carbon atoms and may exist in racemic and optically active forms. All of these compounds and diastereomers are contemplated to be within the scope of the present invention.
• X is selected from the group consisting of halogen, C 1-3 alkyl, C 1-3 alkoxy cyano, CF 3 , and OCF 3 .
• X is halogen
• X is selected from the group consisting of F, Cl and Br.
• X is Cl
• R2 is selected from the group consisting of C 3-6 cycloalkyl, phenyl and heteroaryl, wherein the phenyl or heteroaryl moieties are optionally substituted, once or twice, independently, by a substituent selected from the group consisting of C 1-3 alkyl, halogen, CF 3 , OCF 3 , phenyloxy and benzyloxy; or
• R2 is phenyl substituted by methylenedioxy or by (di-halo-substituted)-methylenedioxy.
• R2 represents phenyl, optionally substituted, independently, once or twice, by a substituent selected from the group consisting of C 1-3 alkyl, halogen, OCF 3 or phenyloxy.
• R2 represents pyridyl, optionally substituted once by halogen.
• R2 represents pyridyl substituted by chloro.
• R2 represents phenyl substituted by difluoromethylenedioxy.
• R2 represents C 3-6 cycloalkyl.
• R2 represents halomethylphenyl, trihalomethyloxyphenyl, dihalophenyl, ethylphenyl or phenyloxyphenyl.
• R2 represents 3-fluoro-2-methylphenyl, 2-trifluoromethyloxyphenyl, 2-chloro-3-fluorophenyl, 2-ethylphenyl or 2-phenyloxyphenyl.
• R2 represents halopyridyl
• R2 represents 2-chloro-3-pyridyl.
• R1 represents C 4-8 heterocyclyl(CH 2 ) n , wherein the heterocyclyl moiety is optionally substituted, independently, once or twice, by a substituent selected from the group consisting of C 1-3 alkyl, C(O)OR4 and C(O)R5; and in which R4 and R5 are, independently, C 1-3 alkyl; and n is 0 or 1;
• R1 is selected from a group consisting of the following ring systems (a-k):
• R3 is H or C 1-3 alkyl.
• the R1 heterocyclyl moiety is pyrrolidinyl.
• the R1 heterocyclyl moiety is selected from the group consisting of azetidinyl, piperidinyl and pyrrolidinyl.
• R1 is selected from the group consisting of pyrrolidinylmethyl, azetidinyl, piperidinyl, pyrrolidinyl and ethyl-1-piperidinylcarboxylate.
• R1 is selected from the group consisting of 3-pyrrolidinylmethyl, 3-azetidinyl, 4-piperidinyl, 3-piperidinyl, 3-pyrrolidinyl and ethyl-1-piperidinylcarboxylate.
• n is 0 or 1.
• n 0.
• n 1
• R1 represents a heterocyclyl moiety selected from the group consisting of 2-azabicyclo[2.2.1]heptyl, 8-azabicyclo[3.2.1]octyl, 8-methyl-8-azabicyclo[3.2.1]octyl, 3-azabicyclo[3.2.1]octyl, 2-azabicyclo[2.2.2]octyl, and 2-oxa-5-azabicyclo[2.2.2]octyl.
• R1 represents 3-exo-8-methyl-8-azabicyclo[3.2.1]oct-3-yl or 3-exo-8-azabicyclo[3.2.1]oct-3-yl.
• Suitable pharmaceutically acceptable salts are well known to those skilled in the art and include basic salts of inorganic and organic salts, such as hydrochloric acid, hydrobromic acid, sulphuric acid, phosphoric acid, methane sulphonic acid, ethane sulphonic acid, acetic acid, malic acid, tartaric acid, citric acid, lactic acid, oxalic acid, succinic acid, fumaric acid, maleic acid, benzoic acid, salicylic acid, phenylacetic acid and mandelic acid.
• pharmaceutically acceptable salts of compounds of Formula (I) may also be formed with a pharmaceutically acceptable cation, for instance, if a substituent group comprises a carboxy moiety.
• Suitable pharmaceutically acceptable cations are well known to those skilled in the art and include alkaline, alkaline earth, ammonium and quaternary ammonium cations.
• Illustrative compounds of the present invention include, but are not limited to:
• the salt is the hydrochloride salt.
• compounds of the present invention include, but are not limited to:
• compounds of the present invention include, but are not limited to:
• compounds of the present invention include, but are not limited to:
• the present compounds may be synthesized by a method comprising the steps of:
• the present invention also involves novel intermediates selected from the group consisting of Formulas (II):
• the compounds of Formula (I) may be obtained by applying synthetic procedures, some of which are illustrated in the Scheme 1 below.
• the synthesis provided for in these Schemes is applicable for the producing compounds of Formula (I) having a variety of different groups which are reacted, employing optional substituents which are suitably protected, to achieve compatibility with the reactions outlined herein. Subsequent deprotection, in those cases, then affords compounds of the nature generally disclosed.
• further compounds of these formulas may be prepared by applying standard techniques for functional group interconversion, well known in the art.
• R1 contain a 3° or an aromatic amine moiety or moieties
• the compounds of Formula (I) may be prepared according to Scheme 1.
• the sulfonyl chloride 1 (prepared according to WO 01/68033A2, incorporated herein by reference to the extent it teaches how to prepare Scheme 1, 1 compounds) is reduced to the corresponding thiol 2 under conditions such as triphenylphosphine in DMF.
• the compound 2 may be prepared by quenching the corresponding lithium anion (see WO 01/68033A2, incorporated herein by reference to the extent it teaches how to prepare Scheme 1, 1 compounds) with sulfur (S 8 ). Alkylation of 2 is then accomplished by treatment with R1-LG, where LG denotes a leaving group such chloro, bromo, iodo or sulfonate, in the presence of base.
• the resulting sulfides 3 are then oxidized to the sulfones 4 by exposure to an oxidizing agent such as hydrogen peroxide. Hydrolysis of the benzoxazole moiety yields the aminophenols 5 which, in turn, is exposed to an isocyanate or a suitable isocyanate precursor which may be transformed to the isocyanate in situ. This reaction produces the final urea 6.
• R1 contains a 1° or 2° amine protected by a Boc group or a similar acid labile protecting group
• the compounds can be prepared as outlined in Scheme 2.
