The invention relates to novel compounds as novel and useful industrial products, which are ligands that activate RAR receptors. The invention also relates to a process for preparing them, and to their use in pharmaceutical compositions for use in human or veterinary medicine, or alternatively in cosmetic compositions, and to the non-therapeutic use of these compositions.

Compounds with activity of retinoid type (vitamin A and its derivatives) are widely described in the literature as having activity in cell proliferation and differentiation processes. These properties give this class of compounds high potential in the treatment or prevention of numerous pathologies, and more particularly in dermatology and cancer. Many biological effects of retinoids are mediated by modulating the nuclear retinoic acid receptors (RAR).

The RAR receptors activate transcription by binding to DNA sequence elements, known as RAR response elements (RARE), in the form of a heterodimer with the retinoid X receptors (known as RXRs).

Three subtypes of human RARs have been identified and described: RARE, RARE and RARy.

Chemical compounds with activating activity

on receptors of RAR type are known from the prior art.

Mention may be made especially of the aromatic heterocyclic biaryl compounds described in patent EP 0 816 352 B1, which find applications in the treatment of dermatological, rheumatic, respiratory and ophthalmological complaints and also in the cosmetics field.

Patent EP 0 952 974 B1 itself describes biphenyl derivatives substituted with an aromatic or heteroaromatic radical. When these molecules contain an aminoalkyl on the phenyl ring, they are more difficult to metabolize at this bond.

It thus appears to be advantageous, more particularly for topical use in man, to have available compounds that are metabolized faster in order to limit the residence time of the product in the body.

It so happens that the Applicant has now discovered, surprisingly and unexpectedly, novel compounds which are ligands that activate retinoic acid receptors containing a bond that is metabolically cleavable at the phenyl, making it possible to satisfy this important criterion in the case of a use in man.

These compounds find applications in human medicine, especially in dermatology, and in the cosmetics field.

Thus, the present invention relates to compounds corresponding to the following general formula (I): in which: - Ar represents a radical chosen from the radicals of formulae (a) to (c) below:

- Ri represents a radical-OR3 or-NR4R5, R3, R4 and R5 having the meanings given below, - R2 represents a hydrogen, fluorine or chlorine atom, a methyl radical or a radical OR6, R6 having the meanings given below, - R3 represents a hydrogen atom, a linear or branched alkyl radical containing from 1 to 20 carbon atoms, a mono-or polyhydroxyalkyl radical containing from 1 to 20 carbon atoms, a monoaminoalkyl radical containing from 1 to 20 carbon atoms, or a sugar residue, - R4 and R5, which may be identical or different, represent a hydrogen atom, a hydroxyl radical, a linear or branched alkyl radical containing from 1 to 6 carbon atoms, a mono-or polyhydroxyalkyl radical containing from 1 to 20 carbon atoms, or R4 and

R5 form, with the nitrogen of the general structure, an amino acid residue or a peptide residue, or alternatively R4 and R5,'taken together, form a heterocycle, - R6 represents a hydrogen atom, a methyl radical or an acetyl radical, - R7 represents a CF3 or methyl radical, - r'and r", which may be identical or different, represent a hydrogen atom, a linear, branched or cyclic alkyl radical, containing from 1 to 4 carbon atoms, or a radical (C=O) R7, or alternatively r'and r", taken together, form a pyrrolidine or piperidine heterocycle, R7 having the above meanings, - A represents an oxygen atom or a sulfur atom, - n is an integer between 1 and 4, - W represents a-CH2-radical, - Y represents an oxygen atom or a sulfur atom, and the salts of the compounds of formula (I) when Ri = OH, and also the optical and geometrical isomers of the compounds of formula (I).

When the compounds according to the invention are in the form of a salt, it is preferably a salt of an alkali metal or alkaline-earth metal, or alternatively a zinc salt or a salt of an organic amine.

According to the present invention, the term "alkyl containing from 1 to 4 carbon atoms"preferably means methyl, ethyl, n-propyl, i-propyl, c-propyl, isopropyl, n-butyl, i-butyl or t-butyl radicals.

According to the present invention, the term "alkyl containing from 1 to 6 carbon atoms"preferably means methyl, ethyl, n-propyl, i-propyl, c-propyl, isopropyl, n-butyl, i-butyl, t-butyl, n-pentyl or n-hexyl radicals.

The term"linear or branched alkyl containing from 1 to 20 carbon atoms"especially means methyl, ethyl, propyl, isopropyl, cyclopropyl, n-butyl, i-butyl, t-butyl, n-pentyl, n-hexyl, 2-ethylhexyl, octyl, dodecyl, hexadecyl or octadecyl radicals.

The term"monohydroxyalkyl"means a radical preferably containing from 1 to 20 carbon atoms, especially a hydroxymethyl, 2-hydroxyethyl, 2-hydroxy- propyl or 3-hydroxypropyl radical.

The term"polyhydroxyalkyl"means a radical preferably containing from 3 to 20 carbon atoms and from 2 to 5 hydroxyl groups, such as 2,3- dihydroxypropyl, 2,3, 4-trihydroxybutyl or 2,3, 4,5- tetrahydroxypentyl radicals or a pentaerythritol residue.

The term"monoaminoalkyl"means a radical preferably containing from 1 to 20 carbon atoms and an amino group, especially a 2-aminoethyl, 3-aminopropyl or 4-aminobutyl radical.

The term"sugar residue"means a residue derived especially from glucose, galactose or mannose, or alternatively from glucuronic acid, such as 6'- mannosyl, 6'-glucosyl or 6'-galactosyl.

The term"amino acid residue"especially means a residue derived from lysine, from glycine or from aspartic acid, and the term"peptide residue"more particularly means a dipeptide or tripeptide residue resulting from the combination of amino acids.

According to the present invention, given that W represents a-CH2-radical, the general formula (I) may be simplified as follows: in which: - Ar, A, r'and r''have the above meanings; - n'is an integer between 2 and 5.

According to the present invention, the compounds of formula (I) that are more particularly preferred are those for which at least one and preferably all of the conditions below are satisfied: A represents an oxygen atom, Ar represents a radical (a), R1 represents a radical-OR3.

Among the compounds of formula (I) falling within the context of the present invention, mention may be made especially of the following: 1. 4'- (4-Isopropylaminobutoxy)-3'- (5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid 2. 4'- (4-Ethylaminobutoxy)-3'- (5, 5,8, 8-tetramethyl- 5,6, 7,8-tetrahydronaphth-2-yl) biphenyl-4-carboxylic acid 3. 4'- (4-Propylaminobutoxy)-3'- (5, 5,8, 8-tetramethyl- 5,6, 7,8-tetrahydronaphth-2-yl) biphenyl-4-carboxylic acid 4. 4'- [4- (Isopropylmethylamino) butoxy]-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid 5. 4'- (4-Diethylaminobutoxy)-3'- (5, 5,8, 8-tetramethyl- 5,6, 7,8-tetrahydronaphth-2-yl) biphenyl-4-carboxylic acid 6. 4'- (4-Acetylaminobutoxy)-3'- (5, 5,8, 8-tetramethyl- 5,6, 7,8-tetrahydronaphth-2-yl) biphenyl-4-carboxylic acid 7. 4'- [4- (Acetylethylamino) butoxy]-3'- (5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid 8. 4'- [4- (Acetylisopropylamino) butoxy]-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid 9. 4'- (4-Acetylaminobutoxy)-3'- (5, 5,8, 8-tetramethyl-

5,6, 7,8-tetrahydronaphth-2-yl) biphenyl-4-carboxylic acid 10. 4'- (4-Pyrrolidin-1-ylbutoxy)-3'- (5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid 11. 4'- (4-Isopropylaminobutylsulfanyl)-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid 12. 4'- (2-Isopropylaminoethoxy)-3'- (5, 5,8, 8-tetramethyl- 5,6, 7,8-tetrahydronaphth-2-yl) biphenyl-4-carboxylic acid 13. 4'- (3-Isopropylaminopropoxy)-3'- (5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid 14. 4'- (5-Isopropylaminopentyloxy)-3'- (5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid 15. 4'- (5-Ethylaminopentyloxy)-3'- (5, 5,8, 8-tetramethyl- 5,6, 7,8-tetrahydronaphth-2-yl) biphenyl-4-carboxylic acid 16. Ethyl 4'- (4-isopropylaminobutoxy)-3'- (5, 5,8, 8-tetra- methyl-5,6, 7, 8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate 17. Propyl 4'- (4-isopropylaminobutoxy)-3'- (5, 5, 8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate 18. Isopropyl-4'- (4-isopropylaminobutoxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl-

4-carboxylate 19. 2,3-Dihydroxypropyl 4'- (4-isopropylaminobutoxy)- 3'- (5, 5,8, 8-tetramethyl-5, 6, 7, 8-tetrahydronaphth- 2-yl) biphenyl-4-carboxylate 20.3-Aminopropyl 4'- (4-isopropylaminobutoxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7, 8-tetrahydronaphth- 2-yl) biphenyl-4-carboxylate 21.6-Glucosyl 4'-(4-isopropylaminobutoxy)-3'-(5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate 22.6-Mannosyl 4'-(4-isopropylaminobutoxy)-3'-(5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate 23. Ethyl 4'- (4-isopropylaminobutoxy)-3'- (5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxamide 24. Diethyl 4'- (4-isopropylaminobutoxy)-3'- (5, 5,8, 8- tetramethyl-5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl- 4-carboxamide 25. [4'- (4-Isopropylaminobutoxy)-3'- (5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl-4-yl]- pyrrolidin-1-ylmethanone 26. {[4'-(4-Isopropylaminobutoxy)-3'-(5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carbonyl] amino} acetic acid 27. 3-Hydroxy-2-1 [4'- (4-isopropylaminobutoxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth- 2-yl) biphenyl-4-carbonyl] amino} propionic acid

