BACKGROUND OF THE INVENTION AP-1 is a transcriptionally active protein heterodimer containing members of the Fos (e. g. c- Fos, FosB, Fra-1, Fra-2) and the Jun (e. g. c-Jun, JunB, JunD) family of proteins. The AP-1 transcription factors are stimulated by e. g. growth factors, cytokines, T cell activators and neurotransmitters and act as dimers binding to DNA in many promoters including proteases and cytokines like IL-2. C-Jun and c-Fos knock-out mice have been produced showing embryonic lethality and osteopetrosis/lymphopenia/behavioural abnormalities, respectively (Johnson et al., 1992). These results emphasise that the AP-1 site is pivotal in many different genes and points out lymphocyte regulation and behaviour, regulation in the central nervous system, as two distinct biological hotspots. Therefore, immune suppression with low capa- bility to produce IL-2 and behavioural disorders are two very different medical indication areas where AP-1 activity is suboptimal and where AP-1 enhancers can be applied.

In US Patent No. 3,177,252 some substituted benzamide derivatives including metoclopra- mide (The Merck Index 12th Ed., entry 6226) are disclosed as being useful for the treatment of emesis.

The compound metoclopramide may be associated with depression and, because of its central as well as peripheral dopamine-blocking properties, may cause most unwanted tardive dys- kinesia. Structure-activity relationship studies have demonstrated the link between the diaminoethylene bridge and the dopamine-D2 blockade.

In GB 1,174,956 quaternary ammonium salts of N-substituted benzamide derivatives and their action to accelerate the automatic motility of digestive tract are disclosed.

In J. Org. Chem. USSR 22,578-582 (1986), the synthesis ofN- (3-dimethylamino-propyl)-3- nitro-4-acetylaminobenzamide is described.

In US Patent No. 4,568,685 some N-[(lH-1, 2,4-triazol-1-yl) alkyl] arylamides are disclosed as being inhibitors of thromboxane synthetase enzyme.

In US Patent No. 4,568,687 some N- [w (lH-imidazole-1-yl) alkyl] arylamides are disclosed as being inhibitors of thromboxane synthetase enzyme and are also useful in the treatment of hypertension and myocardial ischemia.

In Analytical Profiles of Drug Substances vol. 4, K Florey, Ed. (Academic Press, New York, 1975) pp 333-383, procainamide (The Merck Index 12th Ed., entry 7936) is described as an antiarrhytmic agent.

We have now discovered a novel method of stimulating the transcription factor AP-1 using substituted benzamides.

SUMMARY OF THE INVENTION Immune suppression in cancer. autoimmune disease and infectious disease Immune system-based approaches for the treatment of malignant disease have focused on cytolytic effector cells such as cytotoxic T lymphocytes (CTL), and natural killer (NK) cells. It has also been demonstrated that tumour-bearing mice can be cured using a wide variety of approaches, some of which involve IL-2 mediated enhancement of CTL and NK cell activity.

However, the apparent success in mice stands in contrast to the current situation in the clinic, wherein only a minority of patients have thus far benefited from CTL-or NK cell-based anti- tumour approaches. This is probably a result from tumour-induced immune suppression (Whiteside, 1999 ; Kiessling et al., 1999). One of the underlying causes of tumour-associated immune suppression of CTL and NK cell activity, the intracellular signalling deficiency resulting from reduction of the TCR/CD3 zeta chain expression of the T cells, is also shared with HIV infection, leprosy, and rheumatoid arthritis. This signalling deficiency is overrun by IL-2 treatment in vitro. IL-2 is a central cytokine in the development of functional immune responses and it has been clearly shown that the AP-1 site of the IL-2 promoter is pivotal for optimal activity (Sundstedt and Dohlsten, 1998). Distinct benzamides would therefore represent an alternative treatment for immune stimulation and IL-2 enhancement in immune suppressive states of disease. In addition, several treatment regiments such as cytostatic and radiation therapy applied in the treatment of cancer result in unwanted immune suppression, an induced state that would be compensated for by administering compounds of the present invention.