• the sulfone formation and hydrolysis is performed as described above, however, since the latter will result in removal of the Boc group, it has to be reintroduced which can be accomplished under suitable reaction conditions such as Boc anhydride and sodium hydroxide yielding compound 5a.
• the Boc group is then removed for the desired product 7 under acidic conditions such as 4N hydrochloric acid in 1,4-dioxane.
• the resulting amine may be further elaborated by an operation known to those skilled in the art as reductive amination to form the 2° or 3° amines 8.
• ether refers to diethyl ether; brine refers to a saturated aqueous solution of NaCl, DCM refers to dichloromethane, THF refers to tetrahydrofuran, EtOAc refers to ethyl acetate, Hex and Hx refers to hexane, IMS refers to industrial methylated spirit, TBME refers to tert-butylmethyl ether, DMF refers to dimethylformamide, BOC and Boc refers to tert-butyloxycarbonyl. Unless otherwise indicated, all temperatures are expressed in ° C. (degrees Centigrade). All reactions are conducted under an inert atmosphere at room temperature unless otherwise noted.
• flash and column chromatography refers to flash column chromatography on silica using the stated solvent systems.
• LC-MS data were obtained on either a PE Sciex Single Quadrupole LC/MS API-150 combined with a Shimadzu LC system (SCL-10A Controller and dual UV detector) or on a Waters micromass ZQ combined with a Waters 2695 separation module.
• 3,4-dichloroaniline 150 g was dissolved in 1.0 L TBME and the solution was cooled to 10° C.
• Sodium hydroxide 140.7 g of a 30% aqueous solution
• Pivaloyl chloride 125.9 mL was added dropwise while keeping the internal temperature under 35° C.
• the temperature of the reaction was maintained at 30-35° C. for a further 30 min.
• the reaction mixture was then allowed to cool to room temperature and subsequently kept at 0-5° C. for 1 h.
• the resulting precipitate was filtered of and washed with 600 mL water/MeOH (90/10) and then with 900 mL water.
• N-(3,4-dichlorophenyl)-2,2-dimethylpropanamide (121 g) was dissolved in 720 mL THF and the solution was cooled to ⁇ 50° C.
• Butyllithium (433 mL, 2.5N in hex) was added while keeping the internal temperature between ⁇ 45° C. and ⁇ 35° C. (final temp.: ⁇ 35° C.). Held at ⁇ 25° C. for 40 min.
• An hplc check of the reaction mixture revealed that 5-10% of the starting material remained.
• An additional 35 mL of butyllithium was added at ⁇ 30° C. and the reaction was at ⁇ 30 to ⁇ 25° C. for a further 30 min (HPLC: no significant change).
• reaction mixture was cooled to ⁇ 45° C. and SO 2 was bubbled though the solution until saturation appeared to have been reached. Subsequently, the reaction mixture was stirred at ⁇ 10 to 0° C. for 45 min. Argon (2 double-balloon volumes) was bubbled through the solution following which the reaction mixture was cooled to ⁇ 5° C. Sulfuryl chloride (58.8 mL) was added while keeping the temperature below 22° C. Subsequently, the reaction mixture was kept at 10-15° C. for 1 h (HPLC: complete). EtOAc was added and the mixture was concentrated, washed with water, saturated aqueous sodium bicarbonate and brine, dried over MgSO 4 and the solvent was evaporated in vacuo.
• Triphenylphosphine (89 g) was dissolved in DCM (200 ml) and DMF (2.2 ml). The solution was cooled in an ice/methanol bath to ⁇ 1° C. To this was added a solution of the 6-chloro-2-(1,1-dimethylethyl)-1,3-benzoxazole-7-sulfonyl chloride, Starting Material 2, (prepared according to WO01/68033A2, incorporated herein by reference, to the extent that it teaches the synthesis of Starting Material 2, also described above) (35 g) in DCM (100 ml) over 30 minutes maintaining the temperature below 15° C. The reaction mixture was stirred at room temperature under nitrogen for 18 hours.
• N-Boc-nortropinone (6.3 g) was dissolved in MeOH (150 mL) and cooled to 0° C. NaBH 4 was added in portions and the reaction mixture was stirred at 0° C. for 2.5 h. The reaction was quenched with water, acidified to pH3 and extracted with DCM ( ⁇ 3). The combined organic layers were dried over Na 2 SO 4 and concentrated yielding the desired product (5.0 g, 79%, white solid). R f : 0.38 (EtOAc/Hx: 1/1).
• Example 27 (0.20 g) was stirred in CHCl 3 (2 mL) at room temperature under an argon atmosphere. Iodotrimethylsilane (0.21 g) was added and the mixture was heated to reflux overnight. The reaction did not proceed, however, until two batches of chlorotrimethylsilane (0.037 g pr. batch) and NaI (0.051 g pr. batch) were added and the reaction was heated to 75° C. for a further 6 h. At this time, MeOH was added and the mixture was stirred for a further 30 min after which the solvents were removed, ammonia in methanol added. The mixture was extracted with DCM, the organic layer washed with water, dried over Na 2 SO 4 and concentrated. The crude product was triturated with DCM/ether and then purified by column chromatography eluting with methanol. Yield: 10 mg (6%, light brown solid) MS (m/z, ES + , M+H): 502.06.
• Compounds of Formula (I), or a pharmaceutically acceptable salt thereof can be used in the manufacture of a medicine for the prophylactic or therapeutic treatment of any disease state in a human, or other mammal, which is exacerbated or caused by excessive or unregulated IL-8 cytokine production by such mammal's cell, such as, but not limited to, monocytes and/or macrophages, or other chemokines which bind to the IL-8 ⁇ or ⁇ receptor, also referred to as the type I or type II receptor.
• the present invention provides a method of treating a chemokine mediated disease, wherein the chemokine is one which binds to an IL-8 ⁇ or ⁇ receptor and which method comprises administering an effective amount of a compound of Formula (I) or a pharmaceutically acceptable salt thereof.
• the chemokines are IL-8, GRO ⁇ , GRO ⁇ , GRO ⁇ , NAP-2 or ENA-78.
• the compounds of Formula (I) are administered in an amount sufficient to inhibit cytokine function, in particular IL-8, GRO ⁇ , GRO ⁇ , GRO ⁇ , NAP-2 or ENA-78, such that they are biologically regulated down to normal levels of physiological function, or in some case to subnormal levels, so as to ameliorate the disease state.
