WO2001045709A1

WO2001045709A1 - Substituted piperazine and piperidine calcium channel blockers

Info

Publication number: WO2001045709A1
Application number: PCT/CA2000/001557
Authority: WO
Inventors: Terrance P. Snutch
Original assignee: Neuromed Technologies, Inc.
Priority date: 1999-12-20
Filing date: 2000-12-20
Publication date: 2001-06-28
Also published as: EP1244451B1; HK1049969B; ATE333878T1; ES2269220T3; CN100477992C; JP2003518064A; KR100823889B1; BR0016530A; US6387897B1; AU2495601A; US20030045530A1; EP1244451A1; DE60029634D1; AU784206B2; IL150117A0; CN1411374A; DE60029634T2; KR20020075874A; PT1244451E; NO323724B1

Abstract

Compounds of formula (1) and their salts, wherein Cy represents cyclohexyl; Y is CH=CHζ L, CHζ2, ζ or Cy, X is trivalent straight-chain alkylene (3-10C) or trivalent straight-chain 1-alkenylene (3-10C) optionally substituted by oxo at the C adjacent N when n is 0 and Y is ζ2CH; and is otherwise trivalent straight-chain alkylene (5-10C) or trivalent straight-chain 1-alkenylene (5-10C) optionally substituted by oxo at the C adjacent N; Z is N, NCO, CHNCOR1 or CHNR1, wherein R1 is alkyl (1-6C); and n is 0-5; wherein each ζ and Cy independently may optionally be substituted by alkyl (1-6C) or by halo, CF¿3?, OCF3, NO2, NR2, OR, SR, COR, COOR, CONR2, NROCR or OOCR where R is H or alkyl (1-4C), or two substituents may form a 5-7 membered ring with the proviso that the compounds of formula (1) contain at least one aromatic moiety, are useful as calcium channel blockers.

Description

SUBSTITUTED PIPERAZINE AND PIPERIDINE CALCIUM CHANNEL BLOCKERS

Technical Field

The invention relates to compounds useful in treating conditions associated with calcium channel function More specifically, the mvention concerns compounds containing substituted or unsubstituted deπvatives of 6-membered heterocychc moieties that are useful in treatment of conditions such as stroke and pain

Background Art

Native calcium channels have been classified by their electrophysiological and pharmacological properties as T, L, N, P and Q types (for reviews see McCleskey, E W et al Curr Topics Membr (1991) 39 295-326, and Dunlap, K et al Trends Neurosci (1995) 18 89- 98) T-type (or low voltage-activated) channels descπbe a broad class of molecules that transiently activate at negative potentials and are highly sensitive to changes m resting potential The L. N, P and Q-type channels activate at more positive potentials (high voltage activated) and display diverse kinetics and voltage-dependent properties There is some overlap m biophysical properties of the high voltage-activated channels, consequently pharmacological profiles are useful to further distinguish them. L-type channels are sensitive to dihydropyπdme agonists and antagonists, N-type channels are blocked by the Conus geographus peptide toxm, ω-conotoxm GVIA, and P-type channels are blocked by the peptide ω-agatoxm IVA from the venom of the funnel web spider, Agelenopsis aperta A fourth type of high voltage-activated calcium channel (Q-type) has been described, although whether the Q- and P-type channels are distinct molecular entities is controversial (Sather, W A et al Neuron (1995) 11 291-303, Stea, A et al Proc Natl Acad Sci USA (1994) 91 10576-10580, Bouπnet, E. et al Nature Neuroscience (1999) 2 407- 415) Several types of calcium conductances do not fall neatly into any of the above categoπes and there is variability of properties even within a category suggesting that additional calcium channels subtypes remain to be classified

Biochemical analyses show that neuronal high voltage activated calcium channels are heteroo gomeπc complexes consisting of three distinct subunits (a_t, a₂δ and β) (reviewed by De Waard, M et al Ion Channels (1997) vol 4, Narahashi, T ed. Plenum Press, NY) The αi subumt is the major pore-forming subunit and contains the voltage sensor and binding sites for calcium channel antagonists The mainly extracellular α₂ is disulfide-hnked to the transmembrane δ subunit and both are deπved from the same gene and are proteolytically cleaved in vivo The β subumt is a nonglycosylated, hydrophihc protein with a high affinity of binding to a cytoplasmic region of the at subunit. A fourth subumt, γ, is unique to L-type calcium channels expressed in skeletal muscle T-tubules. The isolation and characterization of γ-subunit-encoding cDNAs is described in U.S. Patent No. 5,386,025 which is incorporated herein by reference. Recently, each of these at subtypes has been cloned and expressed, thus permitting more extensive pharmacological studies. These channels have been designated αι_A-αn and α_ts and correlated with the subtypes set forth above. αt_A channels are of the P/Q type; a_te represents N; a_te, ci'i_D, Q.1F and αι_S represent L; αι_E represents a novel type of calcium conductance, and αi_G-c-u represent members of the T-type family, reviewed in Stea, A. et al. in Handbook of Receptors and Channels (1994), North, R.A. ed. CRC Press; Perez-Reyes, et al. Nature (1998) 391 :896-900; Cribbs, L.L. et al. Circulation Research (1998) 83:103-109; Lee, J.H. et al. Journal of euroscience (1999) 19:1912-1921.

Further details concerning the function of N-type channels, which are mainly localized to neurons, have been disclosed, for example, in U.S. Patent No. 5,623,051, the disclosure of which is incorporated herein by reference. As described, N-type channels possess a site for binding syntaxin, a protein anchored in the presynaptic membrane. Blocking this interaction also blocks the presynaptic response to calcium influx. Thus, compounds that block the interaction between syntaxin and this binding site would be useful in neural protection and analgesia. Such compounds have the added advantage of enhanced specificity for presynaptic calcium channel effects.