28. 3-Fluoro-4'- (4-isopropylaminobutoxy)-3'- (5, 5,8, 8- tetramethyl-5, 6,7, 8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid 29. 3-Chloro-4'- (4-isopropylaminobutoxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid 30. 3-Chloro-4'- (4-isopropylaminobutoxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid 31. 3-Hydroxy-4'- (4-isopropylaminobutoxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid 32. 4'- (4-Isopropylaminobutoxy)-3-methoxy-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid 33. 3-Acetoxy-4'- (4-isopropylaminobutoxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid 34. 2-Fluoro-4'- (4-isopropylaminobutoxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid 35. 2-Chloro-4'- (4-isopropylaminobutoxy)-3'- (5, 5, 8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid 36. 2-Hydroxy-4'- (4-isopropylaminobutoxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid 37. 6- [4- (4-Isopropylaminobutoxy)-3- (5, 5,8, 8-tetra-

methyl-5, 6, 7,8-tetrahydronaphth-2-yl) phenyl] - nicotinic acid 38. 5- [4- (4-Isopropylaminobutoxy)-3- (5, 5,8, 8-tetra- methyl-5,6, 7, 8-tetrahydronaphth-2-yl) phenyl- pyridine-2-carboxylic acid 39. 5- [4- (4-Isopropylaminobutoxy)-3- (5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) phenyl- thiophene-2-carboxylic acid 40. 5- [4- (4-Isopropylaminobutoxy)-3- (5, 5, 8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) phenyl] furan- 2-carboxylic acid 41. 4- [4- (4-Isopropylaminobutoxy)-3- (5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) phenyl] furan- 2-carboxylic acid 42. 4- [4- (4-Isopropylaminobutoxy)-3- (5, 5,8, 8-tetra- methyl-5, 6,7, 8-tetrahydronaphth-2-yl) phenyl- thiophene-2-carboxylic acid 43. 5- [4- (4-Isopropylaminobutoxy)-3- (5, 5,8, 8-tetra- methyl-5, 6, 7, 8-tetrahydronaphth-2-yl) phenyl- thiophene-3-carboxylic acid 44. 5- [4- (4-Isopropylaminobutoxy)-3- (5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) phenyl] furan- 3-carboxylic acid 45. 4'- (4-Ethylaminobutoxy)-3-hydroxy-3'- (5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid 46. 3-Hydroxy-4'- (4-propylaminobutoxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl-

4-carboxylic acid 47. 3-Hydroxy-4'- (3-propylaminopropoxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid 48. 4'- (4-Piperidin-1-ylbutoxy)-3'- (5, 5,8, 8-tetramethyl- 5,6, 7, 8-tetrahydronaphth-2-yl) biphenyl-4-carboxylic acid 49. Ethyl 4'- (3-isopropylaminopropoxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7, 8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate 50. Ethyl 4'- (3-cyclopropylaminopropoxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate 51. 4'- (3-Cyclopropylaminopropoxy)-3'- (5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid 52. Ethyl 4'- (3-butylaminopropoxy)-3'- (5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate 53. 4'- (3-Butylaminopropoxy)-3'- (5, 5,8, 8-tetramethyl- 5,6, 7,8-tetrahydronaphth-2-yl) biphenyl-4-carboxylic acid 54. Ethyl 4'- (3-dimethylaminopropoxy)-3'- (5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate 55. 4'- (3-Dimethylaminopropoxy)-3'- (5, 5,8, 8-tetramethyl- 5,6, 7,8-tetrahydronaphth-2-yl) biphenyl-4-carboxylic acid

56. Ethyl 4'- (3-propylaminopropoxy)-3'- (5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate 57. 4'- (3-Propylaminopropoxy)-3'- (5, 5,8, 8-tetramethyl- 5,6, 7,8-tetrahydronaphth-2-yl) biphenyl-4-carboxylic acid 58. Ethyl 4'- (4-cyclopropylaminobutoxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate 59. 4'- (4-Cyclopropylaminobutoxy)-3'- (5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid 60. Ethyl 4'- (3-methylaminopropoxy)-3'- (5, 5,8, 8-tetra- methyl-5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate 61. 4'- (3-Methylaminopropoxy)-3'- (5, 5,8, 8-tetramethyl- 5,6, 7,8-tetrahydronaphth-2-yl) biphenyl-4-carboxylic acid 62. Ethyl 4'- (3-ethylaminopropoxy)-3'- (5, 5,8, 8-tetra- methyl-5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate 63. 4'- (3-Ethylaminopropoxy)-3'- (5, 5,8, 8-tetramethyl- 5,6, 7,8-tetrahydronaphth-2-yl) biphenyl-4-carboxylic acid 64. Ethyl 4'- (3-aminopropoxy)-3'- (5, 5,8, 8-tetramethyl- 5,6, 7,8-tetrahydronaphth-2-yl) biphenyl-4-carboxylate 65. 4'- (3-Aminopropoxy)-3'- (5, 5,8, 8-tetramethyl- 5,6, 7, 8-tetrahydronaphth-2-yl) biphenyl-4-carboxylic

acid 66. Ethyl 4'- (2-cyclopropylaminoethoxy)-3'- (5, 5, 8,8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate 67. 4'-(2-Cyclopropylaminoethoxy)-3'-(5,5,8,8-tetra- methyl-5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid 68. Ethyl 4r- (5-cyclopropylaminopentyloxy)-3r- (5, 5r8r8- tetramethyl-5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate 69. 4'-(5-Cyclopropylaminopentyloxy)-3'-(5,5,8, 8-tetra- methyl-5, 6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid 70. Ethyl 4'- (2-isopropylaminoethoxy)-3'- (5, 5, 8,8-tetra- methyl-5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate 71. Ethyl 4'- (5-ethylaminopentyloxy)-3'- (5, 5, 8, 8-tetra- methyl-5,6, 7, 8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate 72. Ethyl 4'- (5-aminopentyloxy)-3'- (5, 5,8, 8-tetramethyl- 5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl-4-carboxylate 73. 4'-(5-Aminopentyloxy)-3'-(5,5,8,8-tetramethyl- 5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl-4-carboxylic acid 74. Ethyl 4'- (4-aminobutoxy)-3'- (5, 5,8, 8-tetramethyl- 5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl-4-carboxylate 75. 4'- (4-Aminobutoxy)-3'- (5, 5, 8, 8-tetramethyl-5, 6, 7,8- tetrahydronaphth-2-yl) biphenyl-4-carboxylic acid.

A subject of the present invention is also processes for preparing the compounds of formula (I), in particular according to the reaction schemes given in Figure 1.

The claimed compounds may be obtained from starting materials of formula 1. These boronic acid derivatives may be coupled to corresponding aryl halide derivatives in order to obtain the intermediates of formula 2 under Suzuki coupling conditions. The compounds of formula 3 may then be obtained by bromination, for example in the presence of dibromine, and the precursors 5 may then be obtained after a coupling reaction, for example under the conditions described by Suzuki, of 3 with the boronic acid 4.

Nucleophilic substitution of the phenoxide or thiolate derived from 5 on a compound of type 6, in which X is a leaving group of the tosylate, mesylate, triflate or halide type, makes it possible to obtain the compounds of formula (I). Certain products require a deprotection step at this stage, for example in the case where r'or r"is equal to H (P converted into r' or r"). A product of formula (I) in which r'or r''is equal to H may be subjected to a nucleophilic substitution step or, if applicable, to a reductive amination step to obtain another compound in which r' and r"are other than H.

The compounds according to the invention have activating properties on RAR-type receptors. This RAR-

receptor-activating activity is measured in a test of transactivation by means of the dissociation constant Kdapp (apparent).

According to the invention, the expression "activator of RAR-type receptors"means any compound which, for at least one of the RAR subtypes, has a dissociation constant Kdapp of less than or equal to 1 pM, in a transactivation test as described in Example 32.

The preferred compounds of the present invention have, for at least one of the RAR subtypes, a dissociation constant Kdapp of less than or equal to 500 nM and advantageously less than or equal to 100 nM.

A subject of the present invention is also the compounds of formula (I) as described above, as medicinal products.