• Abnormal levels of IL-8, GRO ⁇ , GRO ⁇ , GRO ⁇ , NAP-2 or ENA-78 constitute: (i) levels of free IL-8 greater than or equal to 1 picogram per mL; (ii) any cell associated IL-8, GRO ⁇ , GRO ⁇ , GRO ⁇ , NAP-2 or ENA-78 above normal physiological levels; or (iii) the presence of IL-8, GRO ⁇ , GRO ⁇ , GRO ⁇ , NAP-2 or ENA-78 above basal levels in cells or tissues in which IL-8, GRO ⁇ , GRO ⁇ , GRO ⁇ , NAP-2 or ENA-78 respectively, is produced.
• Chemokine mediated diseases include psoriasis, atopic dermatitis, osteo arthritis, rheumatoid arthritis, asthma, chronic obstructive pulmonary disease, adult respiratory distress syndrome, inflammatory bowel disease, Crohn's disease, ulcerative colitis, stroke, septic shock, endotoxic shock, gram negative sepsis, toxic shock syndrome, cardiac and renal reperfusion injury, glomerulonephritis, thrombosis, graft vs.
• alzheimers disease allograft rejections, malaria, restinosis, angiogenesis, atherosclerosis, osteoporosis, gingivitis, viral diseases such as rhinovirus or undesired hematopoietic stem cell release.
• the ⁇ -chemokines can promote the neovascularization of tumors by promoting the directional growth of endothelial cells. Therefore, the inhibition of IL-8 induced chemotaxis or activation would lead to a direct reduction in the neutrophil infiltration.
• the present invention also provides for a means of treating CNS injuries by the chemokine receptor antagonist compounds of Formula (I). Such treatment is provided in an acute setting, as well as for prevention of injury in those individuals deemed susceptible to injury.
• CNS injuries as defined herein include both open or penetrating head trauma, such as by surgery, or a closed head trauma injury, such as by an injury to the head region. Also included within this definition is ischemic stroke, particularly to the brain area.
• Ischemic stroke may be defined as a focal neurologic disorder that results from insufficient blood supply to a particular brain area, usually as a consequence of an embolus, thrombi, or local atheromatous closure of the blood vessel.
• the role of inflammatory cytokines in this area has been emerging and the present invention provides means for the potential treatment of these injuries. Relatively little treatment, for an acute injury such as these has been available.
• TNF- ⁇ is a cytokine with proinflammatory actions, including endothelial leukocyte adhesion molecule expression.
• Leukocytes infiltrate into ischemic brain lesions and hence compounds which inhibit or decrease levels of TNF would be useful for treatment of ischemic brain injury. See Liu et al., Stroke , Vol. 25., No. 7, pp. 1481-88 (1994) whose disclosure is incorporated herein by reference.
• Compounds of Formula (I) are administered in an amount sufficient to inhibit IL-8, binding to the IL-8 alpha or beta receptors, from binding to these receptors, such as evidenced by a reduction in neutrophil chemotaxis and activation.
• the discovery that the compounds of Formula (I) are inhibitors of IL-8 binding is based upon the effects of the compounds of Formula (I) in the in vitro receptor binding assays which are described herein.
• Compounds of Formula (I) have been shown to be inhibitors of type II IL-8 receptors.
• IL-8 mediated disease or disease state refers to any and all disease states in which IL-8, GRO ⁇ , GRO ⁇ , GRO ⁇ , NAP-2 or ENA-78 plays a role, either by production of IL-8, GRO ⁇ , GRO ⁇ , GRO ⁇ , NAP-2 or ENA-78 themselves, or by IL-8, GRO ⁇ , GRO ⁇ , GRO ⁇ , NAP-2 or ENA-78 causing another monokine to be released, such as but not limited to IL-1, IL-6 or TNF.
• a disease state in which, for instance, IL-1 is a major component, and whose production or action, is exacerbated or secreted in response to IL-8, would therefore be considered a disease state mediated by IL-8.
• chemokine mediated disease or disease state refers to any and all disease states in which a chemokine which binds to an IL-8 ⁇ or ⁇ receptor plays a role, such as but not limited to IL-8, GRO- ⁇ , GRO- ⁇ , GRO ⁇ , NAP-2 or ENA-78.
• a disease state in which, for instance, IL-1 is a major component, and whose production or action, is exacerbated or secreted in response to IL-8, would therefore be considered a disease stated mediated by IL-8.
• cytokine refers to any secreted polypeptide that affects the functions of cells and is a molecule which modulates interactions between cells in the immune, inflammatory or hematopoietic response.
• a cytokine includes, but is not limited to, monokines and lymphokines, regardless of which cells produce them.
• a monokine is generally referred to as being produced and secreted by a mononuclear cell, such as a macrophage and/or monocyte.
• Lymphokines are generally referred to as being produced by lymphocyte cells.
• cytokines include, but are not limited to, Interleukin-1 (IL-1), Interleukin-6 (IL-6), Interleukin-8 (IL-8), Tumor Necrosis Factor-alpha (TNF- ⁇ ) and Tumor Necrosis Factor beta (TNF- ⁇ ).
• chemokine refers to any secreted polypeptide that affects the functions of cells and is a molecule which modulates interactions between cells in the immune, inflammatory or hematopoietic response, similar to the term “cytokine” above.
• a chemokine is primarily secreted through cell transmembranes and causes chemotaxis and activation of specific white blood cells and leukocytes, neutrophils, monocytes, macrophages, T-cells, B-cells, endothelial cells and smooth muscle cells.
• chemokines include, but are not limited to IL-8, GRO- ⁇ , GRO- ⁇ , GRO- ⁇ , NAP-2, ENA-78, IP-10, MIP-1 ⁇ , MIP- ⁇ , PF4, and MCP 1, 2, and 3.
• a compound of Formula (I) or a pharmaceutically acceptable salt thereof in therapy it will normally be formulated into a pharmaceutical composition in accordance with standard pharmaceutical practice.
• This invention also relates to a pharmaceutical composition comprising an effective, non-toxic amount of a compound of Formula (I) and a pharmaceutically acceptable carrier or diluent.
• Compounds of Formula (I), pharmaceutically acceptable salts thereof and pharmaceutical compositions incorporating such may conveniently be administered by any of the routes conventionally used for drug administration, for instance, orally, topically, parenterally or by inhalation.
