Glutamic acid derivatives

STATE OF THE ART
French Patent No. 2,566,410 describes diaminopimelic acid compounds having antibacterial properties and U.S. Pat. No. 4,311,640 describes related compounds.
OBJECTS OF THE INVENTION
It is an object of the invention to provide the novel compounds of formula I and their non-toxic, pharmacutically acceptable addition salts and a process for their preparation.
It is another object of the invention to provide novel immunomodulating compositions and a novel method of inducing immunomodulating activity in warm-blooded animals.
These and other objects and advantages of the invention will become obvious from the following detailed description.
THE INVENTION
The novel compounds of the invention are selected from the group consisting of all isomeric forms and mixtures of isomers of glutamic acid compounds of the formula ##STR5## wherein the glutamic acid is of D- or L- configuration, R.sub.1 is selected from the group consisting of hydrogen, alkyl of 1 to 5 carbon atoms, an amino acid, a peptide of 2 to 4 amino acids and an amino acid or a peptide of 2 to 4 amino acids in which the amine is esterified with an optionally unsaturated aliphatic carboxylic acid of 6 to 24 carbon atoms or R.sub.1 is selected from the group consisting of a residue of a C.sub.6 -C.sub.24 optionally unsaturated aliphatic acid. R.sub.5 is selected from the group consisting of hydrogen and an alkyl of 1 to 5 carbon atoms, R.sub.3 is selected from the group consisting of hydroxy, alkoxy of 1 to 5 carbon atoms and an amino acid with the amine optionally substituted with alkyl of 1 to 5 carbon atoms, Z is ##STR6## R.sub.2 is selected from the group consisting of hydrogen, an amino acid and a peptide of 2 to 4 amino acids, R.sub.4 is selected from the group consisting of hydroxyl, alkoxy of 1 to 5 carbon atoms and an amino acid optionally substituted on the amine with alkyl of 1 to 5 carbon atoms, U is selected from the group consisting of ##STR7## --CH.dbd.CH--CH.sub.2 -- (E or Z isomer), --CH.sub.2 -CH.dbd.CH-- (E or Z isomer) and ##STR8## or U and Y together are .dbd.CH--CH.sub.2 --CH.sub.2 -- (E or Z isomer) and X is hydrogen or U and X together are .dbd.CH--CH.sub.2 --CH.sub.2 -- (E or Z isomer) and Y is hydrogen and their salts with non-toxic, pharmaceutically acceptable acid or bases.
The amino acid in the compounds of formula I is preferably an .alpha.-amino acid and examples of such acids are Ala, Val, Ival, Leu, Ile, Asp, Asn, Glu, Gln, Ser, Thr, Cyc, Met, Lys, Arg, Phe, Tyr, Trp, His and Pro, Nva, Nle, Hyp, Orn, In the D or L form, as well as Sar and Gly, it being possible for all the said acids to be N-esterified or N-alkylated. In the case of a peptide of 2, 3 or 4 amino acids, the latter are chosen from the group consisting of the above amino acids. It will be understood by convention that the symbols for the .alpha.-amino carboxylic acids denote these acids in their D or L configuration (for example, the term Ala denotes alanine in D form or in L form).
The saturated or unsaturated aliphatic acid of 6 to 24 carbon atoms, preferably from 12 to 22 carbon atoms, may be stearic acid, palmitic acid, lauric acid, caprylic acid, myristic acid, .alpha.- or .gamma.-linolenic acid, linoleic acid, arachidonic acid or docosapentaenoic acid.
Examples of alkyl of 1 to 5 carbon atoms are pentyl, isobutyl, butyl and isopropyl, and preferably propyl, ethyl or methyl. Examples of alkoxy of 1 to 5 carbon atoms are pentoxy or butoxy, but preferably propoxy, ethoxy or methoxy.
The products of formula I contain one or more asymmetric carbon atoms and, as stated above, the subject of the invention is the said compounds of formula I in all their possible isomeric forms and in the form of mixtures.
The non-toxic, pharmaceutically acceptable salts of the derivatives of the invention can be formed with organic and inorganic bases such as alkali metal and alkaline earth metal hydroxides such as, for example, sodium, potassium, lithium and calcium hydroxides and magnesium or ammonium hydroxide. Among organic bases, there may be mentioned substituted or unsubstituted alkylamines such as trimethylamine, methylamine, propylamine, N,N-dimethylethanolamine or tris(hydroxymethyl)methylamine. Basic amino acids such as lysine or arginine may also be mentioned as well as glucosamine or procaine may be mentioned.
The addition salts with inorganic or organic acids can be, for example, the salts formed with hydrochloric acid, hydrobromic acid, nitric acid, sulfuric acid, phosphoric acid, acetic acid, formic acid, propionic acid, maleic acid, fumaric acid, succinic acid, tartaric acid, citric acid, oxalic acid, glyoxylic acid and aspartic acid, alkanesulfonic acids such as methane- and ethanesulfonic acid, arylsulfonic acids such as benzene- or p-toluenesulfonic acid, and arylcarboxylic acids such as benzoic acid.
Among the preferred compounds of formula I are those wherein the glutamic acid has the D-configuration, those wherein R.sub.3 and R.sub.4 are hydroxy, those wherein R.sub.5 is hydrogen and their non-toxic, pharmaceutically acceptable acid addition salts. Specific preferred compounds are 2-amino-6-.gamma.-D-glutamylamino)-4-methyleneheptanedioic acid, 2-(L-alanylamino)-6-(.gamma.-Dglutamylamino)-4-methyleneheptanedioic acid, 2-amino-4-methylene -6-[{N-(N-1-oxo-octadecyl)-L-alanyl-.gamma.-D-glutamyl}-amino]heptanedioic acid, 2-amino-4-methylene-6 [[N-(1-oxo-octadecyl) -.gamma.-D-glutamyl]-amino]-heptanedioic acid and their non-toxic, pharmaceutically acceptable acid addition salts.
The novel process of the invention for the preparation of the compounds of formula I comprises reacting a glutamic acid compound of the formula ##STR9## wherein Alk is alkyl of 1 to 3 carbon atoms and R.sub.1 ' has the definition of R.sub.1 other than hydrogen or an amino protective group with a compound of the formula ##STR10## as an individual isomer or mixture of isomers wherein U has the above definition, Alk.sub.1 and Alk.sub.2 are alkyl of 1 to 3 carbon atoms, X' and Y' are hydrogen or --COOAlk.sub.3, Alk.sub.3 is alkyl of 1 to 3 carbon atoms or together with U form an additional bond and R.sub.2 is amine protecting group, an amino acid or a peptide of 2 to 4 amino acids with the amine protected to obtain a compound of the formula ##STR11## in all isomeric forms or isomeric mixtures which is optionally isolated and salified or subjected to the following reactions in any order:
a) if X' or Y' is COO-Alk.sub.3 : decarboyxlation,
b) deprotection of the amino groups,
c) dealkylation of the hydroxyl groups,
d) amidation of the free amino groups with an amino acid or a peptide of 2, 3 or 4 amino acids in which the amino group is protected, followed by deprotection of this amino group,
e) esterificaiton or salification of the carboxy groups with a base, and
f) salification of the amino groups with an acid.