Manic-depressive illness Lithium and sodium valproate (VPA) (The Merck Index 12th Ed., entry 10049) are effective in the treatment of bipolar disorders (manic-depressive illness) and may function through the regulation of signal transduction pathways and transcription factors such as c-Fos and c-Jun, which in turn results to changes in gene expression. The long-term efficacy of lithium and VPA in bipolar disorders suggests that the regulation of gene expression may be an important target for these drugs. These two structurally highly dissimilar agents, lithium and VPA, increase AP-1 DNA binding activity in areas of rodent brain ex vivo and in human neuronal cells in culture (Yuan et al., 1998; Chen et al., 1999). Both treatments also increase the expression of a reporter gene driven by an AP-1-containing promoter, and mutations in the AP-1 sites of the reporter gene promoter markedly attenuate these effects. Both treatments also increase the expression of several endogenous proteins, which genes are known to be regulated by AP-1. These effects suggest that the temporal regulation of AP-1 mediated gene expression in critical neuronal circuits may play a role in the long-term therapeutic efficacy of lithium and VPA and point out that also other AP-1 enhancers like distinct benzamides could potentially act as modulators of e. g. manic-depressive illness.

DESCRIPTION OF THE INVENTION A primary objective of the present invention is to provide benzamide compounds which by virtue of their pharmacological profile, with high potency in experimental models and low level of side-effects, are considered to be of value in the treatment of disease associated with immune suppressive states e. g. for the stimulation, enhancement or modulation of the immune response. Included in the invention is also the use of the compounds for the preparation of a medicament for the stimulation of transcription factor AP-1. In a particular aspect, this invention provides preparation of a medicament for the stimulation of transcription factor AP-1, a method of treating diseases in which the disease pathology may be therapeutically modified by stimulating AP-1. Examples of such diseases are cancer, autoimmune disease and infectious disease. More particularly, the present invention relates to benzamide derivatives suitable for the treatment of, for example, solid tumours, rheumatoid arthritis (RA) and AIDS.

The compounds of the present invention are also suitable for the treatment of manic- depressive illness.

The term"treatment"as used herein includes prophylaxis as well as relieving the symptoms of disease.

It has now surprisingly been found that the compounds of general formula (I) wherein R is selected from methyl, ethyl, n-propyl, iso-propyl, c-propyl, n-butyl, sec.-butyl, iso-butyl, tert.-butyl, c-butyl, n-pentyl, sec.-pentyl, iso-pentyl, tert.-pentyl, neo-pentyl, c-pentyl, c-hexyl and c-heptyl; RNa and RNb are the same or different and selected from hydrogen, methyl and ethyl; R2, R3, R5 and R6 are independently selected from hydrogen, methyl, methoxy, thiomethyl, hydroxy, fluoro, chloro, bromo, trifluoromethyl, phenyl and benzyl; n is 1,2 or 3; R'and R"are the same or different and selected from methyl, ethyl, n-propyl, iso-propyl, n- butyl, sec.-butyl, and iso-butyl or R'and R"together form a saturated heterocyclic ring of 5-7 atoms having the formula wherein p is 1, 2,3; X is selected from CHRhetl, NRhetl and O with the proviso that p is 2 or 3 when X is NRhet and O ; Rhet, is selected from hydrogen and C1 S alkyl, optionally functionalised with OH, halogen (F, Cl and Br), CN, COORhet2, N (Rhet2) 2 wherein Rhet2 independently is selected from H, C1-4 alkyl ; with the proviso that when R'and R"are methyl then R cannot be methyl; and pharmaceutically acceptable salts, hydrates and solvates thereof; are unexpectedly effective and specific in the treatment of individuals suffering from cancer, autoimmune disease, infectious disease and manic-depressive illness.

In a preferred embodiment of the invention R is selected from methyl, ethyl, n-propyl and iso-propyl, RNa and RNb are hydrogen, one of R2, R3, R5 and R6 is selected from methyl, methoxy, thiomethyl, hydroxy, fluoro, chloro, trifluoromethyl and phenyl, R'and R"are selected from methyl, ethyl, n-propyl and n-butyl with the proviso that when R'and R"are methyl then R cannot be methyl;. The compounds of general formula (I) were assayed for AP-1 enhancement. The compounds of this invention were tested in assays for the modulation of stimulated activity of an AP-1- driven reporter gene in the Jurkat T cell line. The activation of this reporter gene results in luciferase production and the amounts of produced luciferase parallels the level of AP-1 activity. A high level of AP-1 activity is pivotal to e. g. high production of IL-2.

