CA2031714C - R-enantiomers of n-propargyl-1-aminoindan compounds, their preparation and pharmaceutical compositions containing them - Google Patents

Abstract

R(+)-N-propargyl-1-aminoindan, its preparation and use and pharmaceutical compositions containing it. The novel compound was found to be useful for the treatment of human patients for Parkinson's disease, memory disorders, dementia of the Alzheimer type (DAT), depression and the hyperactive syndrome.

Description

2~l7~ l~

FIELD OF THE lNv~.~lON
The present invention is in the field of selective irreversible inhibitors of the enzyme monoamine oxidase (hereinafter MAO) and relates to the R(+) enanti n~r of N-propargyl-1-aminoindan (hereinafter, PAI) which is a selective irreversible inhibitor of the B-form of the monoamine oxi~e enzyme (hereinafter, MAO-B). The invention also relates to pharmaceutical compositions containing R(+) PAI which is particularly useful for the treatment of Parkinson's disease, ~ oly disorders and dementia of the Alzheimer type (DAT), depression, and hyperactive syndrome in children.

RA--Y~).~ OF THE lNV~lON AND PRIOR ART
Parkinson's disease is widely considered to be the result of degradation of the pre-synaptic dopaminergic neurons in the brain, with a subsequent decrease in the amount of the neurotransmitter dopamine, that is being released. Inadequate dopamine release, therefore, leads to the onset of voluntary muscle control disturbances symptomatic of Parkinson's disease.

7 1 ~

Various procedures for treating Parkinson's disease have been established and are currently in widespread use, for example, the administration of L-Dopa together with a decarboxylase inhibitor, such as L-carbidopa or benzerazide.
The decarboxylase inhibitor protects the L-Dopa molecule from peripheral decarboxylation and thus ensures L-Dopa uptake by the remaining dopaminergic neurons in the striatum of the brain. Here the L-Dopa is converted into ~op~-lne resulting in increased levels of dopamine in these neurons. In response to physiological impulses these neurons are therefore capable of releasing larger amounts of dopamine, the quantity of which approximates the normal required levels. This treatment therefore alleviates the symptoms of the disease and contributes to the well-being of the patients.
However, this L-Dopa treatment has its drawbacks, the main one being that its effectiveness is optimal only in the first few years following the onset of treatment. After this initial period the clinical response is diminished and is ~ccnmranied by adverse side effects which include dyskinesia, fluctuation in efficacy throughout the day ("on-off effect") and psychiatric ~yl,,~o-,,~ such as confusional states, paranoia and hallucinations. This fall-off in the effect of L-Dopa treatment is attributed to a number of factors, including the natural progre~c;on of the disease, alteration in dopamine re~e~o.~ as a consequence of increased dopamine production or increased levels of dopamine metabolites, and pharmacokinetic problems of L-Dopa absorption (reviewed by Youdim et al., Progress in Medicinal Chemistry, Vol. 21, Chapter 4, pp. 138-167 (1984), Eds. Ellis and West, Elsevier, Amsterdam).
In order to overcome the drawbacks of the L-Dopa treatment, various treatments have been devised in which L-Dopa is combined with MA0 inhibitors, with the aim of reducing the metabolic breakdown of the newly formed dopamine (see for example, U.S. 4,826,875).

8 ~ ~ 3 .~

MAO exists in two forms known as MAO-A and MAO-B
which have selectivity for different substrates and inhibitors. For example, MAO-B metabolizes more efficiently substrates such as 2-phenylethylamine and is selectively and irreversibly inhibited by (-)-deprenyl (as described below).
It should be noted, however, that combining L-Dopa with an inhibitor of both MAO-A and MAO-B is undesirable leading to adverse side effects related to an increased level of catecholamines throughout the neuraxis. Furthermore, complete inhibition of MAO is also undesirable as it potentiates the action of sympathomimetic amines such as tyramine leading to the so-called "cheese effect" (reviewed by Youdim et al., Handbook of Experimental Pharmacology, Vol. 90, Chap. 3 (1988) Eds, Trendelenburg and Weiner, Springer-Verlag). As MAO-B was shown to be the predominant form of MAO
in the brain, selective inhibitors for this form were thus considered to be a possible way for achieving a decrease in dopamine breakdown on the one hand, together with a mi~;m~tion of the systemic effects of total MAO inhibition, on the other.
One of these selective MAO-B inhibitors, (-)-deprenyl, has been extensively studied and has been used as an MAO-B inhibitor to augment L-Dopa treatment. This treatment with (-)-deprenyl is generally favorable, not causing the "cheese effect" at doses causing nearly complete inhibition of MAO-B (Elsworth et al., Physchopharmacology, 57, 33 (1978).
Furthermore, addition of (-)-deprenyl to a combination of L-Dopa and decarboxylase inhibitor to Parkinson's patients leads to i~,~pLov~.,ents in akinesia and overall functional capacity as well as the elimination of "on-off" type fluctuations (reviewed by Birkmayer & Riederer in "Parkinson's Disease" pp.
138-149, Springer-Verlag (1983)).
Thus, (-)-deprenyl enhances and prolongs the effect of L-Dopa and permits a lowering of the dosage of L-Dopa whereby the adverse effects of L-Dopa treatment are limited.

However, (-)-deprenyl is not without its own adverse sides effects which include activation of pre-existing gastric ulcers and occasional hypertensive ep;~o~. Furthermore, (-)-de~ ~l is an amphetamine derivative and is metabolized to yield amphetamine and methamphetamines which may lead to l~n~s;rable side effects associated with these substances, e.g. increased heart rate (Simpson, Biochemical Pharmacology, 27, 1591 (1978); Finberg et al., in "Monoamine Oxidase Inhibitors - The State of the Art", pp. 31-43, Eds. Youdim and Paykel, (1981) Wiley).
Other compounds that are selective irreversible inhibitors of MAO-B but which are free of the undesirable effects associated with (-)-deprenyl have been described. One such compound, namely N-propargyl-l-aminoindan.HCl (racemic-PAI.HCl) was described in GB 1,003,686, GB 1,037,014 and US 3,513,244. It is a potent, selective, irreversible inhibitor of MAO-B, is not metabolized to amphetamines and does not give rise to unwanted sympathom;metic effects.
In comparative animal tests racemic PAI was shown to have considerable advantages over (-)-deprenyl, for example, racemic PAI produced no significant tachycardia, did not increase blood pressure (effects produced by doses of 5 mg/kg of (-)-deprenyl), and did not lead to contraction of nictitating membrane nor to an increase in heart rate at doses up to 5 mg/kg (effects caused by (-)-deprenyl at doses over 0.5 mg/kg). Furthermore, racemic PAI.HCl does not potentiate the cardiovascular effects of tyramine (Finberg et al. in "Enzymes and Neurotransmitters in Mental Disease", pp. 205-219, (1980), Eds. Usdin et al., Pub. John Wiley and sons, NY;
Finberg et al. (1981) in "Monoamine Oxidase Inhibitors - The State of the Art", ibid; Finberg and Youdim, British Journal Pharmacol. 85 451, (1985).
One object of this invention is to separate the racemic PAI compounds and to produce an enantiomer with MAO-B
inhibition activity.