U.S. Patent No. 5,646,149 describes calcium channel antagonists of the formula A-Y-B wherein B contains a piperazine or piperidine ring directly linked to Y. An essential component of these molecules is represented by A, which must be an antioxidant; the piperazine or piperidine itself is said to be important. The exemplified compounds contain a benzhydril substituent, based on known calcium channel blockers (see below). U.S. Patent No. 5,703,071 discloses compounds said to be useful in treating ischemic diseases. A mandatory portion of the molecule is a tropolone residue; among the substituents permitted are piperazine derivatives, including their benzhydril derivatives. U.S. Patent No. 5,428,038 discloses compounds which are said to exert a neural protective and antiallergic effect. These compounds are coumarin derivatives which may include derivatives of piperazine and other six-membered heterocycles. A permitted substituent on the heterocycle is diphenylhydroxymefhyl. Thus, approaches in the art for various indications which may involve calcium channel blocking activity have employed compounds which incidentally contain piperidine or piperazine moieties substituted with benzhydril but mandate additional substituents to maintain functionality.

Certain compounds containing both benzhydril moieties and piperidine or piperazine are known to be calcium channel antagonists and neuroleptic drugs. For example, Gould, R.J. et al. Proc Natl Acad Sci USA (1983) 80:5122-5125 describes antischizophrenic neuroleptic drugs such as lidoflazine, fluspirilene, pimozide, clopimozide, and penfluridol. It has also been shown that fluspirilene binds to sites on L-type calcium channels (King, V.K. et al. J Biol Chem (1989) 264:5633-5641) as well as blocking N-type calcium current (Grantham, CJ. et al. BritJ Pharmacol (1944) 111 :483-488). In addition, Lomerizine, as developed by Kanebo KK, is a known calcium channel blocker; Lomerizine is, however, not specific for N-type channels. A review of publications concerning Lomerizine is found in Dooley, D., Current Opinion in CPNS Investigational Drugs ( 1999) 1 :116-125.

The present invention is based on the recognition that the combination of a six- membered heterocyclic ring containing at least one nitrogen said nitrogen coupled through a linker to a benzhydril moiety results in effective calcium channel blocking activity. In some cases enhanced specificity for N-type channels, or decreased specificity for L-type channels is shown. The compounds are useful for treating stroke and pain and other calcium channel- associated disorders, as further described below. By focusing on these moieties, compounds useful in treating indications associated with calcium channel activity are prepared.

Disclosure of the Invention

The invention relates to compounds useful in treating conditions such as stroke, head trauma, migraine, chronic, neuropathic and acute pain, epilepsy, hypertension, cardiac arrhythmias, and other indications associated with calcium metabolism, including synaptic calcium channel-mediated functions. The compounds of the invention are benzhydril or partly saturated benzhydril derivatives of piperidine or piperazine with substituents which enhance the calcium channel blocking activity of the compounds. Thus, in one aspect, the invention is directed to therapeutic methods that employ compounds of the formula

wherein Cy represents cyclohexyl;

Y is CH=CH , CHΦ₂, Φ or Cy, X is trivalent straight-chain alkylene (3- IOC) or trivalent straight-chain 1-alkenylene (3 -IOC) optionally substituted by oxo at the C adjacent N when n is 0 and Y is Φ CH; and is otherwise trivalent straight-chain alkylene (5- IOC) or trivalent straight-chain 1-alkenylene (5- 10C) optionally substituted by oxo at the C adjacent N; Z is N, NCO, CHNCOR¹ or CHNR¹, wherein R¹ is alkyl (1-6C); and n is 0-5; wherein each Φ and Cy independently may optionally be substituted by alkyl (1-6C) or by halo, CF₃, OCF₃, NO₂, NR₂, OR, SR, COR, COOR, CON ₂, NROCR or OOCR where R is H or alkyl (1-4C), or two substituents may form a 5-7 membered ring with the proviso that the compounds of formula ( 1 ) contain at least one aromatic moiety.

The invention is directed to methods to antagonize calcium channel activity using the compounds of formula (1) and thus to treat associated conditions. It will be noted that the conditions may be associated with abnormal calcium channel activity, or the subject may have normal calcium channel function which nevertheless results in an undesirable physical or metabolic state. In another aspect, the invention is directed to pharmaceutical compositions containing these compounds.

The invention is also directed to combinatorial libraries containing the compounds of formula (1) and to methods to screen these libraries for members containing particularly potent calcium channel blocking activity or for members that antagonize one type of such channels specifically.

Brief Description of the Drawings

Figure 1 shows a comparison of certain preferred embodiments of the compounds of the invention to the known compound Lomerizine. Figure 2 is a graphic representation of the specificity of the compounds shown in

Figure 1 with respect to N-type, L-type and P/Q-type channels.

Figure 3 is a graphic representation of the data shown in Figure 2 based on IC₅o values calculated from the data shown in Figure 2.

Figure 4 shows the effects of MC-34D, 39-1-B4 and 39-45-3 in a hyperalgesia model. Figure 5 shows the effects of MC-34D, 39- 1 -B4 and 39-45-3 in an allodynia model. Modes of Carrying out the Invention

The compounds of formula (1), useful in the methods of the invention, exert their desirable effects through their ability to antagonize the activity of calcium channels. This makes them useful for treatment of certain conditions. Among such conditions are stroke, epilepsy, head trauma, migraine and chronic, neuropathic and acute pain. Calcium flux is also implicated in other neurological disorders such as schizophrenia, anxiety, depression, other psychoses, and certain degenerative disorders. Other treatable conditions include cardiovascular conditions such as hypertension and cardiac arrhythmias.