In a preferred mode of the process of the invention, the glutamic acid compound of formula II is activated by formation of a mixed anhydride such as with isobutyl chloroformate or by the presence of a condensation agent such as dicyclohexylcarbodiimide, N,N'-carbonyldiimidazole or bis(alkylamides) of sulfurous acid such as ##STR12## The decarboxylation is preferably effected with a concentrated inorganic acid such as 12N hydrochloric acid. A direct decarboxylation may be effected directly by the procedure of Krapcho or Keinan et al [J. Org. Chem., Vol. 51 (1986), p. 3615-3619].
The deprotection of the amino groups (formyl or BOC, for example) is preferably carried out with a dilute mineral acid such as hydrochloric acid. The dealkylation of the carboxyl groups is preferably carried out by saponification with an inorganic base such as potassium hydroxide and, preferably sodium hydroxide. It can, if necessary, be performed in two steps in the event of being incomplete. In the latter case, the second dealkylation is preferably carried out after the deprotection of the amino groups and/or the decarboxylation. The amidation of the free amino groups is carried out, for example, using a functional derivative such as a halide of the amino acid or peptide, or in the presence of a condensation agent such as those mentioned above. The esterification of the carboxyl groups is carried out, for example, under the same conditions as above (condensing agents).
The compounds of formula I may have a basic or acidic nature and if so, the addition salts thereof may be prepared by reaction with the appropriate base or acid in substantially stoichiometric form.
In a preferred embodiment of the process, the compound of formula I.sub.A is subjected to the following reactions: dealkylation of the carboxyl groups, deprotection of the amino groups and decarboxylation, amidation or salification of the amino groups with an acid and/or esterification or salification of the carboxyl groups with a base.
Some of the compounds of formula III are known and if they are not known, they may be prepared by reacting a compound of the formula ##STR13## wherein Alk.sub.1, Alk.sub.2, U, X', Y' and R.sub.2 ' have the above definitions with an alkanesulfonyl halide of 1 to 3 alkyl carbon atoms, preferably methane sulfonyl chloride, in the presence of a condensation agent such as pyridine and then with an alkali metal azide such as sodium azide or diphenylphosphoryl azide to form a compound of the formula ##STR14## reducing the latter with triphenyl phosphine, for example, followed by aqueous hydrolysis or by catalytic hydrogenation in the presence of a Lindlar catalyst (poisoned palladium on charcoal) to form a compound of the formula ##STR15## wherein.sub.2, X', Y', U, Alk.sub.1 and Alk.sub.2 have the above definitions and when X' and/or Y' are other than hydrogen, reacting the latter with an agent to protect the amino group to form a compound of the formula ##STR16## wherein R.sub.2 ', Alk.sub.1, Alk.sub.2, U, X' and Y' have the above definitions and Rp is an amino protective group, subjecting the latter to a decarboxylating agent to obtain the corresponding compound with 1 or 2 asymetrical carbon atoms, separating the latter into the isomers or diastereoisomers such as by crystallization or chromatography and then removing the amino protective group to form the compound of formula III in the form of separate isomers or isometric mixtures.
The compounds of formulae II and IV are known.
The novel immunomodulatory compositions of the invention are comprised of an immunomodulatorily effective amount of at least one compound of formula I and its non-toxic, pharmaceutically acceptable salts with acids and bases and an inert pharmaceutical carrier or excipient. The compositions may be in the form of tablets, dragees, gelatin capsules, granules, suppositories and injectable solutions or suspensions.
Examples of suitable excipients are talc, gum arabic, lactose, starch, magnesium stearate, cocoa butter, aqueous or non-aqueous vehicles, fats of animal or vegetable origin, paraffinic derivatives, glycols, the various wetting, dispersing or emulsifying agents and preservatives.
The compositions of the invention have exceptional immuno modulatory properties, particularly by activation of human monocytes and production of monokines such as TNF (tumor necrosis factor) and IL-1, interleukin-1.
They are useful in the treatment of autoimmune diseases, whether conditions affecting organs nonspecifically (rheumatoid polyarthritis, lupus erythematosus, haemolytic anaemia, autoimmune leukopenia, and the like) or specific diseases of organs (thyroiditis, Basedow's disease, Addison's disease, multiple sclerosis, pemphigus, haemorrhagic rectocolitis, some types of nephropathy, and the like). Compositions are also useful in the treatment of haemopathies, cancer, AIDS, viral and microbial conditions, especially those which are chronic and recurrent (bronchitis, influenza and the like), diseases of the oral cavity, and the like. They can constitute adjuvants of viral therapy, antibiotic therapy or anticancer chemotherapy.
The compositions also find use in the treatment of many secondary or acquired immune deficiency states observed during a wide variety of conditions: deficiencies associated with metabolic disorders, deficiencies of iatrogenc origin (corticoids, ionizing radiation, etc.), deficiencies observed in major burns patients, and the like.
The novel method of the invention for inducing immunomodulatory activity in warm-blooded animals, including humans, comprises administering to warm-blooded animals an immunodulatorily effective amount of at least one compound of formula I and its non-toxic, pharmaceutically acceptable salts with acids and bases. The compounds may be administered orally, rectally or parenterally and the usual daily dose is 0.007 to 0.7 mg/kg depending on the compound, condition treated and method of administration. For example, the compound of Example 1 and/or 8 may be orally administered at a dose 0.007 to 0.7 mg/kg for the treatment of rheumatoid polyarthritis.
In the following examples there are described several preferred emobdiments to illustrate the invention. However, it is to be understood that the invention is not intended to be limited to the specific embodiments.

EXAMPLE 1
2-amino-6-(.gamma.-D-glutamylamino)-4-methylene-heptanedioic acid
STEP A: Triethyl 1-formylamino-3-methylene-5-[(N-trifluoroacetyl-0-methyl-.gamma.-D-glutamyl)-amino-1,1,5-pentanetricarboxylate
A solution of 4 g of 1-methyl N-trifluoroacetyl-D-glutamate in 20 ml of dimethoxyethane was added to a solution of 5.1 g of triethyl 5-amino-1-(formylamino)-3-methylene-1,1,5-pentanetricarboxylate in 280 ml of dimethylethylamine and the mixture was cooled to 0.degree. C. 3.2 g of dicyclohexylcarbodiimide were added in small portions and the mixture was stirred for 16 hours at 0.degree. C. and filtered. The filtrate was evaporated to dryness and the residue was taken up with cold dimethoxyethane. The mixture was filtered and the filtrate was taken to dryness. The residue was taken up in methylene chloride and the mixture was washed with N hydrochloric acid, with saturated sodium bicarbonate solution and then with water saturated with sodium chloride, dried and evaporated to dryness. The residue was purified by chromatography on silica (eluant:ethyl acetate/cyclohexane 5:5) to obtain 5 g of the expected product with a specific rotation [.alpha.].sub.D =+8.degree. (c=1% in methylene chloride).
STEP B: 2-amino-6-(.gamma.-D-glutamylamino)-4-methylene-heptanedioic acid
Saponification
10.9 ml of N sodium hydroxide were added dropwise over 5 minutes at 0.degree. C. to a solution of 1.28 g of the product of Step A in 20 ml of ethanol and the mixture was allowed to return to room temperature and stirred for 24 hours. It was neutralized with 0.9 ml of 12N hydrochloric acid and taken to dryness under reduced pressure.
Decarboxylation--deformylation
The residue was taken up in 10 ml of ethanol and 1 ml of 12N hydrochloric acid was added and the mixture was stirred for 40 minutes at 80.degree. C.