All embodiments of the invention as disclosed in the claims are herewith included in the specification.

The following examples are intended to illustrate the invention without restricting the scope thereof.

The compounds of general formula (I) may be prepared by methods well known in the literature. The general solution preparation is shown in Scheme 1 and 2.

Scheme 1 (II) (III) (IV) Scheme 2 A benzamide derivative of general formula (1) may be prepared by conventional methods and, for example, by first the reaction of a 4-amino-benzoic acid methyl ester (II) with an acid chloride (E) or anhydride in an inert solvent such as dichloromethane in the presence of triethylamine (Scheme 1). The resulting 4-acylamino-benzoic acid methyl esters (IV) and a N, N-substituted alkylenediamine (V) is then condensed in an excess of V in the presence of a catalytic amount ammonium chloride to form the compounds of general formula (I) (Scheme 2). Alternatively, the methylester is first hydrolysed and then activated using conventional methods, such as ethylchloroformate, dicyclohexylcarbodiimide (DCC) or 2- (lH-benzotriazol- 1-yl)-1, 1, 3,3-tetramethyluronium tetrafluoroborat (TBTU). The starting materials used herein are commercially available or are prepared by conventional methods found in standard reference books such as the Compendium of Organic Synthetic Methods, vol. I-VI (Wiley- Interscience), well known to those of ordinary skill in the art.

Acid addition salts of the compounds of formula (1) are prepared in a standard manner in a suitable solvent and in excess of an acid, such as hydrochloric, hydrobromic, sulphuric, maleic and succinic acid.

Example 1 4-iso-Butyrylamino-2-methoxv-benzoic acid methyl ester.

1.81 g of 4-amino-2-methoxy-benzoic acid methyl ester and 1.4 g of triethylamine were dissolved in 20 ml of dichloromethane. 1.23 g of isobutyryl chloride in 5 ml of dichlo- romethane was added dropwise at 0°C. The reaction mixture was allowed to reach room temperature and stirred for 3 hours. The reaction mixture was washed with water, dried and the solvents were evaporated to yield 1.9 g of the title product.

1H NMR (CDC13) : 8 1.22 (6H, d), 2.53 (1H, m), 3.83 (3H, s), 3.83 (3H, s), 6.85 (1H, d), 7.70 (1H, s), 7.75 (1H, d), 7.84 (1H, s).

Example 2 N-ff2-Diethylamino') propvn-4-isobutvrvlamino-2-methoxy-benzamide.

0.3 g of 4-iso-butyrylamino-2-methoxy-benzoic acid methyl ester was dissolved in 3 ml of N, N-diethyl-propylenediamine together with a catalytic amount of ammonium chloride. The reaction mixture was refluxed for 3 hours. Dichloromethane was added and washing 4 times with water removed excess diamine. Drying and evaporation of the solvents yielded 0.15 g of the title compound.

1H NMR (CDC13) : 8 0.97 (6H, t), 1.20 (6H, d), 1.71 (2H, m), 2.48 (6H, m), 2.59 (1H, m), 2.46 (2H, q), 3.90 (3H, s), 6.80 (1H, d), 7.94 (1H, s), 8.03 (1H, d), 8.29 (1H, s).

Example 3 N-r3- (Diethylamino) propyl]-4-iso-buturlamino-3-h,ddxy-benzamide 4-iso-Butyrylamino-3-hydroxy-benzoic acid (0.089 g) and TBTU (0.128 g) in chloroform (15 ml) was stirred for 2 hours. N, N-Diethyl-propylenediamine (0.052 g) was added and the mixture was stirred for 1 hour. Evaporation of the solvent gave a residue, which was chro- matographed on a silica gel column first eluted/washed with ethylacetate and then eluted with ethylacetate-methanol-triethylamine (12: 4: 1) to yield 0.03 g, of the title product.

1H NMR (CDC13) : 8 1.14 (t, 6H) 1.25 (m, 6H) 2.01 (m, 2H) 2.61 (m, 1H) 2.98 (m, 2H) 3.04 (m, 2H) 3.44 (m, 2H) 7.35 (m, 1H) 7.80 (d, 1H) 7.92 (m, 1H) 8. 21 (d, 1H) 8.36 (s, 1H).