• the compounds of Formula (I) may be administered in conventional dosage forms prepared by combining a compound of Formula (I) with standard pharmaceutical carriers according to conventional procedures.
• the compounds of Formula (I) may also be administered in conventional dosages in combination with a known, second therapeutically active compound. These procedures may involve mixing, granulating and compressing or dissolving the ingredients as appropriate to the desired preparation.
• the form and character of the pharmaceutically acceptable character or diluent is dictated by the amount of active ingredient with which it is to be combined, the route of administration and other well-known variables.
• the carrier(s) must be “acceptable” in the sense of being compatible with the other ingredients of the formulation and not deleterious to the recipient thereof.
• the pharmaceutical carrier employed may be, for example, either a solid or liquid.
• solid carriers are lactose, terra alba, sucrose, talc, gelatin, agar, pectin, acacia, magnesium stearate, stearic acid and the like.
• liquid carriers are syrup, peanut oil, olive oil, water and the like.
• the carrier or diluent may include time delay material well known to the art, such as glyceryl mono-stearate or glyceryl distearate alone or with a wax.
• the preparation can be tableted, placed in a hard gelatin capsule in powder or pellet form or in the form of a troche or lozenge.
• the amount of solid carrier will vary widely but preferably will be from about 25 mg to about 1 g.
• the preparation will be in the form of a syrup, emulsion, soft gelatin capsule, sterile injectable liquid such as an ampule or nonaqueous liquid suspension.
• Compounds of Formula (I) may be administered topically, that is by non-systemic administration. This includes the application of a compound of Formula (I) externally to the epidermis or the buccal cavity and the instillation of such a compound into the ear, eye and nose, such that the compound does not significantly enter the blood stream.
• systemic administration refers to oral, intravenous, intraperitoneal and intramuscular administration.
• Formulations suitable for topical administration include liquid or semi-liquid preparations suitable for penetration through the skin to the site of inflammation such as liniments, lotions, creams, ointments or pastes, and drops suitable for administration to the eye, ear or nose.
• the active ingredient may comprise, for topical administration, from 0.001% to 10% w/w, for instance from 1% to 2% by weight of the Formulation. It may however comprise as much as 10% w/w but preferably will comprise less than 5% w/w, more preferably from 0.1% to 1% w/w of the Formulation.
• Lotions according to the present invention include those suitable for application to the skin or eye.
• An eye lotion may comprise a sterile aqueous solution optionally containing a bactericide and may be prepared by methods similar to those for the preparation of drops.
• Lotions or liniments for application to the skin may also include an agent to hasten drying and to cool the skin, such as an alcohol or acetone, and/or a moisturizer such as glycerol or an oil such as castor oil or arachis oil.
• Creams, ointments or pastes according to the present invention are semi-solid formulations of the active ingredient for external application. They may be made by mixing the active ingredient in finely-divided or powdered form, alone or in solution or suspension in an aqueous or non-aqueous fluid, with the aid of suitable machinery, with a greasy or non-greasy base.
• the base may comprise hydrocarbons such as hard, soft or liquid paraffin, glycerol, beeswax, a metallic soap; a mucilage; an oil of natural origin such as almond, corn, arachis, castor or olive oil; wool fat or its derivatives or a fatty acid such as steric or oleic acid together with an alcohol such as propylene glycol or a macrogel.
• the formulation may incorporate any suitable surface active agent such as an anionic, cationic or non-ionic surfactant such as a sorbitan ester or a polyoxyethylene derivative thereof.
• Suspending agents such as natural gums, cellulose derivatives or inorganic materials such as silicaceous silicas, and other ingredients such as lanolin, may also be included.
• Drops according to the present invention may comprise sterile aqueous or oily solutions or suspensions and may be prepared by dissolving the active ingredient in a suitable aqueous solution of a bactericidal and/or fungicidal agent and/or any other suitable preservative, and preferably including a surface active agent.
• the resulting solution may then be clarified by filtration, transferred to a suitable container which is then sealed and sterilized by autoclaving or maintaining at 98-100° C. for half an hour.
• the solution may be sterilized by filtration and transferred to the container by an aseptic technique.
• bactericidal and fungicidal agents suitable for inclusion in the drops are phenylmercuric nitrate or acetate (0.002%), benzalkonium chloride (0.01%) and chlorhexidine acetate (0.01%).
• Suitable solvents for the preparation of an oily solution include glycerol, diluted alcohol and propylene glycol.
• Compounds of Formula (I) may be administered parenterally, that is by intravenous, intramuscular, subcutaneous intranasal, intrarectal, intravaginal or intraperitoneal administration.
• the subcutaneous and intramuscular forms of parenteral administration are generally preferred.
• Appropriate dosage forms for such administration may be prepared by conventional techniques.
• Compounds of Formula (I) may also be administered by inhalation, that is by intranasal and oral inhalation administration.
• Appropriate dosage forms for such administration such as an aerosol formulation or a metered dose inhaler, may be prepared by conventional techniques.
• the daily oral dosage regimen will preferably be from about 0.01 to about 80 mg/kg of total body weight.
• the daily parenteral dosage regimen about 0.001 to about 80 mg/kg of total body weight.
• the daily topical dosage regimen will preferably be from 0.1 mg to 150 mg, administered one to four, preferably two or three times daily.
• the daily inhalation dosage regimen will preferably be from about 0.01 mg/kg to about 1 mg/kg per day.
• the optimal quantity and spacing of individual dosages of a compound of Formula (I) or a pharmaceutically acceptable salt thereof will be determined by the nature and extent of the condition being treated, the form, route and site of administration, and the particular patient being treated, and that such optimums can be determined by conventional techniques. It will also be appreciated by one of skill in the art that the optimal course of treatment, i.e., the number of doses of a compound of Formula (I) or a pharmaceutically acceptable salt thereof given per day for a defined number of days, can be ascertained by those skilled in the art using conventional course of treatment determination tests.
• the compound and pharmaceutical formulations according to the invention may be used in combination with or include one or more other therapeutic agents, for example selected from anti-inflammatory agents, anticholinergic agents (particularly an M 1 /M 2 /M 3 receptor antagonist), ⁇ 2 -adrenoreceptor agonists, antiinfective agents, such as antibiotics, antivirals, or antihistamines.
• other therapeutic agents for example selected from anti-inflammatory agents, anticholinergic agents (particularly an M 1 /M 2 /M 3 receptor antagonist), ⁇ 2 -adrenoreceptor agonists, antiinfective agents, such as antibiotics, antivirals, or antihistamines.