Saponification
The above product was chilled and 15.2 ml of 2N sodium hydroxide were added dropwise over 5 minutes. The mixture was stirred for 24 hours at room temperature, brought to pH 6 using 12N hydrochloric acid and taken to dryness.
Purification
The above product was taken up in a few ml of water and the pH was adjusted to 6 with N sodium hydroxide. The mixture was dealkalinized on Dowex 50 W.times.8 H.sup.+ resin (50-100 mesh) and elution was performed first with water and then with N ammonia solution. The product was purified by chromatography on silica eluant:ethanol/ammonia solution 95:5, then ethanol/ammonia solution 8:2) and the eluant was evaporated to dryness. The residue was taken up in 200 ml of water and the mixture was filtered. The filtrate was lyophilized for 16 hours to obtain 400 mg of the expected product with a specific rotation [.alpha.].sub.D =-9.5.degree..+-.1.degree. (c=1% in 4N hydrochloric acid).
A) Preparation of 1-methyl-N-trifluoroacetyl-D-glutamate
Step 1: 5-(1,1-dimethylethyl)-1-methyl-N-trifluoroacetyl-D-glutamate
4.1 ml of triethylamine and then, while cooling 4.1 ml of trifluoroacetic anhydride were added dropwise to a solution of 5.5 g 5-(1,1-dimethylethyl)-1-methyl-D-glutamate in 180 ml of methylene chloride. The mixture was then stirred for 2 hours at room temperature and poured into 70 ml of ice-cold water. The resulting mixture was extracted with methylene chloride and the extract was washed with saline solution, dried and taken to dryness to obtain 7.1 g of the expected product with a specific rotation of [.alpha.].sub.D =+5.degree..+-.1.degree. (c=1.3% in dioxane).
STEP 2: 1-methyl-N-trifluoroacetyl-D-glutamate
6.8 g of the product of Step 1 were dissolved in 50 ml of methylene chloride and 50 ml of trifluoroacetic acid were added. The mixture was stirred for 1 hour and evaporated to dryness. The residue was taken up in ethyl acetate and the mixture was poured into water. The resulting mixture was extracted with ethyl acetate and the extract was washed with saline solution and taken to dryness to obtain 5.5 g of the expected product with specific rotation of [.alpha.].sub.D =+9.degree..+-.2.degree. (c=0.6% in dioxane).
B) Preparation of the starting triethyl 5-amino-1-(formylamino)-3-methylene-1,5-pentanetricarboxylate
STEP 1: Diethyl 2-(formylamino)-(2-methyl-2-propenyl)-propane-dioate
40 g of potassium carbonate, 0.380 g of 18-crown-6-crown ether catalyst and 39.9 g of chloromethylpropene were added to a solution of 30 g of ethyl formamidomalonate in 300 ml of cyanomethyl and the mixture was stirred at reflux for 3 hours and filtered. The filtrate was evaporated to dryness and the residue was cooled to 0.degree. C. to 5.degree. C. and taken up in 10 ml of isopropyl ether. The mixture was filtered, washed with isopropyl ether and dried under reduced pressure to obtain 25.2 g of the expected product with a melting point of 72.degree. C.
STEP 2: Triethyl 1-(formylamino)-5-hydroxy-3-methylene-1,1,5-pentanetricarboxylate (mixture of isomers)
A solution of 26.5 g of ethyl glyoxylate in 180 ml of methylene chloride was added dropwise over 10 minutes to a solution of 84 g of ferric chloride in 180 ml of methylene chloride and the mixture was stirred for 1 hour and cooled to -20.degree. C. A solution of 34 g of the product of Step A in 180 ml of methylene chloride was added dropwise over 20 minutes, and the mixture was stirred for 1 hour at -20.degree. C. and was then poured into 300 ml of ice-cold water. The resulting mixture was extracted with methylene chloride and the extract was washed with 2N NCl and then with saline solution, dried and evaporated to dryness under reduced pressure to obtain 56.5 g of the expected product (mixture of isomers) with a melting point of 68.degree. C. after purification by chromatography on silica (eluant:ethyl acetate/cyclohexane 6:4)
STEP 3: Triethyl 5-azido-1-(formylamino)-3-methylene-1,1,5-pentanetricarboxylate
46 g of the product (mixture of isomers) of Step 2 were dissolved in 500 ml of pyridine and the mixture was cooled to 0.degree. C. 12 ml of methanesulfonyl chloride were added dropwise at 0.degree. C. and the mixture was stirred for 3 hours at room temperature and poured into 400 ml of ice-cold 4N hydrochloric acid and 200 ml of methylene chloride. The resulting mixture was extracted with methylene chloride and the extract was washed with 4N hydrochloric acid, with saturated sodium bicarbonate solution and with saline solution, dried and evaporated to dryness under reduced pressure. The 56 g of residue obtained were dissolved in 250 ml of dimethylformamide and 9.98 g of sodium azide were added. The mixture was stirred for 16 hours at room temperature and the solvent was removed. The residue was taken up in methylene chloride and the mixture was washed with saturated sodium bicarbonate solution and then with saline solution, dried and taken to dryness to obtain 59 g of expected product (mixture of isomers) which was purified by chromatography on silica (eluant:cyclohexane/ethyl acetate 8:2) to obtain 26 g of the expected product.
STEP 4: Triethyl 5-amino-1-(formylamino)-3-methylene-1,1,5-pentanetricarboxylate
10.9 g of triphenylphosphine were added to a solution of 13 g of the product of Step 5 in 250 ml of tetrahydrofuran at approximately -5.degree. C. and the mixture was stirred for 5 hours at room temperature. 8.5 ml of water were added and the mixture was stirred for 24 hours at room temperature. The tetrahydrofuran was evaporated off and the residue was taken up in methylene chloride. The mixture was poured into ice-cold 2N hydrochloric acid, followed by extraction with 2N hydrochloric acid, neutralization with sodium bicarbonate and extraction with methylene chloride. The extract was washed with saline solution, dried and evaporated to dryness to obtain 10 g of the expected product melting at 50.degree. C. after crystallization from isopropyl ether.
EXAMPLE 2
2-(L-Alanylamino)-6-(.gamma.-D-glutamylamino)-4-methyleneheptanedioic acid
STEP A: Triethyl 1-amino-3-methylene-5-(N-trifluoroacetyl-0-methyl-.gamma.-D-glutamyl)-amino]-1,1,5-pentanetricarboxylate
1.5 ml of 12N hydrochloric acid were added to a solution of 1.22 g of product of Step A of Example 1 in 15 ml of ethanol and the mixture was stirred for 40 minutes at 80.degree. C. The solution was removed under reduced pressure and the residue was taken up in 10 ml of water. The mixture was neutralized with sodium bicarbonate and extracted with methylene chloride. The extract was washed with saline solution, dried and taken to dryness. The residue was purified by chromatography on silica (eluant:ethyl acetate/cyclohexane 8:2) to obtain 0.850 g of the expected product.