While the compounds of formula (1) generally have this activity, the availability of a multiplicity of calcium channel blockers permits a nuanced selection of compounds for particular disorders. Thus, the availability of this class of compounds provides not only a genus of general utility in indications that are affected by excessive calcium channel activity, but also provides a large number of compounds which can be mined and manipulated for specific interaction with particular forms of calcium channels. The availability of recombmantly produced calcium channels of the αι_A-αu and αis types set forth above, facilitates this selection process. Dubel, S.J. et al. Proc Natl Acad Sci USA (1992) 89:5058-5062; Fujita, Y. et al. Neuron (1993) 10:585-598; Mikami, A. et al. Nature (1989) 340:230-233; Mori, Y. et al Nature (1991 ) 350:398-402; Snutch, T.P. et al. Neuron (1991 ) 7:45-57; Soong, T. W. et al. Science (1993) 260: 1133-1 136; Tomlinson, W.J. et al Neuropharmacology (1993) 32:11 17-1 126; Williams, M.E. et al Neuron (1992) 8:71 -84; Williams, M.E. et al Science (1992) 257:389-395; Perez-Reyes, et al. Nature (1998) 391:896-900; Cribbs, L.L. et al. Circulation Research (1998) 83: 103-109; Lee, J.H. et al. Journal of Neuroscience (1999) 19: 1912-1921.

Thus, while it is known that calcium channel activity is involved in a multiplicity of disorders, the types of channels associated with particular conditions is the subject of ongoing data collection. For example, the association of N-type channels in conditions associated with neural transmission would indicate that compounds of the invention which target N-type receptors are most useful in these conditions. Many of the members of the genus of compounds of formula (1) exhibit high affinity for N-type channels; other members of the genus may preferentially target other channels. There are two distinguishable types of calcium channel inhibition. The first, designated

"open channel blockage," is conveniently demonstrated when displayed calcium channels are maintained at an artificially negative resting potential of about -100 mV (as distinguished from the typical endogenous resting maintained potential of about -70 mV). When the displayed channels are abruptly depolarized under these conditions, calcium ions are caused to flow through the channel and exhibit a peak current flow which then decays. Open channel blocking inhibitors diminish the current exhibited at the peak flow and can also accelerate the rate of current decay.

This type of inhibition is distinguished from a second type of block, referred to herein as "inactivation inhibition." When maintained at less negative resting potentials, such as the physiologically important potential of -70 mV, a certain percentage of the channels may undergo conformational change, rendering them incapable of being activated — i.e., opened — by the abrupt depolarization. Thus, the peak current due to calcium ion flow will be diminished not because the open channel is blocked, but because some of the channels are unavailable for opening (inactivated). "Inactivation" type inhibitors increase the percentage of receptors that are in an inactived state. Synthesis

The compounds of the invention may be synthesized using conventional methods. Illustrative of such methods are Schemes 1 and 2:

Scheme 1 fZ is N)

Alternatively, a carboxylic acid containing the benzhydril (or ΦCyCH or Cy₂CH) moiety can first be synthesized and then reacted with the piperazine (or piperidine) moiety and subsequently reduced. To synthesize the desired acid, an ω-bromo carboxylic acid is refluxed with, in the case of benzhydril, triphenylphosphine in the presence of methyl nitrile and then treated with lithium hexamethyldisilazide in a solvent such as THF. The resulting unsaturated carboxylic acid containing the two phenyl substituents is then reduced as shown in Scheme 1 with hydrogen on a palladium catalyst and then reacted with derivatized piperazine (or piperidine) to form the amide. The amide can then be reduced as shown above.

Scheme 2 (Z is CHNR')

Φ₂CH — CHj- CH₂-N r ) NHCH₂Y

Preferred Embodiments

The compounds of formula (1) are defined as shown in terms of the embodiments of their various substituents:

Particularly preferred embodiments of the compounds of formula (1) are those wherein

X is coupled to two phenyl groups. Less preferred are instances where X is coupled to one phenyl and one cyclohexyl. Least preferred are those instances wherein X is coupled to two cyclohexyl groups. As defined above, X may be a trivalent straight-chain alkylene of 5- 10C optionally substituted with oxo at the position adjacent the piperidine or piperazine ring nitrogen.

Preferably, the alkylene chain is 5-8C, more preferably 5-7C, and even more preferably 5-6C.

Substitution with oxo is preferred only when the length of the alkylene chain is 6- IOC. In addition, X may be a straight-chain 1-alkenylene (5- IOC) wherein the τ-bond is in the position distal to the piperidine or pyrimidine ring nitrogen. Under these circumstances, the two cyclic moieties are accommodated by the alkenylene chain by virtue of the alkenylene chain as a vinyl substituent to each cyclic moiety. In addition, when n is 0 and Y is Φ CH, the embodiment of X described above may also be shorter and may contain 3- IOC. Preferred embodiments of Z are N, NCO and CHNR¹ where R¹ is preferably H but may also be alkyl (1-6C), preferably 1-4C, more preferably 1-2C, and even more preferably methyl (or H).

Preferred embodiments for n are 0-4, more preferably 1-2.

Any of the phenyl or cyclohexyl moieties contained in the compounds of formula (1) may be substituted, as noted above. Preferred substituents include halo, especially fluoro, NO , alkyl (1-6C), preferably methyl, OR, preferably methoxy, NR₂, preferably dimethylamino, diethylamino, methylamino or ethylamino, acetamido, CF₃, OCF₃ and the like. Two substituted positions may also form a ring. Preferably, where the cyclic moieties coupled to X are both phenyl, the phenyl groups are identically substituted. Where one such moiety is phenyl and the other is cyclohexyl, the presence of a substituent on the phenyl moiety and an unsubstituted cyclohexyl moiety are preferred. It is believed that halogenation of the compounds of the invention is helpful in modulating the in vivo half-fife, and it may be particularly advantageous to include halogen substituents, such as fluoro substitutions on any phenyl moieties.