~ ~ 5 ~ 2 ~ ~ 1 7 1 ~ s Since deprenyl has a similar structure to PAI and it is known that the (-)-enantiomer of deprenyl, i.e. (-)-deprenyl, is considerably more pharmaceutically active than the (+)-enantiomer, it was expected, by those skilled in the art, that only the (-) enantiomer of PAI would be the active MA0-B inhibitor.
However, contrary to such expectations, upon resolution of the enantiomers, it was found, in accordance with the present invention that the (+)-PAI enantiomer was in fact the active MA0-B inhibitor while the (-)enantiomer showed extremely low MA0-B inhibitory activity. Furthermore, the (+)PAI enantiomer surprisingly also had a higher degree of selectivity for MA0-B inhibition than the corresponding racemic form and may thus have less undesirable side effects in the treatment of the indicated disease. These findings are based on both in vitro and in vivo experiments as presented hereinafter in greater detail.
It was subsequently shown that (+)-PAI has the R
absolute configuration. This was also surprising based on the expected structural analogy with deprenyl and the amphetamines.
The high degree of stereoselectivity of pharmacological activity between R(+)-PAI and the S(-) enantiomer is also remarkable. The compounds R(+)-PAI is nearly four orders of magnitude more active than the S(-) enantiomer in MA0-B inhibition. This ratio is significantly higher than that observed between the two deprenyl enantiomers (Knoll and Magyar, Adv. Biochem. Physchopharmacol., 5, 393 (1972); Magyar, et al., Acta Physiol. Acad. Sci. Hung., 32, 377 (1967). Furthermore, in some physiological tests, (+) deprenyl was reported to have equal or even higher activity than the (-) enantiomer (Tekes, et al., Pol. J. Pharmacol.
Pharm. 40, 653 (1988).
N-methyl-N-propargyl-l-aminoindan (MPAI) is a more potent inhibitor of MA0 activity, but with lower selectivity ~ .~

2~34~7 ~ ~

for MA0-B over A (Tipton, et al., Biochem. Pharmacol., 31, 1250 (1982)). Surprisingly, in this case we have found only small degree of difference in the relative activities of the two resolved enantiomers thus further emphasising the remarkableness of the case of R(+)-PAI. (See Table lA).
Another object of the present invention is to provide for the first time use of the pharmaceutically active PAI-enantiomer alone (without L-Dopa) for treatment of Parkinson's disease, dementia and depression (see review by Youdim et al. in Handbook of Experimental Pharmacology, Vol.
90/I, (1988), chap.3, Eds. Trendelenberg and Wiener).
It is yet another object of the invention to provide for the use of the pharmaceutically active PAI-enantiomer for pre-treatment alone or together with synergistic agents, of Parkinson's disease in order to delay the L-Dopa treatment and its associated adverse side effects. This approach has been studied with respect to (-)-deprenyl which was shown to be effective when administered alone to early Parkinsonism patients, and may also have a synergistic effect in these patients when administered together with a-tocopherol (a vitamin E derivative), (The Parkinson's Study Group, New England J. Med., 321 (20), 1364-1371, (1989)).
In addition to its usefulness in treating Parkinson's disease, (-)-deprenyl has also been shown to be useful in the treatment of patients with dementia of the Alzheimer type (DAT) (Tariot et al., Psychopharmacology, 91, 489-495, 1987), and in the treatment of depression (Mendelewicz and Youdim, Brit. J. Psychiat. 142, 508-511, 1983). Thus, the R(+)-PAI compound of this invention has been shown to possess activity in restoration of memory, thus having potential for treatment of Ill~lloly disorders, dementia and especially useful in Alzheimer's disease and for the treatment of the hyperactive syndrome in children.

2 0 3 1 7 1 ~
DFT~TT.F~Tl DESCRIPrION OF '1'~; I~V~ITION
The present lnvention thus provides zs a novel compound the R(+)-enantiomer of N-propargyl-l-aminoindan [R(+)PAI] of the formula (I):

_ / ~ ~ l (I) 0 ~ ci2 - C a~

and pharmaceutically acceptable acid addition salts thereof.
The present invention also relates to the preparation of R(+)PAI, to pharmaceutical compositions comprising the ccmpound R(+)PAI together with suitable carriers and to the use of R(+)PAI for the treatment of human patients for Par~inson's disease, memory disorders, dementia of the Alzheimer type, depression and hyperactive syndrome.
The R(+) PAI may be obtained by optical resolution of racemic mixtures of R and S-enantiomer of PAI. Such a resolution can be accomplished by any conventional resolution method, well known to a person skilled in the art, such as those desc-ibed in "Enantiomers, Racemates and Resolutions" by J. Jacques, A.Collet and S. Wilen, Pub. John Wiley ~ Sons, NY, 1981. For example, the resolution may be carried out by pre?arative chomatography on a chiral column. Another example of a suitable resolution method is the formation of diastereomeric salts with a chiral acid such as tartaric, malic, mandelic acid or N-acetyl derivatives of aminoacids, such as N-acetyl leucine, followed by recrystallisation to isolate the diasterecmeric salt of the desired R enantiomer.
The rzcemic mixture of R and S enantiomers of PAI
may be prepared, e.g. as described in G~ 1,003,676 and GB

3~ 1,037,014. The rac~mic mixture of PAI can also be prepared by A

- 8 - ~ 3~ 7 ~ 4 reacting l-chloroindan or l-bromoindan with propargylamine.
Alternatively, this racemate may be prepared by reacting propargylamine with l-indanone to form the corresponding imine, followed by reduction of the carbon-nitrogen double bond of the imine with a suitable agent, such as sodium borohydride.
In accordance with this invention, the R enantiomer of PAI, can also be prepared directly from the optically active R-enantiomer of l-aminoindan by reaction with propargyl bromide or propargyl chloride in the presence of an organic or inorganic base and optionally in the presence of a suitable solvent.
Suitable organic or inorganic bases for use in the above reaction are, e.g., triethylamine, pyridine, alkali metal carbonates or bicarbonates etc. If the reaction is conducted in the presence of a solvent, this may be chosen from, e.g., toluene, methylene chloride and acetonitrile. A
preferred method of preparation of the afol~.entioned compound is the reaction between R-l-aminoindan with propargyl chloride using potassium bicarbonate as a base and acetonitrile as solvent.
The above described reaction of l-aminoindan generally results in a mixture of unreacted primary amine, the desired secondary amine and the tertiary amine N,N-bispropargylamino product. The desired secondary amine, i.e.N-propagyl-l-aminoindan, can be separated from this mixture by any conventional separation method, such as chlul,a~oyla~hy, distillation, selective extraction, etc.
The R-l-aminoindan starting material can be prepared by methods known from the literature, for example Lawson and Rao, Bichochemistry (1980) 19, 2133 and the references cited therein, and European Patent No. 235,590.
The R-l-aminoindan can also be prepared by resolution of a racemic mixture of the R and S enantiomers, e.g. by formation of diastereomeric salts with chiral acids, 2~317i~