STEP B: Triethyl 1-(N-[(1,1-dimethylethoxy)-carbonyl]-L-alanyl-amino-3-methylene-5-[(N-trifluoroacetyl-0-methyl-.gamma.-D-glutamyl)-amino]-1,1,5-pentanetricarboxylate
0.310 g of BOC-L-alanine were dissolved in 50 ml of tetrahydrofuran and 0.43 ml of triethylamine were added. The mixture was cooled to approximately 5.degree. C. and 0.23 ml of isobutyl chloro formate were added. The mixture was stirred for 30 minutes at approximately +5.degree. C. and a solution of 0.800 g of the product of Step A in 10 ml of tetrahydrofuran was added dropwise over 5 minutes. The mixture was allowed to return to room temperature and was stirred for 16 hours. The tetrahydrofuran was removed and the residue was taken up in a water/methylene chloride mixture. The mixture was extracted with methylene chloride and the extract was washed with saline solution, dried and taken to dryness. The residue was purified by chromatography on silica (eluant:ethyl acetate/cyclohexane 5:5) to obtain the expected product with a specific rotation of [.alpha.].sub.D =12.degree..+-.1.degree. (c=1% in methylene chloride).
STEP C: 2-(L-alanylamino)-6-(.gamma.-D-glutamylamino)-4-methyleneheptanedioic acid
Using the procedure of Step B of Example 1, 700 mg of the product of Step B were reacted. Saponification, deprotection of the BOC-protected amine, saponification and purification were performed to obtain 170 mg of the expected product with a specific rotation of [.alpha.].sub.D =-13.degree..+-.1.degree. (c=1% in 4N HCl).
EXAMPLE 3
2-Amino-4-methylene-6-[N-(1-oxo-octadecyl)-L-alanyl-.gamma.-D-glutamyl-amino]-heptanedioic acid
Using the procedure of Example 1, 1-methyl-N-[N-(1-oxo-octadecyl)-L-alanyl]-D-glutamate was used in place of the corresponding N-trifluoroacetyl derivative obtained in the preparation A of Example 1, to obtain the expected product with a specific rotation of [.alpha.].sub.D =-25.degree. (c=0.6% in water).
Preparation of 1-methyl N-[N-(1-oxo-octadecyl)-L-alanyl]-D-glutamate
STEP 1: Methyl N-(1-oxo-octadecyl)-L-alaninate
24.9 ml of triethylamine were added to a solution of 10 g of L-alanine methyl ester hydrochloride in 250 ml of methylene chloride, followed by dropwise addition over 30 minutes of a solution of 21.7 g of stearyl chloride in 50 ml of methylene chloride. The mixture was stirred for 150 minutes and filtered and the filtrate was washed with 2N hydrochloric acid, then with saline solution, dried and taken to dryness under reduced pressure. The residue was made into a paste with isopropyl ether, vacuum filtered and crystallized in methanol to obtain 22 g of the expected product with melting point of 84.degree. C. and with a specific rotation of [.alpha.].sub.D =-15.degree. (c=1% pyridine).
STEP 2: N-(1-oxo-octadecyl)-L-alanine
A suspension of 21 g of above product in 500 ml of methanol was cooled at 0.degree. C. and 62 ml of N potassium hydroxide were added dropwise. The mixture was stirred for 16 hours at room temperature and 500 ml of methanol were added. The mixture was stirred for 4 hours, cooled to 0.degree. C., brought to a pH of 3 using 2N hydrochloric acid and evaporated. The residue was taken up in methylene chloride and the mixture was washed with saline solution, dried and taken to dryness under reduced pressure. The residue was made into a paste with isopropyl ether vacuum filtered and crystallized from methanol to obtain 11.8 g of the expected product melting at 102.degree. C. and having a specific rotation of [.alpha.].sub.D =-18.degree. (c=0.9% in pyridine).
STEP 3: 5-(1,1-dimethylethyl)-1-methyl N-[N-(1-oxo-octadecyl)-L-alanyl]-D-glutamate
A suspension of 1.77 g of N-(1-oxo-octadecyl)-L-alanine and 1.08 g of 5-(1,1-dimethylethyl)-1-methyl D-glutamate in 170 ml of dimethoxyethane was cooled to 0.degree. C. and a solution of 1.23 g of N,N-dicyclohexylcarbodiimide in 5 ml of dimethoxyethane was added dropwise over 10 minutes. The mixture was stirred for 3 hours at room temperature, cooled and filtrated. The filtrate was evaporated to dryness and the residue was taken up in 250 ml of ether in the heated state. The mixture was filtered and the filtrate was evaporated to dryness under reduced pressure. The residue was made into a paste in isopropyl ether and vacuum filtered to obtain 2.4 g of the expected product melting at .perspectiveto. 100.degree. C. after crystallization in methanol and having a specific rotation of [.alpha.].sub.D =-32.degree..+-.1.degree. (c=1% in CH.sub.2 Cl.sub.2).
STEP 4: 1-Methyl N-[N-(1-oxo-octadecyl)-L-alanyl]-D-glutamate
31 ml of trifluoroacetic acid were added dropwise to a solution of 11.4 g of the product of Step 3 in 150 ml of methylene chloride and the mixture was left for 16 hours with stirring and then evaporated to dryness under reduced pressure. The residue was taken up in methylene chloride and the mixture was washed with saline solution, dried and filtered. The filtrate was evaporated to dryness under reduced pressure and the residue was then crystallized from ethanol to obtain 6.8 g of the expected product melting at .perspectiveto. 110.degree. C. and having a specific rotation of [.alpha.].sub.D =-16.degree..+-.1.degree. (c=0.9% in pyridine).
EXAMPLE 4
2-Amino-6-(.gamma.-D-glutamylamino)-3-heptenedioic acid
Using the procedure of Example 1, triethyl 5-amino-1-formylamino-2-pentene-1,1,5-tricarboxylate was reacted to obtain the expected product.
Preparation of triethyl 5-amino-1-formylamino-2-pentene-1,1,5-tricarboxylate
Using the procedure for the preparation of triethyl 5-amino-1-(formylamino)-3-methylene-1,1,5-pentanetricarboxylate, chloro-methylpropene replaced the allyl bromide to obtain the expected product in the form of an oil with an Rf=0.4 in ethyl acetate/ethanol 4:1.
EXAMPLE 5
2-Glycylamino-6-[N-(1-oxo-dodecyl)-L-alanyl-.gamma.-D-glutamyl]-amino-2-heptenedioic acid
Using the procedure of Example 1, 1-methyl N-[N-(1-oxo-dodecyl)-L-alanyl]-D-glutamate [prepared like 1-methyl N-[N-(1-oxo-octadecyl)-L-alanyl]-D-glutamate in Example 3 by replacing stearyl by lauryl (dodecyl)] was reacted with 7-ethyl-1-methyl-6-amino-2-[(N-formylglycyl)-amino]-3-heptenedioate. In this case, deformylation with hydrochloric acid was not necessary and the neutralization and the desalification were carried out simultaneously using a H.sup.+ resin (Amberlyst 15). The expected product, which became resinous at 150.degree. C., was obtained and had a specific rotation of [.alpha.].sub.D =-14.degree. (c=0.8% in water).
EXAMPLE 6
Mixture of (2D, 6L)- and (2L, 6D)-2-amino-6-(.gamma.-D-glutamylamino)-4-methyleneheptanedioic acid
STEP A: Mixture of (2D, 6L)- and (2L, 6D)-2-formylamino-4-methylene-6-[N-(trifluoroacetyl)-.gamma.-D-glutamylamino]-heptanedioic acid
1.3 g of dicyclohexylcarbodiimide were added at 0.degree. C. to a solution containing 1.5 g of the mixture of diethyl (2D,6L)- and (2L, 6D)-2-formamido-4-methylene-6-amino-1,7-heptanedioate and 1.48 g of D-glutamic acid in 150 ml of dimethoxyethane, and the resulting mixture was stirred for 16 hours while the temperature was maintained at 0.degree. C. The precipitate was filtered off and the filtrate was concentrated to dryness under reduced pressure. The 10.5 g of crude product were purified by chromatography on silica (eluant:cyclohexane/ethyl acetate 2:8) to obtain the expected product with a specific rotation of [.alpha.].sub.D =-14.degree. (c=0.8% in water).