Particularly preferred are compounds MC-34D, JM-G-10, 39-1-B4, and 39-45-3 shown in Figure 1 and variously substituted forms thereof.

Thus, also preferred are forms of these enumerated compounds which contain different substituents on the phenyl or cyclohexyl moieties from those shown. Thus, also preferred are compounds having the general formula of MC-34D wherein the two phenyl moieties attached to X contain fluoro in the para position. Alternative substitutions are as shown below where Φ 1 and Φ2 indicate the 2 phenyl groups attached to X (the numbers being arbitrarily chosen as these phenyl groups are equivalent) and Φ3 represents phenyl group contained in Y. In addition, also preferred are embodiments as set forth herein where Z of MC-34D is NCO or wherein X is - CH(CH₂)-₅.

Φl Φ2 Φ3

2, 4 - dimethyl 2, 4, dimethyl 4 - F

4 - methoxy 3 - chloro 4 - methyl

2, 4, 6 trimethyl 2, 4, 6 trimethyl — amino ammo 4-F 4-F 4-F 4-F 4-F 4 - methoxy 4-F 4-F 3, 4 - OCH₂O-

Similarly, JM-G-10 with substituents on the phenyl groups and cyclohexyl group may be employed in the methods of the invention, preferred embodiments also include those wherein X is -CH(CH₂)-5. Suitable substitutions are shown below:

Φl Φ2 Cy

4-F 4-F

2, 4 - dimethoxy 4 - methyl 3,5- diethyl

3, 5 - diamino 3; 5 - diamino 4-F

Alternatively substituted compounds of formula 39-1-B4 are also included within the preferred embodiments of the invention. In the table below, Φ 1 and Φ2 represent the two equivalent phenyl groups coupled to X and Φ3 and Φ4 represent the two equivalent phenyl groups included in Y. Forms of 39-1-B4 wherein the carbonyl group in X is reduced to methylene are also preferred, including those with the substituents shown below.

Φl Φ2 Φ3 Φ4

4-F 4-F

3, 4-CH₂ CH₂ CH₂- 3, 4 -CH₂ CH₂ CH₂- 4-F 4-F

2, 6 - dimethoxy 3, 5, diamino 3, 5, diamino 2, 6, dimethoxy

4 - COOH 4 - COOH 3, 5 dichloro 3,5- dichloro

Similarly, various alternative substitution patterns on compound 39-45-3 may be employed. Included are those embodiments where a carbonyl is present adjacent the piperazine in the substituent X. Also included are analogs where n = 0. Particularly preferred are embodiments where two substituents on the phenyl group contained in Y form a ring, particularly a 5 -membered ring. Thus, preferred substitution patterns are those set forth below where Φl and Φ2 represent the two equivalent phenyl groups attached to X and Φ3 represents the phenyl group contained in Y.

Φl Φ2 Φ3

4-F 4-F 3, 4, 5 - trimethoxy

4-F 4-F 3, 4, -CH₂ CH₂ -CH₂-

4-F 4-F 3, 4, 5 - tri trifluro-methyl

4-F 4-F 3, 4, -OCH₂O-

2, 4, 6 trimethoxy — 4-F

3, 5 - diethoxy 3,5- diethoxy 3, 5 - diethoxy

4-F 4-F 3, 5-detrifluoromethyl

4-F 4-F 5 - OCF₃

4-f 4-F 3, 4 dimethyl

4-F 4-F 3 - methoxy

4-F 4-F 4-F

4-F 4-F 3 - methyl

4-F 4-F 2 - methoxy

4-F 4-F 4 - acetyl

The pattern of substitution will influence the strength of calcium channel blocking ability as well as specificity.

Where the structure permits, invention compounds may also be supplied as pharmaceutically acceptable salts. Pharmaceutically acceptable salts include the acid addition salts which can be formed from inorganic acids such as hydrochloric, sulfliric, and phosphoric acid or from organic acids such as acetic, propionic, glutamic, glutaric, as well as acid ion- exchange resins.

Libraries and Screening

The compounds of the invention can be synthesized individually using methods known in the art per se, or as members of a combinatorial library. Synthesis of combinatorial libraries is now commonplace in the art. Suitable descriptions of such syntheses are found, for example, in Wentworth, Jr., P. et al. Current Opinion in Biol (1993) 9:109-115; Salemme, F.R. et al Structure (1997) 5:319-324. The libraries contain compounds with various substitutents and various degrees of unsaturation, as well as different chain lengths. The libraries, which contain, as few as 10, but typically several hundred members to several thousand members, may then be screened for compounds which are particularly effective against a specific subtype of calcium channel, i.e., the N-type channel. In addition, using standard screening protocols, the libraries may be screened for compounds which block additional channels or receptors such as sodium channels, potassium channels and the like. Methods of performing these screening functions are well known in the art. Typically, the receptor to be targeted is expressed at the surface of a recombinant host cell such as human embryonic kidney cells. The ability of the members of the library to bind the channel to be tested is measured, for example, by the ability of the compound in the library to displace a labeled binding ligand such as the ligand normally associated with the channel or an antibody to the channel. More typically, ability to antagonize the receptor is measured in the presence of calcium ion and the ability of the compound to interfere with the signal generated is measured using standard techniques.

In more detail, one method involves the binding of radiolabeled agents that interact with the calcium channel and subsequent analysis of equilibrium binding measurements including, but not limited to, on rates, off rates, K values and competitive binding by other molecules. Another method involves the screening for the effects of compounds by electrophysiological assay whereby individual cells are impaled with a microelectrode and currents through the calcium channel are recorded before and after application of the compound of interest. Another method, high-throughput spectrophotometric assay, utilizes loading of the cell lines with a fluorescent dye sensitive to intracellular calcium concentration and subsequent examination of the effects of compounds on the ability of depolarization by potassium chloride or other means to alter intracellular calcium levels.