or by any other known method, such as those reported in the above mentioned "Enantiomers, Racemates and Resolutions" by J.
Jacques et al, Pub. John Wiley & Sons, NY, 1981.
Alternatively, the R-1-aminoindan starting material may be prepared by reacting 1-indanone with an optically active amine, followed by reduction of the carbon-nitrogen double bond of the resulting imine by hydrogenation over a suitable catalyst, such as p~llA~;um on carbon, platinum oxide, Raney-nickel etc. Suitable optically active amines are, for example, one of the antipodes of phenethylamine or an ester of an aminoacid, such as valine or phenylalanine. The benzylic N-C bond may be cleaved subsequently, by hydrogenation under non-vigorous conditions.
Additional methods for preparing R-l-aminoindan are the hydrogenation, as described above, of indan-1-one oxime ethers, wherein the alkyl portion of the ether contains an opti~Ally pure chiral center. Alternatively, a non-chiral derivative of indan-1-one containing a carbon-nitrogen double bond, such as an imine or oxime, can be reduced with a chiral reducing agent, e.g. a complex of lithium aluminium-hydride and ephedrine.
For the preparation of pharmaceutically acce~Lable acid addition salts of the compound of R(+)PAI, the free base can be reacted with the desired acids in the presence of a suitable solvent by co~,v~ltional methods. S;m-l~rily, an acid addition salt may be converted to the free base form in a known manner.
In accordance with the present invention, the compound R(+)PAI may be prepared as pharmaceutical compositions particularly useful for the treatment of Parkinson's disease, dementia of the Alzheimer type (DAT) or depression. Such compositions may comprise the compound of R(+)PAI or pharmaceutically acceptable acid addition salts thereof, together with pharmaceutically acceptable carriers and/or excipients. For example, these compositions may be 2 0 3 ~ 7 1 ~

prepared as medicaments to be administered orally, parenterally, rectally or transdermally. Suitable forms for oral administration include tablets, compressed or coated pills, dragées, sachets, hard or soft gelatin capsules, sublingual tablets, syrups and suspensions; for parenteral administration the invention provides ampoules or vials that include an aqueous or non-aqueous solution or emulsion; for rectal administration there are provided suppositories with hydrophilic or hydrophobic vehicles;
and for topical application as ointments and transdermal delivery there are provided suitable delivery systems as known in the art.
These above compositions may be used alone to treat Parkinson's disease, Alzheimers's disease or depression, or alternatively, in the case of Parkinson's disease, they may be used as an adjunct to the conventional L-Dopa treatments.
The preferred dosages of the active ingredient, i.e., R-PAI compounds, in the above compositions are within the following ranges: for oral or suppository formulations 2-20 mg per dosage unit to be taken daily and more preferably 5-10 mg per dosage unit to be taken daily may be used; and for injectable formulations 1-10 mg/ml per dosage unit to be taken daily and more preferably 2-5 mg/ml per dosage unit to be taken daily may be used.
According to a preferred embodiment, the pharmaceutical composition for oral use in the form of tablets or capsules comprises R(+)-N-propargyl-1-aminoindan, Levodopa and a decarboxylase inhibitor suchas L-Carbidopa or benserazide. Preferably, such a composition comprises 2-10 mg of R(+)-N-propargyl-1-aminoindan, 50-250 mg of Levodopa and 10-25 mg of L-Carbidopa or 12.5-50 mg of benserazide.

- lo 2~7~4 - a -BRIEF DESCRIPTION OF THE DRAWINGS
Fig. 1 is a graphic representation of the results according to Example 19.
Fig. 2 is a graphic representation of the results according to Example 19.
Fig. 3 is a graphic representation of the results according to Example 19.
Fig. 4 is a graphic representation of the results according to Example 20.
Fig. 5 is a graphic representation of the results according to Example 20.

03~1.91 Fig. 6 is a graphic representation of the results according to Example 20.
Fig. 7 is a graphic representation of the results according to Example 20.
Fig. 8 iS a graphic representation of the results according to Example 20.
Fig. 9 iS a graphic representation of the results according to Example 20.
Fig. 10 is a graphic representation of the results according to ~xAmplP 20.
Fig. 11 iS a graphic representation of the results according to Example 20.
Fig. 12 iS a graphic representation of the results according to Example 21.
Fig. 13 is a graphic representation of the results according to Example 21.
Fig. 14 iS a graphic representation of the results according to Example 21.
Fig. 15 is a graphic representation of the results according to Example 21.
Fig. 16 iS a graphic representation of the results according to Example 22.
The invention will now be described in more detail in the following non-limiting ex~mp1es and their ~ccnmpanying Tables and Figures.

Racemic N-propargyl-1-aminoindan hydrochloride Racemic 1-aminoindan (10.0 g) and 10.4 g of potassium carbonate were added to 75 ml of acetonitrile. The resulting suspension was heated to 60~C and 4.5 g of propargyl chloride were added dropwise.
The mixture was stirred at 60~C for 16 hours, whereafter most of the volatiles were removed by distillation in vacuo. The residue was partitioned between 10% aqueous sodium hydroxide and methylene chloride.

- 12 - ~ ~ 3 ~ 7 ~ 4 The organic phase was dried and the solvent removed by distillation. The residue was flash chromatographed on A gel, eluting with 40% ethyl acetate/60~ hexane. The fractions containing the title compound as a free base were combined and the eluant replaced by ether. The ethereal solution was treated with gaseous HCl, the precipitate formed was isolated by suction filtration and recryst~ ed from isopropanol to yield 7.3 g of the title compound, m.p. 182-4~C.
Chromatographic and spectroscopic data were in accordance with the literature (US 3,513,244) and an authentic sample.
MMR (o,CDC13): 2.45 (2H, m), 2.60 (lH, t), 2.90 (lH, m), 3.45 (lH, m), 3.70 (2H, d), 4.95 (lH, t), 7.5 (4H, m) ppm.

S-(-)-N-Propargyl-l-aminoindan hydrochloride The title compound in free base form was isolated by resolving the racemic mixture of the free base of Example 1 on a CHIRACEL o~(cellulose tris[p-methylbenzoate]) preparative HPLC column eluting with 10~ isopropanol/90% hexane and collecting the first eluted major peak. The resulting oil was converted to the title compound (hydrochloride) by treatment of a 10% diethyl ether solution of the oil with gaseous HCl and the resulting precipitate was collected by suction filtration.
~ a]D -29.2~ (1%, ethanol), m.p. 182-184~C. Other chromatographic and spectroscopic properties were identical with the hydrochloride salt of Example 1.

R-(+)-N-Propargyl-l-aminoindan hydrochloride The title compound was prepared as in Example 2 above, except that the second eluted peak from the preparative HPLC was collected; [a]D+29.1~(0.8%, ethanol), m.p. 179-181~C.

* Trade Mark ~.C~
,.

2~31~

-Other chromatographic and spectroscopic properties were identical with the hydrochloride salt of Example 1.