STEP B: Mixture of (2D, 6)- jand (2L, 6D)-2-amino-6-(.gamma.-D-glutamylamino)-4-methyleneheptanedioic acid
5 ml of 12N hydrochloric acid were added to 1.9 g of the product of Step A dissolved in 100 ml of ethanol, and the mixture was stirred for 30 minutes. The solvent was removed under reduced pressure and the residue was taken up in 50 ml of ethanol. The pH was adjusted to 7 with 0.1N sodium hydroxide solution and the mixture was cooled to 0.degree. C. and 16 ml of N sodium hydroxide were added dropwise. The reaction medium was allowed to return to room temperature, stirred for 16 hours and neutralized with N hydrochloric acid. The solvents were removed under reduced pressure and the residue was chromatographed on silica (eluant:ethanol/ammonia solution 95:5, 90:10 and then 80:20). The resin obtained was taken up in water and the mixture was filtered and the filtrate was lyophilized to obtain 0.92 g of expected product with a specific rotation of [.alpha.].sub.D =-13.degree..+-.1.degree. (c=1% in 3N HCl).
EXAMPLE 7
Mixture of (2D, 6D)- and (2L, 6L)-2-amino-6-(.gamma.-D-glutamylamino)-4-methyleneheptanedioic acids
STEP A: Mixture of (2D, 6D)- and (2L, 6L)-2-formylamino-4-methylene-6-[N-(trifluoroacetyl)-.gamma.-D-glutamylamino]-heptanedioic acids
Using the procedure of Step A of Example 6, a mixture of diethyl (2D, 6D)- and (2L, 6L)-2-formamido-4-methylene-6-amino-1,7-heptanedioates was reacted to obtain the expected product.
STEP B: Mixture of (2D,6D)- and (2L,6L)-2-amino-6-amino-6-(.gamma.-D-glutamylamino)-4-methyleneheptanedioic acids
Using the procedure of Step B of Example 6, the product of Step A was reacted to obtain the expected product having a specific rotation of [.alpha.].sub.D =-12.5.degree..+-.1.degree. (c=[1%], 3N HCl).
The mixture of diethyl (2D,6D)- and (2L,6L)-2-formamido-4-methylene-6-amino-1,7-heptanedioates used at the beginning of Example 7 was prepared as described in the preparation of the Example (Step C), starting with the mixture of diethyl (2D,6D)-and (2L,6L)-2-formamido-4-methylene-6-tert-butoxycarbonylamino-1,7-heptanedioates (isomer I) obtained in Step B of this preparation.
Preparation of 7-ethyl 1-methyl 6-amino-2-[(N-formylglycyl)-amino]-3-heptanedioate
Using the procedure of preparation B of Example 1, diethyl-(formylamino)-(2-methyl-2-propenyl)-propanedioate in Step 2 was replaced by methyl 2-[(N-formylglycyl)-amino]-2-(2-propenyl)-ethanoate to obtain the expected product with an Rf=0.2 in a methylene chloride/methanol (9:1) mixture.
Comment
The reduction of the azide to amine (Step 4 of preparation B of Example 1) was carried out by hydrogenation in the presence of palladium on calcium carbonate and of quinoline, instead of triphenyl phosphine.
Preparation of the mixture of diethyl (2D, 6L)- and (2L, 6D)-2-formamido-4-methylene-6-amino-1,7-heptanedioates
STEP A: Triethyl 1-formamido-3-methylene-5-(tert-butoxycarbonylamino)-1,1,5-pentanetricarboxylate
13.6 g of di-tert-butyl pyrocarbonate dissolved in 25 ml of methylene chloride were added at room temperature to 19.5 g of triethyl 1-formamido-3-methylene-5-amino-1,1,5-pentanetricarboxylate dissolved in 75 ml of methylene chloride, and the mixture was maintained with stirring at room temperature for 36 hours. The reaction medium was diluted with 150 ml of methylene chloride and the organic phase was washed with water and dried. The solvents were removed under reduced pressure and the mixture was left to crystallize at +4.degree. C. to obtain 25.8 g of expected product melting at 68.degree. C.
STEP B: Mixture of diethyl (2D,6D)- and (2L,6L)-2-formamido-4-methylene-6-(tert-butoxycarbonylamino)-1,7-heptanedioates and mixture of (2D,6L) and (2L,6D) isomers
2.21 g of cesium carbonate and 9.42 g of p-aminophenol were added to 17.25 g of product of Step A dissolved in 250 ml of dimethylformamide, and the mixture was heated for 3 hours to 85.degree. C. The mixture was allowed to room temperature and was filtered. The solvents were removed under reduced pressure and the residue was taken up in 300 ml of methylene chloride. The organic phase was washed with 0.5N hydrochloric acid and then with aqueous sodium bicarbonate solution and dried. The solvent was removed under reduced pressure and the residue was chromatographed on a silica column (eluant:cyclohexane/ethyl acetate 6:4) to obtain 4.70 g of isomer I (DD,LL isomer), 3.84 g of isomer II (DL, LD isomer) and 2.80 g of a mixture of the 2 isomers.
STEP C: Mixture of diethyl (2D,6L)- and (2L,6D)-2-formamido-4-methylene-6-amino-1,7-heptanedioates
25 ml of 2N hydrochloric acid in ether were added to 3 g of product II of Step B (DL,LD isomer) dissolved in 50 ml of methylene chloride. The mixture was stirred at room temperature for 30 minutes and concentrated under an inert atmosphere. The amine hydrochloride was taken up in methylene chloride to which triethylamine had been added, and the mixture was then evaporated to dryness under reduced pressure. After chromatography on silica (eluant:ethyl acetate/cyclohexane 7:3), 1.86 g of expected product were recovered.
EXAMPLE 8
2-Amino-4-methylene-6-[N-1-oxo-octadecyl)-L-alanyl)-.gamma.-D-glutamyl-amino]-heptanedioic acid and its tri sodium salt
STEP A: Diethyl-2-formamido-(-2-methyl-2-propenyl)-propanedioate
A solution of 30 g of ethyl formamido-malonate in 300 ml of acetonitrile was added to a mixture of 40 g of potassium carbonate, 0.380 g of 18 crown 6 ether catalyst and 39.9 g of chloromethylpropane and the mixture was refluxed for 3 hours and then filtered. The filtrate was dried and cooled to 0.degree. to 5.degree. C. The precipitate was taken up in isopropyl ether and filtered. The product was washed with isopropyl ether and was dried under reduced pressure to obtain 25.2 g of the desired product melting at 72.degree. C.