Example 4 4-(N-iso-ButYrel-N-methYlamino)-benzoic acid 4-Methylamino-benzoic acid methyl ester (0.41 g) were suspended in chloroform (20 ml).

Isobutyryl chloride (0.79 g) in chloroform (10 ml) was added dropwise for 30 minutes and then dropwise triethylamine (1 ml) dissolved in chloroform (5 ml). The reaction mixture was stirred for 3 hours and the solvent was evaporated. 1M NaOH (aq) (40 ml) was added and the mixture stirred overnight. The solution was filtered to remove unsolved material and then acidified with 2M HCl (aq). Filtration and drying in vacuum yielded 0.48 g of the title product.

Example S N- [3-IDiethylamino) propyll-4- (N-iso-butyl-N-methylamino)-benzamide To a stirred solution of 4- (iso-butyryl-N-methylamino)-benzoic acid (0.088 g) and triethyl- amine (0.041 g) in chloroform (4 ml) was added a solution of ethyl chlorformate (0.049 g) in chloroform (1 ml). The mixture was stirred under an N2 atmosphere at room temperature for 1 hours and then cooled to 0 °C. N, N-Diethyl-propylenediamine (0.051 g) in chloroform (1 ml) was added and the mixture was stirred over night. The mixture were washed with 0.5 M NaOH (aq) and water. Drying and evaporation of the solvent gave a residue, which was chromatographed on a silica gel column first eluted/washed with ethylacetate and then eluted with ethylacetate-methanol-triethylamine (12: 4: 1) to yield 0.098 g, of the title product.

1H NMR (CDC13) : 8 1. 01 (t, 6H) 1.04 (t, 6H) 1.77 (m, 2H) 2.48 (m, 1H) 2.61 (m, 6H) 3.23 (s, 3H) 3.57 (m, 2H) 7.21 (m, 1H) 7.83 (m, 1H) 8.80 (s, 1H).

Examples 6 to 12 were prepared by the method described in Example 5.

Example 6 N- [3- (Diethylamino) propvl]-4-iso-butyrylamino-3-methoxy-benzamide 1NMR (CDC13) : 6 1.07 (t, 6H) 1.25 (d, 6H) 1.80 (m, 2H) 2.55 (m, 1H) 2.64 (m, 6H) 3.56 (m, 2H) 3.94 (s, 3H) 7.27 (m, 1H) 7.55 (d, 1H) 7.91 (s, 1H) 8.43 (d, 1H) 8.70 (s, 1H).

Example 7 N- [3- (Diethylamino) propvl]-4- (iso-butvrvl-N-methylamino)-2-methoxy-benzamide 1H NMR (CDC13) : 8 1.04 (m, 12H) 1.80 (m, 2H) 2.56 (m, 7H) 3.24 (s, 3H) 6.75 (s, 1H) 6.88 (m, 1H) 7.99 (m, 1H) 8.17 (d, 1H).

Example 8 N-!-4-iso-butYrYlamino-2-methoxy-benzamide 1H NMR (CDC13) : 8 1.24 (d, 6H) 1.86 (m, 2H) 2.52 (m, 7H) 3.51 (m, 2H) 3.75 (m, 4H) 3.97 (s, 3H) 6.71 (m, 1H) 7.37 (s, 1H) 7.94 (s, lH) 8.09 (d, 1H).

Example 9 N-E4-(Dimethylamino ! butv1]-4-iso-butYrYlamino-2-methoxy-benzamide 1H NMR (CDC13) : 8 1.25 (d, 6H) 1.65 (m, 4H) 2.37 (m, 6H) 2.52 (m, 3H) 3.45 (m, 2H) 3.97 (s, 3H) 6.73 (m, 1H) 7.43 (s, 1H) 7.88 (m, 1H) 7.92 (s, 1H) 8.09 (d, 1H).

Example 10 N-r3-f4-methvlpiperazino)-propvn-4-iso-butvrvlamino-2-methox v-benzamide 1H NMR (CDCI3) : 6 1.25 (d, 6H) 1.83 (m, 3H) 2.35 (s, 3H) 2.52 (m, 3H) 2.60 (m, 7H) 3.49 (m, 2H) 3.96 (s, 3H) 6.71 (m, 1H) 7.37 (s, 1H) 7.94 (m, 2H) 8. 08 (d, 1H).