R-(+)-N-propargyl-1-aminoindan hydrochloride R-(-)-1-aminoindan (12.4 g) and 12.9 g of potassium carbonate were added to 95 ml of acetonitrile. The resulting suspension was heated to 60~ and 5.6 g of propargyl chloride were added dropwise. The mixture was stirred at 60~C for 16 hours, whereafter most of the volatiles were removed by distillation in vacuo. The residue was partitioned between 10% aqueous sodium hydroxide and methylene chloride.
The organic phase was dried and the solvent .~,oved in vacuo, the residue was flash chromatographed on silica gel eluting with 40% ethyl acetate/60% hexane. Fractions con-aining the free base of the title compound were combined and the solvent replaced by ether. The ethereal solution was treated with gaseous HCl and the resulting precipitate was isolated by suction filtration and recrystallized from isopropanol to yield 6.8 g of the title compound, m.p. 183-185~C, [a]D+30.90 (2%, ethanol). Spectral properties were identical to those reported for the compound of Example 1.

S-(-)-N-propargyl-1-aminoindan hydrochloride The title compound was prepared by the method of Example 4, except that S-(+)-1-aminoindan was used as starting material. The product exhibited ta]D-30.3 (2%, ethanol), m.p.
183-5~C. Spectral properties were identical to those reported for the compound of Example 1.

Di (R-(+)-N-propargyl-1-aminoindan)L-tartarate To a solution of L-Tartaric acid (4.4 g) in 48 ml of boiling methanol was added a solution of R-(+)-N-propargyl-1-2i~71~

aminoindan free base (5.0 g) in methanol (48 ml). The solution was heated to reflux and 284 ml of t-butylmethyl ether was added over 20 minutes. The mixture was heated for an additional 30 minutes, cooled, and the resulting precipitate was isolated by suction filtration to yield 6.7 g of the title compound, m.p. 175-177~C.
ta]D (1.5, H20) = +34.3 ; Anal. calcd. for C28H3206N2; C, 68.26, H, 6.56, N, 5.69. Found: C, 68.76; H, 6.57; N, 5.61.

R-(+)-N-Methyl-N-propargyl-l-aminoindan hydrochloride The free base form of R-(+)-N-propargyl-l-aminoindan from Example 4 (1.2 grams), potassium carbonate (0.97 grams) and methyl iodide (1 gram) were added to 15 ml of acetone and the resulting suspension heated to reflux under a nitrogen atmosphere for 8 hrs. Thereafter the volatiles were removed under reduced pressure and the residue partitioned between lOgo-aqueous sodium hydroxide (30 ml) and methylene chloride (30 ml). The organic phase was dried and the solvent lelluved in vacuo. The residue was flash chromatographed on silica gel eluting with 40~ ethyl acetate/60% hexane. Fractions containing the title compound as a free base were combined and the solvent replaced by diethyl ether. The ethereal solution was treated with gaseous HCl, the volatiles ~~lluved in vacuo and the residue re~-y~ ed from isopropanol to yield 400 mg of the title compound as a white ~ly~alline solid, m.p.:
134-136~C [a]D+31.40 (ethanol). NMR(~CDC13):2.55 (2H, m); 2.7 (lH, br.s); 2.8 (3H, s); 3.0 (lH, m); 3.4 (lH, m); 3.9 (2H, br.s): 5.05 (lH, m) 7.7 (4H, m) ppm.

S-(-)-N-methyl-N-propargyl-l-aminoindan hydrochloride The title compound was prepared as in Example 7 above, except that S-(-)-N-propargyl-1-aminoindan (free base) from Example 5 was used as starting material. All of the - - 15 - 2~ i4 physical and spectral properties of the title compound were identical to those in Example 7 except for the [a]D
-34.9~(ethanol).

Tablet Composition R(+)-N-propargyl-l-aminoindan hydrochloride 5.0 mg Pregelatinized starch 47.0 mg Lactose hydrous 66.0 mg 10 Micro~Ly~alline cellulose 20.0 mg Sodium starch glycolate 3.0 mg Talc 1.5 mg Magnesium stearate 0.7 mg Purified water added as required for granulation.

Tablet C~ ,o~ition R(+)-N-propargyl-l-aminoindan hydrochloride 1.0 mg Lactose hydrous 50.0 mg 20 Pregelatinized starch 36.0 mg Micro~Ly~alline cellulose 14.0 mg Sodium starch glycolate 2.2 mg Talc 1.0 mg Magnesium stearate 0.5 mg 25 Purified water added as required for granulation.

Capsule C~mpocition R(+)-N-propargyl-l-aminoindan hydrochloride 5.0 mg 30 Pregelatinized starch 10.0 mg Starch 44.0 mg Microcrystalline cellulose 25.0 mg Ethylcellulose 1.0 mg Talc 1.5 mg 35 Purified water added as required for granulation.

16 2~3:~7~L

Injection Composition R(+)-N-propargyl-1-aminoindan hydLoohloride5.0 mg Dextrose anhydrous 44.0 mg 5 HC1 added to pH 5 Purified water added as required for 1 ml Injection Cnmpo.~;tion 10 R(+)-N-propargyl-1-aminoindan hyd~o~hloride1.0 mg Sodium chloride 8.9 mg HC1 added to pH 5 Purified water added as required to 1 ml Injection Composition R(+)-N-propargyl-l-aminoindan hydrochloride2.0 mg Sodium chloride 8.9 mg HC1 added to pH 5 20 Purified water added as required to 1 ml Syrup Composition R(+)-N-propargyl-1-aminoindan hydrochloride5.0 mg Sucrose 2250.0 mg Saccharin sodium 5.0 mg Methylparaben 6.0 mg Propylparaben 1.0 mg Flavor 20.0 mg 30 Glycerin USP 500 mg Alcohol 95% USP 200 mg Purified water as required to 5.0 ml 2~ 17~

Sl~hl;ngual Tablets R(+)-N-propargyl-1-aminoindan hydrochloride2.5 mg Micro~ly~alline cellulose 20.0 mg 5 Lactose hydrous 5.0 mg Pregelatinized starch 3.0 mg Povidone 0.3 mg Coloring agent q.s.
Flavor q.s.
10 Sweetener q.s.
Talc 0.3 mg Blend the excipients and the active and granulate with an ethanol solution of Povidone. After drying and weighing, it is blended with the talc and cu~ essed~

PAI Sublingual Tablets R(+)-N-propargyl-1-aminoindan hydrochloride5.0 mg 20 Micro~ly~alline cellulose 15.0 mg Pregelatinized starch 12.0 mg Ethyl cellulose 0.3 mg Talc 0.3 mg Purified water added as required for granulation.

Tablet Composition R(+)-N-propargyl-1-aminoindan hydrochloride5.0 mg Levodopa 100.0 mg 30 Carbidopa 25.0 mg Pregelatinized starch 24.0 mg Starch 40.0 mg Mi~l~lys~alline cellulose 49.5 mg Col. D & C Yellow No. 10 0.5 mg 35 Col. D & C Yellow No. 6 0.02 mg Alcohol USP added as required for granulation.

- 18 - 2~ ~ ~ 7 ~4 The following Examples and their accompanying Tables and Figures relate to the Biological Experiments carried out in accordance with this invention.