• the invention thus provides, in a further aspect, a combination comprising a compound of Formula (I) or a pharmaceutically acceptable salt, solvate or physiologically functional derivative thereof together with one or more other therapeutically active agents, for example selected from an anti-inflammatory agent, such as a corticosteroid or an NSAID, an anticholinergic agent, a ⁇ 2 -adrenoreceptor agonist, an antiinfective agent, such as an antibiotic or an antiviral, or an antihistamine.
• an anti-inflammatory agent such as a corticosteroid or an NSAID
• an anticholinergic agent such as a corticosteroid or an NSAID
• an anticholinergic agent such as a ⁇ 2 -adrenoreceptor agonist
• an antiinfective agent such as an antibiotic or an antiviral, or an antihistamine.
• One embodiment of the invention encompasses combinations comprising a compound of Formula (I) or a pharmaceutically acceptable salt, solvate or physiologically functional derivative thereof together with a ⁇ 2 -adrenoreceptor agonist, and/or an anticholinergic, and/or a PDE-4 inhibitor, and/or an antihistamine.
• the other therapeutic ingredient(s) may be used in the form of salts, for example as alkali metal or amine salts or as acid addition salts, or prodrugs, or as esters, for example lower alkyl esters, or as solvates, for example hydrates to optimise the activity and/or stability and/or physical characteristics, such as solubility, of the therapeutic ingredient. It will be clear also that, where appropriate, the therapeutic ingredients may be used in optically pure form.
• the invention encompasses a combination comprising a compound of the invention together with a ⁇ 2 -adrenoreceptor agonist.
• ⁇ 2 -adrenoreceptor agonists include salmeterol (which may be a racemate or a single enantiomer such as the R-enantiomer), salbutamol (which may be a racemate or a single enantiomer such as the R-enantiomer), formoterol (which may be a racemate or a single diastereomer such as the R,R-diastereomer), salmefamol, fenoterol, carmoterol, etanterol, naminterol, clenbuterol, pirbuterol, flerbuterol, reproterol, bambuterol, indacaterol, terbutaline and salts thereof, for example the xinafoate (1-hydroxy-2-naphthalenecarboxylate) salt
• the ⁇ 2 -adrenoreceptor agonists are long-acting ⁇ 2 -adrenoreceptor agonists, for example, compounds which provide effective bronchodilation for about 12 hours or longer.
• Other ⁇ 2 -adrenoreceptor agonists include those described in WO2002/066422, WO2002/070490, WO2002/076933, WO2003/024439, WO2003/072539, WO2003/091204, WO2004/016578, WO2004/022547, WO2004/037807, WO2004/037773, WO2004/037768, WO2004/039762, WO2004/039766, WO2001/42193 and WO2003/042160.
• ⁇ 2 -adrenoreceptor agonists include:
• the ⁇ 2 -adrenoreceptor agonist may be in the form of a salt formed with a pharmaceutically acceptable acid selected from sulphuric, hydrochloric, fumaric, hydroxynaphthoic (for example 1- or 3-hydroxy-2-naphthoic), cinnamic, substituted cinnamic, triphenylacetic, sulphamic, sulphanilic, naphthaleneacrylic, benzoic, 4-methoxybenzoic, 2- or 4-hydroxybenzoic, 4-chlorobenzoic and 4-phenylbenzoic acid.
• a pharmaceutically acceptable acid selected from sulphuric, hydrochloric, fumaric, hydroxynaphthoic (for example 1- or 3-hydroxy-2-naphthoic), cinnamic, substituted cinnamic, triphenylacetic, sulphamic, sulphanilic, naphthaleneacrylic, benzoic, 4-
• Suitable anti-inflammatory agents include corticosteroids.
• corticosteroids which may be used in combination with the compounds of the invention are those oral and inhaled corticosteroids and their pro-drugs which have anti-inflammatory activity.
• Examples include methyl prednisolone, prednisolone, dexamethasone, fluticasone propionate, 6 ⁇ ,9 ⁇ -difluoro-11 ⁇ -hydroxy-16 ⁇ -methyl-17 ⁇ -[(4-methyl-1,3-thiazole-5-carbonyl)oxy]-3-oxo-androsta-1,4-diene-17 ⁇ -carbothioic acid S-fluoromethyl ester, 6 ⁇ ,9 ⁇ -difluoro-17 ⁇ -[(2-furanylcarbonyl)oxy]-11 ⁇ -hydroxy-16 ⁇ -methyl-3-oxo-androsta-1,4-diene-17 ⁇ -carbothioic acid S-fluoromethyl ester (fluticasone furoate), 6 ⁇ ,9 ⁇ -difluoro-11 ⁇ -hydroxy-16 ⁇ -methyl-3-oxo-17 ⁇ -propionyloxy-androsta-1,4-diene-17 ⁇ -carbothioic acid S-(2-oxo-tetrahydro-furan-3S-y
• corticosteroids include fluticasone propionate, 6 ⁇ ,9 ⁇ -difluoro-11 ⁇ -hydroxy-16 ⁇ -methyl-17 ⁇ -[(4-methyl-1,3-thiazole-5-carbonyl)oxy]-3-oxo-androsta-1,4-diene-17 ⁇ -carbothioic acid S-fluoromethyl ester, 6 ⁇ ,9 ⁇ -difluoro-17 ⁇ -[(2-furanylcarbonyl)oxy]-11 ⁇ -hydroxy-16 ⁇ -methyl-3-oxo-androsta-1,4-diene-17 ⁇ -carbothioic acid S-fluoromethyl ester, 6 ⁇ ,9 ⁇ -difluoro-11 ⁇ -hydroxy-16 ⁇ -methyl-3-oxo-17 ⁇ -(2,2,3,3-tetramethycyclopropylcarbonyl)oxy-androsta-1,4-diene-17 ⁇ -carbothioic acid S-cyanomethyl ester and 6 ⁇ ,9 ⁇ -difluoro-11 ⁇ -hydroxy-16 ⁇ -methyl-17 ⁇ -
• the corticosteroid is 6 ⁇ ,9 ⁇ -difluoro-17 ⁇ -[(2-furanylcarbonyl)oxy]-11 ⁇ -hydroxy-16 ⁇ -methyl-3-oxo-androsta-1,4-diene-17 ⁇ -carbothioic acid S-fluoromethyl ester.