STEP B: Triethyl 1-formamido-5-hydroxy-3-methylene-1,1,5-pentane-tridicarboxylate
A solution of 26.5 g of ethyl glycoxylate in 180 ml of methylene chloride was added dropwise over 10 minutes to a solution of 84 g of ferric chloride in 180 ml of methylene chloride and the mixture was stirred for one hour, then cooled to -20.degree. C. A solution of 34 g of the product of Step A was added dropwise over 20 minutes to the mixture which was then stirred at -20.degree. C. for one hour and was poured into 300 ml of ice water. The mixture was extracted with methylene chloride and the organic phase was washed with 2N hydrochloric acid, then aqueous sodium chloride solution, dried and evaporated to dryness under reduced pressure to obtain 56.5 g of a mixture of isomers of the expected product melting at 68.degree. C. after chromatography over silica (6-4 ethyl acetate/cyclohexane).
STEP C: Triethyl 5-azido-1-formamido-3-methylene-1,1,5-pentane-tricarboxylate
12 ml of methanesulfonyl chloride were added dropwise at 0.degree. C. to a solution of 46 g of the mixture of Step B in 500 ml of pyridine and after stirring for 3 hours at room temperature, the mixture was poured into 400 ml of iced 4N hydrochloric acid and 200 ml of methylene chloride. The mixture was extracted with methylene chloride and the organic phase was washed with 4N hydrochloric acid, then with saturated sodium bicarbonte solution, then with aqueous sodium chloride solution, and evaporated to dryness under reduced pressure. The 56 g of residue were dissolved in 250 ml of dimethylformamide and after the addition of 9.98 g of sodium azide, the mixture was stirred at room temperature for 16 hours and evaporated to dryness. The residue was taken up in methylene chloride and the solution was washed with saturated sodium bicarbonate solution, then with aqueous sodium chloride solution, dried and evaporated to dryness to obtain 59 g of the desired mixture of isomers. Chromatography over silica and elution with a 8-2 cyclohexane methyl acetate mixture yielded 26 g of the said product.
STEP D: Triethyl 5-amino-1-formamido-3-methylene-1,1,5-pentane tricarboxylate
10.9 g of triphenylphosphine were added to a solution of 13 g of the product of Step C in 250 ml of tetrahydrofuran at about -5.degree. C. and after stirring for 5 hours at room temperature, 8.5 ml of water were added. The mixture was stirred at room temperature for 24 hours and was evaporated to dryness. The residue was taken up in methylene chloride and the solution was added to iced 2N hydrochloric acid. The mixture was extracted with 2N hydrochloric acid and the extract was neutralized with sodium bicarbonate. The mixture was extracted with methylene chloride and the organic phase was washed with sodium chloride solution, dried and evaporated to dryness to obtain 10 g of the expected product melting at <50.degree. C. after crystallization from isopropyl ether.
STEP E: Triethyl 5-(tert.-butoxycarbonylamino)-1-formamido-3-methylene-1,1,5-pentane-tricarboxylate
A solution of 15.65 g of ditert.-butyl pyrocarbonate (Bo C.sub.2 O) in 25 ml of dichloromethane was added to a solution of 19.5 g of the product of Step D in 75 ml of dichloromethane and the mixture was stirred for 36 hours in a water bath at room temperature. The mixture was diluted with 150 ml of dichloromethane and was washed with water, filtered and dried to obtain 25.8 mg of the expected product melting at 68.degree. C.
STEP F: Diethyl 6-(tert-butoxycarbonylamino)-2-formamido-4-methylene-heptanedioate
2.21 g of cesium carbonate and 9.42 g of p-amino-thiophenol were added all at once to a solution of 17.25 g of the product of Step E in 250 ml of dimethylformamide and the mixture was heated at 85.degree. C. for 3 hours and was then returned to room temperature. The solution was filtered and the filtrate was evaporated to dryness under reduced pressure. The oil residue was taken up in 300 ml of chloromethane and the solution was washed with hydrochloric acid and then with a saturated aqueous sodium bicarbonate solution. The oil was purified by HPLC and elution with a 6-4 cyclohexane-ethyl acetate mixture yielded the expected product.
STEP G: Diethyl 2-amino-6-formamido-4-methylene-heptanedioate
100 ml of a solution of 2.6N hydrochloric acid in anhydrous ether were added to a solution of 6.4 g of the product of Step F in 200 ml of methylene chloride and after stirring at room temperature for one hour, nitrogen was bubbled therethrough The mixture was evaporated to dryness under reduced pressure at 30.degree. C. and the residue was taken up in methylene chloride. The mixture was neutralized and evaporated to dryness to obtain 4.6 g of raw product. The latter was chromatographed over silica and eluted with a 9-1 ethyl acetate-ethanol mixture to obtain the desired product with an Rf=0.06.
STEP H: Diethyl 2-formamido-4-methylene-6-[[0-methyl-N-[N-(1-oxo-octadecyl)-L-alanyl]-.gamma.-D-glutamyl]-amino]-heptanedioate
0.58 ml of triethylamine and 0.3 ml of isobutyl chloroformate were added at 14.degree..+-.1.degree. C. to a solution of 0.992 g of methyl N-[N-(1-oxo-octadecyl)-2-alanyl]-D-glutamate acid, 50 ml of dioxane and 50 ml of tetrahydrofuran and after stirring at 14.degree. C. for 35 minutes, a solution of 0.572 g of the product of Step G in 10 ml of tetrahydrofuran was added. The mixture was stirred at room temperature for 2 hours and was evaporated to dryness at reduced pressure at 30.degree. C. The residue was chromatrographed over silica and eluted with a 2.5-7.5 cyclohexane-ethyl acetate mixture to obtain 480.6 mg of the desired diastereoisomer A and 476 mg of the desired diastereoisomer B.
STEP I: Diethyl 2-amino 6-[[O-ethyl N-[N-(1-oxo-octadecyl)-L-alanyl]-.gamma.-D-glutanyl]amino]4-methylene heptanedioate
403 mg of the product of step H (isomer B) in ethanol were stirred for 45 minutes at 80.degree. C. with 0,41 ml of concentrated hydrochloric acid diluted with 4,1 ml of ethanol. The mixture was then cooled and 2 ml of water were added. The mixture was neutralized with sodium bicarbonate and extracted with methylene chloride dried and evaporated to dryness under reduced pressure. The residue was chromatographed to obtain the desired product which is used as it is for the next step.
STEP J: 2-amino-4-methylene-6-[[N-[N-(1-oxo-octadecyl)-L-alanyl]-.gamma.-D-glutamyl]-amino]-heptanedioic acid and its tri sodium salt
0.43 ml of sodium hydroxide were added at 0.degree. C. to a solution of 107 mg of the product of Step I in 5 ml of ethanol and the mixture was stirred overnight at room temperature and was evaporated to dryness to obtain 117 mg of product which was added to 10 of apyrogen water. The mixture was filtered and lyophylized to obtain 50 mg of the desired product with a specific rotation of [.alpha.].sub.D =-25.degree..+-.2.degree. (c=1% in H.sub.2 O).