Inhibition of MAO activity in vitro Experimental protocol:
The MAO enzyme source was a homogenate of rat brain in 0.3M sucrose, which was centrifuged at 600 g for 15 min. The supernatant was diluted appropriately in 0.05M phosphate buffer, and pre-incubated with serial dilutions of compounds of general formula I: R(+)-PAI, S(-)-PAI and racemic-PAI for 20 min at 37 C. 14C-labelled substrates (2-phenylethylamine, hereinafter PEA; 5-hydroxytryptamine, hereinafter 5-HT) were then added, and the incubation continued for a further 20 min (PEA), or 30-45 min (5-HT). Substrate concentrations used were 50uM (PEA), and lmM (5-HT). In the case of PEA, enzyme concentration was chosen so that not more than 10% of the substrate was metabolized during the course of the reaction. The reaction was then stopped by addition of tranylcypromine (to final concentration lmM), and the incubate filtered over a small column of AMBERLITE* CG-50, buffered to pH 6.3. The column was washed with 1.5ml water, the eluates pooled and the radioactive content determined by liquid scintillation spectrometry. Since the amine substrates are totally retained on the column, radioactivity in the eluate indicates the production of neutral and acidic metabolites formed as a result of MAO activity.
Activity of MAO in the sample was expressed as a percentage of control activity in the absence of inhibitors, after subtraction of appropriate blank values. The activity determined using PEA as substrate is referred to as MAO-B, and that determined using 5-HT
as MAO-A.

* Trade Mark '~' - 19 - 2~317:14 Results:
Inhibitory activity of the R(+)-PAI, S(-)-PAI and racemic-PAI compounds of formula I were examined separately in vitro, and the results of typical experimental runs are shown in Figs. 1 and 2. The entire experiment was repeated three times. Concentration of inhibitor producing 50% inhibition of substrate metabolism (IC-50) was calculated from the inhibition curves, and is shown in Table 1. From this data it can be seen that:
(a) the R(+)-PAI is twice as active as the racemate for inhibiton of MAO-B;
(b) the R(+)-PAI is 29 times more active for inhibition of MAO-B than MAO-A;
(c) the S(-)-PAI is only 1/6,800 as active as the R(+)-PAI
for inhibition of MAO-B, and shows little or no selectivity between MAO-B and MAO-A.

IC-50 (nM) VALUES FOR INHIBITION OF MAO-A AND
MAO-B BY RACEMIC-PAI AND THE R(+) AND S(-) ENANTIOMERS THEREOF IN RAT BRAIN HOMOGENATE
IN VITRO

IC-50 (nM) MAO-A MAO-B
Compound: S(-)PAI R(+)PAI Rac S(-)PAI R(+)PAI Rac 26000 73 140 17000 2.5 5 The results of the same experiment using R(+) and S(-) MPAI (N-methyl-N-propargyl-l-aminoindan) are reported in Table lA. Each of the enantiomers of MPAI is less selective between MAO-B and MAO-A inhibition than R(+)PAI. Furthermore, R(+)MPAI is only five times as active as S(-)MPAI in MAO-B
inhibition, in contrast to R(+)PAI which is about 7000 times as active as S(-)PAI in this assay.

- 20 - 2~3 1 7 ~4 TABLE la IC-50 (nM) VALUES FOR INHIBITION OF MAO-A AND
MAO-B BY THE R(+) AND S(-) ENANTIOMERS OF MPAI
IN RAT BRAIN HOMOGENATE IN VITRO

IC-50 (nM) MAO-A MAO-B
Compound: S(-)MPAI R(+)MPAI S(-)MPAI R(+)MPAI

Some experiments were also carried out with human cerebral cortical tissues, obtained 6 hours post-mortem, and treated as described above. The results of such an experiment are shown in Fig. 3 (where the R(~)PAI, S(-)PAI and racemic PAI compounds were those equivalent to formula I).

Inhibition of MAO activity in vivo: acute treatment Experimental protocol:
Rats (male Sprague-Dawley derived) weighing 250+20g were treated with one of the enantiomers or the racemic form of PAI by intraperitoneal injection (ip) or oral gavage (po) and decapitated lh or 2h later respectively. Groups of three rats were used for each dose level of inhibitor, and MAO
activity determined in brain and liver using the general technique described above. The amount of protein in each incubation was determined using the Folin-Lowry method, and enzyme activity calculated as nmol substrate metabolized per hour incubation for each mg protein. Activity of MAO in tissues from animals treated with inhibitors was expressed as a percentage of the enzyme activity in a group of control animals, administered vehicle (water for oral administration;
0.9% saline for ip injection) and killed as above.
Results:
None of the dose levels used with the inhibitor drugs produced any obvious behavioural alteration. The - 21 - 2~7~

results are depicted in Figs 4 to 11. Following ip administration, compound R(+)-PAI produced 90% inhibition of brain MA0-B activity at a dose of 0.5mg/kg. The same dose produced only 20% inhibition of MA0-A activity. By oral administration, the same dose of R(+)-PAI produced 80%
inhibition of MA0-B with no detectable inhibition of MA0-A.
Essentially similar results were seen for inhibition of hepatic MA0, as for brain MA0. The doses producing 50%
inhibition of MA0-A and MA0-B (IC-50) were r~lr~ ted from the inhibition curves, and are shown in Table 2. These data show :
(a) that MA0 inhibitory activity of compound R(+)-PAI is maintained in vivo in the rat;
(b) that selectivity for inhibition of MA0-B, as opposed to MA0-A, by R(+)-PAI is maintained in vivo;
(c) that the much greater activity of the (+)-as opposed to (-)-enantiomer, is maintained in vivo;
(d) that the compounds are effectively absorbed after oral administration; and (e) that the compounds effectively pass the blood-brain barrier, and effectively inhibit brain MA0. The fact that R(+)-PAI was about twice as active as the racemic compound for inhibition of MA0-B is a reflection of the ex~L~.Iely low activity of S(-)-PAI for inhibition of MA0-B.

- 22 - ~20~1~14 IC-50 VALUES (mg/kg) FOR INHIBITION OF MAO-A
AND MAO-B BY R(+)-PAI, S(-)-PAI OR RACEMIC-PAI, IN THE RAT FOLLOWING INTRAPERITONEAL (IP) INJECTION OR ORAL ADMINISTRATION (PO) IC-50 (mg/kg) MAO-A MAO-B
Compound: S(-)PAI R(+)PAI Rac S(-)PAI R(+)PAI Rac IP BRAIN >10 1.2 2.5 >10 0.07 0.22 IP LIVER >10 5 5 >10 0.06 0.11 PO BRAIN >10 >5 >5 >10 0.17 0.29 PO LIVER >10 >5 >5 >10 0.05 0.09 Inhibition of MAO activity in vivo: chronic treatment Experimental protocol:
Rats (specification as in Example 20: 4 animals for each dose level) were treated with compound R(+)-PAI or r~r~m;c form at three dose levels (0.05, 0.1 and 0.5mg/kg) by oral administration, one dose daily for 21 days, and decapitated 2 hours after the last dose. The activity of MAO
types A and B was determined in brain and liver as described in Example 20.
Results:
A dose of 0.lmg/kg daily of compound R(+)-PAI
produced a good degree of selective inhibition, with more than 80% inhibition of brain MAO-B and 20% or less inhibition of brain MAO-A. At the higher dose of 0.5mg/kg daily, MAO-A was still inhibited by less than 50~ (Figs 12 and 13). Hepatic MAO showed a sim;l~r degree of selective inhibiton (Figs 14 and 15). Compound R(+)-PAI was again more potent than the racemic form of the inhibitor, by a factor of about twofold.