The compounds according to the invention are particularly suitable in the following fields of treatment: 1) for treating dermatological complaints associated with a keratinization disorder relating to cell differentiation and proliferation, especially for treating common acne, comedones, polymorphs, acne rosacea, nodulocystic acne, acne conglobata, senile acne, and secondary acnes such as solar acne, medication-related acne or occupational acne; 2) for treating other types of keratinization disorders, especially ichthyosis, ichthyosiform

conditions, Darier's disease, palmoplantar keratoderma, leukoplakia and leukoplakiform conditions, and cutaneous or mucous (buccal) lichen; 3) for treating other dermatological complaints with an inflammatory immunoallergic component, with or without cell proliferation disorder, and especially all forms of psoriasis, whether cutaneous, mucous or ungual, and even psoriatic rheumatism, or cutaneous atopy, such as eczema, or respiratory atopy, or alternatively gingival hypertrophy; 4) for treating all dermal or epidermal proliferations, whether benign or malignant, and whether of viral origin or otherwise, such as common warts, flat warts and verruciform epidermodysplasia, oral or florid papillomatoses, T lymphoma, and proliferations that may be induced by ultraviolet radiation, especially in the case of basocellular and spinocellular epithelioma, and also any precancerous skin lesion such as keratoacanthomas; 5) for treating other dermatological disorders such as immune dermatoses, such as lupus erythematosus, immune bullous diseases and collagen diseases, such as scleroderma ; 6) in the treatment of dermatological or general complaints with an immunological component; 7) for treating certain ophthalmological disorders, especially corneopathies; 8) for preventing or curing the stigmata of epidermal

and/or dermal atrophy induced by local or systemic corticosteroids, or any other form of cutaneous atrophy; 9) in the treatment of any cutaneous or general complaint of viral origin ; 10) in the treatment of skin disorders caused by exposure to UV radiation, and also for repairing or combating ageing of the skin, whether photoinduced or chronological ageing, or for reducing actinic pigmentations and keratosis, or any pathology associated with chronological or actinic ageing, such as xerosis ; 11) for combating sebaceous function disorders, such as the hyperseborrhoea of acne or simple seborrhoea; 12) for preventing or treating cicatrization disorders, or for preventing or repairing stretch marks, or alternatively for promoting cicatrization ; 13) in the treatment of pigmentation disorders, such as hyperpigmentation, melasma, hypopigmentation or vitiligo ; 14) in the treatment of lipid metabolism complaints, such as obesity, hyperlipidaemia, or non-insulin- dependent diabetes; 15) in the treatment of inflammatory complaints such as arthritis; 16) in the treatment or prevention of cancerous or precancerous conditions ; 17) in the prevention or treatment of alopecia of

various origins, especially alopecia caused by chemotherapy or radiation; 18) in the treatment of disorders of the immune system, such as asthma, type I sugar diabetes, multiple sclerosis or other selective dysfunctions of the immune system; and 19) in the treatment of complaints of the cardiovascular system, such as arteriosclerosis or hypertension.

A subject of the present invention is also a pharmaceutical composition comprising, in a physiologically acceptable medium, at least one compound of formula (I) as defined above.

A subject of the present invention is also a novel medicinal composition intended especially for treating the abovementioned complaints, which is characterized in that it comprises, in a pharmaceutically acceptable support that is compatible with the mode of administration selected for this composition, at least one compound of formula (I), an optical isomer thereof or a salt thereof.

The composition according to the invention may be administered orally, enterally, parenterally, topically or ocularly. The pharmaceutical composition is preferably packaged in a form that is suitable for topical application.

Via the oral route, the composition may be in the form of tablets, gel capsules, dragees, syrups,

suspensions, solutions, powders, granules, emulsions, suspensions of microspheres or nanospheres or lipid or polymer vesicles allowing a controlled release. Via the parenteral route, the composition may be in the form of solutions or suspensions for infusion or for injection.

The compounds according to the invention are generally administered at a daily dose of about 0.01 mg/kg to 100 mg/kg of body weight, in 1 to 3 dosage intakes.

The compounds are used systemically, at a concentration generally of between 0. 001% and 10% by weight and preferably between 0. 01% and 1% by weight, relative to the weight of the composition.

Via the topical route, the pharmaceutical composition according to the invention is more particularly intended for treating the skin and mucous membranes and may be in liquid, pasty or solid form, and more particularly in the form of ointments, creams, milks, pomades, powders, impregnated pads, syndets, solutions, gels, sprays, mousses, suspensions, sticks, shampoos or washing bases. It may also be in the form of suspensions of microspheres or nanospheres or of lipid or polymer vesicles or gelled or polymer patches allowing a controlled release.

The compounds are used topically at a concentration generally of between 0. 001% and 10% by weight and preferably between 0. 01% and 1% by weight, relative to the total weight of the composition.

The compounds of formula (I) according to the invention also find an application in cosmetics, in particular in body and hair hygiene and especially for treating acne-prone skin, for promoting regrowth of the hair or for limiting hair loss, for combating the greasy appearance of the skin or the hair, in protection against the harmful aspects of sunlight or in the treatment of physiologically dry skin, and for preventing and/or combating photoinduced or chronological ageing.

A subject of the invention is thus also a composition comprising, in a cosmetically acceptable support, at least one of the compounds of formula (I).

A subject of the invention is also the cosmetic use of a composition comprising at least one compound of formula (I) for preventing and/or treating the signs of ageing and/or dry skin.

A subject of the invention is also the cosmetic use of a composition comprising at least one compound of formula (I) for body or hair hygiene.

The cosmetic composition according to the invention containing, in a cosmetically acceptable support, at least one compound of formula (I) or an optical or geometrical isomer thereof or a salt thereof, may be especially in the form of a cream, a milk, a gel, suspensions of microspheres or nanospheres or lipid or polymer vesicles, impregnated pads, solutions, sprays, mousses, sticks, soaps, washing

bases or shampoos.

The concentration of compound of formula (I) in the cosmetic composition is preferably between 0. 001% and 3% by weight, relative to the total weight of the composition.

The term"physiologically acceptable medium" means a medium that is compatible with the skin and optionally with its integuments (eyelashes, nails or hair) and/or mucous membranes.

The pharmaceutical and cosmetic compositions as described above may also contain inert additives, or even pharmacodynamically active additives as regards the pharmaceutical compositions, or combinations of these additives, and especially: - wetting agents; - flavour enhancers ; - preserving agents such as para-hydroxybenzoic acid esters; - stabilizers ; - moisture regulators ; - pH regulators ; - osmotic pressure modifiers; - emulsifiers ; - UV-A and UV-B screening agents; - antioxidants such as a-tocopherol, butylhydroxyanisole, butylhydroxytoluene, superoxide dismutase, ubiquinol or certain metal-chelating agents ; - depigmenting agents such as hydroquinone, azelaic

acid, caffeic acid or kojic acid; - emollients ; - moisturizers, for instance glycerol, PEG 400, thiamorpholinone and its derivatives or urea; - antiseborrhoeic or anti-acne agents, such as S-carboxymethylcysteine, S-benzylcysteamine, salts thereof or derivatives thereof, or benzoyl peroxide; - antibiotics, for instance erythromycin and its esters, neomycin, clindamycin and its esters, and tetracyclines; - antifungal agents such as ketoconazole or poly-4,5- methylene-3-isothiazolidones ; - agents for promoting regrowth of the hair, for instance Minoxidil (2,4-diamino-6-piperidinopyrimidine 3-oxide) and its derivatives, Diazoxide (7-chloro-3- methyl-1, 2,4-benzothiadiazine 1,1-dioxide) and Phenytoin (5,4-diphenylimidazolidine-2, 4-dione) ; - non-steroidal anti-inflammatory agents; - carotenoids and especially p-carotene ; - anti-psoriatic agents such as anthralin and its derivatives; - eicosa-5, 8, 11, 14-tetraynoic acid and eicosa-5,8, 11- triynoic acid, and esters and amides thereof ; - retinoids, i. e. natural or synthetic RXR receptor ligands; - corticosteroids or oestrogens ; - a-hydroxy acids and a-keto acids or derivatives thereof, such as lactic acid, malic acid, citric acid,

glycolic acid, mandelic acid, tartaric acid, glyceric acid or ascorbic acid, and also salts, amides or esters thereof, or a-hydroxy acids or derivatives thereof, such as salicylic acid and its salts, amides or esters; - ion-channel blockers such as potassium-channel blockers ; -or alternatively, more particularly for pharmaceutical compositions, in combination with medicinal products known to interfere with the immune system (for example cyclosporin, FK 506, glucocorticoids, monoclonal antibodies, cytokines or growth factors, etc.).

Needless to say, a person skilled in the art will take care to select the optional'compound (s) to be added to these compositions such that the advantageous properties intrinsically attached to the present invention are not, or are not substantially, adversely affected by the envisaged addition.

Another subject of the invention relates to a cosmetic process for enhancing the appearance of the skin, characterized in that a composition comprising at least one compound of formula (I) as defined above is applied to the skin.

Activation of the retinoic acid receptors with the compounds of formula (I) according to the invention makes it possible to obtain skin of enhanced surface appearance.

Several examples of the production of active

compounds of formula (I) according to the invention, biological activity results and also various concrete formulations based on such compounds, will now be given, for illustrative purposes and with no limiting nature.