As described above, a more definitive assay can be used to distinguish inhibitors of calcium flow which operate as open channel blockers, as opposed to those that operate by promoting inactivation of the channel. The methods to distinguish these types of inhibition are more particularly described in the examples below. In general, open-channel blockers are assessed by measuring the level of peak current when depolarization is imposed on a background resting potential of about -100 mV in the presence and absence of the candidate compound. Successful open-channel blockers will reduce the peak current observed and may accelerate the decay of this current. Compounds that are inactivated channel blockers are generally determined by their ability to shift the voltage dependence of inactivation towards more negative potentials. This is also reflected in their ability to reduce peak currents at more depolarized holding potentials (e.g., -70 mV) and at higher frequencies of stimulation, e.g., 0.2 Hz vs. 0.03 Hz.

Utility and Administration

For use as treatment of human and animal subjects, the compounds of the invention can be formulated as pharmaceutical or veterinary compositions. Depending on the subject to be treated, the mode of administration, and the type of treatment desired -- e.g., prevention, prophylaxis, therapy; the compounds are formulated in ways consonant with these parameters. A summary of such techniques is found in Remington's Pharmaceutical Sciences, latest edition, Mack Publishing Co., Easton, PA, incorporated herein by reference. In general, for use in treatment, the compounds of formula (1) may be used alone, as mixtures of two or more compounds of formula (1) or in combination with other pharmaceuticals. Depending on the mode of administration, the compounds will be formulated into suitable compositions to permit facile delivery.

Formulations may be prepared in a manner suitable for systemic administration or topical or local administration. Systemic formulations include those designed for injection (e.g., intramuscular, intravenous or subcutaneous injection) or may be prepared for transdermal, transmucosal, or oral administration. The formulation will generally include a diluent as well as, in some cases, adjuvants, buffers, preservatives and the like. The compounds can be administered also in liposomal compositions or as microemulsions. For injection, formulations can be prepared in conventional forms as liquid solutions or suspensions or as solid forms suitable for solution or suspension in liquid prior to injection or as emulsions. Suitable excipients include, for example, water, saline, dextrose, glycerol and the like. Such compositions may also contain amounts of nontoxic auxiliary substances such as wetting or emulsifying agents, pH buffering agents and the like, such as, for example, sodium acetate, sorbitan monolaurate, and so forth.

Various sustained release systems for drugs have also been devised. See, for example, U.S. Patent No. 5,624,677. Systemic administration may also include relatively noninvasive methods such as the use of suppositories, transdermal patches, transmucosal delivery and intranasal administration. Oral administration is also suitable for compounds of the invention. Suitable forms include syrups, capsules, tablets, as in understood in the art. For administration to animal or human subjects, the dosage of the compounds of the invention is typically 0.1-15 mg/kg, preferably 0.1-1 mg/kg. However, dosage levels are highly dependent on the nature of the condition, the condition of the patient, the judgment of the practitioner, and the frequency and mode of administration.

The following examples are intended to illustrate but not to limit the invention.

Example 1 Assessment of Calcium Channel Blocking Activity Antagonist activity was measured using whole cell patch recordings on human embryonic kidney cells either stably or transiently expressing rat αi_B+α_2b+β_tb channels (N-type channels) with 5 mM barium as a charge carrier.

For transient expression, host cells, such as human embryonic kidney cells, HEK 293 (ATCC# CRL 1573) were grown in standard DMEM medium supplemented with 2 mM glutamine and 10% fetal bovine serum. HEK 293 cells were transfected by a standard calcium- phosphate-DNA coprecipitation method using the rat α_tB + β_lb + α₂δ N-type calcium channel subunits in a vertebrate expression vector (for example, see Current Protocols in Molecular Biology).

After an incubation period of from 24 to 72 hrs the culture medium was removed and replaced with external recording solution (see below). Whole cell patch clamp experiments were performed using an Axopatch 200B amplifier (Axon Instruments, Burlingame, CA) linked to an IBM compatible personal computer equipped with pCLAMP software. Borosilicate glass patch pipettes (Sutter Instrument Co., Novato, CA) were polished (Microforge, Narishige, Japan) to a resistance of about 4 MΩ when filled with cesium methanesulfonate internal solution (composition in MM: 109 CsCH₃SO₄, 4 MgCl₂, 9 EGTA, 9 HEPES, pH 7.2). Cells were bathed in 5 mM Ba^"^ (in mM: 5 BaCl₂, 1 MgCl₂, 10 HEPES, 40 tetraethylammonium chloride,

10 glucose, 87.5 CsCl pH 7.2). Current data shown were elicited by a train of 100 ms test pulses at 0.066 Hz from -100 mV and/or -80 mV to various potentials (min. -20 mV, max. +30 mV). Drugs were perfused directly into the vicinity of the cells using a microperfusion system. Normalized dose-response curves were fit (Sigmaplot 4.0, SPSS Inc., Chicago, IL) by the Hill equation to determine IC₅₀ values. Steady-state inactivation curves were plotted as the normalized test pulse amplitude following 5 s inactivating prepulses at +10 mV increments. Inactivation curves were fit (Sigmaplot 4.0) with the Boltzman equation, Ip_eak (norτnalized)=l/(l+exp((V-V_h)z/25.6)), where V and V), are the conditioning and half inactivation potentials, respectively, and z is the slope factor.