Exaznple11 N- [3- Diethylamino) propyl]-4-iso-butyiylamino-3, 5-dichloro-benzamide 1H NMR (CDC13) : 8 1.10 (t, 6H) 1.29 (d, 6H) 1.82 (m, 2H) 2.69 (m, 7H) 3.55 (m, 2H) 7.03 (s, 1H) 7.82 (s, 2H) 9.22 (s, 1H).

Pharmacological methods Cells from the Jurkat T cell line were transfected with an AP-1-driven luciferase gene reporter construct (Parra et al., 1997) together with a selection gene vector. Selected clones from the resulting stable AP-1 reporter gene transfectants were used in the assays for AP-1 transcription factor activity. These transfected Jurkat cells (Jurkat/AP-lrep) were grown in RPMI 1640 supplemented with glutamine, hepes, sodium pyruvate, gentamicin, 10% FCS and G418. To evaluate distinct compounds for their capacity to enhance the AP-1 activity, Jurkat/AP-lrep cells were stimulated for 5.5 h in the temperature of 37°C with phorbol myristate acetate and ionomycin in the absence and presence of test compounds. The 96 well plates containing the cell cultures were then put on ice until harvested. The supernatants were removed and the cells were lysed. AP-1 activity was measured as luminiscence produced by luciferase substrate, which was added to the wells in conjunction with measurement.

Superantigen responsive mice were treated with Staphylococcal enterotoxin A in accordance with Belfrage et al. (Belfrage et al. 1995,1997a, 1997b). Plasma and splenocytes were collected at different time points to evaluate the induced activity of T cells with and without treatment with the compounds of general formula (1). It is shown that T cell activity as measured as IL-2 production, cytotoxic T cell activity and anergy induction (Belfrage et al.

1995,1997a, 1997b) were modulated by the treatment.

Among preferred compounds is N-[(2-diethylamino) propyl]-4-isobutyrylamino-2- methoxybenzamide, hereinafter called Compound A. Compound A was shown to enhance the activity of the AP-1 driven reporter in a dose dependent fashion down to uM concentrations (Figure 1).

Enhancement of AP-1 activity Concentration of compound A (microM) Figure 1. Percentage enhancement of the reporter gene activity in the assay utilising Jurkat cells with a transfected AP-1-driven luciferase gene reporter.

The compounds of formula (I) are useful as enhancers of AP-1. The present invention provides useful compositions and formulations of said compounds including pharmaceutical compositions and formulations of said compounds.

Effective quantities of the compounds of formula (I) are preferably administered to a patient in need of such treatment according to usual routes of administration and formulated in usual pharmaceutical compositions comprising an effective amount of the active ingredient and a suitable pharmaceutically acceptable carrier. Such compositions may take a variety of forms, e. g. solutions, suspensions, emulsions, tablets, capsules, and powders prepared for oral administration, aerosols for inhalations, sterile solutions for parental administration, supposi- tories for rectal administration or suitable topical formulations. Conventional procedures for the selection and preparation of suitable pharmaceutical formulations are described, for example, in"Pharmaceuticals-The Science of Dosage Form Design", M. B. Aulton, Churchill Livingstone, 1988.

A suitable daily dose for use in the treatment of disease with associated immune suppression or manic-depressive illness is contemplated to vary between 0.0005 mg/kg to about 10 mg/kg body weight, in particular between 0.005 mg/kg to 1 mg/kg body weight, depending upon the specific condition to be treated, the age and weight of the specific patient, and the specific patient's response to the medication. The exact individual dosage, as well as the daily dosage, will be determined according to standard medical principles under the direction of a physician.

Various additives to enhance the stability or ease of administration of the drug are contemplated. The pharmaceutical composition may also contain additional therapeutically useful substances other than a compound of formula (I).

The ability of the compounds of the present invention to enhance the AP-1 activity is clearly evidenced by their ability to enhance the reporter gene activity (see Figure 1). No unacceptable toxicological effects are expected such as tardive dyskinesia when compounds of the present invention are administered in accordance with the present invention.

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