PREPARATION
STEP A: Methyl N-(1-oxo-octadecyl)-L-alaninate
24.9 ml of triethylamine were added to a solution of 10 g of methyl L-alaninate hydrochloride in 250 ml of methylene chloride and then a solution of 21.7 g of stearyl chloride in 50 ml of methylene chloride was added dropwise over 30 minutes. The mixture was stirred for 21/2 hours and filtered. The filtrate was washed and with 2N hydrochloric acid, then with aqueous sodium chloride, dried and evaporated to dryness under reduced pressure. The residue was empasted with isopropyl ether, vacuum filtered and crystallized from methanol to obtain 22 g of the desired product melting at 84.degree. C. and having a specific rotation of [.alpha.].sub.D =-15.degree. (c=1% in pyridine)
STEP B: N-(1-oxo-octadecyl)-L-alaninate
62 ml of N potassium hydroxide solution were added dropwise at 0.degree. C. to a suspension of 21 g of the product of Step A in 500 ml of methanol and after stirring at room temperature for 16 hours, 500 ml of methanol were added. The mixture was stirred for 4 hours, cooled to 0.degree. C. and the pH was adjusted to 3 with 2N hydrochloric acid. The mixture was evaporated to dryness and the residue was taken up in methylene chloride. The solution was washed with aqueous sodium chloride, dried and evaporated to dryness under reduced pressure. The residue was empasted with isopropyl ether, vacuum filtered and crystallized from methanol to obtain 11.8 g of the desired product melting at 102.degree. C. and having a specific rotation of [.alpha.].sub.D =-18.degree. (c=0.9% in pyridine).
STEP C: 1-methyl N-[N-(1-oxo-octadecyl)-L-alanyl]-D-glutamate
A solution of 1.23 g of N,N-dicyclohexylcarbodiimide in 5 ml of dimethoxyethane was added dropwise over 10 minutes at 0.degree. C. to a suspension of 1.77 g of the product of Step B and 1.08 of 1,1-dimethylethyl D-glutamate and after stirring at room temperature for 3 hours, the mixture was cooled and filtered and evaporated to dryness. The residue was taken up in 250 ml of hot ether and the solution was filtered and empasted to dryness under reduced pressure. The residue was evaporated with isopropyl ether, and vacuum filtered to obtain 2.4 g of the desired product melting at 100.degree. C. after crystallization from methanol and a specific rotation of [.alpha.].sub.D =-32.degree..+-.1.degree. (c=1% in CH.sub.2 Cl.sub.2).
STEP D: 1-methyl N-[N-(1-oxo-octadecyl)-L-alanyl]-D-glutamate
31 ml of trifluoroacetic acid were added dropwise to a solution of 11.4 g of the product of Step C in 150 ml of methylene chloride and after stirring for 16 hours, the mixture was evaporated to dryness under reduced pressure. The residue was taken up in methylene chloride and the solution was washed with sodium chloride solution, dried, filtered and evaporated to dryness under reduced pressure. The product was crystallized from ethanol to obtain 6.8 g of the exposed product melting at 110.degree. C. and having a specific rotation of [.alpha.].sub.D =-16.degree..+-.1.degree. (c=0.9% in pyridine)
EXAMPLE 19
2-Amino-4-methylene-6-[[N-(1-oxo-octadecyl)-.gamma.-D-glutamyl]amino]-heptanedioic acid
STEP A: Diethyl 2-formamido-4-methylene-6-[[O-methyl-N-(1-oxo-octadecyl)-.gamma.-D-glutamyl]-amino]-heptanedioate
0.62 ml of triethylamine and 0.3 ml of isobutyl chloroformate were added at 14.degree. C. over 5 minutes to a solution of 615 mg of 1-methyl-N-(1-oxo-octadecyl)-glutamate in a 1-1 mixture of THF and dioxane and after stirring the suspension at 14.degree. C. for 35 minutes, a solution of 915 mg of the product of Step G of Example 8 in 10 ml of tetrahydrofuran was added. The mixture was stirred at room temperature for 2 hours and was then added to ice and was extracted with methylene chloride. The organic phase was washed, dried, filtered and evaporated to dryness at 30.degree. C. to obtain 2.1 g of a mixture of diastereoisomers A and B. The mixture was chromatographed over silica and eluted with a 2.5-7.5 cyclohexane-ethyl acetate mixture to obtain 588 mg of diastereoisomer A of the expected compound and 580 mg of diastereoisomer B.
STEP B: Diethyl 2-amino-4-methylene-6[[O-methyl-N-(1-oxo-octadecyl)-.gamma.-D-glutamyl]-amino]-heptanedioate
0.5 ml of concentrated hydrochloric acid were added to a solution of 470 mg of the diastereoisomer A of Step A in 4.7 ml of ethanol and the mixture was heated to 80.degree. C. for 45 minutes. 20 ml of water were added and the pH was adjusted to 7. The mixture was extracted with methylene chloride and the organic phase was dried, filtered and evaporated to dryness to obtain 500 mg of product which was purified by chromatography over silica to obtain 251 mg of diastereoisomer A of the expected product.
NMR Spectrum (CDCl.sub.3.250 MHz)
Peaks at 3.64 (2-hydrogen of principal chain) and at 4.99 (hydrogen of 4-methylene)
Using the same procedure, 580 mg of the diastereoisomer B of Step A were reacted to obtain 243 mg of the expected diastereoisomer B.
NMR Spectrum (CDCl.sub.3 --250 MHz)
Peaks at 1.65 (hydrogen of 2-substituted amino); at 3.61 (2-hydrogen of principal chain; at 4.94-4.98 (hydrogen of 4-methylene).
STEP C: 2-Amino-4-methylene-6-[[N-(1-oxo-octadecyl)-.gamma.-D-glutamyl]-amino]-heptanedioic acid (A and B diastereoisomers)
1.02 ml of a solution of 0.00102 M of sodium hydroxide were added at 0.degree. C. to a solution of 233 mg of the A isomer product of Step B in ethanol and after stirring overnight at room temperature, the mixture was evaporated to dryness under reduced pressure. The residue was dissolved in 15 ml of water and the solution was filtered and lyophilized to obtain 133 mg of the expected diastereoisomer A with a specific rotation of [.alpha.].sub.D =-9.degree..+-.2.degree. (c=0.7% in H.sub.2 O).
NMR Spectrum (D.sub.2 O)
Peaks at 4.16 and 4.33 (6-hydrogen and hydrogen of CH of .gamma.-D-glutyamyl); at 3.41 (2-hydrogen); at 0.89 (18-hydrogen of octadecyl).
Using the same procedure, 234 mg of the B isomer product of Step B were reacted to obtain 194.4 mg of the expected B isomer product with a specific rotation of [.alpha.].sub.D =-8.5.degree..+-.2.degree. (c=0.7% in H.sub.2 O).
NMR Spectrum (D.sub.2 O)
Peaks at 4.15 and 4.32 (6-hydrogen and hydrogen of --CH-- of .gamma.-D-glutamyl); at 3.46 (2-hydrogen); at 0.88 (18-hydrogen of octadecyl).
The starting (1) methyl N-(1-oxo-octadecyl) acid glutamate used in Step A was prepared by the following reactions ##STR17##
EXAMPLE 10
Tablets were prepared containing 50 mg of 2-amino-6-(.gamma.-D-glutamylamino)-4-methylene-heptanedioic acid and sufficient excipient of lactose, starch, talc, magnesium stearate for a final weight of 100 mg.
EXAMPLE 11
Tablets were prepared containing 50 mg of 2-(L-alanylamino)-6-(.gamma.-D-glutamylamino)-4-methylene-heptanedioic acid and sufficient excipient of lactose, starch, talc and magnesium stearate for a final weight of 100 mg.
EXAMPLE 12
Tablets were prepared containing 50 mg of the product of example 8 and sufficient excipient of lactose starch, talc, magnesium stearate for a final weight of 250 mg.