Example 2 Synthesis of Illustrative Compounds of Formula (1) A. Synthesis of 6,6-Diphenyl Hexanoic Acid. 6-Bromohexanoic acid (7.08g, 36.3 mmole) and triphenylphosphine (lOg, 38.2 mmole) were mixed in dry CH₃CN (40 ml), heated to reflux overnight and allowed to cool to RT. The solution was concentrated under reduced pressure to give a viscous gel. Approximately 75 ml of THF was added to the reaction mixture and the walls of the flask were scratched with a spatula to start crystallization. The resulting solid was filtered under vacuum, washed with THF and dried under reduced pressure and used without further purification.

This product (1.5g) was suspended in dry THF (10ml) and the flask purged with N₂ and cooled to -78°C. To the stirred reaction was added lithium hexamethyldisilazide (LiHMDS) (10ml, IM in THF). The yellow solution was stirred at -78°C for lh over which time the reaction darkened slightly. The cooling bath was removed and the reaction allowed to warm to RT. The reaction was kept at RT for lh during which time the solution turned a dark red color and most of the solids went into solution. Benzophenone (0.54g in 3ml THF) was added to the reaction and allowed to react overnight. The yellow solution was concentrated under reduced pressure to give a yellow solid. The resulting solid was partitioned between ether and 10% HCI. The organic layer was washed with water (2x) and extracted with 10% NaOH (3x). The combined aqueous base fraction was acidified with cone. HCI to a pH of 4. The water layer was extracted with ether (3x) and the combined organic fractions dried over Na₂SO₄.

The ether was evaporated to dryness under reduced pressure to give a colorless oil which crystallized on standing to give a waxy solid, 6,6-diphenyl hex-5-enoic acid, which was dissolved in 30ml MeOH and mixed with 5% Pd-C and placed in a Parr hydrogenator. The reaction vessel was purged with hydrogen and pressurized to 60 PSIG and reacted at RT for 4h. The reaction mixture was sampled and analyzed by TLC. If the TLC when stained with KMnO showed a positive test for alkenes the reaction mixture was resubjected to the reaction conditions. The solution was then filtered through a plug of celite and the methanol filtrate containing 6,6-diphenyl hexanoic acid was concentrated under vacuum.

B. Reaction with Substituted Piperazine.

6,6-Diphenylhexanoic acid (0.4 mmoles) was mixed with the desired substituted piperazine (0.35 mmoles) in dry THF (7ml). EDC (0.5 mmoles) and DMAP (cat) were added and the mixture heated to 40°C with shaking overnight. The reaction was diluted with ethyl acetate and washed with water (4x) and 10% NaOH (3x) and dried over sodium sulfate and evaporated to dryness. The resulting residue was purified by column chromatography (silica gel, 1 :1 hexane:EtOAc), and the products were characterized by HPLC-MS. Piperazines used in the foregoing procedure include phenylpiperazine, benzylpiperazine, benzhydrilpiperazine, and piperazine substituted at the 1 -position with Φ-CH=CH₂-.

The resulting compounds contain a carbonyl adjacent to the ring nitrogen of piperazine. These compounds are of formula (1) and exhibit calcium channel blocking activity.

C. Reduction of CO. The compounds prepared in paragraph B were dissolved in dry THF (5ml) and reacted with LiAlH (IM in THF) and allowed to react for 6h. The reactions were quenched with EtOAc (15ml) and extracted with water (5x) 10% NaOH (lOx), brine (lx), dried over sodium sulfate and concentrated under reduced pressure. Most of the products at this stage were >80% pure. Those <80% were purified for running a short column (silica gel, 1 : 1 hex:EtOAc).

Example 3 Preparation of Compounds of Formula (1) from Benzhydrilpiperazine Derivatives N-(Diphenylmethyl)piperazine (0.5 mmole) was dissolved in dry THF (10ml). To each reaction flask was added powdered K₂CO₃ and acid chloride of the formula Y-CO-C1 (0.7 mmole). The reaction was stirred at RT for 2h and quenched with 105 NaOH (10ml) and extracted with EtOAc (10ml). The organic layer was washed with 10% NaOH (4x) and dried over sodium sulfate, concentrated, and purified by column chromatography (silica gel, 1 : 1 hex:EtOAc) to give the desired amide. Acyl halides used in this procedure included cyclohexyl COC1, ΦCOC1 and ΦCH=CHCOCl. To reduce the resulting amide, the above product was dissolved in dry THF (5ml) and reacted with LiAlFU (IM in THF) and allowed to react for 6h. The reaction was quenched with EtOAc (15ml) and extracted with water (5x) 10% NaOH (lOx), brine (lx), dried over sodium sulfate and concentrated under reduced pressure. Most of the products at this stage were >80% pure. Those <80% were purified for running a short column (silica gel, 1 :1 hex:EtOAc).

Example 4 Channel Blocking Activities of Various Invention Compounds Using the procedure set forth in Example 1, , various compounds of the invention were tested for their ability to block N-type calcium channels. The results are shown in the table below where IC₅₀ is given in μM (micromolar).

Example 5 Additional Methods The methods of Examples 1 and 2 were followed with slight modifications as will be apparent from the description below. A. Transformation of HEK cells:

N-type calcium channel blocking activity was assayed in human embryonic kidney cells, HEK 293, stably transfected with the rat brain N-type calcium channel subunits (αι_B + o^ +β _b cDNA subunits). Alternatively, N-type calcium channels (α_]B + α₂₅ +β_\b cDNA subunits), L- type channels (c-ic + ct2& + β\b cDNA subunits) and P/Q-type channels (a_]A + α_2δ +3_lb cDNA subunits) were transiently expressed in HEK 293 cells. Briefly, cells were cultured in

Dulbecco's modified eagle medium (DMEM) supplemented with 10% fetal bovine serum, 200 U/ml penicillin and 0.2 mg/ml streptomycin at 37°C with 5% CO₂. At 85% confluency cells were split with 0.25% trypsin/1 mM EDTA and plated at 10% confluency on glass coverslips. At 12 hours the medium was replaced and the cells transiently transfected using a standard calcium phosphate protocol and the appropriate calcium channel cDNAs. Fresh DMEM was supplied and the cells transferred to 28°C/5% CO₂. Cells were incubated for 1 to 2 days to whole cell recording.