Example 1: Synthesis of compound 1: <BR> <BR> 4'-(4-Isopropylaminobutoxy)-3'-(5, 5, 8, 8-tetramethyl-<BR> <BR> 5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl-4-carboxylic acid a. 2,2, 2-Trifluoro-N-isopropylacetamide 15 g (260 mmol) of isopropylamine are dissolved in 450 ml of anhydrous THF under an inert atmosphere. 21 ml (260 mmol) of pyridine and 50 mg (cat) of dimethylaminopyridine are added. 40 ml (280 mmol) of trifluoroacetic anhydride are then slowly added dropwise to the reaction medium. The solution is stirred for 15 hours at room temperature and then poured into 500 ml of water and extracted with ethyl acetate. The organic phase is washed with water, dried and concentrated under reduced pressure. A thick oil is obtained, which crystallizes in the form of pink crystals (m = 40.5 g, yield = 100%). b. N- (4-Bromobutyl)-2, 2,2-trifluoro-N- isopropylacetamide 21 g (520 mmol) of 60% sodium hydride are suspended in 700 ml of anhydrous DMF under an inert atmosphere, and the mixture is cooled to 0°C. 40.5 g (260 mmol) of 2,2, 2-trifluoro-N-isopropylacetamide are

slowly added portionwise. After 15 minutes, 62 ml (520 mmol) of 1,4-dibromobutane are added. The reaction medium is then heated at 60°C for 3 hours, and then cooled to room temperature, poured into 1 L of water and extracted with ethyl acetate. The organic phase is washed with water and dried, and the residue obtained is purified by distillation. A colourless oil is obtained (m = 18 g, yield = 24%). c. Ethyl 4'- {4- [isopropyl- (2, 2,2-trifluoro- acetyl) amino] butoxy}-3'- (5, 5,8, 8-tetramethyl-5, 6,7, 8- tetrahydronaphth-2-yl) biphenyl-4-carboxylate 1.6 g (39 mmol) of 60% sodium hydride are suspended in 200 ml of anhydrous DMF under an inert atmosphere, and the mixture is cooled to 0°C. 13.9 g (32 mmol) of ethyl 4'-hydroxy-3'- (5, 5,8, 8-tetramethyl- 5,6, 7,8-tetrahydronaphth-2-yl) biphenyl-4-carboxylate dissolved in 20 ml of DMF are added slowly. After 20 minutes, 11.3 g (39 mmol) of N- (4-bromobutyl)-2, 2,2- trifluoro-N-isopropylacetamide are added. The reaction medium is then heated at 60°C for 3 hours, and then cooled to room temperature and poured into 500 ml of saturated ammonium chloride solution and extracted with ethyl acetate. The organic phase is washed with water and dried, and the residue obtained is purified by chromatography on a column of silica (eluent: 9/1 heptane/ethyl acetate). A pasty white oil is obtained (m = 21.2 g, yield = 100%). d. 4- (4-Isopropylaminobutoxy)-3'- (5, 5,8, 8-

tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid 1 g (1.5 mmol) of ethyl 4'- {4- [isopropyl- (2,2, 2-trifluoroacetyl) amino] butoxy}-3'- (5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate is dissolved in 20 ml of THF. 5 ml of 1N sodium hydroxide solution are added and the reaction medium is refluxed for 5 hours, and then treated with ammonium chloride solution and extracted with ethyl acetate. The residue obtained is triturated from a heptane/isopropyl ether mixture. A white solid is obtained, m. p. = 235°C (m = 520 mg, yield = 60%).

H NMR/DMSO D6: 1. 16 (d, J = 6. 5 Hz, 6H) ; 1.29 (m, 12H) ; 1.68 (m, 4H); 1.72 (m, 2H); 1.81 (m, 2H); 2.87 (m, 2H); 3.19 (m, 1H); 4.11 (m, 2H); 7.23 (d, J = 8.7 Hz, 1H); 7.35 (m, 2H); 7.57 (d, J = 1. 25, 1H) ; 7.32 (d, J = 2.4 Hz, 1H); 7.69 (dd, J1 = 2. 4 Hz, J2 = 8.7 Hz, 1H); 7.81 (d, J = 8. 4 Hz, 2H) ; 7.98 (d, J = 8.4 Hz, 2H); 8.25 (bs, 1H) ; 12.8 (bs, 1H).

Example 2: Synthesis of compound 12: 4'- (5-Isopropylaminoethoxy)-3'- (5, 5, 8, 8-tetramethyl- 5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylic acid a) 4'- (5-Isopropylaminoethoxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid In a manner similar to that of Example 2a, by

reaction of 200 mg (5 mmol) of sodium hydroxide with 250 mg (0.48 mmol) of ethyl 4'- (3-isopropylamino- ethoxy)-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydro- naphth-2-yl) biphenyl-4-carboxylate (Example 23a) in 30 ml of tetrahydrofuran. 180 g of 4'- (3-isopropyl- aminoethoxy)-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetra- hydronaphth-2-yl) biphenyl-4-carboxylic acid are obtained in the form of a white solid (m. p. = 255°C, yield = 76%).

Example 3: Synthesis of compound 13: <BR> <BR> <BR> <BR> 4'- (3-Isopropylaminopropoxy)-3'- (5, 5, 8, 8-tetramethyl- 5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylic acid a) 4'- (3-Isopropylaminopropoxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid 150 mg (3.6 mmol) of sodium hydroxide are added to a solution of 190 mg (0.36 mmol) of ethyl 4'- (3-isopropylaminopropoxy)-3'- (5, 5,8, 8-tetramethyl- 5,6, 7,8-tetrahydronaphth-2-yl) biphenyl-4-carboxylate (obtained in Example lc) in 20 ml of tetrahydrofuran.

The reaction mixture is stirred for one day at room temperature and then overnight at reflux. The reaction is stopped by adding water and 1N hydrochloric acid to pH 5, and then extracted with ethyl acetate. The organic phases are combined and dried over sodium sulfate. The solvents are evaporated off and the

residue is then purified by chromatography on silica gel (eluent: 80/20 ethyl acetate/methanol). 60 mg of 4'- (3-isopropylaminopropoxy)-3'- (5, 5,8, 8-tetramethyl- 5,6, 7, 8-tetrahydronaphth-2-yl) biphenyl-4,4, 4,4- carboxylic acid are obtained in the form of a white solid (m. p. = 233°C, yield = 33%).

Example 4: Synthesis of compound 15: 4'-(5-Ethylaminopentyloxy)-3'-(5,5,8,8-tetramethyl- 5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylic acid a) 4'- (5-Ethylaminopentyloxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid In a manner similar to that of Example 2a, by reaction of 250 mg (6.25 mmol) of sodium hydroxide with 340 mg (0.63 mmol) of ethyl 4'- (3-ethylaminopentyloxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate (Example 21b) in 30 ml of tetrahydrofuran. 290 mg of 4'- (3-ethylaminopentyloxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylic acid are obtained in the form of a white solid (m. p. = 195°C, yield = 90%).

Example 5: Synthesis of compound 49: Ethyl 4'-(3-isopropylaminopropoxy)-3'-(5,5,8,8-tetra- methyl-5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate

a) Ethyl 4'- (3-bromopropoxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate 320 jul (3.14 mmol) of 1,3-dibromopropane and 440 mg (3.18 mmol) of potassium carbonate are added to a solution of 900 mg (2.1 mmol, 1 eq) of ethyl 4'-hydroxy-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydro- naphth-2-yl) biphenyl-4-carboxylate in 30 ml of methyl ethyl ketone. The reaction mixture is stirred overnight at room temperature and then for 1 day at reflux. The medium is cooled to room temperature and then filtered.

The filtrate is evaporated and the residue is purified by chromatography on silica gel (eluent: 90/10 heptane/ ethyl acetate). 640 mg of ethyl 4'- (3-bromopropoxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate are obtained in the form of a white solid (yield = 55%). b) Ethyl 4'- (3-iodopropoxy)-3'- (5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate 260 mg (1.73 mmol) of sodium iodide are added to a solution of 640 mg (1.16 mmol) of ethyl 4'- (3-bromopropoxy)-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8- tetrahydronaphth-2-yl) biphenyl-4-carboxylate in 40 ml of acetone. The reaction mixture is stirred overnight at room temperature. The precipitate formed is filtered off and the filtrate is evaporated. 608 mg of ethyl 4'- (3-iodopropoxy)-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-

tetrahydronaphth-2-yl) biphenyl-4-carboxylate are obtained in the form of a white solid (m. p. = 118°C, yield = 71%). c) Ethyl 4'- (3-isopropylaminopropoxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate 430 jul (5 mmol) of isopropylamine and 420 mg (3 mmol) of potassium carbonate are added to a solution of 600 mg (1 mmol) of ethyl 4'- (3-iodopropoxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate in 50 ml of acetonitrile. The reaction mixture is stirred at reflux overnight. The reaction is stopped by adding water and is then extracted with ethyl acetate. The organic phases are combined and dried over sodium sulfate. The solvents are evaporated off and the residue is then purified by chromatography on silica gel (50/50 heptane/ethyl acetate). 160 mg of ethyl 4'- (3-isopropylaminopropoxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate are obtained in the form of a yellowish solid (m. p. = 171°C, yield = 30%).

Example 6: Synthesis of compound 50: Ethyl 4'-(3-cyclopropylaminopropoxy)-3'-(5,5,8,8-tetra- methyl-5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate a) Ethyl 4'- (3-cyclopropylaminopropoxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)-

biphenyl-4-carboxylate In a manner similar to that of Example lc, by reaction of 1.7 ml (24.5 mmol) of cyclopropylamine with 670 mg (1.12 mmol) of ethyl 41- (3-iodopropoxy)- 3'- (5, 5, 8, 8-tetramethyl-5, 6,7, 8-tetrahydronaphth-2-yl) - biphenyl-4-carboxylate (obtained in Example lb) in 50 ml of ethanol. 350 mg of ethyl 4'- (3-cyclopropyl- aminopropoxy)-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8- tetrahydronaphth-2-yl) biphenyl-4-carboxylate are obtained in the form of a white solid (m. p. = 141°C, yield = 59%).