- 23 - 2 ~ 3 ~ 7 ~4 In the case of brain MA0, R(+)-PAI had a better degree of selectivity for inhibition of MA0-B than the racemic form.
These results show that selectivity of MA0-B
inhibition can be maintained following chronic treatment with the compounds. As with other iL~e~eLsible inhibitors, the degree of enzyme inhibition is greater with chronic treatments than following a single dose of the drug. Compound R(+)-PAI
shows a better degree of selectivity for inhibition of brain MA0-B than the racemic compound.

Irreversible nature of MA0 inhibition Experimental protocol:
A single dose of compound R(+)-PAI (lmg/kg) was administered by ip injection to groups of 4 rats, and the animals killed 2,6,18,24,48 and 72 hours later. Activity of MA0-B was determined in whole brain tissues as described herein before.
Results:
The results are shown in Fig. 16. Maximal inhibition of MA0-B was attained at 6 hours after the injection. MA0 activity had only returned to 30% control activity at 72 hours after the injection. This experiment demonstrates the irreversible nature of the MA0 inhibition by compound R(+)-PAI.

Potentiation of tyramine pressor effect in conscious rats Experimental ~~o~o~ol:
Rats were anesthetised with a mixture of pentobarbital (30mg/kg) and chloral hydrate (120mg/kg) by intraperitoneal injection. The left carotid artery and jugular vein were cannulated with fine polythene tubing (artery) or fine silicone rubber tubing connected to polyethylene tubing (vein), the distal end of which was 2~31714 brought under the skin to an anchor point behind the neck.
The tubing was filled with heparinised saline solution, and plugged with a fine steel rod. The animals were treated with 20mg chloramphenicol by intr~ml-~c~ r injection and allowed to recover from the operation overnight. The following day, the rats were pl~cP~ in a high-walled container permitting free ,o~l,en~. The arterial catheter was connected to a pressure transducer via a 100 cm length of saline-filled, fine-bore polyethylene tubing, and the venous catheter connected to a lml syringe via a s' m; 1 ~r length of tubing, which, together with the syringe, contained a solution of tyramine hydrochloride in saline (1 mg/ml).
Following an equilibration period of 30 to 40 min, tyramine injections (50 or 100 ,ug) were given, and blood pressure responses recorded. At least 15 min was maintained between injections, after return of blood pressure to ~ ol values. Control pressor responses were established, and then one of the drugs injected intra-peritoneally, and tyramine responses repeated over the next 4 hours. Area under the blood pressure response curve was estimated, and the ratio of this area after treatment to before treatment determined, using the average off 3 to 4 values obtained in control period, and 1 to 3 hours after injection of the compounds.
Results:
The results are shown in Table 3. Compound R(+)-PAI
at a dose of lmg/kg, (which causes complete inhibition of MAO-B in brain and liver, and 40 to 50% inhibition of MA0-A in these tissues) caused no significant potentiation of tyramine pressor response. At the higher R(+)-PAI dose of 5mg/kg, (which causes more extensive inhibition of MA0-A in brain and periphery), there was a significant potentiation of the tyramine pressor response, which was s;m;l~r in extent to that produced by the same dose of de~ell~l, and less than that produced by clorgyline (at a dose which inhibits hepatic MA0-A
activity by over 85%).

_ - 25 - ~ 7 ~ ~

POTENTIATION OF TY~A~INE PRESSOR EFFECT IN
CONSCIOUS RATS BY MAO INHIBITORS
InhibitorDoseNo. of ratsRatio Area Under SEM( (mg/kg) (n) Pressor Response Curve; After/Before Saline 12 1.25 0.28 Clorgyline 2 6 10.39 2.13 (-)Deprenyl 1 2 1.15 (-)~eprenyl 5 3 2.36 0.16 R(+)PAI 1 3 1.38 0 7 R(+)PAI 5 3 3 49 0.98 From this experiment it can be concluded that compound R(+)-PAI causes no potentiation of the tyramine pressor effect at a dose which effectively inhibits MAO-B.

EXAMPLE 24~0 Suppression of MPTP-Induced dopaminergic Toxicity by R(+)-PAI
l-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) is a neurotoxin that damages nigrostriatal dopaminergic neurons in several mammalian species including mice and produces a parkinsonian syndrome in humans and primates. A
crucial initial step in the mechanism of its neurotoxicity involves conversion of ~TP to its toxic metabolite l-methyl-4-phenyl pyridinium ion (MPP+). This reaction is catalyzed by the enzyme MAO-B and probably takes place outside of dopaminergic neurons, mainly in glia. It is known that MPTP
is both a substrate and an irreversible inhibitor of MAO-B.
Pretreatment of experimental animals with MAO-B inhibitors such as deprenyl or pargyline protects against and prevents the MP~P-induced damage to nigrostriatal neurons because the oxidative conversion of ~PTP to MPP+ is blocked. One of the major current hypotheses suggests that the progressive (l) SEM: standard error of the mean.
A

- - 26 - 2 0 3 1 71 ~
.
nigrostriatal degeneration in Parkinson's may be due to exposure to environmentally-derived exogenous MPTP-like neurotoxins. In such case, there is an additional strong indication to initiation of sustained treatment with an MAO-B
inhibitor from the very early stages of Parkinson's ~;SQ~e in the hope that it will neutralize the damaging effects of such yet putative MPTP-like toxins and thus arrest or slow down the progression of the illness. A successful MAO-B inhibitor drug is currently judged by its ability to block MPTP-induced damage to nigrostriatal dopaminergic neurons in vivo. We therefore tested the (-) and (+) enantiomers of PAI for their potency in preventing or attenuating the MPTP-i~ ce~ striatal dopamine depletions in mice.
Experimental Protocol:
Male C57 black mice (20-25 g weight) were injected with MPTP.HC1 (30 mg/kg dissolved in distilled water, s.c.) or vehicle alone or one hour after pretreatment with the (-) or (+) isomers of PAI (2.5 mg/kg, i.p.) or with deprenyl (5 mg/kg, i.p.) and decapitated 5 days later. Brains were ~ ved and corpora striata dissected on an ice-cold glass plate and frozen on dry ice. Striatal tissues were homogenized in 0.1 M perchloric acid, and deproteinized aliquots containing dihydroxybenzylamine as an internal standard were assayed for dopamine and its major metabolite 3,4-dihydroxy-phenylacetic acid (DOPAC) using HPLC with electro-chemical detection.
Results:
Table 4 shows the results of this experiment.
Treatment with MPTP alone produced marked striatal dopamine (DA) and DOPAC depletions. Treatment with the (-) and (+) enantiomers of PAI or with (-) deprenyl did not affect striatal DA concentrations. Pretreatment with the (-) isomer of PAI did not affect the MPTP-induced DA and DOPAC levels in striatum. The (+)-isomer of PAI given before MPTP, completely abolished the reduction in striatal DA and DOPAC levels - 27 - 2~ ~ 1 7 ~ ~

produced by the toxin. At a dose of 2.5 mg/kg it was equipotent to (-) deprenyl (5 mg/kg) in its protective effect.