• corticosteroids examples include those described in WO2002/088167, WO2002/100879, WO2002/12265, WO2002/12266, WO2005/005451, WO2005/005452, WO2006/072599 and WO2006/072600.
• Non-steroidal compounds having glucocorticoid agonism that may possess selectivity for transrepression over transactivation and that may be useful in combination therapy include those covered in the following published patent applications and patents: WO2003/082827, WO1998/54159, WO2004/005229, WO2004/009017, WO2004/018429, WO2003/104195, WO2003/082787, WO2003/082280, WO2003/059899, WO2003/101932, WO2002/02565, WO2001/16128, WO2000/66590, WO2003/086294, WO2004/026248, WO2003/061651, WO2003/08277, WO2006/000401, WO2006/000398 and WO2006/015870.
• Non-steroidal compounds having glucocorticoid agonism that may possess selectivity for transrepression over transactivation and that may be useful in combination therapy include those covered in the following patents: WO2003/082827, WO1998/54159, WO2004/005229, WO2004/009017, WO2004/018429, WO2003/104195, WO2003/082787, WO2003/082280, WO2003/059899, WO2003/101932, WO2002/02565, WO2001/16128, WO2000/66590, WO2003/086294, WO2004/026248, WO2003/061651 and WO2003/08277.
• anti-inflammatory agents include non-steroidal anti-inflammatory drugs (NSAID's).
• NSAID's non-steroidal anti-inflammatory drugs
• NSAID's examples include sodium cromoglycate, nedocromil sodium, phosphodiesterase (PDE) inhibitors (for example, theophylline, PDE4 inhibitors or mixed PDE3/PDE4 inhibitors), leukotriene antagonists, inhibitors of leukotriene synthesis (for example montelukast), iNOS inhibitors, tryptase and elastase inhibitors, beta-2 integrin antagonists and adenosine receptor agonists or antagonists (e.g.
• the invention encompasses iNOS (inducible nitric oxide synthase) inhibitors for oral administration.
• iNOS inhibitors include those disclosed in WO1993/13055, WO1998/30537, WO2002/50021, WO1995/34534 and WO1999/62875.
• CCR3 inhibitors include those disclosed in WO2002/26722.
• the invention provides the use of the compounds of Formula (I) in combination with a phosphodiesterase 4 (PDE4) inhibitor, for example in the case of a formulation adapted for inhalation.
• PDE4 inhibitor useful in this aspect of the invention may be any compound that is known to or which is discovered to act as a PDE4 inhibitor, e.g. as an inhibitor of PDE4B and/or PDE4D.
• PDE4 inhibitory compounds include cis-4-cyano-4-(3-cyclopentyloxy-4-methoxyphenyl)cyclohexan-1-carboxylic acid, 2-carbomethoxy-4-cyano-4-(3-cyclopropylmethoxy-4-difluoromethoxyphenyl)cyclohexan-1-one and cis-[4-cyano-4-(3-cyclopropylmethoxy-4-difluoromethoxyphenyl)cyclohexan-1-ol].
• cis-4-cyano-4-[3-(cyclopentyloxy)-4-methoxyphenyl]cyclohexane-1-carboxylic acid also known as cilomilast
• salts, esters, pro-drugs or physical forms which is described in U.S. Pat. No. 5,552,438, issued 3 Sep., 1996.
• PDE4 inhibitory compounds include AWD-12-281 (N-(3,5-dichloro-4-pyridinyl)-1-[4-fluorophenyl)methyl]-5-hydroxy- ⁇ -oxo-1H-indol-3-acetamide) from Elbion (Hofgen, N. et al. 15th EFMC Int Symp Med Chem (September 6-10, Edinburgh) 1998, Abst P.98; CAS reference No.
• a phthalazinone (WO1999/47505) from Byk-Gulden; Pumafentrine, ( ⁇ )-p-[(4aR*,10bS*)-9-ethoxy-1,2,3,4,4a,10b-hexahydro-8-methoxy-2-methylbenzo[c][1,6]naphthyridin-6-yl]-N,N-diisopropylbenzamide which is a mixed PDE3/PDE4 inhibitor which has been prepared and published on by Byk-Gulden, now Altana; arofylline under development by Almirall-Prodesfarma; VM554/UM565 from Vernalis; or T-440 (Tanabe Seiyaku; Fuji, K. et al. J Pharmacol Exp Ther, 1998, 284(1): 162), and T2585.
• PDE4 inhibitory compounds are disclosed in the published international patent applications WO2004/024728, WO2004/056823, WO2004/103998 (e.g. Example 399 or 544 disclosed therein), WO2005/058892, WO2005/090348, WO2005/090353, and WO2005/090354, all in the name of Glaxo Group Limited.
• anticholinergic agents are those compounds that act as antagonists at the muscarinic receptors, in particular those compounds which are antagonists of the M 1 or M 3 receptors, dual antagonists of the M 1 /M 3 or M 2 /M 3 , receptors or pan-antagonists of the M 1 /M 2 /M 3 receptors.
• exemplary compounds for administration via inhalation include ipratropium (for example, as the bromide, CAS 22254-24-6, sold under the name Atrovent), oxitropium (for example, as the bromide, CAS 30286-75-0) and tiotropium (for example, as the bromide, CAS 136310-93-5, sold under the name Spiriva).
• revatropate for example, as the hydrobromide, CAS 262586-79-8) and LAS-34273 which is disclosed in WO2001/04118.
• Exemplary compounds for oral administration include pirenzepine (CAS 28797-61-7), darifenacin (CAS 133099-04-4, or CAS 133099-07-7 for the hydrobromide sold under the name Enablex), oxybutynin (CAS 5633-20-5, sold under the name Ditropan), terodiline (CAS 15793-40-5), tolterodine (CAS 124937-51-5, or CAS 124937-52-6 for the tartrate, sold under the name Detrol), otilonium (for example, as the bromide, CAS 26095-59-0, sold under the name Spasmomen), trospium chloride (CAS 10405-02-4) and solifenacin (CAS 242478-37-1, or CAS 242478-38-2 for the succinate also known as YM
• anticholinergic agents include compounds which are disclosed in U.S. patent application 60/487,981, incorporated herein in its entirety by reference. These include, for example:
• the invention provides a combination comprising a compound of Formula (I) or a pharmaceutically acceptable salt thereof together with an H1 antagonist.