Example 7: Synthesis of compound 51: 4'-(3-Cyclopropylaminopropoxy)-3'-(5,5,8,8-tetramethyl- 5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl-4-carboxylic acid a) 4'- (3-Cyclopropylaminopropoxy)-3'- (5, 5,8, 8- tetramethyl-5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid In a manner similar to that of Example 2a, by reaction of 260 mg (6.5 mmol) of sodium hydroxide with 340 mg (0.65 mmol) of ethyl 4'- (3-cyclopropylamino- propoxy)-3'- (5, 5, 8, 8-tetramethyl-5,6, 7,8-tetrahydro- naphth-2-yl) biphenyl-4-carboxylate (Example 3a) in 30 ml of tetrahydrofuran. 160 mg of 4'- (3-cyclopropyl- aminopropoxy)-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetra- hydronaphth-2-yl) biphenyl-4-carboxylic acid are obtained in the form of a white solid (m. p. = 192°C,

yield = 50%).

Example 8: Synthesis of compound 52: Ethyl 4'-(3-butylaminopropoxy)-3'-(5,5,8,8-tetramethyl- 5, 6, 7, 8-tetrahydronaphth-2-ylJbiphenyl-4-carboxylate a) Ethyl 4'- (3-butylaminopropoxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7, 8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate In a manner similar to that of Example lc, by reaction of 1.9 ml (19. 3 mmol) of n-butylamine and 750 mg (1.29 mmol) of ethyl 4'- (3-iodopropoxy)- 3'- (5, 5,8, 8-tetramethyl-5, 6, 7, 8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate (obtained in Example lb) in 50 ml of ethanol. 380 mg of ethyl 4'- (3-butylamino- propoxy)-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydro- naphth-2-yl) biphenyl-4-carboxylate are obtained in the form of a white solid (m. p. = 174°C, yield = 59%).

Example 9: Synthesis of compound 53: 4'-(3-Butylaminopropoxy)-3'-(5,5,8,8-tetrametyl- 5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl-4-carboxylic acid a) 4'- (3-Butylaminopropoxy)-3'- (5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid In a manner similar to that of Example 2a, by reaction of 410 mg (10 mmol) of sodium hydroxide with 360 mg (0.7 mmol) of ethyl 4'- (3-butylaminopropoxy)-

3'- (5, 5,8, 8-tetramethyl-5, 6, 7, 8-tetrahydronaphth-2-yl) - biphenyl-4-carboxylate (Example 5a) in 30 ml of tetrahydrofuran. 70 mg of 4'- (3-butylaminopropoxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylic acid are obtained in the form of a white solid (m. p. = 238°C, yield = 20%).

Example 10: Synthesis of compound 54: Ethyl 4'- (3-dimethylaminopropoxy)-3'- (5, 5, 8, 8-tetra- methyl-5, 6, 7, 8-tetraXydronaphth-2-yl) biphenyl- 4-carboxylate a) Ethyl 4'- (3-dimethylaminopropoxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7, 8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate 440 mg (2.78 mmol) of 3-dimethylaminopropyl chloride hydrochloride and 970 mg (7 mmol) of potassium carbonate are added to a solution of 1 g (2.33 mmol) of ethyl 4'-hydroxy-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetra- hydronaphth-2-yl) biphenyl-4-carboxylate in 50 ml of acetone. The reaction mixture is stirred for 48 hours at reflux. The reaction is stopped by adding water, and is then extracted with ethyl acetate. The organic phases are combined and dried over sodium sulfate. The solvents are evaporated off and the residue is then purified by chromatography on silica gel (eluent: 90/10 ethyl acetate/methanol). 980 mg of ethyl 4'- (3-dimethyl- aminopropoxy)-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetra- hydronaphth-2-yl) biphenyl-4-carboxylate are obtained in

the form of a yellow oil (yield = 82%).

1H NMR (CDC13,400 MHz) : 1. 30 (s, 12H); 1.44 (t, J = 7.1, 3H) ; 1.75 (s, 4H); 1.96 (m, 2H) ; 2.22 (s, 6H); 2.40 (t, J = 7 Hz, 2H) ; 4.10 (t, J = 7.2 Hz, 2H); 4.42 (q, J = 7.2 Hz, 2H); 7.09 (d, J = 8.5 Hz, 1H) ; 7.36-7. 38 (m, 2H); 7.55-7. 58 (m, 2H); 7.63-7. 69 (m, 2H); 8.10-8. 12 (m, 2H).

Example 11: Synthesis of compound 55: 4'-(3-Dimethylaminopropoxy)-3'-(5,5,8,8-tetramethyl- 5, 6,7, 8-tetrahydronaphth-2-yl) biphenyl-4-carboxylic acid a) 4'- (3-Dimethylaminopropoxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid In a manner similar to that of Example 2a, by reaction of 1.12 g (28 mmol) of sodium hydroxide with 960 mg (1.87 mmol) of ethyl 4'- (3-dimethylamino- propoxy)-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydro- naphth-2-yl) biphenyl-4-carboxylate (Example 7a) in 30 ml of tetrahydrofuran. 820 mg of 4'- (3-dimethyl- aminopropoxy)-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetra- hydronaphth-2-yl) biphenyl-4-carboxylic acid are obtained in the form of a white solid (m. p. = 199°C, yield = 90%).

Example 12: Synthesis of compound 56: Ethyl 4'- (3-propylaminopropoxy)-3- (5, 5, 8, 8-

tetramethyl-5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate a) Ethyl 4'- (3-propylaminopropoxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate In a manner similar to that of Example lc, by reaction of 1.3 ml (15.8 mmol) of n-propylamine and 960 mg (1.6 mmol) of ethyl 4'- (3-iodopropoxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate (obtained in Example lb) in 50 ml of ethanol. 790 mg of ethyl 4'- (3-propylamino- propoxy)-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8- tetrahydronaphth-2-yl) biphenyl-4-carboxylate are obtained in the form of a white solid (m. p. = 120°C, yield = 56%).

Example 13: Synthesis of compound 57: <BR> 4'- (3-propylaminopropoxy)-3l'- (5, 5, 8, 8-tetramethyl<BR> 5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl-4-carboxylic acid a) 4'- (3-Propylaminopropoxy)-3'- (5, 5,8, 8- tetramethyl-5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid In a manner similar to that of Example 2a, by reaction of 584 mg (14.6 mmol) of sodium hydroxide with 770 mg (1.46 mmol) of ethyl 4'- (3-propylaminopropoxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate (Example 9a) in 30 ml of

tetrahydrofuran. 470 mg of 4'- (3-propylaminopropoxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylic acid are obtained in the form of a white solid (m. p. = 226°C, yield = 64%).

Example 14: Synthesis of compound 58: Ethyl 4'- (4-cyclopropylaminobutoxy)-3'-(5,5,8,8-tetra- methyl-5, 6, 7, -tetrahydronapAth-2-yl) biphenyl- 4-carboxylate a) Ethyl 4'- (4-Chlorobutoxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7, 8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate 10 g (23 mmol) of ethyl 4'-hydroxy-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate are dissolved in 400 ml of tetrahydro- furan. 9.2 g (35 mmol) of triphenylphosphine and 6.9 ml (35 mmol) of diisopropyl azodicarboxylate are added and the reaction medium is stirred at room temperature for 30 minutes. 2.8 ml (28 mmol) of 4-chlorobutanol are then added, and the medium is kept stirring for 12 hours, and then poured into 500 ml of water and extracted with ethyl acetate. The residue obtained is purified by chromatography on silica gel (eluent: 80/20 heptane/ethyl acetate). 8.9 g of ethyl 4'- (4-chloro- butoxy)-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydro- naphth-2-yl) biphenyl-4-carboxylate are obtained in the form of a colourless oil (yield = 73%). b) Ethyl 4'- (2-cyclopropylaminobutoxy)-

3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate In a manner similar to that of Example lc, by reaction of 700 mg (1.3 mmol) of ethyl 4'- (4-chloro- butoxy)-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydro- naphth-2-yl) biphenyl-4-carboxylate with 800 pl (11.5 mmol) of cyclopropylamine in 100 ml of ethanol.

180 mg of ethyl 4'-(2-cyclopropylaminobutoxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate are obtained in the form of a yellow oil (yield = 26%).

1H NMR (CDC13, 400 MHz): 0.31-0. 33 (m, 2H); 0.41-0. 44 (m, 2H); 1.42 (s, 12H) ; 1.43 (t, J = 7.4 Hz, 3H) ; 1.60-1. 64 (m, 2H); 1.75 (s, 4H) ; 1.82-1. 86 (m, 2H); 2.07-2. 10 (m, 1H); 2.72 (t, J = 7.1 Hz, 2H); 4.06 (t, J = 7.2 Hz, 2H); 4.42 (q, J = 7.5 Hz, 2H) ; 7.07 (d, J = 8.5 Hz, 1H) ; 7.28-7. 39 (m, 2H); 7.55-7. 60 (m, 2H); 7.64-7. 69 (m, 3H); 8.10-8. 12 (m, 2H).