B. Measurement of Inhibition:

Whole cell patch clamp experiments were performed using an Axopatch 200B amplifier (Axon Instruments, Burlingame, CA) linked to a personal computer equipped with pCLAMP software. The external and internal recording solutions contained, respectively, 5 mM BaCl₂, 1 mM MgCl₂, 10 mM HEPES, 40 mM TEAC1, 10 mM glucose, 87.5 mM CsCl (pH 7.2) and 108 mM CsMS, 4 mM MgCl₂, 9 mM EGTA, 9 mM HEPES (pH 7.2). Currents were typically elicited from a holding potential of -80 mV to +10 mV using Clampex software (Axon Instruments). Typically, currents were first elicited with low frequency stimulation (0.03 Hz) and allowed to stabilize prior to application of the compounds. The compounds were then applied during the low frequency pulse trains for two to three minutes to assess tonic block, and subsequently the pulse frequency was increased to 0.2 Hz to assess frequency dependent block. Data were analyzed using Clampfit (Axon Instruments) and SigmaPlot 4.0 (Jandel Scientific). Specific data obtained for N-type channels are shown in Table 1 below. As indicated by the data in Table 1, the most potent inhibitors at higher frequencies were MC-34D, JM-G-10, 39-1-B4 and 39-45-3 shown in Figure 1. However, all of the compounds tested appeared to be reasonably good blockers at this frequency. Table 1

Tables 2 and 3 show the results of similar experiments conducted with P/Q-type and L-type channels expressed in HEK 293 cells. In general, the IC₅₀ values for MC-34D, JM-G-10, 39-1-B4 and 39-45-3 were higher than those exhibited with respect to N-type channels.

Table 2

Table 3

These data are summarized in Table 4 which show the ratio of IC₅₀ values for P:N and L:N channels. As shown, with respect to specificity for L-type channels in particular, the four compounds mentioned above show much higher affinity for N-type and P/Q-type versus L-type channels.

Table 4

These results are shown graphically in Figures 2 and 3.

Example 5 In Vivo Pain Model

To test the effects of the compounds of the invention on neuropathic pain, a spinal nerve ligation was performed in young adult male rats (~ 300 gm). Under anesthesia adjacent spinal nerves arising from the lumbar spinal cord (L5, L6) of the rat were tightly ligated just distal to the dorsal root ganglia and then allowed to recover from the surgery (S.H. Kim and J.M. Chung, Pain (1992) 50: 355-363). For intrathecal administration, animals were placed under anesthesia and implanted with a spinal catheter essentially as described by Yaksh, T.L. and Rudy, T.A., Physiol Behav. (1976) 17: 1031-1036). After surgery the rats were returned to their cages and allowed to recover. During the recovery period animals subjected to the L5/L6 ligation developed heat hyperalgesia and tactile allodynia in the hind foot innervated by the injured nerves.

Test compounds dissolved in either 10% DMSO (39-45-3) or 100% DMSO (MC-34D and 39-1-B4) were delivered through the implanted catheter in a dose volume of 5 ul followed by a 10 ul saline flush. Each drug was tested at three concentrations and five to six rats were studied per group. To test for thermal stimulation (hyperalgesia), rats were placed in a Plexiglass box upon an elevated glass floor and allowed free to habituate for 10 minutes. An infrared radiant source is focused under the non-lesioned and lesioned hindpaws and the paw-withdrawal latencies were recorded. In order to prevent tissue damage, if no reaction was noted, the test was terminated after 45 seconds. For the tactile stimulation (allodynia), the tip of an electronic Von Frey probe was applied to the non-lesioned and lesioned hindpaws and the force required to induce paw- withdrawal recorded. This procedure was carried out 3 times and the mean force per paw calculated to provide basic scores per animal.

As shown in Figures 4 and 5, all three compounds exhibit significant anti-hyperalgesia and anti-allodynia effects in rat models for neuropathic pain. Figure 4 shows the results for the hyperalgesia model. With a 21 second cut-off, 39-45-3 exhibited a 100% anti-hyperalgesic effect at 30 minutes with 100 ug of drug and a 95% maximal effect at 30 ug of drug delivered. At 30 minutes MC-34D exhibited a 100% anti-hyperalgesic effect with 100 ug of drug and a 98% maximal effect at 30 ug of drug delivered. At 30 minutes 39-1-B4 exhibited a 96% anti-hyperalgesic effect at 30 minutes with 100 ug of drug and a 55% maximal effect at 30 ug of drug delivered. Overall, 39-45-3 exhibited an A50 response = 7.98 ug/animal; MC-34D exhibited an A50 response = 3.05 ug/animal; and 39-1-B4 exhibited an A50 response = 6.95 ug/animal.

Figure 5 shows the results for the allodynia model. Compound 39-45-3 exhibited a maximal 52% anti-allodynic effect at 10 minutes with 100 ug of drug and a 37% maximal effect at 30 minutes with 30 ug of drug delivered. At 10 minutes MC-34D exhibited a maximal 62% anti-allodynic effect with 100 ug of drug and a 57% maximal effect at 60 minutes with 30 ug of drug delivered. At 30 minutes 39-1-B4 exhibited a 50% anti-allodynic effect with 100 ug of drug and a 46% maximal effect at 60 minutes with 30 ug of drug delivered. Overall, 39-45-3 exhibited an A50 response = 104 ug/animal; MC-34D exhibited an A50 response = 60 ug/animal; and 39-1-B4 exhibited an A50 response = 70 ug/animal.