~ ~1 OF PRETREATMENT WITH THE (-) AND (+) ENANTIOMERS OF THE MAO-B INHIBITOR PAI ON THE
STRIATAL DA AND DOPAC DEPLETIONS INDUCED BY
MPTP IN MICE IN VIVO.
DA DOPAC
(ng/mg protein) Control 162.8i 7.2 8.4+0.5 MPTP 53.li 6.2 3.2iO.3 (-)-PAI 174.0i 4.8 7.5+0.2 (-)-PAI + MPTP53.4+ 6.9 7.0+0.6 (+)-PAI 185.0i 6.9 3.3+0.3 (+)-PAI + MPTP177.8il4.4 6.0iO.3 (-) Deprenyl 170.6+ 7.1 5.6iO.3 (-) Deprenyl + MPTP197.0i 8.0 6.4+0.5 Above values for DA and DOPAC expressed as MeaniS.E.M., and No. of rats, n = 7-11 in each group.

These results indicate that the R(+)-PAI is an ~xcellent MAO-B inhibitor in vivo, and is of espe~;~lly great potential for the treatment of Parkinson's disease.
While the invention has been described with reference to the aforementioned Examples and their ~ccomp~nying Tables and Figures, it is not restricted thereto.

Various modifications and applications of the invention are poss;ble, for example, compounds of Formula I may be combined, in a synergistic way, with a-tocopherol (Vit. E. deriv.) for the treatment of Parkinson's disease.

- 28 - 2 ~ 317 ~ ~

Effect of PAI enantiomers on amphetamine induced stereotype behavior in senescent rats Amphetamine is known to induce stereotypic behaviour (Sulser, F. & Sanders-Bush, E. Ann. Rev. Pharmacol. 11:209-230 (1971)) by the mobilization of endogenous dopamine.
Amphetamine is not metabolized by MA0-B. Inhibition of MA0-B
by an effective inhibitor and administration of amphetamine cause release of dopamine which will not undergo degradation by the inhibited MA0-B. Thus, an increase of synaptic dopamine is expected after administration of amphetamine and effective MAO-B inhibitor leading to an increase in stereotype behavior - potentiation of the amphetamine effect. The extent of this bnehavior is rated in accordance with the number of lateral head llov~,ents over a period of 1 minute.
Experimental Protocol:
The test compound was administered at a dose of 0.5 mg/kg/day in drinking water, 24 hours before the infliction of hypoxia (92% nitrogen + 8% oxygen for 6 hours). Following that, amphetamine was injected s.c. at a dose of 0.5 mg/kg 45 min. later, lateral head movements were counted.
Results:
The results of these experiments are shown in Table 5 2g - 2 ~ 3 ~ ~ ~ 4 TABT~ 5 EFFECT OF PAI ISOMERS ON AMPHETAMINE-INDUCED
STEREOTYPE BEHAVIOUR IN SENESCENT RATS
(CONTROL AND HYPOXIALESIONED) 5 Group Treatment Stereotype Behavior Rating Control (6) - 87 + 10 Control (5) (+) PAI 126 + 16*
Control (4) (-) PAI 94 + 18 10 Hypoxia lesioned (5) - 93 + 12 Hypoxia lesioned (6) (+) PAI 143 _ 6*

Numbers in parenthesis are numbers of animals tested *P<O.001 with respect to untreated hypoxia group or untreated control group correspondingly The results in Table 5 indicate that (+)PAI caused significant potentiation of the amphetamine-induced stereotype behavior in both hypoxia-lesioned and control rats. (-)PAI was totally inactive in this respect. These behavioral in vivo results corroborate previous biochemical findings that (+)PAI
is an active inhibitor of MAO-B in the brain while (-)PAI is inactive in this respect.

EXAMP~E 26 Effect on R(+)PAI on the improvement or restoration of memory Newborn rat pups subjected to a brief episode of anoxia and then allowed to resume their growth in a normal way, develop a long-lasting impairment of memory (Speiser, et al., Behav. 8rain Res. 30:89-94, 1988). This memory impairment is expressed as an inferior performance in the passive avoidance test.
The effect of R(+)PAI and S(-l)PAI on the improvement or restoration of memory was investigated in the passive avoidance test. If the drug is effective it increases the latency of response to enter a dark compartment or chamber O ..
.~.

2 0 ~ ~ 7 11 4 li where an electroshoc~ has been experienced earlier by the rat being tested. The latency of the maximal response is 300 seconds.
Experimental Protocol:
Young rats were subjected to post-natal anoxia as described in Example 27. R(+)PAI or S(-)PAI were administered according to one of the following protocols:
Protocol A - Nursing mothers were given a dose of either isomer of 1-1.5 mg/kg/day, in drin~ing water until weanlng at 21 days. ~ollowing that the weaned offsprings were directly dosed with the same dose for 20 days. Treatment was terminated at 40 days and the test was performed at 60 days, that is 20 days after the last dose of the drug.
Protocol B - The dose was reduced to 0.5 mg/kg/day administered to the nursing mother till weaning at 21 days then directly to the young rats to 60 days at which time the test was performed.
Passive Avoidance Test - The apparatus consisted of a lit chamber adjoining a dar~ chamber and a sliding door separating the two. At training, a rat was placed in the lit chamber for 30 sec. then the door was opened. The rat moved to the dark chamber with a latency that was recorded. Upon entry of the rat into the dar~ compartment, the door was closed and a 0.3 mA foot- shoc~ was delivered for 3 sec.
Retention (memory) after 48 hours was determined by repeating the test and recording the latency to step through from light to darkness to an arbitrary maximum of 300 sec.
Results:
The results of these experiments are shown in Table 6.

~' 2~317~ 4 EFFECT OF PAI ISOMERS ON PASSIVE AVOIDANCE
RESPONSE IN YOUNG RATS (60-DAYS OLD) PROTOCOL A
5 Group Treatment Before After Electroshock Electroshock Control - 49 + 13 201 + 111 Control (+)PAI 49 + 19 220 + 100(+9%)*
Control (-)PAI 48 + 13 192 + 116 Anoxia-lesioned - 45 + 11 183 + 109 Anoxia-lesioned (+)PAI 49 + 10 239 + 99(+19%)*
Anoxia-lesioned (-)PAI 55 + 27 179 + 123 PROTOCOL B

Group Treatment Before After , Electroshock Electroshock Control - 53 + 20 104 + 101 Control (+)PAI 48 + 11 128 + 119(+23%)*

Anoxia-lesioned - 45 + 8 119 + 105 Anoxia-lesioned (+)PAI 52 + 12 137 _ 126(+15%)*
Anoxia-lesioned (-)PAI 48 + 19 112 + 112 - Figures represent the latency in seconds for entering a dark compartment where an electroshock had been first experienced by the rat tested.
* The indicated percent increases are with respect to the anoxia or control groups correspondingly.
The experimental results indicated that (+)PAI but not (-)PAI is effective in improving the memory of anoxia-lesioned and control rats. Drugs active in this test are considered to be potentially useful for treatment of various Ill~lloLy impairment disorders, dementia and especially senile dementia of the Alzheimer's type.