Example 15: Synthesis of compound 59: <BR> <BR> <BR> <BR> 4'- (4-Cyclopropylaminobutoxy)-3'- (5, 5, 8, 8-tetramethyl-<BR> <BR> <BR> <BR> <BR> 5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl-4-carboxylic acid In a manner similar to that of Example 2a, by reaction of 130 mg (3 mmol) of sodium hydroxide with 180 mg (0.3 mmol) of ethyl 4'- (4-cyclopropylamino- butoxy)-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydro- naphth-2-yl) biphenyl-4-carboxylate (Example 11) in

30 ml of tetrahydrofuran. 95 mg of 4'- (4-cyclopropyl- aminobutoxy)-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetra- hydronaphth-2-yl) biphenyl-4-carboxylic acid are obtained in the form of a white solid (m. p. = 160°C, yield = 62%).

Example 16: Synthesis of compound 60: Ethyl 4'-(3-methylaminopropoxy)-3'-(5, 5, 8, 8-tetramethyl- 5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl-4-carboxylate a) Ethyl 4'- (3-methylaminopropoxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate In a manner similar to that of Example 1c, by reaction of 905 mg (13.4 mmol) of methylamine hydro- chloride, 1.85 g (13.4 mmol) of potassium carbonate and 800 mg (1.34 mmol) of ethyl 4'-(3-iodopropoxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate (obtained in Example lb) in 50 ml of ethanol. 511 mg of ethyl 4'- (3-methylamino- propoxy)-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydro- naphth-2-yl) biphenyl-4-carboxylate are obtained in the form of a white solid (m. p. = 141°C, yield = 76%).

Example 17: Synthesis of compound 61: 4'-(3-Methylaminopropoxy)-3'-(5,5,8,8-tetramethyl- 5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl-4-carboxylic acid a) 4'- (3-Methylaminopropoxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl-

4-carboxylic acid In a manner similar to that of Example 2a, by reaction of 400 mg (10 mmol) of sodium hydroxide with 500 mg (1 mmol) of ethyl 4'- (3-methylaminopropoxy)- 3'- (5, 5,8, 8-tetramethyl-5, 6,7, 8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate (Example 13a) in 30 ml of tetra- hydrofuran. 310 mg of 4'- (3-methylaminopropoxy)- 3'- (5, 5,8, 8-tetramethyl-5, 6,7, 8-tetrahydronaphth-2-yl) - biphenyl-4-carboxylic acid are obtained in the form of a white solid (m. p. = 242°C, yield = 66%).

Example 18: Synthesis of compound 62: Ethyl 4'-(3-ethylaminopropoxy)-3'-(5,5,8,8-tetramethyl- 5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl-4-carboxylate In a manner similar to that of Example lc, by reaction of 1.1 g (13.4 mmol) of ethylamine hydro- chloride, 1.85 g (13.4 mmol) of potassium carbonate and 800 mg (1.34 mmol) of ethyl 4'- (3-iodopropoxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate (obtained in Example lb) in 50 ml of ethanol. 511 mg of ethyl 4'- (3-ethylamino- propoxy)-3'- (5, 5,8, 8-tetramethyl-5,6, 7, 8-tetrahydro- naphth-2-yl) biphenyl-4-carboxylate are obtained in the form of a white solid (m. p. = 148°C, yield = 74%).

Example 19: Synthesis of compound 63: 4'-(3-Ethylaminopropoxy)-3'-(5,5,8,8-tetramethyl- 5, 6, 7, 8-tetrahydronaphth-2-l) biphenyl-4-carboxylic

acid a) 4'- (3-Ethylaminopropoxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid In a manner similar to that of Example 2a, by reaction of 380 mg (9.5 mmol) of sodium hydroxide with 490 mg (0.95 mmol) of ethyl 4'- (3-ethylaminopropoxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7, 8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate (Example 15a) in 30 ml of tetrahydrofuran. 395 mg of 4'- (3-ethylaminopropoxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylic acid are obtained in the form of a white solid (m. p. = 233°C, yield = 85%).

Example 20: Synthesis of compound 64: Ethyl 4'-(3-aminopropoxy)-3'-(5,5,8,8-tetramethyl- 5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl-4-carboxylate a) Ethyl 4'- [3- (1, 3-dioxo-1, 3-dihydroisoindol- 2-yl) propoxy]-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetra- hydronaphth-2-yl) biphenyl-4-carboxylate 600 mg (2.24 mmol) of N- (3-bromopropyl)- phthalimide and 310 mg (2.24 mmol) of potassium carbonate are added to a solution of 800 mg (1.86 mmol) of ethyl 4'-hydroxy-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8- tetrahydronaphth-2-yl) biphenyl-4-carboxylate in 50 ml of acetone. The reaction mixture is stirred overnight at reflux. The reaction is stopped by adding water, and is then extracted with ethyl acetate. The organic

phases are combined and dried over sodium sulfate. The solvents are evaporated off. The residue is precipitated from a small amount of ethyl acetate. It is filtered off and 700 mg of ethyl 4'- [3- (1, 3-dioxo- 1, 3-dihydroisoindol-2-yl) propoxy]-3'- (5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate are obtained in the form of a white solid (yield = 61%). b) Ethyl 4'- (3-aminopropoxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate 100 pl of hydrazine monohydrate (2.05 mmol) are added to a solution of 650 mg (1 mmol) of ethyl 4'- [3- (1, 3-dioxo-1, 3-dihydroisoindol-2-yl) propoxy]- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate in 50 ml of ethanol. The reaction mixture is stirred overnight at reflux. The reaction is stopped by adding water and hydrochloric acid to pH 4, and then extracted with ethyl acetate.

The organic phases are combined and dried over sodium sulfate. The solvents are evaporated off. The residue is purified by chromatography on silica gel (eluent: 70/30 ethyl acetate/methanol). 180 mg of ethyl 4'- (3-aminopropoxy)-3'- (5, 5, 8, 8-tetramethyl-5, 6,7, 8- tetrahydronaphth-2-yl) biphenyl-4-carboxylate are obtained in the form of a whitish solid (m. p. = 155°C, yield = 35%).

Example 21: Synthesis of compound 65: 4'-(3-Aminopropoxy)-3'-(5,5,8,8-tetramethyl-5,6,7,8- tetrahydronaphth-2-yl) biphenyl-4-carboxylic acid a) 4'- (3-Aminopropoxy)-3'- (5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid In a manner similar to that of Example 2a, by reaction of 140 mg (3.5 mmol) of sodium hydroxide with 170 mg (0.35 mmol) of ethyl 4'- (3-aminopropoxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate (Example 17b) in 30 ml of tetra- hydrofuran. 95 mg of 4'- (3-aminopropoxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid are obtained in the form of a white solid (m. p. = 243°C, yield = 49%).

Example 22: Synthesis of compound 66: Ethyl 4'-(2-cyclopropylaminoethoxy)-3'-(5,5,8,8-tetra- methyl-5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate a) Ethyl 4'- (2-bromoethoxy)-3'- (5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate In a manner similar to that of Example la, by reaction of 6 g (14 mmol) of ethyl 4'-hydroxy- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate with 4 ml (46.2 mmol) of 1, 2-dibromoethane. 2.12 g of ethyl 4'-(2-bromoethoxy)-

3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate are obtained in the form of a white solid (yield = 28%). b) Ethyl 4'- (2-cyclopropylaminoethoxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7, 8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate In a manner similar to that of Example lc, by reaction of 600 mg (1.15 mmol) of ethyl 4'- (2-bromo- ethoxy)-3'- (5, 5,8, 8-tetramethyl-5, 6,7, 8-tetrahydro- naphth-2-yl) biphenyl-4-carboxylate with 800 µl (11.5 mmol) of cyclopropylamine in 100 ml of ethanol.

360 mg of ethyl 4'- (2-cyclopropylaminoethoxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate are obtained in the form of a white solid (m. p. = 141°C, yield = 63%).

Example 23: Synthesis of compound 67: 4'-(2-Cyclopropylaminoethoxy)-3'-(5,5,8,8-tetramethyl- 5, 6, 7, 8-tetrahydronaphth-2-y1) biphenyl-4-carboxylic acid a) 4'- (2-Cyclopropylaminoethoxy)-3'- (5, 5,8, 8- tetramethyl-5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid In a manner similar to that of Example 2a, by reaction of 270 mg (6.75 mmol) of sodium hydroxide with 340 mg (0.66 mmol) of ethyl 4'- (3-cyclopropylamino- ethoxy)-3'- (5, 5,8, 8-tetramethyl-5, 6,7, 8-tetrahydro- naphth-2-yl) biphenyl-4-carboxylate (Example 19b) in

30 ml of tetrahydrofuran. 240 mg of 4'- (3-cyclopropyl- aminoethoxy)-3'- (5, 5,8, 8-tetramethyl-5,6, 7, 8-tetra- hydronaphth-2-yl) biphenyl-4-carboxylic acid are obtained in the form of a white solid (m. p. = 233°C, yield = 75%).