Claims

1. A method to treat conditions associated with calcium channel activity in a subject which method comprises administering to a subject in need of such treatment a compound of the formula

or the salts thereof, wherein Cy represents cyclohexyl;

Y is CH=CHΦ, CHΦ₂, Φ or Cy, X is trivalent straight-chain alkylene (3- 10C) or trivalent straight-chain 1-alkenylene

(3-10C) optionally substituted by oxo at the C adjacent N when n is 0 and Y is Φ₂CH; and is otherwise trivalent straight-chain alkylene (5- 10C) or trivalent straight-chain 1-alkenylene (5- 10C) optionally substituted by oxo at the C adjacent N;

Z is N, NCO, CHNCOR¹ or CHNR¹, wherein R¹ is H or alkyl (1-6C); and n is 0-5; wherein each Φ and Cy independently may optionally be substituted by alkyl (1-6C) or by halo, CF₃, OCF₃, NO₂, NR₂, OR, SR, COR, COOR, CONR₂, NROCR or OOCR where R is H or alkyl (1-4C), or two substituents may form a 5-7 membered ring with the proviso that the compounds of formula (1) contain at least one aromatic moiety.

The method of claim 1 wherein the compound of formula (1) is of the formula

wherein X, Y, Z and n are as defined, and each Φ may optionally be substituted as set forth, in claim 1.

3. The method of claim 2 wherein Y is CH=CHΦ.

4. The method of claim 3 wherein X is CH(CH₂)_mCO or CH(CH₂)_m+t wherein m is 4-10.

5. The method of claim 4 wherein m is 4.

6. The method of claim 3 wherein Z is N and n is 1-3.

7. The method of claim 6 wherein the compound of formula ( 1 ) is MC-34D or a substituted form thereof.

8. The method of claim 2 wherein Y is Cy.

9. The method of claim 8 wherein X is CH(CH₂)_mCO or CH(CH₂)_m+ι wherein m is 4-10.

10. The method of claim 9 wherein m is 4.

11. The method of claim 8 wherein Z is CHNH and n is i.

12. The method of claim 11 wherein the compound of formula ( 1 ) is JM-G- 10 or a substituted form thereof.

13. The method of claim 2 wherein Y is Φ₂CH.

14. The method of claim 13 wherein X is CH(CH₂)ιCO or CH(CH₂)ι₊₁, wherein 1 is 1-10.

15. The method of claim 14 wherein 1 is 1.

16. The method of claim 13 wherein Z is N.

17. The method of claim 16 wherein the compound of formula (1) is 39-1-B4 or a substituted form thereof.

18. The method of claim 2 wherein n is 0 or 1 and Y is Φ.

19. The method of claim 18 wherein X is CH(CH₂)_m+ , or CH(CH₂)_mCO wherein m is 4-10.

20. The method of claim 19 wherein m is 4.

21. The method of claim 20 wherein the compound of formula ( 1 ) is compound 39-45-3 or a differently substituted or unsubstituted form thereof.

22. A pharmaceutical composition for use in treating conditions characterized by calcium channel activity which composition comprises, in admixture with a pharmaceutically acceptable excipient, a dosage amount of at least one compound of the formula

or salts thereof, wherein Cy represents cyclohexyl; Y is CH=CHΦ, CHΦ₂, Φ or Cy,

X is trivalent straight-chain alkylene (3- 10C) or trivalent straight-chain 1-alkenylene (3-10C) optionally substituted by oxo at the C adjacent N when n is 0 and Y is Φ₂CH; and is otherwise trivalent straight-chain alkylene (5- 10C) or trivalent straight-chain 1-alkenylene (5- 10C) optionally substituted by oxo at the C adjacent N; Z is N, NCO, CHNCOR¹ or CHNR¹, wherein R¹ is H or alkyl (1-6C); and n is 0-5; wherein each Φ and Cy independently may optionally be substituted by alkyl (1-6C) or by halo, CF₃, OCF₃,NO₂, NR₂, OR, SR, COR, COOR, CONR₂, NROCR or OOCR where R is H or alkyl (1-4C), or two substituents may form a 5-7 membered ring with the proviso that the compounds of formula (1) contain at least one aromatic moiety.

23. The composition of claim 22 wherein the compound of formula (1) is of the formula

wherein X, Y, Z and n are as defined in claim 1.

24. A compound of the formula

wherein Y is CH=CHΦ, Φ or Cy, wherein each Φ and Cy independently may optionally be substituted by alkyl (1-6C) or by halo, CF₃, OCF₃, NO₂, NR₂, OR, SR, COR, COOR, CONR₂, NROCR or OOCR where R is H or alkyl (1-4C), or two substituents may form a 5-7 membered ring; n is 0-5; and

Z is N or CHNR¹, wherein R¹ is alkyl (1-6C); wherein X is CH(CH₂)_mCO or CH(CH₂)_m+t wherein m is 4-10.

25. The compound of claim 24 wherein Y is CH=CHΦ.

26. The compound of claim 25 wherein m is 4.

27. The compound of claim 24 wherein Z is N and n is 1-3.

28. The compound of claim 27 which is MC-34D or a substituted form thereof.

29. The compound of claim 28 which is MC-34D.

30. The compound of claim 24 wherein Y is Cy.

31. The compound of claim 30 wherein m is 4.

32. The compound of claim 30 wherein Z is CH₂NH and n is 1.

33. The compound of claim 32 which is JM-G-10 or a substituted form thereof.

34. The compound of claim 33 which is JM-G-10.

35. The compound of claim 24 where n is 0 or 1 and Y is Φ.

36. The compound of claim 35 wherein m is 4.

37. The compound of claim 36 which is compound 39-45-3 or a differently substituted or unsubstituted form thereof.

38. The compound of claim 37 which is 39-45-3.