_ - 32 ~ 7 ~ 4 Effect of R(+)PAI on the anoxia-induced hyperactive syndrome in juvenile rats Rats that had been exposed postnatally to anoxia and then left to grow under normal conditions show increased motor activity in the open field at the age of 10-42 days (Hertshkowitz et al., Dev. Brain Res. 7:145-155 (1983)).
The effect of R(+)PAI and S(-)PAI on such hyperactive syndrome was investigated.
Experimental Protocol:
Anoxia was performed on rat pups on the first post-natal day. They were placed in a glass chamber and exposed to 100% nitrogen for 25 min. They were resuscitated by intermittent massage softly applied to the chest and then returned to their respective mothers. Control rats received the same treatment but with air instead of nitrogen.
The R(+)PAI or S(-)PAI (0.5 mg/kg/day) was administered to the nursing mothers in drinking water, thereby transferred to the sucklings through milk.
Locomotion was measured in 6 fully computerized cages (28 x 28 cm) by recording the number of crossing over a given period of time. Crossings of grid infrared beams at 4-cm intervals initiated electrical impulses which fed a counter.
Recordings of motor activity were made at the ages of 15 and 20 days, over a period of 15 min.
Results:
The experimental results are given in Table 7.

~,.

- 33 - ~ Q ~ ~ 7 ~ 4 EFFECT OF EACH OF THE TWO ENANTIOMERS ON THE
ANOXIA-INDUCED HYPERACTIVE SYNDROME
Group Treatment 15-day old 20-day old rats rats Control - 414 + 192(11) 808 + 212(12) Control (+)PAI 254 + 149(11)c 719 + 110(13) Anoxia-lesioned - 482 + 119 (7) 858 + 96 (9) Anoxia-lesioned(~)PAI 276 + 186(15)a 737 + 150(16)b Anoxia-lesioned(-)PAI 334 + 196 (S) 778 + 232 (6j Numbers in parenthesis are numbers of animals tested.
- The figures are the number of crossings of infrared beam grid in the activity cage over a period of 15 minutes.
a P<O.OO1 compared to anoxia untreated group.
b P<0.05 compared to anoxia untreated group.
c P<0.05 compared to control group.
These results indicate that chronic oral treatment with R(+)PAI at dose of 0.5 mg/kg administered to the nursing mother and reaching the milk-fed offspring, significantly ~ o~ed the hyperactive syndrome. Consequently, R(+)PAI is a potentially useful drug for the treatment of the hyperactive syndrome in children.

,

Claims (22)

1. R(+)-N-propargyl-1-aminoindan of the formula:

and pharmaceutically acceptable acid addition salts thereof.

2. Use of R(+)-N-propargyl-1-aminoindan for the treatment of human patients for Parkinson's disease, memory disorders, dementia of the Alzheimer type (DAT), depression and the hyperactive syndrome in children.

3. Use of R(+)-N-propargyl-1-aminoindan for the manufacture of a pharmaceutical composition for the treatment of human patients for Parkinson's disease, memory disorders, dementia of the Alzheimer type (DAT), depression and the hyperactive syndrome in children.

4. A pharmaceutical composition for the treatment of human patients for Parkinson's disease, memory disorders, dementia of the Alzheimer type (DAT), depression and the hyperactive syndrome in children, comprising as active ingredient R(+)-N-propargyl-1-aminoindan or a pharmaceutically acceptable acid addition salt thereof, together with a pharmaceutically acceptable carrier therefor.

5. A pharmaceutical composition according to claim 4, in form suitable for oral administration.

6. A pharmaceutical composition of claim 4, in form of an injectable solution or emulsion.

7. A pharmaceutical composition of claim 4, in form of suppositories for rectal administration.

8. A pharmaceutical composition of claim 4, in a form suitable for transdermal administration.

9. A pharmaceutical composition according to claim 5 or 7, in form of dosage units each containing 2-20 mg of said active ingredient.

10. A pharmaceutical composition according to claim 9, containing 5-10 mg of said active ingredient per dosage unit.

11. A pharmaceutical composition according to claim 6, in form of dosage units each containing 1-10 mg/ml of said active ingredient.

12. A pharmaceutical composition according to claim 11, containing 2-5 mg/ml of said active ingredient per dosage unit.

13. A pharmaceutical composition for oral use in the form of tablets or capsules, for the treatment of human patients for Parkinson's disease, memory disorders, dementia of the Alzheimer type (DAT), depression and the hyperactive syndrome in children, comprising R(+)-N-propargyl-1-aminoindan of formula (I) as defined in claim 1, Levodopa and a decarboxylase inhibitor.

14. A composition according to claim 13, comprising 2-10 mg of R(+)-N-propargyl-1-aminoindan, 50-250 mg Levodopa and 10-25 mg L-Carbidopa.

15. A composition according to claim 13, comprising 2-10 mg R(+)-N-propargyl-1-aminoindan, 50-200 mg Levodopa and 12.5-50 mg benserazide.

16. A method for the preparation of R(+)-N-propargyl-1-aminoindan and an acid addition salt thereof, comprising reacting the R(-)-enantiomer of 1-aminoindan with propargyl bromide or propargyl chloride in the presence of an organic or inorganic base, and isolating the R(+)-enantiomer of the N-propargyl-1-aminoindan by chromatography, distillation, selected extraction and, if a pharmaceutically acceptable acid addition salt is desired, converting the free base obtained into the desired pharmaceutically acceptable acid addition salt thereof.

17. A method according to claim 16, wherein the reaction is carried in the presence of a solvent.

18. A method for the preparation of R(+)-N-propargyl-1-aminoindan and an acid addition salt thereof, comprising reacting racemic 1-aminoindan with propargyl bromide or propargyl chloride in the presence of an organic or inorganic base, and isolating the R(+)-enantiomer of the N-propargyl-1-aminoindan by chromatography, distillation, selected extraction and, if a pharmaceutically acceptable acid addition salt is desired, converting the free base obtained into the desired pharmaceutically acceptable acid addition salt thereof.

19. A method according to claim 18, wherein the reaction is carried in the presence of a solvent.

20. A method according to claim 17, comprising reacting a free base obtained with an optically active acid to produce two diastereomeric salts and separating the desired R(+)-N-propargyl-1-aminoindan salt.

21. A method according to claim 20, further including the step of regenerating the free base.

22. A method according to claim 20 or 21, wherein the separation of the R(+)-N-propargyl-1-aminoindan salt is effected by fractional crystallization.