Example 24: Synthesis of compound 68: Ethyl 4'-(5-cyclopropylaminopentyloxy)-3'-(5,5,8,8- tetramethyl-5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate a) Ethyl 4'- (5-bromopentyloxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate In a manner similar to that of Example la, by reaction of 5 g (11.6 mmol) of ethyl 4'-hydroxy- 3"- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate with 5.2 ml (38.5 mmol) of 1,5-dibromopentane. 4.7 g of ethyl 4'- (5-bromopentyl- oxy)-3'- (5, 5,8, 8-tetramethyl-5, 6,7, 8-tetrahydronaphth- 2-yl) biphenyl-4-carboxylate are obtained in the form of a white solid (yield = 70%). b) Ethyl 4'- (5-cyclopropylaminopentyloxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate In a manner similar to that of Example lb, by reaction of 600 mg (1 mmol) of ethyl 4'- (5-bromopentyl- oxy)-3'-(5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth- 2-yl) biphenyl-4-carboxylate with 720 pl (11.5 mmol) of

cyclopropylamine in 50 ml of ethanol. 420 mg of ethyl 4'- (5-cyclopropylaminopentyloxy)-3'- (5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate are obtained in the form of a white paste (yield = 73%).

1H NMR (CDC13, 400 MHz): 0.72-0. 75 (m, 2H) ; 1.02-1. 04 (m, 2H) ; 1.35 (s, 12H) ; 1.43 (t, J = 7.6 Hz, 3H); 1. 50-1. 54 (m, 2H) ; 1. 75 (s, 4H); 1. 80-1. 87 (m, 4H); 2.41-2. 45 (m, 1H) ; 2.93 (t, J = 7.8 Hz, 2H) ; 4.15 (t, J = 7.4 Hz, 2H) ; 4.41 (q, J = 7.6 Hz, 2H) ; 7.05 (d, J = 8.2 Hz, 1H) ; 7.31-7. 39 (m, 2H); 7.51-7. 58 (m, 2H) ; 7.62-7. 67 (m, 3H) ; 8.09-8. 11 (m, 2H).

Example 25: Synthesis of compound 69: 4'-(5-Cyclopropylaminopentyloxy)-3'-65, 5, 8, 8-tetra- methyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl- 4-carboxylic acid a) 4'- (5-Cyclopropylaminopentyloxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylic acid In a manner similar to that of Example 2a, by reaction of 300 mg (7.5 mmol) of sodium hydroxide with 410 mg (0.74 mmol) of ethyl 4'- (3-cyclopropylamino- pentyloxy)-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydro- naphth-2-yl) biphenyl-4-carboxylate (Example 21b) in 30 ml of tetrahydrofuran. 290 mg of 4'- (3-cyclopropyl- aminopentyloxy)-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetra- hydronaphth-2-yl) biphenyl-4-carboxylic acid are

obtained in the form of a white solid (m. p. = 161°C, yield = 75%).

Example 26: Synthesis of compound 70: Ethyl 4'-(2-isopropylaminoethxoy)-3'-(5,5,8,8-tetra- methyl-5, 6,7, 8-tetrahydronaphth-2-yl)bi henyl- 4-carboxylate a) Ethyl 4'- (2-isopropylaminoethoxy)- 31- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate In a manner similar to that of Example lb, by reaction of 420 mg (0.78 mmol) of ethyl 4'- (5-bromo- ethoxy)-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydro- naphth-2-yl) biphenyl-4-carboxylate (Example 19a) with 670 pl (7. 86 mmol) of isopropylamine in 50 ml of ethanol. 250 mg of ethyl 4'- (5-isopropylaminoethoxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate are obtained in the form of a white solid (m. p. = 104°C, yield = 62%).

Example 27: Synthesis of compound 71: Ethyl 4'-(5-ethylaminopentyloxy)-3'-(5,5,8,8-tetra- methyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl- 4-carboxylate a) Ethyl 4'- (5-ethylaminopentyloxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate In a manner similar to that of Example lb, by

reaction of 600 mg (1 mmol) of ethyl 4'- (5-bromopentyl- oxy)-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth- 2-yl) biphenyl-4-carboxylate with 850 mg (10.4 mmol) of ethylamine hydrochloride and 1.44 g (10.4 mmol) of potassium carbonate in 50 ml of ethanol. 350 mg of ethyl 4'- (5-ethylaminopentyloxy)-3'- (5, 5,8, 8-tetramethyl- 5,6, 7,8-tetrahydronaphth-2-yl) biphenyl-4-carboxylate are obtained in the form of a colourless oil (yield = 62%).

1H NMR (CDC13, 400 MHz) : 1.14 (t, J = 7.3 Hz, 3H); 1.35 (s, 12H) ; 1.43 (t, J = 7.6 Hz, 3H); 1.50-1. 56 (m, 4H); 1.75 (s, 4H); 1.79-1. 85 (m, 2H); 2.61-2. 71 (m, 4H); 4.05 (t, J = 7.4 Hz, 2H); 4.42 (q, J = 7.6 Hz, 2H); 7.06 (d, J = 8.2 Hz, 1H) ; 7.33-7. 39 (m, 2H) ; 7.54- 7.68 (m, 5H); 8.09-8. 12 (m, 2H).

Example 28: Synthesis of compound 72: Ethyl 4"- (5-aminopentyloxy)-31- (5, 5, 8, 8-tetramethyl- 5, 6, 7, 8-tetrahydronaphth-2-yl) biphenyl-4-carboxylate a) Ethyl 4'- [5- (1, 3-dioxo-1, 3-dihydroisoindol- 2-yl) pentyloxy]-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetra- hydronaphth-2-yl) biphenyl-4-carboxylate In a manner similar to that of Example 17a, by reaction of 600 mg (1.4 mmol) of ethyl 4'-hydroxy- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate with 500 mg (1.7 mmol) of N- (5-bromopentyl) phthalimide and 230 mg (1.66 mmol) of potassium carbonate in 50 ml of acetone. 770 mg of

ethyl 4'- [5- (1, 3-dioxo-1, 3-dihydroisoindol-2-yl) pentyl- oxy]-3'- (5, 5,8, 8-tetramethyl-5, 6,7, 8-tetrahydronaphth- 2-yl) biphenyl-4-carboxylate are obtained in the form of a beige-coloured solid (yield = 85%). b) Ethyl 4'- (5-aminopentyloxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate In a manner similar to that of Example 17b, by reaction of 760 mg (1.18 mmol) of ethyl 4'- [5- (1, 3-dioxo-1, 3-dihydroisoindol-2-yl) pentyloxy]- 3'-(5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate with 230 jul (4.72 mmol) of hydrazine monohydrate in 50 ml of ethanol. 280 mg of ethyl 4'- (5-aminopentyloxy)-3'- (5, 5,8, 8-tetramethyl- 5,6, 7,8-tetrahydronaphth-2-yl) biphenyl-4-carboxylate are obtained in the form of a whitish solid (yield = 46%).

1H NMR (CDC13, 400 MHz): 1.32 (s, 6H) ; 1.33 (s, 6H) ; 1.43 (t, J = 7.5 Hz, 3H); 1.53-1. 58 (m, 2H) ; 1.73 (s, 4H); 1.77-1. 81 (m, 4H) ; 2.97 (t, J = 7.8 Hz, 2H) ; 4.00 (t, J = 7.4 Hz, 2H); 4.41 (q, J = 7.6 Hz, 2H) ; 7.02 (d, J = 8.2 Hz, 1H) ; 7. 31-7.38 (m, 2H); 7.51- 7.55 (m, 2H) ; 7.61-7. 65 (m, 3H) ; 8.08-8. 11 (m, 2H).

Example 29: Synthesis of compound 73: <BR> <BR> <BR> <BR> <BR> <BR> 4'-(5-Aminopentyloxy)-3'-(5, 5, 8, 8-tetramethyl-5, 6, 7, 8- tetrahydronaphth-2-yl) biphenyl-4-carboxylic acid a) 4'- (5-Aminopentyloxy)-3'- (5, 5,8, 8-tetra-

methyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid In a manner similar to that of Example 2a, by reaction of 210 mg (5.2 mmol) of sodium hydroxide with 270 mg (0.52 mmol) of ethyl 4'- (5-aminopentyloxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate (Example 27b) in 30 ml of tetrahydrofuran. 165 mg of 4'- (3-ethylaminopentyloxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylic acid are obtained in the form of a white solid (m. p.-252°C, yield = 65%).

Example 30 Synthesis of compound 74: Ethyl 4'-(4-aminobutoxy)-3'-(5,5,8,8-tetramethyl- 5, 6, 7, 8-tetraXydronaphth-2-yl) bíphenyl-4-carboxylate a) Ethyl 4'- [4- (1, 3-dioxo-1, 3-dihydroisoindol- 2-yl) butoxy]-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetra- hydronaphth-2-yl) biphenyl-4-carboxylate In a manner similar to that of Example 17a, by reaction of 600 mg (1.4 mmol) of ethyl 4'-hydroxy- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate with 475 mg (1.68 mmol) of N- (4-bromobutoxy) phthalimide and 230 mg (1.66 mmol) of potassium carbonate in 50 ml of acetone. 790 mg of ethyl 4'- [4- (1, 3-dioxo-1, 3-dihydroisoindol-2-yl) butoxy]- 3'- (5, 5,8, 8-tetramethyl-5, 6,7, 8-tetrahydronaphth-2-yl) - biphenyl-4-carboxylate are obtained in the form of a white solid (yield = 90%).

b) Ethyl 4'- (4-aminobutoxy)-3'- (5, 5,8, 8- tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylate In a manner similar to that of Example 17b, by reaction of 750 mg (1.19 mmol) of ethyl 4'- [4- (1, 3-dioxo-1, 3-dihydroisoindol-2-yl) butoxy]- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylate with 230 all (4.72 mmol) of hydrazine monohydrate in 50 ml of ethanol. 300 mg of 4'- (4-aminobutoxy)-3'- (5, 5,8, 8-tetramethyl-5,6, 7,8- tetrahydronaphth-2-yl) biphenyl-4-carboxylate are obtained in the form of a yellow-brown solid (yield = 50%).