• H1 antagonists include, without limitation, amelexanox, astemizole, azatadine, azelastine, acrivastine, brompheniramine, cetirizine, levocetirizine, efletirizine, chlorpheniramine, clemastine, cyclizine, carebastine, cyproheptadine, carbinoxamine, descarboethoxyloratadine, doxylamine, dimethindene, ebastine, epinastine, efletirizine, fexofenadine, hydroxyzine, ketotifen, loratadine, levocabastine, mizolastine, mequitazine, mianserin, noberastine, meclizine, norastemizole, olopatad
• the invention provides a combination comprising a compound of Formula (I), or a pharmaceutically acceptable salt thereof together with an H3 antagonist (and/or inverse agonist).
• H3 antagonists include, for example, those compounds disclosed in WO2004/035556 and in WO2006/045416.
• Other histamine receptor antagonists which may be used in combination with the compounds of the present invention include antagonists (and/or inverse agonists) of the H4 receptor, for example, the compounds disclosed in Jablonowski et al., J. Med. Chem. 46:3957-3960 (2003).
• the invention provides a combination comprising a compound of Formula (I) or a pharmaceutically acceptable salt thereof together with a CCR5 receptor antagonist, such as 4,4-difluoro-N-((1S)-3- ⁇ 3-[3-methyl-5-(1-methylethyl)-4H-1,2,4-triazol-4-yl]-8-azabicyclo[3.2.1]oct-8-yl ⁇ -1-phenylpropyl)cyclohexanecarboxamide:
• a CCR5 receptor antagonist such as 4,4-difluoro-N-((1S)-3- ⁇ 3-[3-methyl-5-(1-methylethyl)-4H-1,2,4-triazol-4-yl]-8-azabicyclo[3.2.1]oct-8-yl ⁇ -1-phenylpropyl)cyclohexanecarboxamide:
• the invention provides a combination comprising a compound of Formula (I) or a pharmaceutically acceptable salt thereof together with a CXCR3 receptor antagonist such as N-((1R)-1- ⁇ 3-[4-(ethyloxy)phenyl]-4-oxo-3,4-dihydropyrido[2,3-d]pyrimidin-2-yl ⁇ ethyl)-N-(3-pyridinylmethyl)-2- ⁇ 4-[(trifluoromethyl)oxy]phenyl ⁇ acetamide:
• a CXCR3 receptor antagonist such as N-((1R)-1- ⁇ 3-[4-(ethyloxy)phenyl]-4-oxo-3,4-dihydropyrido[2,3-d]pyrimidin-2-yl ⁇ ethyl)-N-(3-pyridinylmethyl)-2- ⁇ 4-[(trifluoromethyl)oxy]phenyl ⁇ acetamide:
• the invention thus provides, in a further aspect, a combination comprising a compound of Formula (I) and/or a pharmaceutically acceptable salt, solvate or physiologically functional derivative thereof together with a PDE4 inhibitor.
• the invention thus provides, in a further aspect, a combination comprising a compound of Formula (I) and/or a pharmaceutically acceptable salt, solvate or physiologically functional derivative thereof together with a ⁇ 2 -adrenoreceptor agonist.
• the invention thus provides, in a further aspect, a combination comprising a compound of Formula (I) and/or a pharmaceutically acceptable salt, solvate or physiologically functional derivative thereof together with a corticosteroid.
• the invention thus provides, in a further aspect, a combination comprising a compound of Formula (I) and/or a pharmaceutically acceptable salt, solvate or physiologically functional derivative thereof together with a non-steroidal GR agonist.
• the invention thus provides, in a further aspect, a combination comprising a compound of Formula (I) and/or a pharmaceutically acceptable salt, solvate or physiologically functional derivative thereof together with an anticholinergic.
• the invention thus provides, in a further aspect, a combination comprising a compound of Formula (I) and/or a pharmaceutically acceptable salt, solvate or physiologically functional derivative thereof together with an antihistamine.
• the invention thus provides, in a further aspect, a combination comprising a compound of Formula (I) and/or a pharmaceutically acceptable salt, solvate or physiologically functional derivative thereof together with a PDE4 inhibitor and a ⁇ 2 -adrenoreceptor agonist.
• the invention thus provides, in a further aspect, a combination comprising a compound of Formula (I) and/or a pharmaceutically acceptable salt, solvate or physiologically functional derivative thereof together with an anticholinergic and a PDE-4 inhibitor.
• compositions comprising a combination as defined above together with a pharmaceutically acceptable diluent or carrier represent a further aspect of the invention.
• the individual compounds of such combinations may be administered either sequentially or simultaneously in separate or combined pharmaceutical formulations.
• the individual compounds will be administered simultaneously in a combined pharmaceutical formulation.
• Appropriate doses of known therapeutic agents will readily be appreciated by those skilled in the art.
• the invention thus provides, in a further aspect, a pharmaceutical composition comprising a combination of a compound of the invention together with another therapeutically active agent.
• the invention thus provides, in a further aspect, a pharmaceutical composition comprising a combination of a compound of the invention together with a PDE4 inhibitor.
• the invention thus provides, in a further aspect, a pharmaceutical composition comprising a combination of a compound of the invention together with a 2-adrenoreceptor agonist.
• the invention thus provides, in a further aspect, a pharmaceutical composition comprising a combination of a compound of the invention together with a corticosteroid.
• the invention thus provides, in a further aspect, a pharmaceutical composition comprising a combination of a compound of the invention together with a non-steroidal GR agonist.
• the invention thus provides, in a further aspect, a pharmaceutical composition comprising a combination of a compound of the invention together with an anticholinergic.
• the invention thus provides, in a further aspect, a pharmaceutical composition
• a pharmaceutical composition comprising a combination of a compound of the invention together with an antihistamine.
• the invention thus provides, in a further aspect, a pharmaceutical composition comprising a combination of a compound of the invention together with CXCR3 receptor antagonist.
• the invention thus provides, in a further aspect, a pharmaceutical combination of the invention together with a CCR5 receptor antagonist.
• IL-8, and GRO- ⁇ chemokine inhibitory effects of compounds of the present invention are determined by the following in vitro assay:
• IL-8 human recombinant
• CXCR1 IL-8 type ⁇
• CXCR2 IL-8 type ⁇ receptors
• IL-8 binding was conducted using Scintillation Proximity Assays (SPA) using wheatgerm agglutinin beads in a 96-well plate format.