PHARMACOLOGICAL STUDY
Stimulation of monocytic cells with an immunostimulant
The mononuclear cells of the circulating blood of normal donors were separated by the classical technique described by Boyum using a Ficoll gradient. After being washed, the mononuclear cells were incubated at 37.degree. C. for 1 hour in the proportion of 5.times.10.sup.6 monocytes (NSE.sup.+ cells) per ml of culture medium, 5 ml per culture bottle. The culture medium used in this experiment was composed of RPMI 1640 to which antibiotics and HEPES buffer had been added. After one hour, the non-adherent cells were removed by washing the bottles with medium previously brought to 37.degree. C., and the adherent cells, composed essentially of monocytes (>90%), were cultured again in the presence of different amounts of test products in a PBS medium (Dulbecco) without Ca.sup.2+ or Mg.sup.2+. Culturing was continued for 24 or 48 hours and the cell supernatants were then withdrawn, centrifuged, aliquoted and stored either at -80.degree. C. or at -20.degree. C. The culture supernatants were replaced in the bottles by the same amount of pyrogen-free distilled water to lyse the cells. The lysate was recovered, aliquoted and also stored at -20.degree. C. The following experiments were carried out in the presence or absence of interferon- (10.sup.3 U/ml) at a dose at which IFN-.gamma. alone was inactive.
Tests for the presence in the supernants of monokines (interleukin-1 and tumor necrosis factor) on the basis of their biological activity.
Interelukin-1 (IL-1) Test
This test was first described by Gery et al in 1972 [Gery et al, 1972 Potentiation of the T Lymphocyte response to mitogens. II. The Cellular Source of Potentiating Mediator(s). J. Exp. Med., 136-143]. It is based on the co-mitogenic action of IL-1 in the presence of an antigen (mimicked by phytohaemagglutinin in the test) on mouse thymocytes. 1.5.times.10.sup.6 thymocytes of C.sub.3 H/HeJ mice (supplied by C.S.E.A.L. of Orleans) were cultured for 3 days in the presence of different dilutions of cell supernatants and lysates likely to contain IL-1 activity, and Wellcome PHA-P (1 .mu.g/ml), in culture plates having 96 flat-bottomed wells, in a final volume of 200 .mu.l of medium composed of RPMI 1640 containing, in addition to antibiotics (penicillin 1 .mu./ml streptomycin 1000 .mu./ml, 1 mM HEPES buffer, 2 mM glutamine, 5% calf serum and 5.times.10.sup.-5 M 2-mercaptoethanol). After 68 hours of culturing, 1 .mu.Ci of tritiated thymidien was added to each well ([methyl.sup.3 H]-thymidine, CEA Saclay, TMM79A, specific activity 1 .mu.Ci/mM), and the radioactivity incorporated by the cells was measured after the cultures had been filtered on a Skaton type semi-automatic collecting apparatus and the filters counted in a scintillation counter (LKB). The results were expressed as the difference between the pulses per minute incorporated by the cultures in the presence of supernatants and the pulses per minute incorporated by the control cultures.
Tumor Necrosis Factor (TNF) Test
TNF activity was demonstrated by the toxicity of this factor on L-929 target cells (sub-clone .alpha.). The technique was sensitized by adding actinomycin D to the test. The L cells were distributed in the proportion of 2.times.10.sup.4 cells per well of a flat-bottomed microplate in 100 .mu.l of RPMI 1640 medium enriched with 5% calf serum, glutamine, HEPES buffer and antibiotics. After 24 hours, different dilutions of the test supernatants were added in a volume of 100 .mu.l, as well as a dose of actinomycin D of 1 .mu.g/ml. After 24 hours of culturing, the number of unlysed viable cells was measured by staining the plates with crystal violet and measuring the optical density of different wells on a multiscan reader.
RESULTS
The products of Examples 1, 2, 8 and 9 stimulated monocytes and their IL-1 and TNF production. In addition, there was synergy between the products of Examples 1, 2, 8 and 9 and interferon-.gamma. and or LPS.
Stimulation of the lymphocyte cells by an immuno stimulant
Test for lymphoblast transformation
The mono-nuclear cells of circulating blood are put in culture at a rate of 2.10.sup.6 cells/ml in flat bottom micro-plates with 96 wells (Nunc) in 100 .mu.l of RPMI 1640 medium enriched with 10% of foetal calf serum (Hyclone), antibiotics, glutamine and Hepes. The products to be tested are added into the wells at a rate of 100 .mu.l to the final dilutions of 1.10 or 100 .mu.g/ml either alone or in presence of phytohemaglutinine PHA-P (Welcome labs) at 1 and/or 10 .mu.g/ml. The plates are put at a temperature of 37.degree. C. in an incubator with CO.sub.2 in an atmosphere saturated with humidity. At the end of 2 and 5 days, the cultures are stopped, an incorporation of tritiated thymidine is carried out in the conditions described above in the detection test for Interleukin-1. The results are given in impulsions per minute.
Summarizing, the products of the chemical examples have been shown to be neither cytotoxic for the lymphocytes in culture nor mitogenetic for these same cells. On the other hand, added at the same time as one product known to be non-specific T mitogenetic such as PHA, they have been shown to be capable of partly inhibiting (especially at 100 .mu.g/ml) the effects of this product. These results could be reproduced on all the donors tested (between 3 and 30 per product).
Production of immuno-globulins
The same cells were cultivated for a week in the presence of different products to be tested at a dose of 0.1, 1 and 10 .mu.g/ml alone or in the presence of two doses of the bacteria Staphylococcus aureus Cowan (SAC) (10.sup.-3 and 10.sup.-4), bacteria known for stimulating the production of immuno-globulins by the human B lymphocytes in a non-specific manner. The supernatants are collected at the end of the culture, and their content of immuno-globulin is evaluated by standard techniques of detection by the ELISA method using a human anti-immunoglobulin anti-body available commercially. The results are given in ng of immuno-globulin per ml of supernatant.
The experiments showed us that the products used on their own are not capable of causing stimulation of lymphocytes of the B type (neither their proliferation, nor their differentiation in plasmocytes) but in the presence of SAC the product from Example 8 is capable of increasing the production of immuno-globulins. On the other hand, the product of the example does not give the same result (see figure).
In vivo activity
Activation of the macrophages
The ability to activate the cells of the monocyte macrophage compartment has been confirmed in vivo in mice. After an injection by intra-peritoneal route of different doses of the products to be tested, the peritoneal cells of the mice BALB/c were collected; the quantity of the cells found had not increased and they were essentially macrophages, which shows that these products are not chemotactic at least in the conditions used. The macrophages have the particularity of being able to respond better to a membranal stimulation which "mimikes" a phagocytosis; in effect, these cells do not spontaneously produce superoxide anions or oxygenated water, but this oxidative metabolism is prepared and is released on the phagocyte signal. The experiments were carried out with different products. The oxidative metabolism is made evident by a chemiluminescence technique in the presence of luminol, using a Berthold LB950 chemiluminometer.
The kinetics of the reaction shows that the phenomenon of activation lasts from 24 to 48 hours following the single injection of the product.
Various modifications of the products and processes of the invention may be made without departing from the spirit or scope thereof and it should be understood that the invention is intended to be limited only as defined in the appended claims.

Number	Date	Country	Kind
87 02547	Feb 1987	FRX
88 11155	Aug 1988	FRX

Number	Name	Date	Kind
4311640	Kuroda et al.	Jan 1982
4730006	Bohme et al.	Mar 1988

Glutamic acid derivatives

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