1H NMR (CDC13, 400 MHz): 1. 33 (s, 6H) ; 1. 34 (s, 6H); 1.43 (t, J = 7.5 Hz, 3H); 1.73 (s, 4H); 1.73- 1.75 (m, 2H); 1.85-1. 89 (m, 2H) ; 2.84 (t, J = 7. 4 Hz, 2H); 3.30 (bs, 2H); 4.04 (t, J = 7.4 Hz, 2H) ; 4. 41 (q, J = 7.6 Hz, 2H) ; 7.03 (d, J = 8.2 Hz, 1H) ; 7.31-7. 40 (m, 2H); 7.52-7. 55 (m, 2H); 7.61-7. 66 (m, 3H) ; 8.09- 8.11 (m, 2H).

Example 31: Synthesis of compound 75: 4'-(4-Aminobutoxy)-3'-(5,5,8,8-tetramethyl-5,6,7,8- tetrahydronaphth-2-yl) biphenyl-4-carboxylic acia' a) 4'- (4-Aminobutoxy)-3'- (5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydronaphth-2-yl) biphenyl- 4-carboxylic acid In a manner similar to that of Example 2a, by

reaction of 300 mg (0.6 mmol) of ethyl 4'- (4-amino- butoxy)-3'- (5, 5-, 8,8-tetramethyl-5, 6,7, 8-tetrahydro- naphth-2-yl) biphenyl-4-carboxylate with 240 mg (6 mmol) of sodium hydroxide. 245 mg of 4'- (4-aminobutoxy)- 3'- (5, 5,8, 8-tetramethyl-5,6, 7,8-tetrahydronaphth-2-yl)- biphenyl-4-carboxylic acid are obtained in the form of a white solid (m. p. = 250°C, yield = 86%).

EXAMPLE 32: TRANSACTIVATION TEST The activation of receptors with an agonist (activator) in HeLa cells leads to the expression of a reporter gene, luciferase, which, in the presence of a substrate, generates light. The activation of the receptors may thus be measured by quantifying the luminescence produced after incubating the cells in the presence of a reference agonist. The activating products displace the agonist from its site, thus preventing activation of the receptor. The activity is measured by quantifying the decrease in light produced.

This measurement makes it possible to determine the activating activity of the compounds according to the invention.

In this study, a constant is determined which represents the affinity of the molecule for the receptor. Since this value can fluctuate depending on the basal activity and the expression of the receptor, it is referred to as the Kd apparent (KdApp).

To determine this constant, the cells are

brought into contact with a concentration of the test product and a concentration of the reference antagonist, 4- (5, 5-dimethyl-8-p-tolyl-5,6-dihydro- 2-naphthalen-2-ylethynyl) benzoic acid. Measurements are also taken for the total agonist (4- [2- (5, 5,8, 8-tetra- methyl-5,6, 7,8-tetrahydro-2-naphthyl) propenyl] benzoic acid) and inverse agonist, 4- { (E)-3- [4- (4-tert-butyl- phenyl) -5,5, 8,8-tetramethyl-5, 6,7, 8-tetrahydro- 2-naphthyl]-3-oxopropenyl} benzoic acid, controls.

These crossed curves make it possible to determine the AC50 values (concentration at which 50% activation is observed) for the reference ligand at various concentrations of test product. These AC50 values are used to calculate the Schild regression by plotting a straight line corresponding to the Schild equation ("Quantitation in Receptor Pharmacology"Terry P. Kenakin, Receptors and Channels, 2001, 7,371-385).

In the case of an agonist, an AC50 value (concentration that gives 50% of the activity) is calculated by plotting the curve of the product at the concentration of the reference ligand that gives 80% activation.

The HeLa cell lines used are stable transfectants containing the plasmids ERE- (3Glob-Luc-SV- Neo (reporter gene) and RAR (a, P, y) ER-DBD-puro. These cells are inoculated into 96-well plates at a rate of 10 000 cells per well in 100 ul of DMEM medium without phenol red, and supplemented with 10% defatted calf

serum. The plates are then incubated at 37°C and 7% COg for 4 hours.

The various dilutions of the test products, of the reference ligand (4- (5, 5-dimethyl-8-p-tolyl-5,6- dihydro-2-naphthalen-2-ylethynyl) benzoic acid), of the 100% control (100 nM 4- [2- (5, 5,8, 8-tetramethyl-5,6, 7,8- tetrahydro-2-naphthyl) propenylbenzoic acid) and of the 0% control (500 nM 4- { (E)-3- [4- (4-tert-butylphenyl)- 5,5, 8,8-tetramethyl-5, 6, 7,8-tetrahydro-2-naphthyl]-3- oxopropenyl} benzoic acid) are added at a rate of 5 p. l per well. The plates are then incubated for 18 hours at 37°C and 7% CO2.

The culture medium is removed by turning over and 100 pl of a 1: 1 PBS/luciferin mixture is added to each well. After 5 minutes, the plates are read using the luminescence reader. Q compound R alpha RAR beta a KD app (nM) Kd app (nM) Kd app (nM) 1 1000 500 15 59 8000 4000 1000 . 61 9999 9999 30 63 nd nd 250 65 nd nd 8 67 1000 60 4 69 2000 500 250 12 9999 4000 120 73 2000 2000 120 75 8000 2000 60

Nd: not determined The results obtained with the compounds according to the invention clearly show Kd app values < 100 nM for at least one of the receptor subtypes, this clearly demonstrating an increase in the signal, and in the luminescence in the presence of the reference antagonist. The compounds according to the invention are thus clearly activators of retinoic acid receptors (RAR).

EXAMPLE 33: FORMULATION EXAMPLES This example illustrates various concrete formulations based on the compounds according to the invention.

A-ORAL ROUTE (a) 0.2 g tablet - Compound of Example 1 0.001 g - Starch 0.114 g - Dicalcium phosphate 0.020 g - Silica 0.020 g - Lactose 0.030 g - Talc 0.010 g - Magnesium stearate 0.005 g (b) Drinkable suspension in 5 ml ampoules - Compound of Example 1 0.001 g

- Glycerol 0.500 g - 70% sorbitol 0.500 g Sodium saccharinate 0.010 g Methyl para-hydroxybenzoate 0.040 g Flavouring qs Purified water qs 5 ml (c) 0.8 g tablet Compound of Example 1 0.500 g Pregelatinized starch 0.100 g -Microcrystalline cellulose 0.115 g Lactose 0.075 g Magnesium stearate 0.010 g (d) Drinkable suspension in 10 ml ampoules Compound of Example 1 0.200 g - Glycerol 1.000 g - 70% sorbitol 1.000 g -Sodium saccharinate 0.010 g Methyl para-hydroxybenzoate 0. 080 g Flavouring qs Purified water qs 10 ml B-PARENTERAL ROUTE (a) Composition - Compound of Example 1 0.002 g - Ethyl oleate qs 10 g (b) Composition - Compound of Example 1 0. 05% - Polyethylene glycol 20% - 0. 9% Nad solution qs 100

(c) Composition - Compound of Example 1 2. 5% - Polyethylene glycol 400 20% -0. 9% NaCl solution qs 100 (d) Injectable cyclodextrin composition Compound of Example 1 0.1 mg - ß-Cyclodextrin 0.10 g Water for injection qs 10.00 g C-TOPICAL ROUTE (a) Ointment - Compound of Example 1 0.020 g - Isopropyl myristate 81.700 g Liquid petroleum jelly oil 9.100 g -Silica ("Aerosil 200"sold by Degussa) 9.180 g (b) Ointment - Compound of Example 1 0.300 g - White petroleum jelly codex qs 100 g (c) Nonionic water-in-oil cream - Compound of Example 4 0.100 g - Mixture of emulsifying lanolin alcohols, waxes and oils ("Anhydrous Eucerin"sold by BDF) 39.900 g -Methyl para-hydroxybenzoate 0.075 g - Propyl para-hydroxybenzoate 0.075 g - Sterile demineralized water qs 100 g (d) Lotion - Compound of Example 1 0.100 g Polyethylene glycol (PEG 400) 69.900 g 95% ethanol 30.000 g (e) Hydrophobic ointment Compound of Example 1 0.300 g Isopropyl myristate 36.400 g Silicone oil ("Rhodorsil 47 V 300" sold by Rhone-Poulenc) 36.400 g Beeswax 13.600 g - Silicone oil ("Abil 300 000 cst" sold by Goldschmidt) qs 100 g (f) Nonionic oil-in-water cream Compound of Example 1 1.000 g - Cetyl alcohol 4.000 g Glyceryl monostearate 2.500 g PEG 50 stearate 2.500 g - Karite butter 9.200 g Propylene glycol 2.000 g Methyl para-hydroxybenzoate 0.075 g Propyl para-hydroxybenzoate 0.075 g Sterile demineralized water qs 100 g