• Membranes CHO-CXCR1 or CHO-CXCR2 were preincubated with the beads in the binding buffer for 30 min. for 4° C.
• Buffer contained 20 mM Bis-Trispropane buffer, pH 8.0, containing 1 mM MgSO 4 , 0.1 mM EDTA and 25 mM NaCl.
• Compounds were diluted in DMSO at 20 ⁇ the final dilution (final compound concentration between 1 nM and 30 uM and final DMSO concentration of 5%).
• Assay was performed in 96-well plates (optiplate 96, Packard) at room temperature, in 0.1 ml binding buffer with membranes and 0.04% CHAPS (3-[(3-cholamidopropyl) dimethylammonio]-1-propanesulfonate), 0.0025% BSA and 0.23 nM [ 125 I] IL-8.
• IL-8 R ⁇ , CXCR1 or Type I, receptor is also referred to herein as the non-permissive receptor and the recombinant IL-8 R ⁇ , CXCR2 or Type II, receptor is referred to as the permissive receptor.
• the in vitro inhibitory properties of these compounds were determined in a neutrophil chemotaxis assay.
• Primary human neutrophils were isolated from peripheral whole blood using percoll discontinuous gradient centrifugation, dextran sedimentation and hypotonic lysis.
• the chemoattractants IL-8 (CXCL8) or GRO- ⁇ (CXCL1) were placed in the bottom chamber of a 96 multi-well chamber (ChemoTx System, Neuro Probe, Gaithersburg, Md.).
• the agonist concentration used was an EC80 concentration.
• the two chambers are separated by a 5 um polycarbonate membrane. When compounds of this invention were tested, they were preincubated with the cells prior to placement on the top of the filter.
• Chemotaxis was allowed to proceed for 45 minutes in a humidified incubator at 37° C. with 5% CO 2 . At the end of the incubation period, the membrane was removed and the migrated cells in the bottom chamber were transferred to a 96-well plate. These cells were measured using a luminescent cell viability assay (Celltiter-Glo, Promega, Madison, Wis.). Each sample was tested in duplicate and each compound repeated at least three times. Positive control cells were cells without compound added and represent the maximum chemotactic response. The negative control (unstimulated) was with no chemokine added to the bottom chamber. The difference between the positive control and the negative control represents the chemotactic activity of the cells.
• Examples 1 to 3 were tested in this assay. A compound would be considered active if IC 50 values were ⁇ 5 uM.
• the compounds indicated were tested for their ability to inhibit the GRO ⁇ -induced expression of the integrin CD11b on neutrophils in human whole blood.
• Blood was drawn (9 ml) using a butterfly line and a 10 ml syringe containing 0.2 ml of working Sodium Heparin. The blood was kept at 37° C. until placed on ice in step 5 below. Compound stock solutions were then diluted to 12 times the maximum final concentration, 120 uM. Half Log serial dilutions were then performed in vehicle. Ten microliters of the compound dilutions or vehicle were then added to the appropriate 12 ⁇ 75 polypropylene tubes. One hundred microliters of whole blood was added per tube and incubated for 10 minutes, in a 37° C. water bath with initial (gentle) agitation and again at 5 minutes.
• the GRO ⁇ stock was diluted 1:166.66 in 0.1% BSA-DPBS to “12 ⁇ ” concentration of 120 nM and 10 ul of the GRO ⁇ dilution or 0.1% BSA-DPBS was added to the appropriate tubes so that the final GRO ⁇ concentration equaled 10 nM.
• the tubes were incubated for 10 min at 37° C. with gentle hand agitation and again at 5 minutes. Samples were then placed on ice and 250 ul of ice cold CellFix working dilution was added followed by a one minute incubation on ice. 1.5 ml Eppendorf tubes were readied during GRO ⁇ incubation by adding the appropriate antibodies.
• Examples 1-3, 12, 17, 18, 23 and 26 exhibited positive inhibitory activity in this assay at IC 50 values of ⁇ 5 uM, and would be considered active.
• Compounds of Examples 1-3, 12, 17, 18, 23 and 26 tested in the above assay had an IC 50 value from about 2 uM to about 0.5 uM.
• CHO-K1 cells stably expressing CXCR2 and G ⁇ 16 were grown to 80% confluency in DMEM/F12 (HAM's) 1:1, w/ 10% FCS (heat inactivated), w/ 2 mM L-glutamine, w/ 0.4 mg/ml G418 while maintained at 37° C. in a 5% CO 2 incubator. Twenty four hours previous to assay, cells were harvested and plated, 40,000 cells per well, in a 96 well, black wall, clear bottom plate (Packard View) and returned to CO 2 incubator. On the day of assay, compounds were serially diluted in 100% DMSO to 300 ⁇ the desired assay concentration.
• Growth media is aspirated off cells and replaced with 100 ul of load media (EMEM with Earl's salts w/ L-Glutamine, 0.1% BSA, (Bovuminar Cohen Fraction V from Seriologicals Corp.), 4 uM Fluo-4-acetoxymethyl ester fluorescent indicator dye (Fluo-4 AM, from Molecular Probes), and 2.5 mM probenecid) and incubated for 1 hour at 37° C. in CO 2 incubator.
• Load media was aspirated and replaced with 100 uL of EMEM with Earl's salts w/ L-Glutamine, 0.1% gelatin, and 2.5 mM probenecid and incubated for an additional 10 min.
• KRH (100 ul) w/ 2.5 mM probenecid with 0.1% gelatin was added to wells then 50 ul of 3 ⁇ compound in KRH w/ 2.5 mM probenecid and 0.1% gelatin was added to wells (compound now at 1 ⁇ ) and incubated at 37° C. in CO 2 incubator for 10 min. Plates were placed onto FLIPR (Fluorometric Imaging Plate Reader, Molecular Devices, Sunnyvale Calif.) for analysis as described previously (Sarau et al., 1999). The percent of maximal human IL-8 induced Ca 2+ mobilization induced by 1.0 nM IL-8, an EC 80 conc.
• Examples 1-38 exhibited positive inhibitory activity in this assay at IC 50 values of ⁇ 10 uM and would be considered active.
• Compounds 1-38 tested by the above assay had an IC 50 from about 600 nM to about 5 nM.

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